Item | Value |
---|---|
geneid | 8492 |
ensemblid | ENSG00000164099.3 |
hgncid | 9477 |
symbol | PRSS12 |
name | serine protease 12 |
refseq_nuc | NM_003619.4 |
refseq_prot | NP_003610.2 |
ensembl_nuc | ENST00000296498.3 |
ensembl_prot | ENSP00000296498.3 |
mane_status | MANE Select |
chr | chr4 |
start | 118280038 |
end | 118353003 |
strand | - |
ver | v1.2 |
region | chr4:118280038-118353003 |
region5000 | chr4:118275038-118358003 |
regionname0 | PRSS12_chr4_118280038_118353003 |
regionname5000 | PRSS12_chr4_118275038_118358003 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 875 | 162 | 46 | 10 | 93 | 0 | 11 | 75 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0002 | 0/0 | 875 | 143 | 20 | 40 | 61 | 7 | 15 | 48 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0003 | 0/0 | 875 | 41 | 7 | 4 | 16 | 2 | 12 | 13 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0004 | 0/0 | 875 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0005 | 0/0 | 875 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0006 | 0/0 | 875 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0007 | 0/0 | 875 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0008 | 0/0 | 875 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0009 | 0/0 | 875 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0010 | 0/0 | 875 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0011 | 0/0 | 875 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
a0012 | 0/0 | 875 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | MTLAR others(870): Show |
chr4 | 118275038 | 118358003 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2625 | 89 | 29 | 6 | 47 | 0 | 5 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0001c0004 | 0/0 | 2625 | 56 | 12 | 3 | 35 | 0 | 6 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0001c0006 | 0/0 | 2625 | 8 | 0 | 1 | 7 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0001c0008 | 0/0 | 2625 | 4 | 0 | 0 | 4 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0001c0009 | 0/0 | 2625 | 4 | 4 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0001c0021 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0002c0002 | 0/0 | 2625 | 83 | 17 | 21 | 37 | 4 | 4 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0002c0003 | 0/0 | 2625 | 57 | 3 | 19 | 21 | 3 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0002c0017 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0002c0018 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0002c0020 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0003c0005 | 0/0 | 2625 | 41 | 7 | 4 | 16 | 2 | 12 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0004c0007 | 0/0 | 2625 | 4 | 1 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0005c0010 | 0/0 | 2625 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0006c0012 | 0/0 | 2625 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0007c0013 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0008c0011 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0009c0015 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0009c0016 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0010c0019 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0011c0022 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 | ||
a0012c0014 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | ATGAC others(2620): Show |
chr4 | 118275038 | 118358003 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4809 | 74 | 25 | 4 | 41 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0002 | 0/0 | 4807 | 2 | 0 | 0 | 1 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4802): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0005 | 0/0 | 4807 | 3 | 3 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4802): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0006 | 0/0 | 4809 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0008 | 0/0 | 4807 | 3 | 0 | 2 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4802): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0013 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0015 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0017 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0001t0023 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0004t0001 | 0/0 | 4809 | 51 | 11 | 2 | 34 | 0 | 4 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0004t0007 | 0/0 | 4809 | 2 | 0 | 0 | 0 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0004t0012 | 0/0 | 4809 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0004t0014 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0004t0020 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0006t0001 | 0/0 | 4809 | 8 | 0 | 1 | 7 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0008t0001 | 0/0 | 4809 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0008t0019 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0009t0001 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0009t0009 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0001c0021t0021 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0002t0001 | 0/0 | 4809 | 79 | 16 | 20 | 36 | 4 | 3 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0002t0007 | 0/0 | 4809 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0002t0016 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0002t0018 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0002t0022 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0003t0001 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0003t0002 | 0/0 | 4807 | 55 | 2 | 19 | 20 | 3 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4802): Show |
chr4 | 118275038 | 118358003 |
a0002c0003t0003 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0002c0017t0002 | 0/0 | 4807 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4802): Show |
chr4 | 118275038 | 118358003 |
a0002c0018t0002 | 0/0 | 4807 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4802): Show |
chr4 | 118275038 | 118358003 |
a0002c0020t0001 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0003c0005t0003 | 0/0 | 4809 | 35 | 2 | 4 | 16 | 2 | 11 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0003c0005t0004 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0003c0005t0010 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0003c0005t0011 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0003c0005t0024 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GTTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0004c0007t0001 | 0/0 | 4809 | 4 | 1 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0005c0010t0001 | 0/0 | 4809 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0006c0012t0003 | 0/0 | 4809 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0007c0013t0004 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0008c0011t0001 | 0/0 | 4809 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0009c0015t0002 | 0/0 | 4807 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4802): Show |
chr4 | 118275038 | 118358003 |
a0009c0016t0001 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0010c0019t0001 | 0/0 | 4809 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0011c0022t0001 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
a0012c0014t0001 | 0/0 | 4809 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | GCTGC others(4804): Show |
chr4 | 118275038 | 118358003 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0036 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0006g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0008g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0008g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0008g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0013g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0017g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0001t0023g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0007g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0007g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0012g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0014g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0004t0020g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0008t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0008t0019g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0009t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0001c0021t0021g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0003 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0007g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0016g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0018g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0002t0022g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0001 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0007 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0010 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0003t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0017t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0018t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0002c0020t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0039 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0011g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0003c0005t0024g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0004c0007t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0005c0010t0001g0014 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0006c0012t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0006c0012t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0007c0013t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0007c0013t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0008c0011t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0008c0011t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0009c0015t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0009c0016t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0010c0019t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0011c0022t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
a0012c0014t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0003 | c0005 | t0003 | g0217 | EUR | GBR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0076 | EUR | GBR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0082 | EUR | FIN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00323 | hp2 | a0002 | c0003 | t0002 | g0010 | EUR | FIN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00408 | hp1 | a0002 | c0003 | t0002 | g0136 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00408 | hp2 | a0002 | c0003 | t0002 | g0130 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00438 | hp1 | a0001 | c0006 | t0001 | g0271 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00438 | hp2 | a0002 | c0017 | t0002 | g0113 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00544 | hp2 | a0001 | c0004 | t0001 | g0260 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00597 | hp2 | a0003 | c0005 | t0003 | g0208 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00609 | hp1 | a0001 | c0006 | t0001 | g0270 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00621 | hp2 | a0001 | c0004 | t0001 | g0265 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00639 | hp1 | a0005 | c0010 | t0001 | g0014 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00639 | hp2 | a0002 | c0003 | t0002 | g0028 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00642 | hp2 | a0002 | c0003 | t0002 | g0134 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0233 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00673 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | CHS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00733 | hp2 | a0002 | c0003 | t0002 | g0016 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0281 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0072 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00738 | hp1 | a0001 | c0004 | t0001 | g0198 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00738 | hp2 | a0002 | c0003 | t0002 | g0139 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00741 | hp1 | a0002 | c0003 | t0002 | g0016 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG00741 | hp2 | a0004 | c0007 | t0001 | g0110 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01071 | hp1 | a0002 | c0003 | t0002 | g0024 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01074 | hp1 | a0002 | c0003 | t0002 | g0141 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01074 | hp2 | a0001 | c0004 | t0012 | g0193 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01109 | hp2 | a0001 | c0006 | t0001 | g0264 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01167 | hp1 | a0006 | c0012 | t0003 | g0227 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01169 | hp1 | a0006 | c0012 | t0003 | g0225 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0120 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0057 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01192 | hp1 | a0004 | c0007 | t0001 | g0109 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01192 | hp2 | a0002 | c0003 | t0002 | g0137 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01243 | hp1 | a0002 | c0003 | t0002 | g0116 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01255 | hp1 | a0003 | c0005 | t0003 | g0201 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01255 | hp2 | a0001 | c0004 | t0001 | g0042 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01256 | hp1 | a0003 | c0005 | t0003 | g0039 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0133 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01261 | hp2 | a0002 | c0003 | t0002 | g0117 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01346 | hp1 | a0002 | c0003 | t0002 | g0025 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0007 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0280 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01496 | hp1 | a0004 | c0007 | t0001 | g0107 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01517 | hp1 | a0010 | c0019 | t0001 | g0091 | EUR | IBS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01517 | hp2 | a0003 | c0005 | t0003 | g0216 | EUR | IBS | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01884 | hp1 | a0002 | c0003 | t0002 | g0138 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01891 | hp2 | a0003 | c0005 | t0003 | g0220 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0090 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01928 | hp2 | a0002 | c0003 | t0002 | g0001 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01934 | hp2 | a0002 | c0003 | t0002 | g0027 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01975 | hp2 | a0002 | c0003 | t0002 | g0001 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01978 | hp2 | a0003 | c0005 | t0003 | g0226 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02027 | hp1 | a0002 | c0003 | t0002 | g0026 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02040 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02055 | hp1 | a0005 | c0010 | t0001 | g0014 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0062 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02080 | hp2 | a0001 | c0004 | t0014 | g0259 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02148 | hp1 | a0002 | c0002 | t0007 | g0142 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02148 | hp2 | a0002 | c0003 | t0002 | g0115 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02155 | hp1 | a0002 | c0002 | t0016 | g0143 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02155 | hp2 | a0001 | c0004 | t0001 | g0041 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02165 | hp1 | a0001 | c0004 | t0001 | g0041 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02258 | hp1 | a0011 | c0022 | t0001 | g0187 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02258 | hp2 | a0001 | c0004 | t0020 | g0279 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02273 | hp1 | a0002 | c0003 | t0002 | g0001 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0183 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0022 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0234 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02572 | hp1 | a0004 | c0007 | t0001 | g0111 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02572 | hp2 | a0002 | c0003 | t0001 | g0065 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02602 | hp1 | a0002 | c0003 | t0002 | g0128 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02602 | hp2 | a0003 | c0005 | t0011 | g0046 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0261 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02647 | hp1 | a0003 | c0005 | t0010 | g0224 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02698 | hp1 | a0002 | c0003 | t0002 | g0024 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02738 | hp2 | a0003 | c0005 | t0003 | g0211 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0188 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02895 | hp2 | a0003 | c0005 | t0010 | g0223 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0244 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02922 | hp1 | a0003 | c0005 | t0004 | g0199 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02922 | hp2 | a0001 | c0004 | t0001 | g0169 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02970 | hp2 | a0008 | c0011 | t0001 | g0145 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02976 | hp2 | a0008 | c0011 | t0001 | g0180 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03017 | hp1 | a0003 | c0005 | t0003 | g0212 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03017 | hp2 | a0002 | c0003 | t0002 | g0010 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03041 | hp1 | a0001 | c0009 | t0009 | g0049 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03041 | hp2 | a0012 | c0014 | t0001 | g0050 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03098 | hp1 | a0001 | c0004 | t0001 | g0170 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0104 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03139 | hp1 | a0001 | c0009 | t0001 | g0275 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03195 | hp2 | a0001 | c0009 | t0001 | g0192 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0172 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03239 | hp1 | a0003 | c0005 | t0003 | g0213 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03486 | hp1 | a0003 | c0005 | t0024 | g0286 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03486 | hp2 | a0001 | c0009 | t0009 | g0048 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03491 | hp1 | a0002 | c0003 | t0002 | g0007 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03491 | hp2 | a0001 | c0004 | t0001 | g0257 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03492 | hp1 | a0009 | c0016 | t0001 | g0051 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03492 | hp2 | a0002 | c0003 | t0002 | g0007 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | ESN | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0042 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03654 | hp2 | a0002 | c0003 | t0002 | g0001 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03669 | hp1 | a0001 | c0004 | t0007 | g0254 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03669 | hp2 | a0003 | c0005 | t0003 | g0040 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03688 | hp1 | a0003 | c0005 | t0003 | g0221 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03688 | hp2 | a0001 | c0004 | t0001 | g0252 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03704 | hp1 | a0001 | c0004 | t0001 | g0182 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03704 | hp2 | a0003 | c0005 | t0003 | g0214 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03710 | hp1 | a0003 | c0005 | t0003 | g0235 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0025 | SAS | PJL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0010 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03834 | hp1 | a0001 | c0001 | t0008 | g0282 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03834 | hp2 | a0003 | c0005 | t0003 | g0222 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03942 | hp1 | a0002 | c0002 | t0022 | g0284 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03942 | hp2 | a0003 | c0005 | t0003 | g0236 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04115 | hp2 | a0009 | c0015 | t0002 | g0052 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04184 | hp1 | a0001 | c0001 | t0013 | g0178 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04184 | hp2 | a0002 | c0003 | t0002 | g0122 | SAS | BEB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04204 | hp1 | a0002 | c0003 | t0002 | g0007 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04204 | hp2 | a0001 | c0004 | t0007 | g0237 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0258 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG04228 | hp2 | a0003 | c0005 | t0003 | g0218 | SAS | STU | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18612 | hp1 | a0003 | c0005 | t0003 | g0215 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18747 | hp2 | a0003 | c0005 | t0003 | g0207 | EAS | CHB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18906 | hp1 | a0001 | c0021 | t0021 | g0283 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18939 | hp1 | a0001 | c0004 | t0001 | g0242 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18943 | hp1 | a0001 | c0004 | t0001 | g0250 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18943 | hp2 | a0001 | c0006 | t0001 | g0273 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18945 | hp1 | a0003 | c0005 | t0003 | g0228 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18946 | hp2 | a0001 | c0004 | t0001 | g0268 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18947 | hp1 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18948 | hp1 | a0003 | c0005 | t0003 | g0249 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18948 | hp2 | a0001 | c0004 | t0001 | g0231 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18952 | hp1 | a0001 | c0004 | t0001 | g0267 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18952 | hp2 | a0003 | c0005 | t0003 | g0206 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18953 | hp1 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18954 | hp2 | a0003 | c0005 | t0003 | g0203 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18957 | hp2 | a0001 | c0004 | t0001 | g0241 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18959 | hp1 | a0001 | c0004 | t0001 | g0251 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18959 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18960 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18960 | hp2 | a0001 | c0006 | t0001 | g0274 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0131 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18961 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18962 | hp1 | a0001 | c0004 | t0001 | g0253 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18962 | hp2 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18963 | hp1 | a0001 | c0004 | t0001 | g0238 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18963 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18964 | hp2 | a0001 | c0004 | t0001 | g0240 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18965 | hp1 | a0001 | c0006 | t0001 | g0272 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0246 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18966 | hp2 | a0003 | c0005 | t0003 | g0210 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18968 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18969 | hp1 | a0001 | c0004 | t0001 | g0044 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18969 | hp2 | a0003 | c0005 | t0003 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18972 | hp1 | a0003 | c0005 | t0003 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18972 | hp2 | a0001 | c0004 | t0001 | g0245 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18973 | hp1 | a0003 | c0005 | t0003 | g0209 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18974 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18974 | hp2 | a0003 | c0005 | t0003 | g0205 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18975 | hp1 | a0003 | c0005 | t0003 | g0204 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18975 | hp2 | a0001 | c0004 | t0001 | g0255 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18978 | hp1 | a0002 | c0018 | t0002 | g0129 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18978 | hp2 | a0001 | c0004 | t0001 | g0247 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18979 | hp2 | a0001 | c0004 | t0001 | g0239 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18980 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18982 | hp1 | a0002 | c0003 | t0002 | g0123 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18982 | hp2 | a0001 | c0004 | t0001 | g0043 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18983 | hp1 | a0001 | c0006 | t0001 | g0269 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18983 | hp2 | a0001 | c0004 | t0001 | g0232 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18987 | hp2 | a0001 | c0001 | t0006 | g0168 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18994 | hp2 | a0001 | c0006 | t0001 | g0263 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA18999 | hp2 | a0002 | c0003 | t0002 | g0114 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19000 | hp1 | a0002 | c0003 | t0002 | g0127 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19001 | hp1 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19002 | hp1 | a0002 | c0003 | t0002 | g0124 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19002 | hp2 | a0001 | c0004 | t0001 | g0248 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19004 | hp2 | a0002 | c0003 | t0002 | g0026 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19007 | hp1 | a0001 | c0008 | t0019 | g0229 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19007 | hp2 | a0002 | c0003 | t0002 | g0135 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19009 | hp1 | a0001 | c0001 | t0023 | g0285 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19012 | hp2 | a0002 | c0003 | t0002 | g0001 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0243 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19054 | hp1 | a0002 | c0003 | t0002 | g0027 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19057 | hp2 | a0003 | c0005 | t0003 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19062 | hp1 | a0001 | c0004 | t0001 | g0266 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19072 | hp1 | a0001 | c0008 | t0001 | g0012 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19072 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19074 | hp1 | a0003 | c0005 | t0003 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19076 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19078 | hp1 | a0002 | c0003 | t0002 | g0126 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19078 | hp2 | a0001 | c0004 | t0001 | g0256 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19079 | hp2 | a0002 | c0003 | t0002 | g0011 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19081 | hp1 | a0001 | c0004 | t0001 | g0230 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19082 | hp1 | a0003 | c0005 | t0003 | g0006 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19082 | hp2 | a0001 | c0008 | t0001 | g0012 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19084 | hp2 | a0001 | c0001 | t0015 | g0162 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19085 | hp1 | a0001 | c0008 | t0001 | g0012 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19085 | hp2 | a0002 | c0020 | t0001 | g0103 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19089 | hp2 | a0002 | c0003 | t0003 | g0132 | EAS | JPT | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19240 | hp1 | a0003 | c0005 | t0004 | g0200 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA19240 | hp2 | a0005 | c0010 | t0001 | g0014 | AFR | YRI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20129 | hp1 | a0007 | c0013 | t0004 | g0277 | AFR | ASW | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ASW | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0106 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20752 | hp2 | a0002 | c0003 | t0002 | g0112 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0023 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20805 | hp2 | a0002 | c0003 | t0002 | g0119 | EUR | TSI | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20905 | hp1 | a0003 | c0005 | t0003 | g0040 | SAS | GIH | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20905 | hp2 | a0002 | c0003 | t0002 | g0121 | SAS | GIH | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG01123 | hp2 | a0003 | c0005 | t0003 | g0219 | AMR | CLM | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02109 | hp1 | a0002 | c0003 | t0002 | g0028 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02109 | hp2 | a0007 | c0013 | t0004 | g0278 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02486 | hp1 | a0002 | c0002 | t0018 | g0084 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0185 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
HG03471 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | MSL | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20300 | hp1 | a0003 | c0005 | t0003 | g0039 | AFR | USA | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | USA | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0150 | REF | REF | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0036 | REF | REF | PRSS12_chr4_118275038_118358003 | PRSS12 | chr4 | 118275038 | 118358003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118282066 | C | T | 1 | a0004 | 4 | HG00741.hp2 HG01192.hp1 HG01496.hp1 others(1): Show |
missense_variant | MODERATE | c.2498G>A | p.Arg833Gln | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2781/4809 | 2498/2628 | 833/875 | chr4 | 118282066 | |||
chr4:118282171 | T | C | 1 | a0010 | 1 | HG01517.hp1 | missense_variant | MODERATE | c.2393A>G | p.Tyr798Cys | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2676/4809 | 2393/2628 | 798/875 | chr4 | 118282171 | |||
chr4:118295806 | G | A | 1 | a0006 | 2 | HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.1888C>T | p.Arg630Trp | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 10/13 | 2171/4809 | 1888/2628 | 630/875 | chr4 | 118295806 | |||
chr4:118298754 | C | A | 4 | a0003 a0006 a0007 others(1): Show |
47 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(44): Show |
missense_variant | MODERATE | c.1816G>T | p.Ala606Ser | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/13 | 2099/4809 | 1816/2628 | 606/875 | chr4 | 118298754 | |||
chr4:118316204 | C | T | 1 | a0008 | 2 | HG02970.hp2 HG02976.hp2 |
missense_variant | MODERATE | c.1270G>A | p.Val424Ile | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/13 | 1553/4809 | 1270/2628 | 424/875 | chr4 | 118316204 | |||
chr4:118338254 | C | T | 1 | a0011 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.563G>A | p.Ser188Asn | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/13 | 846/4809 | 563/2628 | 188/875 | chr4 | 118338254 | |||
chr4:118352281 | G | A | 1 | a0005 | 3 | HG00639.hp1 HG02055.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.440C>T | p.Pro147Leu | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 723/4809 | 440/2628 | 147/875 | chr4 | 118352281 | |||
chr4:118352405 | C | G | 1 | a0009 | 2 | HG03492.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.316G>C | p.Gly106Arg | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 599/4809 | 316/2628 | 106/875 | chr4 | 118352405 | |||
chr4:118352557 | C | G | 4 | a0002 a0004 a0009 others(1): Show |
150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
missense_variant | MODERATE | c.164G>C | p.Arg55Thr | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 447/4809 | 164/2628 | 55/875 | chr4 | 118352557 | |||
chr4:118352657 | C | G | 1 | a0012 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.64G>C | p.Asp22His | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 347/4809 | 64/2628 | 22/875 | chr4 | 118352657 | |||
chr4:118352693 | G | C | 1 | a0007 | 2 | HG02109.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.28C>G | p.Leu10Val | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 311/4809 | 28/2628 | 10/875 | chr4 | 118352693 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118281996 | A | T | 1 | a0001c0008 | 4 | NA19007.hp1 NA19072.hp1 NA19082.hp2 others(1): Show |
synonymous_variant | LOW | c.2568T>A | p.Pro856Pro | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2851/4809 | 2568/2628 | 856/875 | chr4 | 118281996 | |||
chr4:118282029 | G | A | 1 | a0002c0017 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.2535C>T | p.Ser845Ser | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 2818/4809 | 2535/2628 | 845/875 | chr4 | 118282029 | |||
chr4:118298797 | G | A | 1 | a0001c0009 | 4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1773C>T | p.His591His | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/13 | 2056/4809 | 1773/2628 | 591/875 | chr4 | 118298797 | |||
chr4:118313334 | G | A | 1 | a0002c0018 | 1 | NA18978.hp1 | synonymous_variant | LOW | c.1356C>T | p.Asp452Asp | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/13 | 1639/4809 | 1356/2628 | 452/875 | chr4 | 118313334 | |||
chr4:118316193 | T | C | 12 | a0001c0004 a0001c0009 a0001c0021 others(9): Show |
198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
synonymous_variant | LOW | c.1281A>G | p.Gln427Gln | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/13 | 1564/4809 | 1281/2628 | 427/875 | chr4 | 118316193 | |||
chr4:118316202 | A | C | 1 | a0001c0006 | 8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
synonymous_variant | LOW | c.1272T>G | p.Val424Val | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/13 | 1555/4809 | 1272/2628 | 424/875 | chr4 | 118316202 | |||
chr4:118318384 | G | A | 1 | a0002c0020 | 1 | NA19085.hp2 | synonymous_variant | LOW | c.1144C>T | p.Leu382Leu | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/13 | 1427/4809 | 1144/2628 | 382/875 | chr4 | 118318384 | |||
chr4:118352412 | C | G | 1 | a0001c0021 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.309G>C | p.Thr103Thr | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 592/4809 | 309/2628 | 103/875 | chr4 | 118352412 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118280071 | A | G | 1 | a0002c0002t0016 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1865T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1865 | chr4 | 118280071 | ||||||
chr4:118280091 | A | G | 1 | a0003c0005t0011 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1845T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1845 | chr4 | 118280091 | ||||||
chr4:118280171 | G | A | 1 | a0001c0001t0017 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1765C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1765 | chr4 | 118280171 | ||||||
chr4:118280243 | T | G | 1 | a0002c0002t0018 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1693 | chr4 | 118280243 | ||||||
chr4:118280296 | T | C | 1 | a0001c0008t0019 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1640A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1640 | chr4 | 118280296 | ||||||
chr4:118280341 | T | C | 1 | a0001c0004t0012 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1595A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1595 | chr4 | 118280341 | ||||||
chr4:118280374 | A | G | 1 | a0001c0001t0006 | 3 | NA18954.hp1 NA18960.hp1 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1562T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1562 | chr4 | 118280374 | ||||||
chr4:118280376 | GTT | G | 7 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(4): Show |
66 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1558_*1559delAA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1558 | chr4 | 118280376 | ||||||
chr4:118280389 | A | T | 1 | a0001c0001t0015 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1547T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1547 | chr4 | 118280389 | ||||||
chr4:118280432 | C | T | 4 | a0002c0003t0003 a0003c0005t0003 a0003c0005t0011 others(1): Show |
39 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1504G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1504 | chr4 | 118280432 | ||||||
chr4:118280679 | A | G | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1257T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1257 | chr4 | 118280679 | ||||||
chr4:118280731 | A | G | 1 | a0001c0004t0014 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1205T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1205 | chr4 | 118280731 | ||||||
chr4:118280795 | A | G | 1 | a0001c0001t0013 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1141T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1141 | chr4 | 118280795 | ||||||
chr4:118280803 | C | A | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1133G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 1133 | chr4 | 118280803 | ||||||
chr4:118281024 | C | T | 1 | a0003c0005t0010 | 2 | HG02647.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*912G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 912 | chr4 | 118281024 | ||||||
chr4:118281129 | C | T | 2 | a0001c0004t0012 a0001c0004t0020 |
2 | HG01074.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*807G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 807 | chr4 | 118281129 | ||||||
chr4:118281264 | G | A | 3 | a0003c0005t0004 a0003c0005t0024 a0007c0013t0004 |
5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*672C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 672 | chr4 | 118281264 | ||||||
chr4:118281292 | T | C | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*644A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 644 | chr4 | 118281292 | ||||||
chr4:118281517 | T | C | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*419A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 419 | chr4 | 118281517 | ||||||
chr4:118281728 | G | A | 2 | a0001c0004t0007 a0002c0002t0007 |
3 | HG02148.hp1 HG03669.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*208C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 13/13 | 208 | chr4 | 118281728 | ||||||
chr4:118352777 | A | G | 2 | a0001c0001t0005 a0001c0009t0009 |
5 | HG02486.hp2 HG02886.hp2 HG03041.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-57T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 57 | chr4 | 118352777 | ||||||
chr4:118352793 | G | C | 2 | a0001c0001t0008 a0001c0004t0020 |
4 | HG00735.hp1 HG01433.hp2 HG02258.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-73C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 73 | chr4 | 118352793 | ||||||
chr4:118352878 | C | T | 1 | a0003c0005t0011 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-158G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 158 | chr4 | 118352878 | ||||||
chr4:118352885 | T | G | 1 | a0001c0021t0021 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-165A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 165 | chr4 | 118352885 | ||||||
chr4:118352887 | G | A | 1 | a0002c0002t0022 | 1 | HG03942.hp1 | 5_prime_UTR_variant | MODIFIER | c.-167C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 167 | chr4 | 118352887 | ||||||
chr4:118352987 | G | A | 1 | a0001c0001t0023 | 1 | NA19009.hp1 | 5_prime_UTR_variant | MODIFIER | c.-267C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | 267 | chr4 | 118352987 | ||||||
chr4:118353002 | G | A | 1 | a0003c0005t0024 | 1 | HG03486.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-282C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/13 | chr4 | 118353002 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:118282288 | C | T | 1 | a0003c0005t0003g0214 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2321-45G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282288 | |||||||
chr4:118282324 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2321-81A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282324 | |||||||
chr4:118282553 | A | C | 155 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(152): Show |
183 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2320+278T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282553 | |||||||
chr4:118282678 | A | G | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2320+153T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282678 | |||||||
chr4:118282693 | A | C | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2320+138T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 12/12 | chr4 | 118282693 | |||||||
chr4:118283203 | C | G | 1 | a0002c0002t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2040-92G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283203 | |||||||
chr4:118283311 | T | C | 171 | a0001c0001t0001g0146 a0001c0004t0001g0013 a0001c0004t0001g0041 others(168): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2040-200A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283311 | |||||||
chr4:118283390 | C | G | 1 | a0001c0004t0020g0279 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2040-279G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283390 | |||||||
chr4:118283517 | A | G | 1 | a0002c0002t0001g0019 | 2 | NA18984.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2040-406T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283517 | |||||||
chr4:118283535 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2040-424C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283535 | |||||||
chr4:118283565 | A | C | 179 | a0001c0001t0001g0146 a0001c0004t0001g0013 a0001c0004t0001g0041 others(176): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.2040-454T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283565 | |||||||
chr4:118283696 | G | A | 43 | a0001c0001t0002g0202 a0001c0001t0002g0276 a0001c0001t0008g0280 others(40): Show |
63 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.2040-585C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283696 | |||||||
chr4:118283862 | G | A | 7 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(4): Show |
8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-751C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283862 | |||||||
chr4:118283888 | C | T | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-777G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283888 | |||||||
chr4:118283934 | A | C | 1 | a0002c0003t0002g0114 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2040-823T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283934 | |||||||
chr4:118283943 | AATTG | A | 9 | a0001c0001t0001g0146 a0001c0006t0001g0263 a0001c0006t0001g0264 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2040-836_2040-833d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283943 | |||||||
chr4:118283979 | T | C | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-868A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118283979 | |||||||
chr4:118284048 | C | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-937G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284048 | |||||||
chr4:118284281 | C | T | 1 | a0001c0004t0001g0239 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2040-1170G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284281 | |||||||
chr4:118284439 | A | G | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2040-1328T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284439 | |||||||
chr4:118284460 | CCT | C | 2 | a0001c0004t0001g0042 a0001c0004t0001g0244 |
3 | HG01255.hp2 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2040-1351_2040-135 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284460 | |||||||
chr4:118284514 | T | A | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-1403A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284514 | |||||||
chr4:118284566 | A | C | 1 | a0001c0004t0001g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2040-1455T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284566 | |||||||
chr4:118284608 | T | C | 8 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(5): Show |
9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2040-1497A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284608 | |||||||
chr4:118284696 | A | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-1585T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284696 | |||||||
chr4:118284723 | A | G | 113 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(110): Show |
135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.2040-1612T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284723 | |||||||
chr4:118284962 | C | G | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2040-1851G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118284962 | |||||||
chr4:118285062 | G | A | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-1951C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285062 | |||||||
chr4:118285083 | C | T | 1 | a0002c0002t0001g0099 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2040-1972G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285083 | |||||||
chr4:118285386 | T | G | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2040-2275A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285386 | |||||||
chr4:118285663 | GA | G | 6 | a0002c0002t0001g0023 a0003c0005t0004g0199 a0003c0005t0004g0200 others(3): Show |
7 | HG01123.hp1 HG02109.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2040-2553delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285663 | |||||||
chr4:118285952 | A | C | 17 | a0001c0004t0001g0044 a0001c0004t0001g0265 a0001c0004t0001g0266 others(14): Show |
19 | HG00621.hp2 HG02080.hp1 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.2040-2841T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285952 | |||||||
chr4:118285993 | A | G | 1 | a0001c0001t0017g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2040-2882T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118285993 | |||||||
chr4:118286145 | A | G | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-3034T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286145 | |||||||
chr4:118286375 | G | A | 7 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(4): Show |
8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-3264C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286375 | |||||||
chr4:118286397 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2040-3286G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286397 | |||||||
chr4:118286489 | C | T | 1 | a0003c0005t0003g0215 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2040-3378G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286489 | |||||||
chr4:118286706 | T | C | 1 | a0012c0014t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2040-3595A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286706 | |||||||
chr4:118286868 | C | G | 1 | a0001c0004t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2040-3757G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286868 | |||||||
chr4:118286891 | T | G | 1 | a0003c0005t0024g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2040-3780A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286891 | |||||||
chr4:118286917 | T | G | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2040-3806A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118286917 | |||||||
chr4:118287053 | A | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-3942T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287053 | |||||||
chr4:118287141 | A | G | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2040-4030T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287141 | |||||||
chr4:118287147 | C | T | 171 | a0001c0001t0001g0146 a0001c0004t0001g0013 a0001c0004t0001g0041 others(168): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.2040-4036G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287147 | |||||||
chr4:118287207 | C | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-4096G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287207 | |||||||
chr4:118287274 | C | T | 2 | a0001c0004t0001g0231 a0002c0002t0001g0074 |
2 | NA18948.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.2040-4163G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287274 | |||||||
chr4:118287286 | C | A | 1 | a0001c0001t0001g0037 | 2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2040-4175G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118287286 | |||||||
chr4:118288108 | C | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2040-4997G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288108 | |||||||
chr4:118288170 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2040-5059A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288170 | |||||||
chr4:118288183 | G | T | 7 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(4): Show |
8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-5072C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288183 | |||||||
chr4:118288229 | T | C | 1 | a0010c0019t0001g0091 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2040-5118A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288229 | |||||||
chr4:118288287 | CACAAATA others(9): Show |
C | 1 | a0002c0002t0001g0054 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2040-5192_2040-517 others(20): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288287 | |||||||
chr4:118288336 | T | C | 1 | a0002c0002t0001g0023 | 2 | HG01123.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2040-5225A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288336 | |||||||
chr4:118288350 | G | A | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2040-5239C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288350 | |||||||
chr4:118288393 | G | A | 1 | a0001c0004t0001g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2040-5282C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288393 | |||||||
chr4:118288772 | C | T | 7 | a0001c0006t0001g0263 a0001c0006t0001g0269 a0001c0006t0001g0270 others(4): Show |
7 | HG00438.hp1 HG00609.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2040-5661G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288772 | |||||||
chr4:118288881 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2040-5770T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288881 | |||||||
chr4:118288978 | G | A | 2 | a0002c0003t0002g0116 a0002c0003t0002g0117 |
2 | HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2040-5867C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118288978 | |||||||
chr4:118289271 | C | T | 8 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(5): Show |
9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2039+5668G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118289271 | |||||||
chr4:118290001 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2039+4938G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290001 | |||||||
chr4:118290006 | A | G | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2039+4933T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290006 | |||||||
chr4:118290045 | C | T | 3 | a0002c0003t0002g0114 a0002c0003t0002g0115 a0002c0003t0002g0130 |
3 | HG00408.hp2 HG02148.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2039+4894G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290045 | |||||||
chr4:118290115 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2039+4824G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290115 | |||||||
chr4:118290119 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2039+4820C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290119 | |||||||
chr4:118290134 | T | C | 3 | a0003c0005t0003g0219 a0003c0005t0003g0220 a0003c0005t0003g0221 |
3 | HG01123.hp2 HG01891.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.2039+4805A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290134 | |||||||
chr4:118290217 | A | G | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2039+4722T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290217 | |||||||
chr4:118290218 | T | C | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2039+4721A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290218 | |||||||
chr4:118290823 | T | C | 224 | a0001c0001t0001g0146 a0001c0001t0002g0202 a0001c0001t0002g0276 others(221): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.2039+4116A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290823 | |||||||
chr4:118290830 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
62 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.2039+4109T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290830 | |||||||
chr4:118290948 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2039+3991A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118290948 | |||||||
chr4:118291076 | CT | C | 5 | a0003c0005t0004g0199 a0003c0005t0004g0200 a0003c0005t0024g0286 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2039+3862delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291076 | |||||||
chr4:118291197 | A | C | 6 | a0002c0002t0001g0017 a0002c0002t0001g0056 a0002c0002t0001g0066 others(3): Show |
7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2039+3742T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291197 | |||||||
chr4:118291288 | T | C | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2039+3651A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291288 | |||||||
chr4:118291295 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2039+3644A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291295 | |||||||
chr4:118291714 | C | A | 1 | a0001c0004t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2039+3225G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291714 | |||||||
chr4:118291756 | G | A | 1 | a0002c0002t0001g0089 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2039+3183C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291756 | |||||||
chr4:118291796 | A | G | 2 | a0003c0005t0004g0199 a0003c0005t0004g0200 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2039+3143T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118291796 | |||||||
chr4:118292188 | A | G | 7 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(4): Show |
8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2039+2751T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292188 | |||||||
chr4:118292275 | T | C | 1 | a0002c0002t0001g0096 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2039+2664A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292275 | |||||||
chr4:118292374 | G | C | 2 | a0003c0005t0003g0209 a0003c0005t0003g0210 |
2 | NA18966.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2039+2565C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292374 | |||||||
chr4:118292380 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2039+2559C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292380 | |||||||
chr4:118292544 | G | A | 1 | a0003c0005t0003g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2039+2395C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292544 | |||||||
chr4:118292610 | C | T | 1 | a0002c0003t0002g0126 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2039+2329G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292610 | |||||||
chr4:118292613 | A | C | 1 | a0002c0002t0001g0054 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2039+2326T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292613 | |||||||
chr4:118292630 | T | C | 5 | a0002c0003t0002g0024 a0002c0003t0002g0025 a0002c0003t0002g0112 others(2): Show |
7 | HG01071.hp1 HG01175.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.2039+2309A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292630 | |||||||
chr4:118292737 | T | C | 1 | a0001c0004t0001g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2039+2202A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292737 | |||||||
chr4:118292874 | G | A | 1 | a0002c0002t0001g0088 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2039+2065C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292874 | |||||||
chr4:118292875 | C | T | 1 | a0002c0002t0001g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2039+2064G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292875 | |||||||
chr4:118292968 | T | C | 1 | a0002c0002t0016g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2039+1971A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118292968 | |||||||
chr4:118293018 | A | AAAT | 3 | a0002c0002t0001g0100 a0003c0005t0010g0223 a0003c0005t0010g0224 |
3 | HG00609.hp2 HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2039+1918_2039+192 others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293018 | |||||||
chr4:118293167 | T | G | 1 | a0002c0002t0001g0021 | 2 | NA19001.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2039+1772A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293167 | |||||||
chr4:118293776 | CT | C | 90 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(87): Show |
111 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.2039+1162delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293776 | |||||||
chr4:118293957 | T | C | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2039+982A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293957 | |||||||
chr4:118293999 | A | G | 1 | a0002c0003t0002g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2039+940T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118293999 | |||||||
chr4:118294093 | G | T | 1 | a0001c0006t0001g0273 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2039+846C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294093 | |||||||
chr4:118294157 | AT | A | 10 | a0003c0005t0003g0006 a0003c0005t0003g0203 a0003c0005t0003g0204 others(7): Show |
14 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.2039+781delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294157 | |||||||
chr4:118294175 | T | A | 1 | a0003c0005t0003g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2039+764A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294175 | |||||||
chr4:118294267 | T | C | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2039+672A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294267 | |||||||
chr4:118294392 | C | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2039+547G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294392 | |||||||
chr4:118294412 | A | G | 162 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(159): Show |
190 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.2039+527T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294412 | |||||||
chr4:118294495 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2039+444A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294495 | |||||||
chr4:118294613 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2039+326G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294613 | |||||||
chr4:118294614 | G | A | 1 | a0001c0004t0012g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2039+325C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294614 | |||||||
chr4:118294672 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2039+267T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294672 | |||||||
chr4:118294747 | C | G | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2039+192G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294747 | |||||||
chr4:118294770 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0166 |
2 | HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2039+169T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294770 | |||||||
chr4:118294871 | G | A | 1 | a0002c0002t0001g0087 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2039+68C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294871 | |||||||
chr4:118294899 | T | C | 122 | a0001c0001t0001g0146 a0001c0004t0001g0013 a0001c0004t0001g0041 others(119): Show |
144 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.2039+40A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 11/12 | chr4 | 118294899 | |||||||
chr4:118295625 | A | G | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1916+153T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 10/12 | chr4 | 118295625 | |||||||
chr4:118295759 | C | A | 2 | a0002c0003t0002g0124 a0002c0003t0002g0127 |
2 | NA19000.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1916+19G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 10/12 | chr4 | 118295759 | |||||||
chr4:118295900 | CAG | C | 8 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(5): Show |
9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838-46_1838-45del others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118295900 | |||||||
chr4:118295959 | C | G | 283 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
359 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.1838-103G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118295959 | |||||||
chr4:118296063 | C | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1838-207G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296063 | |||||||
chr4:118296100 | G | A | 9 | a0001c0001t0001g0146 a0001c0006t0001g0263 a0001c0006t0001g0264 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838-244C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296100 | |||||||
chr4:118296419 | C | T | 9 | a0001c0001t0001g0146 a0001c0006t0001g0263 a0001c0006t0001g0264 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1838-563G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296419 | |||||||
chr4:118296530 | T | G | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1838-674A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296530 | |||||||
chr4:118296564 | T | G | 1 | a0001c0006t0001g0271 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1838-708A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296564 | |||||||
chr4:118296686 | T | C | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1838-830A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296686 | |||||||
chr4:118296819 | A | G | 10 | a0003c0005t0003g0006 a0003c0005t0003g0203 a0003c0005t0003g0204 others(7): Show |
14 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.1838-963T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296819 | |||||||
chr4:118296881 | T | C | 2 | a0001c0004t0001g0183 a0001c0004t0001g0185 |
2 | HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1838-1025A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296881 | |||||||
chr4:118296892 | A | G | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1838-1036T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118296892 | |||||||
chr4:118297003 | G | A | 1 | a0002c0002t0001g0088 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1838-1147C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297003 | |||||||
chr4:118297128 | T | C | 1 | a0001c0006t0001g0269 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1838-1272A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297128 | |||||||
chr4:118297137 | C | T | 3 | a0002c0003t0002g0024 a0002c0003t0002g0119 a0002c0003t0002g0120 |
4 | HG01071.hp1 HG01175.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1838-1281G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297137 | |||||||
chr4:118297151 | C | T | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1838-1295G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297151 | |||||||
chr4:118297513 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1837+1220A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297513 | |||||||
chr4:118297525 | T | C | 1 | a0003c0005t0003g0205 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1837+1208A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297525 | |||||||
chr4:118297635 | T | C | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1837+1098A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297635 | |||||||
chr4:118297701 | G | C | 1 | a0002c0002t0001g0057 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1837+1032C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297701 | |||||||
chr4:118297818 | T | C | 1 | a0002c0002t0007g0142 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1837+915A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297818 | |||||||
chr4:118297909 | G | T | 26 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(23): Show |
30 | HG00544.hp2 HG00673.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1837+824C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297909 | |||||||
chr4:118297999 | G | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0056 a0002c0002t0001g0066 others(3): Show |
7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1837+734C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118297999 | |||||||
chr4:118298013 | C | T | 46 | a0001c0001t0002g0202 a0001c0001t0002g0276 a0001c0001t0005g0015 others(43): Show |
67 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1837+720G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298013 | |||||||
chr4:118298024 | G | A | 1 | a0001c0004t0001g0041 | 2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1837+709C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298024 | |||||||
chr4:118298032 | G | A | 44 | a0001c0001t0002g0202 a0001c0001t0002g0276 a0001c0001t0008g0280 others(41): Show |
64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1837+701C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298032 | |||||||
chr4:118298086 | C | G | 32 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(29): Show |
38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1837+647G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298086 | |||||||
chr4:118298140 | C | CA | 22 | a0001c0001t0001g0164 a0001c0001t0006g0168 a0001c0001t0008g0281 others(19): Show |
22 | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.1837+592dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298140 | |||||||
chr4:118298345 | T | G | 7 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(4): Show |
8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1837+388A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298345 | |||||||
chr4:118298428 | G | A | 1 | a0002c0003t0002g0122 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1837+305C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298428 | |||||||
chr4:118298529 | T | C | 224 | a0001c0001t0001g0146 a0001c0001t0002g0202 a0001c0001t0002g0276 others(221): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1837+204A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 9/12 | chr4 | 118298529 | |||||||
chr4:118298957 | T | C | 1 | a0003c0005t0003g0206 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1632-19A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118298957 | |||||||
chr4:118298964 | G | T | 1 | a0002c0003t0002g0137 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1632-26C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118298964 | |||||||
chr4:118299199 | C | T | 1 | a0001c0004t0001g0241 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1632-261G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299199 | |||||||
chr4:118299403 | G | A | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1632-465C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299403 | |||||||
chr4:118299408 | C | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1632-470G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299408 | |||||||
chr4:118299452 | G | A | 1 | a0002c0002t0001g0099 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1632-514C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299452 | |||||||
chr4:118299466 | A | G | 2 | a0001c0004t0001g0045 a0002c0002t0001g0070 |
3 | HG02074.hp2 NA18961.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.1632-528T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299466 | |||||||
chr4:118299542 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1632-604A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299542 | |||||||
chr4:118299548 | C | T | 1 | a0002c0003t0002g0117 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1632-610G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299548 | |||||||
chr4:118299689 | T | C | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1632-751A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299689 | |||||||
chr4:118299704 | AAATAAAA others(1): Show |
A | 3 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 |
3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1632-774_1632-767d others(10): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299704 | |||||||
chr4:118299708 | AAAAT | A | 5 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(2): Show |
5 | HG02145.hp2 HG02895.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632-774_1632-771d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299708 | |||||||
chr4:118299712 | T | TA | 4 | a0001c0009t0001g0275 a0001c0009t0009g0048 a0001c0009t0009g0049 others(1): Show |
4 | HG01071.hp1 HG03041.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1632-775dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | |||||||
chr4:118299712 | T | TAAAATAA others(4): Show |
1 | a0001c0009t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1632-775_1632-774i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | |||||||
chr4:118299712 | T | TAAATAAA others(3): Show |
29 | a0001c0001t0002g0276 a0002c0003t0002g0001 a0002c0003t0002g0007 others(26): Show |
43 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1632-784_1632-775d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | |||||||
chr4:118299712 | T | TAAATAAA others(8): Show |
10 | a0001c0001t0002g0202 a0001c0001t0008g0280 a0001c0001t0008g0281 others(7): Show |
12 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1632-789_1632-775d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | |||||||
chr4:118299712 | T | TAATA | 3 | a0001c0004t0007g0237 a0001c0004t0007g0254 a0002c0002t0007g0142 |
3 | HG02148.hp1 HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1632-775_1632-774i others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | |||||||
chr4:118299712 | T | TAATAAAA others(7): Show |
1 | a0001c0004t0001g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1632-775_1632-774i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | |||||||
chr4:118299712 | TAAATAAA others(3): Show |
T | 9 | a0001c0001t0001g0146 a0001c0006t0001g0263 a0001c0006t0001g0264 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1632-784_1632-775d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299712 | |||||||
chr4:118299727 | AAAATAAA others(31): Show |
A | 1 | a0002c0002t0001g0096 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1632-827_1632-790d others(40): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299727 | |||||||
chr4:118299732 | AAAATAAA others(26): Show |
A | 8 | a0001c0004t0001g0198 a0002c0002t0001g0057 a0002c0002t0001g0058 others(5): Show |
8 | HG00738.hp1 HG01175.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.1632-827_1632-795d others(35): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299732 | |||||||
chr4:118299737 | A | AAAAT | 4 | a0001c0001t0001g0033 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
5 | HG02559.hp1 HG03041.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-803_1632-800d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299737 | |||||||
chr4:118299737 | A | AAAATAAA others(12): Show |
2 | a0002c0003t0002g0026 a0002c0003t0002g0116 |
2 | HG01243.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1632-800_1632-799i others(21): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299737 | |||||||
chr4:118299737 | AAAATAAA others(21): Show |
A | 1 | a0002c0002t0001g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1632-827_1632-800d others(30): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299737 | |||||||
chr4:118299741 | TAAAATAA others(22): Show |
T | 3 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 |
3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1632-832_1632-804d others(31): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299741 | |||||||
chr4:118299741 | TAAAATAA others(27): Show |
T | 2 | a0002c0002t0001g0089 a0002c0002t0001g0092 |
2 | HG03831.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1632-837_1632-804d others(36): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299741 | |||||||
chr4:118299742 | AAAAT | A | 7 | a0001c0004t0001g0230 a0001c0004t0001g0240 a0001c0004t0001g0256 others(4): Show |
11 | HG01346.hp2 HG01928.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1632-808_1632-805d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299742 | |||||||
chr4:118299742 | AAAATAAA others(6): Show |
A | 1 | a0002c0002t0001g0140 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1632-817_1632-805d others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299742 | |||||||
chr4:118299742 | AAAATAAA others(16): Show |
A | 68 | a0001c0004t0001g0041 a0001c0004t0001g0043 a0001c0004t0001g0044 others(65): Show |
78 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1632-827_1632-805d others(25): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299742 | |||||||
chr4:118299746 | T | TA | 15 | a0001c0004t0001g0042 a0001c0004t0001g0170 a0001c0004t0001g0188 others(12): Show |
16 | HG00639.hp2 HG01255.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1632-809dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | |||||||
chr4:118299746 | T | TAAAATAA others(4): Show |
3 | a0001c0004t0001g0234 a0001c0004t0001g0243 a0003c0005t0024g0286 |
3 | HG02451.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1632-809_1632-808i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | |||||||
chr4:118299746 | TAAATAAA others(22): Show |
T | 11 | a0001c0004t0001g0255 a0002c0002t0001g0003 a0002c0002t0001g0008 others(8): Show |
14 | HG00323.hp1 HG00642.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1632-837_1632-809d others(31): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | |||||||
chr4:118299746 | TAAATAAA others(32): Show |
T | 1 | a0002c0002t0001g0062 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1632-847_1632-809d others(41): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299746 | |||||||
chr4:118299747 | AAATAAAA others(11): Show |
A | 10 | a0001c0004t0001g0013 a0001c0004t0001g0245 a0001c0004t0001g0246 others(7): Show |
13 | HG01123.hp1 HG01517.hp1 HG03491.hp2 others(10): Show |
intron_variant | MODIFIER | c.1632-827_1632-810d others(20): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299747 | |||||||
chr4:118299750 | T | A | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1632-812A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299750 | |||||||
chr4:118299751 | A | T | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1632-813T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299751 | |||||||
chr4:118299751 | AAAAT | A | 31 | a0001c0001t0001g0262 a0003c0005t0003g0006 a0003c0005t0003g0039 others(28): Show |
37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.1632-817_1632-814d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299751 | |||||||
chr4:118299755 | T | TA | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01243.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632-818dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | |||||||
chr4:118299755 | T | TAAAATAA others(17): Show |
1 | a0002c0003t0002g0028 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1632-818_1632-817i others(26): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | |||||||
chr4:118299755 | T | TAAATA | 40 | a0001c0001t0001g0004 a0001c0001t0001g0167 a0001c0001t0001g0171 others(37): Show |
55 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1632-822_1632-818d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | |||||||
chr4:118299755 | T | TAAATAAA others(3): Show |
2 | a0001c0001t0001g0181 a0001c0001t0006g0035 |
2 | HG02257.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1632-818_1632-817i others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299755 | |||||||
chr4:118299759 | T | A | 9 | a0001c0001t0005g0015 a0001c0001t0005g0047 a0001c0004t0012g0193 others(6): Show |
10 | HG01074.hp2 HG02148.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1632-821A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299759 | |||||||
chr4:118299760 | A | AAAATT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0032 others(10): Show |
18 | HG02165.hp2 NA18939.hp2 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.1632-827_1632-823d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299760 | |||||||
chr4:118299760 | A | T | 10 | a0001c0001t0001g0262 a0001c0001t0005g0015 a0001c0001t0005g0047 others(7): Show |
11 | HG01074.hp2 HG02148.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1632-822T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299760 | |||||||
chr4:118299763 | AT | A | 4 | a0001c0009t0001g0275 a0001c0009t0009g0048 a0001c0009t0009g0049 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-826delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299763 | |||||||
chr4:118299764 | T | A | 7 | a0001c0004t0012g0193 a0001c0004t0020g0279 a0002c0002t0007g0142 others(4): Show |
7 | HG01074.hp2 HG02148.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-826A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299764 | |||||||
chr4:118299764 | TTAAATAA others(22): Show |
T | 5 | a0001c0004t0001g0230 a0002c0002t0001g0003 a0002c0002t0001g0018 others(2): Show |
9 | HG01346.hp2 HG01928.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1632-855_1632-827d others(31): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299764 | |||||||
chr4:118299765 | T | A | 114 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0037 others(111): Show |
147 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1632-827A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | |||||||
chr4:118299765 | T | TAAATA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(16): Show |
30 | HG01256.hp2 HG01258.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.1632-832_1632-828d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | |||||||
chr4:118299765 | T | TAAATAAA others(3): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0165 a0001c0001t0001g0196 |
3 | HG00558.hp1 HG01433.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1632-837_1632-828d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | |||||||
chr4:118299765 | T | TAAATAAA others(8): Show |
1 | a0002c0003t0001g0065 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1632-842_1632-828d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | |||||||
chr4:118299765 | TAAATAAA others(3): Show |
T | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1632-837_1632-828d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299765 | |||||||
chr4:118299769 | TA | T | 35 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(32): Show |
41 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.1632-832delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299769 | |||||||
chr4:118299770 | A | AAAAT | 6 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(3): Show |
7 | HG01255.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-836_1632-833d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299770 | |||||||
chr4:118299774 | TA | T | 83 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(80): Show |
96 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1632-837delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299774 | |||||||
chr4:118299774 | TAAAATA | T | 4 | a0001c0004t0001g0170 a0001c0004t0001g0188 a0001c0004t0001g0240 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-842_1632-837d others(8): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299774 | |||||||
chr4:118299780 | A | T | 1 | a0001c0001t0001g0151 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1632-842T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299780 | |||||||
chr4:118299784 | TA | T | 8 | a0002c0002t0001g0057 a0002c0002t0001g0058 a0002c0002t0001g0059 others(5): Show |
8 | HG01175.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1632-847delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299784 | |||||||
chr4:118299793 | A | T | 7 | a0001c0004t0001g0198 a0002c0002t0001g0096 a0002c0002t0001g0097 others(4): Show |
7 | HG00738.hp1 NA18941.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1632-855T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299793 | |||||||
chr4:118299794 | T | A | 12 | a0001c0004t0001g0198 a0001c0004t0001g0230 a0002c0002t0001g0003 others(9): Show |
16 | HG00738.hp1 HG01346.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.1632-856A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299794 | |||||||
chr4:118299794 | TAAATAAA others(12): Show |
T | 1 | a0003c0005t0010g0223 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1632-875_1632-857d others(21): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299794 | |||||||
chr4:118299798 | T | A | 14 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(11): Show |
15 | HG01074.hp2 HG01255.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1632-860A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299798 | |||||||
chr4:118299799 | A | T | 12 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(9): Show |
13 | HG01255.hp2 HG02451.hp2 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.1632-861T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299799 | |||||||
chr4:118299799 | AAAATAAA others(2): Show |
A | 4 | a0001c0004t0001g0170 a0001c0004t0001g0188 a0001c0004t0001g0240 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-870_1632-862d others(11): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299799 | |||||||
chr4:118299807 | A | T | 5 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 others(2): Show |
6 | HG02027.hp1 NA18966.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632-869T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299807 | |||||||
chr4:118299808 | T | A | 5 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 others(2): Show |
6 | HG02027.hp1 NA18966.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1632-870A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | |||||||
chr4:118299808 | T | TAAATA | 44 | a0001c0001t0001g0029 a0001c0001t0001g0144 a0001c0001t0001g0161 others(41): Show |
64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1632-875_1632-871d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | |||||||
chr4:118299808 | T | TAAATAAA others(3): Show |
4 | a0001c0001t0001g0155 a0001c0001t0005g0015 a0001c0001t0005g0047 others(1): Show |
5 | HG01261.hp2 HG02486.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1632-880_1632-871d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | |||||||
chr4:118299808 | T | TAAATAAA others(8): Show |
1 | a0001c0001t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1632-885_1632-871d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | |||||||
chr4:118299808 | TAAATA | T | 43 | a0001c0001t0001g0146 a0001c0004t0001g0183 a0001c0004t0001g0185 others(40): Show |
49 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.1632-875_1632-871d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | |||||||
chr4:118299808 | TAAATAAA others(3): Show |
T | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-880_1632-871d others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299808 | |||||||
chr4:118299812 | T | A | 16 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(13): Show |
17 | HG01074.hp2 HG01255.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1632-874A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299812 | |||||||
chr4:118299813 | A | T | 16 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(13): Show |
17 | HG01074.hp2 HG01255.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1632-875T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299813 | |||||||
chr4:118299998 | A | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1632-1060T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118299998 | |||||||
chr4:118300017 | C | CT | 5 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0181 others(2): Show |
7 | HG00639.hp1 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-1080dupA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300017 | |||||||
chr4:118300158 | A | G | 1 | a0001c0006t0001g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1632-1220T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300158 | |||||||
chr4:118300253 | T | C | 1 | a0001c0006t0001g0272 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1632-1315A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300253 | |||||||
chr4:118300350 | G | A | 113 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(110): Show |
135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1632-1412C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300350 | |||||||
chr4:118300412 | T | C | 16 | a0001c0004t0001g0044 a0001c0004t0001g0265 a0001c0004t0001g0266 others(13): Show |
18 | HG00621.hp2 HG02080.hp1 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1632-1474A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300412 | |||||||
chr4:118300763 | GAATATAC others(3): Show |
G | 1 | a0002c0003t0003g0132 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1632-1835_1632-182 others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300763 | |||||||
chr4:118300785 | T | G | 178 | a0001c0001t0001g0146 a0001c0004t0001g0013 a0001c0004t0001g0041 others(175): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1632-1847A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300785 | |||||||
chr4:118300824 | A | G | 89 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(86): Show |
110 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.1632-1886T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300824 | |||||||
chr4:118300919 | C | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1632-1981G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118300919 | |||||||
chr4:118301038 | A | C | 34 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(31): Show |
40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1632-2100T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301038 | |||||||
chr4:118301066 | CA | C | 34 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(31): Show |
40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1632-2129delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301066 | |||||||
chr4:118301100 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0191 |
8 | NA18940.hp1 NA18941.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-2162G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301100 | |||||||
chr4:118301505 | C | T | 1 | a0002c0003t0002g0137 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1632-2567G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301505 | |||||||
chr4:118301533 | GA | G | 7 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(4): Show |
8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-2596delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301533 | |||||||
chr4:118301609 | C | T | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1632-2671G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301609 | |||||||
chr4:118301685 | A | C | 1 | a0001c0001t0001g0034 | 2 | NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1632-2747T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301685 | |||||||
chr4:118301815 | T | A | 1 | a0002c0003t0003g0132 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1632-2877A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301815 | |||||||
chr4:118301890 | T | C | 2 | a0001c0004t0001g0157 a0001c0004t0001g0169 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1632-2952A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118301890 | |||||||
chr4:118302039 | A | T | 1 | a0002c0003t0003g0132 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1632-3101T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302039 | |||||||
chr4:118302064 | G | A | 1 | a0002c0003t0002g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1632-3126C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302064 | |||||||
chr4:118302154 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1632-3216G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302154 | |||||||
chr4:118302197 | A | G | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-3259T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302197 | |||||||
chr4:118302491 | A | C | 46 | a0001c0001t0002g0202 a0001c0001t0002g0276 a0001c0001t0005g0015 others(43): Show |
67 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.1632-3553T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302491 | |||||||
chr4:118302491 | A | G | 1 | a0005c0010t0001g0014 | 3 | HG00639.hp1 HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1632-3553T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302491 | |||||||
chr4:118302590 | C | T | 1 | a0002c0002t0022g0284 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1632-3652G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302590 | |||||||
chr4:118302661 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1632-3723C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302661 | |||||||
chr4:118302674 | G | A | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-3736C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302674 | |||||||
chr4:118302707 | G | A | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1632-3769C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302707 | |||||||
chr4:118302765 | T | C | 7 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(4): Show |
8 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-3827A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302765 | |||||||
chr4:118302790 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1632-3852A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302790 | |||||||
chr4:118302806 | TTG | T | 162 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(159): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1632-3870_1632-386 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302806 | |||||||
chr4:118302926 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1632-3988A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302926 | |||||||
chr4:118302981 | A | G | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1632-4043T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118302981 | |||||||
chr4:118303012 | A | C | 1 | a0002c0003t0002g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1632-4074T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303012 | |||||||
chr4:118303194 | C | T | 1 | a0003c0005t0003g0228 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1632-4256G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303194 | |||||||
chr4:118303343 | C | T | 178 | a0001c0001t0001g0146 a0001c0004t0001g0013 a0001c0004t0001g0041 others(175): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1632-4405G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303343 | |||||||
chr4:118303478 | A | G | 5 | a0001c0004t0001g0013 a0001c0004t0001g0245 a0001c0004t0001g0246 others(2): Show |
7 | NA18965.hp2 NA18968.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.1632-4540T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303478 | |||||||
chr4:118303500 | C | T | 1 | a0002c0003t0002g0136 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1632-4562G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303500 | |||||||
chr4:118303656 | T | C | 3 | a0002c0002t0001g0009 a0002c0002t0001g0053 a0002c0002t0001g0054 |
5 | NA18940.hp2 NA18970.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-4718A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303656 | |||||||
chr4:118303696 | C | G | 6 | a0002c0002t0001g0023 a0002c0002t0001g0055 a0002c0002t0001g0083 others(3): Show |
7 | HG01109.hp1 HG01123.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1631+4740G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303696 | |||||||
chr4:118303982 | CT | C | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1631+4453delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118303982 | |||||||
chr4:118304090 | C | G | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1631+4346G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304090 | |||||||
chr4:118304128 | G | A | 1 | a0001c0004t0001g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1631+4308C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304128 | |||||||
chr4:118304138 | G | T | 1 | a0002c0003t0003g0132 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1631+4298C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304138 | |||||||
chr4:118304294 | A | G | 223 | a0001c0001t0001g0146 a0001c0001t0002g0202 a0001c0001t0002g0276 others(220): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1631+4142T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304294 | |||||||
chr4:118304403 | A | G | 169 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(166): Show |
198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1631+4033T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304403 | |||||||
chr4:118304410 | T | C | 1 | a0003c0005t0003g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1631+4026A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304410 | |||||||
chr4:118304572 | T | A | 1 | a0012c0014t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1631+3864A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304572 | |||||||
chr4:118304574 | CA | C | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1631+3861delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304574 | |||||||
chr4:118304785 | C | T | 44 | a0001c0001t0002g0202 a0001c0001t0002g0276 a0001c0001t0008g0280 others(41): Show |
64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1631+3651G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304785 | |||||||
chr4:118304899 | A | C | 8 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(5): Show |
9 | HG01255.hp2 HG02148.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631+3537T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118304899 | |||||||
chr4:118305049 | T | C | 2 | a0003c0005t0004g0199 a0003c0005t0004g0200 |
2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1631+3387A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305049 | |||||||
chr4:118305101 | TTA | T | 16 | a0001c0001t0001g0146 a0001c0004t0001g0042 a0001c0004t0001g0157 others(13): Show |
17 | HG01074.hp2 HG01255.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1631+3333_1631+333 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305101 | |||||||
chr4:118305118 | T | C | 2 | a0001c0001t0005g0015 a0001c0004t0001g0256 |
3 | HG02886.hp2 HG03516.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1631+3318A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305118 | |||||||
chr4:118305120 | T | C | 166 | a0001c0001t0002g0202 a0001c0001t0002g0276 a0001c0001t0005g0015 others(163): Show |
213 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1631+3316A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305120 | |||||||
chr4:118305120 | T | TAC | 3 | a0002c0002t0001g0085 a0003c0005t0003g0215 a0003c0005t0003g0249 |
3 | HG01169.hp2 NA18612.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1631+3314_1631+331 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305120 | |||||||
chr4:118305136 | C | CAT | 18 | a0003c0005t0003g0039 a0003c0005t0003g0201 a0003c0005t0003g0204 others(15): Show |
19 | HG01123.hp2 HG01255.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1631+3298_1631+329 others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305136 | |||||||
chr4:118305136 | C | T | 9 | a0001c0001t0001g0165 a0003c0005t0003g0006 a0003c0005t0003g0203 others(6): Show |
13 | HG00597.hp2 HG01433.hp1 NA18747.hp2 others(10): Show |
intron_variant | MODIFIER | c.1631+3300G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305136 | |||||||
chr4:118305138 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1631+3298A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305138 | |||||||
chr4:118305165 | T | C | 2 | a0001c0004t0001g0157 a0001c0004t0001g0169 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1631+3271A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305165 | |||||||
chr4:118305321 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1631+3115C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305321 | |||||||
chr4:118305505 | T | C | 1 | a0001c0006t0001g0273 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1631+2931A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305505 | |||||||
chr4:118305520 | T | C | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1631+2916A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305520 | |||||||
chr4:118305738 | C | T | 11 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(8): Show |
12 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.1631+2698G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305738 | |||||||
chr4:118305739 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1631+2697C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118305739 | |||||||
chr4:118306104 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1631+2332A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306104 | |||||||
chr4:118306157 | A | G | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1631+2279T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306157 | |||||||
chr4:118306161 | T | C | 1 | a0002c0002t0001g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1631+2275A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306161 | |||||||
chr4:118306258 | T | C | 1 | a0007c0013t0004g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1631+2178A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306258 | |||||||
chr4:118306318 | T | C | 1 | a0002c0003t0002g0131 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1631+2118A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306318 | |||||||
chr4:118306336 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1631+2100G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306336 | |||||||
chr4:118306377 | A | G | 9 | a0001c0001t0001g0146 a0001c0006t0001g0263 a0001c0006t0001g0264 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1631+2059T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306377 | |||||||
chr4:118306441 | C | T | 3 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0069 |
3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1631+1995G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306441 | |||||||
chr4:118306517 | C | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1631+1919G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306517 | |||||||
chr4:118306534 | G | A | 3 | a0003c0005t0024g0286 a0007c0013t0004g0277 a0007c0013t0004g0278 |
3 | HG02109.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1631+1902C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306534 | |||||||
chr4:118306798 | G | A | 224 | a0001c0001t0001g0146 a0001c0001t0002g0202 a0001c0001t0002g0276 others(221): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1631+1638C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118306798 | |||||||
chr4:118307074 | T | C | 1 | a0002c0002t0001g0090 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1631+1362A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307074 | |||||||
chr4:118307198 | T | C | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1631+1238A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307198 | |||||||
chr4:118307205 | T | C | 6 | a0002c0002t0001g0023 a0002c0002t0001g0055 a0002c0002t0001g0083 others(3): Show |
7 | HG01109.hp1 HG01123.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1631+1231A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307205 | |||||||
chr4:118307728 | C | T | 32 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(29): Show |
38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1631+708G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118307728 | |||||||
chr4:118308315 | C | T | 3 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0069 |
3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1631+121G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118308315 | |||||||
chr4:118308338 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1631+98C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118308338 | |||||||
chr4:118308412 | C | G | 1 | a0004c0007t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1631+24G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 8/12 | chr4 | 118308412 | |||||||
chr4:118308584 | C | T | 1 | a0003c0005t0024g0286 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.1490-7G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308584 | |||||||
chr4:118308597 | T | C | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1490-20A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308597 | |||||||
chr4:118308822 | G | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0175 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1490-245C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308822 | |||||||
chr4:118308856 | T | C | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-279A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308856 | |||||||
chr4:118308896 | A | G | 1 | a0001c0006t0001g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1490-319T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308896 | |||||||
chr4:118308910 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1490-333A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118308910 | |||||||
chr4:118309023 | A | G | 12 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(9): Show |
13 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.1490-446T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309023 | |||||||
chr4:118309184 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1490-607A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309184 | |||||||
chr4:118309374 | G | C | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-797C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309374 | |||||||
chr4:118309385 | A | G | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1490-808T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309385 | |||||||
chr4:118309474 | ATC | A | 223 | a0001c0001t0001g0146 a0001c0001t0002g0202 a0001c0001t0002g0276 others(220): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.1490-899_1490-898d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309474 | |||||||
chr4:118309888 | T | C | 1 | a0003c0005t0004g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1490-1311A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118309888 | |||||||
chr4:118310181 | A | C | 1 | a0002c0003t0002g0138 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1490-1604T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310181 | |||||||
chr4:118310467 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1490-1890G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310467 | |||||||
chr4:118310468 | T | C | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1490-1891A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310468 | |||||||
chr4:118310506 | A | G | 2 | a0002c0002t0001g0097 a0002c0002t0001g0098 |
2 | NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1490-1929T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310506 | |||||||
chr4:118310516 | T | C | 114 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(111): Show |
136 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1490-1939A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310516 | |||||||
chr4:118310581 | T | C | 44 | a0001c0001t0002g0202 a0001c0001t0002g0276 a0001c0001t0008g0280 others(41): Show |
64 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.1490-2004A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310581 | |||||||
chr4:118310744 | C | T | 2 | a0002c0002t0001g0081 a0002c0002t0001g0086 |
2 | NA18959.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1490-2167G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310744 | |||||||
chr4:118310879 | C | T | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1490-2302G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310879 | |||||||
chr4:118310905 | G | C | 1 | a0003c0005t0004g0200 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1489+2296C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310905 | |||||||
chr4:118310910 | G | C | 1 | a0009c0015t0002g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1489+2291C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118310910 | |||||||
chr4:118311062 | T | TAATTAAT others(11): Show |
1 | a0001c0006t0001g0274 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1489+2121_1489+213 others(22): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311062 | |||||||
chr4:118311075 | A | T | 6 | a0002c0002t0001g0017 a0002c0002t0001g0056 a0002c0002t0001g0066 others(3): Show |
7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1489+2126T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311075 | |||||||
chr4:118311189 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1489+2012G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311189 | |||||||
chr4:118311198 | C | T | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1489+2003G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311198 | |||||||
chr4:118311237 | A | T | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1489+1964T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311237 | |||||||
chr4:118311282 | T | C | 1 | a0002c0003t0002g0136 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1489+1919A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311282 | |||||||
chr4:118311470 | G | A | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1489+1731C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311470 | |||||||
chr4:118311785 | G | A | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1489+1416C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311785 | |||||||
chr4:118311863 | T | C | 1 | a0002c0003t0002g0131 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1489+1338A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118311863 | |||||||
chr4:118312046 | G | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1489+1155C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312046 | |||||||
chr4:118312070 | G | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1489+1131C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312070 | |||||||
chr4:118312312 | T | C | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1489+889A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312312 | |||||||
chr4:118312470 | CATAT | C | 12 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(9): Show |
13 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.1489+727_1489+730d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312470 | |||||||
chr4:118312614 | A | T | 3 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 |
3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1489+587T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312614 | |||||||
chr4:118312709 | T | A | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1489+492A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312709 | |||||||
chr4:118312791 | T | C | 2 | a0002c0003t0002g0116 a0002c0003t0002g0117 |
2 | HG01243.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1489+410A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118312791 | |||||||
chr4:118313102 | A | G | 13 | a0001c0004t0001g0042 a0001c0004t0001g0234 a0001c0004t0001g0243 others(10): Show |
14 | HG01255.hp2 HG02109.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.1489+99T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 7/12 | chr4 | 118313102 | |||||||
chr4:118313538 | C | T | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1293-141G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313538 | |||||||
chr4:118313714 | A | T | 113 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(110): Show |
135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1293-317T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313714 | |||||||
chr4:118313875 | T | A | 9 | a0001c0001t0001g0146 a0001c0006t0001g0263 a0001c0006t0001g0264 others(6): Show |
9 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1293-478A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313875 | |||||||
chr4:118313898 | C | A | 1 | a0001c0004t0001g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1293-501G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118313898 | |||||||
chr4:118314010 | C | A | 5 | a0003c0005t0004g0199 a0003c0005t0004g0200 a0003c0005t0024g0286 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1293-613G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314010 | |||||||
chr4:118314166 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG02559.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1293-769G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314166 | |||||||
chr4:118314309 | CT | C | 113 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(110): Show |
135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1293-913delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314309 | |||||||
chr4:118314429 | C | G | 228 | a0001c0001t0001g0146 a0001c0001t0001g0171 a0001c0001t0001g0179 others(225): Show |
280 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(277): Show |
intron_variant | MODIFIER | c.1293-1032G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314429 | |||||||
chr4:118314688 | C | T | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1293-1291G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314688 | |||||||
chr4:118314690 | C | T | 113 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(110): Show |
135 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.1293-1293G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314690 | |||||||
chr4:118314714 | C | T | 1 | a0003c0005t0003g0213 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1293-1317G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314714 | |||||||
chr4:118314814 | TA | T | 7 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(4): Show |
7 | HG01169.hp2 HG02486.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1292+1367delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314814 | |||||||
chr4:118314983 | C | A | 1 | a0002c0002t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1292+1199G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118314983 | |||||||
chr4:118315098 | G | A | 178 | a0001c0001t0001g0146 a0001c0004t0001g0013 a0001c0004t0001g0041 others(175): Show |
207 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1292+1084C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315098 | |||||||
chr4:118315182 | T | C | 32 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(29): Show |
38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1292+1000A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315182 | |||||||
chr4:118315187 | T | A | 224 | a0001c0001t0001g0146 a0001c0001t0002g0202 a0001c0001t0002g0276 others(221): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.1292+995A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315187 | |||||||
chr4:118315315 | T | C | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1292+867A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315315 | |||||||
chr4:118315428 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0191 |
8 | NA18940.hp1 NA18941.hp1 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1292+754A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315428 | |||||||
chr4:118315655 | A | T | 1 | a0002c0002t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1292+527T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118315655 | |||||||
chr4:118316159 | C | T | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1292+23G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 6/12 | chr4 | 118316159 | |||||||
chr4:118316533 | T | C | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1151-210A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316533 | |||||||
chr4:118316593 | AG | A | 34 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(31): Show |
40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.1151-271delC | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316593 | |||||||
chr4:118316649 | C | T | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1151-326G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316649 | |||||||
chr4:118316727 | C | T | 3 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0069 |
3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1151-404G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316727 | |||||||
chr4:118316776 | C | T | 2 | a0002c0003t0002g0011 a0002c0003t0002g0135 |
4 | NA18980.hp1 NA19001.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-453G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316776 | |||||||
chr4:118316777 | G | A | 1 | a0001c0001t0013g0178 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1151-454C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316777 | |||||||
chr4:118316808 | C | T | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1151-485G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316808 | |||||||
chr4:118316817 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1151-494C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316817 | |||||||
chr4:118316825 | G | GAAAA | 25 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(22): Show |
31 | HG00597.hp2 HG01123.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.1151-506_1151-503d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316825 | |||||||
chr4:118316825 | G | GAAAAA | 7 | a0003c0005t0003g0206 a0003c0005t0003g0210 a0003c0005t0003g0211 others(4): Show |
7 | HG00099.hp1 HG02738.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-507_1151-503d others(7): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316825 | |||||||
chr4:118316837 | A | AAAAAAAA others(7): Show |
1 | a0002c0002t0001g0068 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAA others(9): Show |
1 | a0002c0002t0001g0067 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(18): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAA others(6): Show |
1 | a0004c0007t0001g0109 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAA others(5): Show |
6 | a0001c0004t0001g0241 a0001c0004t0001g0242 a0001c0004t0001g0248 others(3): Show |
6 | HG03139.hp2 NA18939.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAA others(7): Show |
6 | a0001c0004t0001g0182 a0002c0002t0001g0017 a0002c0002t0001g0056 others(3): Show |
7 | HG01243.hp2 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAA others(13): Show |
1 | a0001c0004t0001g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(22): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAT others(4): Show |
3 | a0001c0004t0001g0257 a0002c0003t0002g0130 a0002c0003t0002g0131 |
3 | HG00408.hp2 HG03491.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAT others(6): Show |
5 | a0001c0004t0001g0246 a0001c0004t0001g0247 a0002c0002t0001g0090 others(2): Show |
5 | HG01928.hp1 HG02080.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAT others(8): Show |
1 | a0001c0004t0001g0250 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAT others(10): Show |
1 | a0001c0004t0001g0183 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(19): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAAAT others(20): Show |
1 | a0001c0004t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(29): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAATA others(3): Show |
2 | a0001c0004t0001g0230 a0010c0019t0001g0091 |
2 | HG01517.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(12): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAATA others(5): Show |
60 | a0001c0001t0005g0047 a0001c0004t0001g0013 a0001c0004t0001g0041 others(57): Show |
76 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAATA others(7): Show |
17 | a0001c0004t0001g0170 a0001c0004t0001g0238 a0001c0004t0001g0245 others(14): Show |
19 | HG00323.hp1 HG01109.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAATA others(9): Show |
5 | a0001c0004t0001g0185 a0001c0004t0001g0198 a0002c0002t0001g0102 others(2): Show |
5 | HG00738.hp1 HG02922.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(18): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAAATA others(13): Show |
1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(22): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAATAT others(4): Show |
18 | a0002c0003t0002g0001 a0002c0003t0002g0007 a0002c0003t0002g0011 others(15): Show |
33 | HG00408.hp1 HG00438.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAATAT others(6): Show |
5 | a0001c0004t0001g0252 a0002c0002t0001g0054 a0002c0003t0002g0123 others(2): Show |
5 | HG03688.hp2 NA18982.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAATAT others(10): Show |
3 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 |
3 | HG00735.hp1 HG01433.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(19): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAAATAT others(12): Show |
1 | a0001c0001t0002g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(21): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAATATA others(5): Show |
10 | a0001c0001t0005g0015 a0001c0004t0001g0266 a0001c0009t0001g0192 others(7): Show |
13 | HG02155.hp1 HG02647.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAATATA others(7): Show |
3 | a0001c0009t0009g0049 a0002c0002t0001g0008 a0002c0002t0001g0061 |
5 | HG00733.hp1 HG01071.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(16): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAAATATA others(9): Show |
2 | a0002c0002t0001g0076 a0002c0003t0002g0139 |
2 | HG00099.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.1151-515_1151-514i others(18): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAATATAT others(4): Show |
7 | a0001c0001t0002g0276 a0002c0003t0002g0010 a0002c0003t0002g0024 others(4): Show |
11 | HG00323.hp2 HG01071.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAATATAT others(6): Show |
1 | a0002c0003t0002g0112 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(15): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAATATAT others(8): Show |
1 | a0002c0003t0002g0121 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1151-515_1151-514i others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AAATATAT others(10): Show |
1 | a0002c0003t0002g0141 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1151-515_1151-514i others(19): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AATATATA others(5): Show |
1 | a0001c0009t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1151-526_1151-515d others(14): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | AT | 4 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0174 others(1): Show |
4 | HG02145.hp2 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-515_1151-514i others(3): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316837 | A | T | 12 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0163 others(9): Show |
12 | HG01109.hp2 HG01975.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1151-514T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316837 | |||||||
chr4:118316839 | T | A | 32 | a0001c0001t0001g0194 a0001c0004t0001g0157 a0003c0005t0003g0006 others(29): Show |
38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1151-516A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316839 | |||||||
chr4:118316841 | T | A | 1 | a0001c0004t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1151-518A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316841 | |||||||
chr4:118316856 | A | C | 1 | a0002c0003t0002g0137 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1151-533T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118316856 | |||||||
chr4:118317063 | GA | G | 114 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(111): Show |
136 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1151-741delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317063 | |||||||
chr4:118317092 | A | T | 1 | a0001c0004t0001g0265 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1151-769T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317092 | |||||||
chr4:118317685 | T | A | 1 | a0003c0005t0003g0228 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1150+693A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317685 | |||||||
chr4:118317809 | T | C | 3 | a0001c0004t0001g0170 a0001c0004t0001g0188 a0001c0004t0001g0198 |
3 | HG00738.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1150+569A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317809 | |||||||
chr4:118317852 | C | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1150+526G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118317852 | |||||||
chr4:118318035 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0186 |
2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1150+343G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318035 | |||||||
chr4:118318071 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1150+307G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318071 | |||||||
chr4:118318112 | T | C | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1150+266A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318112 | |||||||
chr4:118318209 | A | T | 1 | a0001c0009t0009g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1150+169T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318209 | |||||||
chr4:118318234 | T | C | 1 | a0002c0002t0001g0092 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1150+144A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318234 | |||||||
chr4:118318250 | T | C | 32 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(29): Show |
38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.1150+128A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318250 | |||||||
chr4:118318324 | G | A | 1 | a0001c0004t0001g0251 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1150+54C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 5/12 | chr4 | 118318324 | |||||||
chr4:118318633 | A | G | 112 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0043 others(109): Show |
134 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.972-77T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318633 | |||||||
chr4:118318719 | T | C | 1 | a0001c0004t0001g0188 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.972-163A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318719 | |||||||
chr4:118318745 | C | A | 221 | a0001c0001t0001g0146 a0001c0001t0002g0202 a0001c0001t0002g0276 others(218): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.972-189G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318745 | |||||||
chr4:118318748 | T | C | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.972-192A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318748 | |||||||
chr4:118318794 | T | A | 1 | a0002c0002t0001g0093 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.972-238A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318794 | |||||||
chr4:118318834 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0176 |
2 | HG02145.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.972-278A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318834 | |||||||
chr4:118318845 | A | G | 167 | a0001c0001t0001g0161 a0001c0004t0001g0013 a0001c0004t0001g0041 others(164): Show |
196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.972-289T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118318845 | |||||||
chr4:118319050 | A | G | 1 | a0002c0003t0002g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.972-494T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319050 | |||||||
chr4:118319327 | A | C | 34 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(31): Show |
40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.972-771T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319327 | |||||||
chr4:118319368 | A | G | 41 | a0001c0001t0001g0262 a0001c0004t0001g0013 a0001c0004t0001g0041 others(38): Show |
46 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.972-812T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319368 | |||||||
chr4:118319463 | T | C | 87 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0157 others(84): Show |
105 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.972-907A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319463 | |||||||
chr4:118319465 | A | G | 2 | a0001c0004t0007g0237 a0001c0004t0007g0254 |
2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.972-909T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319465 | |||||||
chr4:118319612 | C | T | 6 | a0002c0002t0001g0017 a0002c0002t0001g0056 a0002c0002t0001g0066 others(3): Show |
7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.972-1056G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319612 | |||||||
chr4:118319666 | C | T | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.972-1110G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118319666 | |||||||
chr4:118320341 | C | T | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.972-1785G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320341 | |||||||
chr4:118320503 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972-1947C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320503 | |||||||
chr4:118320615 | T | G | 1 | a0003c0005t0024g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.972-2059A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320615 | |||||||
chr4:118320780 | T | G | 1 | a0001c0004t0007g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.972-2224A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320780 | |||||||
chr4:118320794 | G | T | 32 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(29): Show |
37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-2238C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320794 | |||||||
chr4:118320947 | C | A | 32 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(29): Show |
37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-2391G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118320947 | |||||||
chr4:118321056 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.972-2500T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321056 | |||||||
chr4:118321119 | G | A | 86 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0157 others(83): Show |
104 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.972-2563C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321119 | |||||||
chr4:118321679 | C | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
359 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(356): Show |
intron_variant | MODIFIER | c.972-3123G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321679 | |||||||
chr4:118321812 | T | G | 32 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(29): Show |
37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-3256A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321812 | |||||||
chr4:118321880 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972-3324A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321880 | |||||||
chr4:118321889 | G | A | 165 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(162): Show |
194 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.972-3333C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118321889 | |||||||
chr4:118322164 | G | GTAGT | 34 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(31): Show |
40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.972-3612_972-3609d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322164 | |||||||
chr4:118322214 | A | G | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.972-3658T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322214 | |||||||
chr4:118322271 | T | A | 1 | a0001c0001t0008g0282 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.972-3715A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322271 | |||||||
chr4:118322398 | A | C | 37 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(34): Show |
42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.972-3842T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322398 | |||||||
chr4:118322423 | G | A | 6 | a0002c0002t0001g0057 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
6 | HG01175.hp2 HG01361.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.972-3867C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322423 | |||||||
chr4:118322428 | C | A | 1 | a0003c0005t0003g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.972-3872G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322428 | |||||||
chr4:118322448 | C | T | 37 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(34): Show |
42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.972-3892G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322448 | |||||||
chr4:118322454 | G | A | 1 | a0001c0004t0001g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.972-3898C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322454 | |||||||
chr4:118322482 | G | A | 2 | a0008c0011t0001g0145 a0008c0011t0001g0180 |
2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.972-3926C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322482 | |||||||
chr4:118322549 | TA | T | 173 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0151 others(170): Show |
202 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.972-3994delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322549 | |||||||
chr4:118322724 | A | C | 1 | a0002c0003t0002g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.972-4168T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322724 | |||||||
chr4:118322756 | C | T | 1 | a0003c0005t0003g0212 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.972-4200G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322756 | |||||||
chr4:118322775 | G | A | 86 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0157 others(83): Show |
104 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.972-4219C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322775 | |||||||
chr4:118322852 | A | C | 224 | a0001c0001t0001g0146 a0001c0001t0001g0262 a0001c0001t0002g0202 others(221): Show |
274 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.972-4296T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322852 | |||||||
chr4:118322853 | G | A | 86 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0157 others(83): Show |
104 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.972-4297C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322853 | |||||||
chr4:118322893 | T | G | 10 | a0001c0001t0001g0146 a0001c0006t0001g0263 a0001c0006t0001g0264 others(7): Show |
10 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.972-4337A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118322893 | |||||||
chr4:118323170 | A | T | 1 | a0003c0005t0003g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.972-4614T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323170 | |||||||
chr4:118323448 | A | G | 1 | a0002c0003t0002g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.972-4892T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323448 | |||||||
chr4:118323481 | C | T | 2 | a0003c0005t0003g0218 a0003c0005t0011g0046 |
2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.972-4925G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323481 | |||||||
chr4:118323639 | A | C | 1 | a0001c0001t0001g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.972-5083T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323639 | |||||||
chr4:118323790 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.972-5234A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323790 | |||||||
chr4:118323916 | T | A | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-5360A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118323916 | |||||||
chr4:118324091 | G | A | 4 | a0002c0002t0001g0023 a0002c0002t0001g0093 a0002c0002t0001g0105 others(1): Show |
5 | HG01123.hp1 HG01496.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.972-5535C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324091 | |||||||
chr4:118324233 | T | C | 64 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0265 others(61): Show |
81 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.972-5677A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324233 | |||||||
chr4:118324279 | G | A | 1 | a0002c0002t0001g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.972-5723C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324279 | |||||||
chr4:118324410 | T | G | 34 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(31): Show |
40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.972-5854A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324410 | |||||||
chr4:118324580 | G | A | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-6024C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324580 | |||||||
chr4:118324696 | G | T | 32 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(29): Show |
38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.972-6140C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324696 | |||||||
chr4:118324766 | G | A | 33 | a0001c0001t0001g0146 a0003c0005t0003g0006 a0003c0005t0003g0039 others(30): Show |
39 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.972-6210C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324766 | |||||||
chr4:118324805 | C | T | 32 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(29): Show |
37 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.972-6249G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324805 | |||||||
chr4:118324955 | C | T | 4 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(1): Show |
4 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.972-6399G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324955 | |||||||
chr4:118324983 | G | A | 71 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(68): Show |
82 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.972-6427C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118324983 | |||||||
chr4:118325041 | G | A | 3 | a0003c0005t0024g0286 a0007c0013t0004g0277 a0007c0013t0004g0278 |
3 | HG02109.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.972-6485C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325041 | |||||||
chr4:118325042 | T | A | 8 | a0001c0006t0001g0263 a0001c0006t0001g0264 a0001c0006t0001g0269 others(5): Show |
8 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.972-6486A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325042 | |||||||
chr4:118325081 | A | G | 1 | a0002c0002t0001g0105 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.972-6525T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325081 | |||||||
chr4:118325199 | G | A | 34 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(31): Show |
40 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.971+6517C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325199 | |||||||
chr4:118325238 | C | A | 5 | a0001c0004t0001g0013 a0001c0004t0001g0245 a0001c0004t0001g0246 others(2): Show |
7 | NA18965.hp2 NA18968.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.971+6478G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325238 | |||||||
chr4:118325241 | G | A | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.971+6475C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325241 | |||||||
chr4:118325243 | T | A | 88 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0157 others(85): Show |
106 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.971+6473A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325243 | |||||||
chr4:118325323 | T | TA | 7 | a0001c0006t0001g0264 a0002c0002t0001g0073 a0002c0002t0001g0094 others(4): Show |
7 | HG01109.hp2 HG02080.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.971+6392dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325323 | |||||||
chr4:118325323 | TA | T | 8 | a0001c0001t0001g0032 a0001c0001t0001g0171 a0001c0004t0001g0230 others(5): Show |
9 | HG01169.hp1 HG02109.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.971+6392delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325323 | |||||||
chr4:118325386 | A | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.971+6330T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325386 | |||||||
chr4:118325439 | G | A | 32 | a0003c0005t0003g0006 a0003c0005t0003g0039 a0003c0005t0003g0040 others(29): Show |
38 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.971+6277C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325439 | |||||||
chr4:118325599 | C | T | 2 | a0001c0004t0012g0193 a0001c0004t0020g0279 |
2 | HG01074.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.971+6117G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325599 | |||||||
chr4:118325740 | C | A | 6 | a0002c0002t0001g0017 a0002c0002t0001g0056 a0002c0002t0001g0066 others(3): Show |
7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.971+5976G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325740 | |||||||
chr4:118325831 | T | G | 10 | a0001c0004t0001g0045 a0001c0006t0001g0263 a0001c0006t0001g0264 others(7): Show |
11 | HG00438.hp1 HG00609.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.971+5885A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325831 | |||||||
chr4:118325858 | T | G | 1 | a0003c0005t0003g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.971+5858A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325858 | |||||||
chr4:118325930 | T | C | 3 | a0001c0021t0021g0283 a0003c0005t0010g0223 a0003c0005t0010g0224 |
3 | HG02647.hp1 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.971+5786A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118325930 | |||||||
chr4:118326158 | T | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
97 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.971+5558A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326158 | |||||||
chr4:118326168 | A | G | 5 | a0001c0009t0001g0192 a0001c0009t0001g0275 a0001c0009t0009g0048 others(2): Show |
5 | HG03041.hp1 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+5548T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326168 | |||||||
chr4:118326282 | G | A | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.971+5434C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326282 | |||||||
chr4:118326320 | T | C | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0262 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.971+5396A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326320 | |||||||
chr4:118326341 | T | C | 1 | a0001c0004t0001g0185 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.971+5375A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326341 | |||||||
chr4:118326514 | T | G | 3 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0069 |
3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.971+5202A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326514 | |||||||
chr4:118326590 | G | A | 30 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(27): Show |
36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.971+5126C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326590 | |||||||
chr4:118326599 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.971+5117G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326599 | |||||||
chr4:118326705 | A | G | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.971+5011T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326705 | |||||||
chr4:118326755 | C | A | 1 | a0002c0002t0001g0140 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.971+4961G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326755 | |||||||
chr4:118326831 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
8 | HG00597.hp1 HG02027.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.971+4885G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326831 | |||||||
chr4:118326916 | T | C | 1 | a0002c0002t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.971+4800A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118326916 | |||||||
chr4:118327055 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.971+4661G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327055 | |||||||
chr4:118327068 | A | G | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+4648T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327068 | |||||||
chr4:118327102 | G | A | 31 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(28): Show |
37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.971+4614C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327102 | |||||||
chr4:118327162 | T | A | 5 | a0001c0001t0001g0149 a0001c0009t0001g0192 a0001c0009t0009g0048 others(2): Show |
5 | HG02922.hp1 HG03041.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+4554A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327162 | |||||||
chr4:118327200 | G | A | 4 | a0001c0004t0001g0043 a0001c0004t0001g0250 a0001c0004t0001g0260 others(1): Show |
5 | HG00544.hp2 HG02080.hp2 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.971+4516C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327200 | |||||||
chr4:118327349 | A | T | 1 | a0003c0005t0003g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.971+4367T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327349 | |||||||
chr4:118327432 | G | A | 1 | a0001c0004t0012g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.971+4284C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327432 | |||||||
chr4:118327447 | T | C | 1 | a0001c0004t0001g0251 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.971+4269A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327447 | |||||||
chr4:118327468 | G | C | 115 | a0001c0001t0001g0262 a0001c0001t0002g0276 a0002c0002t0001g0003 others(112): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.971+4248C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327468 | |||||||
chr4:118327556 | C | A | 1 | a0002c0003t0003g0132 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.971+4160G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327556 | |||||||
chr4:118327702 | T | A | 1 | a0004c0007t0001g0110 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.971+4014A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118327702 | |||||||
chr4:118328107 | A | G | 247 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
318 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.971+3609T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328107 | |||||||
chr4:118328197 | T | C | 1 | a0004c0007t0001g0111 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.971+3519A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328197 | |||||||
chr4:118328370 | T | C | 1 | a0003c0005t0010g0224 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.971+3346A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328370 | |||||||
chr4:118328472 | C | T | 2 | a0002c0002t0001g0080 a0002c0002t0001g0102 |
2 | NA18991.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.971+3244G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328472 | |||||||
chr4:118328589 | CAAA | C | 6 | a0002c0003t0002g0007 a0002c0003t0002g0116 a0002c0003t0002g0117 others(3): Show |
9 | HG00642.hp2 HG00738.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.971+3124_971+3126d others(5): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328589 | |||||||
chr4:118328592 | A | C | 207 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(204): Show |
253 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.971+3124T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328592 | |||||||
chr4:118328648 | G | C | 37 | a0001c0001t0001g0262 a0001c0004t0001g0013 a0001c0004t0001g0041 others(34): Show |
42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+3068C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328648 | |||||||
chr4:118328656 | C | T | 37 | a0001c0001t0001g0262 a0001c0004t0001g0013 a0001c0004t0001g0041 others(34): Show |
42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+3060G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328656 | |||||||
chr4:118328680 | G | A | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+3036C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328680 | |||||||
chr4:118328841 | T | C | 3 | a0002c0003t0002g0007 a0002c0003t0002g0133 a0002c0003t0002g0134 |
6 | HG00642.hp2 HG01261.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.971+2875A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328841 | |||||||
chr4:118328860 | C | A | 37 | a0001c0001t0001g0262 a0001c0004t0001g0013 a0001c0004t0001g0041 others(34): Show |
42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+2856G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328860 | |||||||
chr4:118328948 | C | G | 1 | a0002c0003t0002g0115 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.971+2768G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328948 | |||||||
chr4:118328982 | C | T | 206 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(203): Show |
255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.971+2734G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328982 | |||||||
chr4:118328984 | G | A | 37 | a0001c0001t0001g0262 a0001c0004t0001g0013 a0001c0004t0001g0041 others(34): Show |
42 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.971+2732C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328984 | |||||||
chr4:118328996 | G | A | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+2720C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118328996 | |||||||
chr4:118329082 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.971+2634C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329082 | |||||||
chr4:118329103 | A | T | 211 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(208): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.971+2613T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329103 | |||||||
chr4:118329686 | G | C | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+2030C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329686 | |||||||
chr4:118329722 | G | T | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.971+1994C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329722 | |||||||
chr4:118329787 | G | A | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.971+1929C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329787 | |||||||
chr4:118329804 | T | C | 3 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 |
3 | NA18966.hp1 NA18987.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.971+1912A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329804 | |||||||
chr4:118329930 | C | T | 1 | a0001c0004t0001g0233 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.971+1786G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329930 | |||||||
chr4:118329943 | C | A | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.971+1773G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329943 | |||||||
chr4:118329956 | C | G | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.971+1760G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329956 | |||||||
chr4:118329999 | C | T | 1 | a0002c0003t0002g0114 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.971+1717G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118329999 | |||||||
chr4:118330002 | A | G | 114 | a0001c0001t0002g0276 a0002c0002t0001g0003 a0002c0002t0001g0008 others(111): Show |
150 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.971+1714T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330002 | |||||||
chr4:118330018 | A | G | 208 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(205): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.971+1698T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330018 | |||||||
chr4:118330043 | T | C | 1 | a0001c0009t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.971+1673A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330043 | |||||||
chr4:118330055 | C | T | 1 | a0002c0002t0001g0057 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.971+1661G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330055 | |||||||
chr4:118330138 | T | C | 1 | a0002c0002t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.971+1578A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330138 | |||||||
chr4:118330251 | T | C | 1 | a0001c0004t0001g0252 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.971+1465A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330251 | |||||||
chr4:118330393 | A | C | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.971+1323T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330393 | |||||||
chr4:118330460 | G | T | 1 | a0002c0002t0001g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.971+1256C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330460 | |||||||
chr4:118330636 | G | A | 1 | a0001c0004t0001g0230 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.971+1080C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330636 | |||||||
chr4:118330651 | T | C | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.971+1065A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330651 | |||||||
chr4:118330723 | T | G | 1 | a0001c0006t0001g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.971+993A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330723 | |||||||
chr4:118330726 | A | G | 1 | a0008c0011t0001g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.971+990T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330726 | |||||||
chr4:118330780 | G | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(1): Show |
4 | HG02145.hp2 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.971+936C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330780 | |||||||
chr4:118330895 | G | T | 1 | a0002c0002t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.971+821C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330895 | |||||||
chr4:118330941 | AT | A | 121 | a0001c0001t0002g0276 a0002c0002t0001g0003 a0002c0002t0001g0008 others(118): Show |
157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.971+774delA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330941 | |||||||
chr4:118330943 | G | A | 121 | a0001c0001t0002g0276 a0002c0002t0001g0003 a0002c0002t0001g0008 others(118): Show |
157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.971+773C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330943 | |||||||
chr4:118330952 | A | G | 3 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0069 |
3 | HG02630.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.971+764T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330952 | |||||||
chr4:118330978 | C | T | 2 | a0002c0002t0001g0078 a0002c0002t0001g0079 |
2 | HG00621.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.971+738G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118330978 | |||||||
chr4:118331041 | T | A | 215 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(212): Show |
266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.971+675A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331041 | |||||||
chr4:118331099 | C | T | 2 | a0001c0001t0001g0262 a0001c0004t0001g0261 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.971+617G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331099 | |||||||
chr4:118331168 | C | T | 218 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(215): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.971+548G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331168 | |||||||
chr4:118331213 | G | A | 16 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0265 others(13): Show |
18 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.971+503C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331213 | |||||||
chr4:118331344 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.971+372A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331344 | |||||||
chr4:118331352 | C | T | 1 | a0002c0002t0001g0077 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.971+364G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331352 | |||||||
chr4:118331424 | T | A | 1 | a0001c0004t0001g0231 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.971+292A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 4/12 | chr4 | 118331424 | |||||||
chr4:118332002 | C | T | 1 | a0001c0004t0001g0261 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.821-136G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332002 | |||||||
chr4:118332003 | G | GTA | 31 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(28): Show |
37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.821-139_821-138dup others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332003 | |||||||
chr4:118332012 | T | C | 1 | a0002c0002t0001g0100 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.821-146A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332012 | |||||||
chr4:118332025 | G | A | 1 | a0003c0005t0003g0216 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.821-159C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332025 | |||||||
chr4:118332114 | C | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.821-248G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332114 | |||||||
chr4:118332272 | A | G | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.821-406T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332272 | |||||||
chr4:118332293 | T | C | 1 | a0003c0005t0024g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.821-427A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332293 | |||||||
chr4:118332698 | G | A | 1 | a0001c0004t0012g0193 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.821-832C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332698 | |||||||
chr4:118332776 | A | G | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.821-910T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332776 | |||||||
chr4:118332954 | C | T | 1 | a0001c0001t0023g0285 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.821-1088G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118332954 | |||||||
chr4:118333227 | T | TA | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.821-1362dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333227 | |||||||
chr4:118333398 | G | A | 211 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(208): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.821-1532C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333398 | |||||||
chr4:118333849 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.820+1624G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333849 | |||||||
chr4:118333863 | C | A | 1 | a0003c0005t0024g0286 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.820+1610G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118333863 | |||||||
chr4:118334124 | C | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.820+1349G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334124 | |||||||
chr4:118334479 | C | T | 1 | a0001c0004t0001g0256 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.820+994G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334479 | |||||||
chr4:118334671 | T | C | 176 | a0001c0001t0001g0262 a0001c0001t0002g0276 a0001c0004t0001g0013 others(173): Show |
221 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.820+802A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334671 | |||||||
chr4:118334680 | C | T | 1 | a0002c0002t0001g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.820+793G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118334680 | |||||||
chr4:118335063 | T | C | 6 | a0002c0002t0001g0017 a0002c0002t0001g0056 a0002c0002t0001g0066 others(3): Show |
7 | HG01243.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.820+410A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335063 | |||||||
chr4:118335122 | T | G | 1 | a0002c0002t0001g0101 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.820+351A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335122 | |||||||
chr4:118335141 | T | G | 211 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(208): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.820+332A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335141 | |||||||
chr4:118335462 | C | CT | 31 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(28): Show |
37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.820+10dupA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 3/12 | chr4 | 118335462 | |||||||
chr4:118335736 | G | A | 2 | a0003c0005t0003g0218 a0003c0005t0011g0046 |
2 | HG02602.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.642-85C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335736 | |||||||
chr4:118335819 | A | C | 5 | a0003c0005t0004g0199 a0003c0005t0004g0200 a0003c0005t0024g0286 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-168T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335819 | |||||||
chr4:118335834 | C | T | 1 | a0001c0004t0007g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.642-183G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335834 | |||||||
chr4:118335861 | T | C | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.642-210A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335861 | |||||||
chr4:118335913 | T | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0149 a0001c0001t0001g0177 others(1): Show |
5 | HG01256.hp2 HG01258.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-262A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118335913 | |||||||
chr4:118336303 | G | A | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-652C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336303 | |||||||
chr4:118336388 | G | A | 1 | a0003c0005t0010g0224 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.642-737C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336388 | |||||||
chr4:118336399 | TA | T | 215 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(212): Show |
265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.642-749delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336399 | |||||||
chr4:118336557 | A | C | 1 | a0002c0002t0001g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.642-906T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336557 | |||||||
chr4:118336564 | T | C | 31 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(28): Show |
37 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.642-913A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336564 | |||||||
chr4:118336584 | T | G | 1 | a0001c0001t0001g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.642-933A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336584 | |||||||
chr4:118336615 | A | G | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.642-964T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336615 | |||||||
chr4:118336706 | A | G | 1 | a0001c0004t0001g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.642-1055T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336706 | |||||||
chr4:118336724 | T | C | 2 | a0001c0001t0001g0179 a0008c0011t0001g0180 |
2 | HG02976.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.642-1073A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336724 | |||||||
chr4:118336906 | C | A | 1 | a0003c0005t0003g0221 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.642-1255G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336906 | |||||||
chr4:118336946 | C | G | 1 | a0002c0002t0001g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.641+1230G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118336946 | |||||||
chr4:118337323 | A | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.641+853T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337323 | |||||||
chr4:118337330 | A | C | 14 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0265 others(11): Show |
16 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.641+846T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337330 | |||||||
chr4:118337336 | T | C | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+840A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337336 | |||||||
chr4:118337382 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.641+794T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337382 | |||||||
chr4:118337392 | C | G | 1 | a0002c0002t0001g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.641+784G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337392 | |||||||
chr4:118337447 | T | C | 8 | a0001c0001t0001g0038 a0001c0001t0001g0186 a0001c0001t0001g0189 others(5): Show |
9 | HG01975.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.641+729A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337447 | |||||||
chr4:118337560 | A | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+616T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337560 | |||||||
chr4:118337563 | GCAGGA | G | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+608_641+612del others(5): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337563 | |||||||
chr4:118337645 | C | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+531G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337645 | |||||||
chr4:118337993 | T | C | 2 | a0007c0013t0004g0277 a0007c0013t0004g0278 |
2 | HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.641+183A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118337993 | |||||||
chr4:118338044 | C | G | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+132G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118338044 | |||||||
chr4:118338075 | C | T | 10 | a0003c0005t0003g0006 a0003c0005t0003g0203 a0003c0005t0003g0204 others(7): Show |
14 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+101G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118338075 | |||||||
chr4:118338127 | TATTC | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.641+45_641+48delGA others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 2/12 | chr4 | 118338127 | |||||||
chr4:118339090 | C | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-776G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339090 | |||||||
chr4:118339147 | C | T | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.503-833G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339147 | |||||||
chr4:118339654 | C | T | 1 | a0002c0002t0016g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.503-1340G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339654 | |||||||
chr4:118339746 | G | C | 1 | a0001c0004t0001g0253 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.503-1432C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339746 | |||||||
chr4:118339780 | T | C | 1 | a0002c0002t0001g0069 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.503-1466A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339780 | |||||||
chr4:118339964 | C | T | 1 | a0001c0006t0001g0264 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.503-1650G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118339964 | |||||||
chr4:118340158 | A | G | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.503-1844T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340158 | |||||||
chr4:118340544 | G | C | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.503-2230C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340544 | |||||||
chr4:118340572 | C | T | 3 | a0002c0002t0022g0284 a0003c0005t0010g0223 a0003c0005t0010g0224 |
3 | HG02647.hp1 HG02895.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.503-2258G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340572 | |||||||
chr4:118340662 | T | C | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2348A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340662 | |||||||
chr4:118340663 | C | T | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2349G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340663 | |||||||
chr4:118340667 | G | A | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2353C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340667 | |||||||
chr4:118340756 | C | T | 1 | a0002c0002t0001g0073 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.503-2442G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340756 | |||||||
chr4:118340784 | A | G | 214 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(211): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.503-2470T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340784 | |||||||
chr4:118340789 | C | G | 1 | a0002c0002t0001g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.503-2475G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340789 | |||||||
chr4:118340831 | A | G | 1 | a0001c0004t0001g0258 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.503-2517T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340831 | |||||||
chr4:118340833 | G | A | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-2519C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340833 | |||||||
chr4:118340839 | A | T | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2525T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340839 | |||||||
chr4:118340868 | A | T | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2554T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340868 | |||||||
chr4:118340953 | C | T | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2639G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340953 | |||||||
chr4:118340954 | T | C | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2640A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340954 | |||||||
chr4:118340955 | G | T | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-2641C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118340955 | |||||||
chr4:118341211 | T | C | 39 | a0001c0001t0001g0262 a0001c0004t0001g0013 a0001c0004t0001g0041 others(36): Show |
46 | HG00544.hp2 HG00673.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.503-2897A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341211 | |||||||
chr4:118341257 | G | A | 1 | a0001c0004t0007g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.503-2943C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341257 | |||||||
chr4:118341424 | T | G | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-3110A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341424 | |||||||
chr4:118341449 | G | A | 8 | a0003c0005t0003g0040 a0003c0005t0003g0217 a0003c0005t0003g0218 others(5): Show |
9 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.503-3135C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341449 | |||||||
chr4:118341528 | C | T | 1 | a0001c0006t0001g0263 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.503-3214G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341528 | |||||||
chr4:118341624 | G | T | 1 | a0002c0002t0001g0071 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.503-3310C>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341624 | |||||||
chr4:118341642 | A | T | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-3328T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341642 | |||||||
chr4:118341801 | C | A | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.503-3487G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341801 | |||||||
chr4:118341924 | A | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-3610T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118341924 | |||||||
chr4:118342149 | A | G | 5 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(2): Show |
5 | HG01361.hp1 HG02055.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-3835T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342149 | |||||||
chr4:118342250 | T | C | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-3936A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342250 | |||||||
chr4:118342434 | G | A | 1 | a0001c0009t0001g0275 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.503-4120C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342434 | |||||||
chr4:118342531 | G | A | 1 | a0001c0004t0001g0255 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.503-4217C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342531 | |||||||
chr4:118342557 | A | G | 4 | a0001c0001t0001g0031 a0001c0001t0001g0151 a0001c0001t0001g0152 others(1): Show |
5 | NA18945.hp2 NA18956.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-4243T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342557 | |||||||
chr4:118342734 | T | A | 1 | a0002c0002t0001g0102 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.503-4420A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342734 | |||||||
chr4:118342850 | T | TTTTCCTT others(8): Show |
1 | a0002c0020t0001g0103 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.503-4551_503-4537d others(17): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118342850 | |||||||
chr4:118343006 | T | C | 121 | a0001c0001t0002g0276 a0002c0002t0001g0003 a0002c0002t0001g0008 others(118): Show |
157 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.503-4692A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343006 | |||||||
chr4:118343007 | A | T | 5 | a0001c0001t0008g0280 a0001c0001t0008g0281 a0001c0001t0008g0282 others(2): Show |
5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.503-4693T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343007 | |||||||
chr4:118343048 | T | C | 30 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(27): Show |
36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.503-4734A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343048 | |||||||
chr4:118343159 | C | A | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.503-4845G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343159 | |||||||
chr4:118343192 | C | A | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-4878G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343192 | |||||||
chr4:118343258 | G | C | 1 | a0002c0003t0002g0135 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.503-4944C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343258 | |||||||
chr4:118343276 | T | G | 1 | a0002c0003t0002g0136 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.503-4962A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343276 | |||||||
chr4:118343592 | A | G | 1 | a0002c0017t0002g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.503-5278T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343592 | |||||||
chr4:118343697 | G | A | 1 | a0001c0004t0001g0256 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.503-5383C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118343697 | |||||||
chr4:118344038 | T | C | 1 | a0001c0009t0009g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.503-5724A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344038 | |||||||
chr4:118344301 | A | T | 1 | a0001c0004t0001g0232 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.503-5987T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344301 | |||||||
chr4:118344423 | TAA | T | 30 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(27): Show |
36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.503-6111_503-6110d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344423 | |||||||
chr4:118344459 | T | C | 217 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(214): Show |
269 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.503-6145A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344459 | |||||||
chr4:118344460 | G | A | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-6146C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344460 | |||||||
chr4:118344476 | A | G | 2 | a0003c0005t0010g0223 a0003c0005t0010g0224 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.503-6162T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344476 | |||||||
chr4:118344495 | T | C | 1 | a0008c0011t0001g0180 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.503-6181A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344495 | |||||||
chr4:118344933 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0149 |
3 | HG01256.hp2 HG01258.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.503-6619G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118344933 | |||||||
chr4:118345054 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.503-6740C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345054 | |||||||
chr4:118345168 | C | G | 8 | a0003c0005t0003g0006 a0003c0005t0003g0203 a0003c0005t0003g0204 others(5): Show |
12 | HG00597.hp2 NA18747.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.503-6854G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345168 | |||||||
chr4:118345463 | T | C | 3 | a0003c0005t0003g0219 a0003c0005t0003g0220 a0003c0005t0003g0221 |
3 | HG01123.hp2 HG01891.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.502+6756A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345463 | |||||||
chr4:118345477 | T | C | 1 | a0003c0005t0003g0222 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.502+6742A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345477 | |||||||
chr4:118345536 | A | G | 1 | a0002c0002t0001g0058 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502+6683T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345536 | |||||||
chr4:118345611 | C | T | 1 | a0002c0002t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.502+6608G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345611 | |||||||
chr4:118345699 | A | C | 1 | a0002c0002t0001g0057 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.502+6520T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345699 | |||||||
chr4:118345782 | T | G | 1 | a0001c0004t0001g0257 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.502+6437A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345782 | |||||||
chr4:118345809 | T | C | 58 | a0001c0001t0002g0276 a0002c0002t0001g0003 a0002c0002t0001g0008 others(55): Show |
73 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.502+6410A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345809 | |||||||
chr4:118345832 | C | T | 2 | a0001c0004t0001g0230 a0001c0004t0001g0231 |
2 | NA18948.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.502+6387G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345832 | |||||||
chr4:118345835 | A | G | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+6384T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345835 | |||||||
chr4:118345906 | C | A | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+6313G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345906 | |||||||
chr4:118345990 | T | C | 2 | a0002c0002t0007g0142 a0002c0003t0002g0141 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.502+6229A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118345990 | |||||||
chr4:118346275 | G | A | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+5944C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346275 | |||||||
chr4:118346315 | A | C | 1 | a0002c0002t0001g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.502+5904T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346315 | |||||||
chr4:118346384 | TCA | T | 30 | a0001c0001t0002g0202 a0003c0005t0003g0006 a0003c0005t0003g0039 others(27): Show |
36 | HG00099.hp1 HG00597.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+5833_502+5834d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346384 | |||||||
chr4:118346389 | G | A | 2 | a0001c0001t0001g0262 a0001c0004t0001g0261 |
2 | HG02630.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.502+5830C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346389 | |||||||
chr4:118346405 | T | C | 4 | a0002c0002t0001g0104 a0002c0003t0002g0028 a0002c0003t0002g0137 others(1): Show |
5 | HG00639.hp2 HG01192.hp2 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+5814A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346405 | |||||||
chr4:118346458 | T | TTA | 6 | a0001c0001t0001g0181 a0001c0001t0008g0280 a0001c0001t0008g0281 others(3): Show |
6 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+5759_502+5760d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346458 | |||||||
chr4:118346458 | T | TTATA | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+5757_502+5760d others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346458 | |||||||
chr4:118346458 | TTA | T | 205 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(202): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.502+5759_502+5760d others(4): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346458 | |||||||
chr4:118346565 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.502+5654A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346565 | |||||||
chr4:118346651 | CCAGGAGG others(4): Show |
C | 2 | a0001c0001t0005g0015 a0001c0001t0005g0047 |
3 | HG02486.hp2 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.502+5557_502+5567d others(13): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346651 | |||||||
chr4:118346695 | C | A | 40 | a0002c0002t0001g0118 a0002c0002t0007g0142 a0002c0003t0002g0001 others(37): Show |
60 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.502+5524G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346695 | |||||||
chr4:118346721 | C | T | 1 | a0002c0002t0001g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.502+5498G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346721 | |||||||
chr4:118346783 | C | T | 1 | a0001c0001t0002g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.502+5436G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346783 | |||||||
chr4:118346947 | G | A | 3 | a0003c0005t0003g0226 a0006c0012t0003g0225 a0006c0012t0003g0227 |
3 | HG01167.hp1 HG01169.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.502+5272C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118346947 | |||||||
chr4:118347077 | TA | T | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0186 others(3): Show |
6 | HG02280.hp1 HG03704.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+5141delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347077 | |||||||
chr4:118347157 | G | A | 1 | a0002c0003t0002g0139 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.502+5062C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347157 | |||||||
chr4:118347263 | C | A | 214 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(211): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.502+4956G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347263 | |||||||
chr4:118347495 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.502+4724A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347495 | |||||||
chr4:118347551 | G | C | 1 | a0003c0005t0003g0228 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.502+4668C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347551 | |||||||
chr4:118347558 | A | G | 1 | a0003c0005t0004g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.502+4661T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347558 | |||||||
chr4:118347725 | G | A | 4 | a0001c0001t0001g0184 a0001c0004t0001g0182 a0001c0004t0001g0183 others(1): Show |
4 | HG02280.hp2 HG03471.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.502+4494C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347725 | |||||||
chr4:118347750 | A | G | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+4469T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347750 | |||||||
chr4:118347970 | C | T | 1 | a0003c0005t0003g0201 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.502+4249G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118347970 | |||||||
chr4:118348060 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.502+4159A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348060 | |||||||
chr4:118348144 | G | A | 1 | a0001c0004t0001g0258 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.502+4075C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348144 | |||||||
chr4:118348269 | T | G | 217 | a0001c0001t0001g0194 a0001c0001t0001g0262 a0001c0001t0002g0202 others(214): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.502+3950A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348269 | |||||||
chr4:118348344 | C | T | 35 | a0001c0001t0001g0262 a0001c0004t0001g0013 a0001c0004t0001g0041 others(32): Show |
40 | HG00673.hp1 HG01255.hp2 HG02155.hp2 others(37): Show |
intron_variant | MODIFIER | c.502+3875G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348344 | |||||||
chr4:118348355 | A | C | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+3864T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348355 | |||||||
chr4:118348444 | C | T | 5 | a0003c0005t0004g0199 a0003c0005t0004g0200 a0003c0005t0024g0286 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+3775G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348444 | |||||||
chr4:118348651 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.502+3568T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348651 | |||||||
chr4:118348654 | C | CT | 213 | a0001c0001t0001g0194 a0001c0001t0001g0196 a0001c0001t0001g0262 others(210): Show |
261 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.502+3564dupA | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348654 | |||||||
chr4:118348697 | A | G | 217 | a0001c0001t0001g0194 a0001c0001t0001g0262 a0001c0001t0002g0202 others(214): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.502+3522T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348697 | |||||||
chr4:118348720 | C | T | 17 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0260 others(14): Show |
19 | HG00438.hp1 HG00544.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.502+3499G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348720 | |||||||
chr4:118348800 | T | C | 219 | a0001c0001t0001g0194 a0001c0001t0001g0262 a0001c0001t0002g0202 others(216): Show |
271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.502+3419A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348800 | |||||||
chr4:118348927 | C | T | 3 | a0001c0009t0001g0192 a0001c0009t0009g0048 a0001c0009t0009g0049 |
3 | HG03041.hp1 HG03195.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.502+3292G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118348927 | |||||||
chr4:118349074 | TC | T | 33 | a0001c0004t0001g0013 a0001c0004t0001g0041 a0001c0004t0001g0042 others(30): Show |
38 | HG00673.hp1 HG01255.hp2 HG02155.hp2 others(35): Show |
intron_variant | MODIFIER | c.502+3144delG | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349074 | |||||||
chr4:118349346 | G | C | 1 | a0008c0011t0001g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.502+2873C>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349346 | |||||||
chr4:118349395 | A | C | 215 | a0001c0001t0001g0194 a0001c0001t0001g0262 a0001c0001t0002g0202 others(212): Show |
264 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.502+2824T>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349395 | |||||||
chr4:118349403 | CA | C | 67 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(64): Show |
93 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.502+2815delT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349403 | |||||||
chr4:118349615 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.502+2604G>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349615 | |||||||
chr4:118349639 | T | C | 216 | a0001c0001t0001g0194 a0001c0001t0001g0262 a0001c0001t0002g0202 others(213): Show |
265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.502+2580A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349639 | |||||||
chr4:118349873 | G | A | 5 | a0002c0002t0001g0108 a0004c0007t0001g0107 a0004c0007t0001g0109 others(2): Show |
5 | HG00741.hp2 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.502+2346C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118349873 | |||||||
chr4:118350395 | C | G | 1 | a0001c0021t0021g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.502+1824G>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350395 | |||||||
chr4:118350556 | G | A | 15 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0265 others(12): Show |
17 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.502+1663C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350556 | |||||||
chr4:118350641 | A | T | 5 | a0001c0001t0005g0015 a0001c0001t0005g0047 a0001c0009t0009g0048 others(2): Show |
6 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+1578T>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350641 | |||||||
chr4:118350736 | T | TGAAA | 215 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(212): Show |
265 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.502+1482_502+1483i others(6): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350736 | |||||||
chr4:118350752 | G | A | 1 | a0012c0014t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502+1467C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118350752 | |||||||
chr4:118351009 | T | G | 15 | a0001c0004t0001g0044 a0001c0004t0001g0045 a0001c0004t0001g0265 others(12): Show |
17 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.502+1210A>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351009 | |||||||
chr4:118351048 | T | C | 40 | a0002c0002t0001g0118 a0002c0002t0007g0142 a0002c0003t0002g0001 others(37): Show |
60 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.502+1171A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351048 | |||||||
chr4:118351134 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.502+1085A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351134 | |||||||
chr4:118351347 | C | CA | 56 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0262 others(53): Show |
65 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.502+871dupT | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351347 | |||||||
chr4:118351617 | T | C | 1 | a0002c0002t0001g0140 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.502+602A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351617 | |||||||
chr4:118351658 | T | A | 208 | a0001c0001t0001g0262 a0001c0001t0002g0202 a0001c0001t0002g0276 others(205): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.502+561A>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351658 | |||||||
chr4:118351667 | G | A | 2 | a0002c0002t0007g0142 a0002c0003t0002g0141 |
2 | HG01074.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.502+552C>T | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351667 | |||||||
chr4:118351803 | T | C | 115 | a0001c0001t0002g0276 a0002c0002t0001g0003 a0002c0002t0001g0008 others(112): Show |
151 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.502+416A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351803 | |||||||
chr4:118351923 | GCA | G | 5 | a0001c0001t0005g0015 a0001c0001t0005g0047 a0001c0009t0009g0048 others(2): Show |
6 | HG02486.hp2 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.502+294_502+295del others(2): Show |
PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118351923 | |||||||
chr4:118352040 | T | C | 1 | a0002c0002t0016g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.502+179A>G | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118352040 | |||||||
chr4:118352057 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0144 |
3 | NA18970.hp2 NA18989.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.502+162G>A | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118352057 | |||||||
chr4:118352178 | A | G | 1 | a0002c0003t0002g0016 | 2 | HG00733.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.502+41T>C | PRSS12 | ENSG00000164099.3 | transcript | ENST00000296498.3 | protein_coding | 1/12 | chr4 | 118352178 |