Item | Value |
---|---|
geneid | 87178 |
ensemblid | ENSG00000138035.15 |
hgncid | 23166 |
symbol | PNPT1 |
name | polyribonucleotide nucleotidyltransferase 1 |
refseq_nuc | NM_033109.5 |
refseq_prot | NP_149100.2 |
ensembl_nuc | ENST00000447944.7 |
ensembl_prot | ENSP00000400646.2 |
mane_status | MANE Select |
chr | chr2 |
start | 55634061 |
end | 55693844 |
strand | - |
ver | v1.2 |
region | chr2:55634061-55693844 |
region5000 | chr2:55629061-55698844 |
regionname0 | PNPT1_chr2_55634061_55693844 |
regionname5000 | PNPT1_chr2_55629061_55698844 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 783 | 217 | 27 | 37 | 111 | 5 | 36 | 83 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0002 | 0/0 | 783 | 122 | 36 | 30 | 42 | 5 | 9 | 38 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0003 | 0/1 | 783 | 44 | 28 | 5 | 8 | 0 | 2 | 7 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0004 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0005 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0006 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0007 | 0/0 | 783 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0008 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0009 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
a0010 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | MAACR others(778): Show |
chr2 | 55629061 | 55698844 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2349 | 202 | 26 | 31 | 111 | 5 | 28 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0001c0004 | 0/0 | 2349 | 12 | 1 | 5 | 0 | 0 | 6 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0001c0009 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0001c0010 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0001c0017 | 0/0 | 2349 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0002c0002 | 0/0 | 2349 | 115 | 35 | 29 | 37 | 5 | 9 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0002c0005 | 0/0 | 2349 | 5 | 0 | 1 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0002c0011 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0002c0015 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0003c0003 | 0/1 | 2349 | 44 | 28 | 5 | 8 | 0 | 2 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0004c0016 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0005c0013 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0006c0014 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0007c0008 | 0/0 | 2349 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0008c0006 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0009c0012 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 | ||
a0010c0007 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | ATGGC others(2344): Show |
chr2 | 55629061 | 55698844 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4549 | 84 | 13 | 20 | 38 | 4 | 9 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0002 | 0/0 | 4549 | 2 | 0 | 0 | 0 | 0 | 2 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0003 | 1/0 | 4549 | 68 | 0 | 6 | 55 | 0 | 6 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0006 | 0/0 | 4549 | 10 | 1 | 3 | 0 | 1 | 5 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0008 | 0/0 | 4549 | 7 | 7 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0009 | 0/0 | 4550 | 5 | 0 | 1 | 3 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4545): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0011 | 0/0 | 4549 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0012 | 0/0 | 4549 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0013 | 0/0 | 4550 | 2 | 0 | 1 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4545): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0014 | 0/0 | 4550 | 2 | 1 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4545): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0015 | 0/0 | 4549 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0017 | 0/0 | 4549 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0019 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0024 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0025 | 0/0 | 4550 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4545): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0026 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0027 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0028 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0030 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0031 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0033 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0036 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4551): Show |
chr2 | 55629061 | 55698844 |
a0001c0001t0037 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0004t0004 | 0/0 | 4548 | 2 | 1 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0001c0004t0007 | 0/0 | 4549 | 10 | 0 | 5 | 0 | 0 | 5 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0009t0029 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0010t0003 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0001c0017t0001 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0001 | 0/0 | 4549 | 12 | 0 | 0 | 12 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0002 | 0/0 | 4549 | 77 | 28 | 27 | 13 | 3 | 6 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0005 | 0/0 | 4551 | 11 | 0 | 0 | 10 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4546): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0010 | 0/0 | 4549 | 4 | 4 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0021 | 0/0 | 4549 | 2 | 1 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0022 | 0/0 | 4550 | 2 | 0 | 1 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4545): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0023 | 0/0 | 4549 | 2 | 0 | 0 | 0 | 2 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0038 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0039 | 0/0 | 4550 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4545): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0040 | 0/0 | 4551 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4546): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0041 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0002t0042 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4545): Show |
chr2 | 55629061 | 55698844 |
a0002c0005t0001 | 0/0 | 4549 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0005t0002 | 0/0 | 4549 | 4 | 0 | 0 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0011t0001 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0002c0015t0002 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0003c0003t0004 | 0/1 | 4548 | 35 | 21 | 4 | 7 | 0 | 2 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0003c0003t0016 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0003c0003t0018 | 0/0 | 4549 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0003c0003t0020 | 0/0 | 4548 | 2 | 2 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0003c0003t0032 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0003c0003t0034 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0003c0003t0035 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0004c0016t0001 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0005c0013t0004 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0006c0014t0010 | 0/0 | 4549 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0007c0008t0001 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0008c0006t0004 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4543): Show |
chr2 | 55629061 | 55698844 |
a0009c0012t0002 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
a0010c0007t0003 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | GTTGA others(4544): Show |
chr2 | 55629061 | 55698844 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0346 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0009g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0011g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0011g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0012g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0012g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0013g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0013g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0014g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0015g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0017g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0017g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0019g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0024g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0025g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0026g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0027g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0028g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0030g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0031g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0033g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0036g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0001t0037g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0004t0007g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0009t0029g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0010t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0001c0017t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0006 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0368 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0002g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0021g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0021g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0022g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0022g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0023g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0023g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0038g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0039g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0040g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0041g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0002t0042g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0005t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0011t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0002c0015t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0016g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0016g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0018g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0018g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0020g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0020g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0032g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0034g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0003c0003t0035g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0004c0016t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0005c0013t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0006c0014t0010g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0007c0008t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0008c0006t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0009c0012t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
a0010c0007t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0023 | g0227 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00099 | hp2 | a0001 | c0001 | t0006 | g0200 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0236 | EUR | GBR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0361 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0362 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00558 | hp2 | a0001 | c0001 | t0011 | g0144 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00621 | hp1 | a0001 | c0001 | t0036 | g0185 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00621 | hp2 | a0001 | c0001 | t0009 | g0308 | EAS | CHS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00642 | hp1 | a0002 | c0002 | t0022 | g0253 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0218 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0237 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0232 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0213 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01070 | hp2 | a0001 | c0004 | t0007 | g0065 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0366 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01074 | hp2 | a0001 | c0017 | t0001 | g0371 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01081 | hp1 | a0001 | c0004 | t0007 | g0008 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01099 | hp1 | a0001 | c0004 | t0007 | g0008 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0228 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0356 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0229 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0260 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01167 | hp1 | a0002 | c0002 | t0021 | g0254 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0369 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01168 | hp2 | a0003 | c0003 | t0004 | g0078 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01169 | hp1 | a0003 | c0003 | t0004 | g0077 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01175 | hp2 | a0003 | c0003 | t0004 | g0092 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01192 | hp1 | a0001 | c0004 | t0007 | g0063 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01243 | hp1 | a0003 | c0003 | t0034 | g0096 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01255 | hp1 | a0003 | c0003 | t0004 | g0098 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0234 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0206 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01261 | hp2 | a0002 | c0002 | t0002 | g0268 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01346 | hp2 | a0002 | c0005 | t0001 | g0151 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0331 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0221 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0240 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0235 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01433 | hp2 | a0001 | c0004 | t0007 | g0009 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0202 | AMR | CLM | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0370 | EUR | IBS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01884 | hp1 | a0001 | c0001 | t0008 | g0147 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0267 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01891 | hp1 | a0003 | c0003 | t0016 | g0074 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0231 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0336 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01934 | hp1 | a0001 | c0001 | t0006 | g0204 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0350 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0230 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0338 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01978 | hp1 | a0001 | c0001 | t0013 | g0117 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG01978 | hp2 | a0001 | c0001 | t0009 | g0348 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0247 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02056 | hp2 | a0001 | c0001 | t0031 | g0365 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02071 | hp1 | a0001 | c0001 | t0012 | g0184 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02071 | hp2 | a0002 | c0005 | t0002 | g0003 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02074 | hp1 | a0001 | c0001 | t0017 | g0301 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02083 | hp1 | a0001 | c0001 | t0011 | g0194 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02129 | hp2 | a0002 | c0011 | t0001 | g0044 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0251 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02145 | hp2 | a0003 | c0003 | t0018 | g0084 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02257 | hp1 | a0002 | c0002 | t0002 | g0014 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0159 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0321 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0024 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02280 | hp2 | a0001 | c0001 | t0014 | g0154 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0226 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0367 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02451 | hp1 | a0003 | c0003 | t0020 | g0104 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02523 | hp1 | a0004 | c0016 | t0001 | g0053 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0347 | EAS | KHV | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02572 | hp1 | a0002 | c0002 | t0042 | g0241 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02572 | hp2 | a0001 | c0001 | t0024 | g0152 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0259 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0300 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02615 | hp1 | a0003 | c0003 | t0020 | g0070 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02622 | hp1 | a0003 | c0003 | t0004 | g0082 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02622 | hp2 | a0003 | c0003 | t0004 | g0081 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02630 | hp1 | a0003 | c0003 | t0004 | g0075 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02647 | hp1 | a0003 | c0003 | t0004 | g0071 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02683 | hp1 | a0001 | c0009 | t0029 | g0199 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02698 | hp1 | a0001 | c0001 | t0033 | g0323 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0136 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0160 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0244 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02723 | hp2 | a0003 | c0003 | t0004 | g0097 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0225 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0318 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0368 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02809 | hp1 | a0002 | c0002 | t0010 | g0248 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02809 | hp2 | a0001 | c0001 | t0008 | g0161 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02818 | hp2 | a0001 | c0001 | t0019 | g0279 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02886 | hp1 | a0002 | c0002 | t0002 | g0239 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02886 | hp2 | a0001 | c0001 | t0019 | g0278 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02895 | hp1 | a0003 | c0003 | t0004 | g0086 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02895 | hp2 | a0002 | c0002 | t0010 | g0115 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02897 | hp1 | a0002 | c0002 | t0010 | g0116 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02897 | hp2 | a0003 | c0003 | t0004 | g0113 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02922 | hp1 | a0003 | c0003 | t0035 | g0080 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02922 | hp2 | a0002 | c0002 | t0010 | g0245 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02965 | hp1 | a0003 | c0003 | t0004 | g0094 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0148 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02970 | hp1 | a0001 | c0004 | t0004 | g0028 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02970 | hp2 | a0003 | c0003 | t0004 | g0069 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02976 | hp1 | a0003 | c0003 | t0004 | g0088 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03017 | hp1 | a0001 | c0004 | t0007 | g0067 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03017 | hp2 | a0001 | c0004 | t0004 | g0011 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03041 | hp1 | a0005 | c0013 | t0004 | g0012 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0262 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0018 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03130 | hp2 | a0002 | c0002 | t0038 | g0027 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03139 | hp1 | a0003 | c0003 | t0004 | g0085 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03139 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03195 | hp1 | a0003 | c0003 | t0004 | g0079 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0093 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03209 | hp2 | a0003 | c0003 | t0016 | g0073 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03225 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03225 | hp2 | a0003 | c0003 | t0018 | g0103 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0203 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03239 | hp2 | a0001 | c0001 | t0037 | g0118 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03453 | hp2 | a0006 | c0014 | t0010 | g0263 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03486 | hp1 | a0002 | c0002 | t0002 | g0238 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03486 | hp2 | a0003 | c0003 | t0004 | g0101 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03491 | hp1 | a0001 | c0004 | t0007 | g0064 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0332 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03492 | hp1 | a0001 | c0004 | t0007 | g0009 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03516 | hp1 | a0003 | c0003 | t0004 | g0087 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03540 | hp1 | a0001 | c0001 | t0027 | g0155 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03540 | hp2 | a0002 | c0002 | t0002 | g0224 | AFR | GWD | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03579 | hp1 | a0003 | c0003 | t0004 | g0090 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03654 | hp2 | a0002 | c0002 | t0041 | g0271 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0233 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03669 | hp2 | a0007 | c0008 | t0001 | g0055 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03688 | hp2 | a0002 | c0002 | t0039 | g0219 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03704 | hp2 | a0003 | c0003 | t0004 | g0100 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0343 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03710 | hp2 | a0001 | c0001 | t0026 | g0174 | SAS | PJL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03834 | hp1 | a0001 | c0004 | t0007 | g0068 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0354 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03942 | hp1 | a0001 | c0001 | t0025 | g0190 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04115 | hp2 | a0001 | c0004 | t0007 | g0066 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04184 | hp1 | a0003 | c0003 | t0004 | g0072 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0257 | SAS | BEB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0215 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04204 | hp1 | a0001 | c0001 | t0028 | g0114 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04204 | hp2 | a0002 | c0002 | t0005 | g0242 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0207 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0198 | SAS | STU | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0264 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18612 | hp2 | a0003 | c0003 | t0004 | g0107 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | CHB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18906 | hp1 | a0002 | c0015 | t0002 | g0021 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18906 | hp2 | a0008 | c0006 | t0004 | g0109 | AFR | YRI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18940 | hp2 | a0001 | c0001 | t0014 | g0167 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18942 | hp1 | a0001 | c0001 | t0030 | g0040 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18944 | hp2 | a0002 | c0005 | t0002 | g0003 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18946 | hp1 | a0002 | c0002 | t0022 | g0252 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18946 | hp2 | a0003 | c0003 | t0032 | g0112 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18947 | hp1 | a0002 | c0002 | t0040 | g0275 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18950 | hp2 | a0002 | c0005 | t0002 | g0138 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18952 | hp1 | a0002 | c0002 | t0005 | g0002 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18961 | hp1 | a0001 | c0001 | t0009 | g0329 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18963 | hp2 | a0002 | c0005 | t0002 | g0003 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18964 | hp1 | a0001 | c0001 | t0013 | g0168 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18973 | hp1 | a0002 | c0002 | t0005 | g0273 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18979 | hp1 | a0002 | c0002 | t0005 | g0243 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18979 | hp2 | a0003 | c0003 | t0004 | g0111 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18982 | hp2 | a0002 | c0002 | t0005 | g0277 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18983 | hp1 | a0002 | c0002 | t0005 | g0274 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18984 | hp1 | a0003 | c0003 | t0004 | g0106 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18986 | hp1 | a0001 | c0001 | t0017 | g0297 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18990 | hp2 | a0001 | c0001 | t0011 | g0179 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0351 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18998 | hp1 | a0002 | c0002 | t0005 | g0276 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19000 | hp1 | a0001 | c0001 | t0009 | g0349 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19001 | hp1 | a0002 | c0002 | t0005 | g0002 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19002 | hp2 | a0003 | c0003 | t0004 | g0099 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0360 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19003 | hp2 | a0002 | c0002 | t0005 | g0002 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19006 | hp2 | a0001 | c0001 | t0012 | g0177 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19007 | hp2 | a0002 | c0002 | t0005 | g0002 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0076 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0137 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19057 | hp1 | a0001 | c0001 | t0015 | g0033 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19057 | hp2 | a0009 | c0012 | t0002 | g0250 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19063 | hp1 | a0010 | c0007 | t0003 | g0339 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0344 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19074 | hp1 | a0002 | c0002 | t0005 | g0272 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19078 | hp2 | a0003 | c0003 | t0004 | g0108 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19080 | hp1 | a0001 | c0001 | t0012 | g0171 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19089 | hp2 | a0003 | c0003 | t0004 | g0110 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19090 | hp1 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA19091 | hp2 | a0003 | c0003 | t0004 | g0105 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20129 | hp1 | a0003 | c0003 | t0004 | g0095 | AFR | ASW | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ASW | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0181 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20752 | hp2 | a0002 | c0002 | t0023 | g0216 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0265 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20905 | hp1 | a0001 | c0010 | t0003 | g0319 | SAS | GIH | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0201 | SAS | GIH | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02109 | hp2 | a0003 | c0003 | t0004 | g0083 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0266 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02559 | hp1 | a0003 | c0003 | t0004 | g0091 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG03471 | hp2 | a0003 | c0003 | t0004 | g0089 | AFR | MSL | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
HG06807 | hp2 | a0002 | c0002 | t0021 | g0255 | AFR | USA | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
NA21309 | hp2 | a0001 | c0001 | t0008 | g0132 | AFR | LWK | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
homoSapiens | chm13v2 | a0003 | c0003 | t0004 | g0102 | REF | REF | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0346 | REF | REF | PNPT1_chr2_55629061_55698844 | PNPT1 | chr2 | 55629061 | 55698844 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55645391 | A | C | 1 | a0009 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.1780T>G | p.Ser594Ala | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/28 | 1801/4549 | 1780/2352 | 594/783 | chr2 | 55645391 | |||
chr2:55645403 | T | C | 3 | a0003 a0005 a0008 |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
missense_variant | MODERATE | c.1768A>G | p.Asn590Asp | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/28 | 1789/4549 | 1768/2352 | 590/783 | chr2 | 55645403 | |||
chr2:55661972 | C | T | 1 | a0007 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1231G>A | p.Val411Ile | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/28 | 1252/4549 | 1231/2352 | 411/783 | chr2 | 55661972 | |||
chr2:55662008 | A | T | 1 | a0010 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1195T>A | p.Phe399Ile | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/28 | 1216/4549 | 1195/2352 | 399/783 | chr2 | 55662008 | |||
chr2:55667055 | C | T | 1 | a0008 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1112G>A | p.Ser371Asn | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/28 | 1133/4549 | 1112/2352 | 371/783 | chr2 | 55667055 | |||
chr2:55671351 | T | C | 1 | a0006 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.944A>G | p.Lys315Arg | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/28 | 965/4549 | 944/2352 | 315/783 | chr2 | 55671351 | |||
chr2:55684985 | T | C | 5 | a0002 a0004 a0005 others(2): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
missense_variant | MODERATE | c.361A>G | p.Ile121Val | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/28 | 382/4549 | 361/2352 | 121/783 | chr2 | 55684985 | |||
chr2:55685034 | T | A | 1 | a0004 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.312A>T | p.Gln104His | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/28 | 333/4549 | 312/2352 | 104/783 | chr2 | 55685034 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55646272 | A | G | 1 | a0002c0011 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1725T>C | p.Ile575Ile | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/28 | 1746/4549 | 1725/2352 | 575/783 | chr2 | 55646272 | |||
chr2:55656182 | G | T | 7 | a0001c0004 a0002c0002 a0002c0011 others(4): Show |
132 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(129): Show |
synonymous_variant | LOW | c.1390C>A | p.Arg464Arg | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/28 | 1411/4549 | 1390/2352 | 464/783 | chr2 | 55656182 | |||
chr2:55660190 | C | T | 1 | a0001c0009 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1251G>A | p.Gly417Gly | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/28 | 1272/4549 | 1251/2352 | 417/783 | chr2 | 55660190 | |||
chr2:55672007 | G | A | 1 | a0002c0015 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.906C>T | p.Tyr302Tyr | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/28 | 927/4549 | 906/2352 | 302/783 | chr2 | 55672007 | |||
chr2:55672970 | T | C | 1 | a0001c0010 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.789A>G | p.Val263Val | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/28 | 810/4549 | 789/2352 | 263/783 | chr2 | 55672970 | |||
chr2:55693722 | T | C | 1 | a0001c0017 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.102A>G | p.Gln34Gln | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/28 | 123/4549 | 102/2352 | 34/783 | chr2 | 55693722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55634260 | C | CT | 5 | a0001c0001t0009 a0001c0001t0014 a0002c0002t0039 others(2): Show |
11 | HG00621.hp2 HG01978.hp2 HG02145.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1976dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1976 | chr2 | 55634260 | ||||||
chr2:55634260 | C | CTT | 2 | a0002c0002t0005 a0002c0002t0040 |
12 | HG04204.hp2 NA18947.hp1 NA18952.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1975_*1976dupAA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1976 | chr2 | 55634260 | ||||||
chr2:55634318 | A | G | 1 | a0002c0002t0038 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1919T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1919 | chr2 | 55634318 | ||||||
chr2:55634343 | C | T | 1 | a0002c0002t0023 | 2 | HG00099.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1894G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1894 | chr2 | 55634343 | ||||||
chr2:55634367 | T | G | 1 | a0002c0002t0040 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1870A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1870 | chr2 | 55634367 | ||||||
chr2:55634407 | G | T | 1 | a0003c0003t0034 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1830C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1830 | chr2 | 55634407 | ||||||
chr2:55634462 | G | A | 1 | a0001c0001t0017 | 2 | HG02074.hp1 NA18986.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1775C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1775 | chr2 | 55634462 | ||||||
chr2:55634508 | C | A | 1 | a0001c0009t0029 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1729G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1729 | chr2 | 55634508 | ||||||
chr2:55634510 | C | T | 18 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(15): Show |
125 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*1727G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1727 | chr2 | 55634510 | ||||||
chr2:55634561 | A | T | 3 | a0001c0001t0006 a0001c0001t0028 a0001c0009t0029 |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1676T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1676 | chr2 | 55634561 | ||||||
chr2:55634602 | C | T | 1 | a0001c0001t0019 | 2 | HG02818.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1635G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1635 | chr2 | 55634602 | ||||||
chr2:55634619 | G | A | 1 | a0002c0002t0041 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1618 | chr2 | 55634619 | ||||||
chr2:55634802 | C | T | 1 | a0001c0004t0007 | 10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1435G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1435 | chr2 | 55634802 | ||||||
chr2:55634805 | C | T | 1 | a0001c0001t0028 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1432G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1432 | chr2 | 55634805 | ||||||
chr2:55634975 | G | A | 1 | a0001c0001t0033 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1262 | chr2 | 55634975 | ||||||
chr2:55635039 | A | G | 1 | a0001c0001t0012 | 3 | HG02071.hp1 NA19006.hp2 NA19080.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1198T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1198 | chr2 | 55635039 | ||||||
chr2:55635136 | G | A | 1 | a0001c0001t0030 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1101 | chr2 | 55635136 | ||||||
chr2:55635220 | A | T | 10 | a0001c0004t0004 a0002c0002t0021 a0003c0003t0004 others(7): Show |
48 | HG01167.hp1 HG01168.hp2 HG01169.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1017T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 1017 | chr2 | 55635220 | ||||||
chr2:55635298 | A | G | 1 | a0001c0001t0011 | 3 | HG00558.hp2 HG02083.hp1 NA18990.hp2 |
3_prime_UTR_variant | MODIFIER | c.*939T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 939 | chr2 | 55635298 | ||||||
chr2:55635305 | T | C | 50 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(47): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*932A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 932 | chr2 | 55635305 | ||||||
chr2:55635315 | AT | A | 47 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(44): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
3_prime_UTR_variant | MODIFIER | c.*921delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 921 | chr2 | 55635315 | ||||||
chr2:55635336 | C | T | 1 | a0001c0001t0027 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*901G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 901 | chr2 | 55635336 | ||||||
chr2:55635383 | C | T | 2 | a0001c0001t0025 a0001c0001t0026 |
2 | HG03710.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*854G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 854 | chr2 | 55635383 | ||||||
chr2:55635462 | G | A | 1 | a0003c0003t0020 | 2 | HG02451.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*775C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 775 | chr2 | 55635462 | ||||||
chr2:55635490 | C | G | 1 | a0003c0003t0032 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*747G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 747 | chr2 | 55635490 | ||||||
chr2:55635529 | G | A | 1 | a0002c0002t0041 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*708C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 708 | chr2 | 55635529 | ||||||
chr2:55635636 | A | T | 1 | a0001c0001t0024 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*601T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 601 | chr2 | 55635636 | ||||||
chr2:55635640 | C | A | 15 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0005 others(12): Show |
110 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*597G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 597 | chr2 | 55635640 | ||||||
chr2:55635666 | T | C | 3 | a0002c0002t0010 a0002c0002t0042 a0006c0014t0010 |
6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*571A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 571 | chr2 | 55635666 | ||||||
chr2:55635669 | T | TTTGGTAA | 22 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(19): Show |
138 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*561_*567dupTTACCA others(1): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 567 | chr2 | 55635669 | ||||||
chr2:55635726 | C | T | 1 | a0003c0003t0016 | 2 | HG01891.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*511G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 511 | chr2 | 55635726 | ||||||
chr2:55635809 | G | C | 1 | a0001c0001t0015 | 2 | NA19057.hp1 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*428C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 428 | chr2 | 55635809 | ||||||
chr2:55635919 | A | C | 1 | a0001c0001t0031 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 318 | chr2 | 55635919 | ||||||
chr2:55635931 | TTCTA | T | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(18): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*302_*305delTAGA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 302 | chr2 | 55635931 | ||||||
chr2:55635975 | CTA | C | 21 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(18): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*260_*261delTA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 260 | chr2 | 55635975 | ||||||
chr2:55636166 | A | G | 1 | a0001c0001t0008 | 7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*71T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 71 | chr2 | 55636166 | ||||||
chr2:55636225 | T | TA | 18 | a0001c0001t0002 a0001c0001t0037 a0001c0004t0007 others(15): Show |
123 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*11dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 28/28 | 11 | chr2 | 55636225 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55636656 | G | A | 1 | a0001c0001t0003g0336 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2197-264C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636656 | |||||||
chr2:55636733 | T | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2197-341A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636733 | |||||||
chr2:55636741 | A | C | 14 | a0001c0001t0003g0295 a0001c0001t0003g0305 a0001c0001t0003g0321 others(11): Show |
14 | HG01928.hp2 HG01934.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.2197-349T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636741 | |||||||
chr2:55636871 | A | AAAC | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2197-482_2197-480d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636871 | |||||||
chr2:55636871 | AAACAAC | A | 97 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(94): Show |
110 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.2197-485_2197-480d others(8): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636871 | |||||||
chr2:55636871 | AAACAACA others(2): Show |
A | 48 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(45): Show |
48 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.2197-488_2197-480d others(11): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636871 | |||||||
chr2:55636929 | A | G | 47 | a0001c0004t0004g0011 a0001c0004t0004g0028 a0003c0003t0004g0069 others(44): Show |
47 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.2197-537T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55636929 | |||||||
chr2:55637237 | A | G | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2196+315T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55637237 | |||||||
chr2:55637268 | C | T | 6 | a0002c0002t0010g0115 a0002c0002t0010g0116 a0002c0002t0010g0245 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2196+284G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55637268 | |||||||
chr2:55637298 | T | C | 1 | a0002c0002t0002g0019 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2196+254A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 27/27 | chr2 | 55637298 | |||||||
chr2:55637709 | G | A | 1 | a0007c0008t0001g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2149-110C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55637709 | |||||||
chr2:55637903 | G | T | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2149-304C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55637903 | |||||||
chr2:55637999 | C | CA | 15 | a0001c0001t0001g0060 a0001c0001t0001g0162 a0001c0001t0001g0197 others(12): Show |
15 | HG01109.hp2 HG01243.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.2149-401dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55637999 | |||||||
chr2:55638088 | G | A | 1 | a0002c0015t0002g0021 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2149-489C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638088 | |||||||
chr2:55638100 | G | A | 1 | a0001c0001t0003g0343 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2149-501C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638100 | |||||||
chr2:55638303 | G | GA | 9 | a0001c0001t0001g0140 a0001c0001t0003g0306 a0001c0001t0003g0307 others(6): Show |
9 | HG00621.hp2 HG01167.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.2149-705dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638303 | |||||||
chr2:55638303 | GA | G | 234 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(231): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2149-705delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638303 | |||||||
chr2:55638334 | G | C | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.2149-735C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638334 | |||||||
chr2:55638394 | G | A | 4 | a0001c0001t0003g0313 a0001c0001t0003g0314 a0001c0001t0017g0297 others(1): Show |
4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2149-795C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638394 | |||||||
chr2:55638449 | C | T | 1 | a0001c0001t0008g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2149-850G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638449 | |||||||
chr2:55638514 | C | T | 1 | a0001c0001t0026g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2149-915G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638514 | |||||||
chr2:55638576 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2149-977C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638576 | |||||||
chr2:55638817 | C | T | 1 | a0001c0001t0003g0314 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2149-1218G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638817 | |||||||
chr2:55638916 | A | C | 1 | a0002c0002t0002g0217 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2149-1317T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55638916 | |||||||
chr2:55639318 | A | G | 293 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(290): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2148+1309T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639318 | |||||||
chr2:55639382 | G | C | 2 | a0002c0002t0002g0232 a0002c0002t0022g0253 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.2148+1245C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639382 | |||||||
chr2:55639470 | C | G | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.2148+1157G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639470 | |||||||
chr2:55639589 | G | C | 1 | a0001c0001t0003g0335 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2148+1038C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639589 | |||||||
chr2:55639592 | C | G | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2148+1035G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639592 | |||||||
chr2:55639614 | A | G | 4 | a0002c0002t0002g0220 a0002c0002t0002g0222 a0002c0002t0002g0265 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2148+1013T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639614 | |||||||
chr2:55639838 | T | G | 1 | a0001c0001t0003g0342 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2148+789A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639838 | |||||||
chr2:55639862 | G | C | 1 | a0001c0001t0003g0335 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2148+765C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639862 | |||||||
chr2:55639877 | C | A | 1 | a0006c0014t0010g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2148+750G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639877 | |||||||
chr2:55639892 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2148+735T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639892 | |||||||
chr2:55639953 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2148+674A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639953 | |||||||
chr2:55639962 | C | A | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+665G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55639962 | |||||||
chr2:55640016 | A | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2148+611T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640016 | |||||||
chr2:55640129 | T | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2148+498A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640129 | |||||||
chr2:55640144 | T | G | 1 | a0003c0003t0004g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2148+483A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640144 | |||||||
chr2:55640200 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2148+427G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640200 | |||||||
chr2:55640296 | T | C | 1 | a0003c0003t0004g0097 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2148+331A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640296 | |||||||
chr2:55640311 | G | A | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2148+316C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640311 | |||||||
chr2:55640313 | C | T | 1 | a0001c0001t0003g0342 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2148+314G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640313 | |||||||
chr2:55640339 | A | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0165 others(10): Show |
15 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(12): Show |
intron_variant | MODIFIER | c.2148+288T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640339 | |||||||
chr2:55640399 | G | A | 1 | a0002c0002t0010g0245 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2148+228C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640399 | |||||||
chr2:55640482 | T | G | 4 | a0002c0002t0002g0010 a0002c0002t0002g0256 a0002c0002t0002g0258 others(1): Show |
5 | NA18939.hp1 NA19004.hp2 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.2148+145A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 26/27 | chr2 | 55640482 | |||||||
chr2:55640710 | A | G | 1 | a0001c0001t0006g0205 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.2070-5T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640710 | |||||||
chr2:55640803 | A | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(135): Show |
142 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.2070-98T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640803 | |||||||
chr2:55640871 | C | T | 1 | a0007c0008t0001g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2070-166G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640871 | |||||||
chr2:55640889 | G | C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070-184C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55640889 | |||||||
chr2:55641018 | G | A | 2 | a0003c0003t0004g0093 a0003c0003t0004g0095 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2070-313C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641018 | |||||||
chr2:55641093 | G | A | 2 | a0003c0003t0004g0110 a0003c0003t0004g0111 |
2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2070-388C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641093 | |||||||
chr2:55641094 | C | T | 1 | a0002c0002t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2070-389G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641094 | |||||||
chr2:55641127 | G | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2070-422C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641127 | |||||||
chr2:55641137 | T | C | 1 | a0003c0003t0004g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2070-432A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641137 | |||||||
chr2:55641262 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2070-557G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641262 | |||||||
chr2:55641283 | A | AT | 11 | a0001c0001t0003g0300 a0001c0001t0003g0307 a0001c0001t0003g0328 others(8): Show |
11 | HG00544.hp2 HG01358.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.2070-579dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641283 | |||||||
chr2:55641283 | AT | A | 216 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(213): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.2070-579delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641283 | |||||||
chr2:55641283 | ATT | A | 60 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0001g0120 others(57): Show |
60 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.2070-580_2070-579d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641283 | |||||||
chr2:55641310 | C | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0130 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2070-605G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641310 | |||||||
chr2:55641338 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.2070-633C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641338 | |||||||
chr2:55641467 | C | T | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.2070-762G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641467 | |||||||
chr2:55641550 | G | A | 1 | a0001c0001t0026g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2070-845C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641550 | |||||||
chr2:55641831 | T | G | 107 | a0001c0001t0002g0325 a0001c0001t0002g0327 a0001c0004t0007g0008 others(104): Show |
122 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.2070-1126A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641831 | |||||||
chr2:55641836 | C | G | 30 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0056 others(27): Show |
30 | HG00099.hp2 HG01261.hp1 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-1131G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641836 | |||||||
chr2:55641846 | C | CT | 36 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(33): Show |
36 | HG00423.hp2 HG00735.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.2070-1142dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55641846 | |||||||
chr2:55642066 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0058 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2069+1092G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642066 | |||||||
chr2:55642344 | A | C | 1 | a0002c0002t0002g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2069+814T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642344 | |||||||
chr2:55642358 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2069+800C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642358 | |||||||
chr2:55642359 | T | C | 1 | a0002c0002t0002g0233 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2069+799A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642359 | |||||||
chr2:55642377 | G | C | 1 | a0002c0002t0002g0236 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2069+781C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642377 | |||||||
chr2:55642382 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2069+776C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642382 | |||||||
chr2:55642433 | C | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(93): Show |
98 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2069+725G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642433 | |||||||
chr2:55642597 | C | T | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.2069+561G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642597 | |||||||
chr2:55642605 | C | CA | 99 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(96): Show |
99 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.2069+552dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642605 | |||||||
chr2:55642605 | C | CAA | 11 | a0001c0001t0001g0153 a0001c0001t0001g0157 a0001c0004t0004g0028 others(8): Show |
11 | HG02145.hp2 HG02559.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.2069+551_2069+552d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642605 | |||||||
chr2:55642709 | A | G | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.2069+449T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642709 | |||||||
chr2:55642829 | A | T | 1 | a0001c0004t0007g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2069+329T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55642829 | |||||||
chr2:55643036 | C | T | 1 | a0001c0001t0003g0284 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2069+122G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 25/27 | chr2 | 55643036 | |||||||
chr2:55643504 | G | T | 1 | a0001c0001t0003g0340 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1907-79C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643504 | |||||||
chr2:55643562 | T | C | 65 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(62): Show |
67 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1907-137A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643562 | |||||||
chr2:55643692 | A | G | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1907-267T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643692 | |||||||
chr2:55643738 | CA | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1907-314delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643738 | |||||||
chr2:55643790 | T | C | 8 | a0001c0001t0003g0294 a0001c0001t0003g0313 a0001c0001t0003g0314 others(5): Show |
8 | HG00544.hp2 HG02074.hp1 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.1907-365A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55643790 | |||||||
chr2:55644150 | G | A | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1906+487C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55644150 | |||||||
chr2:55644194 | A | G | 13 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(10): Show |
13 | HG00099.hp2 HG01167.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1906+443T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 23/27 | chr2 | 55644194 | |||||||
chr2:55644797 | A | AT | 8 | a0001c0001t0001g0211 a0001c0001t0003g0318 a0002c0002t0010g0115 others(5): Show |
8 | HG02572.hp1 HG02735.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1823-78dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644797 | |||||||
chr2:55644857 | G | C | 1 | a0001c0001t0003g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1823-137C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644857 | |||||||
chr2:55644941 | G | A | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1823-221C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644941 | |||||||
chr2:55644946 | G | A | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1823-226C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55644946 | |||||||
chr2:55645009 | C | T | 1 | a0001c0001t0006g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1823-289G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645009 | |||||||
chr2:55645022 | A | AT | 17 | a0001c0001t0001g0139 a0001c0001t0001g0164 a0001c0001t0001g0175 others(14): Show |
19 | HG00438.hp2 HG01175.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.1823-303dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645022 | |||||||
chr2:55645022 | AT | A | 8 | a0001c0001t0001g0061 a0001c0001t0003g0293 a0001c0001t0003g0318 others(5): Show |
8 | HG01070.hp2 HG02451.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1823-303delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645022 | |||||||
chr2:55645044 | G | A | 1 | a0002c0002t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1822+305C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645044 | |||||||
chr2:55645116 | C | A | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1822+233G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645116 | |||||||
chr2:55645124 | T | C | 62 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
64 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1822+225A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645124 | |||||||
chr2:55645226 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1822+123C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645226 | |||||||
chr2:55645246 | G | A | 3 | a0001c0001t0003g0296 a0003c0003t0004g0069 a0003c0003t0004g0082 |
3 | HG02622.hp1 HG02970.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1822+103C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 22/27 | chr2 | 55645246 | |||||||
chr2:55645582 | T | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1739-150A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645582 | |||||||
chr2:55645834 | ACTT | A | 95 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(92): Show |
106 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1739-405_1739-403d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645834 | |||||||
chr2:55645868 | C | A | 31 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(28): Show |
31 | HG00423.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1738+391G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645868 | |||||||
chr2:55645879 | G | A | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+380C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645879 | |||||||
chr2:55645909 | C | T | 1 | a0003c0003t0004g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1738+350G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645909 | |||||||
chr2:55645931 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0001g0164 a0002c0005t0002g0003 others(1): Show |
6 | HG02071.hp2 NA18944.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1738+328C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645931 | |||||||
chr2:55645988 | C | T | 31 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(28): Show |
31 | HG00423.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1738+271G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55645988 | |||||||
chr2:55646080 | G | A | 95 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(92): Show |
106 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1738+179C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646080 | |||||||
chr2:55646166 | T | A | 97 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(94): Show |
110 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.1738+93A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646166 | |||||||
chr2:55646222 | G | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1738+37C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646222 | |||||||
chr2:55646250 | C | G | 76 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(73): Show |
76 | HG00423.hp2 HG01168.hp2 HG01169.hp1 others(73): Show |
intron_variant | MODIFIER | c.1738+9G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 21/27 | chr2 | 55646250 | |||||||
chr2:55646773 | TGTAA | T | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1603-291_1603-288d others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55646773 | |||||||
chr2:55646863 | C | T | 1 | a0003c0003t0020g0104 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1603-377G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55646863 | |||||||
chr2:55646901 | C | T | 10 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(7): Show |
12 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1603-415G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55646901 | |||||||
chr2:55647158 | A | T | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602+189T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55647158 | |||||||
chr2:55647197 | T | C | 27 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(24): Show |
27 | HG00423.hp2 HG01192.hp2 HG02027.hp2 others(24): Show |
intron_variant | MODIFIER | c.1602+150A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55647197 | |||||||
chr2:55647333 | G | A | 1 | a0001c0001t0003g0341 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1602+14C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 19/27 | chr2 | 55647333 | |||||||
chr2:55647676 | C | T | 42 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(39): Show |
42 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1496-223G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55647676 | |||||||
chr2:55647891 | C | A | 1 | a0003c0003t0004g0072 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1496-438G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55647891 | |||||||
chr2:55648109 | C | T | 1 | a0001c0001t0006g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1496-656G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648109 | |||||||
chr2:55648167 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1496-714G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648167 | |||||||
chr2:55648186 | A | G | 3 | a0001c0001t0001g0169 a0001c0001t0012g0171 a0001c0001t0014g0167 |
3 | NA18940.hp2 NA19056.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1496-733T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648186 | |||||||
chr2:55648233 | C | T | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1496-780G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648233 | |||||||
chr2:55648371 | T | C | 2 | a0001c0001t0003g0296 a0001c0001t0003g0357 |
2 | NA18942.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1496-918A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648371 | |||||||
chr2:55648390 | T | A | 17 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(14): Show |
17 | HG01192.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1496-937A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648390 | |||||||
chr2:55648481 | A | G | 1 | a0003c0003t0020g0104 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1496-1028T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648481 | |||||||
chr2:55648520 | CAATTT | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0165 others(10): Show |
15 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(12): Show |
intron_variant | MODIFIER | c.1496-1072_1496-106 others(9): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648520 | |||||||
chr2:55648539 | T | C | 1 | a0002c0002t0038g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1496-1086A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648539 | |||||||
chr2:55648611 | A | G | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1496-1158T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648611 | |||||||
chr2:55648703 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1496-1250G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648703 | |||||||
chr2:55648939 | T | C | 1 | a0005c0013t0004g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1496-1486A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55648939 | |||||||
chr2:55649256 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0312 |
2 | NA18971.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1496-1803A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649256 | |||||||
chr2:55649376 | C | T | 11 | a0001c0001t0003g0007 a0001c0001t0003g0288 a0001c0001t0003g0293 others(8): Show |
13 | NA18612.hp1 NA18943.hp1 NA18955.hp2 others(10): Show |
intron_variant | MODIFIER | c.1496-1923G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649376 | |||||||
chr2:55649412 | C | G | 1 | a0001c0001t0001g0210 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1496-1959G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649412 | |||||||
chr2:55649421 | T | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1496-1968A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649421 | |||||||
chr2:55649474 | C | T | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-2021G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649474 | |||||||
chr2:55649550 | T | C | 15 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(12): Show |
15 | HG00423.hp2 HG02027.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.1496-2097A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649550 | |||||||
chr2:55649794 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1496-2341C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649794 | |||||||
chr2:55649874 | C | G | 1 | a0001c0001t0003g0332 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1496-2421G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649874 | |||||||
chr2:55649978 | C | T | 92 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(89): Show |
105 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1496-2525G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55649978 | |||||||
chr2:55650036 | G | C | 4 | a0001c0001t0003g0313 a0001c0001t0003g0314 a0001c0001t0017g0297 others(1): Show |
4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1496-2583C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650036 | |||||||
chr2:55650079 | G | A | 122 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(119): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1496-2626C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650079 | |||||||
chr2:55650099 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1496-2646C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650099 | |||||||
chr2:55650111 | A | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1496-2658T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650111 | |||||||
chr2:55650141 | C | CACCTCT | 67 | a0001c0001t0001g0173 a0002c0002t0002g0005 a0002c0002t0002g0006 others(64): Show |
77 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1496-2694_1496-268 others(10): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | |||||||
chr2:55650141 | C | CACCTCTA others(5): Show |
6 | a0002c0002t0010g0115 a0002c0002t0010g0116 a0002c0002t0010g0245 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1496-2700_1496-268 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | |||||||
chr2:55650141 | C | CACCTCTA others(11): Show |
5 | a0002c0002t0002g0001 a0002c0002t0002g0237 a0002c0002t0002g0238 others(2): Show |
8 | HG00738.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1496-2706_1496-268 others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | |||||||
chr2:55650141 | CACCTCTA others(5): Show |
C | 1 | a0001c0001t0002g0325 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1496-2700_1496-268 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650141 | |||||||
chr2:55650167 | C | T | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-2714G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650167 | |||||||
chr2:55650217 | C | T | 121 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(118): Show |
123 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.1496-2764G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650217 | |||||||
chr2:55650268 | G | C | 1 | a0002c0002t0002g0016 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1496-2815C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650268 | |||||||
chr2:55650281 | T | C | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1496-2828A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650281 | |||||||
chr2:55650287 | C | T | 122 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(119): Show |
124 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1496-2834G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650287 | |||||||
chr2:55650341 | C | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1496-2888G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650341 | |||||||
chr2:55650351 | G | T | 1 | a0001c0001t0003g0338 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1496-2898C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650351 | |||||||
chr2:55650387 | C | T | 1 | a0003c0003t0004g0105 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1496-2934G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650387 | |||||||
chr2:55650563 | A | AC | 6 | a0001c0001t0001g0141 a0001c0001t0001g0166 a0001c0001t0006g0206 others(3): Show |
6 | HG01261.hp1 HG01952.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1496-3111dupG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650563 | |||||||
chr2:55650585 | C | T | 1 | a0001c0001t0003g0353 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1496-3132G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650585 | |||||||
chr2:55650639 | C | T | 1 | a0005c0013t0004g0012 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1496-3186G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650639 | |||||||
chr2:55650640 | G | A | 2 | a0001c0001t0001g0363 a0001c0001t0001g0364 |
2 | HG00438.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1496-3187C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650640 | |||||||
chr2:55650702 | G | A | 2 | a0002c0002t0002g0217 a0002c0002t0002g0230 |
2 | HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1496-3249C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650702 | |||||||
chr2:55650721 | G | A | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-3268C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650721 | |||||||
chr2:55650755 | C | T | 1 | a0001c0001t0003g0353 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1496-3302G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650755 | |||||||
chr2:55650837 | C | T | 2 | a0002c0002t0021g0254 a0002c0002t0021g0255 |
2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1496-3384G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650837 | |||||||
chr2:55650849 | AGTGAGGA others(131): Show |
A | 1 | a0001c0001t0003g0340 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1496-3534_1496-339 others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650849 | |||||||
chr2:55650884 | C | G | 5 | a0002c0002t0002g0001 a0002c0002t0002g0237 a0002c0002t0002g0238 others(2): Show |
8 | HG00738.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1496-3431G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650884 | |||||||
chr2:55650893 | G | A | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1496-3440C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650893 | |||||||
chr2:55650899 | G | A | 1 | a0001c0001t0001g0004 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1496-3446C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650899 | |||||||
chr2:55650902 | G | GTCAGCCC others(42): Show |
5 | a0003c0003t0004g0105 a0003c0003t0004g0106 a0003c0003t0004g0107 others(2): Show |
5 | NA18612.hp2 NA18946.hp2 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1496-3498_1496-345 others(53): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650902 | |||||||
chr2:55650912 | C | T | 9 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(6): Show |
11 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.1496-3459G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650912 | |||||||
chr2:55650916 | C | T | 2 | a0001c0001t0011g0144 a0001c0001t0011g0194 |
2 | HG00558.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1496-3463G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650916 | |||||||
chr2:55650930 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1496-3477C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650930 | |||||||
chr2:55650959 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1496-3506G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650959 | |||||||
chr2:55650966 | G | GGCCAGCC others(121): Show |
1 | a0002c0002t0002g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1496-3641_1496-351 others(132): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55650966 | |||||||
chr2:55651135 | G | A | 2 | a0002c0002t0002g0213 a0002c0002t0002g0214 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1496-3682C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651135 | |||||||
chr2:55651179 | C | T | 2 | a0001c0001t0015g0033 a0001c0001t0015g0041 |
2 | NA19057.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1495+3721G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651179 | |||||||
chr2:55651204 | C | T | 111 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(108): Show |
124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+3696G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651204 | |||||||
chr2:55651213 | G | C | 2 | a0003c0003t0004g0110 a0003c0003t0004g0111 |
2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1495+3687C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651213 | |||||||
chr2:55651218 | C | A | 2 | a0003c0003t0004g0110 a0003c0003t0004g0111 |
2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1495+3682G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651218 | |||||||
chr2:55651228 | G | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1495+3672C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651228 | |||||||
chr2:55651250 | G | C | 2 | a0002c0002t0010g0248 a0006c0014t0010g0263 |
2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1495+3650C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651250 | |||||||
chr2:55651497 | A | C | 3 | a0001c0001t0003g0359 a0001c0001t0003g0360 a0001c0001t0003g0361 |
3 | HG00423.hp1 NA19003.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1495+3403T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651497 | |||||||
chr2:55651510 | C | G | 123 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(120): Show |
125 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1495+3390G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651510 | |||||||
chr2:55651542 | A | G | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1495+3358T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651542 | |||||||
chr2:55651564 | C | T | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1495+3336G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651564 | |||||||
chr2:55651645 | C | T | 1 | a0002c0002t0022g0253 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1495+3255G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651645 | |||||||
chr2:55651773 | TA | T | 174 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(171): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1495+3126delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651773 | |||||||
chr2:55651774 | A | T | 7 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495+3126T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651774 | |||||||
chr2:55651789 | A | T | 1 | a0002c0002t0001g0046 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1495+3111T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651789 | |||||||
chr2:55651792 | A | T | 119 | a0001c0001t0001g0156 a0001c0004t0007g0008 a0001c0004t0007g0009 others(116): Show |
134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1495+3108T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651792 | |||||||
chr2:55651828 | T | C | 5 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(2): Show |
5 | HG02257.hp1 HG03139.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495+3072A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651828 | |||||||
chr2:55651885 | C | CA | 17 | a0001c0001t0003g0317 a0001c0001t0003g0324 a0001c0001t0003g0330 others(14): Show |
17 | HG00099.hp1 HG01070.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1495+3014dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | |||||||
chr2:55651885 | C | CAA | 92 | a0001c0004t0007g0064 a0002c0002t0001g0043 a0002c0002t0001g0045 others(89): Show |
105 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.1495+3013_1495+301 others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | |||||||
chr2:55651885 | C | CAAA | 12 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(9): Show |
14 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1495+3012_1495+301 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | |||||||
chr2:55651885 | CA | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(96): Show |
101 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1495+3014delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | |||||||
chr2:55651885 | CAAA | C | 62 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1495+3012_1495+301 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651885 | |||||||
chr2:55651989 | T | C | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495+2911A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55651989 | |||||||
chr2:55652181 | TG | T | 119 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(116): Show |
134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1495+2718delC | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652181 | |||||||
chr2:55652321 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1495+2579G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652321 | |||||||
chr2:55652492 | T | C | 1 | a0002c0002t0002g0239 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1495+2408A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652492 | |||||||
chr2:55652554 | C | T | 2 | a0002c0002t0001g0045 a0002c0002t0001g0057 |
2 | NA18962.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1495+2346G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652554 | |||||||
chr2:55652587 | G | C | 1 | a0004c0016t0001g0053 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1495+2313C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652587 | |||||||
chr2:55652656 | T | C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495+2244A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652656 | |||||||
chr2:55652911 | G | C | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1495+1989C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652911 | |||||||
chr2:55652963 | T | A | 1 | a0001c0001t0026g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1495+1937A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55652963 | |||||||
chr2:55653047 | T | C | 111 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(108): Show |
124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+1853A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653047 | |||||||
chr2:55653173 | A | G | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1495+1727T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653173 | |||||||
chr2:55653307 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1495+1593G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653307 | |||||||
chr2:55653431 | C | T | 10 | a0001c0004t0004g0011 a0001c0004t0004g0028 a0001c0004t0007g0008 others(7): Show |
12 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1495+1469G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653431 | |||||||
chr2:55653544 | T | A | 1 | a0009c0012t0002g0250 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1495+1356A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653544 | |||||||
chr2:55653594 | G | T | 2 | a0002c0002t0002g0225 a0002c0002t0002g0356 |
2 | HG01106.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1495+1306C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55653594 | |||||||
chr2:55654041 | G | A | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1495+859C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654041 | |||||||
chr2:55654072 | T | C | 1 | a0002c0002t0002g0224 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1495+828A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654072 | |||||||
chr2:55654091 | G | A | 6 | a0002c0002t0010g0115 a0002c0002t0010g0116 a0002c0002t0010g0245 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+809C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654091 | |||||||
chr2:55654122 | T | C | 111 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(108): Show |
124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+778A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654122 | |||||||
chr2:55654179 | C | T | 6 | a0002c0002t0010g0115 a0002c0002t0010g0116 a0002c0002t0010g0245 others(3): Show |
6 | HG02572.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+721G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654179 | |||||||
chr2:55654192 | G | A | 4 | a0001c0001t0003g0313 a0001c0001t0003g0314 a0001c0001t0017g0297 others(1): Show |
4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495+708C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654192 | |||||||
chr2:55654194 | T | A | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1495+706A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654194 | |||||||
chr2:55654256 | C | CA | 129 | a0001c0001t0001g0031 a0001c0001t0001g0134 a0001c0001t0001g0149 others(126): Show |
142 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1495+643dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654256 | |||||||
chr2:55654256 | C | CAA | 12 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(9): Show |
14 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1495+642_1495+643d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654256 | |||||||
chr2:55654345 | G | A | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1495+555C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654345 | |||||||
chr2:55654357 | T | C | 1 | a0003c0003t0032g0112 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1495+543A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654357 | |||||||
chr2:55654403 | T | C | 111 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(108): Show |
124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1495+497A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654403 | |||||||
chr2:55654681 | C | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1495+219G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654681 | |||||||
chr2:55654790 | G | C | 1 | a0002c0002t0002g0268 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1495+110C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654790 | |||||||
chr2:55654819 | TCCTGCCT others(19): Show |
T | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1495+55_1495+80del others(26): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 18/27 | chr2 | 55654819 | |||||||
chr2:55654997 | T | A | 2 | a0001c0001t0003g0296 a0001c0001t0003g0357 |
2 | NA18942.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1442-44A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55654997 | |||||||
chr2:55655112 | A | T | 1 | a0003c0003t0004g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1442-159T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655112 | |||||||
chr2:55655172 | A | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1442-219T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655172 | |||||||
chr2:55655336 | A | C | 119 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(116): Show |
134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1442-383T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655336 | |||||||
chr2:55655356 | A | G | 244 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(241): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1442-403T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655356 | |||||||
chr2:55655367 | G | A | 2 | a0002c0002t0002g0213 a0002c0002t0002g0214 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1442-414C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655367 | |||||||
chr2:55655430 | A | C | 111 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(108): Show |
124 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1442-477T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655430 | |||||||
chr2:55655517 | A | G | 10 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0001c0001t0003g0287 others(7): Show |
10 | HG00544.hp1 HG02080.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.1442-564T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655517 | |||||||
chr2:55655537 | T | C | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1442-584A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655537 | |||||||
chr2:55655634 | G | A | 2 | a0002c0002t0021g0254 a0002c0002t0021g0255 |
2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1441+497C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655634 | |||||||
chr2:55655908 | A | G | 1 | a0002c0002t0002g0369 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1441+223T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 17/27 | chr2 | 55655908 | |||||||
chr2:55656405 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1285-34T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656405 | |||||||
chr2:55656430 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1285-59A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656430 | |||||||
chr2:55656458 | T | C | 1 | a0010c0007t0003g0339 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1285-87A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656458 | |||||||
chr2:55656578 | C | A | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1285-207G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656578 | |||||||
chr2:55656598 | C | A | 95 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(92): Show |
99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.1285-227G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656598 | |||||||
chr2:55656896 | G | A | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1285-525C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656896 | |||||||
chr2:55656971 | T | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(123): Show |
130 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1285-600A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55656971 | |||||||
chr2:55657047 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1285-676C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657047 | |||||||
chr2:55657050 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0281 |
2 | NA19000.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1285-679G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657050 | |||||||
chr2:55657117 | T | A | 119 | a0001c0004t0004g0011 a0001c0004t0004g0028 a0001c0004t0007g0008 others(116): Show |
132 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1285-746A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657117 | |||||||
chr2:55657174 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1285-803C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657174 | |||||||
chr2:55657228 | C | T | 103 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(100): Show |
116 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(113): Show |
intron_variant | MODIFIER | c.1285-857G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657228 | |||||||
chr2:55657361 | A | G | 1 | a0001c0001t0003g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1285-990T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657361 | |||||||
chr2:55657474 | T | C | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1285-1103A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657474 | |||||||
chr2:55657593 | T | C | 127 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(124): Show |
131 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1285-1222A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657593 | |||||||
chr2:55657729 | G | A | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1285-1358C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657729 | |||||||
chr2:55657856 | C | CA | 16 | a0002c0002t0002g0006 a0002c0002t0002g0218 a0002c0002t0002g0220 others(13): Show |
18 | HG00639.hp1 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1285-1486dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | C | CAA | 14 | a0001c0001t0001g0056 a0002c0002t0002g0212 a0002c0002t0002g0213 others(11): Show |
14 | HG00140.hp2 HG01069.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1285-1487_1285-148 others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | C | CAAA | 8 | a0002c0002t0002g0014 a0002c0002t0002g0225 a0002c0002t0002g0232 others(5): Show |
8 | HG00642.hp1 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1488_1285-148 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | C | CAAAAAAA others(3): Show |
1 | a0002c0002t0002g0257 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1285-1495_1285-148 others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | C | CAAAAAAA others(5): Show |
2 | a0002c0002t0002g0228 a0002c0002t0005g0242 |
2 | HG01099.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1285-1497_1285-148 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | C | CAAAAAAA others(6): Show |
1 | a0002c0002t0002g0229 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1285-1498_1285-148 others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | C | CAAAAAAA others(8): Show |
1 | a0002c0002t0002g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1285-1500_1285-148 others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | C | CAAAAAAA others(17): Show |
1 | a0002c0002t0002g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1285-1509_1285-148 others(28): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CA | C | 6 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0235 others(3): Show |
6 | HG01433.hp1 HG01516.hp1 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-1486delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAA | C | 8 | a0002c0002t0002g0015 a0002c0002t0002g0016 a0002c0002t0002g0026 others(5): Show |
8 | HG01074.hp1 HG01168.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1487_1285-148 others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAA | C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0124 a0001c0001t0001g0130 others(7): Show |
10 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-1491_1285-148 others(10): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA | C | 10 | a0001c0001t0001g0139 a0001c0001t0001g0153 a0001c0001t0001g0188 others(7): Show |
10 | HG00438.hp2 HG01346.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-1492_1285-148 others(11): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0123 a0001c0001t0001g0134 a0001c0001t0001g0149 others(5): Show |
8 | HG01516.hp2 HG02027.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1285-1493_1285-148 others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(2): Show |
C | 31 | a0001c0001t0001g0121 a0001c0001t0001g0128 a0001c0001t0001g0129 others(28): Show |
33 | HG00558.hp2 HG00621.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1285-1494_1285-148 others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(3): Show |
C | 21 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0122 others(18): Show |
21 | HG00140.hp1 HG00639.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1285-1495_1285-148 others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(5): Show |
C | 9 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
9 | HG01243.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1497_1285-148 others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(6): Show |
C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0059 others(11): Show |
17 | HG00423.hp2 HG01192.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.1285-1498_1285-148 others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(7): Show |
C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0036 others(10): Show |
13 | HG01361.hp2 HG02129.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1285-1499_1285-148 others(18): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(8): Show |
C | 4 | a0001c0001t0001g0034 a0001c0001t0008g0160 a0002c0002t0002g0217 others(1): Show |
4 | HG01952.hp2 HG02293.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-1500_1285-148 others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0159 others(2): Show |
5 | HG02258.hp1 HG02809.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285-1501_1285-148 others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(10): Show |
C | 1 | a0002c0002t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1285-1502_1285-148 others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(13): Show |
C | 2 | a0002c0002t0002g0018 a0002c0002t0002g0019 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1285-1505_1285-148 others(24): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(14): Show |
C | 10 | a0003c0003t0004g0072 a0003c0003t0004g0076 a0003c0003t0004g0092 others(7): Show |
10 | HG01175.hp2 HG02145.hp2 HG03486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1285-1506_1285-148 others(25): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(15): Show |
C | 48 | a0001c0001t0002g0325 a0001c0001t0003g0287 a0001c0001t0003g0290 others(45): Show |
48 | HG01168.hp2 HG01169.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.1285-1507_1285-148 others(26): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(16): Show |
C | 66 | a0001c0001t0002g0327 a0001c0001t0003g0007 a0001c0001t0003g0282 others(63): Show |
68 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1285-1508_1285-148 others(27): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(17): Show |
C | 1 | a0002c0002t0002g0017 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1285-1509_1285-148 others(28): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(18): Show |
C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0165 others(19): Show |
27 | HG00438.hp1 HG00738.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1285-1510_1285-148 others(29): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(21): Show |
C | 1 | a0001c0004t0007g0066 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1285-1513_1285-148 others(32): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(22): Show |
C | 7 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(4): Show |
9 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285-1514_1285-148 others(33): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(26): Show |
C | 2 | a0002c0002t0021g0254 a0002c0002t0021g0255 |
2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1285-1518_1285-148 others(37): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657856 | CAAAAAAA others(27): Show |
C | 1 | a0001c0010t0003g0319 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1285-1519_1285-148 others(38): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657856 | |||||||
chr2:55657892 | A | G | 1 | a0003c0003t0032g0112 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1285-1521T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657892 | |||||||
chr2:55657919 | G | A | 125 | a0001c0001t0002g0325 a0001c0001t0002g0327 a0001c0001t0003g0007 others(122): Show |
127 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1285-1548C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657919 | |||||||
chr2:55657950 | A | G | 65 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(62): Show |
67 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1285-1579T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55657950 | |||||||
chr2:55658093 | G | A | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1285-1722C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658093 | |||||||
chr2:55658128 | G | A | 2 | a0002c0002t0002g0022 a0002c0002t0002g0024 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1285-1757C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658128 | |||||||
chr2:55658373 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0165 others(10): Show |
15 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(12): Show |
intron_variant | MODIFIER | c.1284+1784G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658373 | |||||||
chr2:55658565 | T | C | 1 | a0001c0001t0008g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1284+1592A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658565 | |||||||
chr2:55658775 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1284+1382C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55658775 | |||||||
chr2:55659079 | C | T | 2 | a0002c0002t0021g0254 a0002c0002t0021g0255 |
2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1284+1078G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659079 | |||||||
chr2:55659387 | T | C | 3 | a0001c0004t0007g0009 a0001c0004t0007g0064 a0001c0004t0007g0066 |
4 | HG01433.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+770A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659387 | |||||||
chr2:55659467 | T | C | 95 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(92): Show |
106 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.1284+690A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659467 | |||||||
chr2:55659505 | G | A | 1 | a0001c0001t0003g0342 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1284+652C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659505 | |||||||
chr2:55659521 | CTT | C | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1284+634_1284+635d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659521 | |||||||
chr2:55659543 | C | T | 1 | a0002c0002t0002g0230 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1284+614G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659543 | |||||||
chr2:55659573 | G | A | 1 | a0001c0001t0001g0363 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1284+584C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659573 | |||||||
chr2:55659641 | A | G | 1 | a0001c0001t0033g0323 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1284+516T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659641 | |||||||
chr2:55659645 | C | T | 138 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(135): Show |
142 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1284+512G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659645 | |||||||
chr2:55659658 | C | T | 2 | a0002c0002t0005g0002 a0002c0002t0005g0243 |
5 | NA18952.hp1 NA18979.hp1 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.1284+499G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659658 | |||||||
chr2:55659736 | G | A | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1284+421C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659736 | |||||||
chr2:55659867 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1284+290G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659867 | |||||||
chr2:55659940 | A | G | 2 | a0002c0002t0002g0234 a0002c0002t0002g0261 |
2 | HG01109.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1284+217T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55659940 | |||||||
chr2:55660025 | GC | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.1284+131delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55660025 | |||||||
chr2:55660041 | T | C | 138 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(135): Show |
142 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1284+116A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55660041 | |||||||
chr2:55660057 | C | A | 1 | a0001c0001t0006g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1284+100G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 15/27 | chr2 | 55660057 | |||||||
chr2:55660401 | T | C | 3 | a0001c0001t0003g0307 a0001c0001t0003g0347 a0001c0001t0009g0308 |
3 | HG00621.hp2 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1248-208A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660401 | |||||||
chr2:55660515 | C | T | 1 | a0002c0002t0002g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1248-322G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660515 | |||||||
chr2:55660568 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1248-375G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660568 | |||||||
chr2:55660614 | T | G | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1248-421A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660614 | |||||||
chr2:55660679 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1248-486C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660679 | |||||||
chr2:55660815 | G | C | 1 | a0003c0003t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1248-622C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55660815 | |||||||
chr2:55661091 | C | CT | 19 | a0001c0001t0001g0139 a0001c0001t0001g0175 a0001c0001t0001g0193 others(16): Show |
19 | HG00423.hp1 HG01175.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.1247+864dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | |||||||
chr2:55661091 | CT | C | 138 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(135): Show |
149 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(146): Show |
intron_variant | MODIFIER | c.1247+864delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | |||||||
chr2:55661091 | CTT | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.1247+863_1247+864d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | |||||||
chr2:55661091 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0009g0308 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1247+854_1247+864d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661091 | |||||||
chr2:55661110 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1247+846A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661110 | |||||||
chr2:55661240 | C | T | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1247+716G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661240 | |||||||
chr2:55661260 | T | C | 7 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1247+696A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661260 | |||||||
chr2:55661278 | G | A | 307 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(304): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1247+678C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661278 | |||||||
chr2:55661288 | T | A | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1247+668A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661288 | |||||||
chr2:55661477 | T | A | 183 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(180): Show |
187 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.1247+479A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661477 | |||||||
chr2:55661494 | C | T | 1 | a0001c0001t0003g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1247+462G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661494 | |||||||
chr2:55661740 | T | A | 1 | a0010c0007t0003g0339 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1247+216A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661740 | |||||||
chr2:55661900 | T | C | 1 | a0001c0001t0003g0324 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1247+56A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661900 | |||||||
chr2:55661927 | G | A | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1247+29C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 14/27 | chr2 | 55661927 | |||||||
chr2:55662063 | C | T | 2 | a0001c0001t0012g0177 a0001c0001t0012g0184 |
2 | HG02071.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1177-37G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662063 | |||||||
chr2:55662158 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1177-132G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662158 | |||||||
chr2:55662201 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(4): Show |
7 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1177-175T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662201 | |||||||
chr2:55662208 | A | C | 3 | a0001c0001t0003g0291 a0001c0001t0003g0317 a0001c0001t0009g0349 |
3 | HG00558.hp1 NA19000.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1177-182T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662208 | |||||||
chr2:55662226 | T | C | 1 | a0007c0008t0001g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1177-200A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662226 | |||||||
chr2:55662295 | G | C | 4 | a0001c0001t0003g0313 a0001c0001t0003g0314 a0001c0001t0017g0297 others(1): Show |
4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177-269C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662295 | |||||||
chr2:55662319 | G | A | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177-293C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662319 | |||||||
chr2:55662331 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(121): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1177-305C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662331 | |||||||
chr2:55662533 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(121): Show |
128 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1177-507C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662533 | |||||||
chr2:55662566 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1177-540A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662566 | |||||||
chr2:55662567 | T | C | 1 | a0002c0002t0038g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1177-541A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662567 | |||||||
chr2:55662741 | G | A | 92 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(89): Show |
94 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1177-715C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662741 | |||||||
chr2:55662880 | A | AT | 8 | a0001c0004t0007g0068 a0002c0002t0001g0362 a0002c0002t0002g0256 others(5): Show |
8 | HG00423.hp2 HG01168.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177-855dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662880 | |||||||
chr2:55662880 | AT | A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0140 a0001c0001t0001g0150 others(29): Show |
34 | HG00438.hp1 HG01261.hp1 HG01496.hp2 others(31): Show |
intron_variant | MODIFIER | c.1177-855delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662880 | |||||||
chr2:55662880 | ATT | A | 91 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(88): Show |
93 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1177-856_1177-855d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662880 | |||||||
chr2:55662897 | TG | T | 77 | a0001c0001t0001g0158 a0001c0001t0002g0325 a0001c0001t0002g0327 others(74): Show |
79 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.1177-872delC | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662897 | |||||||
chr2:55662898 | G | T | 6 | a0001c0001t0003g0314 a0001c0001t0003g0351 a0001c0001t0003g0359 others(3): Show |
6 | HG02970.hp1 HG03017.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177-872C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662898 | |||||||
chr2:55662946 | T | C | 1 | a0010c0007t0003g0339 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1177-920A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55662946 | |||||||
chr2:55663175 | C | T | 1 | a0001c0001t0006g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1177-1149G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663175 | |||||||
chr2:55663468 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1177-1442C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663468 | |||||||
chr2:55663468 | G | T | 45 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(42): Show |
45 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(42): Show |
intron_variant | MODIFIER | c.1177-1442C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663468 | |||||||
chr2:55663552 | C | A | 2 | a0003c0003t0004g0093 a0003c0003t0004g0095 |
2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1177-1526G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663552 | |||||||
chr2:55663678 | G | A | 3 | a0001c0001t0003g0307 a0001c0001t0003g0347 a0001c0001t0009g0308 |
3 | HG00621.hp2 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1177-1652C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663678 | |||||||
chr2:55663893 | G | C | 1 | a0002c0002t0002g0368 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1177-1867C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663893 | |||||||
chr2:55663970 | CAGA | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1177-1947_1177-194 others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55663970 | |||||||
chr2:55664005 | T | C | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.1177-1979A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664005 | |||||||
chr2:55664029 | G | A | 1 | a0002c0002t0038g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1177-2003C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664029 | |||||||
chr2:55664185 | T | C | 130 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(127): Show |
134 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1177-2159A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664185 | |||||||
chr2:55664234 | T | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0182 |
2 | HG02080.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1177-2208A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664234 | |||||||
chr2:55664483 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1177-2457C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664483 | |||||||
chr2:55664602 | C | G | 1 | a0003c0003t0004g0099 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1176+2389G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664602 | |||||||
chr2:55664851 | G | A | 1 | a0001c0001t0008g0160 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1176+2140C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55664851 | |||||||
chr2:55665117 | G | A | 1 | a0001c0001t0003g0340 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1176+1874C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665117 | |||||||
chr2:55665126 | A | C | 113 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(110): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1176+1865T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665126 | |||||||
chr2:55665173 | G | T | 2 | a0001c0004t0007g0008 a0001c0004t0007g0063 |
3 | HG01081.hp1 HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1176+1818C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665173 | |||||||
chr2:55665221 | A | G | 113 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(110): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1176+1770T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665221 | |||||||
chr2:55665243 | C | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1176+1748G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665243 | |||||||
chr2:55665375 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1176+1616A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665375 | |||||||
chr2:55665594 | A | C | 1 | a0001c0001t0003g0347 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1176+1397T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665594 | |||||||
chr2:55665628 | CACAACTC others(6): Show |
C | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1176+1350_1176+136 others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665628 | |||||||
chr2:55665672 | G | A | 1 | a0002c0002t0002g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1176+1319C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665672 | |||||||
chr2:55665805 | T | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1176+1186A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665805 | |||||||
chr2:55665882 | G | A | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176+1109C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55665882 | |||||||
chr2:55666130 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1176+861T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666130 | |||||||
chr2:55666201 | C | A | 287 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1176+790G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666201 | |||||||
chr2:55666206 | C | T | 1 | a0001c0001t0009g0349 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1176+785G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666206 | |||||||
chr2:55666587 | C | A | 1 | a0001c0001t0001g0210 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1176+404G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666587 | |||||||
chr2:55666742 | C | T | 1 | a0001c0001t0003g0290 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1176+249G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666742 | |||||||
chr2:55666955 | A | G | 62 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1176+36T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 13/27 | chr2 | 55666955 | |||||||
chr2:55667097 | T | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
splice_region_variant&intron_variant | LOW | c.1074-4A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667097 | |||||||
chr2:55667108 | G | A | 2 | a0002c0002t0002g0232 a0002c0002t0022g0253 |
2 | HG00642.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1074-15C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667108 | |||||||
chr2:55667112 | T | C | 113 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(110): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.1074-19A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667112 | |||||||
chr2:55667284 | T | G | 1 | a0002c0002t0001g0043 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1074-191A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667284 | |||||||
chr2:55667293 | G | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(161): Show |
166 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1074-200C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667293 | |||||||
chr2:55667311 | T | C | 1 | a0002c0002t0002g0269 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1074-218A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667311 | |||||||
chr2:55667321 | G | A | 18 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(15): Show |
18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.1074-228C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667321 | |||||||
chr2:55667349 | C | G | 2 | a0001c0001t0003g0284 a0001c0001t0003g0351 |
2 | NA18994.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1074-256G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667349 | |||||||
chr2:55667410 | C | T | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1074-317G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667410 | |||||||
chr2:55667510 | C | T | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1073+352G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667510 | |||||||
chr2:55667530 | C | T | 4 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0024 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+332G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667530 | |||||||
chr2:55667558 | C | T | 1 | a0003c0003t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1073+304G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667558 | |||||||
chr2:55667585 | CA | C | 174 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(171): Show |
178 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.1073+276delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667585 | |||||||
chr2:55667688 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0015g0033 a0001c0001t0015g0041 others(1): Show |
4 | NA18942.hp1 NA18955.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+174T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 12/27 | chr2 | 55667688 | |||||||
chr2:55668017 | T | C | 1 | a0001c0001t0008g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.977-59A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668017 | |||||||
chr2:55668170 | T | C | 62 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.977-212A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668170 | |||||||
chr2:55668186 | T | C | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.977-228A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668186 | |||||||
chr2:55668275 | T | A | 2 | a0003c0003t0004g0094 a0003c0003t0035g0080 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.977-317A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668275 | |||||||
chr2:55668362 | G | C | 1 | a0001c0001t0003g0347 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.977-404C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668362 | |||||||
chr2:55668439 | T | A | 1 | a0001c0001t0003g0344 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-481A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668439 | |||||||
chr2:55668496 | G | A | 7 | a0002c0002t0002g0213 a0002c0002t0002g0214 a0002c0002t0002g0366 others(4): Show |
7 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.977-538C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668496 | |||||||
chr2:55668518 | G | A | 1 | a0001c0001t0003g0341 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.977-560C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668518 | |||||||
chr2:55668590 | G | A | 1 | a0001c0001t0003g0344 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-632C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668590 | |||||||
chr2:55668707 | C | T | 1 | a0001c0001t0003g0344 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-749G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668707 | |||||||
chr2:55668708 | T | C | 1 | a0001c0001t0003g0344 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-750A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668708 | |||||||
chr2:55668709 | C | T | 1 | a0001c0001t0003g0344 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-751G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668709 | |||||||
chr2:55668719 | C | CCTCCCTA others(5): Show |
1 | a0001c0001t0003g0344 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.977-762_977-761ins others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668719 | |||||||
chr2:55668816 | G | A | 1 | a0002c0002t0002g0259 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.977-858C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668816 | |||||||
chr2:55668857 | C | G | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.977-899G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55668857 | |||||||
chr2:55669161 | G | C | 16 | a0003c0003t0004g0069 a0003c0003t0004g0072 a0003c0003t0004g0077 others(13): Show |
16 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.977-1203C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669161 | |||||||
chr2:55669163 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.977-1205A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669163 | |||||||
chr2:55669177 | A | T | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.977-1219T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669177 | |||||||
chr2:55669185 | AC | A | 43 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(40): Show |
43 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.977-1228delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669185 | |||||||
chr2:55669248 | A | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.977-1290T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669248 | |||||||
chr2:55669270 | T | G | 1 | a0002c0002t0022g0252 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.977-1312A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669270 | |||||||
chr2:55669457 | A | G | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.977-1499T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669457 | |||||||
chr2:55669463 | T | A | 1 | a0002c0002t0002g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.977-1505A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669463 | |||||||
chr2:55669463 | T | C | 135 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.977-1505A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669463 | |||||||
chr2:55669614 | A | G | 2 | a0003c0003t0004g0069 a0003c0003t0004g0082 |
2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.977-1656T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669614 | |||||||
chr2:55669761 | A | T | 1 | a0001c0001t0003g0345 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.976+1558T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | |||||||
chr2:55669761 | AC | A | 99 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(96): Show |
112 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.976+1557delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | |||||||
chr2:55669761 | ACT | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(122): Show |
129 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.976+1556_976+1557d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | |||||||
chr2:55669761 | ACTT | A | 64 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(61): Show |
64 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.976+1555_976+1557d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669761 | |||||||
chr2:55669762 | CT | C | 14 | a0001c0001t0003g0296 a0001c0001t0003g0313 a0001c0001t0003g0314 others(11): Show |
14 | HG00544.hp1 HG00544.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.976+1556delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669762 | |||||||
chr2:55669871 | G | A | 1 | a0001c0001t0008g0147 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.976+1448C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669871 | |||||||
chr2:55669887 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.976+1432A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669887 | |||||||
chr2:55669905 | C | A | 1 | a0002c0002t0002g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.976+1414G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55669905 | |||||||
chr2:55670052 | C | T | 2 | a0003c0003t0004g0110 a0003c0003t0004g0111 |
2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.976+1267G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670052 | |||||||
chr2:55670095 | A | G | 6 | a0001c0001t0006g0136 a0001c0001t0006g0201 a0001c0001t0006g0202 others(3): Show |
6 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.976+1224T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670095 | |||||||
chr2:55670217 | C | T | 1 | a0001c0001t0006g0204 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.976+1102G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670217 | |||||||
chr2:55670287 | C | T | 1 | a0001c0001t0003g0324 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.976+1032G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670287 | |||||||
chr2:55670307 | C | A | 2 | a0001c0001t0003g0296 a0001c0001t0003g0357 |
2 | NA18942.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.976+1012G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670307 | |||||||
chr2:55670337 | C | A | 1 | a0002c0002t0002g0369 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.976+982G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670337 | |||||||
chr2:55670421 | C | T | 6 | a0002c0002t0005g0272 a0002c0002t0005g0273 a0002c0002t0005g0274 others(3): Show |
6 | NA18947.hp1 NA18973.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.976+898G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670421 | |||||||
chr2:55670430 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.976+889A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670430 | |||||||
chr2:55670465 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.976+854G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670465 | |||||||
chr2:55670485 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.976+834G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670485 | |||||||
chr2:55670565 | T | C | 120 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(117): Show |
135 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.976+754A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670565 | |||||||
chr2:55670772 | G | A | 1 | a0001c0001t0008g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.976+547C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670772 | |||||||
chr2:55670861 | T | C | 135 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.976+458A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670861 | |||||||
chr2:55670970 | TAA | T | 276 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(273): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.976+347_976+348del others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670970 | |||||||
chr2:55670970 | TAAA | T | 11 | a0001c0001t0001g0034 a0001c0001t0001g0124 a0001c0001t0028g0114 others(8): Show |
13 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.976+346_976+348del others(3): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670970 | |||||||
chr2:55670995 | C | CT | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.976+323dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55670995 | |||||||
chr2:55671066 | C | T | 1 | a0001c0001t0003g0351 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.976+253G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55671066 | |||||||
chr2:55671068 | A | G | 112 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(109): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.976+251T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55671068 | |||||||
chr2:55671155 | C | G | 110 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(107): Show |
121 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.976+164G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 11/27 | chr2 | 55671155 | |||||||
chr2:55671553 | C | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0165 others(9): Show |
14 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.919-177G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671553 | |||||||
chr2:55671598 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.919-222A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671598 | |||||||
chr2:55671638 | T | A | 1 | a0002c0002t0038g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.919-262A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671638 | |||||||
chr2:55671748 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.918+247G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671748 | |||||||
chr2:55671794 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.918+201T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671794 | |||||||
chr2:55671795 | C | T | 96 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(93): Show |
109 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.918+200G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671795 | |||||||
chr2:55671827 | AAAAAC | A | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.918+163_918+167del others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671827 | |||||||
chr2:55671961 | G | A | 1 | a0003c0003t0020g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.918+34C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 10/27 | chr2 | 55671961 | |||||||
chr2:55672093 | A | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.867-47T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672093 | |||||||
chr2:55672110 | T | C | 1 | a0002c0002t0002g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.867-64A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672110 | |||||||
chr2:55672290 | T | C | 112 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(109): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.867-244A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672290 | |||||||
chr2:55672638 | G | C | 1 | a0001c0001t0033g0323 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.866+255C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672638 | |||||||
chr2:55672661 | T | C | 1 | a0003c0003t0004g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.866+232A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 9/27 | chr2 | 55672661 | |||||||
chr2:55673096 | G | GA | 13 | a0001c0001t0003g0342 a0001c0001t0006g0136 a0001c0001t0006g0198 others(10): Show |
13 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.680-18dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673096 | |||||||
chr2:55673148 | A | G | 112 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(109): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.680-69T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673148 | |||||||
chr2:55673274 | A | G | 1 | a0001c0001t0033g0323 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.680-195T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673274 | |||||||
chr2:55673277 | T | C | 1 | a0002c0002t0002g0226 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.680-198A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673277 | |||||||
chr2:55673324 | A | G | 112 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(109): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.680-245T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673324 | |||||||
chr2:55673355 | C | G | 1 | a0002c0002t0002g0367 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.680-276G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673355 | |||||||
chr2:55673425 | G | A | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.680-346C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673425 | |||||||
chr2:55673493 | C | T | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-414G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673493 | |||||||
chr2:55673664 | G | A | 1 | a0002c0002t0002g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.680-585C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673664 | |||||||
chr2:55673772 | T | C | 1 | a0001c0001t0025g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.680-693A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673772 | |||||||
chr2:55673803 | A | C | 280 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.680-724T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673803 | |||||||
chr2:55673876 | C | T | 2 | a0001c0001t0003g0288 a0001c0001t0003g0299 |
2 | NA18981.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.680-797G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673876 | |||||||
chr2:55673879 | C | T | 1 | a0002c0002t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.680-800G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55673879 | |||||||
chr2:55674182 | T | C | 280 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.680-1103A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674182 | |||||||
chr2:55674258 | G | A | 1 | a0003c0003t0004g0101 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.680-1179C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674258 | |||||||
chr2:55674317 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.680-1238T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674317 | |||||||
chr2:55674355 | A | C | 1 | a0002c0002t0002g0237 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.680-1276T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674355 | |||||||
chr2:55674441 | G | T | 1 | a0002c0002t0002g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.680-1362C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674441 | |||||||
chr2:55674600 | T | A | 1 | a0003c0003t0004g0076 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.680-1521A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674600 | |||||||
chr2:55674906 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-1827G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674906 | |||||||
chr2:55674908 | G | A | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-1829C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674908 | |||||||
chr2:55674913 | T | A | 1 | a0002c0002t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.680-1834A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674913 | |||||||
chr2:55674929 | A | C | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.680-1850T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55674929 | |||||||
chr2:55675094 | C | G | 1 | a0002c0002t0023g0216 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.680-2015G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675094 | |||||||
chr2:55675223 | T | C | 62 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
62 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.680-2144A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675223 | |||||||
chr2:55675234 | C | A | 1 | a0003c0003t0004g0094 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.680-2155G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675234 | |||||||
chr2:55675260 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.680-2181A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675260 | |||||||
chr2:55675281 | A | G | 280 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.680-2202T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675281 | |||||||
chr2:55675360 | G | C | 4 | a0002c0002t0002g0017 a0002c0002t0002g0018 a0002c0002t0002g0019 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-2281C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675360 | |||||||
chr2:55675379 | G | A | 4 | a0001c0001t0003g0313 a0001c0001t0003g0314 a0001c0001t0017g0297 others(1): Show |
4 | HG02074.hp1 NA18975.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.680-2300C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675379 | |||||||
chr2:55675453 | G | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-2374C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675453 | |||||||
chr2:55675611 | T | C | 1 | a0002c0002t0023g0216 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.680-2532A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675611 | |||||||
chr2:55675661 | G | A | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.680-2582C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675661 | |||||||
chr2:55675733 | T | C | 5 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0024 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.680-2654A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675733 | |||||||
chr2:55675881 | A | C | 135 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(132): Show |
137 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.680-2802T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675881 | |||||||
chr2:55675921 | A | G | 9 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0001c0001t0003g0287 others(6): Show |
9 | HG00544.hp1 HG02080.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-2842T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675921 | |||||||
chr2:55675932 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.680-2853G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55675932 | |||||||
chr2:55676113 | A | G | 5 | a0002c0002t0002g0001 a0002c0002t0002g0237 a0002c0002t0002g0238 others(2): Show |
8 | HG00738.hp1 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.680-3034T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676113 | |||||||
chr2:55676128 | T | G | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.680-3049A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676128 | |||||||
chr2:55676132 | C | T | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.680-3053G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676132 | |||||||
chr2:55676164 | T | G | 287 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.680-3085A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676164 | |||||||
chr2:55676174 | C | T | 1 | a0002c0002t0002g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.680-3095G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676174 | |||||||
chr2:55676262 | C | CA | 131 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0035 others(128): Show |
144 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.680-3184dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | |||||||
chr2:55676262 | C | CAA | 65 | a0001c0001t0001g0062 a0001c0001t0006g0136 a0001c0001t0006g0198 others(62): Show |
65 | HG00099.hp1 HG00099.hp2 HG01168.hp2 others(62): Show |
intron_variant | MODIFIER | c.680-3185_680-3184d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | |||||||
chr2:55676262 | C | CAAA | 9 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(6): Show |
9 | HG01175.hp2 HG01346.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.680-3186_680-3184d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | |||||||
chr2:55676262 | CA | C | 8 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 others(5): Show |
8 | HG02080.hp1 HG02273.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.680-3184delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | |||||||
chr2:55676262 | CAAAAAAA others(4): Show |
C | 6 | a0001c0001t0003g0285 a0001c0001t0003g0286 a0001c0001t0003g0287 others(3): Show |
6 | HG02080.hp2 NA18947.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.680-3194_680-3184d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676262 | |||||||
chr2:55676381 | A | G | 1 | a0001c0001t0011g0194 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.679+3301T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676381 | |||||||
chr2:55676451 | A | G | 2 | a0003c0003t0004g0069 a0003c0003t0004g0082 |
2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.679+3231T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676451 | |||||||
chr2:55676485 | G | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.679+3197C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676485 | |||||||
chr2:55676526 | C | T | 5 | a0002c0002t0002g0366 a0002c0002t0002g0367 a0002c0002t0002g0368 others(2): Show |
5 | HG01074.hp1 HG01168.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+3156G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676526 | |||||||
chr2:55676563 | T | TA | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+3118dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676563 | |||||||
chr2:55676576 | G | A | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.679+3106C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676576 | |||||||
chr2:55676612 | G | A | 287 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.679+3070C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676612 | |||||||
chr2:55676642 | A | G | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.679+3040T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676642 | |||||||
chr2:55676643 | C | T | 1 | a0002c0002t0002g0236 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.679+3039G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676643 | |||||||
chr2:55676652 | A | G | 2 | a0003c0003t0016g0073 a0003c0003t0016g0074 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.679+3030T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676652 | |||||||
chr2:55676710 | A | C | 1 | a0002c0002t0005g0273 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.679+2972T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676710 | |||||||
chr2:55676837 | C | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.679+2845G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676837 | |||||||
chr2:55676910 | T | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+2772A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676910 | |||||||
chr2:55676926 | A | G | 31 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(28): Show |
31 | HG00423.hp2 HG01192.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.679+2756T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55676926 | |||||||
chr2:55677035 | C | A | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.679+2647G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677035 | |||||||
chr2:55677217 | T | G | 1 | a0001c0001t0006g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.679+2465A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677217 | |||||||
chr2:55677268 | G | T | 1 | a0002c0002t0002g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.679+2414C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677268 | |||||||
chr2:55677310 | T | C | 1 | a0001c0001t0003g0347 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.679+2372A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677310 | |||||||
chr2:55677336 | A | G | 2 | a0003c0003t0004g0085 a0003c0003t0018g0084 |
2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.679+2346T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677336 | |||||||
chr2:55677365 | G | A | 1 | a0001c0001t0003g0311 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.679+2317C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677365 | |||||||
chr2:55677391 | A | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.679+2291T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677391 | |||||||
chr2:55677391 | A | T | 1 | a0003c0003t0004g0113 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.679+2291T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677391 | |||||||
chr2:55677596 | C | CA | 27 | a0001c0004t0004g0011 a0001c0004t0004g0028 a0002c0002t0002g0013 others(24): Show |
27 | HG01106.hp1 HG01433.hp1 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.679+2085dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | |||||||
chr2:55677596 | C | CAA | 7 | a0001c0001t0001g0061 a0001c0001t0013g0168 a0001c0001t0014g0154 others(4): Show |
7 | HG01109.hp2 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.679+2084_679+2085d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | |||||||
chr2:55677596 | C | CAAA | 92 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(89): Show |
96 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.679+2083_679+2085d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | |||||||
chr2:55677596 | C | CAAAA | 39 | a0001c0001t0001g0042 a0001c0001t0001g0059 a0001c0001t0001g0119 others(36): Show |
39 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.679+2082_679+2085d others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | |||||||
chr2:55677596 | CA | C | 74 | a0001c0001t0002g0325 a0001c0001t0002g0327 a0001c0001t0003g0007 others(71): Show |
76 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.679+2085delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | |||||||
chr2:55677596 | CAAA | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+2083_679+2085d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677596 | |||||||
chr2:55677627 | A | G | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.679+2055T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677627 | |||||||
chr2:55677679 | A | AGG | 18 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(15): Show |
18 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.679+2001_679+2002d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677679 | |||||||
chr2:55677808 | C | T | 1 | a0002c0002t0001g0043 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.679+1874G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677808 | |||||||
chr2:55677827 | C | A | 4 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0024 others(1): Show |
4 | HG02280.hp1 HG02615.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+1855G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677827 | |||||||
chr2:55677835 | G | A | 1 | a0001c0001t0001g0358 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.679+1847C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677835 | |||||||
chr2:55677896 | G | A | 1 | a0003c0003t0004g0082 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.679+1786C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677896 | |||||||
chr2:55677987 | T | G | 112 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(109): Show |
125 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.679+1695A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55677987 | |||||||
chr2:55678021 | G | A | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+1661C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678021 | |||||||
chr2:55678051 | C | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.679+1631G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678051 | |||||||
chr2:55678094 | C | A | 1 | a0003c0003t0016g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.679+1588G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678094 | |||||||
chr2:55678174 | A | G | 1 | a0001c0001t0013g0117 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.679+1508T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678174 | |||||||
chr2:55678214 | G | C | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.679+1468C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678214 | |||||||
chr2:55678240 | C | G | 1 | a0002c0002t0002g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.679+1442G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678240 | |||||||
chr2:55678488 | G | A | 4 | a0002c0002t0002g0217 a0002c0002t0002g0228 a0002c0002t0002g0229 others(1): Show |
4 | HG01099.hp2 HG01106.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.679+1194C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678488 | |||||||
chr2:55678610 | G | T | 2 | a0002c0002t0002g0213 a0002c0002t0002g0214 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.679+1072C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55678610 | |||||||
chr2:55679185 | A | G | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.679+497T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679185 | |||||||
chr2:55679321 | A | G | 2 | a0002c0002t0002g0234 a0002c0002t0002g0261 |
2 | HG01109.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.679+361T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679321 | |||||||
chr2:55679405 | A | T | 1 | a0002c0002t0002g0212 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.679+277T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679405 | |||||||
chr2:55679417 | T | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.679+265A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679417 | |||||||
chr2:55679551 | G | C | 3 | a0001c0001t0003g0307 a0001c0001t0003g0347 a0001c0001t0009g0308 |
3 | HG00621.hp2 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.679+131C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679551 | |||||||
chr2:55679633 | G | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.679+49C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 8/27 | chr2 | 55679633 | |||||||
chr2:55680169 | T | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(5): Show |
8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.566-374A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680169 | |||||||
chr2:55680196 | G | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.566-401C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680196 | |||||||
chr2:55680217 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0165 others(9): Show |
14 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.566-422G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680217 | |||||||
chr2:55680222 | C | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.566-427G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680222 | |||||||
chr2:55680227 | G | A | 1 | a0001c0001t0003g0302 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.566-432C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680227 | |||||||
chr2:55680292 | C | G | 1 | a0002c0002t0023g0216 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.565+420G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680292 | |||||||
chr2:55680328 | C | G | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.565+384G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680328 | |||||||
chr2:55680347 | C | T | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.565+365G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680347 | |||||||
chr2:55680425 | TA | T | 282 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0031 others(279): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.565+286delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680425 | |||||||
chr2:55680425 | TAA | T | 10 | a0001c0001t0001g0120 a0001c0001t0001g0189 a0001c0001t0014g0167 others(7): Show |
10 | HG00639.hp2 HG01069.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.565+285_565+286del others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680425 | |||||||
chr2:55680427 | A | T | 1 | a0001c0001t0014g0154 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.565+285T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680427 | |||||||
chr2:55680622 | G | A | 17 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0034 others(14): Show |
17 | HG01192.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.565+90C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 7/27 | chr2 | 55680622 | |||||||
chr2:55681013 | G | A | 1 | a0002c0002t0005g0277 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.454-95C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681013 | |||||||
chr2:55681152 | A | G | 15 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(12): Show |
15 | HG00423.hp2 HG02027.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.454-234T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681152 | |||||||
chr2:55681182 | G | C | 113 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(110): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.454-264C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681182 | |||||||
chr2:55681239 | G | A | 1 | a0002c0002t0002g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.454-321C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681239 | |||||||
chr2:55681293 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.454-375T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681293 | |||||||
chr2:55681482 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.454-564C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681482 | |||||||
chr2:55681494 | T | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.454-576A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681494 | |||||||
chr2:55681501 | C | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.454-583G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681501 | |||||||
chr2:55681543 | T | C | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-625A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681543 | |||||||
chr2:55681718 | G | A | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.454-800C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681718 | |||||||
chr2:55681798 | C | T | 2 | a0003c0003t0004g0079 a0003c0003t0004g0083 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.454-880G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681798 | |||||||
chr2:55681828 | G | A | 1 | a0001c0001t0003g0311 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.454-910C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681828 | |||||||
chr2:55681844 | C | CA | 280 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(277): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.454-927dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681844 | |||||||
chr2:55681844 | C | CAAA | 8 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(5): Show |
8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.454-929_454-927dup others(3): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681844 | |||||||
chr2:55681869 | C | T | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.454-951G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681869 | |||||||
chr2:55681892 | A | G | 2 | a0002c0002t0002g0231 a0002c0002t0002g0266 |
2 | HG01891.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.454-974T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681892 | |||||||
chr2:55681955 | C | T | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.454-1037G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55681955 | |||||||
chr2:55682016 | G | A | 1 | a0002c0002t0002g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.454-1098C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682016 | |||||||
chr2:55682122 | G | A | 1 | a0002c0002t0002g0262 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.454-1204C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682122 | |||||||
chr2:55682186 | G | A | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.454-1268C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682186 | |||||||
chr2:55682190 | A | G | 290 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(287): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.454-1272T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682190 | |||||||
chr2:55682414 | T | C | 74 | a0001c0001t0001g0004 a0001c0001t0001g0119 a0001c0001t0001g0120 others(71): Show |
76 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.453+1371A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682414 | |||||||
chr2:55682418 | G | A | 1 | a0006c0014t0010g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.453+1367C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682418 | |||||||
chr2:55682473 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.453+1312A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682473 | |||||||
chr2:55682595 | T | C | 6 | a0001c0001t0006g0136 a0001c0001t0006g0201 a0001c0001t0006g0202 others(3): Show |
6 | HG01261.hp1 HG01496.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+1190A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682595 | |||||||
chr2:55682687 | C | G | 2 | a0003c0003t0004g0069 a0003c0003t0004g0082 |
2 | HG02622.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.453+1098G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682687 | |||||||
chr2:55682856 | G | C | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.453+929C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55682856 | |||||||
chr2:55683094 | T | C | 1 | a0001c0001t0006g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.453+691A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683094 | |||||||
chr2:55683179 | G | A | 1 | a0002c0002t0002g0264 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.453+606C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683179 | |||||||
chr2:55683217 | C | G | 1 | a0002c0002t0023g0216 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.453+568G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683217 | |||||||
chr2:55683231 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.453+554A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683231 | |||||||
chr2:55683352 | C | T | 1 | a0001c0001t0006g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.453+433G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683352 | |||||||
chr2:55683383 | G | A | 1 | a0001c0004t0007g0067 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.453+402C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683383 | |||||||
chr2:55683389 | C | T | 1 | a0001c0001t0003g0283 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.453+396G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683389 | |||||||
chr2:55683410 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.453+375G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683410 | |||||||
chr2:55683539 | G | A | 8 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(5): Show |
8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+246C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683539 | |||||||
chr2:55683575 | T | C | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.453+210A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683575 | |||||||
chr2:55683612 | C | CA | 61 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(58): Show |
61 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.453+172dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683612 | |||||||
chr2:55683612 | C | CAA | 6 | a0001c0001t0001g0059 a0001c0001t0006g0198 a0001c0001t0006g0205 others(3): Show |
6 | HG01168.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+171_453+172dup others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 5/27 | chr2 | 55683612 | |||||||
chr2:55684216 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.404-382T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684216 | |||||||
chr2:55684231 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0150 a0001c0001t0001g0165 others(9): Show |
14 | HG00438.hp1 HG03710.hp2 HG03942.hp1 others(11): Show |
intron_variant | MODIFIER | c.404-397C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684231 | |||||||
chr2:55684305 | A | C | 290 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(287): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.404-471T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684305 | |||||||
chr2:55684319 | A | T | 18 | a0002c0002t0002g0217 a0002c0002t0002g0218 a0002c0002t0002g0220 others(15): Show |
18 | HG00099.hp1 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.404-485T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684319 | |||||||
chr2:55684324 | G | A | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.404-490C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684324 | |||||||
chr2:55684388 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG01192.hp2 HG03490.hp2 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.404-554G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684388 | |||||||
chr2:55684519 | T | C | 1 | a0001c0001t0006g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.403+424A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684519 | |||||||
chr2:55684554 | T | G | 1 | a0001c0001t0001g0056 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.403+389A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684554 | |||||||
chr2:55684559 | C | T | 1 | a0001c0001t0003g0315 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.403+384G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684559 | |||||||
chr2:55684736 | G | A | 1 | a0001c0001t0003g0350 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.403+207C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 4/27 | chr2 | 55684736 | |||||||
chr2:55685056 | A | C | 1 | a0002c0002t0002g0026 | 1 | HG02717.hp1 | splice_region_variant&intron_variant | LOW | c.298-8T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685056 | |||||||
chr2:55685229 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.298-181C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685229 | |||||||
chr2:55685527 | TC | T | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-480delG | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685527 | |||||||
chr2:55685619 | T | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.298-571A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685619 | |||||||
chr2:55685826 | T | C | 113 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(110): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.297+544A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685826 | |||||||
chr2:55685996 | G | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(94): Show |
99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.297+374C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55685996 | |||||||
chr2:55686062 | A | G | 1 | a0001c0001t0031g0365 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.297+308T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686062 | |||||||
chr2:55686071 | G | A | 1 | a0002c0002t0002g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.297+299C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686071 | |||||||
chr2:55686128 | C | G | 1 | a0002c0002t0002g0215 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.297+242G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686128 | |||||||
chr2:55686136 | AT | A | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+233delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686136 | |||||||
chr2:55686333 | A | T | 1 | a0003c0003t0004g0092 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.297+37T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 3/27 | chr2 | 55686333 | |||||||
chr2:55686509 | C | A | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-65G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686509 | |||||||
chr2:55686520 | C | T | 4 | a0003c0003t0004g0105 a0003c0003t0004g0106 a0003c0003t0004g0107 others(1): Show |
4 | NA18612.hp2 NA18984.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-76G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686520 | |||||||
chr2:55686762 | A | G | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.223-318T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686762 | |||||||
chr2:55686835 | C | G | 291 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(288): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.223-391G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686835 | |||||||
chr2:55686872 | G | A | 1 | a0002c0002t0041g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.223-428C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686872 | |||||||
chr2:55686874 | A | C | 52 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(49): Show |
52 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.223-430T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686874 | |||||||
chr2:55686890 | G | A | 5 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0024 others(2): Show |
5 | HG02280.hp1 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-446C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686890 | |||||||
chr2:55686990 | G | A | 1 | a0001c0004t0007g0068 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.223-546C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55686990 | |||||||
chr2:55687030 | C | T | 5 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | NA18963.hp1 NA18983.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-586G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687030 | |||||||
chr2:55687048 | A | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0056 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222+597T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687048 | |||||||
chr2:55687075 | G | A | 1 | a0001c0004t0004g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.222+570C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687075 | |||||||
chr2:55687110 | A | C | 2 | a0001c0001t0001g0173 a0001c0001t0026g0174 |
2 | HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.222+535T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687110 | |||||||
chr2:55687147 | G | A | 1 | a0001c0001t0003g0351 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.222+498C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687147 | |||||||
chr2:55687168 | C | T | 2 | a0002c0002t0002g0213 a0002c0002t0002g0214 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.222+477G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687168 | |||||||
chr2:55687169 | G | A | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.222+476C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687169 | |||||||
chr2:55687173 | C | T | 1 | a0003c0003t0004g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.222+472G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687173 | |||||||
chr2:55687213 | C | CA | 139 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0059 others(136): Show |
141 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.222+431dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687213 | |||||||
chr2:55687213 | C | CAA | 137 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(134): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.222+430_222+431dup others(2): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687213 | |||||||
chr2:55687213 | C | CAAA | 7 | a0001c0001t0001g0042 a0001c0001t0028g0114 a0002c0002t0001g0054 others(4): Show |
7 | HG01192.hp2 HG01261.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.222+429_222+431dup others(3): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687213 | |||||||
chr2:55687221 | A | AC | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.222+423_222+424ins others(1): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687221 | |||||||
chr2:55687438 | C | CA | 115 | a0002c0002t0001g0045 a0002c0002t0001g0046 a0002c0002t0001g0047 others(112): Show |
128 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.222+206dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687438 | |||||||
chr2:55687486 | T | C | 113 | a0002c0002t0001g0043 a0002c0002t0001g0045 a0002c0002t0001g0046 others(110): Show |
126 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.222+159A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 2/27 | chr2 | 55687486 | |||||||
chr2:55687745 | C | A | 1 | a0002c0002t0002g0268 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.162-40G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687745 | |||||||
chr2:55687814 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.162-109G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687814 | |||||||
chr2:55687827 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.162-122G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687827 | |||||||
chr2:55687927 | C | T | 1 | a0001c0001t0001g0363 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.162-222G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687927 | |||||||
chr2:55687993 | A | AT | 15 | a0001c0001t0001g0140 a0001c0001t0001g0162 a0001c0001t0001g0166 others(12): Show |
15 | HG02155.hp1 HG02273.hp1 NA18940.hp2 others(12): Show |
intron_variant | MODIFIER | c.162-289dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55687993 | |||||||
chr2:55688020 | T | A | 291 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(288): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.162-315A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688020 | |||||||
chr2:55688232 | T | A | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.162-527A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688232 | |||||||
chr2:55688304 | T | C | 1 | a0007c0008t0001g0055 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.162-599A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688304 | |||||||
chr2:55688309 | G | C | 1 | a0001c0001t0011g0194 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.162-604C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688309 | |||||||
chr2:55688337 | G | C | 2 | a0003c0003t0004g0077 a0003c0003t0004g0078 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.162-632C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688337 | |||||||
chr2:55688383 | T | C | 1 | a0002c0002t0002g0269 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.162-678A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688383 | |||||||
chr2:55688446 | A | T | 3 | a0001c0001t0006g0198 a0001c0001t0006g0207 a0001c0001t0028g0114 |
3 | HG04204.hp1 HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.162-741T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688446 | |||||||
chr2:55688508 | C | T | 1 | a0001c0001t0003g0282 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.162-803G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688508 | |||||||
chr2:55688625 | C | T | 1 | a0003c0003t0004g0099 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.162-920G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688625 | |||||||
chr2:55688691 | G | C | 188 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(185): Show |
192 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.162-986C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688691 | |||||||
chr2:55688760 | C | A | 3 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | NA18969.hp1 NA18985.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.162-1055G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688760 | |||||||
chr2:55688760 | C | CA | 6 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0157 others(3): Show |
6 | HG01346.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-1056dupT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688760 | |||||||
chr2:55688763 | C | A | 88 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0125 others(85): Show |
90 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.162-1058G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688763 | |||||||
chr2:55688766 | C | A | 186 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(183): Show |
190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.162-1061G>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688766 | |||||||
chr2:55688769 | A | C | 99 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(96): Show |
112 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.162-1064T>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688769 | |||||||
chr2:55688873 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.162-1168T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688873 | |||||||
chr2:55688967 | G | C | 1 | a0002c0002t0002g0270 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.162-1262C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688967 | |||||||
chr2:55688975 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0058 |
3 | HG03098.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.162-1270G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55688975 | |||||||
chr2:55689019 | G | A | 12 | a0001c0001t0006g0136 a0001c0001t0006g0198 a0001c0001t0006g0200 others(9): Show |
12 | HG00099.hp2 HG01261.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.162-1314C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689019 | |||||||
chr2:55689168 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.162-1463A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689168 | |||||||
chr2:55689212 | A | G | 1 | a0001c0001t0037g0118 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.162-1507T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689212 | |||||||
chr2:55689268 | T | C | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.162-1563A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689268 | |||||||
chr2:55689284 | T | A | 2 | a0003c0003t0016g0073 a0003c0003t0016g0074 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.162-1579A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689284 | |||||||
chr2:55689371 | C | T | 1 | a0002c0002t0038g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.162-1666G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689371 | |||||||
chr2:55689524 | C | T | 1 | a0003c0003t0020g0104 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.162-1819G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689524 | |||||||
chr2:55689723 | AT | A | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-2019delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55689723 | |||||||
chr2:55690034 | C | G | 2 | a0001c0001t0019g0278 a0001c0001t0019g0279 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.162-2329G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690034 | |||||||
chr2:55690121 | C | T | 7 | a0001c0001t0008g0132 a0001c0001t0008g0137 a0001c0001t0008g0147 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-2416G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690121 | |||||||
chr2:55690348 | CAGAGAA | C | 287 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.162-2649_162-2644d others(8): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690348 | |||||||
chr2:55690408 | C | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(5): Show |
8 | HG01346.hp1 HG02280.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-2703G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690408 | |||||||
chr2:55690469 | A | G | 140 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(137): Show |
153 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.162-2764T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690469 | |||||||
chr2:55690479 | T | C | 1 | a0002c0002t0041g0271 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.162-2774A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690479 | |||||||
chr2:55690607 | T | C | 1 | a0001c0001t0006g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.162-2902A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690607 | |||||||
chr2:55690670 | A | G | 288 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(285): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.162-2965T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690670 | |||||||
chr2:55690961 | G | C | 6 | a0002c0002t0005g0272 a0002c0002t0005g0273 a0002c0002t0005g0274 others(3): Show |
6 | NA18947.hp1 NA18973.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+2702C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690961 | |||||||
chr2:55690967 | C | T | 287 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(284): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.161+2696G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55690967 | |||||||
chr2:55691054 | T | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0119 others(100): Show |
107 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.161+2609A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691054 | |||||||
chr2:55691222 | T | C | 42 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(39): Show |
44 | HG00423.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.161+2441A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691222 | |||||||
chr2:55691247 | A | G | 1 | a0002c0005t0001g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.161+2416T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691247 | |||||||
chr2:55691264 | T | C | 1 | a0002c0002t0002g0026 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.161+2399A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691264 | |||||||
chr2:55691445 | G | T | 2 | a0003c0003t0004g0110 a0003c0003t0004g0111 |
2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.161+2218C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691445 | |||||||
chr2:55691549 | G | A | 1 | a0002c0002t0002g0280 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.161+2114C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691549 | |||||||
chr2:55691718 | T | C | 1 | a0001c0001t0031g0365 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.161+1945A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691718 | |||||||
chr2:55691722 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.161+1941G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691722 | |||||||
chr2:55691848 | T | TATATATA others(4): Show |
1 | a0001c0001t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.161+1814_161+1815i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691848 | T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0056 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02055.hp1 HG02451.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+1805_161+1814d others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691848 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0058 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.161+1803_161+1814d others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691848 | TTA | T | 10 | a0001c0001t0001g0149 a0001c0001t0001g0312 a0001c0001t0003g0309 others(7): Show |
11 | HG01081.hp1 HG01099.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.161+1813_161+1814d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691848 | TTATA | T | 10 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(7): Show |
10 | HG00558.hp2 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161+1811_161+1814d others(6): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691848 | TTATATA | T | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG02698.hp2 HG03688.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1809_161+1814d others(8): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691848 | TTATATAT others(7): Show |
T | 16 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
16 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+1801_161+1814d others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691848 | TTATATAT others(9): Show |
T | 6 | a0001c0001t0003g0306 a0001c0001t0003g0307 a0001c0001t0003g0359 others(3): Show |
6 | HG00423.hp1 HG00621.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+1799_161+1814d others(18): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691848 | |||||||
chr2:55691863 | TATATATA others(6): Show |
T | 1 | a0001c0001t0013g0117 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.161+1787_161+1799d others(15): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691863 | |||||||
chr2:55691864 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0003g0347 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.161+1782_161+1798d others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691864 | |||||||
chr2:55691864 | ATATATAT others(13): Show |
A | 1 | a0002c0002t0002g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.161+1779_161+1798d others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691864 | |||||||
chr2:55691865 | TATATATA others(4): Show |
T | 6 | a0001c0001t0001g0031 a0001c0001t0001g0153 a0001c0001t0001g0156 others(3): Show |
6 | HG01346.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+1787_161+1797d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691865 | |||||||
chr2:55691865 | TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0175 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.161+1785_161+1797d others(15): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691865 | |||||||
chr2:55691866 | ATATATAT others(12): Show |
A | 1 | a0002c0002t0002g0235 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.161+1778_161+1796d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | |||||||
chr2:55691866 | ATATATAT others(13): Show |
A | 46 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(43): Show |
51 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.161+1777_161+1796d others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | |||||||
chr2:55691866 | ATATATAT others(14): Show |
A | 14 | a0002c0002t0002g0001 a0002c0002t0002g0217 a0002c0002t0002g0218 others(11): Show |
14 | HG00735.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.161+1776_161+1796d others(23): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | |||||||
chr2:55691866 | ATATATAT others(15): Show |
A | 1 | a0002c0002t0002g0230 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.161+1775_161+1796d others(24): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691866 | |||||||
chr2:55691867 | TATATA | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0208 a0002c0005t0002g0003 |
3 | HG02071.hp2 NA18963.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.161+1791_161+1795d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691867 | |||||||
chr2:55691867 | TATATATA others(4): Show |
T | 1 | a0001c0001t0024g0152 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.161+1785_161+1795d others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691867 | |||||||
chr2:55691868 | A | G | 1 | a0002c0002t0002g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161+1795T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | |||||||
chr2:55691868 | ATATATAT others(12): Show |
A | 2 | a0002c0002t0002g0001 a0002c0002t0041g0271 |
2 | HG03453.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.161+1776_161+1794d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | |||||||
chr2:55691868 | ATATATAT others(13): Show |
A | 25 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0016 others(22): Show |
28 | HG00099.hp1 HG01074.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.161+1775_161+1794d others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | |||||||
chr2:55691868 | ATATATAT others(14): Show |
A | 3 | a0002c0002t0002g0224 a0002c0002t0002g0225 a0002c0002t0002g0356 |
3 | HG01106.hp1 HG02735.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.161+1774_161+1794d others(23): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691868 | |||||||
chr2:55691869 | TATATA | T | 26 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0169 others(23): Show |
26 | HG00438.hp2 HG00621.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.161+1789_161+1793d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691869 | |||||||
chr2:55691870 | ATATATAT others(11): Show |
A | 1 | a0002c0002t0002g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+1775_161+1792d others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691870 | |||||||
chr2:55691870 | ATATATAT others(12): Show |
A | 3 | a0002c0002t0002g0018 a0002c0002t0002g0019 a0002c0002t0002g0020 |
3 | HG02559.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.161+1774_161+1792d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691870 | |||||||
chr2:55691871 | TATA | T | 6 | a0001c0004t0004g0011 a0001c0004t0007g0009 a0001c0004t0007g0064 others(3): Show |
7 | HG01433.hp2 HG03017.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+1789_161+1791d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691871 | |||||||
chr2:55691871 | TATATA | T | 3 | a0001c0001t0001g0170 a0001c0001t0014g0167 a0002c0005t0001g0151 |
3 | HG01346.hp2 HG02155.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.161+1787_161+1791d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691871 | |||||||
chr2:55691872 | A | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0149 a0001c0001t0006g0136 others(2): Show |
5 | HG02698.hp2 NA18950.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1791T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691872 | |||||||
chr2:55691872 | ATATATAT others(12): Show |
A | 2 | a0002c0002t0021g0254 a0002c0002t0021g0255 |
2 | HG01167.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.161+1772_161+1790d others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691872 | |||||||
chr2:55691873 | TATATA | T | 3 | a0001c0001t0008g0159 a0001c0001t0008g0160 a0001c0001t0008g0161 |
3 | HG02258.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.161+1785_161+1789d others(7): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691873 | |||||||
chr2:55691874 | A | AT | 3 | a0001c0001t0003g0321 a0001c0001t0003g0335 a0001c0001t0003g0351 |
3 | HG02273.hp2 NA18993.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.161+1788dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691874 | |||||||
chr2:55691874 | A | T | 15 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
18 | HG00558.hp2 HG01081.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.161+1789T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691874 | |||||||
chr2:55691876 | A | AT | 6 | a0001c0001t0003g0326 a0001c0001t0003g0336 a0001c0001t0003g0337 others(3): Show |
6 | HG01928.hp2 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+1786dupA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691876 | |||||||
chr2:55691876 | A | T | 57 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(54): Show |
61 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.161+1787T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691876 | |||||||
chr2:55691877 | TA | T | 27 | a0001c0001t0001g0281 a0001c0001t0003g0007 a0001c0001t0003g0282 others(24): Show |
29 | HG00558.hp1 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.161+1785delT | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691877 | |||||||
chr2:55691878 | A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0045 a0002c0002t0001g0047 |
2 | NA18966.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(31): Show |
1 | a0001c0001t0028g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(40): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(24): Show |
1 | a0001c0001t0001g0158 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(33): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(24): Show |
1 | a0001c0001t0006g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(33): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(13): Show |
1 | a0001c0001t0030g0040 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0039 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(14): Show |
1 | a0001c0001t0006g0204 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(23): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0034 a0004c0016t0001g0053 a0007c0008t0001g0055 |
3 | HG02523.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0035 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0030 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0362 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0029 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(15): Show |
1 | a0001c0001t0006g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(24): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0036 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(16): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(12): Show |
2 | a0001c0001t0006g0202 a0001c0001t0006g0205 |
2 | HG01496.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(3): Show |
2 | a0001c0001t0006g0206 a0002c0002t0001g0054 |
2 | HG01261.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0037 a0002c0002t0001g0048 a0002c0002t0001g0050 |
3 | NA19064.hp2 NA19065.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0002c0002t0001g0052 |
3 | HG01192.hp2 HG03834.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0051 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(15): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(10): Show |
1 | a0001c0009t0029g0199 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(19): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(13): Show |
1 | a0001c0001t0006g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(22): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(4): Show |
2 | a0002c0002t0001g0046 a0002c0002t0001g0049 |
2 | NA19002.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(11): Show |
1 | a0001c0001t0006g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(20): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATAT others(12): Show |
1 | a0001c0001t0006g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.161+1784_161+1785i others(21): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATTT others(3): Show |
1 | a0001c0001t0001g0004 | 2 | NA18988.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.161+1784_161+1785i others(12): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATTT others(4): Show |
1 | a0001c0001t0026g0174 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(13): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | ATATATTT others(5): Show |
1 | a0002c0011t0001g0044 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.161+1784_161+1785i others(14): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | A | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0031 a0001c0001t0001g0124 others(98): Show |
105 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.161+1785T>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | AT | A | 17 | a0001c0001t0002g0327 a0001c0001t0003g0313 a0001c0001t0003g0314 others(14): Show |
17 | HG01175.hp2 HG01255.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.161+1784delA | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | ATT | A | 9 | a0001c0001t0003g0318 a0001c0001t0009g0329 a0003c0003t0004g0076 others(6): Show |
9 | HG01168.hp2 HG01169.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+1783_161+1784d others(4): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691878 | ATTT | A | 15 | a0003c0003t0004g0081 a0003c0003t0004g0082 a0003c0003t0004g0083 others(12): Show |
15 | HG02109.hp2 HG02145.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.161+1782_161+1784d others(5): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691878 | |||||||
chr2:55691879 | T | TATATATA others(8): Show |
1 | a0008c0006t0004g0109 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161+1783_161+1784i others(17): Show |
PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691879 | |||||||
chr2:55691880 | T | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(5): Show |
8 | HG01243.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.161+1783A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691880 | |||||||
chr2:55691881 | T | A | 14 | a0001c0001t0003g0355 a0003c0003t0004g0075 a0003c0003t0004g0090 others(11): Show |
14 | HG01175.hp2 HG01243.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.161+1782A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691881 | |||||||
chr2:55691882 | T | A | 12 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
12 | HG01168.hp2 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.161+1781A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691882 | |||||||
chr2:55691882 | T | C | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(1): Show |
4 | NA18963.hp1 NA18983.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+1781A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691882 | |||||||
chr2:55691883 | T | A | 26 | a0003c0003t0004g0081 a0003c0003t0004g0082 a0003c0003t0004g0083 others(23): Show |
26 | HG01175.hp2 HG01243.hp1 HG01255.hp1 others(23): Show |
intron_variant | MODIFIER | c.161+1780A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691883 | |||||||
chr2:55691884 | T | A | 6 | a0003c0003t0004g0099 a0003c0003t0004g0100 a0003c0003t0004g0101 others(3): Show |
6 | HG03225.hp2 HG03486.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+1779A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691884 | |||||||
chr2:55691885 | T | A | 7 | a0003c0003t0004g0105 a0003c0003t0004g0106 a0003c0003t0004g0107 others(4): Show |
7 | HG02451.hp1 NA18612.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+1778A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691885 | |||||||
chr2:55691886 | T | A | 2 | a0003c0003t0004g0110 a0003c0003t0004g0111 |
2 | NA18979.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.161+1777A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691886 | |||||||
chr2:55691887 | T | A | 1 | a0003c0003t0032g0112 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.161+1776A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691887 | |||||||
chr2:55691889 | T | A | 1 | a0003c0003t0032g0112 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.161+1774A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691889 | |||||||
chr2:55691910 | A | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(188): Show |
197 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.161+1753T>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691910 | |||||||
chr2:55691988 | C | T | 2 | a0002c0002t0010g0115 a0002c0002t0010g0116 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.161+1675G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55691988 | |||||||
chr2:55692066 | G | A | 8 | a0001c0004t0007g0008 a0001c0004t0007g0009 a0001c0004t0007g0063 others(5): Show |
10 | HG01070.hp2 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.161+1597C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692066 | |||||||
chr2:55692104 | C | T | 1 | a0001c0001t0028g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.161+1559G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692104 | |||||||
chr2:55692185 | G | A | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.161+1478C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692185 | |||||||
chr2:55692191 | T | A | 1 | a0003c0003t0004g0113 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.161+1472A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692191 | |||||||
chr2:55692266 | G | C | 42 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(39): Show |
44 | HG00423.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.161+1397C>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692266 | |||||||
chr2:55692356 | C | T | 289 | a0001c0001t0001g0004 a0001c0001t0001g0029 a0001c0001t0001g0030 others(286): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.161+1307G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692356 | |||||||
chr2:55692501 | C | G | 44 | a0003c0003t0004g0069 a0003c0003t0004g0071 a0003c0003t0004g0072 others(41): Show |
44 | HG01168.hp2 HG01169.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.161+1162G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692501 | |||||||
chr2:55692523 | T | A | 2 | a0001c0001t0003g0357 a0002c0002t0002g0356 |
2 | HG01106.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.161+1140A>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692523 | |||||||
chr2:55692531 | G | T | 42 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(39): Show |
44 | HG00423.hp2 HG01070.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.161+1132C>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692531 | |||||||
chr2:55692711 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.161+952G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55692711 | |||||||
chr2:55693026 | T | C | 1 | a0001c0001t0001g0358 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.161+637A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693026 | |||||||
chr2:55693125 | T | G | 3 | a0001c0001t0003g0359 a0001c0001t0003g0360 a0001c0001t0003g0361 |
3 | HG00423.hp1 NA19003.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.161+538A>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693125 | |||||||
chr2:55693170 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.161+493G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693170 | |||||||
chr2:55693243 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG02683.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.161+420G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693243 | |||||||
chr2:55693286 | C | T | 2 | a0001c0004t0004g0011 a0001c0004t0004g0028 |
2 | HG02970.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.161+377G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693286 | |||||||
chr2:55693374 | G | A | 1 | a0002c0002t0001g0362 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161+289C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693374 | |||||||
chr2:55693475 | T | C | 2 | a0001c0001t0001g0363 a0001c0001t0001g0364 |
2 | HG00438.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.161+188A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693475 | |||||||
chr2:55693486 | G | A | 1 | a0001c0001t0031g0365 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.161+177C>T | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693486 | |||||||
chr2:55693509 | C | T | 1 | a0002c0002t0038g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.161+154G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693509 | |||||||
chr2:55693528 | T | C | 5 | a0002c0002t0002g0366 a0002c0002t0002g0367 a0002c0002t0002g0368 others(2): Show |
5 | HG01074.hp1 HG01168.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.161+135A>G | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693528 | |||||||
chr2:55693614 | C | T | 15 | a0002c0002t0002g0013 a0002c0002t0002g0014 a0002c0002t0002g0015 others(12): Show |
15 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+49G>A | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693614 | |||||||
chr2:55693646 | C | G | 1 | a0001c0004t0004g0011 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.161+17G>C | PNPT1 | ENSG00000138035.15 | transcript | ENST00000447944.7 | protein_coding | 1/27 | chr2 | 55693646 |