Item | Value |
---|---|
geneid | 23590 |
ensemblid | ENSG00000148459.16 |
hgncid | 17759 |
symbol | PDSS1 |
name | decaprenyl diphosphate synthase subunit 1 |
refseq_nuc | NM_014317.5 |
refseq_prot | NP_055132.2 |
ensembl_nuc | ENST00000376215.10 |
ensembl_prot | ENSP00000365388.5 |
mane_status | MANE Select |
chr | chr10 |
start | 26697701 |
end | 26746798 |
strand | + |
ver | v1.2 |
region | chr10:26697701-26746798 |
region5000 | chr10:26692701-26751798 |
regionname0 | PDSS1_chr10_26697701_26746798 |
regionname5000 | PDSS1_chr10_26692701_26751798 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 415 | 400 | 86 | 77 | 174 | 18 | 43 | 135 | PDSS1_chr10_26692701_26751798 | PDSS1 | MASRW others(410): Show |
chr10 | 26692701 | 26751798 |
a0002 | 0/0 | 415 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | MASRW others(410): Show |
chr10 | 26692701 | 26751798 |
a0003 | 0/0 | 415 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | PDSS1_chr10_26692701_26751798 | PDSS1 | MASRW others(410): Show |
chr10 | 26692701 | 26751798 |
a0004 | 0/0 | 415 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | MASRW others(410): Show |
chr10 | 26692701 | 26751798 |
a0005 | 0/0 | 424 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | MASRW others(419): Show |
chr10 | 26692701 | 26751798 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1245 | 400 | 86 | 77 | 174 | 18 | 43 | PDSS1_chr10_26692701_26751798 | PDSS1 | ATGGC others(1240): Show |
chr10 | 26692701 | 26751798 | ||
a0002c0002 | 0/0 | 1245 | 11 | 10 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | ATGGC others(1240): Show |
chr10 | 26692701 | 26751798 | ||
a0003c0003 | 0/0 | 1245 | 3 | 0 | 0 | 3 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | ATGGC others(1240): Show |
chr10 | 26692701 | 26751798 | ||
a0004c0005 | 0/0 | 1245 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | ATGGC others(1240): Show |
chr10 | 26692701 | 26751798 | ||
a0005c0004 | 0/0 | 1272 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | ATGGC others(1267): Show |
chr10 | 26692701 | 26751798 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1584 | 339 | 71 | 52 | 159 | 13 | 42 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0001c0001t0002 | 0/0 | 1584 | 44 | 0 | 24 | 14 | 5 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0001c0001t0003 | 0/0 | 1584 | 7 | 6 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0001c0001t0004 | 0/0 | 1588 | 5 | 5 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1583): Show |
chr10 | 26692701 | 26751798 |
a0001c0001t0005 | 0/0 | 1584 | 3 | 3 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0001c0001t0007 | 0/0 | 1584 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0001c0001t0008 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0002c0002t0001 | 0/0 | 1584 | 10 | 9 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0002c0002t0003 | 0/0 | 1584 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0003c0003t0001 | 0/0 | 1584 | 3 | 0 | 0 | 3 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0004c0005t0001 | 0/0 | 1584 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1579): Show |
chr10 | 26692701 | 26751798 |
a0005c0004t0006 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | AGACT others(1606): Show |
chr10 | 26692701 | 26751798 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 1/0 | 5 | 0 | 1 | 0 | 2 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0005g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0005g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0002c0002t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0004c0005t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
a0005c0004t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0305 | EUR | GBR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0299 | EUR | GBR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0315 | EUR | FIN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0343 | EUR | FIN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0322 | EUR | FIN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00408 | hp1 | a0001 | c0001 | t0007 | g0056 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0364 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0356 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0358 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0371 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0349 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0350 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0352 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0313 | EUR | IBS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0357 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0361 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0348 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02074 | hp1 | a0003 | c0003 | t0001 | g0287 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CDX | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CDX | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CDX | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CDX | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0335 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0359 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0374 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0369 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0344 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0372 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0291 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0370 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0373 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0238 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0330 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0331 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0327 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0363 | AFR | ESN | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03579 | hp2 | a0002 | c0002 | t0003 | g0329 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03831 | hp2 | a0004 | c0005 | t0001 | g0340 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | STU | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | YRI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18974 | hp1 | a0005 | c0004 | t0006 | g0092 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18978 | hp1 | a0003 | c0003 | t0001 | g0289 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0366 | AFR | LWK | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | LWK | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | LWK | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19067 | hp2 | a0003 | c0003 | t0001 | g0288 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | YRI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ASW | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ASW | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0157 | EUR | TSI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0302 | EUR | TSI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | GIH | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | GIH | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0360 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0326 | AMR | CLM | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0362 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0328 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0368 | AFR | MSL | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | USA | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | USA | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | LWK | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | LWK | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0242 | REF | REF | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | PDSS1_chr10_26692701_26751798 | PDSS1 | chr10 | 26692701 | 26751798 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:26697773 | C | T | 1 | a0004 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.62C>T | p.Pro21Leu | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/12 | 73/1584 | 62/1248 | 21/415 | chr10 | 26697773 | |||
chr10:26697800 | G | T | 1 | a0002 | 11 | HG01123.hp2 HG02055.hp1 HG02717.hp1 others(8): Show |
missense_variant | MODERATE | c.89G>T | p.Gly30Val | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/12 | 100/1584 | 89/1248 | 30/415 | chr10 | 26697800 | |||
chr10:26709708 | T | G | 1 | a0003 | 3 | HG02074.hp1 NA18978.hp1 NA19067.hp2 |
missense_variant | MODERATE | c.407T>G | p.Phe136Cys | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/12 | 418/1584 | 407/1248 | 136/415 | chr10 | 26709708 | |||
chr10:26746438 | C | CGACACCA others(20): Show |
1 | a0005 | 1 | NA18974.hp1 | disruptive_inframe_insertion | MODERATE | c.1213_1214insGACACC others(21): Show |
p.Gln405delinsArgHis others(24): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 1225/1584 | 1214/1248 | 405/415 | chr10 | 26746438 | |||
chr10:26746439 | A | C | 1 | a0005 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1214A>C | p.Gln405Pro | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 1225/1584 | 1214/1248 | 405/415 | chr10 | 26746439 | |||
chr10:26746463 | G | A | 1 | a0005 | 1 | NA18974.hp1 | missense_variant | MODERATE | c.1238G>A | p.Arg413Lys | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 1249/1584 | 1238/1248 | 413/415 | chr10 | 26746463 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:26746476 | A | G | 1 | a0001c0001t0008 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 3 | chr10 | 26746476 | ||||||
chr10:26746479 | C | A | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 6 | chr10 | 26746479 | ||||||
chr10:26746496 | C | G | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*23C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 23 | chr10 | 26746496 | ||||||
chr10:26746528 | T | C | 1 | a0001c0001t0007 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 55 | chr10 | 26746528 | ||||||
chr10:26746549 | C | T | 1 | a0001c0001t0002 | 44 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*76C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 76 | chr10 | 26746549 | ||||||
chr10:26746581 | A | AAGAT | 1 | a0001c0001t0004 | 5 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*110_*113dupGATA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 114 | INFO_REALIGN_3_PRIME | chr10 | 26746581 | |||||
chr10:26746611 | T | A | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 138 | chr10 | 26746611 | ||||||
chr10:26746619 | T | A | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 146 | chr10 | 26746619 | ||||||
chr10:26746623 | G | C | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 150 | chr10 | 26746623 | ||||||
chr10:26746624 | C | A | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*151C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 151 | chr10 | 26746624 | ||||||
chr10:26746627 | A | G | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 154 | chr10 | 26746627 | ||||||
chr10:26746629 | G | T | 1 | a0005c0004t0006 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 156 | chr10 | 26746629 | ||||||
chr10:26746630 | T | G | 3 | a0001c0001t0003 a0001c0001t0005 a0002c0002t0003 |
11 | HG01099.hp2 HG02109.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*157T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 157 | chr10 | 26746630 | ||||||
chr10:26746737 | A | T | 1 | a0001c0001t0005 | 3 | HG02109.hp1 HG02572.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*264A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 12/12 | 264 | chr10 | 26746737 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:26697863 | C | T | 1 | a0001c0001t0001g0375 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.129+23C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26697863 | |||||||
chr10:26697953 | G | C | 1 | a0001c0001t0001g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.129+113G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26697953 | |||||||
chr10:26697969 | AGCTCCGG others(4): Show |
A | 1 | a0001c0001t0005g0374 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129+131_129+141del others(11): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 26697969 | ||||||
chr10:26698003 | T | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
263 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.129+163T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698003 | |||||||
chr10:26698073 | C | T | 13 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0363 others(10): Show |
15 | HG00642.hp1 HG01106.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.129+233C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698073 | |||||||
chr10:26698091 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.129+251G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698091 | |||||||
chr10:26698091 | GT | G | 26 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(23): Show |
26 | HG02015.hp1 HG02135.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.129+255delT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 26698091 | ||||||
chr10:26698131 | G | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(129): Show |
141 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.129+291G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698131 | |||||||
chr10:26698176 | G | GTTAA | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
263 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.129+337_129+340dup others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 26698176 | ||||||
chr10:26698210 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0157 others(1): Show |
6 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+370T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698210 | |||||||
chr10:26698251 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.129+411C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698251 | |||||||
chr10:26698377 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
263 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.129+537C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698377 | |||||||
chr10:26698431 | C | T | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+591C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698431 | |||||||
chr10:26698486 | C | T | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
263 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.129+646C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698486 | |||||||
chr10:26698596 | G | A | 267 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(264): Show |
289 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.129+756G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698596 | |||||||
chr10:26698764 | A | G | 10 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.129+924A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698764 | |||||||
chr10:26698769 | A | G | 109 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(106): Show |
122 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.129+929A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698769 | |||||||
chr10:26698821 | A | G | 1 | a0001c0001t0005g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.129+981A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698821 | |||||||
chr10:26698850 | A | G | 135 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
148 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.129+1010A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26698850 | |||||||
chr10:26699030 | G | C | 1 | a0001c0001t0003g0023 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.129+1190G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699030 | |||||||
chr10:26699063 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG02630.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.129+1223T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699063 | |||||||
chr10:26699142 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.129+1302A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699142 | |||||||
chr10:26699234 | T | C | 241 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
263 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.129+1394T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699234 | |||||||
chr10:26699268 | T | C | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.129+1428T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699268 | |||||||
chr10:26699329 | A | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(129): Show |
141 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.129+1489A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699329 | |||||||
chr10:26699395 | TTC | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.129+1557_129+1558d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 26699395 | ||||||
chr10:26699397 | C | CT | 139 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(136): Show |
151 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.129+1572dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 26699397 | ||||||
chr10:26699416 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.129+1576A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699416 | |||||||
chr10:26699455 | C | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(109): Show |
120 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.129+1615C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699455 | |||||||
chr10:26699459 | A | G | 1 | a0001c0001t0001g0373 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.129+1619A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699459 | |||||||
chr10:26699521 | A | G | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1681A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699521 | |||||||
chr10:26699584 | G | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(88): Show |
104 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.129+1744G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699584 | |||||||
chr10:26699636 | C | G | 16 | a0001c0001t0001g0351 a0001c0001t0002g0001 a0001c0001t0002g0347 others(13): Show |
21 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.129+1796C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699636 | |||||||
chr10:26699638 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(129): Show |
141 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.129+1798A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699638 | |||||||
chr10:26699675 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0002g0281 |
2 | HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.129+1835G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699675 | |||||||
chr10:26699764 | G | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | NA18941.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.129+1924G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699764 | |||||||
chr10:26699816 | C | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(129): Show |
141 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.129+1976C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699816 | |||||||
chr10:26699881 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
265 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.129+2041T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26699881 | |||||||
chr10:26700164 | A | AT | 92 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(89): Show |
105 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.130-1987dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr10 | 26700164 | ||||||
chr10:26700233 | T | C | 26 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(23): Show |
26 | HG02015.hp1 HG02135.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-1929T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700233 | |||||||
chr10:26700267 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.130-1895G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700267 | |||||||
chr10:26700330 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | NA18962.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.130-1832G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700330 | |||||||
chr10:26700330 | G | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
10 | HG01074.hp1 HG01099.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.130-1832G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700330 | |||||||
chr10:26700439 | T | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
262 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.130-1723T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700439 | |||||||
chr10:26700453 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
241 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.130-1709G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700453 | |||||||
chr10:26700477 | T | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(109): Show |
120 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.130-1685T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700477 | |||||||
chr10:26700493 | T | C | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(346): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.130-1669T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700493 | |||||||
chr10:26700600 | G | C | 74 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(71): Show |
84 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.130-1562G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700600 | |||||||
chr10:26700620 | G | A | 10 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.130-1542G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700620 | |||||||
chr10:26700693 | C | T | 109 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(106): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.130-1469C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700693 | |||||||
chr10:26700771 | G | A | 246 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(243): Show |
267 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.130-1391G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700771 | |||||||
chr10:26700904 | A | G | 26 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(23): Show |
26 | HG02015.hp1 HG02135.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-1258A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700904 | |||||||
chr10:26700937 | G | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
262 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.130-1225G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26700937 | |||||||
chr10:26701017 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
241 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.130-1145C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701017 | |||||||
chr10:26701071 | C | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(110): Show |
121 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.130-1091C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701071 | |||||||
chr10:26701142 | T | C | 26 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(23): Show |
26 | HG02015.hp1 HG02135.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-1020T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701142 | |||||||
chr10:26701292 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.130-870T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701292 | |||||||
chr10:26701307 | C | T | 1 | a0001c0001t0005g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130-855C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701307 | |||||||
chr10:26701461 | C | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
247 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.130-701C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701461 | |||||||
chr10:26701646 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.130-516T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701646 | |||||||
chr10:26701656 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
247 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.130-506A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701656 | |||||||
chr10:26701745 | C | T | 26 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(23): Show |
26 | HG02015.hp1 HG02135.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.130-417C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701745 | |||||||
chr10:26701809 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0003g0159 a0001c0001t0003g0160 |
3 | HG02630.hp1 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.130-353C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701809 | |||||||
chr10:26701920 | T | G | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(219): Show |
243 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.130-242T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701920 | |||||||
chr10:26701980 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.130-182C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26701980 | |||||||
chr10:26702104 | CAATACCT others(3): Show |
C | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.130-57_130-48delAA others(8): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26702104 | |||||||
chr10:26702108 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(265): Show |
290 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.130-54A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26702108 | |||||||
chr10:26702116 | T | C | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
291 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.130-46T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26702116 | |||||||
chr10:26702138 | CG | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.130-23delG | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 1/11 | chr10 | 26702138 | |||||||
chr10:26702207 | A | G | 15 | a0001c0001t0001g0022 a0001c0001t0001g0165 a0001c0001t0001g0206 others(12): Show |
16 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.162+13A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702207 | |||||||
chr10:26702234 | T | TGAGTTAA others(302): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
12 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.162+54_162+55insTT others(307): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26702234 | ||||||
chr10:26702234 | T | TGAGTTAA others(302): Show |
3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02965.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.162+54_162+55insTT others(307): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26702234 | ||||||
chr10:26702250 | G | A | 229 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(226): Show |
249 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.162+56G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702250 | |||||||
chr10:26702253 | A | T | 20 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(17): Show |
20 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.162+59A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702253 | |||||||
chr10:26702258 | T | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.162+64T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702258 | |||||||
chr10:26702313 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.162+119G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702313 | |||||||
chr10:26702364 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.162+170T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702364 | |||||||
chr10:26702501 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(30): Show |
37 | HG01123.hp2 HG01243.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.162+307G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702501 | |||||||
chr10:26702504 | C | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(30): Show |
37 | HG01123.hp2 HG01243.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.162+310C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702504 | |||||||
chr10:26702619 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.162+425C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702619 | |||||||
chr10:26702675 | A | G | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(263): Show |
285 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.162+481A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26702675 | |||||||
chr10:26703176 | G | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(116): Show |
123 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.162+982G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703176 | |||||||
chr10:26703196 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.162+1002C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703196 | |||||||
chr10:26703236 | C | T | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0008g0282 |
3 | HG02895.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.162+1042C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703236 | |||||||
chr10:26703237 | G | A | 2 | a0001c0001t0002g0290 a0001c0001t0003g0291 |
2 | HG01361.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.162+1043G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703237 | |||||||
chr10:26703239 | C | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0170 a0001c0001t0001g0171 |
4 | HG00558.hp1 HG02071.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.162+1045C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703239 | |||||||
chr10:26703306 | T | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.162+1112T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703306 | |||||||
chr10:26703342 | TTA | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.162+1151_162+1152d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26703342 | ||||||
chr10:26703354 | A | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.162+1160A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703354 | |||||||
chr10:26703372 | G | A | 5 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
5 | NA18945.hp2 NA18995.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.162+1178G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703372 | |||||||
chr10:26703419 | GAGGATCA others(9): Show |
G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.162+1231_163-1237d others(18): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26703419 | ||||||
chr10:26703483 | T | G | 16 | a0001c0001t0001g0351 a0001c0001t0002g0001 a0001c0001t0002g0347 others(13): Show |
21 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.163-1194T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703483 | |||||||
chr10:26703495 | C | A | 10 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-1182C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703495 | |||||||
chr10:26703727 | A | G | 1 | a0002c0002t0001g0331 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.163-950A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703727 | |||||||
chr10:26703786 | T | C | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.163-891T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703786 | |||||||
chr10:26703799 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | NA18999.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.163-878G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703799 | |||||||
chr10:26703807 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.163-870C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703807 | |||||||
chr10:26703841 | GGAGGCCA others(15): Show |
G | 130 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(127): Show |
134 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.163-831_163-810del others(22): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26703841 | ||||||
chr10:26703878 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.163-799G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703878 | |||||||
chr10:26703909 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.163-768A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703909 | |||||||
chr10:26703925 | C | G | 1 | a0001c0001t0003g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.163-752C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26703925 | |||||||
chr10:26704006 | T | C | 309 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(306): Show |
340 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.163-671T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704006 | |||||||
chr10:26704006 | T | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0323 |
2 | NA19067.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.163-671T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704006 | |||||||
chr10:26704024 | G | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(117): Show |
124 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.163-653G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704024 | |||||||
chr10:26704061 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.163-616G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704061 | |||||||
chr10:26704083 | C | CA | 11 | a0001c0001t0001g0124 a0001c0001t0001g0283 a0001c0001t0001g0284 others(8): Show |
14 | HG01106.hp2 HG01123.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.163-575dupA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(3): Show |
4 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0278 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-584_163-575dup others(10): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0276 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163-585_163-575dup others(11): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0275 |
3 | HG02145.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.163-586_163-575dup others(12): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(6): Show |
28 | a0001c0001t0001g0003 a0001c0001t0001g0247 a0001c0001t0001g0248 others(25): Show |
36 | HG00280.hp1 HG00323.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.163-587_163-575dup others(13): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(7): Show |
40 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0029 others(37): Show |
44 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.163-588_163-575dup others(14): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(8): Show |
14 | a0001c0001t0001g0272 a0001c0001t0001g0294 a0001c0001t0001g0295 others(11): Show |
14 | HG00642.hp1 HG01175.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.163-589_163-575dup others(15): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(9): Show |
15 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0254 others(12): Show |
15 | HG02015.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.163-590_163-575dup others(16): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(10): Show |
21 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0050 others(18): Show |
23 | HG01192.hp2 HG01891.hp1 HG02135.hp1 others(20): Show |
intron_variant | MODIFIER | c.163-591_163-575dup others(17): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(11): Show |
10 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(7): Show |
10 | HG00597.hp2 HG02027.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-592_163-575dup others(18): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(12): Show |
6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01109.hp1 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-593_163-575dup others(19): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(13): Show |
18 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(15): Show |
19 | HG01168.hp1 HG01169.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(20): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(14): Show |
34 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(31): Show |
40 | HG00140.hp1 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(21): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(15): Show |
22 | a0001c0001t0001g0017 a0001c0001t0001g0022 a0001c0001t0001g0094 others(19): Show |
24 | HG00408.hp2 HG00597.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(22): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(16): Show |
6 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0153 others(3): Show |
6 | HG00673.hp2 HG01243.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(23): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(17): Show |
13 | a0001c0001t0001g0015 a0001c0001t0001g0054 a0001c0001t0001g0055 others(10): Show |
14 | HG00558.hp1 HG00741.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(24): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(18): Show |
9 | a0001c0001t0001g0016 a0001c0001t0001g0083 a0001c0001t0001g0084 others(6): Show |
10 | HG02071.hp1 HG02132.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(25): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(19): Show |
16 | a0001c0001t0001g0021 a0001c0001t0001g0053 a0001c0001t0001g0079 others(13): Show |
17 | HG00544.hp1 HG01074.hp2 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(26): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(20): Show |
18 | a0001c0001t0001g0020 a0001c0001t0001g0071 a0001c0001t0001g0072 others(15): Show |
19 | HG01258.hp2 HG01358.hp1 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(27): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(21): Show |
7 | a0001c0001t0001g0009 a0001c0001t0001g0068 a0001c0001t0001g0069 others(4): Show |
8 | HG03492.hp1 NA18612.hp1 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(28): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(22): Show |
6 | a0001c0001t0001g0067 a0001c0001t0001g0213 a0001c0001t0001g0236 others(3): Show |
6 | HG02109.hp1 HG04115.hp1 NA18941.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(29): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0001g0066 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.163-575_163-574ins others(30): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(24): Show |
1 | a0001c0001t0001g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.163-575_163-574ins others(31): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(25): Show |
3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG00438.hp1 HG02004.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.163-575_163-574ins others(32): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(26): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | NA18959.hp1 NA18966.hp1 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(33): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(27): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0058 |
4 | NA18940.hp1 NA18965.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.163-575_163-574ins others(34): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(28): Show |
3 | a0001c0001t0001g0057 a0001c0001t0001g0211 a0001c0001t0007g0056 |
3 | HG00408.hp1 NA18971.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.163-575_163-574ins others(35): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704083 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.163-575_163-574ins others(36): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704083 | ||||||
chr10:26704099 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0134 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.163-575_163-574ins others(29): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704099 | ||||||
chr10:26704099 | A | AAAAAAAA others(21): Show |
1 | a0001c0001t0001g0136 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.163-575_163-574ins others(28): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704099 | ||||||
chr10:26704108 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.163-569C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704108 | |||||||
chr10:26704111 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG02723.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.163-566G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704111 | |||||||
chr10:26704151 | A | G | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.163-526A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704151 | |||||||
chr10:26704178 | C | A | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-499C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704178 | |||||||
chr10:26704227 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.163-450G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704227 | |||||||
chr10:26704262 | G | T | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.163-415G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704262 | |||||||
chr10:26704350 | A | G | 1 | a0001c0001t0002g0361 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.163-327A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704350 | |||||||
chr10:26704433 | TG | T | 12 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(9): Show |
12 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.163-239delG | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704433 | ||||||
chr10:26704461 | T | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.163-216T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704461 | |||||||
chr10:26704482 | A | T | 3 | a0001c0001t0005g0251 a0001c0001t0005g0362 a0001c0001t0005g0374 |
3 | HG02109.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.163-195A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704482 | |||||||
chr10:26704534 | A | C | 1 | a0001c0001t0001g0366 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.163-143A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704534 | |||||||
chr10:26704625 | T | A | 1 | a0001c0001t0001g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.163-52T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | chr10 | 26704625 | |||||||
chr10:26704668 | AT | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(94): Show |
110 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(107): Show |
splice_region_variant&intron_variant | LOW | c.163-5delT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr10 | 26704668 | ||||||
chr10:26704796 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.227+55G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26704796 | |||||||
chr10:26704799 | G | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.227+58G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26704799 | |||||||
chr10:26704808 | A | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.227+67A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26704808 | |||||||
chr10:26704809 | T | A | 10 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.227+68T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26704809 | |||||||
chr10:26704910 | T | C | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.227+169T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26704910 | |||||||
chr10:26704928 | G | C | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG02723.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.227+187G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26704928 | |||||||
chr10:26705026 | C | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.228-260C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26705026 | |||||||
chr10:26705028 | C | G | 1 | a0001c0001t0001g0373 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.228-258C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26705028 | |||||||
chr10:26705032 | G | A | 327 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(324): Show |
358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.228-254G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26705032 | |||||||
chr10:26705105 | G | C | 1 | a0001c0001t0001g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.228-181G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26705105 | |||||||
chr10:26705221 | A | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.228-65A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 3/11 | chr10 | 26705221 | |||||||
chr10:26705416 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+22G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705416 | |||||||
chr10:26705483 | T | C | 98 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(95): Show |
111 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.336+89T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705483 | |||||||
chr10:26705513 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.336+119G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705513 | |||||||
chr10:26705612 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.336+218T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705612 | |||||||
chr10:26705637 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.336+243G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705637 | |||||||
chr10:26705721 | A | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+327A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705721 | |||||||
chr10:26705751 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.336+357A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705751 | |||||||
chr10:26705803 | G | C | 311 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(308): Show |
342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.336+409G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705803 | |||||||
chr10:26705863 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.336+469A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705863 | |||||||
chr10:26705949 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.336+555C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26705949 | |||||||
chr10:26706052 | C | G | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+658C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706052 | |||||||
chr10:26706109 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+715C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706109 | |||||||
chr10:26706119 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
121 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.336+725C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706119 | |||||||
chr10:26706190 | G | A | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0008g0282 |
3 | HG02895.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.336+796G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706190 | |||||||
chr10:26706226 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01074.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.336+832G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706226 | |||||||
chr10:26706321 | C | T | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.336+927C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706321 | |||||||
chr10:26706326 | T | C | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.336+932T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706326 | |||||||
chr10:26706421 | G | T | 1 | a0001c0001t0003g0291 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.336+1027G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706421 | |||||||
chr10:26706493 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.336+1099C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706493 | |||||||
chr10:26706842 | C | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+1448C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26706842 | |||||||
chr10:26707009 | AGT | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+1621_336+1622d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr10 | 26707009 | ||||||
chr10:26707073 | C | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0157 others(5): Show |
10 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.336+1679C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707073 | |||||||
chr10:26707074 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+1680G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707074 | |||||||
chr10:26707084 | A | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(182): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.336+1690A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707084 | |||||||
chr10:26707230 | A | G | 1 | a0001c0001t0001g0368 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.336+1836A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707230 | |||||||
chr10:26707247 | C | A | 1 | a0001c0001t0001g0234 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.336+1853C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707247 | |||||||
chr10:26707249 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.336+1855A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707249 | |||||||
chr10:26707251 | T | G | 1 | a0001c0001t0001g0234 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.336+1857T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707251 | |||||||
chr10:26707252 | T | A | 1 | a0001c0001t0001g0234 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.336+1858T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707252 | |||||||
chr10:26707271 | G | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
9 | HG00408.hp1 HG00544.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.336+1877G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707271 | |||||||
chr10:26707273 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.336+1879T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707273 | |||||||
chr10:26707343 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.336+1949T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707343 | |||||||
chr10:26707392 | C | G | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.336+1998C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707392 | |||||||
chr10:26707403 | A | G | 12 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(9): Show |
12 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.336+2009A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707403 | |||||||
chr10:26707518 | G | A | 10 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.337-2120G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707518 | |||||||
chr10:26707546 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.337-2092C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707546 | |||||||
chr10:26707547 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.337-2091T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707547 | |||||||
chr10:26707588 | C | T | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.337-2050C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707588 | |||||||
chr10:26707663 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(75): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.337-1975C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707663 | |||||||
chr10:26707712 | C | G | 1 | a0001c0001t0001g0308 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.337-1926C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707712 | |||||||
chr10:26707775 | A | G | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-1863A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707775 | |||||||
chr10:26707940 | T | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0369 a0001c0001t0001g0370 others(2): Show |
6 | HG01106.hp2 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-1698T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26707940 | |||||||
chr10:26708039 | A | G | 1 | a0001c0001t0001g0373 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.337-1599A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708039 | |||||||
chr10:26708114 | T | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(114): Show |
121 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.337-1524T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708114 | |||||||
chr10:26708215 | G | T | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-1423G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708215 | |||||||
chr10:26708342 | C | T | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(203): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.337-1296C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708342 | |||||||
chr10:26708362 | T | G | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.337-1276T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708362 | |||||||
chr10:26708501 | T | C | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-1137T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708501 | |||||||
chr10:26708627 | A | G | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-1011A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708627 | |||||||
chr10:26708660 | G | A | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-978G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708660 | |||||||
chr10:26708794 | TG | T | 23 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(20): Show |
23 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(20): Show |
intron_variant | MODIFIER | c.337-841delG | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr10 | 26708794 | ||||||
chr10:26708905 | C | T | 1 | a0002c0002t0001g0006 | 3 | HG02055.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.337-733C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708905 | |||||||
chr10:26708960 | C | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(194): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.337-678C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708960 | |||||||
chr10:26708989 | G | A | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(194): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.337-649G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708989 | |||||||
chr10:26708996 | G | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(217): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.337-642G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26708996 | |||||||
chr10:26709043 | A | C | 327 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(324): Show |
358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.337-595A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26709043 | |||||||
chr10:26709226 | C | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(194): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.337-412C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26709226 | |||||||
chr10:26709317 | T | G | 1 | a0001c0001t0002g0352 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.337-321T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26709317 | |||||||
chr10:26709384 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.337-254A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26709384 | |||||||
chr10:26709429 | C | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(194): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.337-209C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26709429 | |||||||
chr10:26709586 | C | T | 1 | a0001c0001t0003g0023 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.337-52C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 4/11 | chr10 | 26709586 | |||||||
chr10:26709810 | G | C | 98 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(95): Show |
111 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.467+42G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26709810 | |||||||
chr10:26710078 | TGGGAGGC others(3131): Show |
T | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.467+318_467+3455de others(1): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26710078 | ||||||
chr10:26710086 | GGAGGTTG others(3131): Show |
G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(193): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.467+334_467+3471de others(1): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26710086 | ||||||
chr10:26710130 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.467+362G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26710130 | |||||||
chr10:26710155 | A | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(108): Show |
115 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.467+387A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26710155 | |||||||
chr10:26710251 | C | CT | 10 | a0001c0001t0001g0156 a0001c0001t0001g0243 a0001c0001t0001g0244 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.467+495dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26710251 | ||||||
chr10:26710391 | G | A | 1 | a0002c0002t0001g0331 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.467+623G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26710391 | |||||||
chr10:26710495 | A | AT | 13 | a0001c0001t0001g0099 a0001c0001t0001g0106 a0001c0001t0001g0110 others(10): Show |
13 | HG00597.hp2 HG00741.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.467+743dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26710495 | ||||||
chr10:26710777 | C | T | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.467+1009C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26710777 | |||||||
chr10:26710827 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.467+1059C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26710827 | |||||||
chr10:26711002 | A | G | 1 | a0001c0001t0005g0374 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.467+1234A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26711002 | |||||||
chr10:26711584 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0105 |
2 | HG02056.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.467+1816C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26711584 | |||||||
chr10:26711636 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.467+1868G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26711636 | |||||||
chr10:26711817 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.467+2049G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26711817 | |||||||
chr10:26711822 | T | A | 126 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(123): Show |
130 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.467+2054T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26711822 | |||||||
chr10:26711962 | C | T | 78 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(75): Show |
82 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.467+2194C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26711962 | |||||||
chr10:26712001 | C | CTT | 22 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(19): Show |
22 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(19): Show |
intron_variant | MODIFIER | c.467+2250_467+2251d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26712001 | ||||||
chr10:26712001 | CT | C | 87 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(84): Show |
91 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.467+2251delT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26712001 | ||||||
chr10:26712032 | C | T | 4 | a0001c0001t0001g0324 a0003c0003t0001g0287 a0003c0003t0001g0288 others(1): Show |
4 | HG02074.hp1 NA18978.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.467+2264C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26712032 | |||||||
chr10:26712161 | C | G | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.467+2393C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26712161 | |||||||
chr10:26712523 | C | T | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.467+2755C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26712523 | |||||||
chr10:26713030 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0071 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.467+3262C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713030 | |||||||
chr10:26713042 | C | T | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.467+3274C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713042 | |||||||
chr10:26713155 | G | A | 23 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(20): Show |
23 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(20): Show |
intron_variant | MODIFIER | c.467+3387G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713155 | |||||||
chr10:26713249 | G | A | 8 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(5): Show |
8 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.467+3481G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713249 | |||||||
chr10:26713253 | T | C | 23 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(20): Show |
23 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(20): Show |
intron_variant | MODIFIER | c.467+3485T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713253 | |||||||
chr10:26713479 | G | A | 1 | a0001c0001t0001g0346 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.467+3711G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713479 | |||||||
chr10:26713671 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.467+3903T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713671 | |||||||
chr10:26713717 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.467+3949G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713717 | |||||||
chr10:26713727 | G | A | 1 | a0001c0001t0002g0353 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.467+3959G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713727 | |||||||
chr10:26713868 | T | C | 206 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(203): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.467+4100T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713868 | |||||||
chr10:26713970 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.467+4202G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26713970 | |||||||
chr10:26714102 | T | C | 10 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
10 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.467+4334T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714102 | |||||||
chr10:26714113 | C | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(81): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.467+4345C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714113 | |||||||
chr10:26714275 | G | A | 1 | a0001c0001t0005g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.467+4507G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714275 | |||||||
chr10:26714277 | T | C | 1 | a0001c0001t0005g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.467+4509T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714277 | |||||||
chr10:26714309 | A | T | 1 | a0001c0001t0001g0316 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.467+4541A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714309 | |||||||
chr10:26714318 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.467+4550A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714318 | |||||||
chr10:26714335 | G | A | 26 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(23): Show |
26 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(23): Show |
intron_variant | MODIFIER | c.467+4567G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714335 | |||||||
chr10:26714466 | CA | C | 314 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(311): Show |
345 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.467+4714delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26714466 | ||||||
chr10:26714478 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.467+4710A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714478 | |||||||
chr10:26714504 | A | G | 6 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0203 others(3): Show |
7 | HG00639.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.467+4736A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714504 | |||||||
chr10:26714760 | C | T | 2 | a0001c0001t0001g0265 a0001c0001t0001g0271 |
2 | NA18966.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.467+4992C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26714760 | |||||||
chr10:26715142 | C | G | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.468-5076C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715142 | |||||||
chr10:26715280 | C | G | 3 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0008g0282 |
3 | HG02895.hp1 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.468-4938C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715280 | |||||||
chr10:26715303 | G | A | 8 | a0001c0001t0001g0029 a0001c0001t0001g0363 a0001c0001t0001g0364 others(5): Show |
9 | HG00642.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.468-4915G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715303 | |||||||
chr10:26715388 | A | C | 4 | a0001c0001t0001g0324 a0003c0003t0001g0287 a0003c0003t0001g0288 others(1): Show |
4 | HG02074.hp1 NA18978.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.468-4830A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715388 | |||||||
chr10:26715400 | C | G | 2 | a0001c0001t0001g0283 a0001c0001t0008g0282 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.468-4818C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715400 | |||||||
chr10:26715406 | C | CT | 30 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0065 others(27): Show |
30 | HG00558.hp2 HG00597.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.468-4796dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26715406 | ||||||
chr10:26715548 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.468-4670C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715548 | |||||||
chr10:26715554 | G | A | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.468-4664G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715554 | |||||||
chr10:26715589 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.468-4629G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715589 | |||||||
chr10:26715693 | G | C | 23 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(20): Show |
23 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(20): Show |
intron_variant | MODIFIER | c.468-4525G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715693 | |||||||
chr10:26715709 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.468-4509T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715709 | |||||||
chr10:26715769 | C | G | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.468-4449C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715769 | |||||||
chr10:26715828 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-4390A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715828 | |||||||
chr10:26715910 | AC | A | 12 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(9): Show |
12 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.468-4305delC | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26715910 | ||||||
chr10:26715912 | C | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0054 others(46): Show |
50 | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.468-4306C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715912 | |||||||
chr10:26715924 | A | G | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.468-4294A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26715924 | |||||||
chr10:26716280 | T | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.468-3938T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716280 | |||||||
chr10:26716319 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.468-3899G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716319 | |||||||
chr10:26716327 | C | T | 1 | a0001c0001t0005g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.468-3891C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716327 | |||||||
chr10:26716328 | G | A | 1 | a0001c0001t0002g0299 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.468-3890G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716328 | |||||||
chr10:26716343 | G | A | 1 | a0001c0001t0001g0024 | 2 | NA18971.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.468-3875G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716343 | |||||||
chr10:26716354 | A | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(152): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.468-3864A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716354 | |||||||
chr10:26716364 | A | G | 166 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(163): Show |
177 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.468-3854A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716364 | |||||||
chr10:26716407 | T | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-3811T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716407 | |||||||
chr10:26716564 | C | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(154): Show |
168 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.468-3654C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716564 | |||||||
chr10:26716565 | G | A | 8 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0262 others(5): Show |
8 | HG02273.hp2 NA18952.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.468-3653G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716565 | |||||||
chr10:26716697 | A | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-3521A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716697 | |||||||
chr10:26716699 | A | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-3519A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716699 | |||||||
chr10:26716701 | A | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-3517A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716701 | |||||||
chr10:26716703 | G | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-3515G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716703 | |||||||
chr10:26716776 | AG | A | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.468-3440delG | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26716776 | ||||||
chr10:26716818 | G | A | 24 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.468-3400G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26716818 | |||||||
chr10:26717056 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.468-3162G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717056 | |||||||
chr10:26717136 | A | G | 2 | a0001c0001t0001g0365 a0001c0001t0001g0367 |
2 | HG02109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.468-3082A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717136 | |||||||
chr10:26717247 | C | T | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.468-2971C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717247 | |||||||
chr10:26717334 | T | C | 330 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(327): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.468-2884T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717334 | |||||||
chr10:26717429 | G | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-2789G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717429 | |||||||
chr10:26717452 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG01891.hp1 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.468-2766G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717452 | |||||||
chr10:26717471 | A | G | 24 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.468-2747A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717471 | |||||||
chr10:26717478 | C | T | 113 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
121 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.468-2740C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717478 | |||||||
chr10:26717479 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-2739G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717479 | |||||||
chr10:26717487 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.468-2731G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717487 | |||||||
chr10:26717536 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.468-2682A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717536 | |||||||
chr10:26717741 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468-2477A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717741 | |||||||
chr10:26717870 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.468-2348T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717870 | |||||||
chr10:26717907 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02280.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.468-2311A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26717907 | |||||||
chr10:26717990 | ACTCACCT others(11): Show |
A | 1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.468-2224_468-2207d others(20): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26717990 | ||||||
chr10:26718047 | G | GT | 47 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0054 others(44): Show |
48 | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.468-2171_468-2170i others(3): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718047 | |||||||
chr10:26718048 | G | T | 168 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
179 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.468-2170G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718048 | |||||||
chr10:26718054 | T | TG | 65 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(62): Show |
72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.468-2164_468-2163i others(3): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718054 | |||||||
chr10:26718056 | G | GT | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-2161dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26718056 | ||||||
chr10:26718058 | G | T | 162 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(159): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.468-2160G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718058 | |||||||
chr10:26718365 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.468-1853A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718365 | |||||||
chr10:26718480 | G | A | 10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.468-1738G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718480 | |||||||
chr10:26718578 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.468-1640T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718578 | |||||||
chr10:26718761 | C | CA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(48): Show |
61 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.468-1439dupA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26718761 | ||||||
chr10:26718761 | C | CAA | 98 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(95): Show |
111 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.468-1440_468-1439d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26718761 | ||||||
chr10:26718761 | CA | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0132 others(19): Show |
23 | HG01081.hp2 HG01192.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.468-1439delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr10 | 26718761 | ||||||
chr10:26718774 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.468-1444A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718774 | |||||||
chr10:26718835 | A | G | 10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.468-1383A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718835 | |||||||
chr10:26718920 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-1298C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26718920 | |||||||
chr10:26719196 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.468-1022A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719196 | |||||||
chr10:26719245 | G | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-973G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719245 | |||||||
chr10:26719251 | G | C | 1 | a0001c0001t0001g0309 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.468-967G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719251 | |||||||
chr10:26719306 | A | T | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.468-912A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719306 | |||||||
chr10:26719490 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0002g0317 |
2 | HG00438.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.468-728C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719490 | |||||||
chr10:26719497 | C | T | 24 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.468-721C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719497 | |||||||
chr10:26719584 | A | G | 18 | a0001c0001t0001g0057 a0001c0001t0001g0065 a0001c0001t0001g0066 others(15): Show |
18 | HG00558.hp2 HG02056.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.468-634A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719584 | |||||||
chr10:26719658 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-560C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719658 | |||||||
chr10:26719722 | C | T | 10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.468-496C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719722 | |||||||
chr10:26719753 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
179 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.468-465G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719753 | |||||||
chr10:26719773 | A | G | 24 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.468-445A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719773 | |||||||
chr10:26719774 | A | G | 148 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(145): Show |
171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.468-444A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26719774 | |||||||
chr10:26720010 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.468-208G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26720010 | |||||||
chr10:26720069 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.468-149T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26720069 | |||||||
chr10:26720079 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.468-139G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 5/11 | chr10 | 26720079 | |||||||
chr10:26720405 | A | G | 340 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(337): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.609+46A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26720405 | |||||||
chr10:26720733 | A | G | 11 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(8): Show |
11 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.609+374A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26720733 | |||||||
chr10:26721032 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.609+673G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721032 | |||||||
chr10:26721140 | C | T | 340 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(337): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.609+781C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721140 | |||||||
chr10:26721167 | C | T | 340 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(337): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.609+808C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721167 | |||||||
chr10:26721194 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.609+835G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721194 | |||||||
chr10:26721293 | C | A | 1 | a0001c0001t0005g0362 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.609+934C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721293 | |||||||
chr10:26721298 | CA | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(97): Show |
113 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.609+955delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721298 | ||||||
chr10:26721411 | G | A | 32 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(29): Show |
32 | HG00558.hp2 HG00741.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.609+1052G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721411 | |||||||
chr10:26721420 | G | GTA | 13 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0243 others(10): Show |
13 | HG00544.hp1 HG01243.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.609+1064_609+1065d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721420 | ||||||
chr10:26721423 | T | TACAC | 20 | a0001c0001t0001g0113 a0001c0001t0001g0143 a0001c0001t0001g0144 others(17): Show |
20 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.609+1088_609+1091d others(6): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TACACAC | 4 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0149 others(1): Show |
5 | HG01192.hp2 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.609+1086_609+1091d others(8): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0203 a0001c0001t0004g0239 |
2 | HG02300.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.609+1082_609+1091d others(12): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TACACACA others(5): Show |
9 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0208 others(6): Show |
11 | NA18945.hp1 NA18949.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.609+1080_609+1091d others(14): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TACACACA others(7): Show |
3 | a0001c0001t0004g0238 a0001c0001t0004g0240 a0001c0001t0004g0241 |
3 | HG02145.hp2 HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.609+1078_609+1091d others(16): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0196 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.609+1076_609+1091d others(18): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TATAC | 164 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(161): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.609+1065_609+1066i others(6): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TATACAC | 8 | a0001c0001t0001g0093 a0001c0001t0001g0107 a0001c0001t0001g0134 others(5): Show |
9 | HG01243.hp2 HG01978.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.609+1065_609+1066i others(8): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TATACACA others(1): Show |
8 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(5): Show |
8 | HG01099.hp2 HG01884.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.609+1065_609+1066i others(10): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TATACACA others(3): Show |
6 | a0001c0001t0001g0094 a0001c0001t0001g0192 a0001c0001t0001g0204 others(3): Show |
6 | HG01891.hp2 HG01952.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.609+1065_609+1066i others(12): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TATACACA others(5): Show |
6 | a0001c0001t0001g0013 a0001c0001t0001g0157 a0001c0001t0001g0178 others(3): Show |
8 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.609+1065_609+1066i others(14): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TATACACA others(7): Show |
59 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0016 others(56): Show |
67 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.609+1065_609+1066i others(16): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721423 | T | TATACACA others(9): Show |
12 | a0001c0001t0001g0012 a0001c0001t0001g0172 a0001c0001t0001g0182 others(9): Show |
13 | HG01175.hp1 HG01516.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.609+1065_609+1066i others(18): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721423 | ||||||
chr10:26721425 | C | T | 24 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0162 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.609+1066C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721425 | |||||||
chr10:26721468 | ATTG | A | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.609+1112_609+1114d others(5): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26721468 | ||||||
chr10:26721591 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.609+1232C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721591 | |||||||
chr10:26721704 | T | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.609+1345T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721704 | |||||||
chr10:26721834 | T | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.609+1475T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721834 | |||||||
chr10:26721903 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.609+1544C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26721903 | |||||||
chr10:26722111 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.610-1695G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722111 | |||||||
chr10:26722183 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(91): Show |
106 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.610-1623G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722183 | |||||||
chr10:26722207 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.610-1599T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722207 | |||||||
chr10:26722367 | A | G | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.610-1439A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722367 | |||||||
chr10:26722394 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(138): Show |
161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.610-1412G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722394 | |||||||
chr10:26722426 | T | C | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.610-1380T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722426 | |||||||
chr10:26722462 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.610-1344T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722462 | |||||||
chr10:26722568 | G | T | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.610-1238G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722568 | |||||||
chr10:26722594 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(118): Show |
132 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.610-1212C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722594 | |||||||
chr10:26722635 | A | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.610-1171A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722635 | |||||||
chr10:26722703 | CA | C | 16 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0050 others(13): Show |
19 | HG01123.hp2 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.610-1089delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26722703 | ||||||
chr10:26722818 | G | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0202 |
2 | HG01433.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.610-988G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722818 | |||||||
chr10:26722889 | A | C | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.610-917A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722889 | |||||||
chr10:26722898 | C | CT | 49 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(46): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.610-894dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr10 | 26722898 | ||||||
chr10:26722934 | T | C | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(172): Show |
189 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.610-872T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722934 | |||||||
chr10:26722978 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.610-828G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26722978 | |||||||
chr10:26723149 | A | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(92): Show |
107 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.610-657A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723149 | |||||||
chr10:26723154 | T | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.610-652T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723154 | |||||||
chr10:26723167 | C | T | 50 | a0001c0001t0001g0009 a0001c0001t0001g0053 a0001c0001t0001g0055 others(47): Show |
51 | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.610-639C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723167 | |||||||
chr10:26723180 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.610-626G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723180 | |||||||
chr10:26723315 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.610-491A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723315 | |||||||
chr10:26723444 | T | C | 11 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(8): Show |
11 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.610-362T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723444 | |||||||
chr10:26723489 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.610-317C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723489 | |||||||
chr10:26723490 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.610-316G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723490 | |||||||
chr10:26723511 | G | A | 9 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.610-295G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723511 | |||||||
chr10:26723528 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.610-278G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723528 | |||||||
chr10:26723695 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.610-111C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723695 | |||||||
chr10:26723753 | A | G | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.610-53A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 6/11 | chr10 | 26723753 | |||||||
chr10:26724286 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0269 |
2 | NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.831+163C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26724286 | |||||||
chr10:26724326 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.831+203G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26724326 | |||||||
chr10:26724786 | C | T | 330 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(327): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.831+663C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26724786 | |||||||
chr10:26725149 | C | G | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+1026C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725149 | |||||||
chr10:26725250 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.831+1127C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725250 | |||||||
chr10:26725455 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG01099.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.831+1332C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725455 | |||||||
chr10:26725496 | T | C | 5 | a0001c0001t0001g0070 a0001c0001t0001g0097 a0001c0001t0001g0099 others(2): Show |
5 | HG02080.hp2 NA18956.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+1373T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725496 | |||||||
chr10:26725517 | G | GT | 11 | a0001c0001t0001g0233 a0001c0001t0001g0243 a0001c0001t0001g0244 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+1404dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26725517 | ||||||
chr10:26725538 | G | T | 46 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(43): Show |
54 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.831+1415G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725538 | |||||||
chr10:26725694 | CTTAATA | C | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+1575_831+1580d others(8): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26725694 | ||||||
chr10:26725852 | G | A | 10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.831+1729G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725852 | |||||||
chr10:26725884 | T | G | 2 | a0001c0001t0001g0283 a0001c0001t0008g0282 |
2 | HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.831+1761T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725884 | |||||||
chr10:26725984 | C | A | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+1861C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26725984 | |||||||
chr10:26726066 | A | C | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+1943A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726066 | |||||||
chr10:26726262 | T | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(114): Show |
128 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.831+2139T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726262 | |||||||
chr10:26726436 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+2313A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726436 | |||||||
chr10:26726476 | C | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.831+2353C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726476 | |||||||
chr10:26726506 | T | C | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.831+2383T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726506 | |||||||
chr10:26726515 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.831+2392C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726515 | |||||||
chr10:26726673 | C | G | 1 | a0001c0001t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.831+2550C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726673 | |||||||
chr10:26726705 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+2582A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726705 | |||||||
chr10:26726783 | C | T | 1 | a0001c0001t0002g0360 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.831+2660C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726783 | |||||||
chr10:26726832 | C | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(151): Show |
168 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.831+2709C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726832 | |||||||
chr10:26726855 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.831+2732A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726855 | |||||||
chr10:26726949 | C | G | 1 | a0001c0001t0001g0309 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.831+2826C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26726949 | |||||||
chr10:26727059 | C | CA | 17 | a0001c0001t0001g0011 a0001c0001t0001g0083 a0001c0001t0001g0143 others(14): Show |
18 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.831+2946dupA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26727059 | ||||||
chr10:26727069 | AC | A | 254 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(251): Show |
280 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.831+2947delC | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727069 | |||||||
chr10:26727070 | C | A | 74 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(71): Show |
83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.831+2947C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727070 | |||||||
chr10:26727072 | A | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(90): Show |
105 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.831+2949A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727072 | |||||||
chr10:26727171 | T | C | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.831+3048T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727171 | |||||||
chr10:26727174 | T | C | 330 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(327): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.831+3051T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727174 | |||||||
chr10:26727324 | C | T | 24 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.831+3201C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727324 | |||||||
chr10:26727338 | CTCTT | C | 60 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(57): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.831+3217_831+3220d others(6): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26727338 | ||||||
chr10:26727340 | CT | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(98): Show |
113 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.831+3232delT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26727340 | ||||||
chr10:26727340 | CTTTT | C | 6 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+3229_831+3232d others(6): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26727340 | ||||||
chr10:26727342 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.831+3219T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727342 | |||||||
chr10:26727376 | G | C | 1 | a0001c0001t0002g0311 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.831+3253G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727376 | |||||||
chr10:26727485 | C | CT | 60 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(57): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.831+3377dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26727485 | ||||||
chr10:26727485 | CT | C | 12 | a0001c0001t0001g0060 a0001c0001t0001g0120 a0001c0001t0001g0193 others(9): Show |
12 | HG00639.hp2 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.831+3377delT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26727485 | ||||||
chr10:26727526 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.831+3403C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727526 | |||||||
chr10:26727552 | G | A | 5 | a0001c0001t0001g0325 a0002c0002t0001g0328 a0002c0002t0001g0330 others(2): Show |
5 | HG02559.hp2 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.831+3429G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727552 | |||||||
chr10:26727669 | C | CT | 13 | a0001c0001t0001g0011 a0001c0001t0001g0090 a0001c0001t0001g0143 others(10): Show |
14 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.831+3556dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26727669 | ||||||
chr10:26727916 | T | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0045 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.831+3793T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26727916 | |||||||
chr10:26728022 | C | T | 10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.831+3899C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728022 | |||||||
chr10:26728029 | A | G | 329 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(326): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.831+3906A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728029 | |||||||
chr10:26728029 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.831+3906A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728029 | |||||||
chr10:26728093 | C | T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(106): Show |
124 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.831+3970C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728093 | |||||||
chr10:26728263 | A | G | 330 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(327): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.831+4140A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728263 | |||||||
chr10:26728404 | T | G | 1 | a0001c0001t0001g0104 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.831+4281T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728404 | |||||||
chr10:26728772 | ATCTTTTT others(2): Show |
A | 10 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(7): Show |
11 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.831+4651_831+4659d others(11): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26728772 | ||||||
chr10:26728773 | TC | T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02965.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.831+4651delC | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728773 | |||||||
chr10:26728774 | C | CT | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(164): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.831+4673dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26728774 | ||||||
chr10:26728774 | C | CTT | 110 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(107): Show |
120 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.831+4672_831+4673d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26728774 | ||||||
chr10:26728774 | C | CTTT | 20 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0022 others(17): Show |
22 | HG01109.hp1 HG01123.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.831+4671_831+4673d others(5): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26728774 | ||||||
chr10:26728871 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0149 |
3 | HG02615.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.831+4748C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728871 | |||||||
chr10:26728895 | C | T | 6 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.831+4772C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26728895 | |||||||
chr10:26729137 | A | G | 5 | a0001c0001t0001g0189 a0001c0001t0001g0218 a0001c0001t0001g0220 others(2): Show |
5 | HG00609.hp1 HG02129.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+5014A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729137 | |||||||
chr10:26729186 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.831+5063C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729186 | |||||||
chr10:26729213 | G | T | 10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.831+5090G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729213 | |||||||
chr10:26729493 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.831+5370A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729493 | |||||||
chr10:26729550 | C | T | 14 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(11): Show |
17 | HG01123.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.831+5427C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729550 | |||||||
chr10:26729551 | G | A | 65 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(62): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.831+5428G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729551 | |||||||
chr10:26729558 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.831+5435A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729558 | |||||||
chr10:26729587 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0369 a0001c0001t0001g0371 |
4 | HG01106.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.831+5464T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729587 | |||||||
chr10:26729711 | T | G | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-5529T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729711 | |||||||
chr10:26729817 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.832-5423A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729817 | |||||||
chr10:26729841 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-5399A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729841 | |||||||
chr10:26729900 | GTTCCTTT others(4): Show |
G | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-5337_832-5327d others(13): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729900 | ||||||
chr10:26729904 | C | CT | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(104): Show |
115 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.832-5310dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729904 | ||||||
chr10:26729904 | C | CTT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0030 a0001c0001t0001g0038 others(13): Show |
16 | HG00408.hp1 HG00642.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.832-5311_832-5310d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729904 | ||||||
chr10:26729904 | CT | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0181 a0001c0001t0001g0243 others(9): Show |
12 | HG01243.hp1 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-5310delT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729904 | ||||||
chr10:26729904 | CTT | C | 30 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0112 others(27): Show |
30 | HG01928.hp2 HG02015.hp1 HG02273.hp2 others(27): Show |
intron_variant | MODIFIER | c.832-5311_832-5310d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729904 | ||||||
chr10:26729904 | CTTT | C | 107 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0013 others(104): Show |
120 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.832-5312_832-5310d others(5): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729904 | ||||||
chr10:26729904 | CTTTT | C | 13 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(10): Show |
13 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.832-5313_832-5310d others(6): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729904 | ||||||
chr10:26729904 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0332 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.832-5322_832-5310d others(15): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26729904 | ||||||
chr10:26729912 | T | G | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-5328T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729912 | |||||||
chr10:26729915 | T | C | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-5325T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729915 | |||||||
chr10:26729916 | T | A | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-5324T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729916 | |||||||
chr10:26729942 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.832-5298T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26729942 | |||||||
chr10:26730032 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.832-5208C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730032 | |||||||
chr10:26730048 | G | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-5192G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730048 | |||||||
chr10:26730073 | C | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-5167C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730073 | |||||||
chr10:26730086 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.832-5154G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730086 | |||||||
chr10:26730112 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.832-5128T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730112 | |||||||
chr10:26730113 | G | C | 1 | a0001c0001t0001g0301 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.832-5127G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730113 | |||||||
chr10:26730114 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.832-5126G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730114 | |||||||
chr10:26730159 | A | G | 331 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(328): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.832-5081A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730159 | |||||||
chr10:26730201 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.832-5039C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730201 | |||||||
chr10:26730203 | C | T | 24 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-5037C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730203 | |||||||
chr10:26730214 | G | C | 1 | a0001c0001t0001g0370 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.832-5026G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730214 | |||||||
chr10:26730267 | C | T | 10 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0100 others(7): Show |
10 | HG02027.hp2 HG02056.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.832-4973C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730267 | |||||||
chr10:26730284 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.832-4956C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730284 | |||||||
chr10:26730285 | G | A | 24 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0210 others(21): Show |
24 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-4955G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730285 | |||||||
chr10:26730487 | A | T | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-4753A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730487 | |||||||
chr10:26730601 | T | C | 61 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(58): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.832-4639T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730601 | |||||||
chr10:26730624 | TA | T | 59 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(56): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.832-4608delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26730624 | ||||||
chr10:26730649 | A | G | 47 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(44): Show |
55 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.832-4591A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730649 | |||||||
chr10:26730696 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.832-4544C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730696 | |||||||
chr10:26730723 | G | A | 2 | a0001c0001t0001g0345 a0001c0001t0001g0346 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.832-4517G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730723 | |||||||
chr10:26730916 | C | T | 1 | a0002c0002t0003g0329 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.832-4324C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730916 | |||||||
chr10:26730949 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0127 |
2 | HG03239.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.832-4291T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730949 | |||||||
chr10:26730961 | C | A | 32 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(29): Show |
34 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.832-4279C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730961 | |||||||
chr10:26730984 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.832-4256G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26730984 | |||||||
chr10:26731076 | A | G | 26 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
28 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.832-4164A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731076 | |||||||
chr10:26731082 | C | G | 26 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
28 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.832-4158C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731082 | |||||||
chr10:26731147 | G | C | 37 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(34): Show |
39 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-4093G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731147 | |||||||
chr10:26731173 | T | C | 1 | a0004c0005t0001g0340 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.832-4067T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731173 | |||||||
chr10:26731218 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.832-4022G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731218 | |||||||
chr10:26731233 | C | T | 37 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(34): Show |
39 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-4007C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731233 | |||||||
chr10:26731271 | G | C | 37 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(34): Show |
39 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.832-3969G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731271 | |||||||
chr10:26731290 | A | G | 1 | a0001c0001t0001g0346 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.832-3950A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731290 | |||||||
chr10:26731349 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.832-3891T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731349 | |||||||
chr10:26731397 | C | T | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-3843C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731397 | |||||||
chr10:26731480 | C | G | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-3760C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731480 | |||||||
chr10:26731496 | T | C | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-3744T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731496 | |||||||
chr10:26731527 | G | A | 4 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(1): Show |
4 | HG02145.hp1 HG03225.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-3713G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731527 | |||||||
chr10:26731639 | G | A | 329 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(326): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.832-3601G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731639 | |||||||
chr10:26731685 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.832-3555G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731685 | |||||||
chr10:26731691 | GT | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02965.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.832-3544delT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr10 | 26731691 | ||||||
chr10:26731693 | T | A | 1 | a0001c0001t0001g0334 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.832-3547T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731693 | |||||||
chr10:26731780 | T | G | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-3460T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731780 | |||||||
chr10:26731855 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.832-3385G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731855 | |||||||
chr10:26731937 | G | A | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-3303G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26731937 | |||||||
chr10:26732077 | C | T | 290 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.832-3163C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732077 | |||||||
chr10:26732149 | C | T | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-3091C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732149 | |||||||
chr10:26732328 | A | G | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG01433.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.832-2912A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732328 | |||||||
chr10:26732354 | C | T | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-2886C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732354 | |||||||
chr10:26732358 | C | T | 15 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(12): Show |
18 | HG01123.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.832-2882C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732358 | |||||||
chr10:26732515 | CTCCTGT | C | 38 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
40 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-2724_832-2719d others(8): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732515 | |||||||
chr10:26732522 | G | A | 38 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
40 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-2718G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732522 | |||||||
chr10:26732523 | T | G | 38 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
40 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-2717T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732523 | |||||||
chr10:26732524 | T | G | 38 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
40 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-2716T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732524 | |||||||
chr10:26732525 | G | A | 38 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
40 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-2715G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732525 | |||||||
chr10:26732636 | T | C | 38 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
40 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-2604T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732636 | |||||||
chr10:26732671 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.832-2569C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732671 | |||||||
chr10:26732693 | G | A | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
24 | HG00735.hp2 HG01099.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-2547G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732693 | |||||||
chr10:26732699 | A | G | 38 | a0001c0001t0001g0011 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
40 | HG00735.hp2 HG01099.hp2 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.832-2541A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732699 | |||||||
chr10:26732896 | G | A | 292 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(289): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.832-2344G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732896 | |||||||
chr10:26732996 | G | A | 6 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(3): Show |
7 | HG01074.hp1 HG01099.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.832-2244G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26732996 | |||||||
chr10:26733048 | G | A | 4 | a0001c0001t0004g0238 a0001c0001t0004g0239 a0001c0001t0004g0240 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.832-2192G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733048 | |||||||
chr10:26733217 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.832-2023G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733217 | |||||||
chr10:26733429 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(11): Show |
15 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.832-1811G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733429 | |||||||
chr10:26733435 | G | C | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.832-1805G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733435 | |||||||
chr10:26733752 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(12): Show |
16 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.832-1488G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733752 | |||||||
chr10:26733758 | G | A | 1 | a0001c0001t0002g0313 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.832-1482G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733758 | |||||||
chr10:26733826 | T | C | 150 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(147): Show |
170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.832-1414T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733826 | |||||||
chr10:26733895 | G | A | 6 | a0001c0001t0001g0112 a0001c0001t0001g0209 a0001c0001t0001g0256 others(3): Show |
6 | HG02602.hp1 HG03688.hp2 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.832-1345G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733895 | |||||||
chr10:26733974 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.832-1266T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26733974 | |||||||
chr10:26734261 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.832-979C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734261 | |||||||
chr10:26734262 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.832-978G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734262 | |||||||
chr10:26734294 | C | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
12 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.832-946C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734294 | |||||||
chr10:26734473 | G | A | 75 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(72): Show |
78 | HG00558.hp2 HG00741.hp2 HG01123.hp2 others(75): Show |
intron_variant | MODIFIER | c.832-767G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734473 | |||||||
chr10:26734506 | C | G | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.832-734C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734506 | |||||||
chr10:26734553 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.832-687T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734553 | |||||||
chr10:26734648 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.832-592C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734648 | |||||||
chr10:26734651 | T | C | 3 | a0001c0001t0001g0334 a0002c0002t0001g0328 a0002c0002t0001g0330 |
3 | HG03195.hp1 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.832-589T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734651 | |||||||
chr10:26734847 | G | A | 24 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0109 others(21): Show |
24 | HG00597.hp1 HG02027.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.832-393G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734847 | |||||||
chr10:26734953 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0132 others(6): Show |
11 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.832-287T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26734953 | |||||||
chr10:26735132 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.832-108A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26735132 | |||||||
chr10:26735144 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.832-96C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 8/11 | chr10 | 26735144 | |||||||
chr10:26735371 | A | G | 4 | a0001c0001t0003g0023 a0001c0001t0005g0251 a0001c0001t0005g0362 others(1): Show |
5 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.912+51A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 9/11 | chr10 | 26735371 | |||||||
chr10:26735391 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.912+71C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 9/11 | chr10 | 26735391 | |||||||
chr10:26735394 | C | A | 1 | a0001c0001t0001g0039 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.913-72C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 9/11 | chr10 | 26735394 | |||||||
chr10:26735781 | G | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(254): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1026+202G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26735781 | |||||||
chr10:26735888 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0247 |
2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1026+309G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26735888 | |||||||
chr10:26736112 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1026+533G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26736112 | |||||||
chr10:26736190 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0235 |
2 | HG02148.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1026+611A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26736190 | |||||||
chr10:26736214 | G | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0237 |
3 | HG02015.hp2 NA18941.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.1026+635G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26736214 | |||||||
chr10:26736730 | A | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(266): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1026+1151A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26736730 | |||||||
chr10:26737033 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1026+1454G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737033 | |||||||
chr10:26737638 | A | G | 3 | a0001c0001t0005g0251 a0001c0001t0005g0362 a0001c0001t0005g0374 |
3 | HG02109.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1026+2059A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737638 | |||||||
chr10:26737657 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1026+2078G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737657 | |||||||
chr10:26737680 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0044 |
3 | HG01168.hp2 HG01256.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1026+2101G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737680 | |||||||
chr10:26737717 | C | T | 1 | a0001c0001t0004g0335 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1026+2138C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737717 | |||||||
chr10:26737722 | C | CA | 29 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0039 others(26): Show |
31 | HG00735.hp1 HG01106.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1026+2172dupA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CA | C | 45 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0050 others(42): Show |
52 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1026+2172delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAA | C | 15 | a0001c0001t0001g0244 a0001c0001t0001g0246 a0001c0001t0001g0248 others(12): Show |
15 | HG01243.hp1 HG02300.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026+2171_1026+217 others(6): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAAA | C | 8 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0108 others(5): Show |
8 | HG00544.hp1 HG02083.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1026+2170_1026+217 others(7): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAAAA | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(61): Show |
69 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1026+2169_1026+217 others(8): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAAAAA | C | 15 | a0001c0001t0001g0089 a0001c0001t0001g0112 a0001c0001t0001g0209 others(12): Show |
15 | HG01358.hp2 HG02015.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1026+2168_1026+217 others(9): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAAAAAA | C | 20 | a0001c0001t0001g0156 a0001c0001t0001g0171 a0001c0001t0001g0210 others(17): Show |
20 | HG02015.hp1 HG02135.hp1 HG02273.hp2 others(17): Show |
intron_variant | MODIFIER | c.1026+2167_1026+217 others(10): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAAAAAAA others(6): Show |
C | 8 | a0001c0001t0001g0101 a0001c0001t0001g0106 a0001c0001t0001g0162 others(5): Show |
8 | HG01891.hp2 HG02074.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1026+2160_1026+217 others(17): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAAAAAAA others(7): Show |
C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(72): Show |
85 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1026+2159_1026+217 others(18): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737722 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1026+2158_1026+217 others(19): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26737722 | ||||||
chr10:26737753 | G | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0154 a0001c0001t0001g0155 others(1): Show |
4 | HG02602.hp1 HG02965.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1026+2174G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737753 | |||||||
chr10:26737796 | T | C | 3 | a0001c0001t0001g0334 a0002c0002t0001g0328 a0002c0002t0001g0330 |
3 | HG03195.hp1 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1026+2217T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737796 | |||||||
chr10:26737821 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026+2242G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737821 | |||||||
chr10:26737995 | C | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+2416C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26737995 | |||||||
chr10:26738018 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1026+2439A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738018 | |||||||
chr10:26738188 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0231 |
3 | HG00408.hp2 NA18991.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1026+2609G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738188 | |||||||
chr10:26738470 | G | A | 10 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1026+2891G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738470 | |||||||
chr10:26738663 | G | A | 1 | a0002c0002t0001g0326 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1026+3084G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738663 | |||||||
chr10:26738679 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1026+3100C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738679 | |||||||
chr10:26738878 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1026+3299G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738878 | |||||||
chr10:26738889 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1026+3310C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738889 | |||||||
chr10:26738890 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1026+3311G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738890 | |||||||
chr10:26738920 | T | G | 1 | a0001c0001t0001g0278 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1026+3341T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26738920 | |||||||
chr10:26739201 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1027-3296G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739201 | |||||||
chr10:26739220 | C | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(105): Show |
113 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1027-3277C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739220 | |||||||
chr10:26739270 | G | A | 3 | a0001c0001t0001g0334 a0002c0002t0001g0328 a0002c0002t0001g0330 |
3 | HG03195.hp1 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1027-3227G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739270 | |||||||
chr10:26739604 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1027-2893T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739604 | |||||||
chr10:26739618 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1027-2879C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739618 | |||||||
chr10:26739643 | G | A | 8 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0316 others(5): Show |
8 | HG01358.hp2 HG02257.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-2854G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739643 | |||||||
chr10:26739758 | C | G | 1 | a0001c0001t0001g0040 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1027-2739C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739758 | |||||||
chr10:26739875 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1027-2622G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26739875 | |||||||
chr10:26740078 | G | C | 7 | a0001c0001t0001g0029 a0001c0001t0001g0309 a0001c0001t0001g0363 others(4): Show |
8 | HG02109.hp2 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-2419G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740078 | |||||||
chr10:26740086 | C | CA | 8 | a0001c0001t0001g0083 a0001c0001t0001g0100 a0001c0001t0001g0105 others(5): Show |
8 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1027-2410dupA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26740086 | ||||||
chr10:26740141 | C | CA | 31 | a0001c0001t0001g0067 a0001c0001t0001g0089 a0001c0001t0001g0151 others(28): Show |
31 | HG01243.hp1 HG01358.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.1027-2338dupA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26740141 | ||||||
chr10:26740141 | CA | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(95): Show |
103 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1027-2338delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26740141 | ||||||
chr10:26740160 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1027-2337T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740160 | |||||||
chr10:26740161 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1027-2336T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740161 | |||||||
chr10:26740196 | C | A | 4 | a0001c0001t0001g0124 a0001c0001t0001g0132 a0001c0001t0001g0139 others(1): Show |
4 | HG00642.hp2 HG01069.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1027-2301C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740196 | |||||||
chr10:26740201 | C | T | 1 | a0001c0001t0003g0023 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1027-2296C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740201 | |||||||
chr10:26740319 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0247 |
2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1027-2178C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740319 | |||||||
chr10:26740480 | T | A | 3 | a0001c0001t0005g0251 a0001c0001t0005g0362 a0001c0001t0005g0374 |
3 | HG02109.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1027-2017T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740480 | |||||||
chr10:26740559 | C | T | 2 | a0001c0001t0001g0259 a0004c0005t0001g0340 |
2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1027-1938C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740559 | |||||||
chr10:26740591 | T | C | 1 | a0001c0001t0002g0358 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1027-1906T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740591 | |||||||
chr10:26740977 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1027-1520C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740977 | |||||||
chr10:26740996 | A | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0148 others(1): Show |
4 | HG02280.hp2 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-1501A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26740996 | |||||||
chr10:26741109 | A | G | 106 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0014 others(103): Show |
113 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1027-1388A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741109 | |||||||
chr10:26741110 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1027-1387G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741110 | |||||||
chr10:26741211 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1027-1286G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741211 | |||||||
chr10:26741213 | G | A | 1 | a0001c0001t0001g0334 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1027-1284G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741213 | |||||||
chr10:26741275 | A | G | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(227): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.1027-1222A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741275 | |||||||
chr10:26741352 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1027-1145C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741352 | |||||||
chr10:26741431 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1027-1066C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741431 | |||||||
chr10:26741471 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0231 |
3 | HG00408.hp2 NA18991.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1027-1026G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741471 | |||||||
chr10:26741496 | G | GA | 4 | a0001c0001t0001g0058 a0001c0001t0001g0176 a0001c0001t0002g0347 others(1): Show |
4 | HG02074.hp1 NA18940.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-996dupA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26741496 | ||||||
chr10:26741501 | AC | A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(36): Show |
44 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.1027-995delC | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741501 | |||||||
chr10:26741502 | C | A | 172 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(169): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1027-995C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741502 | |||||||
chr10:26741578 | C | G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0063 others(32): Show |
37 | HG00438.hp1 HG00609.hp2 HG02015.hp1 others(34): Show |
intron_variant | MODIFIER | c.1027-919C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741578 | |||||||
chr10:26741626 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1027-871A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741626 | |||||||
chr10:26741641 | T | C | 3 | a0001c0001t0005g0251 a0001c0001t0005g0362 a0001c0001t0005g0374 |
3 | HG02109.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1027-856T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741641 | |||||||
chr10:26741719 | T | G | 36 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0063 others(33): Show |
38 | HG00438.hp1 HG00609.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.1027-778T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741719 | |||||||
chr10:26741852 | G | A | 4 | a0001c0001t0001g0324 a0001c0001t0005g0251 a0001c0001t0005g0362 others(1): Show |
4 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1027-645G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741852 | |||||||
chr10:26741911 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1027-586G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741911 | |||||||
chr10:26741922 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0108 |
2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1027-575T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741922 | |||||||
chr10:26741940 | T | C | 56 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0083 others(53): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1027-557T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741940 | |||||||
chr10:26741944 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1027-553G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26741944 | |||||||
chr10:26742001 | G | A | 31 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0071 others(28): Show |
31 | HG01243.hp2 HG01346.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1027-496G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26742001 | |||||||
chr10:26742101 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1027-396T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26742101 | |||||||
chr10:26742160 | T | A | 27 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0071 others(24): Show |
27 | HG01243.hp2 HG01346.hp1 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.1027-337T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26742160 | |||||||
chr10:26742223 | TA | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(143): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1027-272delA | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26742223 | ||||||
chr10:26742285 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(244): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1027-212A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26742285 | |||||||
chr10:26742456 | A | C | 1 | a0001c0001t0001g0344 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1027-41A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26742456 | |||||||
chr10:26742463 | AGATT | A | 39 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(36): Show |
43 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1027-33_1027-30del others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | chr10 | 26742463 | |||||||
chr10:26742484 | CTT | C | 3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0312 |
5 | NA18957.hp2 NA18964.hp1 NA18965.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1027-7_1027-6delTT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr10 | 26742484 | ||||||
chr10:26742594 | A | T | 4 | a0001c0001t0001g0063 a0001c0001t0005g0251 a0001c0001t0005g0362 others(1): Show |
4 | HG00438.hp1 HG02109.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107+17A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26742594 | |||||||
chr10:26742602 | G | C | 7 | a0001c0001t0003g0023 a0001c0001t0003g0036 a0001c0001t0003g0146 others(4): Show |
8 | HG01099.hp2 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1107+25G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26742602 | |||||||
chr10:26742619 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 |
3 | HG01891.hp1 HG02451.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1107+42C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26742619 | |||||||
chr10:26742745 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0309 a0001c0001t0001g0363 others(4): Show |
8 | HG02109.hp2 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1107+168A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26742745 | |||||||
chr10:26742795 | C | CT | 30 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0071 others(27): Show |
30 | HG01243.hp2 HG01346.hp1 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.1107+220dupT | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26742795 | ||||||
chr10:26742815 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1107+238T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26742815 | |||||||
chr10:26742823 | T | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0171 others(2): Show |
5 | HG02015.hp2 NA18941.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107+246T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26742823 | |||||||
chr10:26743022 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1107+445T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26743022 | |||||||
chr10:26743078 | CAAT | C | 4 | a0002c0002t0001g0006 a0002c0002t0001g0028 a0002c0002t0001g0326 others(1): Show |
7 | HG01123.hp2 HG02055.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1107+504_1107+506d others(5): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26743078 | ||||||
chr10:26743099 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1107+522C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26743099 | |||||||
chr10:26743318 | G | C | 1 | a0001c0001t0001g0286 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1107+741G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26743318 | |||||||
chr10:26743386 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1107+809A>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26743386 | |||||||
chr10:26743533 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0363 a0001c0001t0001g0365 others(3): Show |
7 | HG02109.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1107+956G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26743533 | |||||||
chr10:26743902 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1107+1325A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26743902 | |||||||
chr10:26743910 | A | ACT | 29 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0071 others(26): Show |
29 | HG01243.hp2 HG01346.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1107+1334_1107+133 others(6): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26743910 | ||||||
chr10:26744041 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1107+1464G>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744041 | |||||||
chr10:26744179 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1107+1602C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744179 | |||||||
chr10:26744264 | G | A | 203 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(200): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.1107+1687G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744264 | |||||||
chr10:26744319 | TCACCA | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0198 others(1): Show |
4 | HG01099.hp1 HG01433.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1107+1746_1107+175 others(9): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26744319 | ||||||
chr10:26744360 | CTATTT | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(44): Show |
53 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.1107+1795_1107+179 others(9): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26744360 | ||||||
chr10:26744374 | T | TTTTA | 16 | a0001c0001t0001g0110 a0001c0001t0002g0001 a0001c0001t0002g0347 others(13): Show |
21 | HG00597.hp2 HG01069.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1107+1801_1107+180 others(8): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26744374 | ||||||
chr10:26744485 | G | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0171 others(2): Show |
5 | HG02015.hp2 NA18941.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108-1848G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744485 | |||||||
chr10:26744539 | C | T | 26 | a0001c0001t0001g0057 a0001c0001t0001g0069 a0001c0001t0001g0071 others(23): Show |
26 | HG01243.hp2 HG01346.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.1108-1794C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744539 | |||||||
chr10:26744547 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0284 |
2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1108-1786C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744547 | |||||||
chr10:26744639 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1108-1694G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744639 | |||||||
chr10:26744710 | T | G | 42 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(39): Show |
46 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1108-1623T>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744710 | |||||||
chr10:26744743 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1108-1590A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744743 | |||||||
chr10:26744885 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0198 others(1): Show |
4 | HG01099.hp1 HG01433.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108-1448C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744885 | |||||||
chr10:26744911 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0369 a0001c0001t0001g0371 |
4 | HG01106.hp2 HG01884.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-1422C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744911 | |||||||
chr10:26744941 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1108-1392A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744941 | |||||||
chr10:26744991 | C | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0363 a0001c0001t0001g0365 others(4): Show |
8 | HG01123.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-1342C>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26744991 | |||||||
chr10:26745021 | A | G | 56 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0083 others(53): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.1108-1312A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745021 | |||||||
chr10:26745036 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0363 a0001c0001t0001g0365 others(4): Show |
8 | HG01123.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-1297C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745036 | |||||||
chr10:26745037 | G | A | 7 | a0001c0001t0001g0083 a0001c0001t0001g0100 a0001c0001t0001g0109 others(4): Show |
7 | HG02027.hp2 HG02056.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.1108-1296G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745037 | |||||||
chr10:26745118 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1108-1215C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745118 | |||||||
chr10:26745120 | C | T | 6 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0248 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-1213C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745120 | |||||||
chr10:26745143 | G | A | 1 | a0001c0001t0001g0364 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1108-1190G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745143 | |||||||
chr10:26745174 | T | A | 3 | a0001c0001t0005g0251 a0001c0001t0005g0362 a0001c0001t0005g0374 |
3 | HG02109.hp1 HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1108-1159T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745174 | |||||||
chr10:26745232 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1108-1101T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745232 | |||||||
chr10:26745295 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(51): Show |
60 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1108-1038T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745295 | |||||||
chr10:26745318 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(99): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1108-1015T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745318 | |||||||
chr10:26745339 | T | C | 5 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0171 others(2): Show |
5 | HG02015.hp2 NA18941.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108-994T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745339 | |||||||
chr10:26745372 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0324 |
2 | HG03225.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1108-961A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745372 | |||||||
chr10:26745391 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(244): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.1108-942A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745391 | |||||||
chr10:26745393 | A | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(34): Show |
42 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1108-940A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745393 | |||||||
chr10:26745433 | A | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(39): Show |
46 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1108-900A>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745433 | |||||||
chr10:26745444 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1108-889A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745444 | |||||||
chr10:26745480 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1108-853G>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745480 | |||||||
chr10:26745574 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0363 a0001c0001t0001g0365 others(4): Show |
8 | HG01123.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-759C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745574 | |||||||
chr10:26745662 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1108-671C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745662 | |||||||
chr10:26745673 | C | A | 1 | a0001c0001t0001g0324 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1108-660C>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745673 | |||||||
chr10:26745691 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1108-642A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745691 | |||||||
chr10:26745771 | C | T | 40 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0063 others(37): Show |
42 | HG00438.hp1 HG02015.hp1 HG02015.hp2 others(39): Show |
intron_variant | MODIFIER | c.1108-562C>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745771 | |||||||
chr10:26745791 | G | T | 1 | a0001c0001t0001g0276 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1108-542G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745791 | |||||||
chr10:26745845 | C | CAA | 8 | a0001c0001t0001g0083 a0001c0001t0001g0100 a0001c0001t0001g0109 others(5): Show |
8 | HG00597.hp2 HG02027.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.1108-480_1108-479d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26745845 | ||||||
chr10:26745854 | A | G | 5 | a0001c0001t0001g0089 a0001c0001t0001g0156 a0001c0001t0001g0171 others(2): Show |
5 | HG02015.hp2 NA18941.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108-479A>G | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745854 | |||||||
chr10:26745862 | GAA | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0082 a0001c0001t0001g0293 others(2): Show |
6 | NA18944.hp1 NA18971.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1108-462_1108-461d others(4): Show |
PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr10 | 26745862 | ||||||
chr10:26745876 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0008g0282 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1108-457T>A | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745876 | |||||||
chr10:26745973 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1108-360G>T | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745973 | |||||||
chr10:26745989 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1108-344T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26745989 | |||||||
chr10:26746330 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02056.hp2 | splice_region_variant&intron_variant | LOW | c.1108-3T>C | PDSS1 | ENSG00000148459.16 | transcript | ENST00000376215.10 | protein_coding | 11/11 | chr10 | 26746330 |