Item | Value |
---|---|
geneid | 55748 |
ensemblid | ENSG00000133313.15 |
hgncid | 24437 |
symbol | CNDP2 |
name | carnosine dipeptidase 2 |
refseq_nuc | NM_018235.3 |
refseq_prot | NP_060705.2 |
ensembl_nuc | ENST00000324262.9 |
ensembl_prot | ENSP00000325548.4 |
mane_status | MANE Select |
chr | chr18 |
start | 74496363 |
end | 74523454 |
strand | + |
ver | v1.2 |
region | chr18:74496363-74523454 |
region5000 | chr18:74491363-74528454 |
regionname0 | CNDP2_chr18_74496363_74523454 |
regionname5000 | CNDP2_chr18_74491363_74528454 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 475 | 313 | 82 | 56 | 124 | 16 | 33 | 91 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0002 | 0/0 | 475 | 95 | 9 | 24 | 49 | 2 | 11 | 39 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0003 | 0/0 | 475 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0004 | 0/0 | 475 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0005 | 0/0 | 475 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0006 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0007 | 0/0 | 475 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0008 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0009 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0010 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
a0011 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | MAALT others(470): Show |
chr18 | 74491363 | 74528454 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1425 | 286 | 62 | 55 | 121 | 16 | 30 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0001c0003 | 0/0 | 1425 | 19 | 15 | 1 | 1 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0001c0005 | 0/0 | 1425 | 3 | 3 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0001c0009 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0001c0016 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0001c0017 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0001c0020 | 0/0 | 1425 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0002c0002 | 0/0 | 1425 | 88 | 9 | 23 | 44 | 2 | 10 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0002c0006 | 0/0 | 1425 | 3 | 0 | 1 | 1 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0002c0007 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0002c0008 | 0/0 | 1425 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0003c0004 | 0/0 | 1425 | 8 | 8 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0004c0018 | 0/0 | 1425 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0005c0011 | 0/0 | 1425 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0006c0019 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0007c0012 | 0/0 | 1425 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0008c0015 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0009c0010 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0010c0013 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 | ||
a0011c0014 | 0/0 | 1425 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | ATGGC others(1420): Show |
chr18 | 74491363 | 74528454 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4974 | 174 | 21 | 34 | 91 | 10 | 17 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0002 | 0/0 | 4974 | 18 | 11 | 3 | 0 | 0 | 4 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0003 | 0/0 | 4974 | 15 | 3 | 7 | 0 | 3 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0004 | 0/0 | 4975 | 10 | 0 | 0 | 10 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0005 | 0/0 | 4975 | 3 | 3 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0006 | 0/0 | 4975 | 3 | 3 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0007 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0008 | 0/0 | 4974 | 7 | 7 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0009 | 0/0 | 4974 | 4 | 4 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0010 | 0/0 | 4974 | 2 | 0 | 1 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0011 | 0/0 | 4974 | 6 | 0 | 4 | 0 | 1 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0012 | 1/0 | 4975 | 5 | 3 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0013 | 0/0 | 4974 | 5 | 0 | 0 | 5 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0014 | 0/0 | 4974 | 4 | 0 | 0 | 4 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0015 | 0/0 | 4974 | 2 | 0 | 0 | 0 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0016 | 0/0 | 4974 | 2 | 0 | 0 | 0 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0017 | 0/0 | 4974 | 2 | 1 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0018 | 0/0 | 4974 | 2 | 1 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0019 | 0/0 | 4974 | 2 | 0 | 0 | 1 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0020 | 0/0 | 4974 | 2 | 0 | 2 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0024 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0025 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0026 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0027 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0028 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0029 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0030 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0032 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0033 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0034 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0035 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0036 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0037 | 0/0 | 4975 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0038 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0042 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0046 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0001t0049 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0003t0002 | 0/0 | 4974 | 8 | 6 | 0 | 1 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0003t0006 | 0/0 | 4975 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0001c0003t0007 | 0/0 | 4974 | 4 | 3 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0003t0009 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0003t0021 | 0/0 | 4974 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0003t0023 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0003t0048 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0005t0002 | 0/0 | 4974 | 3 | 3 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0009t0001 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0016t0009 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0017t0002 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0001c0020t0031 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0001 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0002 | 0/0 | 4974 | 67 | 3 | 17 | 40 | 1 | 6 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0006 | 0/0 | 4975 | 4 | 3 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0007 | 0/0 | 4974 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0010 | 0/0 | 4974 | 5 | 0 | 4 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0022 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0039 | 0/0 | 4975 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0040 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0041 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0043 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0044 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0045 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0002t0047 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0006t0002 | 0/0 | 4974 | 2 | 0 | 0 | 1 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0006t0003 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0007t0002 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0002c0008t0001 | 0/0 | 4974 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0003c0004t0005 | 0/0 | 4975 | 7 | 7 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0003c0004t0009 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0004c0018t0001 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0005c0011t0002 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0006c0019t0001 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0007c0012t0007 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0008c0015t0004 | 0/0 | 4975 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4970): Show |
chr18 | 74491363 | 74528454 |
a0009c0010t0001 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0010c0013t0002 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
a0011c0014t0001 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | CGTGG others(4969): Show |
chr18 | 74491363 | 74528454 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 0 | 1 | 13 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0002 | 0/0 | 13 | 2 | 6 | 1 | 3 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0014 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0059 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0004g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0008g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0008g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0010g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0011g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0011g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0011g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0011g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0011g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0011g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0012g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0012g0176 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0012g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0013g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0013g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0013g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0014g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0014g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0014g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0015g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0015g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0016g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0017g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0017g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0018g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0018g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0019g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0019g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0020g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0024g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0025g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0026g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0027g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0028g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0029g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0030g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0032g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0033g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0034g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0035g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0036g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0037g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0038g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0042g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0046g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0001t0049g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0006g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0021g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0023g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0003t0048g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0005t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0005t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0009t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0016t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0017t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0001c0020t0031g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0003 | 0/0 | 8 | 0 | 4 | 2 | 0 | 2 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0005 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0007g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0010g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0010g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0010g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0022g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0022g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0039g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0040g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0041g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0043g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0044g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0045g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0002t0047g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0006t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0006t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0006t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0007t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0007t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0002c0008t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0003c0004t0005g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0003c0004t0005g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0003c0004t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0003c0004t0009g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0004c0018t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0005c0011t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0006c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0007c0012t0007g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0008c0015t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0009c0010t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0010c0013t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
a0011c0014t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | GBR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00280 | hp2 | a0001 | c0001 | t0029 | g0157 | EUR | FIN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00323 | hp1 | a0002 | c0002 | t0010 | g0085 | EUR | FIN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00408 | hp1 | a0001 | c0001 | t0033 | g0004 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00408 | hp2 | a0001 | c0009 | t0001 | g0007 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00544 | hp2 | a0001 | c0001 | t0014 | g0197 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00558 | hp1 | a0001 | c0001 | t0025 | g0007 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00639 | hp1 | a0001 | c0001 | t0011 | g0224 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0075 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00673 | hp1 | a0001 | c0001 | t0027 | g0016 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0155 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01069 | hp1 | a0002 | c0002 | t0010 | g0003 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01074 | hp1 | a0001 | c0003 | t0007 | g0123 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01099 | hp1 | a0001 | c0001 | t0011 | g0215 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0012 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01109 | hp2 | a0002 | c0002 | t0045 | g0137 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01167 | hp1 | a0001 | c0001 | t0012 | g0188 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0222 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01243 | hp1 | a0001 | c0001 | t0038 | g0148 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0012 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01255 | hp2 | a0002 | c0002 | t0039 | g0065 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01256 | hp1 | a0002 | c0002 | t0010 | g0134 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01257 | hp2 | a0001 | c0001 | t0020 | g0050 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01258 | hp1 | a0001 | c0001 | t0020 | g0050 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0107 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01261 | hp2 | a0001 | c0001 | t0028 | g0160 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01346 | hp1 | a0001 | c0001 | t0011 | g0165 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01361 | hp2 | a0002 | c0006 | t0003 | g0277 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01515 | hp1 | a0001 | c0001 | t0049 | g0015 | EUR | IBS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0171 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01891 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0236 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01934 | hp1 | a0004 | c0018 | t0001 | g0004 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0099 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01952 | hp2 | a0005 | c0011 | t0002 | g0003 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01975 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01978 | hp1 | a0002 | c0002 | t0002 | g0131 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01981 | hp1 | a0001 | c0001 | t0017 | g0186 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0129 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02027 | hp1 | a0006 | c0019 | t0001 | g0001 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0030 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02040 | hp2 | a0001 | c0009 | t0001 | g0007 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02055 | hp1 | a0003 | c0004 | t0005 | g0008 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02129 | hp1 | a0001 | c0001 | t0014 | g0285 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0248 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0154 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02148 | hp1 | a0002 | c0002 | t0010 | g0003 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02155 | hp1 | a0001 | c0001 | t0035 | g0284 | EAS | CDX | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02165 | hp1 | a0001 | c0001 | t0014 | g0016 | EAS | CDX | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0249 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02258 | hp1 | a0001 | c0001 | t0012 | g0141 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02258 | hp2 | a0001 | c0003 | t0006 | g0046 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02280 | hp2 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02300 | hp1 | a0002 | c0002 | t0010 | g0003 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02451 | hp2 | a0001 | c0001 | t0018 | g0175 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | KHV | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02572 | hp1 | a0001 | c0001 | t0008 | g0238 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02572 | hp2 | a0001 | c0017 | t0002 | g0073 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02622 | hp2 | a0003 | c0004 | t0005 | g0008 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02630 | hp2 | a0001 | c0001 | t0037 | g0070 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02647 | hp1 | a0002 | c0002 | t0006 | g0102 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02647 | hp2 | a0002 | c0002 | t0006 | g0139 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02683 | hp1 | a0001 | c0001 | t0016 | g0013 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0108 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0098 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0068 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02723 | hp2 | a0001 | c0005 | t0002 | g0047 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02735 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02738 | hp1 | a0001 | c0001 | t0019 | g0201 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02738 | hp2 | a0002 | c0002 | t0043 | g0033 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02809 | hp1 | a0007 | c0012 | t0007 | g0045 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02818 | hp1 | a0001 | c0003 | t0007 | g0045 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02886 | hp1 | a0001 | c0005 | t0002 | g0047 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02886 | hp2 | a0001 | c0003 | t0007 | g0191 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02895 | hp1 | a0001 | c0003 | t0002 | g0194 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02896 | hp1 | a0001 | c0003 | t0021 | g0036 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02896 | hp2 | a0001 | c0001 | t0008 | g0246 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02897 | hp1 | a0001 | c0003 | t0021 | g0036 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02922 | hp1 | a0001 | c0001 | t0034 | g0185 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0168 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02965 | hp2 | a0001 | c0001 | t0012 | g0271 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0170 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02970 | hp2 | a0003 | c0004 | t0005 | g0008 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02976 | hp2 | a0001 | c0003 | t0002 | g0122 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03041 | hp2 | a0001 | c0003 | t0007 | g0138 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03098 | hp1 | a0003 | c0004 | t0005 | g0078 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03098 | hp2 | a0002 | c0002 | t0007 | g0119 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03130 | hp1 | a0003 | c0004 | t0005 | g0029 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03130 | hp2 | a0001 | c0001 | t0046 | g0077 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03139 | hp1 | a0001 | c0003 | t0002 | g0195 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03139 | hp2 | a0003 | c0004 | t0005 | g0008 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03195 | hp2 | a0002 | c0002 | t0007 | g0121 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0037 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03209 | hp2 | a0002 | c0002 | t0040 | g0140 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0074 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03239 | hp1 | a0001 | c0001 | t0011 | g0166 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03239 | hp2 | a0002 | c0002 | t0047 | g0101 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03453 | hp2 | a0002 | c0002 | t0006 | g0120 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03486 | hp1 | a0001 | c0003 | t0002 | g0192 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03486 | hp2 | a0001 | c0001 | t0042 | g0082 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03516 | hp1 | a0001 | c0003 | t0023 | g0037 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0174 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0028 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03579 | hp2 | a0001 | c0005 | t0002 | g0069 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03654 | hp2 | a0001 | c0003 | t0048 | g0152 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03669 | hp1 | a0001 | c0001 | t0015 | g0245 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03669 | hp2 | a0001 | c0001 | t0016 | g0013 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03688 | hp1 | a0001 | c0001 | t0015 | g0244 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03704 | hp1 | a0002 | c0006 | t0002 | g0066 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03710 | hp1 | a0002 | c0002 | t0044 | g0083 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0153 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0151 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04184 | hp1 | a0001 | c0020 | t0031 | g0189 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0067 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG04228 | hp2 | a0001 | c0001 | t0010 | g0064 | SAS | STU | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18522 | hp2 | a0001 | c0001 | t0017 | g0273 | AFR | YRI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | CHB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | CHB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18906 | hp1 | a0003 | c0004 | t0005 | g0029 | AFR | YRI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18940 | hp1 | a0001 | c0001 | t0032 | g0233 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18941 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18943 | hp2 | a0002 | c0002 | t0041 | g0032 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18954 | hp1 | a0002 | c0002 | t0006 | g0112 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0103 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18957 | hp1 | a0001 | c0001 | t0019 | g0052 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18961 | hp2 | a0001 | c0001 | t0013 | g0207 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18968 | hp2 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18969 | hp1 | a0001 | c0001 | t0014 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18969 | hp2 | a0001 | c0001 | t0013 | g0049 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18974 | hp2 | a0001 | c0001 | t0036 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18978 | hp2 | a0001 | c0001 | t0013 | g0211 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18979 | hp2 | a0002 | c0002 | t0022 | g0127 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18980 | hp1 | a0001 | c0001 | t0018 | g0251 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18984 | hp2 | a0001 | c0001 | t0024 | g0221 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18985 | hp1 | a0002 | c0008 | t0001 | g0056 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18987 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18987 | hp2 | a0008 | c0015 | t0004 | g0254 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18988 | hp1 | a0001 | c0003 | t0002 | g0116 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18992 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18995 | hp2 | a0001 | c0001 | t0030 | g0016 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18999 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19000 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19001 | hp1 | a0002 | c0006 | t0002 | g0081 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19002 | hp1 | a0002 | c0002 | t0022 | g0005 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19007 | hp2 | a0009 | c0010 | t0001 | g0227 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | LWK | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0259 | AFR | LWK | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19043 | hp2 | a0001 | c0003 | t0006 | g0046 | AFR | LWK | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19060 | hp2 | a0010 | c0013 | t0002 | g0124 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19063 | hp1 | a0011 | c0014 | t0001 | g0184 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19066 | hp1 | a0001 | c0001 | t0026 | g0002 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19074 | hp2 | a0002 | c0008 | t0001 | g0056 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19081 | hp1 | a0002 | c0007 | t0002 | g0136 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0058 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19089 | hp2 | a0002 | c0007 | t0002 | g0100 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | YRI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ASW | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20129 | hp2 | a0001 | c0003 | t0009 | g0061 | AFR | ASW | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0096 | EUR | TSI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | TSI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20805 | hp2 | a0001 | c0001 | t0011 | g0205 | EUR | TSI | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | GIH | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | GIH | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0109 | AMR | CLM | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02109 | hp2 | a0001 | c0016 | t0009 | g0072 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | MSL | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | USA | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA21309 | hp1 | a0003 | c0004 | t0009 | g0079 | AFR | LWK | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | LWK | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0203 | REF | REF | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0176 | REF | REF | CNDP2_chr18_74491363_74528454 | CNDP2 | chr18 | 74491363 | 74528454 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:74501359 | G | A | 1 | a0009 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.91G>A | p.Val31Met | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/12 | 252/4975 | 91/1428 | 31/475 | chr18 | 74501359 | |||
chr18:74505891 | G | T | 1 | a0006 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.247G>T | p.Gly83Cys | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/12 | 408/4975 | 247/1428 | 83/475 | chr18 | 74505891 | |||
chr18:74505904 | C | T | 1 | a0010 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.260C>T | p.Ser87Phe | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/12 | 421/4975 | 260/1428 | 87/475 | chr18 | 74505904 | |||
chr18:74508848 | T | C | 2 | a0002 a0005 |
96 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(93): Show |
missense_variant | MODERATE | c.376T>C | p.Tyr126His | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/12 | 537/4975 | 376/1428 | 126/475 | chr18 | 74508848 | |||
chr18:74508915 | A | G | 1 | a0004 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.443A>G | p.Gln148Arg | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/12 | 604/4975 | 443/1428 | 148/475 | chr18 | 74508915 | |||
chr18:74510895 | G | A | 1 | a0003 | 8 | HG02055.hp1 HG02622.hp2 HG02970.hp2 others(5): Show |
missense_variant | MODERATE | c.539G>A | p.Arg180Gln | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/12 | 700/4975 | 539/1428 | 180/475 | chr18 | 74510895 | |||
chr18:74513621 | G | A | 1 | a0005 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.805G>A | p.Val269Ile | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/12 | 966/4975 | 805/1428 | 269/475 | chr18 | 74513621 | |||
chr18:74513625 | C | T | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.809C>T | p.Thr270Met | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/12 | 970/4975 | 809/1428 | 270/475 | chr18 | 74513625 | |||
chr18:74516387 | G | A | 1 | a0011 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.1063G>A | p.Glu355Lys | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/12 | 1224/4975 | 1063/1428 | 355/475 | chr18 | 74516387 | |||
chr18:74518949 | T | G | 1 | a0008 | 1 | NA18987.hp2 | missense_variant&splice_region_variant | MODERATE | c.1211T>G | p.Val404Gly | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/12 | 1372/4975 | 1211/1428 | 404/475 | chr18 | 74518949 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:74501373 | G | A | 7 | a0001c0003 a0001c0005 a0002c0002 others(4): Show |
115 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(112): Show |
synonymous_variant | LOW | c.105G>A | p.Pro35Pro | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/12 | 266/4975 | 105/1428 | 35/475 | chr18 | 74501373 | |||
chr18:74505890 | C | T | 1 | a0001c0020 | 1 | HG04184.hp1 | synonymous_variant | LOW | c.246C>T | p.Leu82Leu | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/12 | 407/4975 | 246/1428 | 82/475 | chr18 | 74505890 | |||
chr18:74505938 | G | T | 1 | a0001c0009 | 2 | HG00408.hp2 HG02040.hp2 |
synonymous_variant | LOW | c.294G>T | p.Gly98Gly | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/12 | 455/4975 | 294/1428 | 98/475 | chr18 | 74505938 | |||
chr18:74510878 | C | T | 2 | a0001c0005 a0001c0017 |
4 | HG02572.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
synonymous_variant | LOW | c.522C>T | p.Asp174Asp | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/12 | 683/4975 | 522/1428 | 174/475 | chr18 | 74510878 | |||
chr18:74510926 | T | C | 4 | a0002c0002 a0002c0007 a0002c0008 others(1): Show |
93 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(90): Show |
synonymous_variant | LOW | c.570T>C | p.Tyr190Tyr | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/12 | 731/4975 | 570/1428 | 190/475 | chr18 | 74510926 | |||
chr18:74513572 | C | T | 1 | a0002c0007 | 2 | NA19081.hp1 NA19089.hp2 |
synonymous_variant | LOW | c.756C>T | p.Asp252Asp | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/12 | 917/4975 | 756/1428 | 252/475 | chr18 | 74513572 | |||
chr18:74520020 | C | G | 1 | a0001c0016 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.1380C>G | p.Thr460Thr | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1541/4975 | 1380/1428 | 460/475 | chr18 | 74520020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:74496370 | C | A | 1 | a0001c0003t0023 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/12 | 3604 | chr18 | 74496370 | ||||||
chr18:74496379 | C | G | 1 | a0001c0001t0049 | 1 | HG01515.hp1 | 5_prime_UTR_variant | MODIFIER | c.-145C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/12 | 3595 | chr18 | 74496379 | ||||||
chr18:74499885 | G | A | 1 | a0001c0001t0015 | 2 | HG03669.hp1 HG03688.hp1 |
5_prime_UTR_variant | MODIFIER | c.-89G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/12 | 89 | chr18 | 74499885 | ||||||
chr18:74499889 | C | G | 39 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(36): Show |
161 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(158): Show |
5_prime_UTR_variant | MODIFIER | c.-85C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/12 | 85 | chr18 | 74499889 | ||||||
chr18:74499915 | A | T | 1 | a0001c0001t0036 | 1 | NA18974.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/12 | 59 | chr18 | 74499915 | ||||||
chr18:74499917 | C | T | 1 | a0001c0001t0035 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-57C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/12 | 57 | chr18 | 74499917 | ||||||
chr18:74499949 | C | T | 1 | a0001c0001t0034 | 1 | HG02922.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-25C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/12 | chr18 | 74499949 | |||||||
chr18:74520099 | G | A | 7 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0024 others(4): Show |
22 | HG02027.hp2 HG02258.hp2 HG02451.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*31G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 31 | chr18 | 74520099 | ||||||
chr18:74520236 | C | T | 1 | a0001c0003t0048 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*168C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 168 | chr18 | 74520236 | ||||||
chr18:74520245 | G | A | 1 | a0001c0001t0016 | 2 | HG02683.hp1 HG03669.hp2 |
3_prime_UTR_variant | MODIFIER | c.*177G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 177 | chr18 | 74520245 | ||||||
chr18:74520377 | C | T | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(54): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
3_prime_UTR_variant | MODIFIER | c.*309C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 309 | chr18 | 74520377 | ||||||
chr18:74520404 | G | A | 1 | a0001c0001t0025 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*336G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 336 | chr18 | 74520404 | ||||||
chr18:74520596 | C | T | 3 | a0001c0001t0020 a0001c0001t0046 a0002c0002t0047 |
4 | HG01257.hp2 HG01258.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*528C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 528 | chr18 | 74520596 | ||||||
chr18:74520670 | T | A | 1 | a0001c0001t0038 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*602T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 602 | chr18 | 74520670 | ||||||
chr18:74520841 | G | C | 1 | a0002c0002t0041 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*773G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 773 | chr18 | 74520841 | ||||||
chr18:74520884 | G | A | 1 | a0001c0001t0017 | 2 | HG01981.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*816G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 816 | chr18 | 74520884 | ||||||
chr18:74520911 | C | A | 1 | a0001c0003t0021 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*843C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 843 | chr18 | 74520911 | ||||||
chr18:74521012 | C | G | 1 | a0002c0002t0045 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 944 | chr18 | 74521012 | ||||||
chr18:74521016 | C | T | 58 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(55): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
3_prime_UTR_variant | MODIFIER | c.*948C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 948 | chr18 | 74521016 | ||||||
chr18:74521017 | A | G | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*949A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 949 | chr18 | 74521017 | ||||||
chr18:74521112 | T | C | 6 | a0001c0001t0003 a0001c0001t0010 a0001c0001t0011 others(3): Show |
31 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1044T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1044 | chr18 | 74521112 | ||||||
chr18:74521122 | A | G | 2 | a0001c0003t0048 a0002c0002t0044 |
2 | HG03654.hp2 HG03710.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1054A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1054 | chr18 | 74521122 | ||||||
chr18:74521136 | A | G | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*1068A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1068 | chr18 | 74521136 | ||||||
chr18:74521145 | G | A | 7 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0017 others(4): Show |
18 | HG01074.hp1 HG01891.hp2 HG01981.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1077G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1077 | chr18 | 74521145 | ||||||
chr18:74521339 | TA | T | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*1273delA | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1273 | INFO_REALIGN_3_PRIME | chr18 | 74521339 | |||||
chr18:74521342 | C | T | 1 | a0001c0001t0019 | 2 | HG02738.hp1 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1274C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1274 | chr18 | 74521342 | ||||||
chr18:74521444 | T | C | 1 | a0001c0001t0017 | 2 | HG01981.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1376T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1376 | chr18 | 74521444 | ||||||
chr18:74521508 | G | C | 1 | a0001c0001t0026 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1440 | chr18 | 74521508 | ||||||
chr18:74521544 | G | A | 3 | a0001c0001t0013 a0001c0001t0026 a0001c0001t0027 |
7 | HG00673.hp1 NA18941.hp1 NA18961.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1476G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1476 | chr18 | 74521544 | ||||||
chr18:74521732 | A | G | 1 | a0002c0002t0039 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1664A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1664 | chr18 | 74521732 | ||||||
chr18:74521793 | C | T | 1 | a0001c0001t0033 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1725C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1725 | chr18 | 74521793 | ||||||
chr18:74521815 | A | G | 1 | a0001c0001t0011 | 6 | HG00639.hp1 HG01099.hp1 HG01192.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1747A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1747 | chr18 | 74521815 | ||||||
chr18:74521954 | A | T | 1 | a0001c0001t0032 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1886A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1886 | chr18 | 74521954 | ||||||
chr18:74521955 | C | T | 1 | a0002c0002t0043 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1887C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1887 | chr18 | 74521955 | ||||||
chr18:74521956 | C | A | 1 | a0001c0001t0028 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1888C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1888 | chr18 | 74521956 | ||||||
chr18:74521974 | A | G | 1 | a0001c0020t0031 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1906A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1906 | chr18 | 74521974 | ||||||
chr18:74522015 | C | A | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
3_prime_UTR_variant | MODIFIER | c.*1947C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 1947 | chr18 | 74522015 | ||||||
chr18:74522075 | T | C | 66 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(63): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
3_prime_UTR_variant | MODIFIER | c.*2007T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 2007 | chr18 | 74522075 | ||||||
chr18:74522149 | G | C | 1 | a0001c0001t0029 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2081G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 2081 | chr18 | 74522149 | ||||||
chr18:74522561 | C | G | 1 | a0001c0001t0030 | 1 | NA18995.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2493C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 2493 | chr18 | 74522561 | ||||||
chr18:74522685 | G | A | 1 | a0001c0001t0037 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2617G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 2617 | chr18 | 74522685 | ||||||
chr18:74522979 | G | A | 2 | a0001c0001t0020 a0002c0002t0047 |
3 | HG01257.hp2 HG01258.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2911G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 2911 | chr18 | 74522979 | ||||||
chr18:74523016 | C | A | 1 | a0002c0002t0040 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2948C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 2948 | chr18 | 74523016 | ||||||
chr18:74523320 | A | G | 8 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0017 others(5): Show |
19 | HG01074.hp1 HG01891.hp2 HG01981.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3252A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 3252 | chr18 | 74523320 | ||||||
chr18:74523434 | C | T | 4 | a0001c0001t0014 a0001c0001t0027 a0001c0001t0030 others(1): Show |
8 | HG00544.hp2 HG00673.hp1 HG02129.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3366C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 12/12 | 3366 | chr18 | 74523434 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:74496454 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
7 | HG02129.hp1 HG02155.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-93+23C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496454 | |||||||
chr18:74496458 | C | G | 1 | a0002c0002t0002g0005 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-93+27C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496458 | |||||||
chr18:74496467 | G | C | 1 | a0001c0001t0001g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-93+36G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496467 | |||||||
chr18:74496476 | G | T | 1 | a0002c0002t0002g0281 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-93+45G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496476 | |||||||
chr18:74496542 | G | A | 2 | a0001c0001t0003g0062 a0001c0003t0009g0061 |
2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+111G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496542 | |||||||
chr18:74496594 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-93+163C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496594 | |||||||
chr18:74496798 | C | T | 4 | a0001c0001t0001g0278 a0001c0001t0003g0059 a0001c0001t0003g0279 others(1): Show |
5 | HG01123.hp1 HG01168.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+367C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496798 | |||||||
chr18:74496860 | A | G | 1 | a0001c0001t0001g0276 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-93+429A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496860 | |||||||
chr18:74496862 | G | A | 125 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0276 others(122): Show |
156 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.-93+431G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74496862 | |||||||
chr18:74497091 | T | G | 2 | a0001c0001t0001g0161 a0001c0001t0028g0160 |
2 | HG01261.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-93+660T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497091 | |||||||
chr18:74497301 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-93+870G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497301 | |||||||
chr18:74497377 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-93+946C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497377 | |||||||
chr18:74497556 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-93+1125G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497556 | |||||||
chr18:74497686 | G | A | 3 | a0001c0001t0001g0040 a0001c0001t0011g0165 a0001c0001t0011g0166 |
4 | HG01167.hp2 HG01169.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+1255G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497686 | |||||||
chr18:74497772 | G | A | 1 | a0001c0001t0001g0041 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-93+1341G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497772 | |||||||
chr18:74497823 | T | C | 116 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(113): Show |
146 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(143): Show |
intron_variant | MODIFIER | c.-93+1392T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497823 | |||||||
chr18:74497910 | C | T | 2 | a0001c0003t0002g0151 a0001c0003t0048g0152 |
2 | HG03654.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-93+1479C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497910 | |||||||
chr18:74497950 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-93+1519C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497950 | |||||||
chr18:74497962 | G | A | 4 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0063 others(1): Show |
6 | HG01175.hp1 HG02486.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+1531G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74497962 | |||||||
chr18:74498225 | C | T | 11 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0142 others(8): Show |
13 | HG01243.hp1 HG01358.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-92-1657C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498225 | |||||||
chr18:74498285 | T | C | 1 | a0002c0002t0039g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-92-1597T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498285 | |||||||
chr18:74498341 | T | A | 5 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0009g0168 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-1541T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498341 | |||||||
chr18:74498465 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-92-1417A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498465 | |||||||
chr18:74498506 | A | T | 1 | a0001c0001t0001g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-92-1376A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498506 | |||||||
chr18:74498960 | C | G | 4 | a0001c0003t0007g0138 a0002c0002t0006g0139 a0002c0002t0039g0065 others(1): Show |
4 | HG01255.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-922C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498960 | |||||||
chr18:74498986 | G | A | 1 | a0002c0006t0002g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-92-896G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498986 | |||||||
chr18:74498988 | C | T | 1 | a0001c0001t0017g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-92-894C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74498988 | |||||||
chr18:74499167 | C | T | 5 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0009g0168 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-715C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499167 | |||||||
chr18:74499168 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-92-714G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499168 | |||||||
chr18:74499263 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
7 | HG02129.hp1 HG02155.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-619G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499263 | |||||||
chr18:74499356 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-92-526C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499356 | |||||||
chr18:74499451 | G | A | 1 | a0002c0002t0002g0067 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-92-431G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499451 | |||||||
chr18:74499611 | A | G | 80 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(77): Show |
101 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.-92-271A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499611 | |||||||
chr18:74499721 | A | G | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-161A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499721 | |||||||
chr18:74499722 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-92-160A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499722 | |||||||
chr18:74499803 | G | A | 1 | a0001c0001t0008g0174 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-92-79G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 1/11 | chr18 | 74499803 | |||||||
chr18:74500309 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.60+276C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500309 | |||||||
chr18:74500360 | A | T | 1 | a0001c0001t0042g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.60+327A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500360 | |||||||
chr18:74500411 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
386 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(383): Show |
intron_variant | MODIFIER | c.60+378A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500411 | |||||||
chr18:74500471 | G | A | 7 | a0001c0003t0002g0192 a0001c0003t0002g0193 a0001c0003t0002g0194 others(4): Show |
8 | HG02258.hp2 HG02809.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.60+438G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500471 | |||||||
chr18:74500567 | G | A | 91 | a0001c0001t0018g0175 a0001c0003t0002g0037 a0001c0003t0002g0116 others(88): Show |
114 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(111): Show |
intron_variant | MODIFIER | c.60+534G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500567 | |||||||
chr18:74500589 | T | C | 1 | a0002c0002t0044g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.60+556T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500589 | |||||||
chr18:74500634 | T | C | 31 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(28): Show |
40 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.60+601T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500634 | |||||||
chr18:74500767 | C | T | 34 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(31): Show |
43 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.61-562C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500767 | |||||||
chr18:74500838 | C | T | 1 | a0002c0002t0045g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.61-491C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500838 | |||||||
chr18:74500863 | G | T | 1 | a0002c0007t0002g0136 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.61-466G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500863 | |||||||
chr18:74500948 | T | A | 12 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0196 others(9): Show |
13 | HG00280.hp2 HG00735.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.61-381T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500948 | |||||||
chr18:74500952 | A | T | 2 | a0001c0001t0002g0149 a0001c0001t0038g0148 |
2 | HG01243.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.61-377A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74500952 | |||||||
chr18:74501022 | G | A | 1 | a0002c0002t0002g0084 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.61-307G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501022 | |||||||
chr18:74501050 | T | C | 4 | a0001c0001t0014g0016 a0001c0001t0014g0197 a0001c0001t0027g0016 others(1): Show |
4 | HG00544.hp2 HG00673.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.61-279T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501050 | |||||||
chr18:74501076 | T | G | 1 | a0001c0001t0001g0041 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.61-253T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501076 | |||||||
chr18:74501077 | T | A | 130 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(127): Show |
162 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.61-252T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501077 | |||||||
chr18:74501207 | A | G | 2 | a0002c0002t0002g0135 a0002c0002t0010g0134 |
2 | HG00735.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.61-122A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501207 | |||||||
chr18:74501251 | T | C | 132 | a0001c0001t0001g0196 a0001c0001t0001g0198 a0001c0001t0002g0026 others(129): Show |
164 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(161): Show |
intron_variant | MODIFIER | c.61-78T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501251 | |||||||
chr18:74501259 | C | T | 5 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0009g0168 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.61-70C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501259 | |||||||
chr18:74501294 | T | G | 1 | a0001c0001t0001g0009 | 4 | HG02083.hp1 NA18942.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.61-35T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 2/11 | chr18 | 74501294 | |||||||
chr18:74501555 | G | T | 2 | a0001c0001t0001g0272 a0001c0001t0012g0271 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.204+83G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74501555 | |||||||
chr18:74501622 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.204+150G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74501622 | |||||||
chr18:74501631 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.204+159G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74501631 | |||||||
chr18:74501643 | G | C | 1 | a0001c0001t0005g0068 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.204+171G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74501643 | |||||||
chr18:74501838 | C | T | 33 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(30): Show |
42 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.204+366C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74501838 | |||||||
chr18:74501894 | T | A | 129 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(126): Show |
161 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.204+422T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74501894 | |||||||
chr18:74501933 | G | A | 1 | a0002c0002t0010g0085 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.204+461G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74501933 | |||||||
chr18:74502029 | G | A | 6 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(3): Show |
15 | HG02083.hp1 HG02738.hp1 HG04184.hp2 others(12): Show |
intron_variant | MODIFIER | c.204+557G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502029 | |||||||
chr18:74502032 | A | T | 129 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(126): Show |
161 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.204+560A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502032 | |||||||
chr18:74502034 | C | T | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+562C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502034 | |||||||
chr18:74502139 | G | A | 1 | a0001c0001t0018g0175 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.204+667G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502139 | |||||||
chr18:74502141 | C | T | 4 | a0003c0004t0005g0008 a0003c0004t0005g0029 a0003c0004t0005g0078 others(1): Show |
8 | HG02055.hp1 HG02622.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+669C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502141 | |||||||
chr18:74502160 | A | G | 81 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(78): Show |
102 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.204+688A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502160 | |||||||
chr18:74502269 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.204+797T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502269 | |||||||
chr18:74502298 | G | A | 1 | a0001c0005t0002g0069 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.204+826G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502298 | |||||||
chr18:74502472 | G | GTTT | 86 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(83): Show |
109 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.204+1000_204+1001i others(5): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502472 | |||||||
chr18:74502472 | G | GTTTT | 4 | a0002c0002t0002g0130 a0002c0002t0002g0131 a0002c0002t0002g0132 others(1): Show |
4 | HG01978.hp1 HG02132.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+1000_204+1001i others(6): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502472 | |||||||
chr18:74502472 | G | T | 1 | a0002c0002t0002g0281 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.204+1000G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502472 | |||||||
chr18:74502473 | G | GT | 6 | a0001c0001t0001g0163 a0001c0001t0001g0264 a0001c0001t0001g0266 others(3): Show |
6 | HG00597.hp1 HG03130.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+1012dupT | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74502473 | ||||||
chr18:74502473 | G | T | 92 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(89): Show |
115 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.204+1001G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502473 | |||||||
chr18:74502488 | G | A | 92 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(89): Show |
115 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.204+1016G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502488 | |||||||
chr18:74502491 | A | T | 11 | a0001c0003t0002g0192 a0001c0003t0002g0193 a0001c0003t0002g0194 others(8): Show |
13 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+1019A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502491 | |||||||
chr18:74502622 | A | T | 1 | a0001c0001t0003g0062 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.204+1150A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502622 | |||||||
chr18:74502771 | A | G | 130 | a0001c0001t0001g0196 a0001c0001t0002g0026 a0001c0001t0002g0027 others(127): Show |
162 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.204+1299A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502771 | |||||||
chr18:74502804 | G | A | 2 | a0001c0003t0007g0138 a0002c0002t0006g0139 |
2 | HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.204+1332G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502804 | |||||||
chr18:74502835 | G | A | 5 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0009g0168 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+1363G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74502835 | |||||||
chr18:74503064 | C | T | 81 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(78): Show |
102 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.204+1592C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503064 | |||||||
chr18:74503073 | G | GT | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.204+1614dupT | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503073 | ||||||
chr18:74503073 | G | GTT | 6 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(3): Show |
7 | HG00735.hp2 HG02258.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+1613_204+1614d others(4): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503073 | ||||||
chr18:74503073 | G | GTTTT | 89 | a0001c0001t0001g0196 a0001c0001t0002g0169 a0001c0001t0002g0172 others(86): Show |
112 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.204+1611_204+1614d others(6): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503073 | ||||||
chr18:74503073 | G | GTTTTT | 10 | a0001c0003t0002g0037 a0001c0003t0002g0194 a0001c0003t0023g0037 others(7): Show |
10 | HG02004.hp2 HG02895.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+1610_204+1614d others(7): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503073 | ||||||
chr18:74503075 | T | TTTG | 31 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(28): Show |
40 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.204+1605_204+1606i others(5): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503075 | ||||||
chr18:74503124 | T | C | 69 | a0001c0003t0002g0116 a0001c0003t0002g0151 a0001c0003t0048g0152 others(66): Show |
89 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.204+1652T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503124 | |||||||
chr18:74503162 | G | A | 130 | a0001c0001t0001g0196 a0001c0001t0002g0026 a0001c0001t0002g0027 others(127): Show |
162 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.204+1690G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503162 | |||||||
chr18:74503490 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.204+2018G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503490 | |||||||
chr18:74503675 | G | A | 31 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(28): Show |
40 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.205-2174G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503675 | |||||||
chr18:74503693 | C | T | 5 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0009g0168 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-2156C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503693 | |||||||
chr18:74503748 | ACAGCCAC others(47): Show |
A | 5 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0009g0168 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-2089_205-2036d others(56): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503748 | ||||||
chr18:74503795 | T | C | 2 | a0002c0007t0002g0100 a0002c0007t0002g0136 |
2 | NA19081.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.205-2054T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503795 | |||||||
chr18:74503801 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0264 |
2 | NA19011.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.205-2048C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503801 | |||||||
chr18:74503811 | GTGCCGCT others(47): Show |
G | 1 | a0001c0001t0001g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.205-1951_205-1898d others(56): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503811 | ||||||
chr18:74503820 | G | C | 4 | a0001c0003t0007g0138 a0002c0002t0006g0139 a0002c0002t0039g0065 others(1): Show |
4 | HG01255.hp2 HG02647.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-2029G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503820 | |||||||
chr18:74503847 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.205-2002G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503847 | |||||||
chr18:74503870 | G | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(42): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.205-1979G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503870 | |||||||
chr18:74503901 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.205-1948G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503901 | |||||||
chr18:74503904 | A | ACACACGC others(47): Show |
16 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(13): Show |
19 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-1872_205-1819d others(56): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503904 | ||||||
chr18:74503904 | A | ACACACGC others(47): Show |
251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(248): Show |
357 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.205-1912_205-1911i others(56): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503904 | ||||||
chr18:74503904 | A | ACACACGC others(48): Show |
1 | a0001c0001t0001g0260 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.205-1912_205-1911i others(57): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503904 | ||||||
chr18:74503931 | C | CAAATGAT others(47): Show |
1 | a0001c0001t0009g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205-1912_205-1911i others(56): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503931 | ||||||
chr18:74503938 | G | T | 10 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0009g0168 others(7): Show |
13 | HG00544.hp1 HG01074.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.205-1911G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503938 | |||||||
chr18:74503963 | C | T | 1 | a0001c0003t0048g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.205-1886C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503963 | |||||||
chr18:74503973 | C | CTGCCGCT others(371): Show |
1 | a0001c0003t0021g0036 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.205-1848_205-1847i others(380): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74503973 | ||||||
chr18:74503977 | C | T | 1 | a0002c0002t0002g0117 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.205-1872C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503977 | |||||||
chr18:74503978 | G | A | 1 | a0002c0002t0002g0087 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.205-1871G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74503978 | |||||||
chr18:74504018 | G | A | 2 | a0002c0002t0002g0030 a0002c0002t0002g0084 |
3 | HG02040.hp1 NA18945.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.205-1831G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504018 | |||||||
chr18:74504031 | T | C | 1 | a0001c0001t0011g0205 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.205-1818T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504031 | |||||||
chr18:74504031 | T | TGCTGGGA others(101): Show |
1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.205-1803_205-1696d others(110): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74504031 | ||||||
chr18:74504071 | C | T | 11 | a0001c0003t0002g0192 a0001c0003t0002g0193 a0001c0003t0002g0194 others(8): Show |
13 | HG02258.hp2 HG02723.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-1778C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504071 | |||||||
chr18:74504081 | G | GTGCCGCT others(47): Show |
1 | a0001c0003t0021g0036 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.205-1735_205-1682d others(56): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74504081 | ||||||
chr18:74504134 | A | G | 32 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0038 others(29): Show |
41 | HG00639.hp2 HG01175.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.205-1715A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504134 | |||||||
chr18:74504139 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.205-1710C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504139 | |||||||
chr18:74504140 | GCTGGGAC others(155): Show |
G | 1 | a0001c0020t0031g0189 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.205-1655_205-1494d others(2): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74504140 | ||||||
chr18:74504213 | G | A | 2 | a0002c0002t0006g0120 a0002c0002t0007g0121 |
2 | HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.205-1636G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504213 | |||||||
chr18:74504288 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.205-1561G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504288 | |||||||
chr18:74504316 | G | GGGGCGTC others(101): Show |
1 | a0002c0002t0044g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.205-1494_205-1493i others(110): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74504316 | ||||||
chr18:74504341 | C | T | 6 | a0001c0001t0005g0068 a0001c0001t0006g0028 a0001c0001t0006g0071 others(3): Show |
7 | HG02109.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-1508C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504341 | |||||||
chr18:74504375 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.205-1474G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504375 | |||||||
chr18:74504429 | T | G | 1 | a0002c0002t0002g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.205-1420T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504429 | |||||||
chr18:74504649 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(238): Show |
346 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.205-1200C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504649 | |||||||
chr18:74504650 | G | C | 1 | a0001c0001t0002g0038 | 2 | HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.205-1199G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504650 | |||||||
chr18:74504692 | G | C | 15 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(12): Show |
18 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-1157G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74504692 | |||||||
chr18:74505162 | C | T | 4 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0063 others(1): Show |
6 | HG01175.hp1 HG02486.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-687C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505162 | |||||||
chr18:74505325 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.205-524G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505325 | |||||||
chr18:74505334 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0002g0063 a0001c0001t0010g0064 |
4 | HG03491.hp1 HG03492.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-515C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505334 | |||||||
chr18:74505396 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0266 a0001c0001t0001g0269 others(2): Show |
7 | HG00408.hp2 HG00558.hp1 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-453C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505396 | |||||||
chr18:74505492 | G | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.205-357G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505492 | |||||||
chr18:74505514 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0011g0165 |
3 | HG01167.hp2 HG01169.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.205-335G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505514 | |||||||
chr18:74505556 | G | A | 79 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(76): Show |
100 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(97): Show |
intron_variant | MODIFIER | c.205-293G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505556 | |||||||
chr18:74505564 | G | A | 300 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(297): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.205-285G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505564 | |||||||
chr18:74505598 | C | CA | 7 | a0001c0001t0001g0208 a0001c0001t0001g0260 a0001c0001t0001g0262 others(4): Show |
7 | HG00558.hp2 HG01978.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-233dupA | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74505598 | ||||||
chr18:74505598 | CA | C | 51 | a0001c0001t0001g0057 a0001c0001t0001g0204 a0001c0001t0001g0253 others(48): Show |
64 | HG01175.hp1 HG01243.hp1 HG01257.hp1 others(61): Show |
intron_variant | MODIFIER | c.205-233delA | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74505598 | ||||||
chr18:74505598 | CAA | C | 76 | a0001c0003t0002g0037 a0001c0003t0002g0116 a0001c0003t0002g0122 others(73): Show |
97 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.205-234_205-233del others(2): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 74505598 | ||||||
chr18:74505618 | T | G | 2 | a0001c0001t0001g0225 a0001c0001t0011g0224 |
2 | HG00639.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.205-231T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505618 | |||||||
chr18:74505635 | A | G | 4 | a0003c0004t0005g0008 a0003c0004t0005g0029 a0003c0004t0005g0078 others(1): Show |
8 | HG02055.hp1 HG02622.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-214A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505635 | |||||||
chr18:74505733 | A | G | 1 | a0001c0001t0002g0039 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.205-116A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505733 | |||||||
chr18:74505754 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.205-95G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 3/11 | chr18 | 74505754 | |||||||
chr18:74506018 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00733.hp2 | splice_region_variant&intron_variant | LOW | c.367+7G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506018 | |||||||
chr18:74506025 | G | A | 1 | a0001c0001t0042g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.367+14G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506025 | |||||||
chr18:74506032 | C | T | 1 | a0001c0001t0010g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.367+21C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506032 | |||||||
chr18:74506035 | GC | G | 77 | a0001c0003t0002g0037 a0001c0003t0002g0122 a0001c0003t0002g0151 others(74): Show |
98 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.367+27delC | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 74506035 | ||||||
chr18:74506043 | G | A | 77 | a0001c0003t0002g0037 a0001c0003t0002g0122 a0001c0003t0002g0151 others(74): Show |
98 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.367+32G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506043 | |||||||
chr18:74506079 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.367+68G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506079 | |||||||
chr18:74506286 | C | G | 1 | a0002c0002t0002g0115 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.367+275C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506286 | |||||||
chr18:74506292 | G | A | 2 | a0002c0002t0002g0090 a0002c0002t0002g0091 |
2 | NA18990.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.367+281G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506292 | |||||||
chr18:74506324 | G | A | 3 | a0001c0003t0002g0195 a0001c0005t0002g0047 a0001c0005t0002g0069 |
4 | HG02723.hp2 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+313G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506324 | |||||||
chr18:74506381 | C | T | 2 | a0001c0001t0002g0149 a0001c0001t0008g0259 |
2 | HG02809.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.367+370C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506381 | |||||||
chr18:74506428 | G | A | 1 | a0001c0001t0010g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.367+417G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506428 | |||||||
chr18:74506647 | G | A | 1 | a0001c0001t0042g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.367+636G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506647 | |||||||
chr18:74506749 | C | T | 1 | a0001c0001t0010g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.367+738C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506749 | |||||||
chr18:74506782 | C | T | 13 | a0001c0001t0001g0196 a0001c0001t0002g0038 a0001c0001t0002g0039 others(10): Show |
15 | HG01358.hp2 HG02109.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.367+771C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506782 | |||||||
chr18:74506788 | A | G | 78 | a0001c0001t0001g0223 a0001c0003t0007g0123 a0002c0002t0001g0167 others(75): Show |
99 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.367+777A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506788 | |||||||
chr18:74506856 | T | A | 1 | a0001c0001t0012g0271 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.367+845T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74506856 | |||||||
chr18:74507025 | T | TC | 4 | a0001c0001t0001g0040 a0001c0001t0011g0165 a0001c0001t0011g0166 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+1015dupC | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 74507025 | ||||||
chr18:74507165 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.367+1154G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507165 | |||||||
chr18:74507221 | C | T | 17 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(14): Show |
20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.367+1210C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507221 | |||||||
chr18:74507231 | G | A | 21 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0063 others(18): Show |
28 | HG01175.hp1 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.367+1220G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507231 | |||||||
chr18:74507366 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.367+1355C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507366 | |||||||
chr18:74507466 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(140): Show |
221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.368-1374G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507466 | |||||||
chr18:74507482 | A | G | 1 | a0001c0003t0002g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.368-1358A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507482 | |||||||
chr18:74507592 | C | T | 74 | a0001c0003t0007g0123 a0001c0003t0007g0138 a0002c0002t0001g0167 others(71): Show |
95 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.368-1248C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507592 | |||||||
chr18:74507745 | A | G | 77 | a0001c0003t0007g0123 a0001c0003t0007g0138 a0002c0002t0001g0167 others(74): Show |
98 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.368-1095A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507745 | |||||||
chr18:74507782 | T | G | 2 | a0002c0006t0002g0066 a0002c0006t0002g0081 |
2 | HG03704.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.368-1058T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507782 | |||||||
chr18:74507857 | G | A | 1 | a0002c0002t0002g0031 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.368-983G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507857 | |||||||
chr18:74507917 | A | G | 128 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(125): Show |
160 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.368-923A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507917 | |||||||
chr18:74507935 | A | G | 29 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(26): Show |
33 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.368-905A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507935 | |||||||
chr18:74507983 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.368-857G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74507983 | |||||||
chr18:74508010 | G | T | 1 | a0001c0001t0005g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.368-830G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508010 | |||||||
chr18:74508024 | T | C | 1 | a0009c0010t0001g0227 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.368-816T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508024 | |||||||
chr18:74508027 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.368-813T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508027 | |||||||
chr18:74508168 | C | T | 3 | a0002c0006t0002g0066 a0002c0006t0002g0081 a0002c0006t0003g0277 |
3 | HG01361.hp2 HG03704.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.368-672C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508168 | |||||||
chr18:74508180 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.368-660G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508180 | |||||||
chr18:74508388 | G | T | 1 | a0001c0001t0034g0185 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.368-452G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508388 | |||||||
chr18:74508396 | A | G | 1 | a0001c0001t0024g0221 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.368-444A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508396 | |||||||
chr18:74508579 | A | G | 76 | a0001c0003t0007g0138 a0002c0002t0001g0167 a0002c0002t0002g0003 others(73): Show |
97 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.368-261A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508579 | |||||||
chr18:74508634 | C | T | 1 | a0001c0001t0010g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.368-206C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508634 | |||||||
chr18:74508751 | C | T | 1 | a0001c0001t0042g0082 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.368-89C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508751 | |||||||
chr18:74508836 | C | G | 1 | a0002c0002t0002g0087 | 1 | HG00544.hp1 | splice_region_variant&intron_variant | LOW | c.368-4C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 4/11 | chr18 | 74508836 | |||||||
chr18:74509138 | G | A | 10 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0142 others(7): Show |
12 | HG01358.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.456+210G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509138 | |||||||
chr18:74509174 | A | T | 20 | a0002c0002t0001g0167 a0002c0002t0002g0005 a0002c0002t0002g0012 others(17): Show |
28 | HG00597.hp2 HG01074.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.456+246A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509174 | |||||||
chr18:74509184 | C | T | 1 | a0001c0001t0001g0053 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.456+256C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509184 | |||||||
chr18:74509367 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.456+439G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509367 | |||||||
chr18:74509464 | G | A | 3 | a0002c0002t0002g0032 a0002c0002t0002g0092 a0002c0002t0041g0032 |
3 | NA18943.hp2 NA18961.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.456+536G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509464 | |||||||
chr18:74509547 | C | T | 14 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(11): Show |
17 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.456+619C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509547 | |||||||
chr18:74509582 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.456+654G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509582 | |||||||
chr18:74509622 | G | A | 3 | a0002c0006t0002g0066 a0002c0006t0002g0081 a0002c0006t0003g0277 |
3 | HG01361.hp2 HG03704.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.456+694G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509622 | |||||||
chr18:74509632 | C | CA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.456+719dupA | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 74509632 | ||||||
chr18:74509632 | C | CAA | 14 | a0001c0001t0001g0054 a0001c0001t0001g0060 a0001c0001t0001g0209 others(11): Show |
15 | HG02486.hp1 HG06807.hp2 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.456+718_456+719dup others(2): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 74509632 | ||||||
chr18:74509632 | CA | C | 102 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(99): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.456+719delA | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 74509632 | ||||||
chr18:74509675 | T | TCGTTGTT others(50): Show |
1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.456+748_456+804dup others(57): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 74509675 | ||||||
chr18:74509732 | A | G | 22 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0063 others(19): Show |
29 | HG01175.hp1 HG01884.hp1 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.456+804A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509732 | |||||||
chr18:74509741 | CAGTT | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.456+817_456+820del others(4): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 74509741 | ||||||
chr18:74509916 | G | C | 1 | a0001c0001t0002g0149 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.457-897G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509916 | |||||||
chr18:74509925 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.457-888G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509925 | |||||||
chr18:74509986 | G | C | 5 | a0001c0003t0007g0138 a0002c0002t0006g0139 a0002c0002t0007g0119 others(2): Show |
5 | HG01255.hp2 HG02647.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.457-827G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509986 | |||||||
chr18:74509994 | G | T | 1 | a0001c0001t0018g0251 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.457-819G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509994 | |||||||
chr18:74509997 | G | A | 73 | a0001c0003t0007g0138 a0002c0002t0001g0167 a0002c0002t0002g0003 others(70): Show |
94 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.457-816G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74509997 | |||||||
chr18:74510029 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.457-784C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510029 | |||||||
chr18:74510105 | C | T | 72 | a0002c0002t0001g0167 a0002c0002t0002g0003 a0002c0002t0002g0005 others(69): Show |
93 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.457-708C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510105 | |||||||
chr18:74510116 | C | T | 14 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0142 others(11): Show |
16 | HG01358.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.457-697C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510116 | |||||||
chr18:74510134 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.457-679T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510134 | |||||||
chr18:74510212 | C | G | 1 | a0002c0002t0002g0108 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.457-601C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510212 | |||||||
chr18:74510227 | A | G | 1 | a0002c0002t0002g0107 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.457-586A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510227 | |||||||
chr18:74510230 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.457-583A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510230 | |||||||
chr18:74510246 | TTAGGCCC others(5): Show |
T | 1 | a0011c0014t0001g0184 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.457-565_457-554del others(12): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 74510246 | ||||||
chr18:74510350 | A | T | 7 | a0001c0001t0002g0147 a0001c0001t0005g0068 a0001c0001t0006g0028 others(4): Show |
8 | HG02109.hp2 HG02451.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.457-463A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510350 | |||||||
chr18:74510475 | C | T | 3 | a0002c0006t0002g0066 a0002c0006t0002g0081 a0002c0006t0003g0277 |
3 | HG01361.hp2 HG03704.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.457-338C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510475 | |||||||
chr18:74510578 | C | T | 21 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0063 others(18): Show |
28 | HG01175.hp1 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.457-235C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510578 | |||||||
chr18:74510714 | G | A | 1 | a0002c0002t0010g0085 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.457-99G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510714 | |||||||
chr18:74510726 | A | G | 1 | a0002c0002t0002g0106 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.457-87A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510726 | |||||||
chr18:74510754 | G | T | 3 | a0002c0006t0002g0066 a0002c0006t0002g0081 a0002c0006t0003g0277 |
3 | HG01361.hp2 HG03704.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.457-59G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510754 | |||||||
chr18:74510773 | G | A | 2 | a0002c0002t0002g0094 a0002c0002t0002g0125 |
2 | NA18967.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.457-40G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 5/11 | chr18 | 74510773 | |||||||
chr18:74511054 | T | A | 1 | a0001c0001t0004g0252 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.657+41T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74511054 | |||||||
chr18:74511065 | G | T | 72 | a0002c0002t0001g0167 a0002c0002t0002g0003 a0002c0002t0002g0005 others(69): Show |
93 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.657+52G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74511065 | |||||||
chr18:74511133 | A | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
222 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.657+120A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74511133 | |||||||
chr18:74511175 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(277): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.657+162C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74511175 | |||||||
chr18:74511186 | A | ACAGCAAC others(4): Show |
1 | a0001c0001t0001g0260 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.657+175_657+185dup others(11): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr18 | 74511186 | ||||||
chr18:74511349 | G | A | 1 | a0002c0002t0002g0095 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.657+336G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74511349 | |||||||
chr18:74511622 | C | T | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+609C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74511622 | |||||||
chr18:74511707 | C | CA | 76 | a0001c0003t0007g0138 a0002c0002t0001g0167 a0002c0002t0002g0003 others(73): Show |
98 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.657+709dupA | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr18 | 74511707 | ||||||
chr18:74511980 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.658-468G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74511980 | |||||||
chr18:74512000 | G | A | 2 | a0001c0001t0038g0148 a0002c0002t0002g0118 |
2 | HG01243.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.658-448G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74512000 | |||||||
chr18:74512064 | C | T | 18 | a0002c0002t0002g0035 a0002c0002t0002g0067 a0002c0002t0002g0087 others(15): Show |
20 | HG00544.hp1 HG00609.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.658-384C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74512064 | |||||||
chr18:74512190 | T | G | 1 | a0001c0003t0021g0036 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.658-258T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74512190 | |||||||
chr18:74512275 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.658-173G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74512275 | |||||||
chr18:74512344 | G | A | 74 | a0002c0002t0002g0003 a0002c0002t0002g0005 a0002c0002t0002g0012 others(71): Show |
95 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.658-104G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74512344 | |||||||
chr18:74512400 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.658-48T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 6/11 | chr18 | 74512400 | |||||||
chr18:74512633 | A | G | 5 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0063 others(2): Show |
7 | HG01175.hp1 HG02486.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.742+101A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74512633 | |||||||
chr18:74512927 | G | A | 6 | a0002c0002t0002g0031 a0002c0002t0002g0033 a0002c0002t0002g0096 others(3): Show |
7 | HG00738.hp1 HG01109.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.742+395G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74512927 | |||||||
chr18:74512948 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.742+416C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74512948 | |||||||
chr18:74513284 | C | T | 73 | a0001c0001t0001g0040 a0002c0002t0001g0167 a0002c0002t0002g0003 others(70): Show |
95 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.743-275C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513284 | |||||||
chr18:74513306 | G | A | 23 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(20): Show |
27 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.743-253G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513306 | |||||||
chr18:74513403 | C | T | 2 | a0001c0001t0009g0170 a0001c0001t0009g0171 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.743-156C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513403 | |||||||
chr18:74513419 | T | C | 1 | a0002c0006t0003g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.743-140T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513419 | |||||||
chr18:74513427 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.743-132C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513427 | |||||||
chr18:74513456 | C | A | 1 | a0001c0001t0001g0213 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.743-103C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513456 | |||||||
chr18:74513488 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
214 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.743-71G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513488 | |||||||
chr18:74513504 | G | A | 79 | a0001c0001t0001g0040 a0001c0001t0001g0052 a0001c0001t0001g0212 others(76): Show |
101 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.743-55G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513504 | |||||||
chr18:74513508 | G | A | 21 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0063 others(18): Show |
28 | HG01175.hp1 HG01884.hp1 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.743-51G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 7/11 | chr18 | 74513508 | |||||||
chr18:74513736 | G | A | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+17G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74513736 | |||||||
chr18:74513959 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.903+240C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74513959 | |||||||
chr18:74514076 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0230 others(4): Show |
11 | HG01243.hp2 HG01891.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.903+357G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514076 | |||||||
chr18:74514178 | G | A | 1 | a0002c0002t0002g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.903+459G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514178 | |||||||
chr18:74514199 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.903+480C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514199 | |||||||
chr18:74514248 | T | A | 2 | a0001c0001t0001g0214 a0001c0001t0011g0215 |
2 | HG01099.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.903+529T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514248 | |||||||
chr18:74514370 | A | G | 1 | a0001c0003t0021g0036 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.903+651A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514370 | |||||||
chr18:74514445 | GATGTAAG others(67): Show |
G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
167 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.903+853_903+926del others(74): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514445 | ||||||
chr18:74514480 | T | C | 2 | a0002c0006t0002g0066 a0002c0006t0002g0081 |
2 | HG03704.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.903+761T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514480 | |||||||
chr18:74514482 | G | A | 2 | a0002c0002t0002g0128 a0002c0002t0002g0133 |
2 | NA18940.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.903+763G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514482 | |||||||
chr18:74514494 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.903+775G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514494 | |||||||
chr18:74514519 | T | TATGTAAG others(67): Show |
83 | a0001c0001t0001g0040 a0001c0001t0002g0026 a0001c0001t0002g0063 others(80): Show |
111 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.903+852_903+853ins others(74): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514519 | ||||||
chr18:74514519 | T | TATGTAAG others(215): Show |
1 | a0002c0002t0002g0086 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.903+852_903+853ins others(222): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514519 | ||||||
chr18:74514543 | TTTATGTG others(104): Show |
T | 3 | a0001c0003t0002g0037 a0001c0003t0002g0122 a0001c0003t0023g0037 |
3 | HG02976.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.903+853_903+963del | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514543 | ||||||
chr18:74514554 | T | C | 1 | a0002c0006t0003g0277 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.903+835T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514554 | |||||||
chr18:74514554 | T | TGGATGTA others(30): Show |
2 | a0002c0006t0002g0066 a0002c0006t0002g0081 |
2 | HG03704.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.903+852_903+853ins others(37): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514554 | ||||||
chr18:74514556 | GATGTAAG others(30): Show |
G | 1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.903+853_903+889del others(37): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514556 | ||||||
chr18:74514572 | C | G | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(68): Show |
101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.903+853C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514572 | |||||||
chr18:74514577 | G | A | 24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+858G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514577 | |||||||
chr18:74514577 | GGGCTTAC others(30): Show |
G | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0017 others(44): Show |
73 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.903+861_903+897del others(37): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514577 | ||||||
chr18:74514580 | C | G | 24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+861C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514580 | |||||||
chr18:74514584 | C | T | 24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+865C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514584 | |||||||
chr18:74514591 | C | T | 24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+872C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514591 | |||||||
chr18:74514593 | T | G | 24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+874T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514593 | |||||||
chr18:74514612 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.903+893A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514612 | |||||||
chr18:74514614 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.903+895A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514614 | |||||||
chr18:74514629 | G | GGATGTAA others(30): Show |
24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+921_903+922ins others(37): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr18 | 74514629 | ||||||
chr18:74514649 | G | A | 24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+930G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514649 | |||||||
chr18:74514649 | G | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(21): Show |
34 | HG00544.hp2 HG00673.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.903+930G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514649 | |||||||
chr18:74514654 | G | T | 24 | a0001c0001t0001g0156 a0001c0001t0001g0158 a0001c0001t0001g0179 others(21): Show |
28 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.903+935G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514654 | |||||||
chr18:74514686 | A | G | 3 | a0001c0003t0002g0037 a0001c0003t0002g0122 a0001c0003t0023g0037 |
3 | HG02976.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.903+967A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514686 | |||||||
chr18:74514691 | T | G | 3 | a0001c0003t0002g0037 a0001c0003t0002g0122 a0001c0003t0023g0037 |
3 | HG02976.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.903+972T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514691 | |||||||
chr18:74514735 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.903+1016G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514735 | |||||||
chr18:74514802 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.903+1083G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514802 | |||||||
chr18:74514963 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.903+1244C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74514963 | |||||||
chr18:74515049 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.904-1179C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515049 | |||||||
chr18:74515267 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.904-961G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515267 | |||||||
chr18:74515359 | A | T | 1 | a0001c0001t0008g0249 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.904-869A>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515359 | |||||||
chr18:74515380 | C | G | 2 | a0002c0002t0002g0089 a0002c0002t0002g0114 |
2 | NA18951.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.904-848C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515380 | |||||||
chr18:74515382 | G | A | 1 | a0002c0002t0002g0096 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.904-846G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515382 | |||||||
chr18:74515517 | G | A | 1 | a0001c0001t0001g0010 | 4 | NA18944.hp1 NA18966.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-711G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515517 | |||||||
chr18:74515606 | T | G | 2 | a0001c0001t0006g0028 a0001c0001t0006g0071 |
3 | HG02451.hp1 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.904-622T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515606 | |||||||
chr18:74515643 | G | A | 11 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0142 others(8): Show |
13 | HG01358.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.904-585G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515643 | |||||||
chr18:74515730 | G | A | 72 | a0001c0001t0001g0040 a0002c0002t0001g0167 a0002c0002t0002g0003 others(69): Show |
94 | HG00323.hp1 HG00544.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.904-498G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515730 | |||||||
chr18:74515901 | G | A | 1 | a0002c0002t0002g0094 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.904-327G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515901 | |||||||
chr18:74515918 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.904-310T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515918 | |||||||
chr18:74515956 | T | C | 17 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0142 others(14): Show |
19 | HG01358.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.904-272T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515956 | |||||||
chr18:74515977 | A | C | 2 | a0002c0006t0002g0066 a0002c0006t0003g0277 |
2 | HG01361.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.904-251A>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74515977 | |||||||
chr18:74516164 | C | T | 1 | a0001c0003t0009g0061 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.904-64C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 8/11 | chr18 | 74516164 | |||||||
chr18:74516460 | T | A | 116 | a0001c0001t0001g0040 a0001c0001t0001g0156 a0001c0001t0001g0158 others(113): Show |
148 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1068+68T>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74516460 | |||||||
chr18:74516623 | CCTCA | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(257): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1068+237_1068+240d others(6): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 74516623 | ||||||
chr18:74516671 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1068+279G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74516671 | |||||||
chr18:74516760 | G | A | 16 | a0001c0001t0002g0026 a0001c0001t0002g0063 a0001c0001t0005g0068 others(13): Show |
22 | HG01175.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1068+368G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74516760 | |||||||
chr18:74516972 | A | ACAGACGC others(14): Show |
1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1068+589_1068+609d others(23): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 74516972 | ||||||
chr18:74516972 | ACAGACGC others(14): Show |
A | 1 | a0001c0001t0001g0181 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1068+589_1068+609d others(23): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 74516972 | ||||||
chr18:74516979 | C | T | 1 | a0001c0001t0006g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1068+587C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74516979 | |||||||
chr18:74516981 | GTAGCTTA others(14): Show |
G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.1068+606_1068+626d others(23): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 74516981 | ||||||
chr18:74517002 | A | G | 126 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0156 others(123): Show |
161 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.1068+610A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517002 | |||||||
chr18:74517095 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1068+703C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517095 | |||||||
chr18:74517151 | C | T | 2 | a0001c0001t0015g0244 a0001c0001t0015g0245 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1068+759C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517151 | |||||||
chr18:74517171 | C | G | 1 | a0002c0006t0002g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1068+779C>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517171 | |||||||
chr18:74517284 | C | T | 2 | a0001c0001t0009g0170 a0001c0001t0009g0171 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1068+892C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517284 | |||||||
chr18:74517638 | A | G | 1 | a0001c0001t0008g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1069-861A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517638 | |||||||
chr18:74517767 | A | G | 22 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0196 others(19): Show |
28 | HG01243.hp2 HG01257.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.1069-732A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517767 | |||||||
chr18:74517956 | CTGGGTTT others(7): Show |
C | 1 | a0008c0015t0004g0254 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1069-540_1069-527d others(16): Show |
CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 74517956 | ||||||
chr18:74517996 | C | T | 1 | a0001c0001t0017g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1069-503C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74517996 | |||||||
chr18:74518003 | G | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(281): Show |
399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.1069-496G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518003 | |||||||
chr18:74518044 | G | GC | 4 | a0001c0001t0005g0068 a0001c0001t0009g0074 a0001c0001t0009g0168 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-454dupC | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 74518044 | ||||||
chr18:74518046 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1069-453G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518046 | |||||||
chr18:74518050 | G | A | 1 | a0001c0001t0012g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1069-449G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518050 | |||||||
chr18:74518078 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1069-421C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518078 | |||||||
chr18:74518086 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1069-413C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518086 | |||||||
chr18:74518096 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1069-403A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518096 | |||||||
chr18:74518098 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1069-401T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518098 | |||||||
chr18:74518111 | A | C | 4 | a0001c0001t0001g0196 a0001c0001t0002g0149 a0001c0003t0009g0061 others(1): Show |
4 | HG02109.hp2 HG02809.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-388A>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518111 | |||||||
chr18:74518115 | G | T | 2 | a0001c0001t0002g0149 a0001c0016t0009g0072 |
2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1069-384G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518115 | |||||||
chr18:74518121 | T | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(89): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1069-378T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518121 | |||||||
chr18:74518122 | G | A | 1 | a0002c0002t0006g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1069-377G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518122 | |||||||
chr18:74518123 | T | C | 1 | a0001c0001t0001g0048 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1069-376T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518123 | |||||||
chr18:74518124 | G | A | 7 | a0001c0001t0008g0174 a0001c0001t0008g0238 a0001c0003t0007g0045 others(4): Show |
7 | HG01074.hp1 HG02572.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1069-375G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518124 | |||||||
chr18:74518127 | G | A | 3 | a0001c0001t0015g0244 a0001c0001t0029g0157 a0001c0003t0048g0152 |
3 | HG00280.hp2 HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1069-372G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518127 | |||||||
chr18:74518128 | G | A | 2 | a0001c0003t0002g0193 a0002c0002t0002g0111 |
2 | HG03471.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1069-371G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518128 | |||||||
chr18:74518129 | C | T | 6 | a0001c0001t0001g0237 a0001c0001t0003g0154 a0002c0002t0002g0067 others(3): Show |
6 | HG02145.hp2 HG04199.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-370C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518129 | |||||||
chr18:74518130 | G | A | 1 | a0002c0002t0006g0120 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1069-369G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518130 | |||||||
chr18:74518134 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1069-365G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518134 | |||||||
chr18:74518150 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1069-349G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518150 | |||||||
chr18:74518169 | G | A | 3 | a0001c0001t0008g0246 a0001c0001t0008g0248 a0001c0001t0008g0249 |
3 | HG02145.hp1 HG02257.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1069-330G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518169 | |||||||
chr18:74518210 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG00642.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1069-289C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518210 | |||||||
chr18:74518217 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(123): Show |
185 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1069-282A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518217 | |||||||
chr18:74518226 | T | C | 2 | a0001c0001t0014g0197 a0002c0002t0002g0087 |
2 | HG00544.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.1069-273T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518226 | |||||||
chr18:74518227 | G | A | 2 | a0001c0001t0014g0197 a0002c0002t0002g0087 |
2 | HG00544.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.1069-272G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518227 | |||||||
chr18:74518239 | A | G | 4 | a0001c0001t0001g0199 a0001c0001t0004g0255 a0002c0002t0006g0102 others(1): Show |
4 | HG02647.hp1 HG03453.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-260A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518239 | |||||||
chr18:74518241 | A | G | 6 | a0001c0001t0001g0199 a0001c0001t0004g0255 a0001c0001t0014g0197 others(3): Show |
6 | HG00544.hp1 HG00544.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1069-258A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518241 | |||||||
chr18:74518249 | G | A | 42 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0023 others(39): Show |
55 | HG00673.hp1 HG01192.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.1069-250G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518249 | |||||||
chr18:74518257 | A | G | 4 | a0001c0001t0014g0197 a0002c0002t0002g0087 a0002c0002t0006g0102 others(1): Show |
4 | HG00544.hp1 HG00544.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-242A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518257 | |||||||
chr18:74518357 | T | G | 4 | a0001c0001t0006g0071 a0001c0001t0007g0076 a0001c0001t0046g0077 others(1): Show |
4 | HG02451.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069-142T>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518357 | |||||||
chr18:74518369 | C | A | 1 | a0002c0002t0002g0099 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1069-130C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518369 | |||||||
chr18:74518403 | G | A | 3 | a0001c0001t0001g0242 a0002c0002t0002g0031 a0010c0013t0002g0124 |
4 | HG01891.hp1 HG02615.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1069-96G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518403 | |||||||
chr18:74518403 | G | T | 12 | a0001c0001t0006g0071 a0001c0001t0012g0141 a0001c0001t0012g0271 others(9): Show |
17 | HG01255.hp2 HG01257.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1069-96G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518403 | |||||||
chr18:74518453 | G | A | 28 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0040 others(25): Show |
38 | HG00280.hp2 HG00738.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1069-46G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 9/11 | chr18 | 74518453 | |||||||
chr18:74518647 | C | T | 16 | a0001c0001t0004g0024 a0001c0001t0004g0058 a0001c0001t0004g0173 others(13): Show |
20 | HG02027.hp2 HG02451.hp1 HG02630.hp2 others(17): Show |
splice_region_variant&intron_variant | LOW | c.1210+7C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518647 | |||||||
chr18:74518648 | G | A | 3 | a0001c0001t0001g0052 a0001c0001t0001g0212 a0001c0001t0019g0052 |
3 | HG02132.hp2 NA18957.hp1 NA19075.hp1 |
splice_region_variant&intron_variant | LOW | c.1210+8G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518648 | |||||||
chr18:74518670 | C | T | 2 | a0002c0002t0006g0102 a0002c0002t0006g0120 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1210+30C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518670 | |||||||
chr18:74518683 | G | A | 3 | a0001c0001t0008g0238 a0001c0003t0007g0191 a0002c0002t0002g0117 |
3 | HG02015.hp1 HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1210+43G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518683 | |||||||
chr18:74518737 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1210+97G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518737 | |||||||
chr18:74518753 | G | T | 1 | a0001c0001t0001g0055 | 2 | HG01496.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1210+113G>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518753 | |||||||
chr18:74518824 | G | A | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(294): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1211-125G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518824 | |||||||
chr18:74518825 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG03710.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1211-124C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518825 | |||||||
chr18:74518826 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1211-123G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518826 | |||||||
chr18:74518940 | T | TC | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(247): Show |
354 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(351): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1211-3dupC | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 74518940 | ||||||
chr18:74518941 | C | A | 4 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0018g0175 others(1): Show |
4 | HG01884.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1211-8C>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518941 | |||||||
chr18:74518947 | A | C | 1 | a0008c0015t0004g0254 | 1 | NA18987.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1211-2A>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518947 | |||||||
chr18:74518948 | G | A | 1 | a0008c0015t0004g0254 | 1 | NA18987.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1211-1G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 10/11 | chr18 | 74518948 | |||||||
chr18:74519169 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(185): Show |
280 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.1358+73G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/11 | chr18 | 74519169 | |||||||
chr18:74519264 | C | T | 29 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0040 others(26): Show |
39 | HG00280.hp2 HG00738.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.1358+168C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/11 | chr18 | 74519264 | |||||||
chr18:74519326 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1358+230A>G | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/11 | chr18 | 74519326 | |||||||
chr18:74519395 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1358+299T>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/11 | chr18 | 74519395 | |||||||
chr18:74519474 | G | C | 5 | a0001c0001t0009g0170 a0001c0001t0009g0171 a0001c0001t0018g0175 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1358+378G>C | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/11 | chr18 | 74519474 | |||||||
chr18:74519543 | G | A | 1 | a0001c0001t0015g0244 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1358+447G>A | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/11 | chr18 | 74519543 | |||||||
chr18:74519925 | C | T | 17 | a0001c0001t0007g0076 a0001c0001t0008g0174 a0001c0001t0008g0236 others(14): Show |
17 | HG01074.hp1 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1359-74C>T | CNDP2 | ENSG00000133313.15 | transcript | ENST00000324262.9 | protein_coding | 11/11 | chr18 | 74519925 |