Item | Value |
---|---|
geneid | 64430 |
ensemblid | ENSG00000126773.13 |
hgncid | 20349 |
symbol | PCNX4 |
name | pecanex 4 |
refseq_nuc | NM_001330177.2 |
refseq_prot | NP_001317106.1 |
ensembl_nuc | ENST00000406854.6 |
ensembl_prot | ENSP00000384801.1 |
mane_status | MANE Select |
chr | chr14 |
start | 60091923 |
end | 60148221 |
strand | + |
ver | v1.2 |
region | chr14:60091923-60148221 |
region5000 | chr14:60086923-60153221 |
regionname0 | PCNX4_chr14_60091923_60148221 |
regionname5000 | PCNX4_chr14_60086923_60153221 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1172 | 134 | 28 | 25 | 58 | 7 | 15 | 49 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0002 | 0/0 | 1172 | 65 | 33 | 13 | 9 | 0 | 10 | 4 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0003 | 0/0 | 1172 | 40 | 2 | 0 | 37 | 0 | 1 | 30 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0004 | 0/0 | 1172 | 24 | 0 | 0 | 24 | 0 | 0 | 24 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0005 | 0/0 | 1172 | 8 | 0 | 2 | 3 | 1 | 2 | 3 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0006 | 0/0 | 1172 | 8 | 0 | 1 | 7 | 0 | 0 | 5 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0007 | 0/0 | 1173 | 7 | 4 | 1 | 0 | 0 | 2 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1168): Show |
chr14 | 60086923 | 60153221 |
a0008 | 0/0 | 1172 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0009 | 0/0 | 1172 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0010 | 1/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0011 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0012 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0013 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0014 | 0/0 | 1172 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0015 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0016 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0017 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0018 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0019 | 0/0 | 1172 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0020 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0021 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0022 | 0/0 | 724 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(719): Show |
chr14 | 60086923 | 60153221 |
a0023 | 0/0 | 1172 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0024 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
a0025 | 0/0 | 1172 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | MSPDV others(1167): Show |
chr14 | 60086923 | 60153221 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3516 | 131 | 27 | 25 | 57 | 7 | 14 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0001c0021 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0001c0023 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0001c0030 | 0/0 | 3516 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0002c0002 | 0/0 | 3516 | 50 | 20 | 11 | 9 | 0 | 10 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0002c0007 | 0/0 | 3516 | 7 | 6 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0002c0009 | 0/0 | 3516 | 6 | 6 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0002c0013 | 0/0 | 3516 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0002c0025 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0003c0003 | 0/0 | 3516 | 40 | 2 | 0 | 37 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0004c0004 | 0/0 | 3516 | 24 | 0 | 0 | 24 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0005c0006 | 0/0 | 3516 | 8 | 0 | 2 | 3 | 1 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0006c0005 | 0/0 | 3516 | 8 | 0 | 1 | 7 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0007c0008 | 0/0 | 3519 | 7 | 4 | 1 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3514): Show |
chr14 | 60086923 | 60153221 | ||
a0008c0010 | 0/0 | 3516 | 4 | 0 | 0 | 4 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0009c0011 | 0/0 | 3516 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0010c0015 | 1/0 | 3516 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0011c0022 | 0/0 | 3516 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0012c0029 | 0/0 | 3516 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0013c0032 | 0/0 | 3516 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0014c0024 | 0/0 | 3516 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0015c0027 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0016c0014 | 0/0 | 3516 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0017c0031 | 0/0 | 3516 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0018c0017 | 0/0 | 3516 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0019c0016 | 0/0 | 3516 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0020c0026 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0021c0019 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0022c0020 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0023c0028 | 0/0 | 3516 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0024c0018 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 | ||
a0025c0012 | 0/0 | 3516 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | ATGAG others(3511): Show |
chr14 | 60086923 | 60153221 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 18069 | 68 | 20 | 10 | 23 | 4 | 10 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0006 | 0/0 | 18067 | 4 | 0 | 0 | 4 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18062): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0007 | 0/0 | 18069 | 7 | 0 | 0 | 7 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0008 | 0/0 | 18069 | 8 | 1 | 7 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0010 | 0/0 | 18069 | 5 | 0 | 0 | 5 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0011 | 0/0 | 18069 | 4 | 0 | 4 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0012 | 0/0 | 18069 | 4 | 1 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0015 | 0/0 | 18067 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18062): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0018 | 0/0 | 18069 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0019 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0020 | 0/0 | 18069 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0021 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0022 | 0/0 | 18069 | 2 | 0 | 1 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0023 | 0/0 | 18069 | 2 | 0 | 0 | 0 | 2 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0024 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0030 | 0/0 | 18069 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0033 | 0/0 | 18069 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0034 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0036 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0038 | 0/0 | 18158 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18153): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0040 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0042 | 0/0 | 18070 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18065): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0043 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0044 | 0/0 | 18067 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18062): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0046 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0047 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0048 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0001t0049 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0021t0032 | 0/0 | 18067 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18062): Show |
chr14 | 60086923 | 60153221 |
a0001c0023t0001 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0001c0030t0006 | 0/0 | 18067 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18062): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0003 | 0/0 | 18062 | 23 | 15 | 6 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0005 | 0/0 | 18062 | 9 | 0 | 1 | 6 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0014 | 0/0 | 18062 | 3 | 0 | 3 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0017 | 0/0 | 18062 | 3 | 3 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0028 | 0/0 | 18062 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0031 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0065 | 0/0 | 18058 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18053): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0067 | 0/0 | 18060 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18055): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0068 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0069 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0070 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0071 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0075 | 0/0 | 18062 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0078 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0002t0079 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0007t0003 | 0/0 | 18062 | 5 | 4 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0007t0061 | 0/0 | 18065 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18060): Show |
chr14 | 60086923 | 60153221 |
a0002c0007t0064 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0009t0027 | 0/0 | 18062 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0009t0029 | 0/0 | 18068 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0002c0009t0055 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0009t0073 | 0/0 | 18068 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0002c0013t0003 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0002c0025t0077 | 0/0 | 18068 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0003c0003t0002 | 0/0 | 18068 | 36 | 2 | 0 | 33 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0003c0003t0059 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0003c0003t0060 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0003c0003t0062 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0003c0003t0074 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0004c0004t0004 | 0/0 | 18075 | 18 | 0 | 0 | 18 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18070): Show |
chr14 | 60086923 | 60153221 |
a0004c0004t0016 | 0/0 | 18076 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18071): Show |
chr14 | 60086923 | 60153221 |
a0004c0004t0025 | 0/0 | 18069 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0004c0004t0053 | 0/0 | 18075 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18070): Show |
chr14 | 60086923 | 60153221 |
a0005c0006t0009 | 0/0 | 18064 | 5 | 0 | 2 | 2 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18059): Show |
chr14 | 60086923 | 60153221 |
a0005c0006t0051 | 0/0 | 18064 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18059): Show |
chr14 | 60086923 | 60153221 |
a0005c0006t0058 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0005c0006t0063 | 0/0 | 18064 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18059): Show |
chr14 | 60086923 | 60153221 |
a0006c0005t0001 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0006c0005t0006 | 0/0 | 18067 | 6 | 0 | 1 | 5 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18062): Show |
chr14 | 60086923 | 60153221 |
a0006c0005t0039 | 0/0 | 18067 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18062): Show |
chr14 | 60086923 | 60153221 |
a0007c0008t0013 | 0/0 | 18061 | 4 | 4 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18056): Show |
chr14 | 60086923 | 60153221 |
a0007c0008t0026 | 0/0 | 18061 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18056): Show |
chr14 | 60086923 | 60153221 |
a0007c0008t0056 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0008c0010t0005 | 0/0 | 18062 | 4 | 0 | 0 | 4 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0009c0011t0001 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0009c0011t0037 | 0/0 | 18069 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0010c0015t0052 | 1/0 | 18069 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0011c0022t0041 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0012c0029t0057 | 0/0 | 18062 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0013c0032t0009 | 0/0 | 18064 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18059): Show |
chr14 | 60086923 | 60153221 |
a0014c0024t0045 | 0/0 | 18069 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0015c0027t0002 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0016c0014t0066 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0017c0031t0035 | 0/0 | 18069 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0018c0017t0003 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0019c0016t0005 | 0/0 | 18062 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
a0020c0026t0072 | 0/0 | 18061 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18056): Show |
chr14 | 60086923 | 60153221 |
a0021c0019t0050 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0022c0020t0007 | 0/0 | 18069 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18064): Show |
chr14 | 60086923 | 60153221 |
a0023c0028t0054 | 0/0 | 18068 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18063): Show |
chr14 | 60086923 | 60153221 |
a0024c0018t0076 | 0/0 | 18072 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18067): Show |
chr14 | 60086923 | 60153221 |
a0025c0012t0003 | 0/0 | 18062 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | GCGTA others(18057): Show |
chr14 | 60086923 | 60153221 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0003 | 0/0 | 10 | 8 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0031 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0175 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0002 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0008g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0010g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0011g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0011g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0012g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0012g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0015g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0015g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0018g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0018g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0019g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0020g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0020g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0021g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0022g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0022g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0023g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0023g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0024g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0024g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0030g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0033g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0036g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0038g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0040g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0042g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0043g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0044g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0046g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0047g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0048g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0001t0049g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0021t0032g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0023t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0001c0030t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0014g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0014g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0017g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0017g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0017g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0028g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0028g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0031g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0065g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0067g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0068g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0069g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0070g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0071g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0075g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0078g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0002t0079g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0061g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0007t0064g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0027g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0027g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0029g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0029g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0055g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0009t0073g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0013t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0002c0025t0077g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0004 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0059g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0060g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0062g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0003c0003t0074g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0016g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0016g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0016g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0025g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0025g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0004c0004t0053g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0006t0009g0017 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0006t0009g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0006t0051g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0006t0058g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0005c0006t0063g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0005t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0005t0006g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0005t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0005t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0005t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0005t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0006c0005t0039g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0013g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0026g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0026g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0007c0008t0056g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0008c0010t0005g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0008c0010t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0009c0011t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0009c0011t0037g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0010c0015t0052g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0011c0022t0041g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0012c0029t0057g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0013c0032t0009g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0014c0024t0045g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0015c0027t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0016c0014t0066g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0017c0031t0035g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0018c0017t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0019c0016t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0020c0026t0072g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0021c0019t0050g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0022c0020t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0023c0028t0054g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0024c0018t0076g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
a0025c0012t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0023 | g0144 | EUR | GBR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00280 | hp2 | a0001 | c0001 | t0023 | g0162 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00323 | hp2 | a0005 | c0006 | t0063 | g0018 | EUR | FIN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00558 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00609 | hp1 | a0003 | c0003 | t0002 | g0068 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00639 | hp1 | a0002 | c0002 | t0003 | g0014 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00642 | hp1 | a0005 | c0006 | t0009 | g0017 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00642 | hp2 | a0001 | c0001 | t0046 | g0125 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00673 | hp1 | a0002 | c0002 | t0075 | g0008 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00673 | hp2 | a0001 | c0001 | t0049 | g0173 | EAS | CHS | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00735 | hp1 | a0011 | c0022 | t0041 | g0153 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG00735 | hp2 | a0005 | c0006 | t0009 | g0017 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01081 | hp2 | a0002 | c0007 | t0003 | g0079 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01109 | hp1 | a0002 | c0002 | t0003 | g0082 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01109 | hp2 | a0002 | c0002 | t0079 | g0008 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01175 | hp1 | a0001 | c0001 | t0022 | g0143 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0182 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01192 | hp1 | a0001 | c0001 | t0011 | g0011 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01192 | hp2 | a0002 | c0002 | t0014 | g0022 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01243 | hp1 | a0002 | c0013 | t0003 | g0056 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01243 | hp2 | a0012 | c0029 | t0057 | g0110 | AMR | PUR | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01255 | hp1 | a0002 | c0002 | t0005 | g0008 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01257 | hp2 | a0002 | c0002 | t0003 | g0038 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01258 | hp1 | a0002 | c0002 | t0003 | g0038 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01258 | hp2 | a0001 | c0001 | t0036 | g0003 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01346 | hp1 | a0002 | c0002 | t0003 | g0014 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01358 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01358 | hp2 | a0007 | c0008 | t0056 | g0111 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01361 | hp1 | a0013 | c0032 | t0009 | g0105 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0136 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01433 | hp2 | a0002 | c0002 | t0014 | g0022 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01496 | hp1 | a0014 | c0024 | t0045 | g0116 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01496 | hp2 | a0006 | c0005 | t0006 | g0150 | AMR | CLM | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01884 | hp1 | a0002 | c0007 | t0064 | g0077 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01928 | hp1 | a0001 | c0001 | t0008 | g0142 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01928 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01934 | hp2 | a0001 | c0001 | t0011 | g0138 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0132 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0036 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01978 | hp1 | a0001 | c0001 | t0008 | g0146 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01981 | hp1 | a0002 | c0002 | t0014 | g0014 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG01981 | hp2 | a0001 | c0001 | t0011 | g0011 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02004 | hp1 | a0001 | c0001 | t0008 | g0002 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02004 | hp2 | a0001 | c0001 | t0047 | g0011 | AMR | PEL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02015 | hp1 | a0003 | c0003 | t0002 | g0026 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02040 | hp1 | a0015 | c0027 | t0002 | g0074 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02055 | hp2 | a0007 | c0008 | t0013 | g0028 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02071 | hp1 | a0003 | c0003 | t0002 | g0066 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02074 | hp1 | a0002 | c0002 | t0005 | g0091 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02074 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02080 | hp1 | a0002 | c0002 | t0005 | g0015 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02080 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02132 | hp1 | a0003 | c0003 | t0002 | g0007 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02132 | hp2 | a0002 | c0002 | t0068 | g0099 | EAS | KHV | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02145 | hp1 | a0007 | c0008 | t0013 | g0113 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02145 | hp2 | a0002 | c0007 | t0003 | g0027 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02155 | hp1 | a0001 | c0001 | t0012 | g0129 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02155 | hp2 | a0001 | c0001 | t0044 | g0013 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02165 | hp1 | a0003 | c0003 | t0002 | g0071 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02165 | hp2 | a0006 | c0005 | t0006 | g0151 | EAS | CDX | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02257 | hp2 | a0002 | c0025 | t0077 | g0054 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0058 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02280 | hp1 | a0007 | c0008 | t0013 | g0112 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02572 | hp1 | a0003 | c0003 | t0002 | g0114 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02572 | hp2 | a0001 | c0001 | t0018 | g0134 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02602 | hp1 | a0002 | c0002 | t0003 | g0022 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02615 | hp2 | a0002 | c0007 | t0061 | g0060 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02683 | hp1 | a0002 | c0002 | t0005 | g0094 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02683 | hp2 | a0001 | c0001 | t0022 | g0127 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02717 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02723 | hp1 | a0002 | c0002 | t0069 | g0025 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0184 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02735 | hp2 | a0007 | c0008 | t0026 | g0108 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02738 | hp1 | a0001 | c0030 | t0006 | g0174 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02738 | hp2 | a0002 | c0002 | t0078 | g0092 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02818 | hp2 | a0002 | c0002 | t0003 | g0085 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02895 | hp2 | a0002 | c0002 | t0003 | g0010 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0087 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02896 | hp2 | a0001 | c0001 | t0038 | g0128 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02922 | hp1 | a0002 | c0009 | t0055 | g0055 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02970 | hp1 | a0002 | c0007 | t0003 | g0076 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02970 | hp2 | a0002 | c0002 | t0070 | g0179 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02976 | hp1 | a0001 | c0001 | t0020 | g0003 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03139 | hp1 | a0009 | c0011 | t0037 | g0034 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03139 | hp2 | a0002 | c0009 | t0027 | g0075 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03195 | hp2 | a0002 | c0002 | t0017 | g0083 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03209 | hp1 | a0001 | c0023 | t0001 | g0119 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03209 | hp2 | a0002 | c0002 | t0003 | g0088 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03453 | hp1 | a0002 | c0009 | t0073 | g0103 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0090 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03486 | hp1 | a0002 | c0002 | t0003 | g0180 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03486 | hp2 | a0002 | c0002 | t0017 | g0084 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03490 | hp1 | a0001 | c0001 | t0030 | g0030 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03490 | hp2 | a0002 | c0002 | t0031 | g0181 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03491 | hp1 | a0001 | c0001 | t0030 | g0030 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03491 | hp2 | a0002 | c0002 | t0005 | g0096 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03516 | hp2 | a0002 | c0002 | t0017 | g0081 | AFR | ESN | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03540 | hp2 | a0007 | c0008 | t0013 | g0028 | AFR | GWD | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03579 | hp1 | a0001 | c0001 | t0020 | g0019 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03579 | hp2 | a0002 | c0002 | t0003 | g0061 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03654 | hp2 | a0002 | c0002 | t0065 | g0008 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03669 | hp1 | a0002 | c0002 | t0028 | g0100 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03688 | hp1 | a0016 | c0014 | t0066 | g0097 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03704 | hp1 | a0003 | c0003 | t0002 | g0007 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03704 | hp2 | a0017 | c0031 | t0035 | g0002 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03710 | hp2 | a0005 | c0006 | t0058 | g0107 | SAS | PJL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03831 | hp2 | a0002 | c0002 | t0028 | g0101 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0014 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03942 | hp1 | a0007 | c0008 | t0026 | g0109 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04115 | hp1 | a0002 | c0002 | t0071 | g0093 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04115 | hp2 | a0018 | c0017 | t0003 | g0183 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04204 | hp1 | a0005 | c0006 | t0009 | g0017 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04204 | hp2 | a0001 | c0001 | t0042 | g0139 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04228 | hp1 | a0019 | c0016 | t0005 | g0095 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18522 | hp2 | a0002 | c0002 | t0003 | g0059 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18612 | hp1 | a0006 | c0005 | t0039 | g0172 | EAS | CHB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18612 | hp2 | a0002 | c0002 | t0005 | g0015 | EAS | CHB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18906 | hp2 | a0020 | c0026 | t0072 | g0178 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18939 | hp2 | a0004 | c0004 | t0025 | g0024 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18940 | hp1 | a0004 | c0004 | t0016 | g0051 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18940 | hp2 | a0021 | c0019 | t0050 | g0157 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18941 | hp1 | a0004 | c0004 | t0004 | g0024 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18941 | hp2 | a0002 | c0002 | t0067 | g0008 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18942 | hp1 | a0022 | c0020 | t0007 | g0039 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18942 | hp2 | a0003 | c0003 | t0002 | g0062 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18943 | hp1 | a0003 | c0003 | t0059 | g0009 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18944 | hp1 | a0008 | c0010 | t0005 | g0016 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18944 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18945 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18945 | hp2 | a0004 | c0004 | t0004 | g0044 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18946 | hp1 | a0005 | c0006 | t0009 | g0018 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18946 | hp2 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18948 | hp2 | a0005 | c0006 | t0051 | g0106 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18950 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18960 | hp1 | a0001 | c0001 | t0040 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18960 | hp2 | a0004 | c0004 | t0025 | g0048 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18961 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18961 | hp2 | a0001 | c0001 | t0048 | g0035 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18962 | hp1 | a0023 | c0028 | t0054 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18962 | hp2 | a0005 | c0006 | t0009 | g0018 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18964 | hp1 | a0004 | c0004 | t0004 | g0050 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18964 | hp2 | a0003 | c0003 | t0002 | g0073 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18966 | hp1 | a0006 | c0005 | t0006 | g0171 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18968 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18968 | hp2 | a0001 | c0001 | t0010 | g0168 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18975 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18975 | hp2 | a0004 | c0004 | t0004 | g0041 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18977 | hp1 | a0006 | c0005 | t0006 | g0118 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18977 | hp2 | a0004 | c0004 | t0004 | g0047 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18978 | hp1 | a0002 | c0002 | t0005 | g0029 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18979 | hp1 | a0001 | c0021 | t0032 | g0165 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18979 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18980 | hp2 | a0001 | c0001 | t0015 | g0013 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18981 | hp1 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18981 | hp2 | a0003 | c0003 | t0002 | g0069 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18982 | hp1 | a0001 | c0001 | t0015 | g0163 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18983 | hp2 | a0004 | c0004 | t0004 | g0023 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18984 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18986 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18986 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18988 | hp1 | a0004 | c0004 | t0053 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18988 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18989 | hp1 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18989 | hp2 | a0003 | c0003 | t0002 | g0067 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18990 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18992 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18992 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0169 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18994 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18995 | hp2 | a0004 | c0004 | t0004 | g0045 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18998 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18999 | hp1 | a0001 | c0001 | t0024 | g0170 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA18999 | hp2 | a0004 | c0004 | t0004 | g0043 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19002 | hp1 | a0002 | c0002 | t0005 | g0029 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19002 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19004 | hp1 | a0004 | c0004 | t0016 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19004 | hp2 | a0001 | c0001 | t0024 | g0035 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19006 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19006 | hp2 | a0006 | c0005 | t0001 | g0020 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19007 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19007 | hp2 | a0003 | c0003 | t0060 | g0065 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19009 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19009 | hp2 | a0001 | c0001 | t0021 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19011 | hp2 | a0001 | c0001 | t0012 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19012 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19043 | hp1 | a0002 | c0007 | t0003 | g0027 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19043 | hp2 | a0001 | c0001 | t0018 | g0123 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19057 | hp1 | a0003 | c0003 | t0062 | g0007 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19059 | hp1 | a0003 | c0003 | t0002 | g0104 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19059 | hp2 | a0001 | c0001 | t0043 | g0135 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19065 | hp1 | a0004 | c0004 | t0016 | g0046 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19065 | hp2 | a0008 | c0010 | t0005 | g0098 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19066 | hp1 | a0001 | c0001 | t0006 | g0021 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19066 | hp2 | a0008 | c0010 | t0005 | g0016 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19068 | hp1 | a0001 | c0001 | t0019 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19068 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19070 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19075 | hp1 | a0008 | c0010 | t0005 | g0016 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19075 | hp2 | a0003 | c0003 | t0002 | g0070 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19078 | hp1 | a0003 | c0003 | t0074 | g0009 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19079 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19079 | hp2 | a0006 | c0005 | t0006 | g0020 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19080 | hp1 | a0003 | c0003 | t0002 | g0064 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19080 | hp2 | a0001 | c0001 | t0010 | g0147 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19081 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19081 | hp2 | a0004 | c0004 | t0004 | g0049 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19082 | hp1 | a0002 | c0002 | t0005 | g0015 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19083 | hp1 | a0001 | c0001 | t0007 | g0133 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19083 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19084 | hp2 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19085 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19086 | hp1 | a0004 | c0004 | t0004 | g0042 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19086 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19087 | hp1 | a0006 | c0005 | t0006 | g0020 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19087 | hp2 | a0003 | c0003 | t0002 | g0063 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19088 | hp1 | a0004 | c0004 | t0004 | g0023 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19088 | hp2 | a0001 | c0001 | t0034 | g0001 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19090 | hp1 | a0003 | c0003 | t0002 | g0026 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19090 | hp2 | a0001 | c0001 | t0010 | g0148 | EAS | JPT | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA19240 | hp2 | a0024 | c0018 | t0076 | g0115 | AFR | YRI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0057 | AFR | ASW | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20805 | hp1 | a0001 | c0001 | t0033 | g0037 | EUR | TSI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | TSI | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0086 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02486 | hp2 | a0002 | c0009 | t0029 | g0052 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02559 | hp1 | a0009 | c0011 | t0001 | g0034 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG02559 | hp2 | a0003 | c0003 | t0002 | g0072 | AFR | ACB | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03471 | hp1 | a0002 | c0007 | t0003 | g0078 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
HG03471 | hp2 | a0002 | c0009 | t0029 | g0053 | AFR | MSL | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20300 | hp1 | a0002 | c0009 | t0027 | g0102 | AFR | USA | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0002 | AFR | USA | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
NA21309 | hp2 | a0025 | c0012 | t0003 | g0080 | AFR | LWK | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0175 | REF | REF | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
homoSapiens | grch38p0 | a0010 | c0015 | t0052 | g0089 | REF | REF | PCNX4_chr14_60086923_60153221 | PCNX4 | chr14 | 60086923 | 60153221 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60107708 | G | A | 1 | a0006 | 8 | HG01496.hp2 HG02165.hp2 NA18612.hp1 others(5): Show |
missense_variant | MODERATE | c.70G>A | p.Val24Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 620/18069 | 70/3519 | 24/1172 | chr14 | 60107708 | |||
chr14:60107730 | A | G | 2 | a0005 a0013 |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
missense_variant | MODERATE | c.92A>G | p.Lys31Arg | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 642/18069 | 92/3519 | 31/1172 | chr14 | 60107730 | |||
chr14:60107789 | C | A | 1 | a0025 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.151C>A | p.Pro51Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 701/18069 | 151/3519 | 51/1172 | chr14 | 60107789 | |||
chr14:60108087 | C | T | 1 | a0017 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.449C>T | p.Ala150Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 999/18069 | 449/3519 | 150/1172 | chr14 | 60108087 | |||
chr14:60108279 | T | C | 1 | a0021 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.641T>C | p.Met214Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 1191/18069 | 641/3519 | 214/1172 | chr14 | 60108279 | |||
chr14:60115091 | A | C | 1 | a0012 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.987A>C | p.Leu329Phe | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1537/18069 | 987/3519 | 329/1172 | chr14 | 60115091 | |||
chr14:60115188 | A | G | 1 | a0004 | 24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
missense_variant | MODERATE | c.1084A>G | p.Ile362Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1634/18069 | 1084/3519 | 362/1172 | chr14 | 60115188 | |||
chr14:60115335 | G | A | 7 | a0001 a0006 a0009 others(4): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
missense_variant | MODERATE | c.1231G>A | p.Val411Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1781/18069 | 1231/3519 | 411/1172 | chr14 | 60115335 | |||
chr14:60115743 | T | A | 1 | a0013 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1382T>A | p.Phe461Tyr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 5/11 | 1932/18069 | 1382/3519 | 461/1172 | chr14 | 60115743 | |||
chr14:60116008 | G | A | 1 | a0016 | 1 | HG03688.hp1 | missense_variant | MODERATE | c.1526G>A | p.Ser509Asn | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/11 | 2076/18069 | 1526/3519 | 509/1172 | chr14 | 60116008 | |||
chr14:60118413 | A | G | 15 | a0002 a0003 a0004 others(12): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
missense_variant | MODERATE | c.1663A>G | p.Lys555Glu | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2213/18069 | 1663/3519 | 555/1172 | chr14 | 60118413 | |||
chr14:60118564 | G | A | 1 | a0009 | 2 | HG02559.hp1 HG03139.hp1 |
missense_variant | MODERATE | c.1814G>A | p.Arg605Gln | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2364/18069 | 1814/3519 | 605/1172 | chr14 | 60118564 | |||
chr14:60118621 | C | T | 1 | a0018 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1871C>T | p.Thr624Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2421/18069 | 1871/3519 | 624/1172 | chr14 | 60118621 | |||
chr14:60121226 | G | T | 1 | a0011 | 1 | HG00735.hp1 | missense_variant | MODERATE | c.1973G>T | p.Gly658Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/11 | 2523/18069 | 1973/3519 | 658/1172 | chr14 | 60121226 | |||
chr14:60124345 | T | A | 1 | a0022 | 1 | NA18942.hp1 | stop_gained | HIGH | c.2174T>A | p.Leu725* | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2724/18069 | 2174/3519 | 725/1172 | chr14 | 60124345 | |||
chr14:60124446 | G | A | 1 | a0020 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.2275G>A | p.Asp759Asn | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2825/18069 | 2275/3519 | 759/1172 | chr14 | 60124446 | |||
chr14:60124481 | A | T | 3 | a0003 a0015 a0023 |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
missense_variant | MODERATE | c.2310A>T | p.Gln770His | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2860/18069 | 2310/3519 | 770/1172 | chr14 | 60124481 | |||
chr14:60124509 | G | A | 1 | a0015 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.2338G>A | p.Glu780Lys | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2888/18069 | 2338/3519 | 780/1172 | chr14 | 60124509 | |||
chr14:60124746 | T | C | 1 | a0022 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2575T>C | p.Ser859Pro | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3125/18069 | 2575/3519 | 859/1172 | chr14 | 60124746 | |||
chr14:60124899 | G | A | 1 | a0025 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2728G>A | p.Val910Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3278/18069 | 2728/3519 | 910/1172 | chr14 | 60124899 | |||
chr14:60124983 | T | C | 1 | a0008 | 4 | NA18944.hp1 NA19065.hp2 NA19066.hp2 others(1): Show |
missense_variant | MODERATE | c.2812T>C | p.Tyr938His | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3362/18069 | 2812/3519 | 938/1172 | chr14 | 60124983 | |||
chr14:60125088 | C | T | 1 | a0019 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2917C>T | p.His973Tyr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3467/18069 | 2917/3519 | 973/1172 | chr14 | 60125088 | |||
chr14:60125169 | G | A | 17 | a0002 a0003 a0004 others(14): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
missense_variant | MODERATE | c.2998G>A | p.Gly1000Ser | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3548/18069 | 2998/3519 | 1000/1172 | chr14 | 60125169 | |||
chr14:60125235 | G | A | 1 | a0024 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.3064G>A | p.Ala1022Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3614/18069 | 3064/3519 | 1022/1172 | chr14 | 60125235 | |||
chr14:60125677 | C | CTAT | 1 | a0007 | 7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
disruptive_inframe_insertion | MODERATE | c.3121_3122insTAT | p.Pro1041delinsLeuSe others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/11 | 3672/18069 | 3122/3519 | 1041/1172 | chr14 | 60125677 | |||
chr14:60134160 | C | T | 1 | a0023 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.3458C>T | p.Ala1153Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4008/18069 | 3458/3519 | 1153/1172 | chr14 | 60134160 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60107821 | A | G | 24 | a0001c0001 a0001c0021 a0001c0023 others(21): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
synonymous_variant | LOW | c.183A>G | p.Leu61Leu | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 733/18069 | 183/3519 | 61/1172 | chr14 | 60107821 | |||
chr14:60108148 | A | G | 1 | a0001c0030 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.510A>G | p.Thr170Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 1060/18069 | 510/3519 | 170/1172 | chr14 | 60108148 | |||
chr14:60108157 | T | C | 1 | a0024c0018 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.519T>C | p.Thr173Thr | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/11 | 1069/18069 | 519/3519 | 173/1172 | chr14 | 60108157 | |||
chr14:60115145 | G | A | 15 | a0001c0001 a0001c0021 a0001c0023 others(12): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
synonymous_variant | LOW | c.1041G>A | p.Pro347Pro | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1591/18069 | 1041/3519 | 347/1172 | chr14 | 60115145 | |||
chr14:60115217 | C | T | 23 | a0001c0001 a0001c0021 a0001c0023 others(20): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
synonymous_variant | LOW | c.1113C>T | p.Ser371Ser | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1663/18069 | 1113/3519 | 371/1172 | chr14 | 60115217 | |||
chr14:60115391 | G | C | 1 | a0002c0013 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1287G>C | p.Val429Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/11 | 1837/18069 | 1287/3519 | 429/1172 | chr14 | 60115391 | |||
chr14:60118385 | G | T | 1 | a0013c0032 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.1635G>T | p.Val545Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2185/18069 | 1635/3519 | 545/1172 | chr14 | 60118385 | |||
chr14:60118508 | C | T | 1 | a0001c0023 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1758C>T | p.Leu586Leu | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2308/18069 | 1758/3519 | 586/1172 | chr14 | 60118508 | |||
chr14:60118610 | G | A | 1 | a0002c0025 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1860G>A | p.Val620Val | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/11 | 2410/18069 | 1860/3519 | 620/1172 | chr14 | 60118610 | |||
chr14:60124538 | G | A | 1 | a0001c0021 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.2367G>A | p.Gly789Gly | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 2917/18069 | 2367/3519 | 789/1172 | chr14 | 60124538 | |||
chr14:60125111 | T | C | 18 | a0002c0002 a0002c0007 a0002c0009 others(15): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
synonymous_variant | LOW | c.2940T>C | p.Phe980Phe | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/11 | 3490/18069 | 2940/3519 | 980/1172 | chr14 | 60125111 | |||
chr14:60134014 | C | A | 1 | a0024c0018 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.3312C>A | p.Ile1104Ile | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3862/18069 | 3312/3519 | 1104/1172 | chr14 | 60134014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60091946 | A | T | 3 | a0001c0001t0030 a0002c0002t0078 a0002c0002t0079 |
4 | HG01109.hp2 HG02738.hp2 HG03490.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-527A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15693 | chr14 | 60091946 | ||||||
chr14:60091961 | C | A | 2 | a0002c0002t0014 a0002c0002t0031 |
4 | HG01192.hp2 HG01433.hp2 HG01981.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-512C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15678 | chr14 | 60091961 | ||||||
chr14:60091966 | T | C | 39 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(36): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-507T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15673 | chr14 | 60091966 | ||||||
chr14:60092011 | G | T | 5 | a0001c0001t0010 a0001c0001t0024 a0001c0001t0048 others(2): Show |
10 | HG00673.hp2 NA18940.hp2 NA18944.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-462G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15628 | chr14 | 60092011 | ||||||
chr14:60092048 | C | T | 1 | a0001c0001t0047 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-425C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15591 | chr14 | 60092048 | ||||||
chr14:60092081 | C | T | 1 | a0001c0001t0046 | 1 | HG00642.hp2 | 5_prime_UTR_variant | MODIFIER | c.-392C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15558 | chr14 | 60092081 | ||||||
chr14:60092120 | C | G | 1 | a0002c0025t0077 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-353C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15519 | chr14 | 60092120 | ||||||
chr14:60092314 | T | A | 2 | a0001c0001t0007 a0022c0020t0007 |
8 | HG02074.hp2 NA18942.hp1 NA18945.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-159T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15325 | chr14 | 60092314 | ||||||
chr14:60092315 | C | T | 2 | a0001c0001t0007 a0022c0020t0007 |
8 | HG02074.hp2 NA18942.hp1 NA18945.hp1 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-158C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | chr14 | 60092315 | |||||||
chr14:60092342 | G | T | 39 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(36): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-131G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15297 | chr14 | 60092342 | ||||||
chr14:60092354 | A | G | 39 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(36): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(139): Show |
5_prime_UTR_variant | MODIFIER | c.-119A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15285 | chr14 | 60092354 | ||||||
chr14:60092362 | T | A | 1 | a0001c0021t0032 | 1 | NA18979.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/11 | 15277 | chr14 | 60092362 | ||||||
chr14:60134490 | T | C | 1 | a0005c0006t0051 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 269 | chr14 | 60134490 | ||||||
chr14:60134501 | C | T | 52 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(49): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*280C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 280 | chr14 | 60134501 | ||||||
chr14:60134590 | G | A | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*369G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 369 | chr14 | 60134590 | ||||||
chr14:60134618 | T | C | 1 | a0014c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*397T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 397 | chr14 | 60134618 | ||||||
chr14:60134793 | T | C | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*572T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 572 | chr14 | 60134793 | ||||||
chr14:60134828 | T | C | 1 | a0014c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*607T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 607 | chr14 | 60134828 | ||||||
chr14:60134900 | A | G | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*679A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 679 | chr14 | 60134900 | ||||||
chr14:60134986 | A | C | 1 | a0001c0001t0044 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*765A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 765 | chr14 | 60134986 | ||||||
chr14:60134987 | C | A | 1 | a0023c0028t0054 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*766C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 766 | chr14 | 60134987 | ||||||
chr14:60135079 | C | A | 1 | a0002c0009t0055 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*858C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 858 | chr14 | 60135079 | ||||||
chr14:60135087 | G | A | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*866G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 866 | chr14 | 60135087 | ||||||
chr14:60135272 | T | C | 1 | a0001c0001t0018 | 2 | HG02572.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1051T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1051 | chr14 | 60135272 | ||||||
chr14:60135300 | C | T | 1 | a0002c0002t0075 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1079C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1079 | chr14 | 60135300 | ||||||
chr14:60135338 | G | A | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1117 | chr14 | 60135338 | ||||||
chr14:60135381 | C | CT | 5 | a0005c0006t0009 a0005c0006t0051 a0005c0006t0058 others(2): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1167dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1168 | INFO_REALIGN_3_PRIME | chr14 | 60135381 | |||||
chr14:60135418 | G | A | 1 | a0014c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1197G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1197 | chr14 | 60135418 | ||||||
chr14:60135556 | C | CT | 4 | a0001c0001t0042 a0001c0001t0043 a0003c0003t0074 others(1): Show |
6 | HG04204.hp2 NA18940.hp1 NA19004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1347dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1348 | INFO_REALIGN_3_PRIME | chr14 | 60135556 | |||||
chr14:60135698 | G | A | 4 | a0007c0008t0013 a0007c0008t0026 a0007c0008t0056 others(1): Show |
8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1477G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1477 | chr14 | 60135698 | ||||||
chr14:60135705 | A | G | 3 | a0002c0009t0029 a0002c0009t0073 a0002c0025t0077 |
4 | HG02257.hp2 HG02486.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1484A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1484 | chr14 | 60135705 | ||||||
chr14:60135771 | C | T | 1 | a0011c0022t0041 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1550C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1550 | chr14 | 60135771 | ||||||
chr14:60135796 | C | T | 2 | a0012c0029t0057 a0014c0024t0045 |
2 | HG01243.hp2 HG01496.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1575C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1575 | chr14 | 60135796 | ||||||
chr14:60135886 | TGATA | T | 26 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(23): Show |
69 | HG00639.hp1 HG00673.hp1 HG01081.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1670_*1673delGATA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1670 | INFO_REALIGN_3_PRIME | chr14 | 60135886 | |||||
chr14:60135921 | A | G | 1 | a0001c0001t0023 | 2 | HG00099.hp1 HG00280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1700A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1700 | chr14 | 60135921 | ||||||
chr14:60136058 | C | T | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1837C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1837 | chr14 | 60136058 | ||||||
chr14:60136069 | A | G | 1 | a0001c0001t0022 | 2 | HG01175.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1848A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1848 | chr14 | 60136069 | ||||||
chr14:60136107 | TA | T | 51 | a0001c0001t0040 a0001c0001t0043 a0002c0002t0003 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*1899delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 1899 | INFO_REALIGN_3_PRIME | chr14 | 60136107 | |||||
chr14:60136650 | C | T | 1 | a0001c0001t0015 | 3 | NA18946.hp2 NA18980.hp2 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2429C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2429 | chr14 | 60136650 | ||||||
chr14:60136668 | C | T | 1 | a0005c0006t0063 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2447C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2447 | chr14 | 60136668 | ||||||
chr14:60136686 | TGA | T | 7 | a0001c0001t0006 a0001c0001t0015 a0001c0001t0044 others(4): Show |
17 | HG01496.hp2 HG02155.hp2 HG02165.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2469_*2470delAG | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2469 | INFO_REALIGN_3_PRIME | chr14 | 60136686 | |||||
chr14:60136694 | G | C | 2 | a0001c0001t0011 a0001c0001t0047 |
5 | HG01192.hp1 HG01928.hp2 HG01934.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2473G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2473 | chr14 | 60136694 | ||||||
chr14:60136746 | G | T | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2525G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2525 | chr14 | 60136746 | ||||||
chr14:60136787 | T | C | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2566T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2566 | chr14 | 60136787 | ||||||
chr14:60136913 | T | A | 1 | a0001c0001t0019 | 2 | NA18975.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2692T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2692 | chr14 | 60136913 | ||||||
chr14:60136941 | G | A | 1 | a0001c0001t0033 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2720G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2720 | chr14 | 60136941 | ||||||
chr14:60137046 | T | C | 1 | a0001c0001t0034 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2825T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2825 | chr14 | 60137046 | ||||||
chr14:60137086 | A | G | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2865A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2865 | chr14 | 60137086 | ||||||
chr14:60137165 | G | C | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2944G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 2944 | chr14 | 60137165 | ||||||
chr14:60137315 | G | A | 2 | a0002c0009t0027 a0002c0009t0055 |
3 | HG02922.hp1 HG03139.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3094G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3094 | chr14 | 60137315 | ||||||
chr14:60137353 | C | G | 1 | a0003c0003t0062 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3132C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3132 | chr14 | 60137353 | ||||||
chr14:60137579 | A | G | 91 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(88): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
3_prime_UTR_variant | MODIFIER | c.*3358A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3358 | chr14 | 60137579 | ||||||
chr14:60137899 | C | G | 1 | a0020c0026t0072 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3678C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3678 | chr14 | 60137899 | ||||||
chr14:60137931 | T | TA | 3 | a0007c0008t0013 a0007c0008t0026 a0007c0008t0056 |
7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3721dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3722 | INFO_REALIGN_3_PRIME | chr14 | 60137931 | |||||
chr14:60137952 | G | A | 1 | a0007c0008t0026 | 2 | HG02735.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3731G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3731 | chr14 | 60137952 | ||||||
chr14:60138050 | C | T | 1 | a0002c0009t0055 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3829C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3829 | chr14 | 60138050 | ||||||
chr14:60138069 | C | T | 3 | a0007c0008t0013 a0007c0008t0026 a0007c0008t0056 |
7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3848C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3848 | chr14 | 60138069 | ||||||
chr14:60138078 | G | A | 5 | a0005c0006t0009 a0005c0006t0051 a0005c0006t0058 others(2): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3857G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3857 | chr14 | 60138078 | ||||||
chr14:60138126 | G | A | 1 | a0002c0002t0017 | 3 | HG03195.hp2 HG03486.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3905G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 3905 | chr14 | 60138126 | ||||||
chr14:60138245 | A | G | 1 | a0002c0002t0028 | 2 | HG03669.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4024A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4024 | chr14 | 60138245 | ||||||
chr14:60138446 | A | T | 1 | a0014c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4225A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4225 | chr14 | 60138446 | ||||||
chr14:60138453 | G | A | 1 | a0002c0007t0064 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4232G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4232 | chr14 | 60138453 | ||||||
chr14:60138998 | TAAAAC | T | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*4780_*4784delAACA others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4780 | INFO_REALIGN_3_PRIME | chr14 | 60138998 | |||||
chr14:60139070 | A | G | 24 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(21): Show |
66 | HG00639.hp1 HG00673.hp1 HG01081.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4849A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4849 | chr14 | 60139070 | ||||||
chr14:60139123 | T | C | 1 | a0002c0002t0078 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4902T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4902 | chr14 | 60139123 | ||||||
chr14:60139184 | AAAAG | A | 4 | a0002c0002t0065 a0007c0008t0013 a0007c0008t0026 others(1): Show |
8 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4971_*4974delGAAA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4971 | INFO_REALIGN_3_PRIME | chr14 | 60139184 | |||||
chr14:60139208 | C | G | 1 | a0020c0026t0072 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4987C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 4987 | chr14 | 60139208 | ||||||
chr14:60139225 | T | C | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*5004T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5004 | chr14 | 60139225 | ||||||
chr14:60139320 | G | C | 7 | a0003c0003t0002 a0003c0003t0059 a0003c0003t0060 others(4): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*5099G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5099 | chr14 | 60139320 | ||||||
chr14:60139370 | C | T | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*5149C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5149 | chr14 | 60139370 | ||||||
chr14:60139378 | GAC | G | 5 | a0005c0006t0009 a0005c0006t0051 a0005c0006t0058 others(2): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5159_*5160delCA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5159 | INFO_REALIGN_3_PRIME | chr14 | 60139378 | |||||
chr14:60139809 | T | C | 52 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(49): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*5588T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5588 | chr14 | 60139809 | ||||||
chr14:60139914 | C | T | 1 | a0002c0002t0031 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5693C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5693 | chr14 | 60139914 | ||||||
chr14:60139952 | T | TA | 48 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(45): Show |
155 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*5741dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5742 | INFO_REALIGN_3_PRIME | chr14 | 60139952 | |||||
chr14:60139999 | A | G | 1 | a0014c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5778A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5778 | chr14 | 60139999 | ||||||
chr14:60140098 | G | A | 46 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(43): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*5877G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5877 | chr14 | 60140098 | ||||||
chr14:60140119 | A | G | 1 | a0002c0002t0071 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5898A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 5898 | chr14 | 60140119 | ||||||
chr14:60140248 | A | C | 1 | a0012c0029t0057 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6027A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6027 | chr14 | 60140248 | ||||||
chr14:60140308 | G | C | 2 | a0007c0008t0013 a0007c0008t0056 |
5 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6087G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6087 | chr14 | 60140308 | ||||||
chr14:60140341 | G | A | 52 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(49): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*6120G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6120 | chr14 | 60140341 | ||||||
chr14:60140350 | A | C | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6129A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6129 | chr14 | 60140350 | ||||||
chr14:60140521 | T | C | 12 | a0002c0002t0005 a0002c0002t0028 a0002c0002t0065 others(9): Show |
24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6300T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6300 | chr14 | 60140521 | ||||||
chr14:60140601 | T | TAC | 36 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(33): Show |
87 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6397_*6398dupAC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6399 | INFO_REALIGN_3_PRIME | chr14 | 60140601 | |||||
chr14:60140601 | T | TACAC | 10 | a0002c0009t0029 a0002c0009t0073 a0002c0025t0077 others(7): Show |
46 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*6395_*6398dupACAC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6399 | INFO_REALIGN_3_PRIME | chr14 | 60140601 | |||||
chr14:60140601 | T | TACACAC | 3 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0053 |
22 | NA18940.hp1 NA18941.hp1 NA18945.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*6393_*6398dupACAC others(2): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6399 | INFO_REALIGN_3_PRIME | chr14 | 60140601 | |||||
chr14:60140696 | C | G | 6 | a0002c0009t0029 a0002c0009t0073 a0007c0008t0013 others(3): Show |
11 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6475C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6475 | chr14 | 60140696 | ||||||
chr14:60140814 | C | T | 1 | a0004c0004t0053 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6593C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6593 | chr14 | 60140814 | ||||||
chr14:60140858 | A | G | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6637A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6637 | chr14 | 60140858 | ||||||
chr14:60140899 | A | C | 5 | a0005c0006t0009 a0005c0006t0051 a0005c0006t0058 others(2): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6678A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6678 | chr14 | 60140899 | ||||||
chr14:60140947 | GA | G | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6729delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6729 | INFO_REALIGN_3_PRIME | chr14 | 60140947 | |||||
chr14:60141047 | A | G | 52 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(49): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*6826A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6826 | chr14 | 60141047 | ||||||
chr14:60141165 | G | T | 1 | a0002c0025t0077 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6944G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 6944 | chr14 | 60141165 | ||||||
chr14:60141267 | A | G | 52 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(49): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*7046A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7046 | chr14 | 60141267 | ||||||
chr14:60141356 | A | G | 1 | a0021c0019t0050 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7135A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7135 | chr14 | 60141356 | ||||||
chr14:60141359 | ACAAT | A | 4 | a0007c0008t0013 a0007c0008t0026 a0007c0008t0056 others(1): Show |
8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7142_*7145delTCAA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7142 | INFO_REALIGN_3_PRIME | chr14 | 60141359 | |||||
chr14:60141361 | A | G | 1 | a0004c0004t0016 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7140A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7140 | chr14 | 60141361 | ||||||
chr14:60141364 | C | G | 1 | a0003c0003t0060 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7143C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7143 | chr14 | 60141364 | ||||||
chr14:60141367 | G | T | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7146G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7146 | chr14 | 60141367 | ||||||
chr14:60141622 | T | A | 2 | a0001c0001t0024 a0001c0001t0048 |
3 | NA18961.hp2 NA18999.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7401T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7401 | chr14 | 60141622 | ||||||
chr14:60141635 | TAAAAG | T | 46 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(43): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*7418_*7422delAGAA others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7418 | INFO_REALIGN_3_PRIME | chr14 | 60141635 | |||||
chr14:60141739 | G | T | 48 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(45): Show |
135 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*7518G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7518 | chr14 | 60141739 | ||||||
chr14:60142006 | A | C | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7785A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7785 | chr14 | 60142006 | ||||||
chr14:60142089 | G | A | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7868G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 7868 | chr14 | 60142089 | ||||||
chr14:60142369 | G | C | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8148G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8148 | chr14 | 60142369 | ||||||
chr14:60142478 | T | TA | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*8261dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8262 | INFO_REALIGN_3_PRIME | chr14 | 60142478 | |||||
chr14:60142528 | A | T | 1 | a0001c0001t0043 | 1 | NA19059.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8307A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8307 | chr14 | 60142528 | ||||||
chr14:60142590 | G | A | 1 | a0017c0031t0035 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8369G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8369 | chr14 | 60142590 | ||||||
chr14:60142681 | T | C | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8460T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8460 | chr14 | 60142681 | ||||||
chr14:60142969 | G | A | 50 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(47): Show |
156 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*8748G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8748 | chr14 | 60142969 | ||||||
chr14:60142985 | G | A | 1 | a0001c0001t0020 | 2 | HG02976.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*8764G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8764 | chr14 | 60142985 | ||||||
chr14:60142989 | A | G | 1 | a0001c0001t0038 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8768A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8768 | chr14 | 60142989 | ||||||
chr14:60143000 | C | G | 1 | a0005c0006t0051 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8779C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8779 | chr14 | 60143000 | ||||||
chr14:60143046 | T | C | 41 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(38): Show |
124 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*8825T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 8825 | chr14 | 60143046 | ||||||
chr14:60143276 | G | C | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*9055G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9055 | chr14 | 60143276 | ||||||
chr14:60143404 | C | T | 1 | a0001c0001t0030 | 2 | HG03490.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9183C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9183 | chr14 | 60143404 | ||||||
chr14:60143449 | C | T | 2 | a0001c0001t0049 a0021c0019t0050 |
2 | HG00673.hp2 NA18940.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9228C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9228 | chr14 | 60143449 | ||||||
chr14:60143496 | C | CTAATTAG others(82): Show |
1 | a0001c0001t0038 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9277_*9365dupAATT others(85): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9366 | INFO_REALIGN_3_PRIME | chr14 | 60143496 | |||||
chr14:60143598 | C | T | 46 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(43): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*9377C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9377 | chr14 | 60143598 | ||||||
chr14:60143679 | G | A | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9458G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9458 | chr14 | 60143679 | ||||||
chr14:60143760 | T | C | 1 | a0002c0002t0069 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9539T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9539 | chr14 | 60143760 | ||||||
chr14:60143825 | A | G | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9604A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9604 | chr14 | 60143825 | ||||||
chr14:60143839 | C | T | 1 | a0002c0002t0070 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9618C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9618 | chr14 | 60143839 | ||||||
chr14:60143881 | T | C | 1 | a0012c0029t0057 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9660T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9660 | chr14 | 60143881 | ||||||
chr14:60144087 | A | G | 1 | a0009c0011t0037 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9866A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 9866 | chr14 | 60144087 | ||||||
chr14:60144383 | C | T | 1 | a0002c0002t0068 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10162C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10162 | chr14 | 60144383 | ||||||
chr14:60144399 | G | C | 1 | a0002c0002t0068 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10178G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10178 | chr14 | 60144399 | ||||||
chr14:60144476 | C | T | 1 | a0014c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10255C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10255 | chr14 | 60144476 | ||||||
chr14:60144675 | G | A | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10454G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10454 | chr14 | 60144675 | ||||||
chr14:60144810 | T | C | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10589T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10589 | chr14 | 60144810 | ||||||
chr14:60144867 | T | C | 46 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(43): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*10646T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10646 | chr14 | 60144867 | ||||||
chr14:60144930 | C | T | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10709C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10709 | chr14 | 60144930 | ||||||
chr14:60144957 | G | A | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10736G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10736 | chr14 | 60144957 | ||||||
chr14:60145029 | A | C | 1 | a0012c0029t0057 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10808A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10808 | chr14 | 60145029 | ||||||
chr14:60145075 | T | C | 1 | a0001c0001t0048 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*10854T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10854 | chr14 | 60145075 | ||||||
chr14:60145120 | T | C | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*10899T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10899 | chr14 | 60145120 | ||||||
chr14:60145184 | C | T | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*10963C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 10963 | chr14 | 60145184 | ||||||
chr14:60145312 | A | G | 1 | a0014c0024t0045 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11091A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11091 | chr14 | 60145312 | ||||||
chr14:60145401 | A | G | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11180A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11180 | chr14 | 60145401 | ||||||
chr14:60145683 | T | C | 1 | a0003c0003t0059 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11462T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11462 | chr14 | 60145683 | ||||||
chr14:60145689 | GA | G | 3 | a0007c0008t0013 a0007c0008t0026 a0007c0008t0056 |
7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11477delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11477 | INFO_REALIGN_3_PRIME | chr14 | 60145689 | |||||
chr14:60145697 | A | C | 3 | a0007c0008t0013 a0007c0008t0026 a0007c0008t0056 |
7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*11476A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11476 | chr14 | 60145697 | ||||||
chr14:60145744 | A | G | 1 | a0024c0018t0076 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11523A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11523 | chr14 | 60145744 | ||||||
chr14:60145969 | G | A | 6 | a0002c0009t0029 a0002c0009t0073 a0007c0008t0013 others(3): Show |
11 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*11748G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11748 | chr14 | 60145969 | ||||||
chr14:60145996 | C | T | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11775C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11775 | chr14 | 60145996 | ||||||
chr14:60146048 | G | A | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11827G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11827 | chr14 | 60146048 | ||||||
chr14:60146132 | T | TATC | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*11913_*11914insCA others(1): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 11914 | INFO_REALIGN_3_PRIME | chr14 | 60146132 | |||||
chr14:60146245 | C | T | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*12024C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12024 | chr14 | 60146245 | ||||||
chr14:60146605 | T | C | 1 | a0001c0001t0036 | 1 | HG01258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12384T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12384 | chr14 | 60146605 | ||||||
chr14:60146683 | G | GTC | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*12463_*12464insCT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12464 | INFO_REALIGN_3_PRIME | chr14 | 60146683 | |||||
chr14:60146687 | G | A | 5 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(2): Show |
25 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*12466G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12466 | chr14 | 60146687 | ||||||
chr14:60146687 | G | GTA | 44 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(41): Show |
131 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*12467_*12468insAT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12468 | INFO_REALIGN_3_PRIME | chr14 | 60146687 | |||||
chr14:60146689 | G | A | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*12468G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12468 | chr14 | 60146689 | ||||||
chr14:60146846 | C | A | 52 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(49): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*12625C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12625 | chr14 | 60146846 | ||||||
chr14:60147134 | G | A | 5 | a0005c0006t0009 a0005c0006t0051 a0005c0006t0058 others(2): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*12913G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12913 | chr14 | 60147134 | ||||||
chr14:60147173 | G | C | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*12952G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 12952 | chr14 | 60147173 | ||||||
chr14:60147222 | G | A | 1 | a0002c0009t0073 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13001G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13001 | chr14 | 60147222 | ||||||
chr14:60147279 | T | G | 8 | a0002c0007t0061 a0002c0009t0029 a0002c0009t0073 others(5): Show |
13 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*13058T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13058 | chr14 | 60147279 | ||||||
chr14:60147293 | T | C | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*13072T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13072 | chr14 | 60147293 | ||||||
chr14:60147320 | C | A | 52 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(49): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*13099C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13099 | chr14 | 60147320 | ||||||
chr14:60147320 | C | T | 2 | a0001c0001t0021 a0001c0001t0034 |
3 | NA18986.hp2 NA19009.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13099C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13099 | chr14 | 60147320 | ||||||
chr14:60147401 | A | C | 12 | a0002c0002t0005 a0002c0002t0028 a0002c0002t0065 others(9): Show |
24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*13180A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13180 | chr14 | 60147401 | ||||||
chr14:60147458 | G | C | 51 | a0002c0002t0003 a0002c0002t0005 a0002c0002t0014 others(48): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*13237G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13237 | chr14 | 60147458 | ||||||
chr14:60147596 | A | G | 1 | a0016c0014t0066 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13375A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13375 | chr14 | 60147596 | ||||||
chr14:60148028 | T | A | 4 | a0004c0004t0004 a0004c0004t0016 a0004c0004t0025 others(1): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*13807T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13807 | chr14 | 60148028 | ||||||
chr14:60148169 | T | C | 1 | a0006c0005t0039 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13948T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 11/11 | 13948 | chr14 | 60148169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:60092494 | T | G | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+75T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092494 | |||||||
chr14:60092511 | A | G | 4 | a0001c0001t0007g0039 a0001c0001t0007g0040 a0001c0001t0007g0185 others(1): Show |
5 | HG02074.hp2 NA18942.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+92A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092511 | |||||||
chr14:60092521 | G | T | 11 | a0001c0001t0012g0184 a0002c0002t0003g0014 a0002c0002t0003g0022 others(8): Show |
15 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.-54+102G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092521 | |||||||
chr14:60092769 | C | T | 1 | a0020c0026t0072g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-54+350C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092769 | |||||||
chr14:60092855 | C | A | 3 | a0002c0009t0029g0052 a0002c0009t0029g0053 a0002c0025t0077g0054 |
3 | HG02257.hp2 HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+436C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092855 | |||||||
chr14:60092943 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.-54+524C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092943 | |||||||
chr14:60092966 | G | A | 1 | a0002c0009t0055g0055 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-54+547G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60092966 | |||||||
chr14:60093114 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-54+695T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093114 | |||||||
chr14:60093238 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-54+819C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093238 | |||||||
chr14:60093272 | C | A | 7 | a0002c0002t0003g0025 a0002c0002t0003g0057 a0002c0002t0003g0058 others(4): Show |
7 | HG01243.hp1 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-54+853C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093272 | |||||||
chr14:60093445 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.-54+1026G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093445 | |||||||
chr14:60093465 | C | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-54+1046C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093465 | |||||||
chr14:60093854 | T | G | 2 | a0020c0026t0072g0178 a0024c0018t0076g0115 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-54+1435T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093854 | |||||||
chr14:60093889 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-54+1470A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60093889 | |||||||
chr14:60094064 | A | C | 1 | a0003c0003t0002g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-54+1645A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094064 | |||||||
chr14:60094151 | T | A | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+1732T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094151 | |||||||
chr14:60094318 | T | TC | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-54+1904dupC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094318 | ||||||
chr14:60094428 | C | A | 1 | a0002c0002t0003g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-54+2009C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094428 | |||||||
chr14:60094447 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-54+2028T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094447 | |||||||
chr14:60094611 | C | G | 1 | a0002c0002t0005g0029 | 2 | NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-54+2192C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094611 | |||||||
chr14:60094624 | C | T | 4 | a0007c0008t0013g0028 a0007c0008t0013g0112 a0007c0008t0013g0113 others(1): Show |
5 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-54+2205C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094624 | |||||||
chr14:60094657 | G | GCC | 7 | a0007c0008t0013g0028 a0007c0008t0013g0112 a0007c0008t0013g0113 others(4): Show |
8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.-54+2240_-54+2241d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094657 | ||||||
chr14:60094761 | G | GC | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(74): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.-54+2351dupC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | ||||||
chr14:60094761 | G | GCC | 39 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0036 others(36): Show |
50 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-54+2350_-54+2351d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | ||||||
chr14:60094761 | G | GCCC | 13 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0167 others(10): Show |
14 | HG00673.hp2 HG02071.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.-54+2349_-54+2351d others(5): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | ||||||
chr14:60094761 | GC | G | 23 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(20): Show |
41 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(38): Show |
intron_variant | MODIFIER | c.-54+2351delC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60094761 | ||||||
chr14:60094770 | C | A | 1 | a0006c0005t0006g0118 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-54+2351C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094770 | |||||||
chr14:60094771 | A | C | 2 | a0001c0001t0001g0176 a0018c0017t0003g0183 |
2 | HG01884.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-54+2352A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094771 | |||||||
chr14:60094805 | A | T | 1 | a0003c0003t0002g0104 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-54+2386A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094805 | |||||||
chr14:60094912 | T | C | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+2493T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094912 | |||||||
chr14:60094943 | T | C | 24 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(21): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.-54+2524T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60094943 | |||||||
chr14:60095162 | G | A | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+2743G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095162 | |||||||
chr14:60095256 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+2837A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095256 | |||||||
chr14:60095342 | A | G | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+2923A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095342 | |||||||
chr14:60095372 | G | A | 1 | a0002c0009t0027g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-54+2953G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095372 | |||||||
chr14:60095411 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-54+2992G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095411 | |||||||
chr14:60095455 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(104): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-54+3036T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095455 | |||||||
chr14:60095463 | G | A | 8 | a0003c0003t0002g0004 a0003c0003t0002g0009 a0003c0003t0002g0062 others(5): Show |
17 | HG00558.hp2 NA18942.hp2 NA18943.hp1 others(14): Show |
intron_variant | MODIFIER | c.-54+3044G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095463 | |||||||
chr14:60095509 | G | T | 11 | a0002c0009t0029g0052 a0002c0009t0029g0053 a0002c0009t0073g0103 others(8): Show |
12 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54+3090G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095509 | |||||||
chr14:60095600 | C | T | 1 | a0004c0004t0004g0050 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-54+3181C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095600 | |||||||
chr14:60095655 | C | T | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+3236C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095655 | |||||||
chr14:60095694 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-54+3275G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095694 | |||||||
chr14:60095882 | C | G | 1 | a0001c0001t0001g0166 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-54+3463C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095882 | |||||||
chr14:60095996 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0121 |
4 | HG00280.hp1 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+3577G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60095996 | |||||||
chr14:60096076 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+3657T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096076 | |||||||
chr14:60096147 | A | ATCTGGGT others(2): Show |
108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+3731_-54+3739d others(11): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60096147 | ||||||
chr14:60096151 | G | A | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+3732G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096151 | |||||||
chr14:60096236 | G | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-54+3817G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096236 | |||||||
chr14:60096254 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-54+3835C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096254 | |||||||
chr14:60096317 | G | C | 1 | a0002c0013t0003g0056 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-54+3898G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096317 | |||||||
chr14:60096361 | G | A | 2 | a0004c0004t0004g0023 a0004c0004t0004g0041 |
3 | NA18975.hp2 NA18983.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-54+3942G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096361 | |||||||
chr14:60096423 | A | G | 2 | a0002c0009t0027g0075 a0002c0009t0027g0102 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-54+4004A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096423 | |||||||
chr14:60096521 | C | T | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+4102C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096521 | |||||||
chr14:60096585 | A | G | 1 | a0012c0029t0057g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-54+4166A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096585 | |||||||
chr14:60096766 | T | A | 1 | a0002c0007t0003g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-54+4347T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096766 | |||||||
chr14:60096947 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-54+4528G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60096947 | |||||||
chr14:60097050 | T | TTTAAA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+4634_-54+4638d others(7): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60097050 | ||||||
chr14:60097275 | A | G | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-54+4856A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097275 | |||||||
chr14:60097284 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0120 a0001c0001t0001g0121 |
4 | HG00280.hp1 HG02257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+4865A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097284 | |||||||
chr14:60097350 | G | A | 1 | a0001c0001t0008g0146 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-54+4931G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097350 | |||||||
chr14:60097392 | A | G | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+4973A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097392 | |||||||
chr14:60097648 | T | TA | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54+5232dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60097648 | ||||||
chr14:60097669 | G | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-54+5250G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097669 | |||||||
chr14:60097768 | A | G | 1 | a0001c0021t0032g0165 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-54+5349A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097768 | |||||||
chr14:60097837 | A | T | 1 | a0004c0004t0004g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-54+5418A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097837 | |||||||
chr14:60097843 | A | G | 1 | a0003c0003t0002g0026 | 2 | HG02015.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-54+5424A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097843 | |||||||
chr14:60097855 | C | G | 2 | a0002c0002t0028g0100 a0002c0002t0028g0101 |
2 | HG03669.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-54+5436C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097855 | |||||||
chr14:60097933 | C | A | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+5514C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097933 | |||||||
chr14:60097946 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+5527G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60097946 | |||||||
chr14:60098006 | C | T | 1 | a0004c0004t0025g0048 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-54+5587C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098006 | |||||||
chr14:60098010 | G | A | 5 | a0002c0007t0003g0027 a0002c0007t0003g0076 a0002c0007t0003g0078 others(2): Show |
6 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-54+5591G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098010 | |||||||
chr14:60098074 | A | G | 19 | a0002c0002t0005g0008 a0002c0002t0005g0015 a0002c0002t0005g0029 others(16): Show |
24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.-54+5655A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098074 | |||||||
chr14:60098090 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-54+5671T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098090 | |||||||
chr14:60098109 | A | C | 1 | a0002c0002t0031g0181 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-54+5690A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098109 | |||||||
chr14:60098162 | C | T | 1 | a0003c0003t0002g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-54+5743C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098162 | |||||||
chr14:60098312 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-54+5893C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098312 | |||||||
chr14:60098395 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-54+5976T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098395 | |||||||
chr14:60098525 | C | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-54+6106C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098525 | |||||||
chr14:60098559 | G | C | 3 | a0002c0009t0029g0052 a0002c0009t0029g0053 a0002c0009t0073g0103 |
3 | HG02486.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+6140G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098559 | |||||||
chr14:60098648 | A | G | 1 | a0012c0029t0057g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-54+6229A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098648 | |||||||
chr14:60098768 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54+6349T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098768 | |||||||
chr14:60098843 | C | G | 2 | a0001c0001t0001g0164 a0001c0001t0015g0163 |
2 | NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-54+6424C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098843 | |||||||
chr14:60098856 | T | C | 1 | a0001c0001t0018g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-54+6437T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60098856 | |||||||
chr14:60099009 | T | C | 3 | a0002c0009t0027g0075 a0002c0009t0027g0102 a0002c0009t0055g0055 |
3 | HG02922.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-54+6590T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099009 | |||||||
chr14:60099023 | G | A | 3 | a0002c0007t0003g0027 a0002c0007t0003g0078 a0002c0007t0064g0077 |
4 | HG01884.hp1 HG02145.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54+6604G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099023 | |||||||
chr14:60099094 | C | G | 3 | a0002c0009t0029g0052 a0002c0009t0029g0053 a0002c0009t0073g0103 |
3 | HG02486.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+6675C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099094 | |||||||
chr14:60099251 | A | G | 3 | a0002c0009t0029g0052 a0002c0009t0029g0053 a0002c0009t0073g0103 |
3 | HG02486.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-54+6832A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099251 | |||||||
chr14:60099415 | T | G | 3 | a0004c0004t0004g0042 a0004c0004t0004g0049 a0004c0004t0004g0050 |
3 | NA18964.hp1 NA19081.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-54+6996T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099415 | |||||||
chr14:60099795 | G | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-54+7376G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099795 | |||||||
chr14:60099897 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-54+7478C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099897 | |||||||
chr14:60099947 | C | T | 2 | a0001c0001t0023g0144 a0001c0001t0023g0162 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.-54+7528C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099947 | |||||||
chr14:60099949 | C | T | 1 | a0002c0002t0003g0090 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-54+7530C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60099949 | |||||||
chr14:60100143 | A | G | 5 | a0002c0007t0061g0060 a0002c0009t0029g0052 a0002c0009t0029g0053 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-7443A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60100143 | |||||||
chr14:60100258 | A | G | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53-7328A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60100258 | |||||||
chr14:60100371 | T | A | 1 | a0025c0012t0003g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-53-7215T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60100371 | |||||||
chr14:60101083 | T | C | 1 | a0004c0004t0004g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-53-6503T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101083 | |||||||
chr14:60101140 | T | A | 1 | a0001c0001t0015g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-53-6446T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101140 | |||||||
chr14:60101168 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-53-6418T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101168 | |||||||
chr14:60101226 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-53-6360G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101226 | |||||||
chr14:60101412 | CAGATT | C | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-6172_-53-6168d others(7): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60101412 | ||||||
chr14:60101421 | G | C | 1 | a0020c0026t0072g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-53-6165G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101421 | |||||||
chr14:60101697 | T | TA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-53-5881dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60101697 | ||||||
chr14:60101710 | T | A | 1 | a0003c0003t0002g0104 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-53-5876T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101710 | |||||||
chr14:60101711 | A | T | 1 | a0003c0003t0002g0104 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-53-5875A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101711 | |||||||
chr14:60101828 | T | C | 25 | a0002c0025t0077g0054 a0003c0003t0002g0004 a0003c0003t0002g0006 others(22): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(40): Show |
intron_variant | MODIFIER | c.-53-5758T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60101828 | |||||||
chr14:60102329 | T | TTAAAAA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-53-5256_-53-5255i others(8): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60102329 | ||||||
chr14:60102446 | A | G | 1 | a0002c0007t0061g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-53-5140A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102446 | |||||||
chr14:60102557 | C | A | 1 | a0020c0026t0072g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-53-5029C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102557 | |||||||
chr14:60102661 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-53-4925T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102661 | |||||||
chr14:60102773 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-53-4813G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102773 | |||||||
chr14:60102796 | T | A | 1 | a0003c0003t0002g0104 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-53-4790T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102796 | |||||||
chr14:60102842 | T | C | 3 | a0001c0001t0010g0147 a0001c0001t0010g0148 a0001c0001t0010g0168 |
3 | NA18968.hp2 NA19080.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-53-4744T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102842 | |||||||
chr14:60102914 | AT | A | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-4668delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60102914 | ||||||
chr14:60102940 | A | G | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53-4646A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60102940 | |||||||
chr14:60103088 | G | A | 2 | a0001c0001t0001g0149 a0001c0001t0006g0169 |
2 | NA18994.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-53-4498G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103088 | |||||||
chr14:60103276 | A | G | 1 | a0003c0003t0002g0062 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-53-4310A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103276 | |||||||
chr14:60103330 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-53-4256C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103330 | |||||||
chr14:60103357 | T | G | 29 | a0002c0007t0061g0060 a0002c0009t0029g0052 a0002c0009t0029g0053 others(26): Show |
47 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(44): Show |
intron_variant | MODIFIER | c.-53-4229T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103357 | |||||||
chr14:60103395 | T | C | 1 | a0001c0001t0046g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-53-4191T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103395 | |||||||
chr14:60103446 | G | A | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-4140G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103446 | |||||||
chr14:60103509 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-53-4077C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103509 | |||||||
chr14:60103816 | G | A | 24 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(21): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.-53-3770G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103816 | |||||||
chr14:60103858 | T | C | 1 | a0001c0001t0046g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-53-3728T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103858 | |||||||
chr14:60103925 | G | A | 2 | a0002c0009t0027g0075 a0002c0009t0027g0102 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-53-3661G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60103925 | |||||||
chr14:60104012 | C | A | 5 | a0002c0002t0003g0082 a0002c0002t0003g0085 a0002c0002t0017g0081 others(2): Show |
5 | HG01109.hp1 HG02818.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53-3574C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104012 | |||||||
chr14:60104092 | G | A | 1 | a0003c0003t0002g0064 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-53-3494G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104092 | |||||||
chr14:60104154 | A | G | 1 | a0001c0030t0006g0174 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-53-3432A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104154 | |||||||
chr14:60104203 | C | A | 1 | a0001c0001t0001g0032 | 2 | NA18984.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-53-3383C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104203 | |||||||
chr14:60104228 | A | T | 1 | a0005c0006t0058g0107 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-53-3358A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104228 | |||||||
chr14:60104250 | C | T | 1 | a0002c0002t0068g0099 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-53-3336C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104250 | |||||||
chr14:60104318 | C | CA | 16 | a0002c0002t0003g0059 a0002c0002t0003g0086 a0002c0002t0005g0015 others(13): Show |
22 | HG02071.hp1 HG02080.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.-53-3239dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | ||||||
chr14:60104318 | C | CAA | 7 | a0002c0002t0003g0025 a0002c0002t0003g0057 a0002c0002t0003g0058 others(4): Show |
7 | HG01243.hp1 HG02074.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53-3240_-53-3239d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | ||||||
chr14:60104318 | CA | C | 34 | a0002c0002t0003g0022 a0002c0002t0003g0038 a0002c0002t0003g0082 others(31): Show |
44 | HG01081.hp2 HG01109.hp1 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.-53-3239delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | ||||||
chr14:60104318 | CAAAAAAA others(4): Show |
C | 8 | a0002c0009t0027g0075 a0002c0009t0027g0102 a0005c0006t0009g0017 others(5): Show |
11 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.-53-3249_-53-3239d others(13): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | ||||||
chr14:60104318 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0024g0035 a0001c0001t0024g0170 a0001c0001t0048g0035 |
3 | NA18961.hp2 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-53-3253_-53-3239d others(17): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | ||||||
chr14:60104318 | CAAAAAAA others(9): Show |
C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(100): Show |
144 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-53-3254_-53-3239d others(18): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60104318 | ||||||
chr14:60104366 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-53-3220C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104366 | |||||||
chr14:60104511 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-53-3075T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104511 | |||||||
chr14:60104752 | G | T | 1 | a0001c0001t0022g0143 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-53-2834G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104752 | |||||||
chr14:60104772 | A | C | 1 | a0002c0002t0071g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-53-2814A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104772 | |||||||
chr14:60104776 | T | A | 4 | a0002c0002t0003g0082 a0002c0002t0017g0081 a0002c0002t0017g0083 others(1): Show |
4 | HG01109.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53-2810T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104776 | |||||||
chr14:60104939 | T | A | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-2647T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60104939 | |||||||
chr14:60105301 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-53-2285A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105301 | |||||||
chr14:60105320 | G | C | 1 | a0002c0007t0064g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-53-2266G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105320 | |||||||
chr14:60105409 | AT | A | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-2174delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60105409 | ||||||
chr14:60105455 | T | C | 7 | a0006c0005t0001g0020 a0006c0005t0006g0020 a0006c0005t0006g0118 others(4): Show |
8 | HG01496.hp2 HG02165.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.-53-2131T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105455 | |||||||
chr14:60105514 | C | CTA | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-53-2063_-53-2062d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60105514 | ||||||
chr14:60105539 | T | C | 1 | a0004c0004t0004g0045 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-53-2047T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105539 | |||||||
chr14:60105642 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-53-1944T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105642 | |||||||
chr14:60105753 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-53-1833T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60105753 | |||||||
chr14:60106019 | A | T | 1 | a0006c0005t0039g0172 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-53-1567A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106019 | |||||||
chr14:60106058 | G | T | 1 | a0002c0009t0029g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-53-1528G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106058 | |||||||
chr14:60106065 | A | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-53-1521A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106065 | |||||||
chr14:60106105 | T | G | 6 | a0007c0008t0013g0028 a0007c0008t0013g0112 a0007c0008t0013g0113 others(3): Show |
7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-53-1481T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106105 | |||||||
chr14:60106168 | A | G | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53-1418A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106168 | |||||||
chr14:60106205 | C | T | 1 | a0002c0007t0064g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-53-1381C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106205 | |||||||
chr14:60106275 | G | A | 24 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(21): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.-53-1311G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106275 | |||||||
chr14:60106282 | C | G | 1 | a0001c0001t0008g0142 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-53-1304C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106282 | |||||||
chr14:60106403 | T | A | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53-1183T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106403 | |||||||
chr14:60106472 | A | G | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-1114A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106472 | |||||||
chr14:60106494 | G | A | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.-53-1092G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106494 | |||||||
chr14:60106591 | G | A | 1 | a0002c0002t0078g0092 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-53-995G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106591 | |||||||
chr14:60106767 | TTTAA | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-53-816_-53-813del others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr14 | 60106767 | ||||||
chr14:60106945 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-53-641A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60106945 | |||||||
chr14:60107084 | A | T | 1 | a0001c0001t0001g0141 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-53-502A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107084 | |||||||
chr14:60107249 | C | T | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53-337C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107249 | |||||||
chr14:60107288 | G | A | 1 | a0002c0025t0077g0054 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-53-298G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107288 | |||||||
chr14:60107520 | G | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-53-66G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 1/10 | chr14 | 60107520 | |||||||
chr14:60108431 | A | G | 1 | a0007c0008t0013g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.689+104A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108431 | |||||||
chr14:60108472 | C | A | 2 | a0003c0003t0002g0068 a0003c0003t0002g0073 |
2 | HG00609.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.689+145C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108472 | |||||||
chr14:60108522 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.689+195T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108522 | |||||||
chr14:60108768 | A | AATATTGA others(301): Show |
1 | a0001c0001t0001g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.689+454_689+455ins others(308): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | ||||||
chr14:60108768 | A | AATATTGA others(307): Show |
5 | a0001c0001t0007g0039 a0001c0001t0022g0127 a0001c0001t0022g0143 others(2): Show |
5 | HG01175.hp1 HG02683.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+454_689+455ins others(314): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | ||||||
chr14:60108768 | A | AATATTGA others(308): Show |
71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(68): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.689+454_689+455ins others(315): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | ||||||
chr14:60108768 | A | AATATTGA others(309): Show |
29 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0036 others(26): Show |
34 | HG00609.hp2 HG01361.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.689+454_689+455ins others(316): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60108768 | ||||||
chr14:60108794 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0031 others(31): Show |
47 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.689+467G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60108794 | |||||||
chr14:60109083 | A | G | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+756A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109083 | |||||||
chr14:60109113 | G | T | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+786G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109113 | |||||||
chr14:60109151 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.689+824A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109151 | |||||||
chr14:60109321 | T | C | 1 | a0001c0001t0012g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.689+994T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109321 | |||||||
chr14:60109377 | G | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.689+1050G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109377 | |||||||
chr14:60109523 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.689+1196G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109523 | |||||||
chr14:60109590 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.689+1263G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109590 | |||||||
chr14:60109632 | G | T | 1 | a0002c0009t0055g0055 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.689+1305G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109632 | |||||||
chr14:60109919 | A | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.689+1592A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60109919 | |||||||
chr14:60110032 | T | G | 24 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(21): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.689+1705T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110032 | |||||||
chr14:60110068 | A | G | 2 | a0001c0001t0023g0144 a0001c0001t0023g0162 |
2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.689+1741A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110068 | |||||||
chr14:60110071 | A | G | 2 | a0008c0010t0005g0016 a0008c0010t0005g0098 |
4 | NA18944.hp1 NA19065.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+1744A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110071 | |||||||
chr14:60110121 | C | A | 1 | a0002c0002t0005g0094 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.689+1794C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110121 | |||||||
chr14:60110143 | A | G | 4 | a0001c0001t0007g0039 a0001c0001t0007g0040 a0001c0001t0007g0185 others(1): Show |
5 | HG02074.hp2 NA18942.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+1816A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110143 | |||||||
chr14:60110233 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.689+1906A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110233 | |||||||
chr14:60110300 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.689+1973C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110300 | |||||||
chr14:60110366 | A | C | 1 | a0001c0001t0018g0123 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.689+2039A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110366 | |||||||
chr14:60110500 | T | G | 1 | a0002c0002t0003g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.689+2173T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110500 | |||||||
chr14:60110930 | G | T | 1 | a0003c0003t0002g0072 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.689+2603G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110930 | |||||||
chr14:60110994 | A | G | 30 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(27): Show |
49 | HG00558.hp2 HG00609.hp1 HG01358.hp2 others(46): Show |
intron_variant | MODIFIER | c.689+2667A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60110994 | |||||||
chr14:60111084 | A | T | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.689+2757A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111084 | |||||||
chr14:60111155 | C | G | 24 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(21): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.689+2828C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111155 | |||||||
chr14:60111243 | T | G | 1 | a0025c0012t0003g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.689+2916T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111243 | |||||||
chr14:60111355 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.689+3028G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111355 | |||||||
chr14:60111437 | A | G | 1 | a0002c0009t0073g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.689+3110A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111437 | |||||||
chr14:60111634 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.690-3066G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111634 | |||||||
chr14:60111847 | A | G | 12 | a0002c0007t0061g0060 a0002c0009t0029g0052 a0002c0009t0029g0053 others(9): Show |
13 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.690-2853A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60111847 | |||||||
chr14:60112004 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.690-2696T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112004 | |||||||
chr14:60112167 | AAGAC | A | 6 | a0007c0008t0013g0028 a0007c0008t0013g0112 a0007c0008t0013g0113 others(3): Show |
7 | HG01358.hp2 HG02055.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-2527_690-2524d others(6): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60112167 | ||||||
chr14:60112271 | T | C | 1 | a0003c0003t0002g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.690-2429T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112271 | |||||||
chr14:60112323 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.690-2377T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112323 | |||||||
chr14:60112352 | A | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0032 others(26): Show |
41 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.690-2348A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112352 | |||||||
chr14:60112430 | T | C | 2 | a0002c0002t0003g0057 a0002c0002t0003g0059 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.690-2270T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112430 | |||||||
chr14:60112451 | A | T | 2 | a0002c0002t0003g0057 a0002c0002t0003g0059 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.690-2249A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112451 | |||||||
chr14:60112623 | G | T | 2 | a0001c0001t0018g0123 a0001c0001t0018g0134 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.690-2077G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112623 | |||||||
chr14:60112646 | A | G | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.690-2054A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112646 | |||||||
chr14:60112910 | G | A | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.690-1790G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112910 | |||||||
chr14:60112921 | C | T | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.690-1779C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112921 | |||||||
chr14:60112955 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.690-1745A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60112955 | |||||||
chr14:60113038 | T | C | 1 | a0020c0026t0072g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.690-1662T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113038 | |||||||
chr14:60113270 | G | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(167): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.690-1430G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113270 | |||||||
chr14:60113280 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.690-1420A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113280 | |||||||
chr14:60113568 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.690-1132C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113568 | |||||||
chr14:60113661 | G | A | 1 | a0001c0001t0022g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.690-1039G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113661 | |||||||
chr14:60113780 | C | T | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.690-920C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113780 | |||||||
chr14:60113785 | A | G | 7 | a0007c0008t0013g0028 a0007c0008t0013g0112 a0007c0008t0013g0113 others(4): Show |
8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.690-915A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113785 | |||||||
chr14:60113890 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.690-810T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113890 | |||||||
chr14:60113952 | C | T | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.690-748C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113952 | |||||||
chr14:60113982 | T | C | 1 | a0001c0001t0008g0132 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.690-718T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60113982 | |||||||
chr14:60114086 | A | G | 2 | a0001c0001t0049g0173 a0021c0019t0050g0157 |
2 | HG00673.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.690-614A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114086 | |||||||
chr14:60114228 | G | C | 1 | a0001c0001t0010g0147 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.690-472G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114228 | |||||||
chr14:60114591 | G | GT | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(106): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.690-100dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr14 | 60114591 | ||||||
chr14:60114652 | C | T | 1 | a0002c0009t0029g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.690-48C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114652 | |||||||
chr14:60114659 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.690-41A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 2/10 | chr14 | 60114659 | |||||||
chr14:60114885 | T | C | 1 | a0003c0003t0060g0065 | 1 | NA19007.hp2 | splice_region_variant&intron_variant | LOW | c.869+6T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 3/10 | chr14 | 60114885 | |||||||
chr14:60114955 | CT | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.870-9delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr14 | 60114955 | ||||||
chr14:60114965 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0038g0128 |
3 | HG02615.hp1 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.870-9T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 3/10 | chr14 | 60114965 | |||||||
chr14:60115558 | A | G | 1 | a0002c0007t0003g0027 | 2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1357+97A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/10 | chr14 | 60115558 | |||||||
chr14:60115598 | T | C | 1 | a0001c0023t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1358-121T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/10 | chr14 | 60115598 | |||||||
chr14:60115611 | G | T | 1 | a0002c0007t0003g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1358-108G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 4/10 | chr14 | 60115611 | |||||||
chr14:60115842 | A | G | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1458+23A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 5/10 | chr14 | 60115842 | |||||||
chr14:60116344 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1578+284A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116344 | |||||||
chr14:60116456 | C | T | 1 | a0003c0003t0002g0071 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1578+396C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116456 | |||||||
chr14:60116519 | T | C | 1 | a0002c0002t0003g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1578+459T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116519 | |||||||
chr14:60116535 | T | C | 3 | a0003c0003t0002g0066 a0003c0003t0002g0069 a0015c0027t0002g0074 |
3 | HG02040.hp1 HG02071.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1578+475T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116535 | |||||||
chr14:60116625 | G | A | 116 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(113): Show |
158 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.1578+565G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116625 | |||||||
chr14:60116641 | A | C | 1 | a0005c0006t0051g0106 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1578+581A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116641 | |||||||
chr14:60116650 | T | G | 3 | a0002c0002t0003g0057 a0002c0002t0003g0059 a0002c0007t0061g0060 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1578+590T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60116650 | |||||||
chr14:60117055 | G | T | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1578+995G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117055 | |||||||
chr14:60117112 | A | G | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1578+1052A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117112 | |||||||
chr14:60117363 | G | A | 1 | a0002c0002t0003g0182 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1579-966G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117363 | |||||||
chr14:60117367 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1579-962A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117367 | |||||||
chr14:60117456 | C | T | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1579-873C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117456 | |||||||
chr14:60117497 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1579-832A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117497 | |||||||
chr14:60117508 | C | T | 1 | a0004c0004t0004g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1579-821C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117508 | |||||||
chr14:60117533 | T | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1579-796T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117533 | |||||||
chr14:60117549 | C | G | 117 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(114): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.1579-780C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117549 | |||||||
chr14:60117695 | G | A | 1 | a0004c0004t0016g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1579-634G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117695 | |||||||
chr14:60117744 | G | T | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1579-585G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117744 | |||||||
chr14:60117808 | G | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1579-521G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117808 | |||||||
chr14:60117851 | A | G | 92 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(89): Show |
124 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(121): Show |
intron_variant | MODIFIER | c.1579-478A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117851 | |||||||
chr14:60117924 | G | A | 1 | a0020c0026t0072g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1579-405G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60117924 | |||||||
chr14:60118117 | G | GT | 88 | a0001c0001t0001g0122 a0002c0002t0003g0010 a0002c0002t0003g0014 others(85): Show |
123 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.1579-200dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr14 | 60118117 | ||||||
chr14:60118117 | G | GTT | 9 | a0002c0002t0003g0025 a0002c0002t0003g0058 a0002c0002t0069g0025 others(6): Show |
9 | HG01243.hp1 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1579-201_1579-200d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr14 | 60118117 | ||||||
chr14:60118244 | T | A | 1 | a0019c0016t0005g0095 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1579-85T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60118244 | |||||||
chr14:60118317 | A | T | 1 | a0012c0029t0057g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1579-12A>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 6/10 | chr14 | 60118317 | |||||||
chr14:60118929 | T | G | 36 | a0002c0007t0003g0027 a0002c0007t0003g0076 a0002c0007t0003g0078 others(33): Show |
58 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1942+237T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60118929 | |||||||
chr14:60118963 | C | A | 1 | a0013c0032t0009g0105 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1942+271C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60118963 | |||||||
chr14:60119328 | A | G | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1942+636A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119328 | |||||||
chr14:60119360 | T | G | 117 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(114): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.1942+668T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119360 | |||||||
chr14:60119615 | T | TA | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.1942+924dupA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr14 | 60119615 | ||||||
chr14:60119677 | C | T | 1 | a0012c0029t0057g0110 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1942+985C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119677 | |||||||
chr14:60119919 | T | C | 2 | a0002c0002t0003g0025 a0002c0002t0069g0025 |
2 | HG02723.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1942+1227T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119919 | |||||||
chr14:60119922 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1942+1230A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119922 | |||||||
chr14:60119943 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1942+1251A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119943 | |||||||
chr14:60119975 | G | A | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1943-1221G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60119975 | |||||||
chr14:60120032 | A | G | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.1943-1164A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120032 | |||||||
chr14:60120311 | C | T | 7 | a0007c0008t0013g0028 a0007c0008t0013g0112 a0007c0008t0013g0113 others(4): Show |
8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1943-885C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120311 | |||||||
chr14:60120338 | G | C | 117 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(114): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.1943-858G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120338 | |||||||
chr14:60120428 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1943-768A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120428 | |||||||
chr14:60120429 | T | TCAGGTAG others(15): Show |
1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1943-762_1943-741d others(24): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr14 | 60120429 | ||||||
chr14:60120513 | A | G | 1 | a0003c0003t0002g0067 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1943-683A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120513 | |||||||
chr14:60120781 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0043g0135 |
2 | NA19059.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1943-415G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120781 | |||||||
chr14:60120957 | T | G | 1 | a0003c0003t0060g0065 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1943-239T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60120957 | |||||||
chr14:60121071 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1943-125T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60121071 | |||||||
chr14:60121161 | C | CT | 16 | a0003c0003t0002g0007 a0005c0006t0009g0017 a0005c0006t0009g0018 others(13): Show |
21 | HG00323.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1943-15dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr14 | 60121161 | ||||||
chr14:60121166 | T | C | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1943-30T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60121166 | |||||||
chr14:60121181 | T | C | 10 | a0002c0002t0003g0014 a0002c0002t0003g0022 a0002c0002t0003g0038 others(7): Show |
14 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1943-15T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 7/10 | chr14 | 60121181 | |||||||
chr14:60121328 | A | G | 25 | a0002c0025t0077g0054 a0003c0003t0002g0004 a0003c0003t0002g0006 others(22): Show |
43 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(40): Show |
intron_variant | MODIFIER | c.2046+29A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121328 | |||||||
chr14:60121448 | A | G | 115 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(112): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.2046+149A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121448 | |||||||
chr14:60121519 | C | CT | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.2046+224dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr14 | 60121519 | ||||||
chr14:60121532 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0164 |
2 | NA18982.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2046+233C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121532 | |||||||
chr14:60121584 | AT | A | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.2046+294delT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr14 | 60121584 | ||||||
chr14:60121632 | A | G | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.2046+333A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121632 | |||||||
chr14:60121726 | A | G | 2 | a0002c0009t0027g0075 a0002c0009t0027g0102 |
2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2046+427A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121726 | |||||||
chr14:60121851 | T | C | 1 | a0002c0002t0005g0029 | 2 | NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2046+552T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121851 | |||||||
chr14:60121912 | A | C | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.2046+613A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60121912 | |||||||
chr14:60122013 | C | T | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2046+714C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122013 | |||||||
chr14:60122061 | C | T | 2 | a0014c0024t0045g0116 a0024c0018t0076g0115 |
2 | HG01496.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2046+762C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122061 | |||||||
chr14:60122238 | C | A | 1 | a0011c0022t0041g0153 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2046+939C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122238 | |||||||
chr14:60122436 | G | A | 1 | a0002c0002t0003g0087 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2046+1137G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122436 | |||||||
chr14:60122447 | T | G | 2 | a0002c0002t0028g0100 a0002c0002t0028g0101 |
2 | HG03669.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2046+1148T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122447 | |||||||
chr14:60122454 | G | T | 115 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(112): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.2046+1155G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122454 | |||||||
chr14:60122619 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0164 |
2 | NA18982.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2046+1320A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122619 | |||||||
chr14:60122848 | C | A | 1 | a0001c0001t0007g0133 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2047-1370C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122848 | |||||||
chr14:60122848 | C | T | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2047-1370C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60122848 | |||||||
chr14:60123063 | A | G | 3 | a0003c0003t0002g0066 a0003c0003t0002g0069 a0015c0027t0002g0074 |
3 | HG02040.hp1 HG02071.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2047-1155A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123063 | |||||||
chr14:60123102 | A | C | 1 | a0003c0003t0002g0064 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2047-1116A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123102 | |||||||
chr14:60123240 | T | G | 115 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(112): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.2047-978T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123240 | |||||||
chr14:60123504 | C | CAATATTT others(1): Show |
117 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(114): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.2047-709_2047-702d others(10): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr14 | 60123504 | ||||||
chr14:60123928 | C | G | 117 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(114): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.2047-290C>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 8/10 | chr14 | 60123928 | |||||||
chr14:60125312 | A | G | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3080+61A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/10 | chr14 | 60125312 | |||||||
chr14:60125403 | A | G | 19 | a0002c0002t0005g0008 a0002c0002t0005g0015 a0002c0002t0005g0029 others(16): Show |
24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.3080+152A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 9/10 | chr14 | 60125403 | |||||||
chr14:60126146 | G | A | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.3267+323G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126146 | |||||||
chr14:60126309 | T | G | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3267+486T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126309 | |||||||
chr14:60126631 | G | A | 1 | a0003c0003t0002g0114 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3267+808G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126631 | |||||||
chr14:60126732 | A | G | 1 | a0002c0002t0017g0084 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3267+909A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126732 | |||||||
chr14:60126817 | A | G | 1 | a0001c0001t0042g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3267+994A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126817 | |||||||
chr14:60126971 | A | G | 1 | a0002c0002t0003g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3267+1148A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60126971 | |||||||
chr14:60127607 | A | G | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.3267+1784A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127607 | |||||||
chr14:60127622 | A | C | 1 | a0016c0014t0066g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3267+1799A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127622 | |||||||
chr14:60127759 | A | G | 1 | a0006c0005t0006g0151 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3267+1936A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127759 | |||||||
chr14:60127971 | G | A | 1 | a0008c0010t0005g0098 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3267+2148G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127971 | |||||||
chr14:60127985 | T | C | 7 | a0007c0008t0013g0028 a0007c0008t0013g0112 a0007c0008t0013g0113 others(4): Show |
8 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.3267+2162T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60127985 | |||||||
chr14:60128034 | T | C | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3267+2211T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128034 | |||||||
chr14:60128061 | A | G | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3267+2238A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128061 | |||||||
chr14:60128098 | G | A | 1 | a0020c0026t0072g0178 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3267+2275G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128098 | |||||||
chr14:60128164 | GA | G | 114 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(111): Show |
156 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(153): Show |
intron_variant | MODIFIER | c.3267+2349delA | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60128164 | ||||||
chr14:60128236 | G | A | 1 | a0024c0018t0076g0115 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3267+2413G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128236 | |||||||
chr14:60128464 | C | T | 10 | a0002c0002t0003g0014 a0002c0002t0003g0022 a0002c0002t0003g0038 others(7): Show |
14 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.3267+2641C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128464 | |||||||
chr14:60128465 | A | G | 117 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(114): Show |
159 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(156): Show |
intron_variant | MODIFIER | c.3267+2642A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128465 | |||||||
chr14:60128564 | T | C | 6 | a0005c0006t0009g0017 a0005c0006t0009g0018 a0005c0006t0051g0106 others(3): Show |
9 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.3267+2741T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128564 | |||||||
chr14:60128615 | T | C | 2 | a0014c0024t0045g0116 a0024c0018t0076g0115 |
2 | HG01496.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3267+2792T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128615 | |||||||
chr14:60128784 | G | C | 1 | a0005c0006t0051g0106 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3267+2961G>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128784 | |||||||
chr14:60128784 | G | T | 1 | a0001c0023t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3267+2961G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128784 | |||||||
chr14:60128807 | A | G | 19 | a0002c0002t0005g0008 a0002c0002t0005g0015 a0002c0002t0005g0029 others(16): Show |
24 | HG00673.hp1 HG01109.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.3267+2984A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128807 | |||||||
chr14:60128841 | A | G | 5 | a0002c0007t0061g0060 a0002c0009t0029g0052 a0002c0009t0029g0053 others(2): Show |
5 | HG02257.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3267+3018A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128841 | |||||||
chr14:60128978 | C | T | 1 | a0002c0002t0003g0180 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3267+3155C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128978 | |||||||
chr14:60128987 | C | T | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3267+3164C>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60128987 | |||||||
chr14:60129240 | C | CAA | 109 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(106): Show |
151 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.3267+3429_3267+343 others(6): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60129240 | ||||||
chr14:60129363 | G | A | 1 | a0025c0012t0003g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3267+3540G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60129363 | |||||||
chr14:60129958 | CAAAG | C | 2 | a0005c0006t0009g0017 a0005c0006t0058g0107 |
4 | HG00642.hp1 HG00735.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3268-4008_3268-400 others(8): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60129958 | ||||||
chr14:60130229 | A | G | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3268-3741A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130229 | |||||||
chr14:60130342 | AC | A | 47 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(44): Show |
59 | HG00639.hp1 HG00673.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.3268-3626delC | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60130342 | ||||||
chr14:60130479 | T | C | 6 | a0002c0002t0003g0014 a0002c0002t0003g0022 a0002c0002t0014g0014 others(3): Show |
9 | HG00639.hp1 HG01192.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.3268-3491T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130479 | |||||||
chr14:60130487 | A | C | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-3483A>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130487 | |||||||
chr14:60130689 | T | C | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-3281T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60130689 | |||||||
chr14:60130794 | A | AT | 28 | a0002c0007t0061g0060 a0002c0009t0029g0052 a0002c0009t0029g0053 others(25): Show |
36 | HG01243.hp2 HG01358.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.3268-3164dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60130794 | ||||||
chr14:60131016 | C | A | 5 | a0002c0007t0003g0027 a0002c0007t0003g0076 a0002c0007t0003g0078 others(2): Show |
6 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.3268-2954C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131016 | |||||||
chr14:60131039 | G | T | 1 | a0002c0002t0003g0082 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3268-2931G>T | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131039 | |||||||
chr14:60131041 | T | TG | 115 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(112): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.3268-2929_3268-292 others(5): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131041 | |||||||
chr14:60131466 | G | A | 24 | a0003c0003t0002g0004 a0003c0003t0002g0006 a0003c0003t0002g0007 others(21): Show |
42 | HG00558.hp2 HG00609.hp1 HG02015.hp1 others(39): Show |
intron_variant | MODIFIER | c.3268-2504G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131466 | |||||||
chr14:60131559 | C | A | 115 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(112): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.3268-2411C>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131559 | |||||||
chr14:60131618 | A | G | 8 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0041 others(5): Show |
15 | NA18940.hp1 NA18975.hp2 NA18983.hp2 others(12): Show |
intron_variant | MODIFIER | c.3268-2352A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131618 | |||||||
chr14:60131771 | G | A | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-2199G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60131771 | |||||||
chr14:60132211 | T | C | 3 | a0001c0001t0011g0011 a0001c0001t0011g0138 a0001c0001t0047g0011 |
5 | HG01192.hp1 HG01928.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.3268-1759T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60132211 | |||||||
chr14:60132260 | A | G | 1 | a0014c0024t0045g0116 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3268-1710A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60132260 | |||||||
chr14:60132805 | T | C | 2 | a0009c0011t0001g0034 a0009c0011t0037g0034 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3268-1165T>C | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60132805 | |||||||
chr14:60133019 | GAA | G | 4 | a0002c0002t0003g0082 a0002c0002t0017g0081 a0002c0002t0017g0083 others(1): Show |
4 | HG01109.hp1 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3268-948_3268-947d others(4): Show |
PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60133019 | ||||||
chr14:60133117 | A | G | 1 | a0003c0003t0002g0069 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3268-853A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133117 | |||||||
chr14:60133175 | G | A | 115 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(112): Show |
157 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(154): Show |
intron_variant | MODIFIER | c.3268-795G>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133175 | |||||||
chr14:60133503 | T | G | 1 | a0002c0007t0061g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3268-467T>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133503 | |||||||
chr14:60133637 | A | G | 5 | a0002c0002t0003g0010 a0002c0002t0003g0086 a0002c0002t0003g0087 others(2): Show |
8 | HG02486.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.3268-333A>G | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133637 | |||||||
chr14:60133759 | T | A | 98 | a0002c0002t0003g0010 a0002c0002t0003g0014 a0002c0002t0003g0022 others(95): Show |
133 | HG00323.hp2 HG00558.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.3268-211T>A | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | chr14 | 60133759 | |||||||
chr14:60133890 | C | CT | 17 | a0004c0004t0004g0005 a0004c0004t0004g0023 a0004c0004t0004g0024 others(14): Show |
24 | NA18939.hp2 NA18940.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.3268-79dupT | PCNX4 | ENSG00000126773.13 | transcript | ENST00000406854.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr14 | 60133890 |