Item | Value |
---|---|
geneid | 400668 |
ensemblid | ENSG00000185198.12 |
hgncid | 31397 |
symbol | PRSS57 |
name | serine protease 57 |
refseq_nuc | NM_001308209.2 |
refseq_prot | NP_001295138.2 |
ensembl_nuc | ENST00000329267.9 |
ensembl_prot | ENSP00000327386.6 |
mane_status | MANE Select |
chr | chr19 |
start | 685546 |
end | 695452 |
strand | - |
ver | v1.2 |
region | chr19:685546-695452 |
region5000 | chr19:680546-700452 |
regionname0 | PRSS57_chr19_685546_695452 |
regionname5000 | PRSS57_chr19_680546_700452 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 282 | 376 | 86 | 76 | 154 | 18 | 41 | 118 | PRSS57_chr19_680546_700452 | PRSS57 | MGLGL others(277): Show |
chr19 | 680546 | 700452 |
a0002 | 0/0 | 282 | 45 | 10 | 1 | 31 | 0 | 3 | 22 | PRSS57_chr19_680546_700452 | PRSS57 | MGLGL others(277): Show |
chr19 | 680546 | 700452 |
a0003 | 0/0 | 282 | 16 | 0 | 0 | 16 | 0 | 0 | 11 | PRSS57_chr19_680546_700452 | PRSS57 | MGLGL others(277): Show |
chr19 | 680546 | 700452 |
a0004 | 1/0 | 282 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | MGLGL others(277): Show |
chr19 | 680546 | 700452 |
a0005 | 0/0 | 282 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | MGLGL others(277): Show |
chr19 | 680546 | 700452 |
a0006 | 0/0 | 282 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | MGLGL others(277): Show |
chr19 | 680546 | 700452 |
a0007 | 0/0 | 282 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | MGLRL others(277): Show |
chr19 | 680546 | 700452 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 846 | 203 | 51 | 42 | 75 | 16 | 19 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0002 | 0/1 | 846 | 149 | 34 | 29 | 71 | 0 | 14 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0005 | 0/0 | 846 | 15 | 0 | 3 | 4 | 2 | 6 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0006 | 0/0 | 846 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0009 | 0/0 | 846 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0010 | 0/0 | 846 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0012 | 0/0 | 846 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0015 | 0/0 | 846 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0016 | 0/0 | 846 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0001c0017 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0002c0003 | 0/0 | 846 | 44 | 10 | 1 | 30 | 0 | 3 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0002c0011 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0003c0004 | 0/0 | 846 | 16 | 0 | 0 | 16 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0004c0007 | 1/0 | 846 | 2 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0005c0013 | 0/0 | 846 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0006c0014 | 0/0 | 846 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 | ||
a0007c0008 | 0/0 | 846 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | ATGGG others(841): Show |
chr19 | 680546 | 700452 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1041 | 194 | 44 | 40 | 75 | 16 | 19 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0001t0002 | 0/0 | 1041 | 5 | 4 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0001t0003 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0001t0004 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0001t0006 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAT others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0002t0001 | 0/1 | 1041 | 126 | 20 | 26 | 71 | 0 | 8 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0002t0002 | 0/0 | 1041 | 23 | 14 | 3 | 0 | 0 | 6 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0005t0001 | 0/0 | 1041 | 15 | 0 | 3 | 4 | 2 | 6 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0006t0001 | 0/0 | 1041 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0009t0001 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0010t0001 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0012t0005 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0015t0001 | 0/0 | 1041 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0016t0001 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0001c0017t0001 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0002c0003t0001 | 0/0 | 1041 | 44 | 10 | 1 | 30 | 0 | 3 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0002c0011t0001 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0003c0004t0001 | 0/0 | 1041 | 16 | 0 | 0 | 16 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0004c0007t0001 | 1/0 | 1041 | 2 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0005c0013t0001 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0006c0014t0001 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
a0007c0008t0001 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | GAGAC others(1036): Show |
chr19 | 680546 | 700452 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 34 | 2 | 1 | 28 | 1 | 2 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0003 | 0/0 | 31 | 3 | 16 | 1 | 6 | 5 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0004 | 0/0 | 15 | 4 | 1 | 7 | 1 | 2 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0005 | 0/0 | 12 | 1 | 5 | 4 | 1 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0001t0006g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0001 | 0/0 | 51 | 1 | 14 | 32 | 0 | 4 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0007 | 0/0 | 10 | 0 | 4 | 3 | 0 | 3 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0008 | 0/0 | 9 | 8 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0013 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0033 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0005t0001g0011 | 0/0 | 6 | 0 | 1 | 1 | 2 | 2 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0005t0001g0018 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0005t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0006t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0009t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0010t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0012t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0015t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0016t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0001c0017t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0010 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0002c0011t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0003c0004t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0003c0004t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0003c0004t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0003c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0003c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0003c0004t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0004c0007t0001g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0004c0007t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0005c0013t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0006c0014t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
a0007c0008t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00408 | hp1 | a0002 | c0003 | t0001 | g0081 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00423 | hp2 | a0003 | c0004 | t0001 | g0029 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0027 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00558 | hp1 | a0002 | c0003 | t0001 | g0086 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00558 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00597 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00609 | hp1 | a0003 | c0004 | t0001 | g0006 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0019 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00735 | hp2 | a0005 | c0013 | t0001 | g0164 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00741 | hp1 | a0002 | c0003 | t0001 | g0085 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01074 | hp1 | a0001 | c0016 | t0001 | g0201 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0141 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01109 | hp2 | a0006 | c0014 | t0001 | g0054 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01175 | hp2 | a0004 | c0007 | t0001 | g0132 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0105 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01255 | hp2 | a0001 | c0005 | t0001 | g0011 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01257 | hp2 | a0001 | c0009 | t0001 | g0072 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01261 | hp2 | a0001 | c0005 | t0001 | g0032 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0066 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01516 | hp1 | a0001 | c0005 | t0001 | g0011 | EUR | IBS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | IBS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0138 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0206 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02040 | hp1 | a0003 | c0004 | t0001 | g0006 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0097 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0059 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02074 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02080 | hp1 | a0001 | c0005 | t0001 | g0011 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02129 | hp1 | a0002 | c0003 | t0001 | g0083 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02129 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0009 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02135 | hp1 | a0001 | c0005 | t0001 | g0018 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02135 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02258 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02300 | hp1 | a0001 | c0005 | t0001 | g0032 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0055 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0101 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02602 | hp2 | a0001 | c0005 | t0001 | g0011 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0057 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0203 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02698 | hp1 | a0001 | c0005 | t0001 | g0096 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02723 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0130 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02818 | hp1 | a0002 | c0003 | t0001 | g0135 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02818 | hp2 | a0002 | c0003 | t0001 | g0067 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02922 | hp2 | a0002 | c0003 | t0001 | g0093 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0045 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03209 | hp2 | a0002 | c0003 | t0001 | g0142 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0205 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0019 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03491 | hp2 | a0001 | c0015 | t0001 | g0167 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0019 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03540 | hp1 | a0002 | c0003 | t0001 | g0074 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0122 | AFR | GWD | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03579 | hp1 | a0001 | c0012 | t0005 | g0056 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03831 | hp1 | a0002 | c0003 | t0001 | g0031 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0031 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0189 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03927 | hp2 | a0001 | c0005 | t0001 | g0011 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04115 | hp2 | a0001 | c0005 | t0001 | g0095 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0115 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04184 | hp2 | a0001 | c0010 | t0001 | g0106 | SAS | BEB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04199 | hp2 | a0001 | c0005 | t0001 | g0018 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04228 | hp1 | a0001 | c0005 | t0001 | g0018 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | YRI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | CHB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | YRI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | YRI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18947 | hp1 | a0001 | c0006 | t0001 | g0020 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18947 | hp2 | a0002 | c0011 | t0001 | g0128 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18949 | hp2 | a0002 | c0003 | t0001 | g0136 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18950 | hp1 | a0001 | c0017 | t0001 | g0194 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18951 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18952 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18954 | hp1 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18965 | hp2 | a0002 | c0003 | t0001 | g0075 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18969 | hp1 | a0002 | c0003 | t0001 | g0091 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0027 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18971 | hp2 | a0001 | c0006 | t0001 | g0020 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18974 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18977 | hp1 | a0001 | c0005 | t0001 | g0113 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18978 | hp2 | a0002 | c0003 | t0001 | g0080 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18979 | hp2 | a0001 | c0005 | t0001 | g0094 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18980 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18983 | hp1 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18987 | hp2 | a0003 | c0004 | t0001 | g0089 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18995 | hp1 | a0001 | c0006 | t0001 | g0020 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18998 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18999 | hp1 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19003 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19004 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19010 | hp2 | a0003 | c0004 | t0001 | g0145 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19012 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | LWK | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | LWK | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | LWK | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19055 | hp1 | a0003 | c0004 | t0001 | g0088 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19056 | hp1 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19059 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19062 | hp1 | a0003 | c0004 | t0001 | g0076 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0009 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19064 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19067 | hp1 | a0002 | c0003 | t0001 | g0078 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19082 | hp1 | a0003 | c0004 | t0001 | g0029 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19085 | hp1 | a0002 | c0003 | t0001 | g0084 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19086 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19087 | hp2 | a0007 | c0008 | t0001 | g0049 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19088 | hp2 | a0003 | c0004 | t0001 | g0006 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | YRI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ASW | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20752 | hp1 | a0001 | c0005 | t0001 | g0011 | EUR | TSI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0090 | SAS | GIH | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG02559 | hp2 | a0002 | c0003 | t0001 | g0082 | AFR | ACB | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0197 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | USA | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA18955 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | USA | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | LWK | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | LWK | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0033 | REF | REF | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
homoSapiens | grch38p0 | a0004 | c0007 | t0001 | g0126 | REF | REF | PRSS57_chr19_680546_700452 | PRSS57 | chr19 | 680546 | 700452 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:686965 | C | T | 1 | a0006 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.602G>A | p.Cys201Tyr | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/5 | 624/1041 | 602/849 | 201/282 | chr19 | 686965 | |||
chr19:687104 | G | A | 1 | a0005 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.463C>T | p.Arg155Trp | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/5 | 485/1041 | 463/849 | 155/282 | chr19 | 687104 | |||
chr19:687112 | G | A | 4 | a0002 a0003 a0006 others(1): Show |
63 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(60): Show |
missense_variant | MODERATE | c.455C>T | p.Ala152Val | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/5 | 477/1041 | 455/849 | 152/282 | chr19 | 687112 | |||
chr19:687142 | G | A | 6 | a0001 a0002 a0003 others(3): Show |
439 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(436): Show |
missense_variant | MODERATE | c.425C>T | p.Pro142Leu | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/5 | 447/1041 | 425/849 | 142/282 | chr19 | 687142 | |||
chr19:691995 | G | A | 1 | a0003 | 16 | HG00423.hp2 HG00597.hp2 HG00609.hp1 others(13): Show |
missense_variant | MODERATE | c.241C>T | p.Arg81Cys | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/5 | 263/1041 | 241/849 | 81/282 | chr19 | 691995 | |||
chr19:695421 | C | T | 1 | a0007 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.10G>A | p.Gly4Arg | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/5 | 32/1041 | 10/849 | 4/282 | chr19 | 695421 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:685761 | G | A | 1 | a0001c0006 | 3 | NA18947.hp1 NA18971.hp2 NA18995.hp1 |
synonymous_variant | LOW | c.804C>T | p.Pro268Pro | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 5/5 | 826/1041 | 804/849 | 268/282 | chr19 | 685761 | |||
chr19:685833 | G | T | 1 | a0001c0005 | 15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
synonymous_variant | LOW | c.732C>A | p.Pro244Pro | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 5/5 | 754/1041 | 732/849 | 244/282 | chr19 | 685833 | |||
chr19:687015 | C | T | 1 | a0001c0012 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.552G>A | p.Pro184Pro | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/5 | 574/1041 | 552/849 | 184/282 | chr19 | 687015 | |||
chr19:687078 | G | A | 6 | a0001c0010 a0002c0003 a0002c0011 others(3): Show |
64 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(61): Show |
synonymous_variant | LOW | c.489C>T | p.Phe163Phe | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/5 | 511/1041 | 489/849 | 163/282 | chr19 | 687078 | |||
chr19:687183 | G | A | 1 | a0001c0015 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.384C>T | p.Asn128Asn | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/5 | 406/1041 | 384/849 | 128/282 | chr19 | 687183 | |||
chr19:691909 | T | C | 10 | a0001c0001 a0001c0005 a0001c0012 others(7): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
synonymous_variant | LOW | c.327A>G | p.Thr109Thr | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/5 | 349/1041 | 327/849 | 109/282 | chr19 | 691909 | |||
chr19:691972 | G | A | 1 | a0001c0016 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.264C>T | p.Gly88Gly | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/5 | 286/1041 | 264/849 | 88/282 | chr19 | 691972 | |||
chr19:694837 | C | G | 1 | a0001c0009 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.210G>C | p.Ser70Ser | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/5 | 232/1041 | 210/849 | 70/282 | chr19 | 694837 | |||
chr19:694873 | G | A | 1 | a0001c0017 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.174C>T | p.Cys58Cys | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/5 | 196/1041 | 174/849 | 58/282 | chr19 | 694873 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:685661 | C | T | 2 | a0001c0001t0002 a0001c0002t0002 |
28 | HG00733.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 5/5 | 55 | chr19 | 685661 | ||||||
chr19:685715 | C | T | 1 | a0001c0012t0005 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 5/5 | 1 | chr19 | 685715 | ||||||
chr19:695432 | G | T | 1 | a0001c0001t0003 | 2 | HG02896.hp2 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-2C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/5 | 2 | chr19 | 695432 | ||||||
chr19:695447 | C | T | 1 | a0001c0001t0004 | 1 | NA20129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/5 | 17 | chr19 | 695447 | ||||||
chr19:695448 | G | A | 1 | a0001c0001t0006 | 1 | HG02004.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-18C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/5 | chr19 | 695448 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:685935 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0060 others(1): Show |
7 | HG02055.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-13C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 685935 | |||||||
chr19:685985 | G | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(41): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.643-63C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 685985 | |||||||
chr19:686079 | C | G | 4 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0001g0060 others(1): Show |
7 | HG02055.hp1 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-157G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686079 | |||||||
chr19:686109 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.643-187G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686109 | |||||||
chr19:686162 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(94): Show |
164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.643-240G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686162 | |||||||
chr19:686181 | G | A | 97 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(94): Show |
164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.643-259C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686181 | |||||||
chr19:686234 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(94): Show |
164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.643-312G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686234 | |||||||
chr19:686286 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0143 |
3 | HG02559.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.643-364A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686286 | |||||||
chr19:686304 | G | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0066 a0001c0002t0001g0109 |
7 | HG00621.hp1 HG01123.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-382C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686304 | |||||||
chr19:686317 | G | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-395C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686317 | |||||||
chr19:686344 | T | A | 19 | a0001c0001t0002g0092 a0001c0001t0002g0137 a0001c0001t0002g0155 others(16): Show |
28 | HG00733.hp1 HG00738.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.643-422A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686344 | |||||||
chr19:686574 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(94): Show |
164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.642+351G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686574 | |||||||
chr19:686597 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.642+328C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686597 | |||||||
chr19:686715 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.642+210A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686715 | |||||||
chr19:686791 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(87): Show |
149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.642+134G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686791 | |||||||
chr19:686862 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.642+63T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 4/4 | chr19 | 686862 | |||||||
chr19:687204 | G | T | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-16C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687204 | |||||||
chr19:687220 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.379-32C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687220 | |||||||
chr19:687279 | T | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0042 others(16): Show |
37 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.379-91A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687279 | |||||||
chr19:687287 | A | G | 1 | a0002c0003t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.379-99T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687287 | |||||||
chr19:687358 | C | T | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-170G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687358 | |||||||
chr19:687378 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.379-190C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687378 | |||||||
chr19:687381 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.379-193T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687381 | |||||||
chr19:687397 | TTTCTG | T | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-214_379-210del others(5): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687397 | |||||||
chr19:687407 | G | GTTCTT | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-224_379-220dup others(5): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687407 | |||||||
chr19:687412 | T | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0143 |
3 | HG02559.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379-224A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687412 | |||||||
chr19:687428 | T | C | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-240A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687428 | |||||||
chr19:687466 | C | T | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-278G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687466 | |||||||
chr19:687467 | A | G | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-279T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687467 | |||||||
chr19:687469 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0058 |
3 | HG02145.hp1 HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.379-281T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687469 | |||||||
chr19:687552 | G | T | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-364C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687552 | |||||||
chr19:687696 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.379-508G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687696 | |||||||
chr19:687701 | A | G | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-513T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687701 | |||||||
chr19:687729 | T | G | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-541A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687729 | |||||||
chr19:687760 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(1): Show |
5 | HG01891.hp2 HG02145.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.379-572G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687760 | |||||||
chr19:687773 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(95): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.379-585T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687773 | |||||||
chr19:687784 | C | G | 1 | a0004c0007t0001g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.379-596G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687784 | |||||||
chr19:687799 | A | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(88): Show |
150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.379-611T>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687799 | |||||||
chr19:687829 | T | C | 1 | a0001c0002t0001g0127 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.379-641A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687829 | |||||||
chr19:687835 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(98): Show |
168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.379-647A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687835 | |||||||
chr19:687855 | T | G | 1 | a0001c0002t0001g0127 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.379-667A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687855 | |||||||
chr19:687881 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0053 |
5 | HG02055.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-693G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687881 | |||||||
chr19:687973 | A | C | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-785T>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 687973 | |||||||
chr19:688109 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.379-921G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688109 | |||||||
chr19:688168 | T | C | 3 | a0001c0002t0001g0045 a0001c0002t0001g0204 a0001c0002t0001g0205 |
4 | HG02258.hp2 HG02630.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-980A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688168 | |||||||
chr19:688182 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0002g0092 |
4 | HG02109.hp1 HG02886.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-994G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688182 | |||||||
chr19:688243 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0036 others(37): Show |
71 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.379-1055G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688243 | |||||||
chr19:688249 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.379-1061G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688249 | |||||||
chr19:688298 | G | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0143 |
3 | HG02559.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379-1110C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688298 | |||||||
chr19:688328 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-1140C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688328 | |||||||
chr19:688344 | C | CT | 82 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0025 others(79): Show |
137 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.379-1157dupA | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688344 | |||||||
chr19:688344 | C | CTT | 5 | a0001c0001t0001g0183 a0001c0001t0001g0187 a0001c0001t0001g0190 others(2): Show |
6 | HG02135.hp2 NA18940.hp2 NA18956.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-1158_379-1157d others(4): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688344 | |||||||
chr19:688355 | G | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(95): Show |
165 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.379-1167C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688355 | |||||||
chr19:688379 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(98): Show |
168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.379-1191A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688379 | |||||||
chr19:688401 | C | T | 1 | a0002c0003t0001g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.379-1213G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688401 | |||||||
chr19:688427 | G | A | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-1239C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688427 | |||||||
chr19:688504 | A | AG | 97 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(94): Show |
163 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.379-1317dupC | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688504 | |||||||
chr19:688511 | G | A | 3 | a0001c0002t0001g0008 a0001c0002t0001g0120 a0001c0002t0001g0203 |
11 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.379-1323C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688511 | |||||||
chr19:688536 | C | CGGGTCTG others(18): Show |
1 | a0001c0002t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.379-1373_379-1349d others(27): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688536 | |||||||
chr19:688547 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.379-1359C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688547 | |||||||
chr19:688602 | C | CT | 8 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0002t0001g0024 others(5): Show |
9 | HG01433.hp2 HG02738.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.379-1415dupA | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTT | 6 | a0001c0001t0001g0025 a0001c0001t0001g0065 a0001c0001t0001g0146 others(3): Show |
7 | HG01891.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-1417_379-1415d others(5): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTT | 26 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0023 others(23): Show |
48 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.379-1418_379-1415d others(6): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0053 |
5 | HG02055.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.379-1425_379-1415d others(13): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(5): Show |
2 | a0001c0002t0002g0122 a0002c0003t0001g0084 |
2 | HG03540.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.379-1426_379-1415d others(14): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(6): Show |
43 | a0001c0001t0002g0137 a0001c0001t0002g0155 a0001c0001t0002g0156 others(40): Show |
69 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.379-1427_379-1415d others(15): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(7): Show |
10 | a0001c0002t0002g0068 a0001c0002t0002g0104 a0001c0002t0002g0197 others(7): Show |
19 | HG00423.hp2 HG00438.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.379-1428_379-1415d others(16): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(8): Show |
2 | a0001c0005t0001g0032 a0003c0004t0001g0088 |
3 | HG01261.hp2 HG02300.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.379-1415_379-1414i others(17): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(9): Show |
1 | a0001c0005t0001g0011 | 6 | HG01255.hp2 HG01516.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1415_379-1414i others(18): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(10): Show |
4 | a0001c0005t0001g0018 a0001c0005t0001g0094 a0001c0005t0001g0095 others(1): Show |
6 | HG02135.hp1 HG02698.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.379-1415_379-1414i others(19): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688602 | C | CTTTTTTT others(11): Show |
1 | a0001c0005t0001g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.379-1415_379-1414i others(20): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688602 | |||||||
chr19:688661 | C | T | 1 | a0002c0003t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.379-1473G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688661 | |||||||
chr19:688724 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-1536C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688724 | |||||||
chr19:688765 | ATTT | A | 13 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(10): Show |
22 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.379-1580_379-1578d others(5): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688765 | |||||||
chr19:688800 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.379-1612G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688800 | |||||||
chr19:688846 | G | A | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.379-1658C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688846 | |||||||
chr19:688870 | G | A | 1 | a0001c0001t0001g0044 | 2 | NA19007.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.379-1682C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688870 | |||||||
chr19:688925 | C | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379-1737G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 688925 | |||||||
chr19:689004 | G | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(89): Show |
158 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.379-1816C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689004 | |||||||
chr19:689024 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.379-1836A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689024 | |||||||
chr19:689025 | C | CCCTGCCC others(5): Show |
1 | a0002c0003t0001g0078 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.379-1838_379-1837i others(14): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689025 | |||||||
chr19:689053 | G | A | 1 | a0001c0002t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.379-1865C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689053 | |||||||
chr19:689054 | A | G | 1 | a0001c0002t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.379-1866T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689054 | |||||||
chr19:689088 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0143 |
3 | HG02559.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379-1900C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689088 | |||||||
chr19:689101 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0003g0047 a0001c0001t0003g0048 |
3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.379-1913G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689101 | |||||||
chr19:689104 | C | CGGGGCCG others(32): Show |
1 | a0001c0002t0002g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.379-1917_379-1916i others(41): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689104 | |||||||
chr19:689104 | C | CGGGGGCC others(150): Show |
1 | a0002c0003t0001g0078 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.379-1917_379-1916i others(159): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689104 | |||||||
chr19:689114 | A | G | 1 | a0001c0002t0001g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.379-1926T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689114 | |||||||
chr19:689114 | AGGGTGGT others(101): Show |
A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0036 others(26): Show |
49 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.379-2034_379-1927d others(2): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689114 | |||||||
chr19:689137 | T | A | 60 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(57): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.379-1949A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689137 | |||||||
chr19:689140 | C | T | 60 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(57): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.379-1952G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689140 | |||||||
chr19:689143 | C | T | 60 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(57): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.379-1955G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689143 | |||||||
chr19:689146 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(48): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.379-1958A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689146 | |||||||
chr19:689146 | T | G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(59): Show |
108 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.379-1958A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689146 | |||||||
chr19:689149 | T | C | 60 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(57): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.379-1961A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689149 | |||||||
chr19:689150 | A | AGAAGGGT others(188): Show |
5 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(2): Show |
6 | HG01891.hp2 HG02145.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.379-1963_379-1962i others(197): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689150 | |||||||
chr19:689150 | A | G | 60 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(57): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.379-1962T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689150 | |||||||
chr19:689150 | AGAAGGGT others(32): Show |
A | 1 | a0001c0002t0001g0007 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.379-2001_379-1963d others(41): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689150 | |||||||
chr19:689150 | AGAAGGGT others(101): Show |
A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0143 |
3 | HG02559.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.379-2070_379-1963d others(2): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689150 | |||||||
chr19:689176 | T | A | 2 | a0001c0002t0002g0197 a0002c0003t0001g0078 |
2 | HG03471.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.379-1988A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689176 | |||||||
chr19:689179 | C | T | 2 | a0001c0002t0002g0197 a0002c0003t0001g0078 |
2 | HG03471.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.379-1991G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689179 | |||||||
chr19:689182 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.379-1994G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689182 | |||||||
chr19:689185 | G | C | 65 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0053 others(62): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.379-1997C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689185 | |||||||
chr19:689188 | T | C | 2 | a0001c0002t0002g0197 a0002c0003t0001g0078 |
2 | HG03471.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.379-2000A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689188 | |||||||
chr19:689189 | G | A | 65 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0053 others(62): Show |
112 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.379-2001C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689189 | |||||||
chr19:689203 | C | G | 2 | a0001c0002t0002g0197 a0002c0003t0001g0078 |
2 | HG03471.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.379-2015G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689203 | |||||||
chr19:689204 | A | G | 2 | a0001c0002t0002g0197 a0002c0003t0001g0078 |
2 | HG03471.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.379-2016T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689204 | |||||||
chr19:689222 | G | GGGGCTGG others(2): Show |
6 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0065 others(3): Show |
7 | HG01891.hp2 HG02145.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.379-2035_379-2034i others(11): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689222 | |||||||
chr19:689222 | G | GGGGCTGG others(158): Show |
52 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(49): Show |
90 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.379-2035_379-2034i others(167): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689222 | |||||||
chr19:689222 | G | GGGGCTGG others(197): Show |
1 | a0006c0014t0001g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.379-2035_379-2034i others(206): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689222 | |||||||
chr19:689222 | G | GGGGCTGG others(80): Show |
6 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(3): Show |
14 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-2035_379-2034i others(89): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689222 | |||||||
chr19:689233 | G | C | 60 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(57): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.379-2045C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689233 | |||||||
chr19:689234 | G | A | 60 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0001t0002g0137 others(57): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.379-2046C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689234 | |||||||
chr19:689251 | C | CGGGGCCG others(71): Show |
1 | a0001c0002t0002g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.379-2064_379-2063i others(80): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689251 | |||||||
chr19:689251 | C | T | 90 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(87): Show |
156 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.379-2063G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689251 | |||||||
chr19:689258 | G | A | 6 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(3): Show |
14 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.379-2070C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689258 | |||||||
chr19:689263 | G | GGTGGTCC others(71): Show |
1 | a0001c0005t0001g0094 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.379-2076_379-2075i others(80): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689263 | |||||||
chr19:689376 | C | A | 1 | a0006c0014t0001g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.379-2188G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689376 | |||||||
chr19:689377 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0148 |
4 | HG01175.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-2189C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689377 | |||||||
chr19:689392 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0148 |
4 | HG01175.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.379-2204G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689392 | |||||||
chr19:689395 | G | A | 1 | a0002c0003t0001g0087 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.379-2207C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689395 | |||||||
chr19:689431 | G | A | 10 | a0001c0002t0001g0030 a0001c0002t0001g0079 a0001c0002t0001g0123 others(7): Show |
19 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.379-2243C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689431 | |||||||
chr19:689438 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.379-2250A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689438 | |||||||
chr19:689440 | G | A | 70 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0053 others(67): Show |
118 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.379-2252C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689440 | |||||||
chr19:689445 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.379-2257C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689445 | |||||||
chr19:689476 | C | T | 70 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0053 others(67): Show |
118 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.379-2288G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689476 | |||||||
chr19:689485 | T | G | 1 | a0001c0002t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.379-2297A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689485 | |||||||
chr19:689487 | C | T | 70 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0053 others(67): Show |
118 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.379-2299G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689487 | |||||||
chr19:689590 | C | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.378+2268G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689590 | |||||||
chr19:689618 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378+2240C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689618 | |||||||
chr19:689684 | T | G | 1 | a0001c0002t0001g0110 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.378+2174A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689684 | |||||||
chr19:689791 | C | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0036 others(28): Show |
51 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.378+2067G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689791 | |||||||
chr19:689803 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.378+2055G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689803 | |||||||
chr19:689804 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0147 |
3 | HG01099.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.378+2054C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689804 | |||||||
chr19:689818 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.378+2040G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689818 | |||||||
chr19:689828 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0150 a0001c0001t0004g0046 others(1): Show |
5 | HG01243.hp2 HG01978.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.378+2030G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689828 | |||||||
chr19:689829 | G | A | 1 | a0001c0001t0001g0021 | 3 | HG02572.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.378+2029C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689829 | |||||||
chr19:689836 | T | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(59): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.378+2022A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689836 | |||||||
chr19:689844 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
6 | HG02559.hp1 HG02572.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+2014G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689844 | |||||||
chr19:689858 | G | T | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+2000C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689858 | |||||||
chr19:689925 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.378+1933A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689925 | |||||||
chr19:689977 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(57): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.378+1881G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 689977 | |||||||
chr19:690000 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(35): Show |
63 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.378+1858G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690000 | |||||||
chr19:690039 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(75): Show |
136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378+1819A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690039 | |||||||
chr19:690040 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(75): Show |
136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378+1818C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690040 | |||||||
chr19:690045 | T | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(75): Show |
136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378+1813A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690045 | |||||||
chr19:690080 | AG | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0023 others(75): Show |
136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.378+1777delC | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690080 | |||||||
chr19:690167 | C | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(94): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.378+1691G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690167 | |||||||
chr19:690203 | C | CG | 46 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0037 others(43): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.378+1654dupC | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690203 | |||||||
chr19:690211 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.378+1647A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690211 | |||||||
chr19:690243 | A | G | 13 | a0002c0003t0001g0009 a0002c0003t0001g0010 a0002c0003t0001g0026 others(10): Show |
27 | HG00408.hp1 HG00558.hp2 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.378+1615T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690243 | |||||||
chr19:690256 | A | C | 5 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0195 others(2): Show |
5 | HG02896.hp2 HG02897.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.378+1602T>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690256 | |||||||
chr19:690270 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.378+1588A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690270 | |||||||
chr19:690285 | T | TG | 146 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(143): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.378+1572dupC | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690285 | |||||||
chr19:690309 | G | GA | 19 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0037 others(16): Show |
34 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.378+1548dupT | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690309 | |||||||
chr19:690309 | G | GAA | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(86): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.378+1547_378+1548d others(4): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690309 | |||||||
chr19:690309 | G | GAAA | 6 | a0001c0001t0001g0170 a0001c0001t0001g0187 a0001c0001t0001g0200 others(3): Show |
6 | HG01074.hp1 HG01257.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+1546_378+1548d others(5): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690309 | |||||||
chr19:690369 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.378+1489A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690369 | |||||||
chr19:690383 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.378+1475G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690383 | |||||||
chr19:690426 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.378+1432C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690426 | |||||||
chr19:690510 | G | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.378+1348C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690510 | |||||||
chr19:690526 | A | AAAGATCA others(28): Show |
1 | a0001c0002t0001g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.378+1297_378+1331d others(37): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690526 | |||||||
chr19:690548 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.378+1310T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690548 | |||||||
chr19:690561 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.378+1297G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690561 | |||||||
chr19:690620 | G | A | 2 | a0001c0001t0001g0202 a0001c0016t0001g0201 |
2 | HG01074.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.378+1238C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690620 | |||||||
chr19:690633 | T | A | 1 | a0001c0002t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.378+1225A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690633 | |||||||
chr19:690639 | C | T | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(80): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.378+1219G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690639 | |||||||
chr19:690679 | C | T | 1 | a0002c0003t0001g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.378+1179G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690679 | |||||||
chr19:690684 | C | T | 5 | a0001c0002t0002g0019 a0001c0002t0002g0115 a0001c0002t0002g0130 others(2): Show |
7 | HG00733.hp1 HG01099.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.378+1174G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690684 | |||||||
chr19:690699 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.378+1159C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690699 | |||||||
chr19:690719 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0148 |
4 | HG01175.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+1139C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690719 | |||||||
chr19:690761 | A | T | 97 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(94): Show |
164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.378+1097T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690761 | |||||||
chr19:690762 | T | G | 97 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(94): Show |
164 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.378+1096A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690762 | |||||||
chr19:690763 | C | T | 1 | a0001c0002t0001g0116 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.378+1095G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690763 | |||||||
chr19:690814 | C | T | 38 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0058 others(35): Show |
66 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.378+1044G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690814 | |||||||
chr19:690817 | G | A | 1 | a0001c0002t0001g0129 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.378+1041C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690817 | |||||||
chr19:690829 | C | T | 1 | a0001c0001t0001g0023 | 3 | HG02109.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.378+1029G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690829 | |||||||
chr19:690837 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.378+1021G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690837 | |||||||
chr19:690902 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(48): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.378+956A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690902 | |||||||
chr19:690926 | C | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(41): Show |
70 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.378+932G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 690926 | |||||||
chr19:691025 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(45): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.378+833G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691025 | |||||||
chr19:691061 | C | T | 1 | a0002c0003t0001g0136 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.378+797G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691061 | |||||||
chr19:691138 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG00735.hp2 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+720G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691138 | |||||||
chr19:691146 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0002g0137 a0002c0003t0001g0138 others(1): Show |
6 | HG01884.hp1 HG02572.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.378+712G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691146 | |||||||
chr19:691213 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0064 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.378+645T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691213 | |||||||
chr19:691243 | C | T | 7 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(4): Show |
15 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.378+615G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691243 | |||||||
chr19:691257 | A | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0148 |
4 | HG01175.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.378+601T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691257 | |||||||
chr19:691263 | T | C | 1 | a0001c0001t0001g0023 | 3 | HG02109.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.378+595A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691263 | |||||||
chr19:691310 | C | T | 6 | a0001c0001t0001g0058 a0002c0003t0001g0059 a0002c0003t0001g0067 others(3): Show |
6 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.378+548G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691310 | |||||||
chr19:691322 | A | G | 2 | a0001c0002t0002g0115 a0001c0002t0002g0130 |
2 | HG02735.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.378+536T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691322 | |||||||
chr19:691391 | G | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(41): Show |
70 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.378+467C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691391 | |||||||
chr19:691461 | C | A | 1 | a0001c0002t0002g0130 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.378+397G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691461 | |||||||
chr19:691504 | C | CA | 34 | a0001c0001t0001g0028 a0001c0001t0001g0058 a0001c0002t0001g0111 others(31): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.378+353dupT | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691504 | |||||||
chr19:691504 | CA | C | 9 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(6): Show |
9 | HG01168.hp1 HG01496.hp2 HG01517.hp1 others(6): Show |
intron_variant | MODIFIER | c.378+353delT | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691504 | |||||||
chr19:691520 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.378+338C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691520 | |||||||
chr19:691557 | C | T | 8 | a0001c0005t0001g0011 a0001c0005t0001g0018 a0001c0005t0001g0032 others(5): Show |
16 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.378+301G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691557 | |||||||
chr19:691687 | C | G | 1 | a0001c0002t0001g0131 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.378+171G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691687 | |||||||
chr19:691687 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.378+171G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691687 | |||||||
chr19:691759 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.378+99G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691759 | |||||||
chr19:691793 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.378+65G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691793 | |||||||
chr19:691833 | C | T | 42 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0058 others(39): Show |
79 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.378+25G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 3/4 | chr19 | 691833 | |||||||
chr19:692092 | G | C | 1 | a0001c0002t0002g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234-90C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692092 | |||||||
chr19:692160 | G | A | 1 | a0001c0002t0002g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.234-158C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692160 | |||||||
chr19:692177 | CTGATCAA others(65): Show |
C | 1 | a0001c0002t0001g0033 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.234-247_234-176del others(72): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692177 | |||||||
chr19:692238 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0064 others(1): Show |
6 | HG02109.hp1 HG02976.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.234-236T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692238 | |||||||
chr19:692261 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0160 a0002c0003t0001g0081 |
4 | HG00408.hp1 HG02145.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-259G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692261 | |||||||
chr19:692279 | G | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0160 a0001c0001t0001g0198 others(4): Show |
8 | HG01074.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-277C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692279 | |||||||
chr19:692300 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.234-298G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692300 | |||||||
chr19:692347 | C | T | 16 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0050 others(13): Show |
28 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.234-345G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692347 | |||||||
chr19:692350 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.234-348G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692350 | |||||||
chr19:692363 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.234-361G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692363 | |||||||
chr19:692376 | C | CA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0021 others(42): Show |
71 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.234-375dupT | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692376 | |||||||
chr19:692400 | A | T | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.234-398T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692400 | |||||||
chr19:692419 | C | CCTTTTTT | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0021 others(81): Show |
154 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.234-424_234-418dup others(7): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692419 | |||||||
chr19:692427 | C | CTTTTTTC others(1): Show |
16 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0053 others(13): Show |
23 | HG01074.hp1 HG01109.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.234-426_234-425ins others(8): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692427 | |||||||
chr19:692428 | T | TTTTTTC | 41 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(38): Show |
109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.234-427_234-426ins others(6): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692428 | |||||||
chr19:692453 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.234-451G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692453 | |||||||
chr19:692461 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0035 others(31): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.234-459C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692461 | |||||||
chr19:692517 | A | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0060 others(4): Show |
10 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-515T>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692517 | |||||||
chr19:692530 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0035 others(33): Show |
103 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.234-528G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692530 | |||||||
chr19:692635 | T | A | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.234-633A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692635 | |||||||
chr19:692635 | T | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0064 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.234-633A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692635 | |||||||
chr19:692696 | C | T | 4 | a0001c0002t0002g0015 a0001c0002t0002g0068 a0001c0002t0002g0069 others(1): Show |
7 | HG02630.hp2 HG02809.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-694G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692696 | |||||||
chr19:692790 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0071 others(13): Show |
50 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.234-788C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692790 | |||||||
chr19:692797 | T | A | 1 | a0001c0002t0001g0133 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.234-795A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692797 | |||||||
chr19:692816 | C | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
5 | NA18943.hp1 NA18972.hp1 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-814G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692816 | |||||||
chr19:692877 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.234-875A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692877 | |||||||
chr19:692934 | A | AT | 7 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG02976.hp1 HG03195.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-933dupA | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 692934 | |||||||
chr19:693015 | C | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA18941.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.234-1013G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693015 | |||||||
chr19:693023 | GT | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-1022delA | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693023 | |||||||
chr19:693048 | C | G | 1 | a0001c0002t0001g0112 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.234-1046G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693048 | |||||||
chr19:693055 | A | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0160 a0001c0001t0001g0198 others(4): Show |
8 | HG01074.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-1053T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693055 | |||||||
chr19:693102 | T | A | 1 | a0001c0002t0001g0134 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.234-1100A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693102 | |||||||
chr19:693145 | A | T | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.234-1143T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693145 | |||||||
chr19:693166 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(36): Show |
72 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.234-1164G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693166 | |||||||
chr19:693186 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0022 others(22): Show |
47 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.234-1184G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693186 | |||||||
chr19:693210 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-1208G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693210 | |||||||
chr19:693215 | G | C | 1 | a0001c0001t0001g0023 | 3 | HG02109.hp1 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.234-1213C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693215 | |||||||
chr19:693221 | G | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | NA18972.hp1 NA18991.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.234-1219C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693221 | |||||||
chr19:693228 | GC | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG02976.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.234-1227delG | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693228 | |||||||
chr19:693229 | C | CT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0186 others(10): Show |
22 | HG01261.hp2 HG01516.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.234-1228_234-1227i others(3): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693229 | |||||||
chr19:693229 | C | CTT | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
129 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.234-1228_234-1227i others(4): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693229 | |||||||
chr19:693229 | C | CTTT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(52): Show |
96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.234-1228_234-1227i others(5): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693229 | |||||||
chr19:693229 | C | CTTTT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0035 others(13): Show |
39 | HG00597.hp1 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.234-1228_234-1227i others(6): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693229 | |||||||
chr19:693229 | C | CTTTTT | 4 | a0001c0001t0001g0003 a0002c0003t0001g0080 a0002c0003t0001g0138 others(1): Show |
4 | HG01261.hp1 HG01884.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-1228_234-1227i others(7): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693229 | |||||||
chr19:693230 | C | CT | 12 | a0001c0002t0001g0007 a0001c0002t0001g0101 a0001c0002t0001g0102 others(9): Show |
21 | HG00438.hp2 HG01192.hp2 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.234-1229dupA | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693230 | |||||||
chr19:693230 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.234-1228G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693230 | |||||||
chr19:693259 | G | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0037 others(45): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.234-1257C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693259 | |||||||
chr19:693425 | G | T | 8 | a0001c0001t0001g0098 a0001c0005t0001g0011 a0001c0005t0001g0018 others(5): Show |
16 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.233+1389C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693425 | |||||||
chr19:693454 | C | T | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.233+1360G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693454 | |||||||
chr19:693470 | T | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.233+1344A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693470 | |||||||
chr19:693503 | G | A | 1 | a0002c0003t0001g0091 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.233+1311C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693503 | |||||||
chr19:693509 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.233+1305C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693509 | |||||||
chr19:693562 | A | G | 1 | a0001c0002t0001g0079 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.233+1252T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693562 | |||||||
chr19:693712 | A | C | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.233+1102T>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693712 | |||||||
chr19:693770 | C | T | 1 | a0006c0014t0001g0054 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.233+1044G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693770 | |||||||
chr19:693802 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1012G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693802 | |||||||
chr19:693823 | G | C | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0035 others(32): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.233+991C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693823 | |||||||
chr19:693906 | A | T | 9 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
10 | HG01074.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.233+908T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693906 | |||||||
chr19:693975 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.233+839G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693975 | |||||||
chr19:693991 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.233+823G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693991 | |||||||
chr19:693992 | G | C | 8 | a0001c0001t0001g0098 a0001c0005t0001g0011 a0001c0005t0001g0018 others(5): Show |
16 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.233+822C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 693992 | |||||||
chr19:694005 | G | T | 2 | a0001c0001t0001g0023 a0001c0002t0002g0197 |
4 | HG02109.hp1 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+809C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694005 | |||||||
chr19:694042 | A | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02976.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+772T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694042 | |||||||
chr19:694058 | T | C | 1 | a0001c0002t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.233+756A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694058 | |||||||
chr19:694121 | C | A | 3 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | NA18972.hp1 NA18991.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.233+693G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694121 | |||||||
chr19:694121 | C | G | 17 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0036 others(14): Show |
37 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.233+693G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694121 | |||||||
chr19:694121 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(50): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.233+693G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694121 | |||||||
chr19:694156 | G | A | 1 | a0002c0003t0001g0093 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.233+658C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694156 | |||||||
chr19:694172 | G | C | 2 | a0001c0001t0002g0092 a0002c0003t0001g0093 |
2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.233+642C>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694172 | |||||||
chr19:694177 | C | A | 1 | a0001c0005t0001g0032 | 2 | HG01261.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.233+637G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694177 | |||||||
chr19:694177 | CCAGGACC others(26): Show |
C | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+604_233+636del others(33): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694177 | |||||||
chr19:694195 | G | A | 1 | a0001c0002t0001g0205 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.233+619C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694195 | |||||||
chr19:694214 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+600C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694214 | |||||||
chr19:694217 | G | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+597C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694217 | |||||||
chr19:694221 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+593C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694221 | |||||||
chr19:694222 | G | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+592C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694222 | |||||||
chr19:694226 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.233+588G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694226 | |||||||
chr19:694227 | C | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+587G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694227 | |||||||
chr19:694228 | A | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+586T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694228 | |||||||
chr19:694230 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+584G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694230 | |||||||
chr19:694231 | C | T | 10 | a0001c0001t0001g0098 a0001c0001t0004g0046 a0001c0002t0001g0140 others(7): Show |
18 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.233+583G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694231 | |||||||
chr19:694232 | A | C | 1 | a0002c0003t0001g0078 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.233+582T>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694232 | |||||||
chr19:694233 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+581G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694233 | |||||||
chr19:694234 | C | G | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+580G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694234 | |||||||
chr19:694237 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+577C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694237 | |||||||
chr19:694239 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+575G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694239 | |||||||
chr19:694241 | C | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+573G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694241 | |||||||
chr19:694241 | C | G | 9 | a0001c0001t0001g0098 a0001c0001t0004g0046 a0001c0005t0001g0011 others(6): Show |
17 | HG01255.hp2 HG01261.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.233+573G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694241 | |||||||
chr19:694242 | C | G | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+572G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694242 | |||||||
chr19:694247 | T | G | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+567A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694247 | |||||||
chr19:694252 | T | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+562A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694252 | |||||||
chr19:694256 | A | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+558T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694256 | |||||||
chr19:694259 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+555C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694259 | |||||||
chr19:694260 | T | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+554A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694260 | |||||||
chr19:694261 | T | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+553A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694261 | |||||||
chr19:694263 | T | G | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+551A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694263 | |||||||
chr19:694264 | T | G | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+550A>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694264 | |||||||
chr19:694272 | T | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+542A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694272 | |||||||
chr19:694275 | G | GACAGATG others(29): Show |
1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+538_233+539ins others(36): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694275 | |||||||
chr19:694278 | T | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+536A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694278 | |||||||
chr19:694279 | A | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+535T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694279 | |||||||
chr19:694281 | A | C | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+533T>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694281 | |||||||
chr19:694284 | G | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+530C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694284 | |||||||
chr19:694286 | G | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+528C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694286 | |||||||
chr19:694288 | C | G | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+526G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694288 | |||||||
chr19:694289 | A | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+525T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694289 | |||||||
chr19:694292 | G | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+522C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694292 | |||||||
chr19:694293 | C | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+521G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694293 | |||||||
chr19:694297 | G | T | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+517C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694297 | |||||||
chr19:694298 | C | A | 1 | a0001c0002t0001g0140 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.233+516G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694298 | |||||||
chr19:694405 | T | TAAAAATG others(370): Show |
1 | a0001c0001t0001g0077 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.233+408_233+409ins others(377): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694405 | |||||||
chr19:694442 | C | A | 1 | a0001c0002t0002g0141 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.233+372G>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694442 | |||||||
chr19:694466 | G | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(67): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.233+348C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694466 | |||||||
chr19:694492 | C | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0051 a0001c0001t0001g0148 |
4 | HG01175.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+322G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694492 | |||||||
chr19:694528 | G | A | 1 | a0002c0003t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233+286C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694528 | |||||||
chr19:694529 | T | C | 1 | a0002c0003t0001g0142 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.233+285A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694529 | |||||||
chr19:694534 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.233+280G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694534 | |||||||
chr19:694555 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.233+259G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694555 | |||||||
chr19:694561 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0060 a0001c0001t0001g0077 others(3): Show |
8 | HG02109.hp1 HG02976.hp1 HG03486.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+242_233+252dup others(11): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694561 | |||||||
chr19:694561 | C | CAAAAAAA others(5): Show |
32 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0058 others(29): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.233+241_233+252dup others(12): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694561 | |||||||
chr19:694561 | C | CAAAAAAA others(6): Show |
5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0146 others(2): Show |
6 | HG01891.hp2 HG02055.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+252_233+253ins others(13): Show |
PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694561 | |||||||
chr19:694575 | A | G | 43 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(40): Show |
74 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.233+239T>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694575 | |||||||
chr19:694579 | T | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0025 others(54): Show |
95 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.233+235A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694579 | |||||||
chr19:694586 | A | T | 42 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(39): Show |
73 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.233+228T>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694586 | |||||||
chr19:694604 | T | C | 1 | a0001c0002t0001g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.233+210A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694604 | |||||||
chr19:694617 | C | G | 1 | a0001c0002t0001g0073 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.233+197G>C | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694617 | |||||||
chr19:694646 | TC | T | 9 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
10 | HG01074.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.233+167delG | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694646 | |||||||
chr19:694649 | CT | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(77): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.233+164delA | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694649 | |||||||
chr19:694650 | T | C | 10 | a0001c0001t0001g0035 a0001c0001t0001g0098 a0001c0001t0004g0046 others(7): Show |
18 | HG01255.hp2 HG01261.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.233+164A>G | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694650 | |||||||
chr19:694682 | T | A | 6 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0012t0005g0056 others(3): Show |
6 | HG01109.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.233+132A>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694682 | |||||||
chr19:694731 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0150 a0001c0001t0001g0160 others(1): Show |
5 | HG02145.hp1 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+83G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 2/4 | chr19 | 694731 | |||||||
chr19:695001 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.80-34G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695001 | |||||||
chr19:695002 | G | T | 5 | a0001c0002t0002g0015 a0001c0002t0002g0068 a0001c0002t0002g0069 others(2): Show |
8 | HG02630.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-35C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695002 | |||||||
chr19:695036 | G | T | 4 | a0001c0001t0001g0021 a0001c0001t0002g0137 a0002c0003t0001g0138 others(1): Show |
6 | HG01884.hp1 HG02572.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-69C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695036 | |||||||
chr19:695149 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.80-182G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695149 | |||||||
chr19:695153 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.80-186G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695153 | |||||||
chr19:695167 | G | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0058 a0001c0001t0001g0060 others(7): Show |
12 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.79+185C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695167 | |||||||
chr19:695189 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
6 | HG02109.hp1 HG02572.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.79+163C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695189 | |||||||
chr19:695209 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0053 a0001c0012t0005g0056 others(3): Show |
9 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.79+143G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695209 | |||||||
chr19:695225 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.79+127G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695225 | |||||||
chr19:695234 | G | A | 9 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(6): Show |
10 | HG01074.hp1 HG02258.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+118C>T | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695234 | |||||||
chr19:695272 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.79+80G>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695272 | |||||||
chr19:695279 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.79+73C>A | PRSS57 | ENSG00000185198.12 | transcript | ENST00000329267.9 | protein_coding | 1/4 | chr19 | 695279 |