Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22803 |
| ensemblid | ENSG00000088930.8 |
| hgncid | 12836 |
| symbol | XRN2 |
| name | 5'-3' exoribonuclease 2 |
| refseq_nuc | NM_012255.5 |
| refseq_prot | NP_036387.2 |
| ensembl_nuc | ENST00000377191.5 |
| ensembl_prot | ENSP00000366396.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 21303331 |
| end | 21389825 |
| strand | + |
| ver | v1.2 |
| region | chr20:21303331-21389825 |
| region5000 | chr20:21298331-21394825 |
| regionname0 | XRN2_chr20_21303331_21389825 |
| regionname5000 | XRN2_chr20_21298331_21394825 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 950 | 275 | 84 | 46 | 105 | 14 | 24 | 79 | XRN2_chr20_21298331_21394825 | XRN2 | MGVPA others(945): Show |
chr20 | 21298331 | 21394825 |
| a0002 | 0/0 | 950 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | MGVPA others(945): Show |
chr20 | 21298331 | 21394825 |
| a0003 | 0/0 | 950 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | MGVPA others(945): Show |
chr20 | 21298331 | 21394825 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2850 | 257 | 68 | 44 | 105 | 14 | 24 | XRN2_chr20_21298331_21394825 | XRN2 | ATGGG others(2845): Show |
chr20 | 21298331 | 21394825 | ||
| a0001c0002 | 0/0 | 2850 | 16 | 15 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | ATGGG others(2845): Show |
chr20 | 21298331 | 21394825 | ||
| a0001c0004 | 0/0 | 2850 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | ATGGG others(2845): Show |
chr20 | 21298331 | 21394825 | ||
| a0001c0006 | 0/0 | 2850 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | ATGGG others(2845): Show |
chr20 | 21298331 | 21394825 | ||
| a0002c0003 | 0/0 | 2850 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | ATGGG others(2845): Show |
chr20 | 21298331 | 21394825 | ||
| a0003c0005 | 0/0 | 2850 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | ATGGG others(2845): Show |
chr20 | 21298331 | 21394825 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3410 | 175 | 48 | 32 | 71 | 10 | 13 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| a0001c0001t0002 | 0/0 | 3410 | 62 | 17 | 5 | 31 | 4 | 5 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| a0001c0001t0003 | 1/0 | 3408 | 19 | 3 | 7 | 3 | 0 | 5 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3403): Show |
chr20 | 21298331 | 21394825 |
| a0001c0001t0004 | 0/0 | 3410 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| a0001c0002t0001 | 0/0 | 3410 | 16 | 15 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| a0001c0004t0001 | 0/0 | 3410 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| a0001c0006t0001 | 0/0 | 3410 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| a0002c0003t0001 | 0/0 | 3410 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| a0003c0005t0002 | 0/0 | 3410 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | GCCGC others(3405): Show |
chr20 | 21298331 | 21394825 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0001c0006t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0002c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| a0003c0005t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0173 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00639 | hp1 | a0001 | c0006 | t0001 | g0221 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0161 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0135 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0099 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CDX | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CDX | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0119 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0105 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0097 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ESN | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0085 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0094 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18963 | hp2 | a0003 | c0005 | t0002 | g0143 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | YRI | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ASW | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0120 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | MSL | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | USA | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | USA | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0199 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | LWK | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0264 | REF | REF | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0167 | REF | REF | XRN2_chr20_21298331_21394825 | XRN2 | chr20 | 21298331 | 21394825 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:21356665 | A | G | 1 | a0002 | 2 | HG03209.hp1 NA21309.hp1 |
missense_variant&splice_region_variant | MODERATE | c.2198A>G | p.Gln733Arg | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/30 | 2266/3408 | 2198/2853 | 733/950 | chr20 | 21356665 | |||
| chr20:21386972 | A | G | 1 | a0003 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.2753A>G | p.Tyr918Cys | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/30 | 2821/3408 | 2753/2853 | 918/950 | chr20 | 21386972 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:21331620 | T | C | 1 | a0001c0004 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.636T>C | p.Ile212Ile | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/30 | 704/3408 | 636/2853 | 212/950 | chr20 | 21331620 | |||
| chr20:21333579 | A | G | 1 | a0001c0006 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.894A>G | p.Glu298Glu | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 10/30 | 962/3408 | 894/2853 | 298/950 | chr20 | 21333579 | |||
| chr20:21365603 | C | T | 1 | a0001c0002 | 16 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
synonymous_variant | LOW | c.2355C>T | p.Asp785Asp | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/30 | 2423/3408 | 2355/2853 | 785/950 | chr20 | 21365603 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:21303376 | G | A | 1 | a0001c0001t0004 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/30 | 23 | chr20 | 21303376 | ||||||
| chr20:21389696 | C | CTT | 8 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(5): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*358_*359insTT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 30/30 | 359 | chr20 | 21389696 | ||||||
| chr20:21389808 | G | C | 2 | a0001c0001t0002 a0003c0005t0002 |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*470G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 30/30 | 470 | chr20 | 21389808 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:21303598 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(75): Show |
81 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.75+125T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21303598 | |||||||
| chr20:21303824 | CTGT | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(6): Show |
9 | HG00423.hp1 NA18944.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.75+357_75+359delTT others(1): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21303824 | ||||||
| chr20:21304065 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.75+592C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304065 | |||||||
| chr20:21304127 | G | A | 1 | a0001c0001t0002g0084 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.75+654G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304127 | |||||||
| chr20:21304196 | T | G | 1 | a0001c0001t0001g0018 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.75+723T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304196 | |||||||
| chr20:21304348 | C | CT | 6 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0270 others(3): Show |
6 | HG02622.hp1 HG03669.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+891dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21304348 | ||||||
| chr20:21304348 | CT | C | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(54): Show |
59 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.75+891delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21304348 | ||||||
| chr20:21304453 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+980C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304453 | |||||||
| chr20:21304459 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.75+986T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304459 | |||||||
| chr20:21304620 | T | C | 6 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
6 | HG02809.hp2 HG02886.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+1147T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21304620 | |||||||
| chr20:21305028 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.75+1555T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305028 | |||||||
| chr20:21305249 | A | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+1776A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305249 | |||||||
| chr20:21305335 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.75+1862A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305335 | |||||||
| chr20:21305415 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.75+1942C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305415 | |||||||
| chr20:21305452 | GCCATGTT others(2675): Show |
G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.75+1989_75+4670del | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305452 | ||||||
| chr20:21305483 | G | C | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+2010G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305483 | |||||||
| chr20:21305553 | C | CT | 29 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0201 others(26): Show |
29 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.75+2103dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | ||||||
| chr20:21305553 | C | CTT | 5 | a0001c0001t0001g0200 a0001c0001t0002g0157 a0001c0001t0002g0159 others(2): Show |
5 | HG01361.hp2 HG02965.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2102_75+2103dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | ||||||
| chr20:21305553 | C | CTTTTT | 9 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(6): Show |
9 | HG00741.hp1 HG01256.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+2099_75+2103dup others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | ||||||
| chr20:21305553 | C | CTTTTTT | 5 | a0001c0001t0003g0005 a0001c0001t0003g0116 a0001c0001t0003g0117 others(2): Show |
5 | HG00738.hp2 HG01192.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+2098_75+2103dup others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305553 | ||||||
| chr20:21305614 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.75+2141A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305614 | |||||||
| chr20:21305747 | CT | C | 50 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(47): Show |
52 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.75+2290delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21305747 | ||||||
| chr20:21305795 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.75+2322G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305795 | |||||||
| chr20:21305808 | C | T | 1 | a0001c0001t0003g0005 | 2 | NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.75+2335C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21305808 | |||||||
| chr20:21306134 | G | GT | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+2671dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21306134 | ||||||
| chr20:21306159 | C | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+2686C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306159 | |||||||
| chr20:21306206 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.75+2733G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306206 | |||||||
| chr20:21306241 | G | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+2768G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306241 | |||||||
| chr20:21306893 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.75+3420C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21306893 | |||||||
| chr20:21307071 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.75+3598C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307071 | |||||||
| chr20:21307073 | C | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+3600C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307073 | |||||||
| chr20:21307359 | T | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG00140.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.75+3886T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307359 | |||||||
| chr20:21307462 | A | G | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.75+3989A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21307462 | |||||||
| chr20:21308156 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.75+4683T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308156 | |||||||
| chr20:21308173 | G | A | 5 | a0001c0001t0003g0113 a0001c0001t0003g0114 a0001c0001t0003g0115 others(2): Show |
5 | HG01192.hp2 HG01943.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.75+4700G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308173 | |||||||
| chr20:21308279 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.75+4806G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308279 | |||||||
| chr20:21308345 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.75+4872T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308345 | |||||||
| chr20:21308497 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.75+5024G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308497 | |||||||
| chr20:21308497 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+5024G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308497 | |||||||
| chr20:21308631 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.75+5158A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308631 | |||||||
| chr20:21308641 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
37 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.75+5168A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308641 | |||||||
| chr20:21308674 | G | A | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+5201G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308674 | |||||||
| chr20:21308873 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75+5400A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308873 | |||||||
| chr20:21308924 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.75+5451G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308924 | |||||||
| chr20:21308947 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+5474C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308947 | |||||||
| chr20:21308964 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+5491A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21308964 | |||||||
| chr20:21309152 | T | G | 1 | a0001c0001t0001g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.75+5679T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309152 | |||||||
| chr20:21309223 | A | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.75+5750A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309223 | |||||||
| chr20:21309243 | A | G | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+5770A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309243 | |||||||
| chr20:21309668 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(12): Show |
16 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+6195G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309668 | |||||||
| chr20:21309850 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.75+6377A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309850 | |||||||
| chr20:21309947 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.75+6474A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309947 | |||||||
| chr20:21309964 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
37 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.75+6491C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309964 | |||||||
| chr20:21309996 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.75+6523T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21309996 | |||||||
| chr20:21310263 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.75+6790C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310263 | |||||||
| chr20:21310528 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.75+7055A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310528 | |||||||
| chr20:21310784 | G | A | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+7311G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310784 | |||||||
| chr20:21310831 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.75+7358G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310831 | |||||||
| chr20:21310842 | T | G | 1 | a0001c0001t0001g0207 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.75+7369T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310842 | |||||||
| chr20:21310893 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+7420C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310893 | |||||||
| chr20:21310986 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+7513C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21310986 | |||||||
| chr20:21311003 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.75+7530T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311003 | |||||||
| chr20:21311200 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+7727C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311200 | |||||||
| chr20:21311454 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75+7981G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311454 | |||||||
| chr20:21311590 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+8117G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311590 | |||||||
| chr20:21311606 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | NA18995.hp1 NA19056.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+8133T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311606 | |||||||
| chr20:21311625 | T | C | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75+8152T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311625 | |||||||
| chr20:21311632 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.75+8159A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311632 | |||||||
| chr20:21311721 | C | T | 4 | a0001c0001t0002g0140 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+8248C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21311721 | |||||||
| chr20:21312153 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.75+8680C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312153 | |||||||
| chr20:21312173 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+8700C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312173 | |||||||
| chr20:21312188 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8715C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312188 | |||||||
| chr20:21312191 | C | A | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8718C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312191 | |||||||
| chr20:21312192 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8719A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312192 | |||||||
| chr20:21312195 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8722C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312195 | |||||||
| chr20:21312196 | T | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8723T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312196 | |||||||
| chr20:21312197 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8724C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312197 | |||||||
| chr20:21312198 | T | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8725T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312198 | |||||||
| chr20:21312205 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8732C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312205 | |||||||
| chr20:21312206 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8733A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312206 | |||||||
| chr20:21312235 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8762C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312235 | |||||||
| chr20:21312237 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8764C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312237 | |||||||
| chr20:21312275 | GCTAAGTT others(9): Show |
G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8803_75+8818del others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312275 | |||||||
| chr20:21312293 | T | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8820T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312293 | |||||||
| chr20:21312297 | T | G | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8824T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312297 | |||||||
| chr20:21312299 | T | A | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8826T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312299 | |||||||
| chr20:21312302 | T | A | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8829T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312302 | |||||||
| chr20:21312324 | C | A | 1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8851C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312324 | |||||||
| chr20:21312325 | C | CCGGTTAG others(16): Show |
1 | a0001c0001t0002g0194 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+8852_75+8853ins others(23): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312325 | |||||||
| chr20:21312363 | G | C | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.75+8890G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312363 | |||||||
| chr20:21312391 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+8918G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312391 | |||||||
| chr20:21312441 | T | A | 2 | a0001c0001t0002g0142 a0003c0005t0002g0143 |
2 | NA18963.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.75+8968T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312441 | |||||||
| chr20:21312597 | C | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+9124C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312597 | |||||||
| chr20:21312602 | A | AT | 8 | a0001c0001t0002g0187 a0001c0001t0002g0188 a0001c0001t0002g0189 others(5): Show |
8 | HG00423.hp2 HG00738.hp1 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+9153dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | ||||||
| chr20:21312602 | AT | A | 27 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(24): Show |
28 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.75+9153delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | ||||||
| chr20:21312602 | ATT | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(30): Show |
34 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.75+9152_75+9153del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | ||||||
| chr20:21312602 | ATTTTTTT others(2): Show |
A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
152 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.75+9145_75+9153del others(9): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21312602 | ||||||
| chr20:21312901 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.75+9428C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21312901 | |||||||
| chr20:21313178 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0186 |
2 | NA19058.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.75+9705C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21313178 | |||||||
| chr20:21313246 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+9773C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21313246 | |||||||
| chr20:21313952 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.75+10479C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21313952 | |||||||
| chr20:21314179 | C | A | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.75+10706C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314179 | |||||||
| chr20:21314277 | T | C | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+10804T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314277 | |||||||
| chr20:21314429 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.75+10956G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314429 | |||||||
| chr20:21314588 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.75+11115G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314588 | |||||||
| chr20:21314589 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0185 |
2 | NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.75+11116C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314589 | |||||||
| chr20:21314804 | G | A | 1 | a0001c0001t0003g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.75+11331G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314804 | |||||||
| chr20:21314871 | G | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.75+11398G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314871 | |||||||
| chr20:21314958 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.76-11321C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21314958 | |||||||
| chr20:21315012 | C | G | 1 | a0001c0001t0002g0184 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.76-11267C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315012 | |||||||
| chr20:21315350 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-10929C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315350 | |||||||
| chr20:21315487 | G | A | 1 | a0001c0002t0001g0086 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.76-10792G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315487 | |||||||
| chr20:21315845 | T | C | 1 | a0001c0001t0003g0120 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-10434T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315845 | |||||||
| chr20:21315869 | TC | T | 2 | a0001c0001t0003g0005 a0001c0001t0003g0127 |
3 | HG03654.hp2 NA18941.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.76-10407delC | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21315869 | ||||||
| chr20:21315921 | C | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.76-10358C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315921 | |||||||
| chr20:21315991 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.76-10288G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315991 | |||||||
| chr20:21315993 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.76-10286T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21315993 | |||||||
| chr20:21316001 | G | A | 1 | a0001c0001t0002g0149 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.76-10278G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316001 | |||||||
| chr20:21316022 | G | C | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.76-10257G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316022 | |||||||
| chr20:21316042 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.76-10237C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316042 | |||||||
| chr20:21316186 | G | A | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.76-10093G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316186 | |||||||
| chr20:21316670 | C | A | 1 | a0001c0001t0003g0120 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-9609C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316670 | |||||||
| chr20:21316741 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(16): Show |
20 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.76-9538T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316741 | |||||||
| chr20:21316748 | T | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-9531T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316748 | |||||||
| chr20:21316863 | A | T | 3 | a0001c0001t0002g0183 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.76-9416A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21316863 | |||||||
| chr20:21317031 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.76-9248A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317031 | |||||||
| chr20:21317047 | C | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.76-9232C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317047 | |||||||
| chr20:21317301 | AT | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
158 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.76-8967delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21317301 | ||||||
| chr20:21317340 | C | T | 1 | a0002c0003t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.76-8939C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317340 | |||||||
| chr20:21317496 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.76-8783T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317496 | |||||||
| chr20:21317564 | G | T | 1 | a0001c0002t0001g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.76-8715G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317564 | |||||||
| chr20:21317808 | C | T | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-8471C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21317808 | |||||||
| chr20:21318076 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0002g0183 a0001c0001t0002g0193 others(1): Show |
4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-8203C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318076 | |||||||
| chr20:21318093 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.76-8186T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318093 | |||||||
| chr20:21318094 | G | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.76-8185G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318094 | |||||||
| chr20:21318385 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.76-7894A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318385 | |||||||
| chr20:21318399 | A | G | 2 | a0001c0001t0002g0191 a0001c0001t0002g0192 |
2 | NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.76-7880A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318399 | |||||||
| chr20:21318412 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.76-7867C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318412 | |||||||
| chr20:21318536 | T | TTA | 8 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(5): Show |
8 | HG01934.hp2 HG01943.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-7742_76-7741ins others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21318536 | ||||||
| chr20:21318544 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.76-7735G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318544 | |||||||
| chr20:21318603 | G | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.76-7676G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318603 | |||||||
| chr20:21318716 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.76-7563A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318716 | |||||||
| chr20:21318762 | A | T | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.76-7517A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318762 | |||||||
| chr20:21318861 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.76-7418C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21318861 | |||||||
| chr20:21319024 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-7255T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319024 | |||||||
| chr20:21319241 | C | T | 1 | a0001c0001t0003g0120 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.76-7038C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319241 | |||||||
| chr20:21319302 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-6977C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319302 | |||||||
| chr20:21319392 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.76-6887G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319392 | |||||||
| chr20:21319493 | T | C | 1 | a0001c0001t0003g0121 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.76-6786T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319493 | |||||||
| chr20:21319586 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.76-6693A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319586 | |||||||
| chr20:21319617 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.76-6662C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319617 | |||||||
| chr20:21319751 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.76-6528G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21319751 | |||||||
| chr20:21320029 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-6250T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320029 | |||||||
| chr20:21320066 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-6213C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320066 | |||||||
| chr20:21320137 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-6142T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320137 | |||||||
| chr20:21320264 | CATTTATT others(9): Show |
C | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-5984_76-5969del others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320264 | ||||||
| chr20:21320267 | T | TTATTTAT others(5): Show |
137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
142 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.76-6000_76-5989dup others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320267 | ||||||
| chr20:21320279 | G | GTATT | 14 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(11): Show |
15 | HG00738.hp2 HG01192.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-5988_76-5985dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320279 | ||||||
| chr20:21320279 | G | GTATTTAT others(9): Show |
12 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0043 others(9): Show |
12 | HG02148.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-5989_76-5988ins others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320279 | ||||||
| chr20:21320279 | G | GTATTTAT others(17): Show |
1 | a0001c0001t0001g0243 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.76-5989_76-5988ins others(24): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21320279 | ||||||
| chr20:21320295 | G | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.76-5984G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320295 | |||||||
| chr20:21320540 | C | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-5739C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320540 | |||||||
| chr20:21320722 | G | C | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-5557G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320722 | |||||||
| chr20:21320815 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0258 |
3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.76-5464C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320815 | |||||||
| chr20:21320839 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.76-5440C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21320839 | |||||||
| chr20:21321058 | C | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-5221C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321058 | |||||||
| chr20:21321078 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0258 |
3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.76-5201C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321078 | |||||||
| chr20:21321207 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.76-5072A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321207 | |||||||
| chr20:21321240 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.76-5039C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321240 | |||||||
| chr20:21321256 | G | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-5023G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321256 | |||||||
| chr20:21321263 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.76-5016G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321263 | |||||||
| chr20:21321301 | C | CTG | 18 | a0001c0001t0001g0073 a0001c0001t0002g0006 a0001c0001t0002g0173 others(15): Show |
19 | HG00099.hp2 HG00738.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-4930_76-4929dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | C | CTGTG | 6 | a0001c0001t0002g0142 a0001c0001t0002g0148 a0001c0001t0002g0180 others(3): Show |
6 | HG01981.hp1 NA18941.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-4932_76-4929dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | C | CTGTGTGT others(3): Show |
1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.76-4938_76-4929dup others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTG | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
39 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.76-4930_76-4929del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTG | C | 47 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0019 others(44): Show |
47 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.76-4932_76-4929del others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTGTG | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(107): Show |
115 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-4934_76-4929del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTGTGT others(1): Show |
C | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0098 others(8): Show |
11 | HG00280.hp2 HG00639.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-4936_76-4929del others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTGTGT others(3): Show |
C | 11 | a0001c0001t0001g0139 a0001c0001t0001g0204 a0001c0001t0001g0208 others(8): Show |
11 | HG00639.hp2 HG01074.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-4938_76-4929del others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0216 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.76-4940_76-4929del others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTGTGT others(9): Show |
C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-4944_76-4929del others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTGTGT others(11): Show |
C | 3 | a0001c0001t0001g0200 a0001c0001t0002g0144 a0001c0001t0002g0145 |
3 | HG01167.hp1 HG01169.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.76-4946_76-4929del others(18): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321301 | CTGTGTGT others(25): Show |
C | 1 | a0001c0001t0001g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.76-4960_76-4929del others(32): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21321301 | ||||||
| chr20:21321353 | G | A | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-4926G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321353 | |||||||
| chr20:21321358 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(36): Show |
40 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.76-4921C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321358 | |||||||
| chr20:21321689 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.76-4590G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321689 | |||||||
| chr20:21321713 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.76-4566G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321713 | |||||||
| chr20:21321772 | T | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.76-4507T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321772 | |||||||
| chr20:21321814 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | NA18946.hp2 NA18986.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.76-4465G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321814 | |||||||
| chr20:21321847 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.76-4432T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321847 | |||||||
| chr20:21321851 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0001g0252 |
3 | HG00280.hp2 HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.76-4428A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321851 | |||||||
| chr20:21321927 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.76-4352C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321927 | |||||||
| chr20:21321943 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.76-4336T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21321943 | |||||||
| chr20:21322009 | T | G | 1 | a0001c0001t0002g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-4270T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322009 | |||||||
| chr20:21322096 | C | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-4183C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322096 | |||||||
| chr20:21322247 | G | A | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.76-4032G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322247 | |||||||
| chr20:21322299 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-3980C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322299 | |||||||
| chr20:21322732 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.76-3547C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322732 | |||||||
| chr20:21322802 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.76-3477A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322802 | |||||||
| chr20:21322867 | A | G | 1 | a0001c0001t0003g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.76-3412A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21322867 | |||||||
| chr20:21324192 | A | G | 3 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0032 |
3 | NA18991.hp2 NA19064.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.76-2087A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324192 | |||||||
| chr20:21324202 | A | G | 2 | a0001c0001t0002g0164 a0001c0001t0002g0165 |
2 | HG00140.hp1 HG00280.hp1 |
intron_variant | MODIFIER | c.76-2077A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324202 | |||||||
| chr20:21324497 | C | CT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(106): Show |
113 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.76-1769dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21324497 | ||||||
| chr20:21324497 | C | CTT | 38 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
39 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.76-1770_76-1769dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr20 | 21324497 | ||||||
| chr20:21324514 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.76-1765C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324514 | |||||||
| chr20:21324670 | G | C | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.76-1609G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324670 | |||||||
| chr20:21324762 | T | C | 15 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(12): Show |
15 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-1517T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324762 | |||||||
| chr20:21324776 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.76-1503C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21324776 | |||||||
| chr20:21325393 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.76-886G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325393 | |||||||
| chr20:21325499 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-780T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325499 | |||||||
| chr20:21325609 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.76-670G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325609 | |||||||
| chr20:21325653 | G | T | 1 | a0001c0001t0002g0185 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.76-626G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325653 | |||||||
| chr20:21325675 | A | G | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.76-604A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325675 | |||||||
| chr20:21325819 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.76-460A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325819 | |||||||
| chr20:21325857 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.76-422T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 1/29 | chr20 | 21325857 | |||||||
| chr20:21326469 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.204-21A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 2/29 | chr20 | 21326469 | |||||||
| chr20:21326813 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.315+212G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21326813 | |||||||
| chr20:21327058 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.315+457G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327058 | |||||||
| chr20:21327066 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(53): Show |
58 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.315+465G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327066 | |||||||
| chr20:21327090 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.315+489C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327090 | |||||||
| chr20:21327116 | C | T | 4 | a0001c0001t0002g0118 a0001c0001t0002g0147 a0001c0001t0002g0163 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+515C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327116 | |||||||
| chr20:21327173 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.315+572G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327173 | |||||||
| chr20:21327243 | G | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(2): Show |
5 | HG00423.hp1 NA18944.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.315+642G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327243 | |||||||
| chr20:21327480 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.315+879G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327480 | |||||||
| chr20:21327884 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.316-675A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327884 | |||||||
| chr20:21327934 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.316-625A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21327934 | |||||||
| chr20:21328174 | G | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.316-385G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 3/29 | chr20 | 21328174 | |||||||
| chr20:21328832 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.427+162A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21328832 | |||||||
| chr20:21329123 | C | T | 6 | a0001c0001t0002g0084 a0001c0001t0002g0150 a0001c0001t0002g0151 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.427+453C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329123 | |||||||
| chr20:21329188 | G | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.427+518G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329188 | |||||||
| chr20:21329516 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.427+846C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329516 | |||||||
| chr20:21329677 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.428-804C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329677 | |||||||
| chr20:21329698 | AATAGTG | A | 5 | a0001c0001t0002g0187 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG01891.hp1 HG02976.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.428-778_428-773del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329698 | ||||||
| chr20:21329770 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(1): Show |
4 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.428-711G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329770 | |||||||
| chr20:21329835 | CA | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.428-640delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329835 | ||||||
| chr20:21329856 | G | GGT | 24 | a0001c0001t0001g0108 a0001c0001t0001g0111 a0001c0001t0001g0128 others(21): Show |
24 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.428-584_428-583dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | G | GGTGT | 8 | a0001c0001t0001g0106 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
8 | HG01934.hp1 HG01975.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.428-586_428-583dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | G | GGTGTGT | 6 | a0001c0001t0001g0132 a0001c0001t0001g0267 a0001c0001t0002g0152 others(3): Show |
6 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.428-588_428-583dup others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.428-596_428-583dup others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | GGT | G | 35 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0040 others(32): Show |
35 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.428-584_428-583del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | GGTGT | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.428-586_428-583del others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | GGTGTGT | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(51): Show |
56 | HG00280.hp2 HG00621.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.428-588_428-583del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(4): Show |
8 | HG01884.hp2 HG02015.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.428-590_428-583del others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0002g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.428-592_428-583del others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329856 | GGTGTGTG others(5): Show |
G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(4): Show |
7 | HG00423.hp1 HG03239.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.428-594_428-583del others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr20 | 21329856 | ||||||
| chr20:21329908 | C | T | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.428-573C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21329908 | |||||||
| chr20:21330204 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.428-277A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21330204 | |||||||
| chr20:21330367 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.428-114C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21330367 | |||||||
| chr20:21330468 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.428-13C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 4/29 | chr20 | 21330468 | |||||||
| chr20:21331003 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.576+298A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331003 | |||||||
| chr20:21331268 | G | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.577-293G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331268 | |||||||
| chr20:21331350 | C | T | 1 | a0001c0001t0003g0123 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.577-211C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331350 | |||||||
| chr20:21331399 | T | TCA | 19 | a0001c0001t0001g0050 a0001c0001t0001g0073 a0001c0001t0001g0109 others(16): Show |
19 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.577-124_577-123dup others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | ||||||
| chr20:21331399 | T | TCACA | 17 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0129 others(14): Show |
18 | HG00140.hp2 HG00741.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.577-126_577-123dup others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | ||||||
| chr20:21331399 | T | TCACACA | 5 | a0001c0001t0001g0128 a0001c0001t0001g0267 a0001c0001t0001g0268 others(2): Show |
5 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-128_577-123dup others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | ||||||
| chr20:21331399 | TCA | T | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(101): Show |
109 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.577-124_577-123del others(2): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | ||||||
| chr20:21331399 | TCACA | T | 41 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(38): Show |
41 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.577-126_577-123del others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | ||||||
| chr20:21331399 | TCACACA | T | 14 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(11): Show |
14 | HG00621.hp2 HG00673.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.577-128_577-123del others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr20 | 21331399 | ||||||
| chr20:21331470 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.577-91T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 6/29 | chr20 | 21331470 | |||||||
| chr20:21331644 | C | T | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 |
3 | HG02965.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.649+11C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/29 | chr20 | 21331644 | |||||||
| chr20:21331650 | A | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.649+17A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/29 | chr20 | 21331650 | |||||||
| chr20:21331687 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(33): Show |
37 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.649+54G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 7/29 | chr20 | 21331687 | |||||||
| chr20:21332015 | C | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.700+197C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 8/29 | chr20 | 21332015 | |||||||
| chr20:21332206 | G | T | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.701-77G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 8/29 | chr20 | 21332206 | |||||||
| chr20:21332255 | C | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(15): Show |
19 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.701-28C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 8/29 | chr20 | 21332255 | |||||||
| chr20:21332471 | T | TA | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.858+42dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr20 | 21332471 | ||||||
| chr20:21332743 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.858+303C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332743 | |||||||
| chr20:21332806 | T | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.858+366T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332806 | |||||||
| chr20:21332880 | A | G | 4 | a0001c0001t0002g0140 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+440A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332880 | |||||||
| chr20:21332994 | G | T | 1 | a0001c0001t0002g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.859-550G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21332994 | |||||||
| chr20:21333019 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0258 |
3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.859-525G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333019 | |||||||
| chr20:21333021 | G | C | 1 | a0001c0001t0001g0018 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.859-523G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333021 | |||||||
| chr20:21333137 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.859-407C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333137 | |||||||
| chr20:21333199 | A | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(204): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.859-345A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333199 | |||||||
| chr20:21333201 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.859-343C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333201 | |||||||
| chr20:21333217 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.859-327G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333217 | |||||||
| chr20:21333441 | T | C | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.859-103T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333441 | |||||||
| chr20:21333457 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.859-87G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333457 | |||||||
| chr20:21333503 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.859-41C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333503 | |||||||
| chr20:21333521 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.859-23C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333521 | |||||||
| chr20:21333538 | T | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(12): Show |
16 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.859-6T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 9/29 | chr20 | 21333538 | |||||||
| chr20:21333902 | G | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG02896.hp1 HG03098.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1068-35G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 11/29 | chr20 | 21333902 | |||||||
| chr20:21334218 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1233+33C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334218 | |||||||
| chr20:21334444 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1233+259C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334444 | |||||||
| chr20:21334493 | A | G | 2 | a0001c0001t0001g0249 a0001c0004t0001g0105 |
2 | HG02976.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1233+308A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334493 | |||||||
| chr20:21334595 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1233+410G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334595 | |||||||
| chr20:21334933 | AGAG | A | 15 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(12): Show |
15 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1233+749_1233+751d others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21334933 | |||||||
| chr20:21335022 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1233+837T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335022 | |||||||
| chr20:21335151 | A | T | 1 | a0001c0001t0003g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1233+966A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335151 | |||||||
| chr20:21335281 | G | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1096G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335281 | |||||||
| chr20:21335516 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
173 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.1233+1331G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335516 | |||||||
| chr20:21335562 | G | C | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1233+1377G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335562 | |||||||
| chr20:21335736 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1233+1551T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335736 | |||||||
| chr20:21335898 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1233+1713G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335898 | |||||||
| chr20:21335961 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1233+1776C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21335961 | |||||||
| chr20:21336335 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1233+2150G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21336335 | |||||||
| chr20:21336851 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1234-2193G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21336851 | |||||||
| chr20:21336860 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1234-2184T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21336860 | |||||||
| chr20:21337210 | A | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1234-1834A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337210 | |||||||
| chr20:21337212 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1234-1832G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337212 | |||||||
| chr20:21337263 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(32): Show |
36 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1234-1781A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337263 | |||||||
| chr20:21337285 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1234-1759G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21337285 | |||||||
| chr20:21338060 | T | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1234-984T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338060 | |||||||
| chr20:21338188 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1234-856A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338188 | |||||||
| chr20:21338339 | A | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0047 others(28): Show |
32 | HG00621.hp2 HG00673.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1234-705A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338339 | |||||||
| chr20:21338340 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1234-704G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338340 | |||||||
| chr20:21338623 | T | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1234-421T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338623 | |||||||
| chr20:21338731 | T | C | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1234-313T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338731 | |||||||
| chr20:21338896 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1234-148T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338896 | |||||||
| chr20:21338910 | G | C | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1234-134G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 13/29 | chr20 | 21338910 | |||||||
| chr20:21339180 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1278+92A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339180 | |||||||
| chr20:21339190 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.1278+102A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339190 | |||||||
| chr20:21339611 | G | C | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1278+523G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339611 | |||||||
| chr20:21339697 | C | A | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0230 others(2): Show |
5 | HG00735.hp1 HG02723.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+609C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339697 | |||||||
| chr20:21339916 | A | C | 4 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0265 others(1): Show |
4 | HG01256.hp1 HG02683.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279-805A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339916 | |||||||
| chr20:21339966 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | NA18959.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.1279-755A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21339966 | |||||||
| chr20:21340015 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(110): Show |
117 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.1279-706T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340015 | |||||||
| chr20:21340255 | A | C | 1 | a0001c0001t0004g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1279-466A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340255 | |||||||
| chr20:21340656 | C | T | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(210): Show |
220 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.1279-65C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340656 | |||||||
| chr20:21340696 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1279-25T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 14/29 | chr20 | 21340696 | |||||||
| chr20:21341054 | C | CGTA | 18 | a0001c0001t0001g0076 a0001c0001t0003g0005 a0001c0001t0003g0113 others(15): Show |
19 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1410+204_1410+206d others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr20 | 21341054 | ||||||
| chr20:21341264 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1410+412G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341264 | |||||||
| chr20:21341572 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1410+720C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341572 | |||||||
| chr20:21341584 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1410+732G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341584 | |||||||
| chr20:21341652 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+800A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341652 | |||||||
| chr20:21341653 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+801C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341653 | |||||||
| chr20:21341654 | A | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+802A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341654 | |||||||
| chr20:21341655 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1410+803C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21341655 | |||||||
| chr20:21342320 | C | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 |
3 | HG01069.hp2 HG02683.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1410+1468C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342320 | |||||||
| chr20:21342342 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1410+1490A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342342 | |||||||
| chr20:21342438 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1410+1586C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342438 | |||||||
| chr20:21342755 | C | T | 2 | a0001c0002t0001g0087 a0001c0002t0001g0088 |
2 | HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1411-1335C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342755 | |||||||
| chr20:21342907 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1411-1183G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342907 | |||||||
| chr20:21342976 | A | T | 1 | a0001c0001t0001g0042 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1411-1114A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21342976 | |||||||
| chr20:21343356 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1411-734G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343356 | |||||||
| chr20:21343410 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1411-680C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343410 | |||||||
| chr20:21343820 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1411-270T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343820 | |||||||
| chr20:21343872 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1411-218G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343872 | |||||||
| chr20:21343884 | A | G | 1 | a0001c0002t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1411-206A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 15/29 | chr20 | 21343884 | |||||||
| chr20:21344251 | A | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0024 a0001c0001t0001g0026 others(6): Show |
10 | HG01978.hp1 HG02004.hp2 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.1529+43A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344251 | |||||||
| chr20:21344382 | A | T | 1 | a0001c0001t0002g0179 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1529+174A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344382 | |||||||
| chr20:21344384 | G | A | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1529+176G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344384 | |||||||
| chr20:21344560 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1529+352T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344560 | |||||||
| chr20:21344584 | T | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1529+376T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344584 | |||||||
| chr20:21344667 | A | C | 1 | a0001c0001t0003g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1529+459A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344667 | |||||||
| chr20:21344796 | C | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0235 a0001c0001t0001g0251 |
3 | HG00099.hp1 HG01496.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1529+588C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344796 | |||||||
| chr20:21344965 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1529+757C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344965 | |||||||
| chr20:21344983 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1529+775C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21344983 | |||||||
| chr20:21345073 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(109): Show |
116 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.1529+865T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345073 | |||||||
| chr20:21345222 | G | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1529+1014G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345222 | |||||||
| chr20:21345355 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1530-1060A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345355 | |||||||
| chr20:21345429 | G | C | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1530-986G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345429 | |||||||
| chr20:21345460 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1530-955T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21345460 | |||||||
| chr20:21345940 | AT | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1530-468delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | INFO_REALIGN_3_PRIME | chr20 | 21345940 | ||||||
| chr20:21346044 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1530-371T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346044 | |||||||
| chr20:21346127 | G | A | 1 | a0002c0003t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1530-288G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346127 | |||||||
| chr20:21346152 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0065 |
3 | HG02572.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1530-263A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346152 | |||||||
| chr20:21346240 | C | T | 7 | a0001c0001t0001g0059 a0001c0001t0001g0062 a0001c0001t0001g0068 others(4): Show |
7 | HG00621.hp2 HG02132.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530-175C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 16/29 | chr20 | 21346240 | |||||||
| chr20:21346568 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1665+18T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346568 | |||||||
| chr20:21346611 | C | T | 1 | a0002c0003t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1665+61C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346611 | |||||||
| chr20:21346632 | G | C | 1 | a0001c0001t0002g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1665+82G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346632 | |||||||
| chr20:21346807 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1665+257C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346807 | |||||||
| chr20:21346867 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1665+317T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21346867 | |||||||
| chr20:21347004 | G | A | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1665+454G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347004 | |||||||
| chr20:21347071 | T | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1665+521T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347071 | |||||||
| chr20:21347079 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1665+529A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347079 | |||||||
| chr20:21347269 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1665+719T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347269 | |||||||
| chr20:21347549 | C | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1666-597C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347549 | |||||||
| chr20:21347648 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1666-498A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347648 | |||||||
| chr20:21347740 | G | A | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1666-406G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347740 | |||||||
| chr20:21347749 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(53): Show |
58 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1666-397C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347749 | |||||||
| chr20:21347789 | G | A | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1666-357G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 17/29 | chr20 | 21347789 | |||||||
| chr20:21348314 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(31): Show |
35 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.1774-27G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 18/29 | chr20 | 21348314 | |||||||
| chr20:21348329 | T | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1774-12T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 18/29 | chr20 | 21348329 | |||||||
| chr20:21348811 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(15): Show |
19 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1863+381T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348811 | |||||||
| chr20:21348871 | G | A | 31 | a0001c0001t0001g0003 a0001c0001t0001g0043 a0001c0001t0001g0047 others(28): Show |
32 | HG00621.hp2 HG00673.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.1863+441G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348871 | |||||||
| chr20:21348904 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1863+474A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348904 | |||||||
| chr20:21348949 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1864-440A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21348949 | |||||||
| chr20:21349142 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1864-247T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21349142 | |||||||
| chr20:21349312 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(32): Show |
36 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1864-77A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 19/29 | chr20 | 21349312 | |||||||
| chr20:21349476 | T | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(34): Show |
38 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.1936+15T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349476 | |||||||
| chr20:21349537 | T | G | 1 | a0001c0001t0001g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1936+76T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349537 | |||||||
| chr20:21349664 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1936+203G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349664 | |||||||
| chr20:21349677 | T | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1936+216T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21349677 | |||||||
| chr20:21350298 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | NA18995.hp1 NA19056.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936+837G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350298 | |||||||
| chr20:21350353 | C | T | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1936+892C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350353 | |||||||
| chr20:21350394 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1936+933C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350394 | |||||||
| chr20:21350395 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(202): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.1936+934G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350395 | |||||||
| chr20:21350399 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1936+938G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350399 | |||||||
| chr20:21350404 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1936+943T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350404 | |||||||
| chr20:21350441 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1936+980G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350441 | |||||||
| chr20:21350504 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1936+1043C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350504 | |||||||
| chr20:21350525 | C | CA | 77 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0019 others(74): Show |
79 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1936+1092dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350525 | C | CAA | 25 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0043 others(22): Show |
27 | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1936+1091_1936+109 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350525 | CA | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0021 others(30): Show |
34 | HG00323.hp1 HG00558.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1936+1092delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350525 | CAA | C | 22 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(19): Show |
22 | HG00423.hp1 HG01891.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1936+1091_1936+109 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350525 | CAAA | C | 31 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0128 others(28): Show |
33 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1936+1090_1936+109 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350525 | CAAAA | C | 9 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
9 | HG01975.hp2 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1936+1089_1936+109 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350525 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1936+1081_1936+109 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350525 | CAAAAAAA others(9): Show |
C | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1936+1077_1936+109 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21350525 | ||||||
| chr20:21350695 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1936+1234T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350695 | |||||||
| chr20:21350734 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1936+1273G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350734 | |||||||
| chr20:21350768 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1936+1307C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350768 | |||||||
| chr20:21350796 | T | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | NA18962.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1936+1335T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350796 | |||||||
| chr20:21350903 | T | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1936+1442T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21350903 | |||||||
| chr20:21351041 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1936+1580A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351041 | |||||||
| chr20:21351224 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1936+1763T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351224 | |||||||
| chr20:21351264 | T | C | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1936+1803T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351264 | |||||||
| chr20:21351627 | G | A | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG00099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1936+2166G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351627 | |||||||
| chr20:21351709 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1936+2248C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351709 | |||||||
| chr20:21351811 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1936+2350A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21351811 | |||||||
| chr20:21352016 | C | T | 1 | a0001c0006t0001g0221 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1936+2555C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352016 | |||||||
| chr20:21352024 | G | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1936+2563G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352024 | |||||||
| chr20:21352071 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1936+2610A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352071 | |||||||
| chr20:21352228 | A | G | 17 | a0001c0001t0003g0005 a0001c0001t0003g0113 a0001c0001t0003g0114 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1937-2561A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352228 | |||||||
| chr20:21352279 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0258 |
3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1937-2510A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352279 | |||||||
| chr20:21352432 | A | G | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1937-2357A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352432 | |||||||
| chr20:21352448 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(203): Show |
213 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1937-2341T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352448 | |||||||
| chr20:21352573 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1937-2216C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352573 | |||||||
| chr20:21352804 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1937-1985A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21352804 | |||||||
| chr20:21353013 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1937-1776G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353013 | |||||||
| chr20:21353030 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
155 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.1937-1759G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353030 | |||||||
| chr20:21353223 | G | GAT | 8 | a0001c0001t0001g0106 a0001c0001t0002g0190 a0001c0001t0002g0197 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1937-1525_1937-152 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | G | GATAT | 5 | a0001c0001t0001g0138 a0001c0002t0001g0087 a0001c0002t0001g0094 others(2): Show |
5 | HG02965.hp2 HG03041.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1937-1527_1937-152 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GAT | G | 11 | a0001c0001t0001g0134 a0001c0001t0002g0161 a0001c0001t0002g0175 others(8): Show |
11 | HG00738.hp2 HG01192.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1937-1525_1937-152 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GATAT | G | 16 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0133 others(13): Show |
17 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1937-1527_1937-152 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GATATAT | G | 26 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0001g0108 others(23): Show |
28 | HG00438.hp1 HG00735.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1937-1529_1937-152 others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GATATATA others(1): Show |
G | 19 | a0001c0001t0002g0146 a0001c0001t0002g0156 a0001c0001t0002g0157 others(16): Show |
19 | HG00423.hp2 HG00558.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1937-1531_1937-152 others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GATATATA others(3): Show |
G | 17 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0002g0084 others(14): Show |
17 | HG00099.hp2 HG00741.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1937-1533_1937-152 others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GATATATA others(5): Show |
G | 3 | a0001c0001t0002g0118 a0001c0001t0002g0140 a0001c0001t0002g0160 |
3 | HG02257.hp2 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1937-1535_1937-152 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GATATATA others(9): Show |
G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1937-1539_1937-152 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353223 | GATATATA others(23): Show |
G | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1937-1553_1937-152 others(34): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353223 | ||||||
| chr20:21353240 | ATATATAT others(19): Show |
A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1937-1547_1937-152 others(30): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353240 | ||||||
| chr20:21353242 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1937-1545_1937-152 others(28): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353242 | ||||||
| chr20:21353252 | ATATATAT others(7): Show |
A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1937-1535_1937-152 others(18): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353252 | ||||||
| chr20:21353266 | C | A | 1 | a0001c0002t0001g0086 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1937-1523C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353266 | |||||||
| chr20:21353301 | A | T | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1937-1488A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353301 | |||||||
| chr20:21353794 | T | TA | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
148 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1937-979dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21353794 | ||||||
| chr20:21353817 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1937-972T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353817 | |||||||
| chr20:21353824 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1937-965G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353824 | |||||||
| chr20:21353889 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1937-900C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21353889 | |||||||
| chr20:21354014 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1937-775T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354014 | |||||||
| chr20:21354034 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1937-755C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354034 | |||||||
| chr20:21354159 | T | A | 4 | a0001c0001t0001g0098 a0001c0001t0001g0139 a0002c0003t0001g0085 others(1): Show |
4 | HG03209.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1937-630T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354159 | |||||||
| chr20:21354264 | TTAG | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0258 |
3 | HG01515.hp1 HG01517.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1937-521_1937-519d others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr20 | 21354264 | ||||||
| chr20:21354326 | A | T | 55 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(52): Show |
56 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.1937-463A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354326 | |||||||
| chr20:21354414 | A | G | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1937-375A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354414 | |||||||
| chr20:21354475 | T | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(251): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1937-314T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354475 | |||||||
| chr20:21354591 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1937-198G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 20/29 | chr20 | 21354591 | |||||||
| chr20:21355126 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2020+254C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355126 | |||||||
| chr20:21355162 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2020+290C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355162 | |||||||
| chr20:21355367 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2020+495C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355367 | |||||||
| chr20:21355674 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2021-406C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355674 | |||||||
| chr20:21355705 | T | A | 4 | a0001c0001t0001g0214 a0001c0001t0001g0238 a0001c0001t0002g0184 others(1): Show |
4 | HG02273.hp2 HG02818.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2021-375T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355705 | |||||||
| chr20:21355771 | T | A | 1 | a0001c0001t0001g0080 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2021-309T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 21/29 | chr20 | 21355771 | |||||||
| chr20:21356186 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2118+9C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 22/29 | chr20 | 21356186 | |||||||
| chr20:21356187 | G | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(75): Show |
81 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.2118+10G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 22/29 | chr20 | 21356187 | |||||||
| chr20:21356430 | T | G | 3 | a0001c0001t0002g0183 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2119-156T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 22/29 | chr20 | 21356430 | |||||||
| chr20:21356755 | A | C | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2198+90A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/29 | chr20 | 21356755 | |||||||
| chr20:21356867 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2198+202G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/29 | chr20 | 21356867 | |||||||
| chr20:21357138 | G | GT | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.2198+474dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr20 | 21357138 | ||||||
| chr20:21358063 | G | T | 2 | a0001c0002t0001g0090 a0001c0002t0001g0097 |
2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2255+271G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358063 | |||||||
| chr20:21358703 | G | C | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2255+911G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358703 | |||||||
| chr20:21358748 | CGTTTATC others(17): Show |
C | 3 | a0001c0001t0002g0183 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2255+969_2255+992d others(26): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21358748 | ||||||
| chr20:21358760 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2255+968C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358760 | |||||||
| chr20:21358950 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2255+1158C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21358950 | |||||||
| chr20:21359078 | A | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0243 |
2 | NA19000.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2255+1286A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359078 | |||||||
| chr20:21359124 | G | A | 61 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2255+1332G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359124 | |||||||
| chr20:21359219 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2255+1427A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359219 | |||||||
| chr20:21359253 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0139 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2255+1461C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359253 | |||||||
| chr20:21359254 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2255+1462G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359254 | |||||||
| chr20:21359365 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2255+1573T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359365 | |||||||
| chr20:21359409 | G | T | 1 | a0001c0001t0003g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2255+1617G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359409 | |||||||
| chr20:21359468 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2255+1676C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359468 | |||||||
| chr20:21359524 | C | CA | 62 | a0001c0001t0001g0238 a0001c0001t0001g0258 a0001c0001t0002g0006 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2255+1746dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21359524 | ||||||
| chr20:21359834 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0001g0226 |
2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2255+2042A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359834 | |||||||
| chr20:21359913 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2255+2121A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21359913 | |||||||
| chr20:21360061 | A | G | 61 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2255+2269A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21360061 | |||||||
| chr20:21360353 | C | T | 62 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2255+2561C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21360353 | |||||||
| chr20:21360457 | G | GT | 18 | a0001c0001t0001g0025 a0001c0001t0001g0136 a0001c0001t0001g0138 others(15): Show |
18 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.2255+2679dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21360457 | ||||||
| chr20:21360695 | A | AT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(14): Show |
18 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2255+2909dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21360695 | ||||||
| chr20:21361348 | T | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2255+3556T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361348 | |||||||
| chr20:21361695 | A | G | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2256-3726A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361695 | |||||||
| chr20:21361740 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2256-3681T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361740 | |||||||
| chr20:21361840 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2256-3581A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361840 | |||||||
| chr20:21361912 | T | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2256-3509T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21361912 | |||||||
| chr20:21362088 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2256-3333G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362088 | |||||||
| chr20:21362153 | A | G | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2256-3268A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362153 | |||||||
| chr20:21362332 | G | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2256-3089G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362332 | |||||||
| chr20:21362691 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2256-2730C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362691 | |||||||
| chr20:21362834 | G | A | 1 | a0002c0003t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2256-2587G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362834 | |||||||
| chr20:21362997 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2256-2424T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21362997 | |||||||
| chr20:21363228 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2256-2193T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363228 | |||||||
| chr20:21363306 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2256-2115G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363306 | |||||||
| chr20:21363780 | T | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2256-1641T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363780 | |||||||
| chr20:21363808 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2256-1613A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363808 | |||||||
| chr20:21363815 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2256-1606T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363815 | |||||||
| chr20:21363816 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2256-1605G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21363816 | |||||||
| chr20:21364010 | C | T | 60 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.2256-1411C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364010 | |||||||
| chr20:21364153 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2256-1268G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364153 | |||||||
| chr20:21364804 | C | CA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0074 others(32): Show |
36 | HG00140.hp2 HG00621.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2256-601dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21364804 | ||||||
| chr20:21364804 | CA | C | 11 | a0001c0001t0001g0207 a0001c0001t0002g0141 a0001c0001t0003g0005 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.2256-601delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr20 | 21364804 | ||||||
| chr20:21364935 | A | C | 19 | a0001c0001t0002g0169 a0001c0001t0002g0173 a0001c0001t0002g0174 others(16): Show |
20 | HG00099.hp2 HG00738.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2256-486A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364935 | |||||||
| chr20:21364942 | C | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0043 others(23): Show |
27 | HG00621.hp2 HG00673.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2256-479C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21364942 | |||||||
| chr20:21365079 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2256-342C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21365079 | |||||||
| chr20:21365184 | C | G | 1 | a0001c0001t0001g0248 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2256-237C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 24/29 | chr20 | 21365184 | |||||||
| chr20:21365770 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0073 |
2 | HG02258.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2456+66G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21365770 | |||||||
| chr20:21365800 | A | ATATATAT others(26): Show |
1 | a0001c0001t0002g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2456+111_2456+143d others(35): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365800 | ||||||
| chr20:21365803 | TATATA | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2456+105_2456+109d others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365803 | ||||||
| chr20:21365877 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2456+173A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21365877 | |||||||
| chr20:21365881 | T | TTATATAA others(19): Show |
1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2456+184_2456+209d others(28): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365881 | ||||||
| chr20:21365896 | TTA | T | 3 | a0001c0001t0002g0183 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2456+201_2456+202d others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21365896 | ||||||
| chr20:21365966 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2456+262T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21365966 | |||||||
| chr20:21366012 | A | ATATATAA others(30): Show |
1 | a0001c0001t0001g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2456+352_2456+388d others(39): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366012 | ||||||
| chr20:21366020 | T | TATATATA others(71): Show |
1 | a0001c0001t0002g0181 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2456+352_2456+429d others(80): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366020 | ||||||
| chr20:21366057 | T | C | 1 | a0001c0001t0002g0175 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2456+353T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366057 | |||||||
| chr20:21366057 | T | TATATATA others(34): Show |
3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0002c0003t0001g0199 |
3 | HG01361.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2456+412_2456+452d others(43): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366057 | ||||||
| chr20:21366057 | T | TATATATA others(75): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0202 |
2 | HG02965.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2456+371_2456+452d others(84): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366057 | ||||||
| chr20:21366094 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2456+390A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366094 | |||||||
| chr20:21366109 | ATATAT | A | 31 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(28): Show |
32 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2456+412_2456+416d others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366109 | ||||||
| chr20:21366120 | T | A | 1 | a0001c0001t0001g0021 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2456+416T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366120 | |||||||
| chr20:21366125 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0021 |
2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+421G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366125 | |||||||
| chr20:21366126 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0021 |
2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+422T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366126 | |||||||
| chr20:21366128 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0021 |
2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+424T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366128 | |||||||
| chr20:21366139 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(28): Show |
32 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.2456+435C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366139 | |||||||
| chr20:21366147 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2456+443A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366147 | |||||||
| chr20:21366150 | A | ATATAT | 30 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(27): Show |
31 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.2456+448_2456+452d others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366150 | ||||||
| chr20:21366150 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0021 |
2 | HG01071.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2456+446A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366150 | |||||||
| chr20:21366163 | T | TTATA | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2456+462_2456+465d others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366163 | ||||||
| chr20:21366192 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2456+488T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366192 | |||||||
| chr20:21366218 | T | TTA | 4 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0190 others(1): Show |
4 | HG01891.hp1 HG02976.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2456+526_2456+527d others(4): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr20 | 21366218 | ||||||
| chr20:21366469 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2456+765A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366469 | |||||||
| chr20:21366737 | A | C | 59 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.2456+1033A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366737 | |||||||
| chr20:21366762 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2456+1058T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21366762 | |||||||
| chr20:21367076 | G | T | 1 | a0001c0001t0001g0013 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2456+1372G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367076 | |||||||
| chr20:21367340 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2457-1123A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367340 | |||||||
| chr20:21367561 | G | A | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2457-902G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367561 | |||||||
| chr20:21367643 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2457-820G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367643 | |||||||
| chr20:21367792 | C | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2457-671C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367792 | |||||||
| chr20:21367990 | A | G | 2 | a0001c0002t0001g0093 a0001c0004t0001g0105 |
2 | HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2457-473A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21367990 | |||||||
| chr20:21368344 | T | C | 16 | a0001c0001t0001g0203 a0001c0002t0001g0086 a0001c0002t0001g0087 others(13): Show |
16 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2457-119T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 26/29 | chr20 | 21368344 | |||||||
| chr20:21368974 | C | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2584+384C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21368974 | |||||||
| chr20:21369091 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2584+501G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369091 | |||||||
| chr20:21369211 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2584+621C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369211 | |||||||
| chr20:21369491 | T | G | 1 | a0001c0001t0001g0251 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2584+901T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369491 | |||||||
| chr20:21369518 | C | A | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2584+928C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369518 | |||||||
| chr20:21369523 | C | G | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02559.hp2 HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2584+933C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21369523 | |||||||
| chr20:21370254 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2584+1664A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21370254 | |||||||
| chr20:21370577 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2584+1987A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21370577 | |||||||
| chr20:21370698 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2584+2108G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21370698 | |||||||
| chr20:21371025 | TC | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0067 a0001c0001t0001g0075 others(1): Show |
4 | HG01884.hp1 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2584+2436delC | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371025 | |||||||
| chr20:21371092 | ACC | A | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584+2505_2584+250 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21371092 | ||||||
| chr20:21371120 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2584+2530C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371120 | |||||||
| chr20:21371180 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2584+2590A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371180 | |||||||
| chr20:21371274 | C | G | 1 | a0001c0001t0001g0231 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2584+2684C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371274 | |||||||
| chr20:21371598 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2584+3008A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371598 | |||||||
| chr20:21371667 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2584+3077C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371667 | |||||||
| chr20:21371735 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2584+3145T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371735 | |||||||
| chr20:21371862 | G | A | 4 | a0001c0001t0002g0118 a0001c0001t0002g0147 a0001c0001t0002g0163 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2584+3272G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21371862 | |||||||
| chr20:21372326 | C | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2584+3736C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372326 | |||||||
| chr20:21372373 | G | T | 3 | a0001c0001t0002g0183 a0001c0001t0002g0193 a0001c0001t0002g0194 |
3 | HG00738.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2584+3783G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372373 | |||||||
| chr20:21372382 | T | TA | 7 | a0001c0001t0001g0062 a0001c0001t0001g0068 a0001c0001t0001g0069 others(4): Show |
7 | HG00621.hp1 HG00621.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2584+3794dupA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21372382 | ||||||
| chr20:21372450 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2584+3860G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372450 | |||||||
| chr20:21372538 | G | T | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2584+3948G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372538 | |||||||
| chr20:21372706 | A | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2584+4116A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372706 | |||||||
| chr20:21372764 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2584+4174G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372764 | |||||||
| chr20:21372771 | A | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2584+4181A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372771 | |||||||
| chr20:21372841 | G | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2584+4251G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372841 | |||||||
| chr20:21372882 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2584+4292T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372882 | |||||||
| chr20:21372929 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2584+4339C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21372929 | |||||||
| chr20:21373012 | CT | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2584+4431delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21373012 | ||||||
| chr20:21373277 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2584+4687C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21373277 | |||||||
| chr20:21373540 | G | A | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2584+4950G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21373540 | |||||||
| chr20:21374086 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2584+5496T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374086 | |||||||
| chr20:21374243 | C | T | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2584+5653C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374243 | |||||||
| chr20:21374422 | T | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2584+5832T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374422 | |||||||
| chr20:21374981 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2584+6391G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21374981 | |||||||
| chr20:21375010 | C | CT | 88 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0019 others(85): Show |
90 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.2584+6445dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | ||||||
| chr20:21375010 | C | CTT | 40 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(37): Show |
42 | HG00140.hp2 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.2584+6444_2584+644 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | ||||||
| chr20:21375010 | CTTT | C | 30 | a0001c0001t0001g0200 a0001c0001t0002g0006 a0001c0001t0002g0118 others(27): Show |
31 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(28): Show |
intron_variant | MODIFIER | c.2584+6443_2584+644 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | ||||||
| chr20:21375010 | CTTTT | C | 33 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0002g0084 others(30): Show |
33 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.2584+6442_2584+644 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | ||||||
| chr20:21375010 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0068 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2584+6436_2584+644 others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | ||||||
| chr20:21375010 | CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0021 others(13): Show |
16 | HG01071.hp2 HG02132.hp1 HG02965.hp2 others(13): Show |
intron_variant | MODIFIER | c.2584+6435_2584+644 others(15): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | ||||||
| chr20:21375010 | CTTTTTTT others(5): Show |
C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(23): Show |
27 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.2584+6434_2584+644 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375010 | ||||||
| chr20:21375056 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2584+6466A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375056 | |||||||
| chr20:21375187 | AT | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0079 a0001c0001t0002g0168 others(2): Show |
5 | HG00558.hp2 HG01884.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.2584+6609delT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375187 | ||||||
| chr20:21375189 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2584+6599T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375189 | |||||||
| chr20:21375208 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2584+6618A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375208 | |||||||
| chr20:21375618 | T | C | 5 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
5 | HG01975.hp1 NA18948.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-6376T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375618 | |||||||
| chr20:21375818 | ATTTATTT others(4): Show |
A | 1 | a0001c0001t0001g0023 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2585-6164_2585-615 others(15): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375818 | ||||||
| chr20:21375826 | ATTT | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0039 others(10): Show |
13 | HG00621.hp1 HG00621.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.2585-6164_2585-616 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375826 | ||||||
| chr20:21375829 | T | TA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(110): Show |
117 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.2585-6165_2585-616 others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375829 | |||||||
| chr20:21375829 | T | TATTTA | 19 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0028 others(16): Show |
19 | HG01361.hp1 HG01884.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.2585-6165_2585-616 others(9): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375829 | |||||||
| chr20:21375829 | T | TTTTA | 5 | a0001c0001t0002g0187 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG01891.hp1 HG02976.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2585-6141_2585-613 others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375829 | ||||||
| chr20:21375829 | T | TTTTATTT others(5): Show |
3 | a0001c0001t0001g0139 a0001c0001t0002g0150 a0001c0001t0002g0152 |
3 | HG02559.hp2 HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2585-6149_2585-613 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375829 | ||||||
| chr20:21375829 | T | TTTTATTT others(9): Show |
1 | a0001c0001t0002g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2585-6153_2585-613 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21375829 | ||||||
| chr20:21375907 | C | T | 34 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(31): Show |
35 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2585-6087C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21375907 | |||||||
| chr20:21376039 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2585-5955C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376039 | |||||||
| chr20:21376040 | G | A | 8 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(5): Show |
8 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.2585-5954G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376040 | |||||||
| chr20:21376418 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2585-5576A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376418 | |||||||
| chr20:21376499 | A | G | 62 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2585-5495A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376499 | |||||||
| chr20:21376649 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2585-5345C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376649 | |||||||
| chr20:21376849 | G | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(11): Show |
15 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2585-5145G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21376849 | |||||||
| chr20:21377006 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2585-4988C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377006 | |||||||
| chr20:21377022 | TA | T | 15 | a0001c0002t0001g0086 a0001c0002t0001g0087 a0001c0002t0001g0088 others(12): Show |
15 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2585-4964delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377022 | ||||||
| chr20:21377080 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2585-4914T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377080 | |||||||
| chr20:21377110 | G | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0212 |
2 | NA18946.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2585-4884G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377110 | |||||||
| chr20:21377243 | C | CATATGAT | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-4750_2585-474 others(11): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377243 | ||||||
| chr20:21377255 | C | T | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-4739C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377255 | |||||||
| chr20:21377264 | C | CTTT | 15 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(12): Show |
16 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.2585-4718_2585-471 others(7): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTCT others(6): Show |
1 | a0001c0001t0001g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2585-4725_2585-472 others(17): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTCT others(14): Show |
1 | a0001c0001t0002g0159 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2585-4725_2585-472 others(25): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0196 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2585-4725_2585-471 others(14): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0136 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2585-4726_2585-471 others(15): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(5): Show |
71 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(68): Show |
73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.2585-4727_2585-471 others(16): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(6): Show |
79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
82 | HG00280.hp2 HG00621.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.2585-4728_2585-471 others(17): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(7): Show |
17 | a0001c0001t0001g0039 a0001c0001t0001g0064 a0001c0001t0001g0081 others(14): Show |
17 | HG00438.hp2 HG02027.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2585-4729_2585-471 others(18): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(23): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0139 a0001c0006t0001g0221 |
2 | HG00639.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(19): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(9): Show |
1 | a0002c0003t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(20): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0002g0188 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(21): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0002g0154 a0001c0001t0002g0186 |
2 | NA18948.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(23): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(13): Show |
4 | a0001c0001t0002g0084 a0001c0001t0002g0141 a0001c0001t0002g0157 others(1): Show |
4 | NA18968.hp2 NA18985.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(24): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(14): Show |
5 | a0001c0001t0002g0162 a0001c0001t0002g0183 a0001c0001t0002g0185 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(25): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(15): Show |
8 | a0001c0001t0002g0140 a0001c0001t0002g0142 a0001c0001t0002g0146 others(5): Show |
8 | HG00423.hp2 HG00558.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(26): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(16): Show |
9 | a0001c0001t0002g0006 a0001c0001t0002g0118 a0001c0001t0002g0147 others(6): Show |
10 | HG00438.hp1 HG02615.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(27): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(17): Show |
5 | a0001c0001t0002g0160 a0001c0001t0002g0173 a0001c0001t0002g0175 others(2): Show |
5 | HG00099.hp2 HG02165.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(28): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(18): Show |
12 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0164 others(9): Show |
12 | HG00140.hp1 HG00280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(29): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0002g0172 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(30): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(20): Show |
4 | a0001c0001t0002g0151 a0001c0001t0002g0168 a0001c0001t0002g0171 others(1): Show |
4 | HG01891.hp1 HG03540.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(31): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0002g0161 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(32): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(22): Show |
1 | a0001c0001t0002g0269 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2585-4716_2585-471 others(33): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377264 | C | CTTTTTTT others(23): Show |
3 | a0001c0001t0002g0150 a0001c0001t0002g0177 a0001c0001t0002g0187 |
3 | HG02559.hp2 HG02976.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.2585-4716_2585-471 others(34): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377264 | ||||||
| chr20:21377295 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2585-4699C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377295 | |||||||
| chr20:21377339 | C | G | 1 | a0001c0001t0002g0160 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2585-4655C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377339 | |||||||
| chr20:21377528 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2585-4466G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377528 | |||||||
| chr20:21377537 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2585-4457C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377537 | |||||||
| chr20:21377538 | G | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG01361.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2585-4456G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21377538 | |||||||
| chr20:21377561 | G | GT | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(201): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2585-4422dupT | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377561 | ||||||
| chr20:21377561 | G | GTT | 62 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2585-4423_2585-442 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21377561 | ||||||
| chr20:21378353 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2585-3641C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378353 | |||||||
| chr20:21378389 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2585-3605C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378389 | |||||||
| chr20:21378723 | T | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-3271T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378723 | |||||||
| chr20:21378906 | A | G | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2585-3088A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378906 | |||||||
| chr20:21378907 | C | T | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2585-3087C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21378907 | |||||||
| chr20:21379002 | T | C | 16 | a0001c0001t0001g0203 a0001c0002t0001g0086 a0001c0002t0001g0087 others(13): Show |
16 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2585-2992T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379002 | |||||||
| chr20:21379027 | A | G | 61 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2585-2967A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379027 | |||||||
| chr20:21379035 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2585-2959C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379035 | |||||||
| chr20:21379149 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2585-2845A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379149 | |||||||
| chr20:21379535 | C | G | 3 | a0001c0001t0002g0084 a0001c0001t0002g0154 a0001c0001t0002g0185 |
3 | NA18948.hp1 NA18995.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2585-2459C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379535 | |||||||
| chr20:21379570 | A | G | 16 | a0001c0001t0001g0203 a0001c0002t0001g0086 a0001c0002t0001g0087 others(13): Show |
16 | HG00741.hp2 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.2585-2424A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379570 | |||||||
| chr20:21379617 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2585-2377T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379617 | |||||||
| chr20:21379623 | G | A | 61 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(58): Show |
62 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.2585-2371G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379623 | |||||||
| chr20:21379624 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2585-2370G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379624 | |||||||
| chr20:21379828 | A | C | 2 | a0001c0001t0002g0187 a0001c0001t0002g0189 |
2 | HG02976.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2585-2166A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379828 | |||||||
| chr20:21379890 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
154 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.2585-2104A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21379890 | |||||||
| chr20:21380023 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2585-1971C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380023 | |||||||
| chr20:21380092 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2585-1902A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380092 | |||||||
| chr20:21380163 | G | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0048 |
4 | HG02027.hp2 NA18963.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2585-1831G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380163 | |||||||
| chr20:21380228 | A | G | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-1766A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380228 | |||||||
| chr20:21380523 | T | C | 5 | a0001c0001t0002g0187 a0001c0001t0002g0189 a0001c0001t0002g0190 others(2): Show |
5 | HG01891.hp1 HG02976.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.2585-1471T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380523 | |||||||
| chr20:21380849 | G | C | 3 | a0001c0001t0002g0169 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG00099.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2585-1145G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380849 | |||||||
| chr20:21380990 | T | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0001g0252 |
3 | HG00280.hp2 HG00639.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2585-1004T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380990 | |||||||
| chr20:21380999 | G | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-995G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21380999 | |||||||
| chr20:21381046 | G | A | 3 | a0001c0001t0002g0169 a0001c0001t0002g0173 a0001c0001t0002g0174 |
3 | HG00099.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2585-948G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381046 | |||||||
| chr20:21381100 | TTTTC | T | 10 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(7): Show |
10 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.2585-890_2585-887d others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381100 | ||||||
| chr20:21381180 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2585-814G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381180 | |||||||
| chr20:21381262 | T | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-732T>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381262 | |||||||
| chr20:21381284 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2585-710C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381284 | |||||||
| chr20:21381324 | T | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-670T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381324 | |||||||
| chr20:21381424 | C | G | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2585-570C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381424 | |||||||
| chr20:21381466 | T | C | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2585-528T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381466 | |||||||
| chr20:21381713 | TACACAC | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2585-257_2585-252d others(8): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381713 | ||||||
| chr20:21381713 | TACACACA others(1): Show |
T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0066 a0001c0001t0001g0098 others(21): Show |
24 | HG00741.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.2585-259_2585-252d others(10): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381713 | ||||||
| chr20:21381713 | TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0180 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2585-261_2585-252d others(12): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr20 | 21381713 | ||||||
| chr20:21381815 | G | T | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2585-179G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381815 | |||||||
| chr20:21381861 | A | G | 5 | a0001c0001t0001g0098 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2585-133A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381861 | |||||||
| chr20:21381961 | A | C | 1 | a0001c0001t0002g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2585-33A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 27/29 | chr20 | 21381961 | |||||||
| chr20:21382065 | TA | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2648+12delA | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr20 | 21382065 | ||||||
| chr20:21382120 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2648+63T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382120 | |||||||
| chr20:21382125 | A | C | 2 | a0002c0003t0001g0085 a0002c0003t0001g0199 |
2 | HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2648+68A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382125 | |||||||
| chr20:21382183 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2648+126C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382183 | |||||||
| chr20:21382284 | A | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(38): Show |
42 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.2648+227A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382284 | |||||||
| chr20:21382323 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(37): Show |
41 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2648+266T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382323 | |||||||
| chr20:21382338 | G | A | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2648+281G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382338 | |||||||
| chr20:21382344 | G | C | 1 | a0001c0001t0001g0239 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2648+287G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382344 | |||||||
| chr20:21382440 | G | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(37): Show |
41 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2648+383G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382440 | |||||||
| chr20:21382797 | A | T | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2648+740A>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382797 | |||||||
| chr20:21382799 | T | G | 3 | a0001c0001t0002g0149 a0001c0001t0002g0162 a0001c0001t0002g0195 |
3 | HG00423.hp2 HG00438.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.2648+742T>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382799 | |||||||
| chr20:21382940 | C | A | 1 | a0001c0001t0003g0120 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2648+883C>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21382940 | |||||||
| chr20:21383017 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2648+960A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383017 | |||||||
| chr20:21383166 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2648+1109A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383166 | |||||||
| chr20:21383176 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2648+1119C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383176 | |||||||
| chr20:21383228 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2648+1171A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383228 | |||||||
| chr20:21383602 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2648+1545G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383602 | |||||||
| chr20:21383651 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2648+1594C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21383651 | |||||||
| chr20:21384281 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2648+2224A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384281 | |||||||
| chr20:21384325 | C | G | 63 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0002g0006 others(60): Show |
64 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.2648+2268C>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384325 | |||||||
| chr20:21384341 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(36): Show |
40 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.2648+2284C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384341 | |||||||
| chr20:21384423 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2648+2366A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384423 | |||||||
| chr20:21384742 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2649-2126C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384742 | |||||||
| chr20:21384774 | G | C | 1 | a0001c0004t0001g0105 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2649-2094G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384774 | |||||||
| chr20:21384825 | G | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(99): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2649-2043G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384825 | |||||||
| chr20:21384882 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2649-1986T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384882 | |||||||
| chr20:21384920 | G | A | 62 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2649-1948G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21384920 | |||||||
| chr20:21385396 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2649-1472T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385396 | |||||||
| chr20:21385622 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2649-1246T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385622 | |||||||
| chr20:21385639 | C | CAA | 62 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2649-1225_2649-122 others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr20 | 21385639 | ||||||
| chr20:21385775 | C | T | 1 | a0001c0002t0001g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2649-1093C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385775 | |||||||
| chr20:21385791 | A | G | 25 | a0001c0001t0002g0006 a0001c0001t0002g0142 a0001c0001t0002g0148 others(22): Show |
26 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2649-1077A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385791 | |||||||
| chr20:21385857 | A | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(11): Show |
15 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2649-1011A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385857 | |||||||
| chr20:21385869 | G | C | 1 | a0002c0003t0001g0199 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2649-999G>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21385869 | |||||||
| chr20:21386162 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2649-706C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386162 | |||||||
| chr20:21386195 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2649-673A>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386195 | |||||||
| chr20:21386803 | C | T | 1 | a0002c0003t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2649-65C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386803 | |||||||
| chr20:21386822 | G | A | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2649-46G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 28/29 | chr20 | 21386822 | |||||||
| chr20:21387103 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
37 | HG00323.hp2 HG00423.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.2787+97A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387103 | |||||||
| chr20:21387369 | AAAGT | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0001g0106 others(37): Show |
41 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.2787+368_2787+371d others(6): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr20 | 21387369 | ||||||
| chr20:21387502 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2787+496A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387502 | |||||||
| chr20:21387524 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2787+518G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387524 | |||||||
| chr20:21387948 | C | T | 25 | a0001c0001t0002g0006 a0001c0001t0002g0142 a0001c0001t0002g0148 others(22): Show |
26 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2787+942C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21387948 | |||||||
| chr20:21387955 | G | GAGT | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(248): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2787+950_2787+951i others(5): Show |
XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr20 | 21387955 | ||||||
| chr20:21388294 | G | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.2788-979G>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388294 | |||||||
| chr20:21388375 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2788-898G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388375 | |||||||
| chr20:21388670 | T | C | 62 | a0001c0001t0002g0006 a0001c0001t0002g0084 a0001c0001t0002g0118 others(59): Show |
63 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2788-603T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388670 | |||||||
| chr20:21388701 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0057 a0001c0001t0001g0058 |
3 | HG00673.hp1 NA18946.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2788-572A>G | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388701 | |||||||
| chr20:21388874 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2788-399T>C | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21388874 | |||||||
| chr20:21389023 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0106 a0001c0001t0001g0107 others(14): Show |
18 | HG00140.hp2 HG00735.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2788-250G>A | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21389023 | |||||||
| chr20:21389072 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2788-201C>T | XRN2 | ENSG00000088930.8 | transcript | ENST00000377191.5 | protein_coding | 29/29 | chr20 | 21389072 |