Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 63929 |
| ensemblid | ENSG00000196236.13 |
| hgncid | 28052 |
| symbol | XPNPEP3 |
| name | X-prolyl aminopeptidase 3 |
| refseq_nuc | NM_022098.4 |
| refseq_prot | NP_071381.1 |
| ensembl_nuc | ENST00000357137.9 |
| ensembl_prot | ENSP00000349658.4 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 40857148 |
| end | 40932815 |
| strand | + |
| ver | v1.2 |
| region | chr22:40857148-40932815 |
| region5000 | chr22:40852148-40937815 |
| regionname0 | XPNPEP3_chr22_40857148_40932815 |
| regionname5000 | XPNPEP3_chr22_40852148_40937815 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 507 | 246 | 82 | 40 | 84 | 10 | 28 | 61 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | MPWLL others(502): Show |
chr22 | 40852148 | 40937815 |
| a0002 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | MPWLL others(502): Show |
chr22 | 40852148 | 40937815 |
| a0003 | 0/0 | 507 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | MPWLL others(502): Show |
chr22 | 40852148 | 40937815 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1521 | 241 | 77 | 40 | 84 | 10 | 28 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | ATGCC others(1516): Show |
chr22 | 40852148 | 40937815 | ||
| a0001c0002 | 0/0 | 1521 | 4 | 4 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | ATGCC others(1516): Show |
chr22 | 40852148 | 40937815 | ||
| a0001c0005 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | ATGCC others(1516): Show |
chr22 | 40852148 | 40937815 | ||
| a0002c0003 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | ATGCC others(1516): Show |
chr22 | 40852148 | 40937815 | ||
| a0003c0004 | 0/0 | 1521 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | ATGCC others(1516): Show |
chr22 | 40852148 | 40937815 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7939 | 60 | 5 | 10 | 31 | 4 | 10 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0002 | 1/0 | 7938 | 55 | 12 | 16 | 12 | 4 | 10 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0003 | 0/0 | 7938 | 21 | 16 | 2 | 3 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0004 | 0/0 | 7937 | 15 | 0 | 0 | 15 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0005 | 0/0 | 7937 | 9 | 9 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0006 | 0/0 | 7940 | 7 | 1 | 2 | 3 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7935): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0007 | 0/0 | 7939 | 6 | 1 | 2 | 3 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0008 | 0/0 | 7936 | 6 | 4 | 2 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7931): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0009 | 0/0 | 7939 | 4 | 3 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0010 | 0/0 | 7938 | 4 | 0 | 0 | 4 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0011 | 0/0 | 7924 | 4 | 3 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7919): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0012 | 0/0 | 7938 | 3 | 1 | 1 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0013 | 0/0 | 7938 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0014 | 0/0 | 7939 | 3 | 1 | 0 | 0 | 0 | 2 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0015 | 0/0 | 7938 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0016 | 0/0 | 7938 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0017 | 0/0 | 7937 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0018 | 0/1 | 7938 | 2 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0019 | 0/0 | 7938 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0020 | 0/0 | 7938 | 2 | 0 | 0 | 0 | 0 | 2 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0021 | 0/0 | 7937 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0022 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0023 | 0/0 | 7938 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0024 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0025 | 0/0 | 7938 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0026 | 0/0 | 7941 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7936): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0027 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0028 | 0/0 | 7938 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0029 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0030 | 0/0 | 7938 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0031 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0032 | 0/0 | 7938 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0033 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0034 | 0/0 | 7939 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0035 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0036 | 0/0 | 7940 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7935): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0037 | 0/0 | 7939 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0038 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0039 | 0/0 | 7940 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7935): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0040 | 0/0 | 7940 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7935): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0041 | 0/0 | 7936 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7931): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0042 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0043 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0044 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0045 | 0/0 | 7939 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0047 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0049 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0001t0051 | 0/0 | 7939 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7934): Show |
chr22 | 40852148 | 40937815 |
| a0001c0002t0005 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0002t0046 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0002t0048 | 0/0 | 7937 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0001c0002t0050 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0001c0005t0003 | 0/0 | 7938 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7933): Show |
chr22 | 40852148 | 40937815 |
| a0002c0003t0004 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| a0003c0004t0004 | 0/0 | 7937 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | CTCTT others(7932): Show |
chr22 | 40852148 | 40937815 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0099 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0006g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0006g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0006g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0007g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0009g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0009g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0010g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0010g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0011g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0011g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0011g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0012g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0012g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0012g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0014g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0014g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0015g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0016g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0016g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0017g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0017g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0018g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0018g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0019g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0019g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0020g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0020g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0021g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0021g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0022g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0023g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0024g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0025g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0026g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0027g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0028g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0029g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0030g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0031g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0032g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0033g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0034g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0035g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0036g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0037g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0038g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0039g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0040g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0041g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0042g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0043g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0044g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0045g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0047g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0049g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0001t0051g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0002t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0002t0046g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0002t0048g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0002t0050g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0001c0005t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0002c0003t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| a0003c0004t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0012 | g0040 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0140 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0150 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0052 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00597 | hp1 | a0001 | c0001 | t0016 | g0008 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00609 | hp1 | a0001 | c0001 | t0010 | g0050 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0220 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01109 | hp2 | a0001 | c0001 | t0025 | g0171 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01192 | hp1 | a0001 | c0001 | t0007 | g0186 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0185 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01243 | hp2 | a0001 | c0001 | t0008 | g0168 | AMR | PUR | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01346 | hp2 | a0001 | c0001 | t0037 | g0034 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01433 | hp1 | a0001 | c0001 | t0012 | g0037 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0068 | AMR | CLM | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | IBS | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01884 | hp1 | a0001 | c0001 | t0035 | g0035 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01884 | hp2 | a0001 | c0002 | t0046 | g0212 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01934 | hp2 | a0001 | c0001 | t0009 | g0213 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0163 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02132 | hp1 | a0002 | c0003 | t0004 | g0046 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02257 | hp2 | a0001 | c0001 | t0024 | g0143 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0055 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0074 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02293 | hp2 | a0001 | c0001 | t0030 | g0117 | AMR | PEL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02451 | hp2 | a0001 | c0005 | t0003 | g0191 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0065 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02602 | hp2 | a0001 | c0001 | t0020 | g0142 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02622 | hp1 | a0001 | c0001 | t0008 | g0066 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0200 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02630 | hp1 | a0001 | c0002 | t0048 | g0209 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02683 | hp2 | a0001 | c0001 | t0014 | g0029 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0187 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0084 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02809 | hp1 | a0001 | c0001 | t0049 | g0204 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0215 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02886 | hp1 | a0001 | c0001 | t0022 | g0013 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02895 | hp2 | a0001 | c0001 | t0019 | g0014 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02897 | hp1 | a0001 | c0001 | t0019 | g0015 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02897 | hp2 | a0001 | c0001 | t0014 | g0016 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0127 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02976 | hp1 | a0001 | c0001 | t0013 | g0128 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02976 | hp2 | a0001 | c0001 | t0033 | g0058 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0221 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03098 | hp2 | a0001 | c0001 | t0047 | g0012 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0067 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | ESN | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0210 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03209 | hp2 | a0001 | c0001 | t0029 | g0217 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0199 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03453 | hp1 | a0001 | c0001 | t0021 | g0206 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03453 | hp2 | a0001 | c0001 | t0031 | g0172 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03486 | hp1 | a0001 | c0001 | t0021 | g0205 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03579 | hp1 | a0001 | c0001 | t0027 | g0223 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03579 | hp2 | a0001 | c0001 | t0017 | g0216 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03654 | hp2 | a0001 | c0001 | t0020 | g0184 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03669 | hp2 | a0001 | c0001 | t0034 | g0089 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03704 | hp2 | a0001 | c0001 | t0028 | g0141 | SAS | PJL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03831 | hp2 | a0001 | c0001 | t0026 | g0030 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | BEB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0219 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18906 | hp1 | a0001 | c0001 | t0045 | g0036 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18944 | hp1 | a0001 | c0001 | t0023 | g0087 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18975 | hp1 | a0001 | c0001 | t0036 | g0177 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18980 | hp1 | a0001 | c0001 | t0015 | g0120 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18994 | hp1 | a0003 | c0004 | t0004 | g0007 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18995 | hp1 | a0001 | c0001 | t0010 | g0164 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18995 | hp2 | a0001 | c0001 | t0038 | g0095 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA18997 | hp2 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19000 | hp2 | a0001 | c0001 | t0007 | g0230 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19009 | hp2 | a0001 | c0001 | t0044 | g0049 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19010 | hp1 | a0001 | c0001 | t0010 | g0190 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19030 | hp2 | a0001 | c0001 | t0040 | g0098 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19043 | hp1 | a0001 | c0002 | t0050 | g0208 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19054 | hp1 | a0001 | c0001 | t0042 | g0165 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19060 | hp1 | a0001 | c0001 | t0043 | g0001 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19060 | hp2 | a0001 | c0001 | t0051 | g0027 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19063 | hp2 | a0001 | c0001 | t0039 | g0166 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19065 | hp2 | a0001 | c0001 | t0015 | g0121 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0192 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19087 | hp1 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19087 | hp2 | a0001 | c0001 | t0041 | g0041 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0009 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19090 | hp2 | a0001 | c0001 | t0016 | g0045 | EAS | JPT | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0183 | AFR | YRI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ASW | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0201 | AFR | ASW | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20752 | hp2 | a0001 | c0001 | t0032 | g0039 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0138 | EUR | TSI | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | GIH | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | GIH | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG02559 | hp2 | a0001 | c0001 | t0012 | g0038 | AFR | ACB | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG03471 | hp2 | a0001 | c0001 | t0011 | g0222 | AFR | MSL | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0135 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0214 | AFR | USA | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA21309 | hp1 | a0001 | c0001 | t0017 | g0134 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | LWK | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0136 | REF | REF | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0099 | REF | REF | XPNPEP3_chr22_40852148_40937815 | XPNPEP3 | chr22 | 40852148 | 40937815 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40881790 | T | C | 1 | a0002 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.202T>C | p.Ser68Pro | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/10 | 236/7938 | 202/1524 | 68/507 | chr22 | 40881790 | |||
| chr22:40886424 | G | A | 1 | a0003 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.701G>A | p.Arg234Gln | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/10 | 735/7938 | 701/1524 | 234/507 | chr22 | 40886424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40857244 | A | G | 1 | a0001c0005 | 1 | HG02451.hp2 | splice_region_variant&synonymous_variant | LOW | c.63A>G | p.Ser21Ser | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/10 | 97/7938 | 63/1524 | 21/507 | chr22 | 40857244 | |||
| chr22:40869045 | A | G | 1 | a0001c0002 | 4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.111A>G | p.Pro37Pro | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/10 | 145/7938 | 111/1524 | 37/507 | chr22 | 40869045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40857159 | C | T | 1 | a0001c0001t0051 | 1 | NA19060.hp2 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/10 | 23 | chr22 | 40857159 | ||||||
| chr22:40926825 | A | G | 1 | a0001c0002t0050 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*390A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 390 | chr22 | 40926825 | ||||||
| chr22:40926902 | C | T | 8 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0047 others(5): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*467C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 467 | chr22 | 40926902 | ||||||
| chr22:40926966 | T | G | 1 | a0001c0001t0022 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 531 | chr22 | 40926966 | ||||||
| chr22:40927312 | A | G | 2 | a0001c0001t0011 a0001c0001t0045 |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*877A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 877 | chr22 | 40927312 | ||||||
| chr22:40927331 | G | C | 1 | a0001c0001t0023 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*896G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 896 | chr22 | 40927331 | ||||||
| chr22:40927485 | T | C | 1 | a0001c0002t0046 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1050T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1050 | chr22 | 40927485 | ||||||
| chr22:40927638 | G | A | 2 | a0001c0001t0021 a0001c0001t0047 |
3 | HG03098.hp2 HG03453.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1203G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1203 | chr22 | 40927638 | ||||||
| chr22:40927650 | G | A | 1 | a0001c0001t0047 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1215G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1215 | chr22 | 40927650 | ||||||
| chr22:40927651 | G | A | 1 | a0001c0001t0015 | 2 | NA18980.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1216G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1216 | chr22 | 40927651 | ||||||
| chr22:40927670 | T | C | 1 | a0001c0001t0015 | 2 | NA18980.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1235T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1235 | chr22 | 40927670 | ||||||
| chr22:40927671 | G | A | 1 | a0001c0001t0015 | 2 | NA18980.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1236G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1236 | chr22 | 40927671 | ||||||
| chr22:40927874 | C | CA | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0016 others(4): Show |
19 | HG00597.hp1 HG00597.hp2 HG01106.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1457dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1458 | INFO_REALIGN_3_PRIME | chr22 | 40927874 | |||||
| chr22:40927874 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0011 | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1445_*1457delAAAA others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1445 | INFO_REALIGN_3_PRIME | chr22 | 40927874 | |||||
| chr22:40927887 | A | G | 1 | a0001c0001t0020 | 2 | HG02602.hp2 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1452A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1452 | chr22 | 40927887 | ||||||
| chr22:40927966 | A | G | 1 | a0001c0001t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1531A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1531 | chr22 | 40927966 | ||||||
| chr22:40928041 | GC | G | 10 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(7): Show |
33 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1607delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1607 | chr22 | 40928041 | ||||||
| chr22:40928201 | C | CT | 13 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0010 others(10): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1784dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1785 | INFO_REALIGN_3_PRIME | chr22 | 40928201 | |||||
| chr22:40928201 | CT | C | 11 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0021 others(8): Show |
23 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1784delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 1784 | INFO_REALIGN_3_PRIME | chr22 | 40928201 | |||||
| chr22:40928683 | A | G | 1 | a0001c0001t0033 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2248A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2248 | chr22 | 40928683 | ||||||
| chr22:40929046 | G | T | 2 | a0001c0001t0019 a0001c0001t0022 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2611G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2611 | chr22 | 40929046 | ||||||
| chr22:40929064 | G | A | 43 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(40): Show |
170 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*2629G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2629 | chr22 | 40929064 | ||||||
| chr22:40929192 | C | CT | 4 | a0001c0001t0019 a0001c0001t0022 a0001c0001t0040 others(1): Show |
5 | HG02886.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2774dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2775 | INFO_REALIGN_3_PRIME | chr22 | 40929192 | |||||
| chr22:40929197 | T | C | 1 | a0001c0001t0013 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2762T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2762 | chr22 | 40929197 | ||||||
| chr22:40929316 | C | G | 8 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0047 others(5): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2881C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2881 | chr22 | 40929316 | ||||||
| chr22:40929393 | G | A | 10 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0021 others(7): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2958G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2958 | chr22 | 40929393 | ||||||
| chr22:40929413 | G | A | 8 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0047 others(5): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2978G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 2978 | chr22 | 40929413 | ||||||
| chr22:40929438 | G | A | 1 | a0001c0001t0008 | 6 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3003G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3003 | chr22 | 40929438 | ||||||
| chr22:40929562 | A | G | 1 | a0001c0002t0046 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3127A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3127 | chr22 | 40929562 | ||||||
| chr22:40929572 | C | G | 10 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0021 others(7): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3137C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3137 | chr22 | 40929572 | ||||||
| chr22:40929611 | T | C | 1 | a0001c0001t0042 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3176T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3176 | chr22 | 40929611 | ||||||
| chr22:40929755 | T | G | 1 | a0001c0001t0043 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3320T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3320 | chr22 | 40929755 | ||||||
| chr22:40929767 | G | A | 1 | a0001c0001t0034 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3332G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3332 | chr22 | 40929767 | ||||||
| chr22:40929786 | C | T | 2 | a0001c0001t0012 a0001c0001t0032 |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3351C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3351 | chr22 | 40929786 | ||||||
| chr22:40929801 | C | T | 10 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0021 others(7): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3366C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3366 | chr22 | 40929801 | ||||||
| chr22:40929846 | T | C | 4 | a0001c0001t0009 a0001c0001t0019 a0001c0001t0022 others(1): Show |
8 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3411T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3411 | chr22 | 40929846 | ||||||
| chr22:40930125 | G | T | 9 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0021 others(6): Show |
21 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3690G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3690 | chr22 | 40930125 | ||||||
| chr22:40930133 | G | GT | 4 | a0001c0001t0011 a0001c0001t0026 a0001c0001t0028 others(1): Show |
7 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3712dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3713 | INFO_REALIGN_3_PRIME | chr22 | 40930133 | |||||
| chr22:40930240 | C | T | 1 | a0001c0001t0038 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3805C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3805 | chr22 | 40930240 | ||||||
| chr22:40930390 | A | G | 2 | a0001c0001t0019 a0001c0001t0022 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3955A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 3955 | chr22 | 40930390 | ||||||
| chr22:40930797 | C | G | 9 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0021 others(6): Show |
21 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4362C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4362 | chr22 | 40930797 | ||||||
| chr22:40930965 | C | T | 2 | a0001c0001t0025 a0001c0001t0031 |
2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4530C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4530 | chr22 | 40930965 | ||||||
| chr22:40930996 | G | A | 2 | a0001c0001t0012 a0001c0001t0032 |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4561G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4561 | chr22 | 40930996 | ||||||
| chr22:40931021 | G | A | 8 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0047 others(5): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4586G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4586 | chr22 | 40931021 | ||||||
| chr22:40931137 | G | A | 11 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0010 others(8): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4702G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 4702 | chr22 | 40931137 | ||||||
| chr22:40931806 | T | C | 1 | a0001c0001t0044 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5371T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5371 | chr22 | 40931806 | ||||||
| chr22:40931880 | G | A | 1 | a0001c0001t0027 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5445G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5445 | chr22 | 40931880 | ||||||
| chr22:40931962 | A | G | 1 | a0001c0001t0037 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5527A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5527 | chr22 | 40931962 | ||||||
| chr22:40931982 | C | G | 1 | a0001c0001t0018 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5547C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5547 | chr22 | 40931982 | ||||||
| chr22:40932049 | C | A | 1 | a0001c0002t0048 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5614C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5614 | chr22 | 40932049 | ||||||
| chr22:40932078 | C | G | 1 | a0001c0001t0011 | 4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5643C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5643 | chr22 | 40932078 | ||||||
| chr22:40932204 | T | A | 1 | a0001c0001t0049 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5769T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5769 | chr22 | 40932204 | ||||||
| chr22:40932206 | C | A | 1 | a0001c0001t0049 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5771C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5771 | chr22 | 40932206 | ||||||
| chr22:40932337 | G | GT | 3 | a0001c0001t0009 a0001c0001t0036 a0001c0001t0045 |
6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5915dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5916 | INFO_REALIGN_3_PRIME | chr22 | 40932337 | |||||
| chr22:40932337 | GT | G | 8 | a0001c0001t0008 a0001c0001t0011 a0001c0001t0017 others(5): Show |
18 | HG00639.hp2 HG01109.hp2 HG01243.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5915delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5915 | INFO_REALIGN_3_PRIME | chr22 | 40932337 | |||||
| chr22:40932350 | T | A | 1 | a0001c0001t0030 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5915T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 5915 | chr22 | 40932350 | ||||||
| chr22:40932490 | A | C | 1 | a0001c0001t0013 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6055A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 6055 | chr22 | 40932490 | ||||||
| chr22:40932614 | G | A | 2 | a0001c0001t0025 a0001c0001t0031 |
2 | HG01109.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6179G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 6179 | chr22 | 40932614 | ||||||
| chr22:40932636 | A | T | 8 | a0001c0001t0005 a0001c0001t0021 a0001c0001t0047 others(5): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*6201A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 10/10 | 6201 | chr22 | 40932636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:40857280 | G | T | 1 | a0001c0001t0005g0233 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.64+35G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857280 | |||||||
| chr22:40857362 | C | T | 2 | a0001c0001t0002g0004 a0001c0001t0002g0232 |
4 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+117C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857362 | |||||||
| chr22:40857708 | C | G | 1 | a0001c0001t0002g0231 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.64+463C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857708 | |||||||
| chr22:40857811 | A | C | 8 | a0001c0001t0002g0011 a0001c0001t0002g0225 a0001c0001t0002g0226 others(5): Show |
9 | NA18949.hp1 NA18969.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+566A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857811 | |||||||
| chr22:40857818 | C | A | 1 | a0001c0001t0047g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64+573C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40857818 | |||||||
| chr22:40858242 | G | C | 3 | a0001c0001t0019g0014 a0001c0001t0019g0015 a0001c0001t0022g0013 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.64+997G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858242 | |||||||
| chr22:40858293 | A | G | 31 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(28): Show |
31 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.64+1048A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858293 | |||||||
| chr22:40858303 | TGCCACGT others(2): Show |
T | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+1063_64+1071del others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858303 | ||||||
| chr22:40858373 | C | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+1128C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858373 | |||||||
| chr22:40858522 | C | CT | 21 | a0001c0001t0001g0178 a0001c0001t0002g0179 a0001c0001t0002g0180 others(18): Show |
23 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+1301dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | ||||||
| chr22:40858522 | C | CTT | 5 | a0001c0001t0002g0193 a0001c0001t0003g0194 a0001c0001t0003g0195 others(2): Show |
5 | HG02572.hp1 HG02630.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+1300_64+1301dup others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | ||||||
| chr22:40858522 | CT | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0018 others(64): Show |
70 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.64+1301delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | ||||||
| chr22:40858522 | CTT | C | 13 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(10): Show |
13 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+1300_64+1301del others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40858522 | ||||||
| chr22:40858546 | T | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0008g0065 others(3): Show |
6 | HG00733.hp1 HG01496.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1301T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858546 | |||||||
| chr22:40858646 | C | T | 1 | a0001c0001t0047g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.64+1401C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858646 | |||||||
| chr22:40858980 | G | T | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | NA18967.hp1 NA18968.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+1735G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40858980 | |||||||
| chr22:40859030 | A | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1785A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859030 | |||||||
| chr22:40859159 | G | A | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+1914G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859159 | |||||||
| chr22:40859233 | G | A | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.64+1988G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859233 | |||||||
| chr22:40859386 | A | T | 2 | a0001c0001t0025g0171 a0001c0001t0031g0172 |
2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.64+2141A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859386 | |||||||
| chr22:40859557 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64+2312A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859557 | |||||||
| chr22:40859667 | A | G | 15 | a0001c0001t0003g0003 a0001c0001t0003g0055 a0001c0001t0003g0056 others(12): Show |
17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+2422A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859667 | |||||||
| chr22:40859741 | C | T | 1 | a0001c0001t0005g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.64+2496C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859741 | |||||||
| chr22:40859815 | G | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0055 a0001c0001t0003g0056 others(12): Show |
17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+2570G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859815 | |||||||
| chr22:40859957 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG01515.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.64+2712G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40859957 | |||||||
| chr22:40860157 | A | C | 2 | a0001c0001t0025g0171 a0001c0001t0031g0172 |
2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.64+2912A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860157 | |||||||
| chr22:40860181 | A | G | 1 | a0001c0001t0008g0168 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.64+2936A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860181 | |||||||
| chr22:40860363 | C | T | 32 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(29): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.64+3118C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860363 | |||||||
| chr22:40860656 | CT | C | 7 | a0001c0001t0001g0002 a0001c0001t0005g0207 a0001c0001t0011g0219 others(4): Show |
9 | HG00639.hp2 HG03041.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.64+3425delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40860656 | ||||||
| chr22:40860676 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.64+3431A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860676 | |||||||
| chr22:40860708 | A | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+3463A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860708 | |||||||
| chr22:40860798 | A | G | 158 | a0001c0001t0001g0144 a0001c0001t0002g0004 a0001c0001t0002g0010 others(155): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.64+3553A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860798 | |||||||
| chr22:40860879 | C | G | 1 | a0001c0001t0005g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64+3634C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40860879 | |||||||
| chr22:40861047 | T | C | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.64+3802T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861047 | |||||||
| chr22:40861209 | G | A | 5 | a0001c0001t0002g0113 a0001c0001t0009g0213 a0001c0001t0009g0214 others(2): Show |
5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+3964G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861209 | |||||||
| chr22:40861389 | C | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG00733.hp1 HG01109.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.64+4144C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861389 | |||||||
| chr22:40861616 | A | C | 4 | a0001c0001t0005g0207 a0001c0001t0021g0205 a0001c0001t0021g0206 others(1): Show |
4 | HG03098.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+4371A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861616 | |||||||
| chr22:40861655 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.64+4410C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861655 | |||||||
| chr22:40861735 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.64+4490C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861735 | |||||||
| chr22:40861830 | T | TA | 7 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0118 others(4): Show |
7 | HG00423.hp1 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+4586dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40861830 | ||||||
| chr22:40861873 | T | G | 14 | a0001c0001t0002g0011 a0001c0001t0002g0114 a0001c0001t0002g0119 others(11): Show |
15 | HG01167.hp1 HG04228.hp1 NA18949.hp1 others(12): Show |
intron_variant | MODIFIER | c.64+4628T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40861873 | |||||||
| chr22:40862140 | A | G | 68 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(65): Show |
70 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.64+4895A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862140 | |||||||
| chr22:40862404 | G | A | 6 | a0001c0001t0008g0065 a0001c0001t0008g0066 a0001c0001t0008g0067 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+5159G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862404 | |||||||
| chr22:40862427 | C | G | 2 | a0001c0001t0015g0120 a0001c0001t0015g0121 |
2 | NA18980.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.64+5182C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862427 | |||||||
| chr22:40862657 | T | C | 7 | a0001c0001t0004g0001 a0001c0001t0004g0042 a0001c0001t0010g0164 others(4): Show |
8 | NA18949.hp2 NA18960.hp1 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+5412T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40862657 | |||||||
| chr22:40862673 | GC | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+5430delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40862673 | ||||||
| chr22:40863619 | A | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-5380A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40863619 | |||||||
| chr22:40864133 | G | C | 4 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(1): Show |
4 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-4866G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864133 | |||||||
| chr22:40864420 | A | G | 2 | a0001c0001t0025g0171 a0001c0001t0031g0172 |
2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.65-4579A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864420 | |||||||
| chr22:40864701 | T | C | 1 | a0001c0001t0037g0034 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.65-4298T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864701 | |||||||
| chr22:40864708 | G | A | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-4291G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864708 | |||||||
| chr22:40864822 | T | A | 1 | a0001c0001t0002g0122 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.65-4177T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864822 | |||||||
| chr22:40864842 | C | G | 5 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(2): Show |
5 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-4157C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864842 | |||||||
| chr22:40864927 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.65-4072C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864927 | |||||||
| chr22:40864989 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.65-4010C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40864989 | |||||||
| chr22:40865005 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.65-3994A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865005 | |||||||
| chr22:40865311 | G | A | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.65-3688G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865311 | |||||||
| chr22:40865325 | CT | C | 134 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0033 others(131): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.65-3654delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40865325 | ||||||
| chr22:40865325 | CTT | C | 33 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0126 others(30): Show |
33 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.65-3655_65-3654del others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40865325 | ||||||
| chr22:40865555 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.65-3444C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865555 | |||||||
| chr22:40865699 | G | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.65-3300G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865699 | |||||||
| chr22:40865742 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.65-3257G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865742 | |||||||
| chr22:40865743 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.65-3256C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865743 | |||||||
| chr22:40865815 | A | G | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-3184A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40865815 | |||||||
| chr22:40866099 | A | G | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-2900A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866099 | |||||||
| chr22:40866123 | A | T | 6 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0108 others(3): Show |
6 | HG00639.hp1 HG01515.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-2876A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866123 | |||||||
| chr22:40866149 | T | C | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-2850T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866149 | |||||||
| chr22:40866353 | G | A | 6 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(3): Show |
6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-2646G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866353 | |||||||
| chr22:40866460 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-2539C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866460 | |||||||
| chr22:40866575 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.65-2424A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866575 | |||||||
| chr22:40866644 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.65-2355A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866644 | |||||||
| chr22:40866847 | G | A | 1 | a0001c0001t0010g0164 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.65-2152G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866847 | |||||||
| chr22:40866848 | C | T | 21 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0124 others(18): Show |
24 | HG00140.hp1 HG00733.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.65-2151C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866848 | |||||||
| chr22:40866947 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-2052C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866947 | |||||||
| chr22:40866994 | G | A | 4 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(1): Show |
4 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-2005G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40866994 | |||||||
| chr22:40867363 | A | G | 2 | a0001c0001t0025g0171 a0001c0001t0031g0172 |
2 | HG01109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.65-1636A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867363 | |||||||
| chr22:40867368 | C | T | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-1631C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867368 | |||||||
| chr22:40867419 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.65-1580A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867419 | |||||||
| chr22:40867769 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0077 |
4 | HG00544.hp2 NA18964.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1230T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40867769 | |||||||
| chr22:40867936 | C | CA | 17 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0112 others(14): Show |
17 | HG00438.hp2 HG00639.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.65-1045dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40867936 | ||||||
| chr22:40867936 | CA | C | 15 | a0001c0001t0002g0126 a0001c0001t0005g0198 a0001c0001t0005g0199 others(12): Show |
15 | HG01167.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-1045delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40867936 | ||||||
| chr22:40868139 | T | G | 3 | a0001c0001t0013g0127 a0001c0001t0013g0128 a0001c0001t0013g0183 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.65-860T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868139 | |||||||
| chr22:40868428 | C | CGT | 52 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0003g0197 others(49): Show |
54 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.65-546_65-545dupGT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868428 | ||||||
| chr22:40868428 | C | CGTGT | 3 | a0001c0001t0003g0031 a0001c0001t0011g0221 a0001c0001t0011g0222 |
3 | HG01981.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.65-548_65-545dupGT others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868428 | ||||||
| chr22:40868428 | CGT | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0022 others(10): Show |
14 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.65-546_65-545delGT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868428 | ||||||
| chr22:40868446 | T | TGA | 9 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.65-552_65-551insAG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | 40868446 | ||||||
| chr22:40868537 | T | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.65-462T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868537 | |||||||
| chr22:40868658 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | NA18961.hp1 NA19054.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-341C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868658 | |||||||
| chr22:40868705 | A | G | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.65-294A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 1/9 | chr22 | 40868705 | |||||||
| chr22:40869139 | C | T | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.181+24C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869139 | |||||||
| chr22:40869331 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.181+216T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869331 | |||||||
| chr22:40869770 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.181+655T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869770 | |||||||
| chr22:40869816 | G | A | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+701G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869816 | |||||||
| chr22:40869896 | A | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.181+781A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869896 | |||||||
| chr22:40869999 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.181+884T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40869999 | |||||||
| chr22:40870406 | A | G | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181+1291A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40870406 | |||||||
| chr22:40870526 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0007g0186 |
2 | HG01192.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.181+1411A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40870526 | |||||||
| chr22:40870968 | G | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0194 a0001c0001t0003g0195 |
5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.181+1853G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40870968 | |||||||
| chr22:40871034 | A | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.181+1919A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871034 | |||||||
| chr22:40871058 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.181+1943T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871058 | |||||||
| chr22:40871360 | C | A | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+2245C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871360 | |||||||
| chr22:40871665 | G | C | 2 | a0001c0001t0003g0061 a0001c0001t0003g0062 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.181+2550G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40871665 | |||||||
| chr22:40872215 | G | T | 2 | a0001c0002t0005g0210 a0001c0002t0048g0209 |
2 | HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.181+3100G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872215 | |||||||
| chr22:40872489 | C | T | 18 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(15): Show |
18 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.181+3374C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872489 | |||||||
| chr22:40872611 | C | T | 2 | a0001c0001t0002g0116 a0001c0001t0002g0118 |
2 | HG01934.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.181+3496C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872611 | |||||||
| chr22:40872921 | T | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0017 others(178): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.181+3806T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872921 | |||||||
| chr22:40872980 | G | A | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.181+3865G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40872980 | |||||||
| chr22:40873098 | C | CT | 13 | a0001c0001t0001g0032 a0001c0001t0001g0102 a0001c0001t0001g0178 others(10): Show |
13 | HG00423.hp2 HG01192.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.181+4008dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40873098 | ||||||
| chr22:40873098 | CT | C | 42 | a0001c0001t0001g0017 a0001c0001t0001g0063 a0001c0001t0001g0071 others(39): Show |
44 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.181+4008delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40873098 | ||||||
| chr22:40873098 | CTT | C | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG01884.hp2 HG01934.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.181+4007_181+4008d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40873098 | ||||||
| chr22:40873103 | T | C | 3 | a0001c0001t0005g0202 a0001c0001t0005g0203 a0001c0001t0049g0204 |
3 | HG02109.hp1 HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.181+3988T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873103 | |||||||
| chr22:40873104 | T | C | 14 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(11): Show |
14 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.181+3989T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873104 | |||||||
| chr22:40873208 | A | G | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.181+4093A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873208 | |||||||
| chr22:40873877 | A | G | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.181+4762A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873877 | |||||||
| chr22:40873924 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.181+4809A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40873924 | |||||||
| chr22:40874164 | A | G | 1 | a0001c0001t0003g0083 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.181+5049A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874164 | |||||||
| chr22:40874421 | G | GTGTTTT | 29 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(26): Show |
29 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.181+5320_181+5325d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40874421 | ||||||
| chr22:40874435 | G | GT | 32 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(29): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.181+5328dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40874435 | ||||||
| chr22:40874518 | G | T | 29 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(26): Show |
29 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.181+5403G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874518 | |||||||
| chr22:40874632 | C | T | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+5517C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874632 | |||||||
| chr22:40874713 | A | G | 1 | a0001c0001t0005g0201 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.181+5598A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874713 | |||||||
| chr22:40874726 | G | A | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.181+5611G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874726 | |||||||
| chr22:40874960 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.181+5845A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40874960 | |||||||
| chr22:40875144 | C | A | 1 | a0001c0001t0002g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.181+6029C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875144 | |||||||
| chr22:40875229 | G | T | 1 | a0001c0001t0022g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.181+6114G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875229 | |||||||
| chr22:40875273 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.181+6158G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875273 | |||||||
| chr22:40875663 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.182-6107T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875663 | |||||||
| chr22:40875850 | T | TA | 6 | a0001c0001t0001g0102 a0001c0001t0001g0174 a0001c0001t0002g0130 others(3): Show |
6 | HG02027.hp1 HG03654.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.182-5900dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40875850 | ||||||
| chr22:40875850 | TA | T | 30 | a0001c0001t0004g0051 a0001c0001t0005g0198 a0001c0001t0005g0199 others(27): Show |
30 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.182-5900delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40875850 | ||||||
| chr22:40875931 | A | G | 5 | a0001c0001t0002g0154 a0001c0001t0002g0157 a0001c0001t0002g0158 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.182-5839A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40875931 | |||||||
| chr22:40876072 | T | G | 1 | a0001c0001t0002g0119 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.182-5698T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876072 | |||||||
| chr22:40876139 | T | C | 154 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0011 others(151): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.182-5631T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876139 | |||||||
| chr22:40876260 | T | G | 1 | a0001c0001t0004g0044 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.182-5510T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876260 | |||||||
| chr22:40876411 | C | T | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.182-5359C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876411 | |||||||
| chr22:40876556 | TAGTGAAT others(104): Show |
T | 1 | a0001c0001t0001g0071 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.182-5139_182-5029d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40876556 | ||||||
| chr22:40876585 | C | T | 1 | a0001c0001t0014g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.182-5185C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876585 | |||||||
| chr22:40876879 | T | A | 2 | a0001c0001t0003g0086 a0001c0001t0023g0087 |
2 | NA18942.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.182-4891T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40876879 | |||||||
| chr22:40877194 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | NA18961.hp1 NA19054.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-4576C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877194 | |||||||
| chr22:40877219 | C | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-4551C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877219 | |||||||
| chr22:40877350 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.182-4420A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877350 | |||||||
| chr22:40877356 | C | T | 3 | a0001c0001t0010g0164 a0001c0001t0010g0190 a0001c0001t0042g0165 |
3 | NA18995.hp1 NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.182-4414C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877356 | |||||||
| chr22:40877717 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.182-4053T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877717 | |||||||
| chr22:40877762 | A | G | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.182-4008A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877762 | |||||||
| chr22:40877926 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.182-3844T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877926 | |||||||
| chr22:40877979 | G | A | 1 | a0001c0001t0006g0081 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.182-3791G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40877979 | |||||||
| chr22:40878137 | C | T | 1 | a0001c0001t0006g0084 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.182-3633C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40878137 | |||||||
| chr22:40878206 | C | CA | 20 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(17): Show |
20 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.182-3547dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40878206 | ||||||
| chr22:40878388 | CAT | C | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-3380_182-3379d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40878388 | ||||||
| chr22:40878523 | CAT | C | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-3245_182-3244d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40878523 | ||||||
| chr22:40878840 | G | A | 1 | a0001c0001t0017g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.182-2930G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40878840 | |||||||
| chr22:40879120 | A | C | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2650A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40879120 | |||||||
| chr22:40879241 | T | C | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-2529T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40879241 | |||||||
| chr22:40879255 | C | G | 3 | a0001c0001t0013g0127 a0001c0001t0013g0128 a0001c0001t0013g0183 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.182-2515C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40879255 | |||||||
| chr22:40880028 | C | CA | 22 | a0001c0001t0001g0022 a0001c0001t0001g0088 a0001c0001t0001g0174 others(19): Show |
22 | HG00639.hp2 HG01192.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.182-1720dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40880028 | ||||||
| chr22:40880117 | G | A | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.182-1653G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880117 | |||||||
| chr22:40880264 | AG | A | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1505delG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880264 | |||||||
| chr22:40880267 | T | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1503T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880267 | |||||||
| chr22:40880268 | A | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1502A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880268 | |||||||
| chr22:40880271 | G | A | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1499G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880271 | |||||||
| chr22:40880273 | C | T | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1497C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880273 | |||||||
| chr22:40880657 | G | A | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-1113G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880657 | |||||||
| chr22:40880712 | C | T | 4 | a0001c0001t0005g0207 a0001c0001t0021g0205 a0001c0001t0021g0206 others(1): Show |
4 | HG03098.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.182-1058C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880712 | |||||||
| chr22:40880772 | A | T | 32 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(29): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.182-998A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880772 | |||||||
| chr22:40880784 | T | A | 1 | a0001c0001t0002g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.182-986T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880784 | |||||||
| chr22:40880787 | C | CA | 24 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0088 others(21): Show |
26 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.182-966dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40880787 | ||||||
| chr22:40880787 | CA | C | 12 | a0001c0001t0002g0125 a0001c0001t0009g0215 a0001c0001t0011g0219 others(9): Show |
12 | HG00639.hp2 HG02809.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.182-966delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40880787 | ||||||
| chr22:40880956 | G | A | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.182-814G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40880956 | |||||||
| chr22:40881162 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.182-608C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40881162 | |||||||
| chr22:40881170 | C | G | 1 | a0001c0001t0004g0042 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.182-600C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | chr22 | 40881170 | |||||||
| chr22:40881456 | C | CA | 15 | a0001c0001t0001g0025 a0001c0001t0002g0124 a0001c0001t0002g0126 others(12): Show |
15 | HG00140.hp1 HG00733.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.182-298dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40881456 | ||||||
| chr22:40881456 | CA | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0002g0125 others(34): Show |
37 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(34): Show |
intron_variant | MODIFIER | c.182-298delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr22 | 40881456 | ||||||
| chr22:40882243 | A | C | 9 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.589+66A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882243 | |||||||
| chr22:40882322 | C | T | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.589+145C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882322 | |||||||
| chr22:40882491 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.589+314G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882491 | |||||||
| chr22:40882503 | C | A | 4 | a0001c0001t0002g0130 a0001c0001t0002g0133 a0001c0001t0002g0156 others(1): Show |
4 | HG01361.hp1 HG02027.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+326C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882503 | |||||||
| chr22:40882527 | C | T | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.589+350C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882527 | |||||||
| chr22:40882634 | T | TA | 31 | a0001c0001t0003g0003 a0001c0001t0003g0055 a0001c0001t0003g0056 others(28): Show |
33 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.589+470dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 40882634 | ||||||
| chr22:40882752 | T | A | 9 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.589+575T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882752 | |||||||
| chr22:40882971 | C | A | 1 | a0001c0001t0013g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.589+794C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40882971 | |||||||
| chr22:40883598 | G | A | 3 | a0001c0001t0019g0014 a0001c0001t0019g0015 a0001c0001t0022g0013 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.589+1421G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40883598 | |||||||
| chr22:40883665 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.589+1488G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40883665 | |||||||
| chr22:40883904 | G | T | 9 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.589+1727G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40883904 | |||||||
| chr22:40884494 | G | A | 1 | a0001c0001t0022g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.590-1819G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884494 | |||||||
| chr22:40884722 | C | G | 1 | a0001c0001t0012g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.590-1591C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884722 | |||||||
| chr22:40884855 | G | A | 4 | a0001c0002t0005g0210 a0001c0002t0046g0212 a0001c0002t0048g0209 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-1458G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884855 | |||||||
| chr22:40884889 | G | A | 2 | a0001c0001t0002g0004 a0001c0001t0002g0232 |
4 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.590-1424G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884889 | |||||||
| chr22:40884963 | G | A | 6 | a0001c0001t0008g0065 a0001c0001t0008g0066 a0001c0001t0008g0067 others(3): Show |
6 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-1350G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40884963 | |||||||
| chr22:40885091 | A | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.590-1222A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885091 | |||||||
| chr22:40885418 | A | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-895A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885418 | |||||||
| chr22:40885588 | A | T | 1 | a0001c0001t0006g0021 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.590-725A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885588 | |||||||
| chr22:40885647 | C | T | 6 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(3): Show |
6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-666C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885647 | |||||||
| chr22:40885760 | G | A | 2 | a0001c0001t0017g0134 a0001c0001t0024g0143 |
2 | HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.590-553G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885760 | |||||||
| chr22:40885880 | G | T | 9 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.590-433G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885880 | |||||||
| chr22:40885977 | A | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-336A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40885977 | |||||||
| chr22:40885987 | TAAAG | T | 4 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0161 others(1): Show |
4 | HG02015.hp2 NA18747.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-324_590-321del others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr22 | 40885987 | ||||||
| chr22:40886043 | C | A | 5 | a0001c0001t0002g0115 a0001c0001t0002g0179 a0001c0001t0002g0180 others(2): Show |
5 | HG00423.hp1 HG00735.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.590-270C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886043 | |||||||
| chr22:40886061 | C | G | 1 | a0001c0001t0001g0100 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.590-252C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886061 | |||||||
| chr22:40886246 | T | C | 1 | a0001c0001t0003g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.590-67T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886246 | |||||||
| chr22:40886304 | C | T | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.590-9C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886304 | |||||||
| chr22:40886305 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.590-8A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 3/9 | chr22 | 40886305 | |||||||
| chr22:40886588 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.792+73G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886588 | |||||||
| chr22:40886783 | G | T | 32 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(29): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.792+268G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886783 | |||||||
| chr22:40886826 | C | CA | 17 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0024 others(14): Show |
17 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+328dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40886826 | ||||||
| chr22:40886826 | CA | C | 29 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(26): Show |
29 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(26): Show |
intron_variant | MODIFIER | c.792+328delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40886826 | ||||||
| chr22:40886902 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG00733.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.792+387A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886902 | |||||||
| chr22:40886974 | A | G | 9 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(6): Show |
9 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+459A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40886974 | |||||||
| chr22:40887197 | G | C | 6 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(3): Show |
6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+682G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887197 | |||||||
| chr22:40887480 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0014g0016 |
2 | HG02559.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.792+965C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887480 | |||||||
| chr22:40887705 | C | A | 31 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(28): Show |
31 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.792+1190C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887705 | |||||||
| chr22:40887747 | G | C | 1 | a0001c0001t0018g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.792+1232G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887747 | |||||||
| chr22:40887845 | CT | C | 9 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(6): Show |
9 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+1331delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887845 | |||||||
| chr22:40887980 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(162): Show |
172 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.792+1465G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40887980 | |||||||
| chr22:40888000 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.792+1485A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888000 | |||||||
| chr22:40888005 | A | G | 1 | a0001c0001t0005g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.792+1490A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888005 | |||||||
| chr22:40888042 | G | A | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+1527G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888042 | |||||||
| chr22:40888531 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.792+2016G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888531 | |||||||
| chr22:40888636 | CT | C | 13 | a0001c0001t0005g0207 a0001c0001t0009g0213 a0001c0001t0009g0214 others(10): Show |
13 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.792+2135delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40888636 | ||||||
| chr22:40888832 | C | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0125 a0001c0001t0002g0151 others(2): Show |
6 | HG01433.hp2 HG02280.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+2317C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888832 | |||||||
| chr22:40888864 | C | G | 3 | a0001c0001t0011g0220 a0001c0001t0011g0221 a0001c0001t0011g0222 |
3 | HG00639.hp2 HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.792+2349C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40888864 | |||||||
| chr22:40889014 | T | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(29): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.792+2499T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889014 | |||||||
| chr22:40889192 | G | GGCTCAT | 31 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(28): Show |
31 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(28): Show |
intron_variant | MODIFIER | c.792+2677_792+2678i others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889192 | |||||||
| chr22:40889555 | T | C | 1 | a0001c0001t0014g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.792+3040T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889555 | |||||||
| chr22:40889938 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.792+3423G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40889938 | |||||||
| chr22:40890163 | T | C | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+3648T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890163 | |||||||
| chr22:40890187 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.792+3672A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890187 | |||||||
| chr22:40890392 | A | T | 1 | a0001c0001t0024g0143 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.792+3877A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890392 | |||||||
| chr22:40890413 | G | GTGGT | 5 | a0001c0001t0001g0032 a0001c0001t0001g0097 a0001c0001t0014g0016 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+3899_792+3902d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40890413 | ||||||
| chr22:40890740 | ACCTGTAG others(486): Show |
A | 1 | a0001c0001t0006g0192 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.792+4244_792+4736d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40890740 | ||||||
| chr22:40890972 | G | A | 6 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(3): Show |
6 | HG02622.hp2 HG02886.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+4457G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40890972 | |||||||
| chr22:40891179 | C | CA | 15 | a0001c0001t0001g0077 a0001c0001t0001g0102 a0001c0001t0001g0178 others(12): Show |
15 | HG00423.hp2 HG00544.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.792+4687dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40891179 | ||||||
| chr22:40891179 | CA | C | 13 | a0001c0001t0001g0069 a0001c0001t0001g0112 a0001c0001t0002g0115 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(10): Show |
intron_variant | MODIFIER | c.792+4687delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40891179 | ||||||
| chr22:40891264 | A | T | 1 | a0001c0001t0002g0122 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.792+4749A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40891264 | |||||||
| chr22:40891514 | G | A | 1 | a0001c0001t0010g0043 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.792+4999G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40891514 | |||||||
| chr22:40891532 | A | G | 2 | a0001c0001t0005g0211 a0001c0001t0005g0233 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.792+5017A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40891532 | |||||||
| chr22:40892006 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.792+5491C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892006 | |||||||
| chr22:40892274 | T | C | 1 | a0001c0001t0007g0185 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.792+5759T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892274 | |||||||
| chr22:40892375 | C | T | 2 | a0001c0001t0003g0086 a0001c0001t0023g0087 |
2 | NA18942.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.792+5860C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892375 | |||||||
| chr22:40892477 | G | A | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+5962G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892477 | |||||||
| chr22:40892882 | T | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(29): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.792+6367T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892882 | |||||||
| chr22:40892931 | CATATT | C | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+6420_792+6424d others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40892931 | ||||||
| chr22:40892950 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.792+6435C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40892950 | |||||||
| chr22:40893039 | T | C | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.792+6524T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40893039 | |||||||
| chr22:40893064 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.792+6549A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40893064 | |||||||
| chr22:40893096 | TTATATAT others(3): Show |
T | 28 | a0001c0001t0001g0085 a0001c0001t0004g0001 a0001c0001t0004g0006 others(25): Show |
30 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.792+6599_792+6608d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893096 | ||||||
| chr22:40893105 | AAT | A | 1 | a0001c0001t0001g0002 | 3 | NA18964.hp1 NA18970.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.792+6598_792+6599d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893105 | ||||||
| chr22:40893505 | C | CA | 27 | a0001c0001t0001g0092 a0001c0001t0001g0174 a0001c0001t0002g0137 others(24): Show |
27 | HG00733.hp2 HG00735.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.792+7013dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893505 | ||||||
| chr22:40893505 | CA | C | 6 | a0001c0001t0001g0075 a0001c0001t0001g0162 a0001c0001t0002g0146 others(3): Show |
6 | HG01257.hp2 HG02015.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+7013delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40893505 | ||||||
| chr22:40893822 | G | A | 4 | a0001c0002t0005g0210 a0001c0002t0046g0212 a0001c0002t0048g0209 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+7307G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40893822 | |||||||
| chr22:40894466 | C | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+7951C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40894466 | |||||||
| chr22:40894624 | A | G | 6 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(3): Show |
6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+8109A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40894624 | |||||||
| chr22:40894909 | C | T | 6 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(3): Show |
6 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+8394C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40894909 | |||||||
| chr22:40895100 | T | G | 1 | a0001c0001t0002g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.792+8585T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895100 | |||||||
| chr22:40895104 | A | T | 1 | a0001c0001t0017g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.792+8589A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895104 | |||||||
| chr22:40895126 | AATTGCCT others(342): Show |
A | 2 | a0001c0001t0002g0182 a0001c0001t0002g0193 |
2 | NA18967.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.792+8613_792+8961d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40895126 | ||||||
| chr22:40895288 | T | A | 1 | a0001c0001t0002g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.792+8773T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895288 | |||||||
| chr22:40895342 | C | CT | 6 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(3): Show |
6 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+8838dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40895342 | ||||||
| chr22:40895392 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.792+8877A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895392 | |||||||
| chr22:40895726 | T | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(162): Show |
172 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.792+9211T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895726 | |||||||
| chr22:40895985 | G | A | 1 | a0001c0001t0021g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.792+9470G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895985 | |||||||
| chr22:40895998 | T | C | 1 | a0001c0001t0007g0224 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.792+9483T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40895998 | |||||||
| chr22:40896205 | A | C | 1 | a0001c0001t0002g0157 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.792+9690A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896205 | |||||||
| chr22:40896244 | C | A | 16 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(13): Show |
16 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.792+9729C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896244 | |||||||
| chr22:40896351 | G | A | 10 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(7): Show |
10 | HG01934.hp2 HG02630.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.792+9836G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896351 | |||||||
| chr22:40896399 | C | T | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.792+9884C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896399 | |||||||
| chr22:40896440 | C | T | 4 | a0001c0001t0004g0001 a0001c0001t0004g0042 a0001c0001t0041g0041 others(1): Show |
5 | NA18949.hp2 NA18960.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+9925C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896440 | |||||||
| chr22:40896524 | G | C | 2 | a0001c0001t0002g0119 a0001c0001t0002g0124 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.792+10009G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896524 | |||||||
| chr22:40896659 | A | G | 7 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(4): Show |
7 | HG01934.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+10144A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896659 | |||||||
| chr22:40896702 | A | G | 16 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(13): Show |
16 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.792+10187A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896702 | |||||||
| chr22:40896817 | C | T | 2 | a0001c0001t0012g0037 a0001c0001t0012g0040 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.792+10302C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896817 | |||||||
| chr22:40896834 | A | G | 4 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(1): Show |
4 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+10319A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40896834 | |||||||
| chr22:40896918 | TACTTC | T | 3 | a0001c0001t0013g0127 a0001c0001t0013g0128 a0001c0001t0013g0183 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.792+10408_792+1041 others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40896918 | ||||||
| chr22:40897029 | C | CT | 80 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(77): Show |
83 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.792+10536dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40897029 | ||||||
| chr22:40897029 | C | CTT | 7 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0002g0182 others(4): Show |
7 | HG01884.hp1 HG02602.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+10535_792+1053 others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40897029 | ||||||
| chr22:40897071 | G | T | 1 | a0001c0001t0035g0035 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.793-10516G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40897071 | |||||||
| chr22:40897113 | G | C | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-10474G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40897113 | |||||||
| chr22:40897401 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.793-10186A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40897401 | |||||||
| chr22:40898095 | G | GTTT | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-9487_793-9485d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898095 | ||||||
| chr22:40898100 | T | TTTG | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-9478_793-9476d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898100 | ||||||
| chr22:40898167 | G | A | 3 | a0001c0001t0021g0205 a0001c0001t0021g0206 a0001c0001t0047g0012 |
3 | HG03098.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.793-9420G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898167 | |||||||
| chr22:40898219 | TGACCCAT others(326): Show |
T | 32 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(29): Show |
32 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.793-9357_793-9025d others(2): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898219 | ||||||
| chr22:40898225 | A | AT | 18 | a0001c0001t0002g0010 a0001c0001t0002g0131 a0001c0001t0002g0148 others(15): Show |
19 | HG00140.hp1 HG00733.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.793-9323dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATT | 8 | a0001c0001t0002g0004 a0001c0001t0002g0125 a0001c0001t0002g0129 others(5): Show |
10 | HG02280.hp2 HG02451.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.793-9324_793-9323d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTT | 10 | a0001c0001t0001g0103 a0001c0001t0003g0003 a0001c0001t0003g0056 others(7): Show |
10 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.793-9325_793-9323d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTT | 6 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0001c0001t0004g0052 others(3): Show |
6 | HG00544.hp1 HG00609.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.793-9327_793-9323d others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0078 others(6): Show |
9 | HG01257.hp1 HG01257.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.793-9328_793-9323d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT | 18 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0024 others(15): Show |
18 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.793-9329_793-9323d others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(1): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0079 others(5): Show |
8 | HG02257.hp1 HG02559.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.793-9330_793-9323d others(10): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0001g0088 a0001c0001t0002g0154 a0001c0001t0003g0062 |
3 | HG01256.hp2 HG02055.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.793-9332_793-9323d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0101 |
2 | HG03654.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.793-9333_793-9323d others(13): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(5): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0096 others(2): Show |
5 | HG01109.hp1 HG01258.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-9334_793-9323d others(14): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(6): Show |
2 | a0001c0001t0001g0076 a0001c0001t0001g0106 |
2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.793-9335_793-9323d others(15): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(7): Show |
7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0069 others(4): Show |
7 | HG00544.hp2 HG01943.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-9336_793-9323d others(16): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(8): Show |
5 | a0001c0001t0001g0023 a0001c0001t0001g0073 a0001c0001t0001g0082 others(2): Show |
5 | HG01169.hp1 NA18944.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-9337_793-9323d others(17): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0108 a0001c0001t0003g0090 |
2 | HG03492.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.793-9338_793-9323d others(18): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.793-9339_793-9323d others(19): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(13): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0107 |
2 | HG01243.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.793-9342_793-9323d others(22): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(14): Show |
1 | a0001c0001t0036g0177 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.793-9343_793-9323d others(23): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0003g0031 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.793-9345_793-9323d others(25): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | A | ATTTTTTT others(18): Show |
1 | a0001c0001t0001g0070 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.793-9347_793-9323d others(27): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | AT | A | 17 | a0001c0001t0001g0005 a0001c0001t0002g0113 a0001c0001t0002g0115 others(14): Show |
17 | HG01943.hp2 HG01981.hp1 HG02293.hp1 others(14): Show |
intron_variant | MODIFIER | c.793-9323delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATT | A | 22 | a0001c0001t0002g0011 a0001c0001t0002g0122 a0001c0001t0002g0126 others(19): Show |
22 | HG00099.hp2 HG00423.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.793-9324_793-9323d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTT | A | 12 | a0001c0001t0002g0011 a0001c0001t0002g0114 a0001c0001t0002g0118 others(9): Show |
12 | HG00099.hp1 HG01934.hp1 HG03654.hp2 others(9): Show |
intron_variant | MODIFIER | c.793-9325_793-9323d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0006g0176 a0001c0001t0035g0035 |
2 | HG00597.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.793-9332_793-9323d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0102 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.793-9334_793-9323d others(14): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02015.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.793-9335_793-9323d others(15): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0001g0100 a0001c0001t0003g0055 |
2 | HG02258.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.793-9337_793-9323d others(17): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(9): Show |
A | 1 | a0001c0001t0001g0002 | 3 | NA18964.hp1 NA18970.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.793-9338_793-9323d others(18): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0178 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.793-9339_793-9323d others(19): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(11): Show |
A | 3 | a0001c0001t0001g0144 a0001c0001t0003g0145 a0001c0001t0051g0027 |
3 | HG00735.hp1 HG01256.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.793-9340_793-9323d others(20): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(12): Show |
A | 2 | a0001c0001t0001g0173 a0001c0001t0006g0192 |
2 | NA18989.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.793-9341_793-9323d others(21): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898225 | ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0033g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.793-9342_793-9323d others(22): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40898225 | ||||||
| chr22:40898277 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.793-9310C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898277 | |||||||
| chr22:40898285 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0094 a0001c0001t0001g0144 others(1): Show |
4 | HG00735.hp1 HG01256.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-9302C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898285 | |||||||
| chr22:40898474 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(187): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.793-9113T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898474 | |||||||
| chr22:40898994 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG01243.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-8593C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40898994 | |||||||
| chr22:40899085 | G | T | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-8502G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899085 | |||||||
| chr22:40899145 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.793-8442T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899145 | |||||||
| chr22:40899208 | C | T | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-8379C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899208 | |||||||
| chr22:40899220 | C | CA | 5 | a0001c0001t0010g0164 a0001c0001t0011g0219 a0001c0001t0011g0220 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-8360dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899220 | ||||||
| chr22:40899380 | C | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-8207C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899380 | |||||||
| chr22:40899430 | A | G | 1 | a0001c0001t0002g0193 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.793-8157A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899430 | |||||||
| chr22:40899616 | T | C | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-7971T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899616 | |||||||
| chr22:40899623 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.793-7964A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899623 | |||||||
| chr22:40899680 | G | A | 3 | a0001c0001t0013g0127 a0001c0001t0013g0128 a0001c0001t0013g0183 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.793-7907G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899680 | |||||||
| chr22:40899767 | G | A | 1 | a0001c0001t0021g0206 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.793-7820G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899767 | |||||||
| chr22:40899812 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.793-7775T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899812 | |||||||
| chr22:40899817 | C | CA | 13 | a0001c0001t0002g0148 a0001c0001t0009g0218 a0001c0001t0010g0164 others(10): Show |
13 | HG00639.hp2 HG01884.hp2 HG03041.hp2 others(10): Show |
intron_variant | MODIFIER | c.793-7750dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899817 | ||||||
| chr22:40899817 | CA | C | 19 | a0001c0001t0003g0003 a0001c0001t0003g0055 a0001c0001t0003g0056 others(16): Show |
21 | HG01496.hp2 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.793-7750delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899817 | ||||||
| chr22:40899837 | AG | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(72): Show |
78 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.793-7748delG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40899837 | ||||||
| chr22:40899838 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0085 a0001c0001t0001g0092 others(1): Show |
4 | HG01109.hp1 HG02056.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-7749G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40899838 | |||||||
| chr22:40900307 | G | GA | 10 | a0001c0001t0002g0148 a0001c0001t0007g0186 a0001c0001t0007g0230 others(7): Show |
10 | HG00639.hp2 HG01109.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.793-7265dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40900307 | ||||||
| chr22:40900308 | A | G | 2 | a0001c0001t0003g0061 a0001c0001t0003g0062 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.793-7279A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900308 | |||||||
| chr22:40900330 | T | C | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-7257T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900330 | |||||||
| chr22:40900407 | C | A | 3 | a0001c0001t0012g0037 a0001c0001t0012g0040 a0001c0001t0032g0039 |
3 | HG00099.hp1 HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.793-7180C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900407 | |||||||
| chr22:40900474 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.793-7113C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900474 | |||||||
| chr22:40900555 | G | A | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-7032G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900555 | |||||||
| chr22:40900757 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.793-6830C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40900757 | |||||||
| chr22:40901097 | A | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(80): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.793-6490A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901097 | |||||||
| chr22:40901233 | G | T | 1 | a0001c0001t0003g0197 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.793-6354G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901233 | |||||||
| chr22:40901236 | C | CTTTTTTT | 21 | a0001c0001t0001g0025 a0001c0001t0002g0011 a0001c0001t0002g0150 others(18): Show |
22 | HG00140.hp1 HG02257.hp2 HG02738.hp2 others(19): Show |
intron_variant | MODIFIER | c.793-6344_793-6338d others(9): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40901236 | ||||||
| chr22:40901299 | A | G | 1 | a0001c0001t0033g0058 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.793-6288A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901299 | |||||||
| chr22:40901301 | C | G | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(80): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.793-6286C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901301 | |||||||
| chr22:40901493 | C | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-6094C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901493 | |||||||
| chr22:40901501 | C | G | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-6086C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901501 | |||||||
| chr22:40901915 | G | T | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-5672G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901915 | |||||||
| chr22:40901916 | G | A | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-5671G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901916 | |||||||
| chr22:40901920 | C | G | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-5667C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40901920 | |||||||
| chr22:40901931 | TG | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0132 a0001c0001t0002g0232 |
5 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-5654delG | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40901931 | ||||||
| chr22:40902071 | C | CTTT | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-5499_793-5497d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902071 | ||||||
| chr22:40902071 | C | CTTTTT | 12 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(9): Show |
12 | HG00639.hp2 HG01934.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.793-5501_793-5497d others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902071 | ||||||
| chr22:40902111 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-5476C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902111 | |||||||
| chr22:40902134 | G | A | 68 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(65): Show |
70 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.793-5453G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902134 | |||||||
| chr22:40902246 | A | AT | 23 | a0001c0001t0002g0119 a0001c0001t0002g0124 a0001c0001t0002g0179 others(20): Show |
23 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.793-5319dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902246 | ||||||
| chr22:40902246 | A | ATT | 6 | a0001c0001t0005g0200 a0001c0001t0011g0219 a0001c0001t0011g0220 others(3): Show |
6 | HG00639.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-5320_793-5319d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902246 | ||||||
| chr22:40902246 | AT | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(75): Show |
81 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.793-5319delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902246 | ||||||
| chr22:40902485 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0170 a0001c0001t0038g0095 |
3 | HG02080.hp2 NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.793-5102C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902485 | |||||||
| chr22:40902649 | T | C | 1 | a0001c0001t0012g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.793-4938T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902649 | |||||||
| chr22:40902651 | G | A | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-4936G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902651 | |||||||
| chr22:40902733 | G | A | 6 | a0001c0001t0004g0006 a0001c0001t0004g0053 a0001c0001t0010g0043 others(3): Show |
7 | HG02015.hp1 HG02027.hp2 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-4854G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902733 | |||||||
| chr22:40902847 | G | A | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-4740G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902847 | |||||||
| chr22:40902871 | CCT | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(160): Show |
170 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.793-4713_793-4712d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40902871 | ||||||
| chr22:40902969 | T | C | 1 | a0002c0003t0004g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.793-4618T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902969 | |||||||
| chr22:40902973 | A | G | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-4614A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40902973 | |||||||
| chr22:40903042 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.793-4545C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903042 | |||||||
| chr22:40903062 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.793-4525A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903062 | |||||||
| chr22:40903483 | C | G | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-4104C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903483 | |||||||
| chr22:40903530 | G | A | 1 | a0001c0001t0003g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.793-4057G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903530 | |||||||
| chr22:40903688 | C | T | 1 | a0001c0001t0011g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.793-3899C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903688 | |||||||
| chr22:40903874 | T | TCA | 4 | a0001c0001t0003g0059 a0001c0001t0004g0048 a0001c0001t0014g0187 others(1): Show |
4 | HG02738.hp1 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-3676_793-3675d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | ||||||
| chr22:40903874 | T | TCACA | 6 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0062 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-3678_793-3675d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | ||||||
| chr22:40903874 | T | TCACACA | 9 | a0001c0001t0003g0003 a0001c0001t0003g0055 a0001c0001t0003g0061 others(6): Show |
11 | HG02258.hp1 HG02280.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.793-3680_793-3675d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | ||||||
| chr22:40903874 | T | TCACACAC others(3): Show |
3 | a0001c0001t0011g0219 a0001c0001t0011g0222 a0001c0005t0003g0191 |
3 | HG02451.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.793-3684_793-3675d others(12): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | ||||||
| chr22:40903874 | TCA | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0023 others(75): Show |
81 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.793-3676_793-3675d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | ||||||
| chr22:40903874 | TCACA | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0017 others(71): Show |
76 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.793-3678_793-3675d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | ||||||
| chr22:40903874 | TCACACA | T | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-3680_793-3675d others(8): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40903874 | ||||||
| chr22:40903989 | A | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0170 a0001c0001t0038g0095 |
3 | HG02080.hp2 NA18995.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.793-3598A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40903989 | |||||||
| chr22:40904181 | A | T | 1 | a0001c0001t0001g0024 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.793-3406A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904181 | |||||||
| chr22:40904232 | A | G | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0014g0187 |
3 | HG01515.hp2 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.793-3355A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904232 | |||||||
| chr22:40904308 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.793-3279G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904308 | |||||||
| chr22:40904366 | A | G | 2 | a0001c0001t0012g0037 a0001c0001t0012g0040 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.793-3221A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904366 | |||||||
| chr22:40904423 | A | G | 1 | a0001c0001t0036g0177 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.793-3164A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40904423 | |||||||
| chr22:40905084 | T | A | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.793-2503T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905084 | |||||||
| chr22:40905237 | G | A | 1 | a0001c0001t0005g0207 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.793-2350G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905237 | |||||||
| chr22:40905501 | C | T | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-2086C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905501 | |||||||
| chr22:40905728 | C | G | 1 | a0001c0001t0018g0135 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.793-1859C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905728 | |||||||
| chr22:40905765 | C | T | 1 | a0001c0001t0030g0117 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.793-1822C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905765 | |||||||
| chr22:40905926 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.793-1661G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905926 | |||||||
| chr22:40905940 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.793-1647C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905940 | |||||||
| chr22:40905983 | G | T | 3 | a0001c0001t0019g0014 a0001c0001t0019g0015 a0001c0001t0022g0013 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.793-1604G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40905983 | |||||||
| chr22:40906067 | A | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG02132.hp2 NA18942.hp2 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1520A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906067 | |||||||
| chr22:40906090 | C | CTGTT | 18 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(15): Show |
18 | HG01934.hp2 HG02109.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.793-1471_793-1468d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40906090 | ||||||
| chr22:40906215 | C | T | 1 | a0001c0001t0034g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.793-1372C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906215 | |||||||
| chr22:40906420 | C | CA | 10 | a0001c0001t0001g0026 a0001c0001t0002g0129 a0001c0001t0002g0137 others(7): Show |
10 | HG01106.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.793-1151dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40906420 | ||||||
| chr22:40906420 | C | CAA | 13 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(10): Show |
13 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.793-1152_793-1151d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40906420 | ||||||
| chr22:40906588 | A | G | 1 | a0001c0001t0002g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.793-999A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906588 | |||||||
| chr22:40906628 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-959C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906628 | |||||||
| chr22:40906784 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.793-803A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906784 | |||||||
| chr22:40906907 | T | A | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.793-680T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906907 | |||||||
| chr22:40906969 | A | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(163): Show |
173 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.793-618A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40906969 | |||||||
| chr22:40907159 | C | T | 2 | a0001c0001t0002g0119 a0001c0001t0002g0124 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.793-428C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907159 | |||||||
| chr22:40907217 | C | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.793-370C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907217 | |||||||
| chr22:40907256 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.793-331C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907256 | |||||||
| chr22:40907290 | G | A | 3 | a0001c0001t0019g0014 a0001c0001t0019g0015 a0001c0001t0022g0013 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.793-297G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907290 | |||||||
| chr22:40907382 | C | T | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.793-205C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | chr22 | 40907382 | |||||||
| chr22:40907420 | C | CA | 7 | a0001c0001t0001g0028 a0001c0001t0002g0137 a0001c0001t0002g0148 others(4): Show |
7 | HG01496.hp1 HG02615.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-157dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr22 | 40907420 | ||||||
| chr22:40907918 | G | A | 32 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(29): Show |
32 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.855+269G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40907918 | |||||||
| chr22:40908121 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.855+472C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40908121 | |||||||
| chr22:40908301 | C | G | 2 | a0001c0001t0017g0134 a0001c0001t0024g0143 |
2 | HG02257.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.855+652C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40908301 | |||||||
| chr22:40908459 | A | G | 4 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(1): Show |
4 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-663A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 5/9 | chr22 | 40908459 | |||||||
| chr22:40909625 | C | T | 1 | a0001c0001t0045g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.969+390C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909625 | |||||||
| chr22:40909631 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18961.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.969+396G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909631 | |||||||
| chr22:40909691 | G | A | 5 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(2): Show |
5 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+456G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909691 | |||||||
| chr22:40909772 | CTAAA | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0153 a0001c0001t0002g0232 |
5 | HG02258.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+560_969+563del others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40909772 | ||||||
| chr22:40909791 | A | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0094 a0001c0001t0001g0144 others(1): Show |
4 | HG00735.hp1 HG01256.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+556A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909791 | |||||||
| chr22:40909792 | A | T | 4 | a0001c0001t0001g0088 a0001c0001t0001g0094 a0001c0001t0001g0144 others(1): Show |
4 | HG00735.hp1 HG01256.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+557A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909792 | |||||||
| chr22:40909899 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.969+664C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40909899 | |||||||
| chr22:40910175 | G | A | 5 | a0001c0001t0004g0007 a0001c0001t0004g0048 a0001c0001t0004g0051 others(2): Show |
5 | NA18961.hp2 NA18968.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+940G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910175 | |||||||
| chr22:40910541 | C | CA | 7 | a0001c0001t0002g0115 a0001c0001t0002g0116 a0001c0001t0002g0118 others(4): Show |
7 | HG00423.hp1 HG00735.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.969+1313dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40910541 | ||||||
| chr22:40910583 | C | G | 1 | a0001c0001t0029g0217 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.969+1348C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910583 | |||||||
| chr22:40910724 | G | A | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.969+1489G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910724 | |||||||
| chr22:40910956 | C | T | 36 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(33): Show |
38 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.969+1721C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40910956 | |||||||
| chr22:40911481 | G | A | 1 | a0001c0001t0034g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.969+2246G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40911481 | |||||||
| chr22:40911789 | C | G | 1 | a0001c0001t0002g0137 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.970-2450C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40911789 | |||||||
| chr22:40911803 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG00639.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.970-2436G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40911803 | |||||||
| chr22:40912000 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.970-2239C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912000 | |||||||
| chr22:40912585 | G | A | 3 | a0001c0001t0019g0014 a0001c0001t0019g0015 a0001c0001t0022g0013 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.970-1654G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912585 | |||||||
| chr22:40912699 | A | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(29): Show |
34 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.970-1540A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912699 | |||||||
| chr22:40912731 | G | T | 4 | a0001c0002t0005g0210 a0001c0002t0046g0212 a0001c0002t0048g0209 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-1508G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912731 | |||||||
| chr22:40912794 | CAGGAGGC others(13): Show |
C | 1 | a0001c0001t0002g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.970-1442_970-1423d others(22): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40912794 | ||||||
| chr22:40912936 | T | G | 1 | a0001c0001t0003g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.970-1303T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40912936 | |||||||
| chr22:40913131 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.970-1108A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913131 | |||||||
| chr22:40913348 | G | C | 1 | a0002c0003t0004g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.970-891G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913348 | |||||||
| chr22:40913426 | A | C | 2 | a0001c0001t0012g0037 a0001c0001t0012g0040 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.970-813A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913426 | |||||||
| chr22:40913437 | C | CA | 7 | a0001c0001t0001g0102 a0001c0001t0009g0213 a0001c0001t0009g0214 others(4): Show |
7 | HG01934.hp2 HG02809.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.970-785dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40913437 | ||||||
| chr22:40913456 | A | C | 1 | a0001c0002t0048g0209 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.970-783A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913456 | |||||||
| chr22:40913693 | C | G | 1 | a0001c0001t0005g0198 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.970-546C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913693 | |||||||
| chr22:40913698 | C | T | 13 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(10): Show |
13 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.970-541C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913698 | |||||||
| chr22:40913882 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.970-357C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913882 | |||||||
| chr22:40913896 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.970-343G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40913896 | |||||||
| chr22:40914003 | TGTG | T | 22 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(19): Show |
22 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.970-231_970-229del others(3): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40914003 | ||||||
| chr22:40914056 | C | T | 2 | a0001c0001t0009g0215 a0001c0001t0009g0218 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.970-183C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914056 | |||||||
| chr22:40914059 | T | C | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.970-180T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914059 | |||||||
| chr22:40914064 | C | T | 1 | a0001c0001t0014g0016 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.970-175C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914064 | |||||||
| chr22:40914144 | G | GA | 7 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0109 others(4): Show |
7 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.970-79dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr22 | 40914144 | ||||||
| chr22:40914180 | AC | A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0153 a0001c0001t0002g0232 |
5 | HG02258.hp2 HG03130.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.970-58delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914180 | |||||||
| chr22:40914199 | C | G | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.970-40C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914199 | |||||||
| chr22:40914218 | A | T | 2 | a0001c0001t0020g0142 a0001c0001t0020g0184 |
2 | HG02602.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.970-21A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 6/9 | chr22 | 40914218 | |||||||
| chr22:40914339 | G | A | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+15G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914339 | |||||||
| chr22:40914404 | C | A | 1 | a0001c0001t0007g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1055+80C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914404 | |||||||
| chr22:40914528 | A | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1055+204A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914528 | |||||||
| chr22:40914531 | A | AT | 46 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0104 others(43): Show |
46 | HG00140.hp1 HG00544.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1055+238dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | ||||||
| chr22:40914531 | A | ATT | 5 | a0001c0001t0004g0047 a0001c0001t0015g0121 a0001c0001t0019g0015 others(2): Show |
5 | HG02080.hp1 HG02897.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+237_1055+238d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | ||||||
| chr22:40914531 | AT | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(50): Show |
54 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.1055+238delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | ||||||
| chr22:40914531 | ATT | A | 14 | a0001c0001t0001g0033 a0001c0001t0001g0070 a0001c0001t0001g0079 others(11): Show |
14 | HG00609.hp2 HG01515.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1055+237_1055+238d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | ||||||
| chr22:40914531 | ATTT | A | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+236_1055+238d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40914531 | ||||||
| chr22:40914572 | C | T | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1055+248C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914572 | |||||||
| chr22:40914890 | G | T | 3 | a0001c0001t0019g0014 a0001c0001t0019g0015 a0001c0001t0022g0013 |
3 | HG02886.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1055+566G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40914890 | |||||||
| chr22:40915050 | C | CT | 200 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(197): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.1055+745dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40915050 | ||||||
| chr22:40915050 | C | CTT | 12 | a0001c0001t0003g0169 a0001c0001t0005g0199 a0001c0001t0005g0207 others(9): Show |
12 | HG00639.hp2 HG03041.hp2 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.1055+744_1055+745d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40915050 | ||||||
| chr22:40915116 | A | T | 7 | a0001c0001t0004g0007 a0001c0001t0004g0008 a0001c0001t0004g0048 others(4): Show |
7 | HG00597.hp1 NA18961.hp2 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.1055+792A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915116 | |||||||
| chr22:40915233 | G | A | 2 | a0001c0001t0006g0021 a0001c0001t0006g0081 |
2 | HG01106.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1055+909G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915233 | |||||||
| chr22:40915512 | T | C | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1055+1188T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915512 | |||||||
| chr22:40915732 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1055+1408C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915732 | |||||||
| chr22:40915869 | A | T | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+1545A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40915869 | |||||||
| chr22:40916058 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0077 |
4 | HG00544.hp2 NA18964.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+1734C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916058 | |||||||
| chr22:40916308 | A | G | 1 | a0001c0002t0050g0208 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1055+1984A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916308 | |||||||
| chr22:40916313 | A | G | 3 | a0001c0001t0006g0084 a0001c0001t0026g0030 a0001c0001t0037g0034 |
3 | HG01346.hp2 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1055+1989A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916313 | |||||||
| chr22:40916346 | A | G | 68 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0007 others(65): Show |
70 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1055+2022A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916346 | |||||||
| chr22:40916578 | T | C | 5 | a0001c0001t0008g0065 a0001c0001t0008g0066 a0001c0001t0008g0067 others(2): Show |
5 | HG01243.hp2 HG01496.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+2254T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916578 | |||||||
| chr22:40916764 | G | A | 3 | a0001c0001t0013g0127 a0001c0001t0013g0128 a0001c0001t0013g0183 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1055+2440G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40916764 | |||||||
| chr22:40917088 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1055+2764A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917088 | |||||||
| chr22:40917201 | C | T | 1 | a0001c0001t0028g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1055+2877C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917201 | |||||||
| chr22:40917570 | TATG | T | 3 | a0001c0001t0003g0003 a0001c0001t0003g0194 a0001c0001t0003g0195 |
5 | HG02280.hp2 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055+3249_1055+325 others(7): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40917570 | ||||||
| chr22:40917610 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1055+3286G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917610 | |||||||
| chr22:40917698 | C | T | 3 | a0001c0001t0017g0134 a0001c0001t0017g0216 a0001c0001t0024g0143 |
3 | HG02257.hp2 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1055+3374C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917698 | |||||||
| chr22:40917720 | A | G | 1 | a0001c0001t0017g0216 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1055+3396A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917720 | |||||||
| chr22:40917776 | G | A | 3 | a0001c0001t0002g0132 a0001c0001t0002g0138 a0001c0001t0007g0185 |
3 | HG01192.hp2 HG06807.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1055+3452G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917776 | |||||||
| chr22:40917839 | A | T | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3515A>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917839 | |||||||
| chr22:40917998 | G | T | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3674G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40917998 | |||||||
| chr22:40918006 | G | GT | 5 | a0001c0001t0001g0017 a0001c0001t0001g0101 a0001c0001t0001g0175 others(2): Show |
5 | HG01109.hp1 HG01981.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055+3683dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918006 | ||||||
| chr22:40918007 | TC | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0170 a0001c0001t0038g0095 others(1): Show |
4 | HG02080.hp2 NA18984.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3684delC | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918007 | |||||||
| chr22:40918008 | C | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0101 a0001c0001t0001g0175 others(2): Show |
5 | HG01109.hp1 HG01981.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1055+3684C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918008 | |||||||
| chr22:40918008 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(68): Show |
74 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1055+3684C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918008 | |||||||
| chr22:40918009 | T | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(73): Show |
79 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1055+3685T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918009 | |||||||
| chr22:40918009 | T | TA | 7 | a0001c0001t0002g0118 a0001c0001t0002g0139 a0001c0001t0002g0160 others(4): Show |
7 | HG01934.hp1 HG02683.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1055+3705dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918009 | ||||||
| chr22:40918009 | TA | T | 83 | a0001c0001t0002g0010 a0001c0001t0002g0125 a0001c0001t0002g0151 others(80): Show |
88 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1055+3705delA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918009 | ||||||
| chr22:40918029 | A | G | 1 | a0001c0001t0012g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1055+3705A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918029 | |||||||
| chr22:40918242 | C | T | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1055+3918C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918242 | |||||||
| chr22:40918633 | G | A | 2 | a0001c0001t0002g0151 a0001c0001t0002g0152 |
2 | HG01433.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1056-3700G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918633 | |||||||
| chr22:40918764 | G | A | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-3569G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918764 | |||||||
| chr22:40918783 | G | GT | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(85): Show |
91 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1056-3540dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40918783 | ||||||
| chr22:40918783 | G | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1056-3550G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918783 | |||||||
| chr22:40918875 | C | T | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-3458C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40918875 | |||||||
| chr22:40919079 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(167): Show |
177 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.1056-3254T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919079 | |||||||
| chr22:40919081 | A | G | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-3252A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919081 | |||||||
| chr22:40919151 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1056-3182C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919151 | |||||||
| chr22:40919326 | G | A | 1 | a0001c0001t0004g0047 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1056-3007G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919326 | |||||||
| chr22:40919373 | G | T | 1 | a0001c0001t0004g0047 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1056-2960G>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919373 | |||||||
| chr22:40919526 | G | A | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056-2807G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919526 | |||||||
| chr22:40919534 | T | C | 4 | a0001c0001t0004g0001 a0001c0001t0004g0042 a0001c0001t0041g0041 others(1): Show |
5 | NA18949.hp2 NA18960.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-2799T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919534 | |||||||
| chr22:40919590 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(80): Show |
86 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.1056-2743C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919590 | |||||||
| chr22:40919856 | G | A | 3 | a0001c0001t0013g0127 a0001c0001t0013g0128 a0001c0001t0013g0183 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1056-2477G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40919856 | |||||||
| chr22:40920241 | G | A | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-2092G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40920241 | |||||||
| chr22:40920534 | GT | G | 3 | a0001c0001t0013g0127 a0001c0001t0013g0128 a0001c0001t0013g0183 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1056-1797delT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40920534 | ||||||
| chr22:40920904 | T | A | 17 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(14): Show |
17 | HG01884.hp2 HG02109.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056-1429T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40920904 | |||||||
| chr22:40921012 | G | A | 15 | a0001c0001t0003g0003 a0001c0001t0003g0055 a0001c0001t0003g0056 others(12): Show |
17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056-1321G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921012 | |||||||
| chr22:40921079 | A | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0009 others(78): Show |
84 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1056-1254A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921079 | |||||||
| chr22:40921221 | T | C | 9 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(6): Show |
9 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1056-1112T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921221 | |||||||
| chr22:40921393 | G | A | 1 | a0001c0001t0003g0057 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1056-940G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921393 | |||||||
| chr22:40921440 | T | C | 32 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(29): Show |
32 | HG00639.hp2 HG01884.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.1056-893T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921440 | |||||||
| chr22:40921486 | T | TA | 34 | a0001c0001t0001g0092 a0001c0001t0001g0102 a0001c0001t0001g0174 others(31): Show |
34 | HG00639.hp2 HG01106.hp2 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1056-827dupA | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40921486 | ||||||
| chr22:40921507 | C | A | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1056-826C>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921507 | |||||||
| chr22:40921536 | T | TGTG | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-792_1056-790d others(5): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr22 | 40921536 | ||||||
| chr22:40921812 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1056-521A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40921812 | |||||||
| chr22:40922150 | C | T | 4 | a0001c0002t0005g0210 a0001c0002t0046g0212 a0001c0002t0048g0209 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056-183C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40922150 | |||||||
| chr22:40922273 | G | A | 5 | a0001c0001t0011g0219 a0001c0001t0011g0220 a0001c0001t0011g0221 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1056-60G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 7/9 | chr22 | 40922273 | |||||||
| chr22:40922669 | T | C | 3 | a0001c0001t0017g0134 a0001c0001t0017g0216 a0001c0001t0024g0143 |
3 | HG02257.hp2 HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1236+156T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922669 | |||||||
| chr22:40922715 | GAT | G | 9 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 others(6): Show |
9 | HG02055.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1236+208_1236+209d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922715 | ||||||
| chr22:40922719 | TATAC | T | 6 | a0001c0001t0003g0003 a0001c0001t0003g0194 a0001c0001t0003g0195 others(3): Show |
8 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1236+208_1236+211d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922719 | ||||||
| chr22:40922721 | T | C | 5 | a0001c0001t0002g0114 a0001c0001t0002g0122 a0001c0001t0002g0126 others(2): Show |
5 | HG01167.hp2 HG01361.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236+208T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922721 | |||||||
| chr22:40922721 | T | TAC | 6 | a0001c0001t0001g0100 a0001c0001t0002g0131 a0001c0001t0002g0232 others(3): Show |
6 | HG02723.hp1 HG02886.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1236+232_1236+233d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922721 | ||||||
| chr22:40922721 | T | TACAC | 3 | a0001c0001t0006g0084 a0001c0001t0026g0030 a0001c0001t0037g0034 |
3 | HG01346.hp2 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1236+230_1236+233d others(6): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922721 | ||||||
| chr22:40922721 | TAC | T | 18 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(15): Show |
18 | HG01934.hp2 HG02109.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.1236+232_1236+233d others(4): Show |
XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922721 | ||||||
| chr22:40922747 | T | C | 15 | a0001c0001t0003g0003 a0001c0001t0003g0055 a0001c0001t0003g0056 others(12): Show |
17 | HG02055.hp1 HG02258.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1236+234T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922747 | |||||||
| chr22:40922767 | C | T | 1 | a0001c0001t0027g0223 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1236+254C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922767 | |||||||
| chr22:40922795 | G | GT | 3 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0023 |
4 | HG01243.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1236+288dupT | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr22 | 40922795 | ||||||
| chr22:40922893 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0006g0176 |
2 | HG00597.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.1236+380T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922893 | |||||||
| chr22:40922955 | C | T | 1 | a0001c0001t0003g0169 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1236+442C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40922955 | |||||||
| chr22:40923313 | C | G | 23 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(20): Show |
23 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1236+800C>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40923313 | |||||||
| chr22:40923649 | C | T | 8 | a0001c0001t0009g0213 a0001c0001t0009g0214 a0001c0001t0009g0215 others(5): Show |
8 | HG01934.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1237-713C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40923649 | |||||||
| chr22:40924116 | T | A | 23 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(20): Show |
23 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1237-246T>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40924116 | |||||||
| chr22:40924142 | G | A | 4 | a0001c0002t0005g0210 a0001c0002t0046g0212 a0001c0002t0048g0209 others(1): Show |
4 | HG01884.hp2 HG02630.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1237-220G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 8/9 | chr22 | 40924142 | |||||||
| chr22:40924670 | C | T | 9 | a0001c0001t0005g0198 a0001c0001t0005g0199 a0001c0001t0005g0200 others(6): Show |
9 | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1357+188C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40924670 | |||||||
| chr22:40924790 | T | G | 1 | a0001c0001t0003g0090 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1357+308T>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40924790 | |||||||
| chr22:40924895 | A | G | 4 | a0001c0001t0002g0113 a0001c0001t0002g0137 a0001c0001t0020g0142 others(1): Show |
4 | HG02602.hp2 HG03654.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1357+413A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40924895 | |||||||
| chr22:40925377 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1358-892G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925377 | |||||||
| chr22:40925674 | G | C | 1 | a0001c0001t0014g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1358-595G>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925674 | |||||||
| chr22:40925690 | C | T | 7 | a0001c0001t0003g0055 a0001c0001t0003g0056 a0001c0001t0003g0057 others(4): Show |
7 | HG02258.hp1 HG02615.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1358-579C>T | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925690 | |||||||
| chr22:40925756 | T | C | 1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1358-513T>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925756 | |||||||
| chr22:40925890 | G | A | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-379G>A | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925890 | |||||||
| chr22:40925892 | A | G | 4 | a0001c0001t0012g0037 a0001c0001t0012g0038 a0001c0001t0012g0040 others(1): Show |
4 | HG00099.hp1 HG01433.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1358-377A>G | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925892 | |||||||
| chr22:40925944 | A | C | 2 | a0001c0001t0002g0004 a0001c0001t0002g0232 |
4 | HG03130.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1358-325A>C | XPNPEP3 | ENSG00000196236.13 | transcript | ENST00000357137.9 | protein_coding | 9/9 | chr22 | 40925944 |