Item | Value |
---|---|
geneid | 9651 |
ensemblid | ENSG00000149527.18 |
hgncid | 29037 |
symbol | PLCH2 |
name | phospholipase C eta 2 |
refseq_nuc | NM_014638.4 |
refseq_prot | NP_055453.2 |
ensembl_nuc | ENST00000378486.8 |
ensembl_prot | ENSP00000367747.3 |
mane_status | MANE Select |
chr | chr1 |
start | 2476289 |
end | 2505532 |
strand | + |
ver | v1.2 |
region | chr1:2476289-2505532 |
region5000 | chr1:2471289-2510532 |
regionname0 | PLCH2_chr1_2476289_2505532 |
regionname5000 | PLCH2_chr1_2471289_2510532 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1416 | 318 | 69 | 64 | 138 | 13 | 34 | 96 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0002 | 0/0 | 1416 | 12 | 0 | 0 | 12 | 0 | 0 | 11 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0003 | 0/0 | 1416 | 10 | 7 | 0 | 1 | 0 | 2 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0004 | 0/0 | 1416 | 7 | 6 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0005 | 0/0 | 1416 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0006 | 0/1 | 1416 | 2 | 0 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0007 | 0/0 | 1416 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0008 | 0/0 | 1416 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0009 | 0/0 | 1416 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0010 | 0/0 | 1416 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0011 | 0/0 | 1416 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0012 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0013 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0014 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0015 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0016 | 0/0 | 1416 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0017 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0018 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0019 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0020 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0021 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0022 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0023 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0024 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0025 | 0/0 | 1416 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0026 | 0/0 | 1416 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0027 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0028 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0029 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
a0030 | 0/0 | 1416 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | MSGPW others(1411): Show |
chr1 | 2471289 | 2510532 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4248 | 166 | 49 | 33 | 57 | 8 | 19 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0002 | 0/0 | 4248 | 81 | 8 | 13 | 49 | 4 | 7 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0003 | 0/0 | 4248 | 53 | 7 | 11 | 27 | 1 | 7 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0009 | 0/0 | 4248 | 3 | 0 | 2 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0010 | 0/0 | 4248 | 3 | 1 | 2 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0014 | 0/0 | 4248 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0023 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0025 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0028 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0041 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0043 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0044 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0045 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0047 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0049 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0001c0050 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0002c0004 | 0/0 | 4248 | 9 | 0 | 0 | 9 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0002c0011 | 0/0 | 4248 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0002c0019 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0003c0005 | 0/0 | 4248 | 7 | 4 | 0 | 1 | 0 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0003c0008 | 0/0 | 4248 | 3 | 3 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0004c0006 | 0/0 | 4248 | 6 | 6 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0004c0024 | 0/0 | 4248 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0005c0007 | 0/0 | 4248 | 5 | 0 | 0 | 4 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0006c0012 | 0/1 | 4248 | 2 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0007c0017 | 0/0 | 4248 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0008c0036 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0008c0046 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0009c0016 | 0/0 | 4248 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0010c0015 | 0/0 | 4248 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0011c0013 | 0/0 | 4248 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0012c0022 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0013c0035 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0014c0027 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0015c0034 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0016c0026 | 0/0 | 4248 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0017c0033 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0018c0038 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0019c0021 | 0/0 | 4248 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0020c0037 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0021c0048 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0022c0020 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0023c0032 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0024c0030 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0025c0029 | 0/0 | 4248 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0026c0042 | 0/0 | 4248 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0027c0039 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0028c0018 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0029c0031 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 | ||
a0030c0040 | 0/0 | 4248 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | ATGTC others(4243): Show |
chr1 | 2471289 | 2510532 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4870 | 42 | 13 | 8 | 7 | 4 | 10 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0001t0002 | 0/0 | 4870 | 111 | 33 | 18 | 49 | 3 | 8 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0001t0003 | 0/0 | 4870 | 8 | 1 | 6 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0001t0007 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0001t0008 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0001t0009 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0001t0010 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0001t0011 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0002t0001 | 0/0 | 4870 | 77 | 8 | 13 | 45 | 4 | 7 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0002t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0002t0005 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0003t0001 | 0/0 | 4870 | 53 | 7 | 11 | 27 | 1 | 7 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0009t0002 | 0/0 | 4870 | 3 | 0 | 2 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0010t0001 | 0/0 | 4870 | 3 | 1 | 2 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0014t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0023t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0025t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0028t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0041t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0043t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0044t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0045t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0047t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0049t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0001c0050t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0002c0004t0002 | 0/0 | 4870 | 9 | 0 | 0 | 9 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0002c0011t0001 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0002c0019t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0003c0005t0002 | 0/0 | 4870 | 7 | 4 | 0 | 1 | 0 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0003c0008t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0003c0008t0002 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0004c0006t0002 | 0/0 | 4870 | 5 | 5 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0004c0006t0006 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0004c0024t0001 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0005c0007t0001 | 0/0 | 4870 | 5 | 0 | 0 | 4 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0006c0012t0001 | 0/1 | 4870 | 2 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0007c0017t0001 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0008c0036t0004 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0008c0046t0004 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0009c0016t0001 | 0/0 | 4870 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0010c0015t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0011c0013t0002 | 0/0 | 4870 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0012c0022t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0013c0035t0001 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0014c0027t0003 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0015c0034t0002 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0016c0026t0003 | 0/0 | 4870 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0017c0033t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0018c0038t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0019c0021t0001 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0020c0037t0001 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0021c0048t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0022c0020t0004 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0023c0032t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0024c0030t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0025c0029t0002 | 0/0 | 4870 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0026c0042t0001 | 0/0 | 4870 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0027c0039t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0028c0018t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0029c0031t0002 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
a0030c0040t0001 | 0/0 | 4870 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | GTCCT others(4865): Show |
chr1 | 2471289 | 2510532 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0009 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0016 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0001 | 0/0 | 24 | 0 | 2 | 16 | 0 | 6 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0045 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0003g0006 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0008g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0001t0011g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0002 | 0/0 | 16 | 0 | 1 | 15 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0007 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0008 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0002t0005g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0003 | 0/0 | 10 | 0 | 3 | 3 | 1 | 3 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0004 | 0/0 | 11 | 1 | 2 | 8 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0009t0002g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0009t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0009t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0010t0001g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0014t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0014t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0023t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0025t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0028t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0041t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0043t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0044t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0045t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0047t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0049t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0001c0050t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0002c0004t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0002c0004t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0002c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0002c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0002c0011t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0002c0011t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0002c0019t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0005t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0005t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0005t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0005t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0005t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0005t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0008t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0008t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0003c0008t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0004c0006t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0004c0006t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0004c0006t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0004c0006t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0004c0006t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0004c0006t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0004c0024t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0005c0007t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0005c0007t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0006c0012t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0006c0012t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0007c0017t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0007c0017t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0008c0036t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0008c0046t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0009c0016t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0009c0016t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0010c0015t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0011c0013t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0011c0013t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0012c0022t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0013c0035t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0014c0027t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0015c0034t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0016c0026t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0017c0033t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0018c0038t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0019c0021t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0020c0037t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0021c0048t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0022c0020t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0023c0032t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0024c0030t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0025c0029t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0026c0042t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0027c0039t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0028c0018t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0029c0031t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
a0030c0040t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | GBR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0224 | EUR | GBR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0019 | EUR | FIN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | FIN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0163 | EUR | FIN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | FIN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00408 | hp1 | a0012 | c0022 | t0002 | g0187 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00438 | hp1 | a0005 | c0007 | t0001 | g0002 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00438 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00558 | hp2 | a0001 | c0014 | t0002 | g0217 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00597 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00733 | hp1 | a0001 | c0009 | t0002 | g0219 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01070 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01074 | hp1 | a0001 | c0009 | t0002 | g0001 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0175 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01099 | hp2 | a0001 | c0010 | t0001 | g0013 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01106 | hp2 | a0013 | c0035 | t0001 | g0086 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0003 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0227 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01243 | hp1 | a0001 | c0010 | t0001 | g0013 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01255 | hp1 | a0014 | c0027 | t0003 | g0094 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01258 | hp1 | a0001 | c0043 | t0001 | g0007 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01261 | hp1 | a0015 | c0034 | t0002 | g0197 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0079 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01358 | hp1 | a0016 | c0026 | t0003 | g0095 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0065 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01515 | hp1 | a0006 | c0012 | t0001 | g0003 | EUR | IBS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0206 | EUR | IBS | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01891 | hp1 | a0004 | c0006 | t0006 | g0161 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0176 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01993 | hp1 | a0001 | c0001 | t0011 | g0012 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02015 | hp1 | a0001 | c0025 | t0001 | g0194 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02040 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02056 | hp2 | a0007 | c0017 | t0001 | g0081 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0067 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0075 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02145 | hp1 | a0003 | c0005 | t0002 | g0137 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CDX | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | CDX | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02165 | hp1 | a0001 | c0041 | t0001 | g0164 | EAS | CDX | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | CDX | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02300 | hp2 | a0001 | c0028 | t0001 | g0084 | AMR | PEL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02451 | hp1 | a0004 | c0006 | t0002 | g0203 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02523 | hp1 | a0002 | c0004 | t0002 | g0029 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02572 | hp1 | a0003 | c0005 | t0002 | g0150 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0122 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02615 | hp1 | a0003 | c0008 | t0001 | g0056 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02622 | hp1 | a0001 | c0010 | t0001 | g0013 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02622 | hp2 | a0017 | c0033 | t0001 | g0205 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02630 | hp2 | a0018 | c0038 | t0001 | g0225 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02647 | hp2 | a0001 | c0045 | t0002 | g0082 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02683 | hp1 | a0019 | c0021 | t0001 | g0007 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02717 | hp1 | a0003 | c0005 | t0002 | g0139 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0120 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02723 | hp1 | a0003 | c0008 | t0002 | g0054 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02723 | hp2 | a0008 | c0046 | t0004 | g0119 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0080 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02735 | hp2 | a0001 | c0009 | t0002 | g0191 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0003 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0032 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02818 | hp1 | a0001 | c0047 | t0002 | g0087 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02922 | hp1 | a0001 | c0001 | t0008 | g0210 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02922 | hp2 | a0004 | c0006 | t0002 | g0136 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02965 | hp2 | a0020 | c0037 | t0001 | g0125 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02976 | hp1 | a0021 | c0048 | t0002 | g0124 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0121 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03098 | hp2 | a0004 | c0006 | t0002 | g0192 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03130 | hp2 | a0004 | c0006 | t0002 | g0154 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03139 | hp1 | a0022 | c0020 | t0004 | g0026 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03209 | hp2 | a0023 | c0032 | t0002 | g0035 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03225 | hp1 | a0004 | c0006 | t0002 | g0160 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03453 | hp1 | a0024 | c0030 | t0002 | g0144 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03453 | hp2 | a0025 | c0029 | t0002 | g0092 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0178 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03491 | hp1 | a0003 | c0005 | t0002 | g0025 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03492 | hp1 | a0003 | c0005 | t0002 | g0025 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03540 | hp2 | a0001 | c0050 | t0002 | g0143 | AFR | GWD | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0003 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0003 | SAS | STU | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0022 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03831 | hp1 | a0001 | c0001 | t0010 | g0001 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03831 | hp2 | a0005 | c0007 | t0001 | g0002 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03942 | hp2 | a0026 | c0042 | t0001 | g0218 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG04184 | hp1 | a0004 | c0024 | t0001 | g0152 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | STU | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0200 | SAS | STU | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | YRI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | YRI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18906 | hp1 | a0003 | c0008 | t0002 | g0055 | AFR | YRI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18941 | hp1 | a0002 | c0019 | t0002 | g0118 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18944 | hp2 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18945 | hp1 | a0010 | c0015 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18947 | hp2 | a0002 | c0011 | t0001 | g0168 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18948 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18954 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18960 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18962 | hp1 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18966 | hp1 | a0002 | c0004 | t0002 | g0112 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18967 | hp2 | a0002 | c0004 | t0002 | g0029 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18973 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18983 | hp2 | a0001 | c0014 | t0002 | g0208 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18984 | hp1 | a0001 | c0044 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18985 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18986 | hp2 | a0002 | c0011 | t0001 | g0113 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18990 | hp2 | a0027 | c0039 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18995 | hp1 | a0028 | c0018 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18997 | hp1 | a0001 | c0001 | t0009 | g0116 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0073 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18998 | hp2 | a0003 | c0005 | t0002 | g0123 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18999 | hp1 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19002 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19005 | hp1 | a0011 | c0013 | t0002 | g0057 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19005 | hp2 | a0029 | c0031 | t0002 | g0189 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19007 | hp1 | a0007 | c0017 | t0001 | g0221 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19007 | hp2 | a0001 | c0002 | t0005 | g0047 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19009 | hp2 | a0011 | c0013 | t0002 | g0058 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19010 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19011 | hp2 | a0030 | c0040 | t0001 | g0038 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19012 | hp2 | a0010 | c0015 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19030 | hp1 | a0009 | c0016 | t0001 | g0089 | AFR | LWK | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19030 | hp2 | a0003 | c0005 | t0002 | g0110 | AFR | LWK | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | LWK | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19054 | hp2 | a0002 | c0004 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19060 | hp2 | a0002 | c0004 | t0002 | g0114 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19064 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19067 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19074 | hp2 | a0005 | c0007 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19077 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19080 | hp2 | a0001 | c0002 | t0005 | g0047 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19091 | hp2 | a0005 | c0007 | t0001 | g0146 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | YRI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | YRI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ASW | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ASW | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | TSI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0014 | EUR | TSI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0003 | EUR | TSI | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0066 | SAS | GIH | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG01123 | hp2 | a0001 | c0023 | t0001 | g0002 | AMR | CLM | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0032 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | ACB | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG03471 | hp2 | a0001 | c0049 | t0002 | g0131 | AFR | MSL | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | USA | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
HG06807 | hp2 | a0009 | c0016 | t0001 | g0088 | AFR | USA | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20300 | hp1 | a0008 | c0036 | t0004 | g0026 | AFR | USA | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
NA21309 | hp2 | a0001 | c0002 | t0001 | g0129 | AFR | LWK | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
homoSapiens | chm13v2 | a0006 | c0012 | t0001 | g0071 | REF | REF | PLCH2_chr1_2471289_2510532 | PLCH2 | chr1 | 2471289 | 2510532 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2476671 | G | C | 2 | a0002 a0028 |
13 | HG02523.hp1 NA18941.hp1 NA18944.hp2 others(10): Show |
missense_variant | MODERATE | c.83G>C | p.Gly28Ala | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | 383/4870 | 83/4251 | 28/1416 | chr1 | 2476671 | |||
chr1:2478482 | G | A | 1 | a0022 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.131G>A | p.Arg44Gln | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/22 | 431/4870 | 131/4251 | 44/1416 | chr1 | 2478482 | |||
chr1:2479806 | G | A | 1 | a0006 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.344G>A | p.Ser115Asn | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 3/22 | 644/4870 | 344/4251 | 115/1416 | chr1 | 2479806 | |||
chr1:2484536 | A | T | 1 | a0021 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.734A>T | p.Tyr245Phe | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/22 | 1034/4870 | 734/4251 | 245/1416 | chr1 | 2484536 | |||
chr1:2484571 | C | A | 1 | a0019 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.769C>A | p.His257Asn | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/22 | 1069/4870 | 769/4251 | 257/1416 | chr1 | 2484571 | |||
chr1:2487298 | G | A | 1 | a0012 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.1036G>A | p.Val346Met | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 7/22 | 1336/4870 | 1036/4251 | 346/1416 | chr1 | 2487298 | |||
chr1:2491312 | C | T | 1 | a0026 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.1636C>T | p.Pro546Ser | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/22 | 1936/4870 | 1636/4251 | 546/1416 | chr1 | 2491312 | |||
chr1:2494871 | G | A | 1 | a0007 | 2 | HG02056.hp2 NA19007.hp1 |
missense_variant | MODERATE | c.1675G>A | p.Asp559Asn | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/22 | 1975/4870 | 1675/4251 | 559/1416 | chr1 | 2494871 | |||
chr1:2494874 | G | A | 1 | a0004 | 7 | HG01891.hp1 HG02451.hp1 HG02922.hp2 others(4): Show |
missense_variant | MODERATE | c.1678G>A | p.Val560Met | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/22 | 1978/4870 | 1678/4251 | 560/1416 | chr1 | 2494874 | |||
chr1:2498564 | C | A | 1 | a0016 | 1 | HG01358.hp1 | missense_variant | MODERATE | c.2266C>A | p.Leu756Ile | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 17/22 | 2566/4870 | 2266/4251 | 756/1416 | chr1 | 2498564 | |||
chr1:2502190 | C | T | 1 | a0013 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.2740C>T | p.Arg914Trp | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/22 | 3040/4870 | 2740/4251 | 914/1416 | chr1 | 2502190 | |||
chr1:2502197 | C | T | 2 | a0015 a0017 |
2 | HG01261.hp1 HG02622.hp2 |
missense_variant | MODERATE | c.2747C>T | p.Pro916Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/22 | 3047/4870 | 2747/4251 | 916/1416 | chr1 | 2502197 | |||
chr1:2502203 | G | T | 1 | a0009 | 2 | HG06807.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.2753G>T | p.Arg918Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/22 | 3053/4870 | 2753/4251 | 918/1416 | chr1 | 2502203 | |||
chr1:2502271 | C | T | 1 | a0015 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.2821C>T | p.Arg941Cys | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/22 | 3121/4870 | 2821/4251 | 941/1416 | chr1 | 2502271 | |||
chr1:2502334 | G | A | 1 | a0005 | 5 | HG00438.hp1 HG03831.hp2 NA18999.hp1 others(2): Show |
missense_variant | MODERATE | c.2884G>A | p.Asp962Asn | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/22 | 3184/4870 | 2884/4251 | 962/1416 | chr1 | 2502334 | |||
chr1:2502370 | G | A | 1 | a0014 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.2920G>A | p.Ala974Thr | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/22 | 3220/4870 | 2920/4251 | 974/1416 | chr1 | 2502370 | |||
chr1:2504012 | C | T | 1 | a0010 | 2 | NA18945.hp1 NA19012.hp2 |
missense_variant | MODERATE | c.3050C>T | p.Pro1017Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3350/4870 | 3050/4251 | 1017/1416 | chr1 | 2504012 | |||
chr1:2504035 | A | G | 1 | a0023 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.3073A>G | p.Ser1025Gly | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3373/4870 | 3073/4251 | 1025/1416 | chr1 | 2504035 | |||
chr1:2504299 | G | A | 2 | a0018 a0020 |
2 | HG02630.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.3337G>A | p.Ala1113Thr | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3637/4870 | 3337/4251 | 1113/1416 | chr1 | 2504299 | |||
chr1:2504320 | G | A | 2 | a0008 a0022 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.3358G>A | p.Val1120Met | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3658/4870 | 3358/4251 | 1120/1416 | chr1 | 2504320 | |||
chr1:2504461 | C | T | 1 | a0030 | 1 | NA19011.hp2 | missense_variant | MODERATE | c.3499C>T | p.Arg1167Cys | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3799/4870 | 3499/4251 | 1167/1416 | chr1 | 2504461 | |||
chr1:2504519 | C | T | 1 | a0029 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.3557C>T | p.Ser1186Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3857/4870 | 3557/4251 | 1186/1416 | chr1 | 2504519 | |||
chr1:2504689 | G | T | 1 | a0028 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.3727G>T | p.Val1243Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4027/4870 | 3727/4251 | 1243/1416 | chr1 | 2504689 | |||
chr1:2504864 | A | C | 1 | a0018 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.3902A>C | p.Glu1301Ala | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4202/4870 | 3902/4251 | 1301/1416 | chr1 | 2504864 | |||
chr1:2504965 | G | C | 4 | a0003 a0008 a0021 others(1): Show |
14 | HG02145.hp1 HG02572.hp1 HG02615.hp1 others(11): Show |
missense_variant | MODERATE | c.4003G>C | p.Val1335Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4303/4870 | 4003/4251 | 1335/1416 | chr1 | 2504965 | |||
chr1:2505038 | G | C | 1 | a0011 | 2 | NA19005.hp1 NA19009.hp2 |
missense_variant | MODERATE | c.4076G>C | p.Arg1359Pro | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4376/4870 | 4076/4251 | 1359/1416 | chr1 | 2505038 | |||
chr1:2505067 | C | G | 1 | a0024 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.4105C>G | p.Gln1369Glu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4405/4870 | 4105/4251 | 1369/1416 | chr1 | 2505067 | |||
chr1:2505166 | G | A | 1 | a0027 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.4204G>A | p.Gly1402Arg | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4504/4870 | 4204/4251 | 1402/1416 | chr1 | 2505166 | |||
chr1:2505205 | C | T | 1 | a0025 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4243C>T | p.Arg1415Cys | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4543/4870 | 4243/4251 | 1415/1416 | chr1 | 2505205 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2476606 | C | T | 1 | a0001c0050 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.18C>T | p.Pro6Pro | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | 318/4870 | 18/4251 | 6/1416 | chr1 | 2476606 | |||
chr1:2476609 | C | T | 1 | a0001c0049 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.21C>T | p.Ser7Ser | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | 321/4870 | 21/4251 | 7/1416 | chr1 | 2476609 | |||
chr1:2479840 | C | T | 1 | a0001c0010 | 3 | HG01099.hp2 HG01243.hp1 HG02622.hp1 |
synonymous_variant | LOW | c.378C>T | p.His126His | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 3/22 | 678/4870 | 378/4251 | 126/1416 | chr1 | 2479840 | |||
chr1:2486924 | C | T | 1 | a0001c0047 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.834C>T | p.Leu278Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 6/22 | 1134/4870 | 834/4251 | 278/1416 | chr1 | 2486924 | |||
chr1:2487186 | C | T | 6 | a0001c0003 a0001c0045 a0002c0019 others(3): Show |
59 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
synonymous_variant | LOW | c.924C>T | p.Tyr308Tyr | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 7/22 | 1224/4870 | 924/4251 | 308/1416 | chr1 | 2487186 | |||
chr1:2487620 | C | T | 1 | a0001c0044 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.1137C>T | p.Asp379Asp | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/22 | 1437/4870 | 1137/4251 | 379/1416 | chr1 | 2487620 | |||
chr1:2489795 | G | A | 1 | a0001c0023 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1443G>A | p.Ala481Ala | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/22 | 1743/4870 | 1443/4251 | 481/1416 | chr1 | 2489795 | |||
chr1:2489840 | C | T | 2 | a0001c0043 a0019c0021 |
2 | HG01258.hp1 HG02683.hp1 |
synonymous_variant | LOW | c.1488C>T | p.Asp496Asp | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/22 | 1788/4870 | 1488/4251 | 496/1416 | chr1 | 2489840 | |||
chr1:2495520 | C | T | 1 | a0001c0041 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.1785C>T | p.Ser595Ser | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/22 | 2085/4870 | 1785/4251 | 595/1416 | chr1 | 2495520 | |||
chr1:2496979 | G | A | 1 | a0001c0025 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.2085G>A | p.Pro695Pro | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 15/22 | 2385/4870 | 2085/4251 | 695/1416 | chr1 | 2496979 | |||
chr1:2499178 | C | T | 16 | a0001c0002 a0001c0003 a0001c0023 others(13): Show |
154 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(151): Show |
synonymous_variant | LOW | c.2529C>T | p.Ile843Ile | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 19/22 | 2829/4870 | 2529/4251 | 843/1416 | chr1 | 2499178 | |||
chr1:2499660 | A | G | 3 | a0008c0036 a0008c0046 a0022c0020 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2601A>G | p.Leu867Leu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/22 | 2901/4870 | 2601/4251 | 867/1416 | chr1 | 2499660 | |||
chr1:2499663 | A | G | 3 | a0008c0036 a0008c0046 a0022c0020 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.2604A>G | p.Glu868Glu | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/22 | 2904/4870 | 2604/4251 | 868/1416 | chr1 | 2499663 | |||
chr1:2504337 | G | A | 1 | a0003c0008 | 3 | HG02615.hp1 HG02723.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.3375G>A | p.Thr1125Thr | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3675/4870 | 3375/4251 | 1125/1416 | chr1 | 2504337 | |||
chr1:2504613 | C | T | 1 | a0001c0014 | 2 | HG00558.hp2 NA18983.hp2 |
synonymous_variant | LOW | c.3651C>T | p.Asp1217Asp | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3951/4870 | 3651/4251 | 1217/1416 | chr1 | 2504613 | |||
chr1:2504817 | G | A | 1 | a0001c0009 | 3 | HG00733.hp1 HG01074.hp1 HG02735.hp2 |
synonymous_variant | LOW | c.3855G>A | p.Gly1285Gly | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4155/4870 | 3855/4251 | 1285/1416 | chr1 | 2504817 | |||
chr1:2504832 | G | A | 1 | a0001c0028 | 1 | HG02300.hp2 | synonymous_variant | LOW | c.3870G>A | p.Ser1290Ser | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 4170/4870 | 3870/4251 | 1290/1416 | chr1 | 2504832 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2476342 | C | T | 4 | a0001c0001t0003 a0001c0001t0011 a0014c0027t0003 others(1): Show |
11 | HG00642.hp2 HG00738.hp1 HG00741.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-247C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | 247 | chr1 | 2476342 | ||||||
chr1:2476402 | A | G | 1 | a0001c0001t0010 | 1 | HG03831.hp1 | 5_prime_UTR_variant | MODIFIER | c.-187A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | 187 | chr1 | 2476402 | ||||||
chr1:2476488 | C | T | 1 | a0001c0001t0009 | 1 | NA18997.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-101C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | chr1 | 2476488 | |||||||
chr1:2476500 | C | T | 1 | a0001c0001t0008 | 1 | HG02922.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-89C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | chr1 | 2476500 | |||||||
chr1:2476513 | A | G | 1 | a0001c0001t0007 | 1 | HG02559.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/22 | 76 | chr1 | 2476513 | ||||||
chr1:2505216 | G | A | 3 | a0008c0036t0004 a0008c0046t0004 a0022c0020t0004 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 3 | chr1 | 2505216 | ||||||
chr1:2505276 | C | T | 1 | a0001c0002t0005 | 2 | NA19007.hp2 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*63C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 63 | chr1 | 2505276 | ||||||
chr1:2505281 | G | A | 1 | a0004c0006t0006 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 68 | chr1 | 2505281 | ||||||
chr1:2505339 | A | G | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(30): Show |
168 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*126A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 22/22 | 126 | chr1 | 2505339 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:2476879 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0229 |
3 | HG03195.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.124+167C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2476879 | |||||||
chr1:2476930 | C | T | 1 | a0001c0003t0001g0228 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.124+218C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2476930 | |||||||
chr1:2476940 | C | A | 4 | a0001c0010t0001g0013 a0003c0008t0001g0056 a0003c0008t0002g0054 others(1): Show |
6 | HG01099.hp2 HG01243.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+228C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2476940 | |||||||
chr1:2477032 | G | A | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.124+320G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477032 | |||||||
chr1:2477132 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+420T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477132 | |||||||
chr1:2477146 | G | A | 3 | a0001c0001t0002g0053 a0001c0001t0002g0060 a0001c0001t0002g0229 |
4 | HG03195.hp1 HG03209.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+434G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477146 | |||||||
chr1:2477186 | G | T | 1 | a0001c0001t0002g0052 | 2 | HG00639.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.124+474G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477186 | |||||||
chr1:2477210 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.124+498C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477210 | |||||||
chr1:2477222 | A | G | 186 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0031 others(183): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.124+510A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477222 | |||||||
chr1:2477395 | G | A | 3 | a0001c0002t0001g0008 a0001c0002t0001g0105 a0001c0002t0001g0106 |
7 | HG00323.hp2 HG00639.hp1 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+683G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477395 | |||||||
chr1:2477456 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0002g0028 a0001c0001t0002g0062 others(3): Show |
8 | HG00642.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+744G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477456 | |||||||
chr1:2477491 | G | A | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.124+779G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477491 | |||||||
chr1:2477539 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.124+827G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477539 | |||||||
chr1:2477747 | G | A | 2 | a0001c0001t0001g0111 a0003c0005t0002g0110 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.125-729G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477747 | |||||||
chr1:2477770 | A | G | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.125-706A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477770 | |||||||
chr1:2477796 | G | A | 10 | a0001c0001t0002g0005 a0001c0001t0009g0116 a0001c0002t0002g0115 others(7): Show |
18 | HG02523.hp1 NA18612.hp1 NA18944.hp2 others(15): Show |
intron_variant | MODIFIER | c.125-680G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477796 | |||||||
chr1:2477799 | G | A | 1 | a0001c0002t0001g0030 | 2 | NA18941.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.125-677G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477799 | |||||||
chr1:2477837 | A | G | 162 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(159): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.125-639A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477837 | |||||||
chr1:2477871 | G | T | 1 | a0001c0001t0002g0226 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.125-605G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477871 | |||||||
chr1:2477891 | G | A | 1 | a0001c0001t0002g0135 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.125-585G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477891 | |||||||
chr1:2477901 | G | C | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.125-575G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477901 | |||||||
chr1:2477921 | G | A | 150 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(147): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.125-555G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477921 | |||||||
chr1:2477944 | G | A | 36 | a0001c0001t0001g0117 a0001c0003t0001g0003 a0001c0003t0001g0004 others(33): Show |
60 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.125-532G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477944 | |||||||
chr1:2477946 | G | C | 1 | a0001c0010t0001g0013 | 3 | HG01099.hp2 HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.125-530G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477946 | |||||||
chr1:2477970 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.125-506C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477970 | |||||||
chr1:2477971 | G | A | 1 | a0001c0003t0001g0064 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.125-505G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2477971 | |||||||
chr1:2478341 | GGTGAGGA others(35): Show |
G | 1 | a0003c0005t0002g0123 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.125-99_125-58delTT others(40): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 2478341 | ||||||
chr1:2478385 | TGAGGAGT others(35): Show |
T | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.125-80_125-39delCG others(40): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 2478385 | ||||||
chr1:2478417 | GTC | G | 4 | a0001c0010t0001g0013 a0003c0008t0001g0056 a0003c0008t0002g0054 others(1): Show |
6 | HG01099.hp2 HG01243.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-54_125-53delTC | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 2478417 | ||||||
chr1:2478444 | T | C | 1 | a0021c0048t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.125-32T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2478444 | |||||||
chr1:2478453 | A | G | 179 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(176): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.125-23A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 1/21 | chr1 | 2478453 | |||||||
chr1:2478790 | A | T | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.271+168A>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2478790 | |||||||
chr1:2478847 | C | T | 1 | a0001c0001t0002g0050 | 2 | NA18979.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.271+225C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2478847 | |||||||
chr1:2478915 | A | G | 2 | a0001c0002t0001g0134 a0021c0048t0002g0124 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.271+293A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2478915 | |||||||
chr1:2479012 | G | A | 1 | a0001c0003t0001g0065 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.271+390G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479012 | |||||||
chr1:2479045 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.271+423G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479045 | |||||||
chr1:2479158 | C | T | 1 | a0001c0009t0002g0219 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.271+536C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479158 | |||||||
chr1:2479168 | G | T | 2 | a0001c0001t0001g0111 a0003c0005t0002g0110 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.271+546G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479168 | |||||||
chr1:2479239 | C | T | 1 | a0021c0048t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.272-495C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479239 | |||||||
chr1:2479259 | G | A | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.272-475G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479259 | |||||||
chr1:2479272 | C | T | 6 | a0001c0010t0001g0013 a0003c0008t0001g0056 a0003c0008t0002g0054 others(3): Show |
8 | HG01099.hp2 HG01243.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.272-462C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479272 | |||||||
chr1:2479350 | C | T | 153 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(150): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.272-384C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479350 | |||||||
chr1:2479688 | G | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0060 a0001c0001t0002g0229 others(1): Show |
5 | HG02717.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.272-46G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479688 | |||||||
chr1:2479723 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.272-11C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 2/21 | chr1 | 2479723 | |||||||
chr1:2480012 | A | G | 164 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(161): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.515+35A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 3/21 | chr1 | 2480012 | |||||||
chr1:2480084 | G | T | 9 | a0001c0001t0001g0133 a0001c0001t0002g0033 a0001c0002t0001g0032 others(6): Show |
11 | HG02109.hp1 HG02280.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.516-99G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 3/21 | chr1 | 2480084 | |||||||
chr1:2480148 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.516-35C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 3/21 | chr1 | 2480148 | |||||||
chr1:2480350 | G | A | 3 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 |
4 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+38G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480350 | |||||||
chr1:2480358 | C | G | 1 | a0001c0014t0002g0217 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.645+46C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480358 | |||||||
chr1:2480507 | T | C | 1 | a0001c0028t0001g0084 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.645+195T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480507 | |||||||
chr1:2480682 | G | C | 4 | a0001c0001t0001g0133 a0001c0001t0002g0033 a0001c0002t0001g0132 others(1): Show |
5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.645+370G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480682 | |||||||
chr1:2480740 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.645+428A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480740 | |||||||
chr1:2480786 | C | T | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | NA19088.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.645+474C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480786 | |||||||
chr1:2480840 | A | T | 158 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(155): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.645+528A>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480840 | |||||||
chr1:2480854 | C | T | 33 | a0001c0003t0001g0003 a0001c0003t0001g0004 a0001c0003t0001g0020 others(30): Show |
57 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.645+542C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480854 | |||||||
chr1:2480894 | G | A | 1 | a0001c0002t0001g0141 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.645+582G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2480894 | |||||||
chr1:2481003 | C | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0212 a0001c0001t0001g0213 |
4 | NA18956.hp1 NA18973.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+691C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481003 | |||||||
chr1:2481014 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0212 a0001c0001t0001g0213 |
4 | NA18956.hp1 NA18973.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+702G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481014 | |||||||
chr1:2481128 | A | G | 1 | a0001c0003t0001g0064 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.645+816A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481128 | |||||||
chr1:2481137 | C | T | 2 | a0001c0001t0001g0211 a0001c0002t0001g0048 |
3 | HG00544.hp1 HG02056.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.645+825C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481137 | |||||||
chr1:2481148 | C | CCCTGCCA others(3): Show |
1 | a0001c0001t0002g0034 | 2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.645+857_645+866dup others(10): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2481148 | ||||||
chr1:2481211 | G | A | 2 | a0001c0001t0002g0035 a0023c0032t0002g0035 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.645+899G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481211 | |||||||
chr1:2481408 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.645+1096G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481408 | |||||||
chr1:2481490 | C | T | 3 | a0001c0001t0001g0213 a0001c0001t0002g0209 a0001c0001t0008g0210 |
3 | HG02647.hp1 HG02922.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.645+1178C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481490 | |||||||
chr1:2481547 | C | T | 5 | a0001c0001t0001g0111 a0003c0005t0002g0110 a0003c0008t0001g0056 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.645+1235C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481547 | |||||||
chr1:2481645 | G | C | 1 | a0001c0001t0002g0142 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.645+1333G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481645 | |||||||
chr1:2481710 | C | T | 5 | a0001c0001t0001g0111 a0003c0005t0002g0110 a0003c0008t0001g0056 others(2): Show |
5 | HG02559.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.645+1398C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481710 | |||||||
chr1:2481727 | A | G | 1 | a0001c0002t0001g0224 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.645+1415A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481727 | |||||||
chr1:2481795 | G | A | 1 | a0011c0013t0002g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.645+1483G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481795 | |||||||
chr1:2481812 | C | T | 1 | a0003c0008t0001g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.645+1500C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481812 | |||||||
chr1:2481848 | C | T | 1 | a0003c0005t0002g0123 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.645+1536C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2481848 | |||||||
chr1:2482025 | G | C | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.645+1713G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482025 | |||||||
chr1:2482195 | G | C | 156 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(153): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.645+1883G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482195 | |||||||
chr1:2482288 | A | G | 2 | a0001c0002t0001g0134 a0021c0048t0002g0124 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.645+1976A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482288 | |||||||
chr1:2482357 | C | G | 1 | a0001c0014t0002g0208 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.645+2045C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482357 | |||||||
chr1:2482357 | C | T | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.645+2045C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482357 | |||||||
chr1:2482561 | C | T | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.646-1887C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482561 | |||||||
chr1:2482567 | G | C | 2 | a0001c0002t0001g0134 a0021c0048t0002g0124 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.646-1881G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482567 | |||||||
chr1:2482579 | G | A | 1 | a0001c0003t0001g0064 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.646-1869G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482579 | |||||||
chr1:2482668 | G | T | 1 | a0001c0002t0005g0047 | 2 | NA19007.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.646-1780G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482668 | |||||||
chr1:2482680 | T | C | 1 | a0001c0010t0001g0013 | 3 | HG01099.hp2 HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.646-1768T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482680 | |||||||
chr1:2482682 | G | C | 1 | a0001c0003t0001g0085 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.646-1766G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2482682 | |||||||
chr1:2483012 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.646-1436A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483012 | |||||||
chr1:2483046 | A | C | 1 | a0001c0002t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.646-1402A>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483046 | |||||||
chr1:2483150 | C | T | 1 | a0001c0002t0005g0047 | 2 | NA19007.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.646-1298C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483150 | |||||||
chr1:2483367 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.646-1081G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483367 | |||||||
chr1:2483457 | T | C | 7 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 others(4): Show |
10 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-991T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483457 | |||||||
chr1:2483489 | G | A | 154 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0044 others(151): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.646-959G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483489 | |||||||
chr1:2483589 | T | C | 1 | a0001c0003t0001g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.646-859T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483589 | |||||||
chr1:2483606 | G | A | 1 | a0003c0005t0002g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.646-842G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483606 | |||||||
chr1:2483669 | T | C | 2 | a0001c0001t0001g0059 a0013c0035t0001g0086 |
2 | HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.646-779T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483669 | |||||||
chr1:2483752 | TTGACCCC others(15): Show |
T | 33 | a0001c0001t0001g0117 a0001c0001t0001g0133 a0001c0001t0002g0033 others(30): Show |
57 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.646-663_646-642del others(22): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483752 | ||||||
chr1:2483757 | C | T | 1 | a0024c0030t0002g0144 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.646-691C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483757 | |||||||
chr1:2483760 | C | T | 1 | a0001c0001t0002g0180 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.646-688C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483760 | |||||||
chr1:2483763 | T | G | 156 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(153): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.646-685T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483763 | |||||||
chr1:2483764 | TG | T | 156 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(153): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.646-677delG | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483764 | ||||||
chr1:2483769 | G | T | 2 | a0001c0002t0001g0134 a0021c0048t0002g0124 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.646-679G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483769 | |||||||
chr1:2483769 | GGGCGCTG others(38): Show |
G | 6 | a0001c0001t0001g0111 a0001c0001t0001g0126 a0001c0001t0002g0128 others(3): Show |
7 | HG02155.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.646-663_646-619del others(45): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483769 | ||||||
chr1:2483774 | C | T | 89 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0155 others(86): Show |
137 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.646-674C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483774 | |||||||
chr1:2483779 | C | T | 148 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(145): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.646-669C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483779 | |||||||
chr1:2483785 | T | G | 10 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 others(7): Show |
11 | HG00738.hp2 HG02109.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-663T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483785 | |||||||
chr1:2483787 | GGGGGGGC others(14): Show |
G | 1 | a0001c0003t0001g0070 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.646-655_646-635del others(21): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483787 | ||||||
chr1:2483791 | G | GT | 7 | a0001c0002t0001g0032 a0001c0002t0001g0130 a0001c0002t0001g0134 others(4): Show |
8 | HG00738.hp2 HG02109.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.646-657_646-656ins others(1): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483791 | |||||||
chr1:2483791 | G | GTGGCGCT others(15): Show |
1 | a0001c0002t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-657_646-656ins others(22): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483791 | |||||||
chr1:2483791 | GGGCGCTG others(16): Show |
G | 5 | a0001c0001t0001g0101 a0003c0008t0001g0056 a0003c0008t0002g0054 others(2): Show |
5 | HG02615.hp1 HG02723.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-612_646-590del others(23): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483791 | ||||||
chr1:2483807 | G | T | 147 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(144): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.646-641G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483807 | |||||||
chr1:2483810 | G | GGGTGGCG others(98): Show |
1 | a0003c0005t0002g0110 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.646-636_646-635ins others(105): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483810 | ||||||
chr1:2483813 | GT | G | 151 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(148): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.646-634delT | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483813 | |||||||
chr1:2483813 | GTGGCGCT others(17): Show |
G | 1 | a0018c0038t0001g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.646-634_646-611del others(24): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483813 | |||||||
chr1:2483814 | T | G | 1 | a0001c0001t0002g0046 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.646-634T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483814 | |||||||
chr1:2483818 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.646-630G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483818 | |||||||
chr1:2483824 | C | T | 1 | a0001c0002t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-624C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483824 | |||||||
chr1:2483831 | TG | T | 4 | a0001c0003t0001g0068 a0001c0003t0001g0069 a0001c0045t0002g0082 others(1): Show |
4 | HG00738.hp2 HG02056.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-612delG | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483831 | ||||||
chr1:2483833 | G | GGGGGGCG others(35): Show |
1 | a0001c0002t0001g0032 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.646-612_646-611ins others(42): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483833 | ||||||
chr1:2483836 | GT | G | 4 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0003c0005t0002g0110 others(1): Show |
4 | HG02976.hp1 HG02976.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-611delT | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483836 | |||||||
chr1:2483836 | GTGGCGCT others(37): Show |
G | 7 | a0001c0001t0002g0035 a0001c0001t0002g0046 a0001c0002t0001g0018 others(4): Show |
9 | HG01109.hp2 HG02622.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.646-611_646-568del others(44): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483836 | |||||||
chr1:2483837 | T | G | 1 | a0001c0002t0001g0032 | 2 | HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.646-611T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483837 | |||||||
chr1:2483840 | C | T | 1 | a0004c0006t0002g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.646-608C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483840 | |||||||
chr1:2483847 | C | T | 3 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 |
4 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-601C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483847 | |||||||
chr1:2483847 | CCCCGTGT others(36): Show |
C | 21 | a0001c0001t0001g0211 a0001c0001t0002g0039 a0001c0001t0002g0151 others(18): Show |
45 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.646-589_646-547del others(43): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483847 | ||||||
chr1:2483855 | G | C | 2 | a0001c0001t0002g0196 a0001c0002t0001g0206 |
2 | HG01515.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.646-593G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483855 | |||||||
chr1:2483855 | G | T | 3 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0010t0001g0013 |
6 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-593G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483855 | |||||||
chr1:2483855 | GGGGTGGC others(14): Show |
G | 2 | a0001c0045t0002g0082 a0007c0017t0001g0081 |
2 | HG02056.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.646-579_646-559del others(21): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483855 | ||||||
chr1:2483856 | GGGTGGCG others(13): Show |
G | 1 | a0001c0001t0002g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.646-589_646-570del others(20): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483856 | ||||||
chr1:2483859 | T | G | 134 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(131): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.646-589T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483859 | |||||||
chr1:2483869 | C | T | 7 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 others(4): Show |
10 | HG01099.hp2 HG01243.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-579C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483869 | |||||||
chr1:2483869 | CCCCGTGT others(14): Show |
C | 112 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(109): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.646-568_646-548del others(21): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483869 | ||||||
chr1:2483876 | T | TC | 19 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0010 others(16): Show |
28 | HG00408.hp1 HG00609.hp1 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.646-572_646-571ins others(1): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483876 | |||||||
chr1:2483876 | T | TG | 31 | a0001c0001t0001g0117 a0001c0002t0001g0206 a0001c0003t0001g0003 others(28): Show |
55 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.646-569dupG | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483876 | ||||||
chr1:2483877 | GGGTGGCG others(57): Show |
G | 1 | a0021c0048t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646-568_646-505del others(64): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483877 | ||||||
chr1:2483880 | T | G | 29 | a0001c0001t0001g0155 a0001c0001t0002g0001 a0001c0001t0002g0010 others(26): Show |
41 | HG00408.hp1 HG00609.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.646-568T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483880 | |||||||
chr1:2483880 | T | TGGCGCTG others(101): Show |
2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.646-559_646-558ins others(108): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483880 | ||||||
chr1:2483890 | T | C | 38 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0155 others(35): Show |
49 | HG00408.hp1 HG00609.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.646-558T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483890 | |||||||
chr1:2483897 | T | TTGGGGGG others(14): Show |
2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.646-551_646-550ins others(21): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483897 | |||||||
chr1:2483897 | TGGGGGGG others(81): Show |
T | 1 | a0001c0002t0001g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.646-544_646-457del others(88): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483897 | ||||||
chr1:2483898 | G | C | 146 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(143): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.646-550G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483898 | |||||||
chr1:2483898 | G | T | 3 | a0001c0002t0001g0130 a0008c0036t0004g0026 a0022c0020t0004g0026 |
3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.646-550G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483898 | |||||||
chr1:2483902 | G | T | 4 | a0001c0001t0002g0202 a0001c0001t0002g0229 a0001c0003t0001g0122 others(1): Show |
4 | HG01934.hp2 HG02572.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-546G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483902 | |||||||
chr1:2483902 | GGGCGCTG others(36): Show |
G | 1 | a0001c0002t0001g0206 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.646-503_646-461del others(43): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483902 | ||||||
chr1:2483912 | T | C | 154 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(151): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.646-536T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483912 | |||||||
chr1:2483919 | TGGGGGGG others(37): Show |
T | 1 | a0001c0001t0002g0202 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.646-522_646-479del others(44): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483919 | ||||||
chr1:2483920 | G | C | 2 | a0001c0001t0007g0103 a0003c0005t0002g0150 |
2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.646-528G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483920 | |||||||
chr1:2483920 | G | GGGGGGCG others(35): Show |
1 | a0001c0002t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.646-523_646-522ins others(42): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483920 | ||||||
chr1:2483924 | G | GGCGCTGA others(14): Show |
4 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0011c0013t0002g0057 others(1): Show |
5 | HG02109.hp1 HG02809.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-523_646-522ins others(21): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483924 | ||||||
chr1:2483924 | G | GGGCGCTG others(15): Show |
1 | a0001c0002t0001g0130 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.646-504_646-503ins others(22): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483924 | ||||||
chr1:2483924 | G | T | 149 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(146): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.646-524G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483924 | |||||||
chr1:2483934 | T | C | 151 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(148): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.646-514T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483934 | |||||||
chr1:2483941 | T | TG | 5 | a0001c0001t0002g0135 a0001c0001t0002g0229 a0008c0036t0004g0026 others(2): Show |
5 | HG02630.hp2 HG03139.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.646-504dupG | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483941 | ||||||
chr1:2483941 | TGGGTGGC others(15): Show |
T | 5 | a0001c0001t0001g0155 a0001c0001t0002g0010 a0001c0001t0002g0153 others(2): Show |
10 | HG01099.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.646-503_646-482del others(22): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483941 | ||||||
chr1:2483945 | T | G | 151 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(148): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.646-503T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483945 | |||||||
chr1:2483945 | TGGCGCTG others(15): Show |
T | 1 | a0001c0001t0002g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.646-438_646-417del others(22): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483945 | ||||||
chr1:2483945 | TGGCGCTG others(59): Show |
T | 1 | a0001c0003t0001g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.646-482_646-417del others(66): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2483945 | ||||||
chr1:2483955 | T | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(146): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.646-493T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483955 | |||||||
chr1:2483974 | G | A | 1 | a0021c0048t0002g0124 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646-474G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483974 | |||||||
chr1:2483976 | C | A | 150 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(147): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.646-472C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483976 | |||||||
chr1:2483977 | T | C | 7 | a0001c0001t0001g0155 a0001c0001t0002g0010 a0001c0001t0002g0153 others(4): Show |
10 | HG01891.hp2 HG01934.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-471T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483977 | |||||||
chr1:2483986 | G | C | 149 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(146): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.646-462G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483986 | |||||||
chr1:2483992 | C | T | 1 | a0001c0003t0001g0023 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.646-456C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483992 | |||||||
chr1:2483998 | C | A | 7 | a0001c0001t0001g0155 a0001c0001t0002g0010 a0001c0001t0002g0153 others(4): Show |
10 | HG01891.hp2 HG01934.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.646-450C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2483998 | |||||||
chr1:2484008 | G | C | 164 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(161): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.646-440G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484008 | |||||||
chr1:2484040 | A | G | 2 | a0001c0001t0002g0201 a0001c0002t0001g0224 |
2 | HG00140.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.646-408A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484040 | |||||||
chr1:2484053 | T | G | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.646-395T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484053 | |||||||
chr1:2484056 | C | T | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.646-392C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484056 | |||||||
chr1:2484058 | T | C | 153 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(150): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.646-390T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484058 | |||||||
chr1:2484066 | CGTGTGGG others(14): Show |
C | 1 | a0001c0001t0002g0220 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.646-372_646-352del others(21): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 2484066 | ||||||
chr1:2484106 | C | T | 2 | a0001c0010t0001g0013 a0018c0038t0001g0225 |
4 | HG01099.hp2 HG01243.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-342C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484106 | |||||||
chr1:2484183 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.646-265G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484183 | |||||||
chr1:2484236 | G | C | 7 | a0001c0001t0002g0011 a0001c0001t0002g0046 a0001c0001t0002g0142 others(4): Show |
11 | HG00423.hp2 HG02155.hp1 NA18956.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-212G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484236 | |||||||
chr1:2484273 | T | C | 1 | a0001c0003t0001g0072 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.646-175T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484273 | |||||||
chr1:2484286 | C | T | 2 | a0011c0013t0002g0057 a0011c0013t0002g0058 |
2 | NA19005.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.646-162C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484286 | |||||||
chr1:2484444 | G | C | 3 | a0004c0006t0002g0136 a0004c0006t0002g0160 a0004c0006t0006g0161 |
3 | HG01891.hp1 HG02922.hp2 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.646-4G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 4/21 | chr1 | 2484444 | |||||||
chr1:2484629 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.816+11C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2484629 | |||||||
chr1:2484630 | G | A | 2 | a0001c0001t0002g0162 a0001c0049t0002g0131 |
2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.816+12G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2484630 | |||||||
chr1:2484664 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.816+46G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2484664 | |||||||
chr1:2484719 | G | A | 1 | a0003c0005t0002g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.816+101G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2484719 | |||||||
chr1:2484918 | G | A | 153 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(150): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.816+300G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2484918 | |||||||
chr1:2484949 | C | T | 1 | a0001c0010t0001g0013 | 3 | HG01099.hp2 HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.816+331C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2484949 | |||||||
chr1:2484964 | G | C | 1 | a0001c0001t0002g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.816+346G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2484964 | |||||||
chr1:2485091 | G | A | 1 | a0001c0001t0002g0036 | 2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.816+473G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2485091 | |||||||
chr1:2485223 | T | TGCTCTCT others(4): Show |
212 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(209): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.816+608_816+609ins others(11): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 2485223 | ||||||
chr1:2485546 | TGCCTCAG others(35): Show |
T | 1 | a0001c0002t0001g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.816+1018_816+1059d others(44): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr1 | 2485546 | ||||||
chr1:2485693 | C | G | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.816+1075C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2485693 | |||||||
chr1:2485771 | C | G | 1 | a0001c0001t0002g0199 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.817-1136C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2485771 | |||||||
chr1:2485979 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.817-928C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2485979 | |||||||
chr1:2485984 | G | A | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.817-923G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2485984 | |||||||
chr1:2486023 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0002g0033 a0001c0002t0001g0132 others(1): Show |
5 | HG02280.hp1 HG03471.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.817-884G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486023 | |||||||
chr1:2486182 | C | T | 1 | a0001c0002t0001g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.817-725C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486182 | |||||||
chr1:2486191 | C | T | 2 | a0001c0002t0001g0134 a0021c0048t0002g0124 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.817-716C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486191 | |||||||
chr1:2486244 | C | A | 1 | a0001c0002t0001g0040 | 2 | NA18964.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.817-663C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486244 | |||||||
chr1:2486463 | G | A | 1 | a0002c0004t0002g0112 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.817-444G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486463 | |||||||
chr1:2486491 | G | C | 2 | a0001c0010t0001g0013 a0018c0038t0001g0225 |
4 | HG01099.hp2 HG01243.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.817-416G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486491 | |||||||
chr1:2486500 | G | C | 2 | a0001c0001t0001g0133 a0001c0002t0001g0132 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.817-407G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486500 | |||||||
chr1:2486519 | G | A | 155 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(152): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.817-388G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486519 | |||||||
chr1:2486593 | C | T | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.817-314C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486593 | |||||||
chr1:2486635 | C | G | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.817-272C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 5/21 | chr1 | 2486635 | |||||||
chr1:2487163 | C | T | 4 | a0001c0002t0001g0134 a0011c0013t0002g0057 a0011c0013t0002g0058 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.911-10C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 6/21 | chr1 | 2487163 | |||||||
chr1:2487451 | C | T | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1114+75C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 7/21 | chr1 | 2487451 | |||||||
chr1:2487496 | C | T | 157 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(154): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1115-102C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 7/21 | chr1 | 2487496 | |||||||
chr1:2487976 | C | G | 4 | a0001c0002t0001g0134 a0011c0013t0002g0057 a0011c0013t0002g0058 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1235+258C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2487976 | |||||||
chr1:2488155 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1235+437C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488155 | |||||||
chr1:2488211 | T | C | 1 | a0001c0001t0007g0103 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1235+493T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488211 | |||||||
chr1:2488325 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1235+607C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488325 | |||||||
chr1:2488332 | G | A | 5 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 others(2): Show |
6 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1235+614G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488332 | |||||||
chr1:2488555 | C | G | 1 | a0001c0001t0002g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1236-652C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488555 | |||||||
chr1:2488630 | T | G | 2 | a0001c0002t0001g0141 a0001c0041t0001g0164 |
2 | HG02074.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1236-577T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488630 | |||||||
chr1:2488659 | A | T | 36 | a0001c0001t0001g0117 a0001c0003t0001g0003 a0001c0003t0001g0004 others(33): Show |
60 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1236-548A>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488659 | |||||||
chr1:2488670 | C | T | 1 | a0003c0005t0002g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1236-537C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488670 | |||||||
chr1:2488758 | ACCAATGT others(56): Show |
A | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1236-447_1236-385d others(65): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 2488758 | ||||||
chr1:2488794 | G | T | 4 | a0001c0002t0001g0134 a0011c0013t0002g0057 a0011c0013t0002g0058 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236-413G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488794 | |||||||
chr1:2488826 | T | C | 1 | a0001c0002t0001g0017 | 3 | HG00597.hp2 HG00673.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1236-381T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488826 | |||||||
chr1:2488868 | C | G | 1 | a0018c0038t0001g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1236-339C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488868 | |||||||
chr1:2488954 | G | C | 1 | a0001c0002t0001g0145 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1236-253G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488954 | |||||||
chr1:2488971 | C | G | 4 | a0001c0002t0001g0134 a0011c0013t0002g0057 a0011c0013t0002g0058 others(1): Show |
4 | HG02976.hp1 HG03098.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236-236C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2488971 | |||||||
chr1:2489056 | C | A | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1236-151C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2489056 | |||||||
chr1:2489092 | G | A | 2 | a0001c0003t0001g0068 a0001c0003t0001g0073 |
2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1236-115G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2489092 | |||||||
chr1:2489151 | T | C | 225 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0027 others(222): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.1236-56T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2489151 | |||||||
chr1:2489180 | C | A | 1 | a0001c0003t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1236-27C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 8/21 | chr1 | 2489180 | |||||||
chr1:2489474 | A | G | 172 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(169): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1407+96A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 9/21 | chr1 | 2489474 | |||||||
chr1:2489587 | G | A | 2 | a0001c0001t0007g0103 a0003c0005t0002g0150 |
2 | HG02559.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1408-173G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 9/21 | chr1 | 2489587 | |||||||
chr1:2489621 | C | T | 1 | a0003c0005t0002g0137 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1408-139C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 9/21 | chr1 | 2489621 | |||||||
chr1:2489682 | C | T | 4 | a0001c0001t0002g0142 a0003c0005t0002g0025 a0003c0005t0002g0123 others(1): Show |
5 | HG00423.hp2 HG02145.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408-78C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 9/21 | chr1 | 2489682 | |||||||
chr1:2489982 | T | C | 1 | a0001c0001t0002g0165 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1515+115T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2489982 | |||||||
chr1:2490402 | C | T | 3 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 |
4 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+535C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2490402 | |||||||
chr1:2490419 | C | T | 3 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 |
4 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+552C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2490419 | |||||||
chr1:2490503 | A | C | 1 | a0001c0003t0001g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1515+636A>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2490503 | |||||||
chr1:2490522 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1515+655G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2490522 | |||||||
chr1:2490555 | G | A | 1 | a0001c0014t0002g0217 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1516-637G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2490555 | |||||||
chr1:2490626 | G | A | 1 | a0001c0001t0002g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1516-566G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2490626 | |||||||
chr1:2490988 | G | A | 1 | a0001c0003t0001g0067 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1516-204G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2490988 | |||||||
chr1:2491005 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1516-187G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2491005 | |||||||
chr1:2491019 | G | A | 1 | a0001c0001t0003g0014 | 3 | HG00642.hp2 HG01433.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1516-173G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2491019 | |||||||
chr1:2491081 | C | T | 1 | a0015c0034t0002g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1516-111C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2491081 | |||||||
chr1:2491175 | G | A | 196 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0111 others(193): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.1516-17G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 10/21 | chr1 | 2491175 | |||||||
chr1:2491375 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1659+40C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491375 | |||||||
chr1:2491487 | C | T | 1 | a0003c0005t0002g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1659+152C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491487 | |||||||
chr1:2491522 | C | T | 6 | a0004c0006t0002g0136 a0004c0006t0002g0154 a0004c0006t0002g0160 others(3): Show |
6 | HG01891.hp1 HG02451.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1659+187C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491522 | |||||||
chr1:2491622 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1659+287G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491622 | |||||||
chr1:2491623 | T | C | 1 | a0014c0027t0003g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1659+288T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491623 | |||||||
chr1:2491821 | G | A | 3 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 |
4 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1659+486G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491821 | |||||||
chr1:2491877 | G | A | 1 | a0001c0041t0001g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1659+542G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491877 | |||||||
chr1:2491924 | G | C | 5 | a0003c0005t0002g0025 a0003c0005t0002g0123 a0003c0005t0002g0137 others(2): Show |
6 | HG02145.hp1 HG02572.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1659+589G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491924 | |||||||
chr1:2491979 | G | A | 10 | a0001c0001t0002g0015 a0001c0001t0002g0035 a0001c0001t0002g0036 others(7): Show |
13 | HG01109.hp2 HG01255.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1659+644G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2491979 | |||||||
chr1:2492127 | C | G | 213 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0117 others(210): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1659+792C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492127 | |||||||
chr1:2492235 | C | T | 1 | a0001c0001t0002g0045 | 2 | HG00099.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1659+900C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492235 | |||||||
chr1:2492316 | A | C | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1659+981A>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492316 | |||||||
chr1:2492317 | G | A | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1659+982G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492317 | |||||||
chr1:2492320 | C | G | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1659+985C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492320 | |||||||
chr1:2492534 | C | T | 1 | a0003c0008t0002g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1659+1199C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492534 | |||||||
chr1:2492576 | CT | C | 2 | a0001c0002t0001g0037 a0002c0011t0001g0168 |
3 | NA18947.hp1 NA18947.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1659+1242delT | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492576 | |||||||
chr1:2492587 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1659+1252C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492587 | |||||||
chr1:2492683 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0003g0006 others(3): Show |
14 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1659+1348G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492683 | |||||||
chr1:2492746 | C | T | 1 | a0001c0009t0002g0191 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1659+1411C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492746 | |||||||
chr1:2492807 | G | T | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1659+1472G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492807 | |||||||
chr1:2492868 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1659+1533C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492868 | |||||||
chr1:2492880 | G | A | 7 | a0001c0001t0002g0012 a0001c0001t0002g0151 a0001c0001t0002g0169 others(4): Show |
9 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1659+1545G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492880 | |||||||
chr1:2492978 | T | C | 216 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0097 others(213): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1659+1643T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2492978 | |||||||
chr1:2493102 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1660-1754T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493102 | |||||||
chr1:2493194 | G | A | 2 | a0001c0001t0001g0126 a0020c0037t0001g0125 |
2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1660-1662G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493194 | |||||||
chr1:2493272 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0002t0001g0132 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1660-1584C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493272 | |||||||
chr1:2493277 | G | A | 1 | a0003c0005t0002g0137 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1660-1579G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493277 | |||||||
chr1:2493326 | G | A | 93 | a0001c0001t0001g0007 a0001c0001t0001g0126 a0001c0001t0001g0172 others(90): Show |
155 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1660-1530G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493326 | |||||||
chr1:2493402 | T | A | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1660-1454T>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493402 | |||||||
chr1:2493403 | A | T | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1660-1453A>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493403 | |||||||
chr1:2493455 | T | C | 111 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0001g0133 others(108): Show |
167 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1660-1401T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493455 | |||||||
chr1:2493508 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1660-1348C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493508 | |||||||
chr1:2493572 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1660-1284C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493572 | |||||||
chr1:2493679 | T | C | 1 | a0001c0010t0001g0013 | 3 | HG01099.hp2 HG01243.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1660-1177T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493679 | |||||||
chr1:2493728 | C | T | 1 | a0024c0030t0002g0144 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1660-1128C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493728 | |||||||
chr1:2493733 | G | A | 2 | a0001c0002t0001g0170 a0001c0002t0001g0171 |
2 | NA18952.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1660-1123G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493733 | |||||||
chr1:2493793 | G | C | 1 | a0001c0001t0002g0180 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1660-1063G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493793 | |||||||
chr1:2493935 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1660-921G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2493935 | |||||||
chr1:2494026 | C | A | 2 | a0001c0003t0001g0068 a0001c0003t0001g0073 |
2 | NA18998.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1660-830C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494026 | |||||||
chr1:2494120 | T | A | 1 | a0001c0001t0002g0181 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1660-736T>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494120 | |||||||
chr1:2494121 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1660-735G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494121 | |||||||
chr1:2494170 | G | A | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1660-686G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494170 | |||||||
chr1:2494171 | A | G | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1660-685A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494171 | |||||||
chr1:2494226 | G | A | 1 | a0002c0004t0002g0112 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1660-630G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494226 | |||||||
chr1:2494502 | C | T | 1 | a0029c0031t0002g0189 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1660-354C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494502 | |||||||
chr1:2494553 | C | T | 213 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0117 others(210): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1660-303C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494553 | |||||||
chr1:2494638 | C | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0079 |
3 | HG01346.hp1 HG01496.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1660-218C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494638 | |||||||
chr1:2494687 | C | T | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1660-169C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494687 | |||||||
chr1:2494710 | C | A | 101 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0002g0001 others(98): Show |
154 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1660-146C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494710 | |||||||
chr1:2494809 | G | C | 1 | a0018c0038t0001g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1660-47G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494809 | |||||||
chr1:2494825 | C | T | 1 | a0001c0002t0001g0042 | 2 | HG02074.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.1660-31C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 11/21 | chr1 | 2494825 | |||||||
chr1:2494962 | C | T | 1 | a0025c0029t0002g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1752+14C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2494962 | |||||||
chr1:2494989 | AGTGTCCT others(18): Show |
A | 22 | a0001c0001t0001g0126 a0001c0001t0002g0043 a0001c0001t0002g0090 others(19): Show |
25 | HG01255.hp2 HG02109.hp1 HG02129.hp1 others(22): Show |
intron_variant | MODIFIER | c.1752+92_1752+116de others(26): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 2494989 | ||||||
chr1:2495026 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1752+78G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495026 | |||||||
chr1:2495159 | C | G | 5 | a0003c0005t0002g0110 a0003c0005t0002g0139 a0003c0008t0001g0056 others(2): Show |
5 | HG02615.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1752+211C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495159 | |||||||
chr1:2495164 | G | C | 1 | a0001c0003t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1752+216G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495164 | |||||||
chr1:2495231 | G | C | 2 | a0001c0001t0002g0142 a0001c0001t0002g0157 |
2 | HG00423.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1753-257G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495231 | |||||||
chr1:2495238 | T | C | 1 | a0001c0002t0001g0200 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1753-250T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495238 | |||||||
chr1:2495250 | C | T | 101 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0002g0001 others(98): Show |
154 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1753-238C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495250 | |||||||
chr1:2495318 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1753-170C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495318 | |||||||
chr1:2495327 | A | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0126 others(95): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1753-161A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495327 | |||||||
chr1:2495329 | C | T | 1 | a0012c0022t0002g0187 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1753-159C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495329 | |||||||
chr1:2495374 | G | C | 2 | a0007c0017t0001g0081 a0007c0017t0001g0221 |
2 | HG02056.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1753-114G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495374 | |||||||
chr1:2495379 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1753-109G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495379 | |||||||
chr1:2495455 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1753-33G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 12/21 | chr1 | 2495455 | |||||||
chr1:2495589 | G | A | 1 | a0001c0003t0001g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1835+19G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2495589 | |||||||
chr1:2495828 | C | T | 1 | a0001c0002t0001g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1835+258C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2495828 | |||||||
chr1:2495836 | G | A | 1 | a0003c0005t0002g0137 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1835+266G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2495836 | |||||||
chr1:2495901 | T | C | 116 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0002g0001 others(113): Show |
179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1835+331T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2495901 | |||||||
chr1:2495929 | T | C | 103 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0002g0001 others(100): Show |
156 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1835+359T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2495929 | |||||||
chr1:2496226 | C | G | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1836-381C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496226 | |||||||
chr1:2496228 | G | C | 1 | a0001c0001t0009g0116 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1836-379G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496228 | |||||||
chr1:2496233 | C | A | 1 | a0004c0006t0002g0160 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1836-374C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496233 | |||||||
chr1:2496235 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1836-372C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496235 | |||||||
chr1:2496273 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0179 a0001c0001t0001g0188 others(78): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1836-334C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496273 | |||||||
chr1:2496354 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1836-253G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496354 | |||||||
chr1:2496387 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1836-220C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496387 | |||||||
chr1:2496528 | C | T | 1 | a0001c0001t0002g0107 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1836-79C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 13/21 | chr1 | 2496528 | |||||||
chr1:2497045 | G | A | 5 | a0003c0005t0002g0110 a0003c0005t0002g0150 a0003c0008t0001g0056 others(2): Show |
5 | HG02572.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116+35G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 15/21 | chr1 | 2497045 | |||||||
chr1:2497053 | G | A | 1 | a0001c0001t0002g0050 | 2 | NA18979.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2116+43G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 15/21 | chr1 | 2497053 | |||||||
chr1:2497280 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2117-222C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 15/21 | chr1 | 2497280 | |||||||
chr1:2497404 | C | T | 1 | a0001c0025t0001g0194 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2117-98C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 15/21 | chr1 | 2497404 | |||||||
chr1:2497435 | T | C | 218 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0102 others(215): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.2117-67T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 15/21 | chr1 | 2497435 | |||||||
chr1:2497497 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.2117-5C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 15/21 | chr1 | 2497497 | |||||||
chr1:2497733 | C | T | 1 | a0009c0016t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2224+124C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2497733 | |||||||
chr1:2497977 | T | C | 1 | a0001c0002t0001g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2224+368T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2497977 | |||||||
chr1:2498044 | C | A | 1 | a0001c0003t0001g0020 | 2 | NA18985.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.2224+435C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498044 | |||||||
chr1:2498065 | G | T | 1 | a0001c0001t0002g0109 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2224+456G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498065 | |||||||
chr1:2498076 | G | A | 1 | a0001c0003t0001g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2225-447G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498076 | |||||||
chr1:2498090 | A | G | 2 | a0001c0002t0001g0093 a0001c0003t0001g0023 |
3 | HG02145.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2225-433A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498090 | |||||||
chr1:2498093 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2225-430G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498093 | |||||||
chr1:2498269 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2225-254C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498269 | |||||||
chr1:2498283 | G | A | 10 | a0003c0005t0002g0025 a0003c0005t0002g0110 a0003c0005t0002g0123 others(7): Show |
11 | HG02145.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.2225-240G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498283 | |||||||
chr1:2498361 | C | A | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2225-162C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498361 | |||||||
chr1:2498475 | G | T | 1 | a0001c0002t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2225-48G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498475 | |||||||
chr1:2498510 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2225-13G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 16/21 | chr1 | 2498510 | |||||||
chr1:2498647 | G | GGTGGGGG others(2): Show |
13 | a0001c0003t0001g0003 a0001c0003t0001g0022 a0001c0003t0001g0066 others(10): Show |
23 | HG00423.hp1 HG00544.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.2349+1_2349+9dupGT others(7): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr1 | 2498647 | ||||||
chr1:2498666 | C | T | 1 | a0001c0003t0001g0077 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2349+19C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 17/21 | chr1 | 2498666 | |||||||
chr1:2498899 | G | A | 1 | a0004c0024t0001g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2434+71G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 18/21 | chr1 | 2498899 | |||||||
chr1:2499031 | G | T | 2 | a0001c0001t0001g0126 a0001c0010t0001g0013 |
4 | HG01099.hp2 HG01243.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2435-53G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 18/21 | chr1 | 2499031 | |||||||
chr1:2499267 | C | T | 2 | a0001c0001t0001g0133 a0001c0002t0001g0132 |
2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2581+37C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 19/21 | chr1 | 2499267 | |||||||
chr1:2499402 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2581+172G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 19/21 | chr1 | 2499402 | |||||||
chr1:2499432 | C | G | 3 | a0008c0036t0004g0026 a0008c0046t0004g0119 a0022c0020t0004g0026 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2581+202C>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 19/21 | chr1 | 2499432 | |||||||
chr1:2499434 | GGAAGAGG others(22): Show |
G | 1 | a0001c0001t0002g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2581+205_2582-178d others(31): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 19/21 | chr1 | 2499434 | |||||||
chr1:2499450 | G | A | 4 | a0001c0002t0001g0002 a0001c0002t0001g0037 a0001c0003t0001g0004 others(1): Show |
7 | NA18947.hp1 NA18960.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582-191G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 19/21 | chr1 | 2499450 | |||||||
chr1:2499618 | C | T | 102 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0002g0001 others(99): Show |
155 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.2582-23C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 19/21 | chr1 | 2499618 | |||||||
chr1:2499792 | T | G | 1 | a0001c0001t0002g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2661+72T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2499792 | |||||||
chr1:2499924 | T | C | 1 | a0003c0005t0002g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2661+204T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2499924 | |||||||
chr1:2499936 | T | G | 3 | a0008c0036t0004g0026 a0008c0046t0004g0119 a0022c0020t0004g0026 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2661+216T>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2499936 | |||||||
chr1:2500415 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2661+695C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2500415 | |||||||
chr1:2500452 | C | T | 2 | a0001c0002t0001g0145 a0001c0002t0001g0149 |
2 | NA18943.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2661+732C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2500452 | |||||||
chr1:2500614 | G | T | 2 | a0001c0003t0001g0022 a0001c0003t0001g0079 |
3 | HG01346.hp1 HG01496.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2661+894G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2500614 | |||||||
chr1:2500757 | C | T | 13 | a0001c0001t0001g0044 a0001c0001t0002g0005 a0001c0001t0002g0044 others(10): Show |
20 | NA18612.hp1 NA18944.hp2 NA18945.hp1 others(17): Show |
intron_variant | MODIFIER | c.2661+1037C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2500757 | |||||||
chr1:2500779 | C | CCCCTCCC others(13): Show |
2 | a0001c0001t0001g0061 a0001c0001t0001g0179 |
2 | HG03017.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2661+1136_2661+115 others(24): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr1 | 2500779 | ||||||
chr1:2500779 | CCCCTCCC others(13): Show |
C | 93 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0117 others(90): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.2661+1136_2661+115 others(24): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr1 | 2500779 | ||||||
chr1:2500779 | CCCCTCCC others(33): Show |
C | 105 | a0001c0001t0001g0044 a0001c0001t0002g0001 a0001c0001t0002g0005 others(102): Show |
158 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.2661+1116_2661+115 others(44): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr1 | 2500779 | ||||||
chr1:2500789 | CCCTCAGT others(32): Show |
C | 1 | a0001c0001t0002g0182 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2661+1072_2661+111 others(43): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr1 | 2500789 | ||||||
chr1:2500892 | C | A | 87 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0179 others(84): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2661+1172C>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2500892 | |||||||
chr1:2501025 | A | C | 108 | a0001c0001t0001g0044 a0001c0001t0001g0117 a0001c0001t0002g0001 others(105): Show |
161 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.2662-1087A>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501025 | |||||||
chr1:2501096 | G | A | 5 | a0001c0001t0002g0034 a0001c0001t0002g0108 a0001c0001t0002g0109 others(2): Show |
6 | HG00642.hp1 HG02615.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2662-1016G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501096 | |||||||
chr1:2501137 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2662-975G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501137 | |||||||
chr1:2501210 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2662-902C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501210 | |||||||
chr1:2501310 | G | A | 101 | a0001c0001t0001g0044 a0001c0001t0002g0001 a0001c0001t0002g0005 others(98): Show |
153 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.2662-802G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501310 | |||||||
chr1:2501322 | C | T | 3 | a0008c0036t0004g0026 a0008c0046t0004g0119 a0022c0020t0004g0026 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2662-790C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501322 | |||||||
chr1:2501323 | G | A | 85 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0179 others(82): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2662-789G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501323 | |||||||
chr1:2501412 | G | A | 1 | a0001c0047t0002g0087 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2662-700G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501412 | |||||||
chr1:2501518 | G | C | 1 | a0001c0002t0001g0149 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2662-594G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501518 | |||||||
chr1:2501571 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2662-541G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501571 | |||||||
chr1:2501605 | G | A | 2 | a0001c0002t0001g0175 a0001c0002t0001g0224 |
2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2662-507G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501605 | |||||||
chr1:2501605 | G | C | 3 | a0001c0002t0001g0041 a0001c0002t0001g0173 a0001c0002t0001g0207 |
4 | HG00673.hp2 HG02027.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.2662-507G>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501605 | |||||||
chr1:2501729 | G | A | 1 | a0001c0014t0002g0208 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2662-383G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501729 | |||||||
chr1:2501768 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2662-344G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501768 | |||||||
chr1:2501788 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2662-324G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501788 | |||||||
chr1:2501848 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0002g0186 |
2 | HG02451.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2662-264C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501848 | |||||||
chr1:2501937 | C | T | 1 | a0001c0002t0001g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2662-175C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501937 | |||||||
chr1:2501986 | C | T | 2 | a0008c0036t0004g0026 a0022c0020t0004g0026 |
2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2662-126C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2501986 | |||||||
chr1:2502017 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2662-95C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 20/21 | chr1 | 2502017 | |||||||
chr1:2502455 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2959+46G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502455 | |||||||
chr1:2502461 | C | T | 93 | a0001c0001t0001g0007 a0001c0001t0001g0133 a0001c0001t0001g0172 others(90): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2959+52C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502461 | |||||||
chr1:2502475 | G | A | 2 | a0001c0001t0002g0091 a0025c0029t0002g0092 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2959+66G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502475 | |||||||
chr1:2502534 | C | T | 1 | a0024c0030t0002g0144 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2959+125C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502534 | |||||||
chr1:2502535 | G | A | 5 | a0003c0005t0002g0110 a0003c0005t0002g0139 a0003c0008t0001g0056 others(2): Show |
5 | HG02615.hp1 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2959+126G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502535 | |||||||
chr1:2502536 | G | A | 3 | a0001c0002t0001g0032 a0001c0002t0001g0129 a0001c0002t0001g0130 |
4 | HG02109.hp1 HG02809.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2959+127G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502536 | |||||||
chr1:2502537 | C | T | 3 | a0003c0008t0001g0056 a0003c0008t0002g0054 a0003c0008t0002g0055 |
3 | HG02615.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2959+128C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502537 | |||||||
chr1:2502701 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2959+292A>G | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2502701 | |||||||
chr1:2502732 | C | CG | 16 | a0001c0001t0002g0158 a0001c0001t0002g0163 a0001c0001t0002g0169 others(13): Show |
17 | HG00323.hp1 HG00438.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.2959+325dupG | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 2502732 | ||||||
chr1:2503002 | GCCT | G | 4 | a0001c0001t0002g0053 a0001c0001t0002g0060 a0001c0001t0002g0229 others(1): Show |
5 | HG02922.hp1 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2959+595_2959+597d others(5): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 2503002 | ||||||
chr1:2503021 | G | T | 2 | a0001c0003t0001g0066 a0001c0003t0001g0080 |
2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2959+612G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503021 | |||||||
chr1:2503034 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2959+625C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503034 | |||||||
chr1:2503065 | T | C | 1 | a0001c0003t0001g0064 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2959+656T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503065 | |||||||
chr1:2503084 | T | C | 2 | a0001c0001t0002g0033 a0001c0049t0002g0131 |
3 | HG03471.hp2 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2959+675T>C | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503084 | |||||||
chr1:2503142 | G | A | 1 | a0001c0002t0001g0147 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2959+733G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503142 | |||||||
chr1:2503160 | G | A | 1 | a0001c0003t0001g0066 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2959+751G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503160 | |||||||
chr1:2503222 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2960-700C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503222 | |||||||
chr1:2503245 | ACCTCCTG others(35): Show |
A | 1 | a0001c0002t0001g0204 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2960-673_2960-632d others(44): Show |
PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 2503245 | ||||||
chr1:2503263 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | NA19088.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2960-659G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503263 | |||||||
chr1:2503301 | G | A | 1 | a0001c0002t0001g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2960-621G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503301 | |||||||
chr1:2503305 | C | T | 33 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0016 others(30): Show |
49 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.2960-617C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503305 | |||||||
chr1:2503462 | G | T | 1 | a0003c0005t0002g0025 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2960-460G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503462 | |||||||
chr1:2503571 | C | T | 1 | a0001c0002t0001g0148 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2960-351C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503571 | |||||||
chr1:2503633 | G | T | 2 | a0001c0002t0001g0145 a0001c0002t0001g0149 |
2 | NA18943.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2960-289G>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503633 | |||||||
chr1:2503634 | C | T | 1 | a0001c0001t0002g0185 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2960-288C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503634 | |||||||
chr1:2503648 | C | T | 1 | a0001c0003t0001g0076 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2960-274C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503648 | |||||||
chr1:2503712 | C | T | 1 | a0029c0031t0002g0189 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2960-210C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503712 | |||||||
chr1:2503761 | G | A | 2 | a0001c0001t0009g0116 a0001c0002t0002g0174 |
2 | NA18997.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.2960-161G>A | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503761 | |||||||
chr1:2503762 | C | T | 3 | a0008c0036t0004g0026 a0008c0046t0004g0119 a0022c0020t0004g0026 |
3 | HG02723.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2960-160C>T | PLCH2 | ENSG00000149527.18 | transcript | ENST00000378486.8 | protein_coding | 21/21 | chr1 | 2503762 |