Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9601 |
| ensemblid | ENSG00000155660.11 |
| hgncid | 30167 |
| symbol | PDIA4 |
| name | protein disulfide isomerase family A member 4 |
| refseq_nuc | NM_004911.5 |
| refseq_prot | NP_004902.1 |
| ensembl_nuc | ENST00000652332.1 |
| ensembl_prot | ENSP00000499129.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 149003062 |
| end | 149028505 |
| strand | - |
| ver | v1.2 |
| region | chr7:149003062-149028505 |
| region5000 | chr7:148998062-149033505 |
| regionname0 | PDIA4_chr7_149003062_149028505 |
| regionname5000 | PDIA4_chr7_148998062_149033505 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 645 | 322 | 91 | 57 | 129 | 12 | 31 | 96 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0002 | 0/0 | 645 | 12 | 2 | 0 | 10 | 0 | 0 | 7 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0003 | 0/0 | 645 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0004 | 0/0 | 645 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0005 | 0/0 | 645 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0006 | 0/0 | 645 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0007 | 0/0 | 645 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0008 | 0/0 | 645 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0009 | 0/0 | 645 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0010 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0011 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0012 | 0/0 | 645 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| a0013 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | MRPRK others(640): Show |
chr7 | 148998062 | 149033505 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1935 | 285 | 61 | 53 | 129 | 11 | 29 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0002 | 0/0 | 1935 | 28 | 22 | 4 | 0 | 0 | 2 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0006 | 0/0 | 1935 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0009 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0011 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0017 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0018 | 0/0 | 1935 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0019 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0001c0020 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0002c0003 | 0/0 | 1935 | 12 | 2 | 0 | 10 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0003c0004 | 0/0 | 1935 | 4 | 0 | 0 | 4 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0004c0005 | 0/0 | 1935 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0005c0007 | 0/0 | 1935 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0006c0008 | 0/0 | 1935 | 2 | 0 | 0 | 0 | 0 | 2 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0007c0014 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0008c0012 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0009c0016 | 0/0 | 1935 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0010c0015 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0011c0021 | 0/0 | 1935 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0012c0013 | 0/0 | 1935 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 | ||
| a0013c0010 | 0/0 | 1935 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | ATGAG others(1930): Show |
chr7 | 148998062 | 149033505 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2767 | 228 | 34 | 39 | 125 | 8 | 20 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0002 | 0/0 | 2767 | 24 | 3 | 10 | 0 | 3 | 8 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0003 | 0/0 | 2767 | 4 | 4 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0004 | 0/0 | 2767 | 4 | 4 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0005 | 0/0 | 2766 | 6 | 6 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2761): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0006 | 0/0 | 2768 | 6 | 6 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2763): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0007 | 0/0 | 2766 | 4 | 0 | 1 | 3 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2761): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0008 | 0/0 | 2767 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0010 | 0/0 | 2767 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0014 | 0/0 | 2767 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0016 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0018 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0019 | 0/0 | 2768 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2763): Show |
chr7 | 148998062 | 149033505 |
| a0001c0001t0022 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0002t0002 | 0/0 | 2767 | 26 | 20 | 4 | 0 | 0 | 2 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0002t0011 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2761): Show |
chr7 | 148998062 | 149033505 |
| a0001c0002t0012 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0006t0009 | 0/0 | 2767 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0006t0015 | 0/0 | 2766 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2761): Show |
chr7 | 148998062 | 149033505 |
| a0001c0009t0004 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0011t0004 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0017t0003 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0018t0001 | 0/0 | 2767 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0001c0019t0013 | 0/0 | 2768 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2763): Show |
chr7 | 148998062 | 149033505 |
| a0001c0020t0017 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0002c0003t0003 | 0/0 | 2767 | 11 | 2 | 0 | 9 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0002c0003t0021 | 0/0 | 2766 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2761): Show |
chr7 | 148998062 | 149033505 |
| a0003c0004t0001 | 0/0 | 2767 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0003c0004t0020 | 0/0 | 2767 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0004c0005t0001 | 0/0 | 2767 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0005c0007t0001 | 0/0 | 2767 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0006c0008t0001 | 0/0 | 2767 | 2 | 0 | 0 | 0 | 0 | 2 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0007c0014t0001 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0008c0012t0001 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0009c0016t0004 | 0/0 | 2767 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0010c0015t0004 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0011c0021t0001 | 0/0 | 2767 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0012c0013t0002 | 0/0 | 2767 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| a0013c0010t0001 | 0/0 | 2767 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | GCGTC others(2762): Show |
chr7 | 148998062 | 149033505 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 1 | 7 | 14 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0002 | 0/0 | 10 | 3 | 0 | 7 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0003 | 0/0 | 9 | 1 | 4 | 1 | 1 | 2 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 0 | 4 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0012 | 0/0 | 4 | 1 | 0 | 2 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0016 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0008 | 0/0 | 6 | 1 | 2 | 0 | 0 | 3 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 0 | 0 | 4 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0003g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0006g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0010g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0016g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0018g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0019g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0001t0022g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0013 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0002t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0006t0009g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0006t0015g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0009t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0011t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0017t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0018t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0019t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0001c0020t0017g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0002c0003t0021g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0003c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0003c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0003c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0003c0004t0020g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0004c0005t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0005c0007t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0006c0008t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0007c0014t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0008c0012t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0009c0016t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0010c0015t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0011c0021t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0012c0013t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| a0013c0010t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | GBR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00323 | hp2 | a0001 | c0018 | t0001 | g0078 | EUR | FIN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00423 | hp1 | a0001 | c0001 | t0019 | g0126 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00558 | hp1 | a0002 | c0003 | t0003 | g0160 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00558 | hp2 | a0001 | c0001 | t0007 | g0069 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01167 | hp1 | a0005 | c0007 | t0001 | g0033 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01168 | hp2 | a0001 | c0001 | t0010 | g0026 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01169 | hp1 | a0001 | c0001 | t0010 | g0026 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01169 | hp2 | a0005 | c0007 | t0001 | g0033 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01243 | hp2 | a0007 | c0014 | t0001 | g0125 | AMR | PUR | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0208 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0186 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0196 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0050 | EUR | IBS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0079 | EUR | IBS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0201 | EUR | IBS | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01884 | hp1 | a0002 | c0003 | t0003 | g0164 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01891 | hp2 | a0001 | c0009 | t0004 | g0053 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01928 | hp1 | a0008 | c0012 | t0001 | g0121 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01952 | hp1 | a0009 | c0016 | t0004 | g0057 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02027 | hp1 | a0002 | c0003 | t0003 | g0044 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0081 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02135 | hp2 | a0002 | c0003 | t0003 | g0044 | EAS | KHV | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0190 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0113 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0061 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02300 | hp2 | a0001 | c0001 | t0022 | g0218 | AMR | PEL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0192 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0168 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02622 | hp2 | a0001 | c0019 | t0013 | g0182 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02717 | hp2 | a0010 | c0015 | t0004 | g0184 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02738 | hp2 | a0001 | c0001 | t0014 | g0102 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0187 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0197 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02896 | hp1 | a0001 | c0006 | t0015 | g0207 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0180 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02897 | hp1 | a0001 | c0002 | t0011 | g0181 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02965 | hp2 | a0001 | c0002 | t0012 | g0206 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02970 | hp1 | a0011 | c0021 | t0001 | g0129 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03041 | hp1 | a0001 | c0017 | t0003 | g0194 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03098 | hp1 | a0001 | c0006 | t0009 | g0052 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0191 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03195 | hp1 | a0004 | c0005 | t0001 | g0015 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03209 | hp1 | a0001 | c0020 | t0017 | g0213 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03209 | hp2 | a0001 | c0001 | t0016 | g0058 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0025 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0178 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03486 | hp1 | a0004 | c0005 | t0001 | g0015 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03491 | hp2 | a0006 | c0008 | t0001 | g0034 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03492 | hp2 | a0006 | c0008 | t0001 | g0034 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03516 | hp1 | a0002 | c0003 | t0003 | g0163 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | ESN | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03669 | hp2 | a0012 | c0013 | t0002 | g0210 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | STU | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | YRI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18944 | hp2 | a0002 | c0003 | t0003 | g0215 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18947 | hp2 | a0002 | c0003 | t0003 | g0158 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18963 | hp2 | a0003 | c0004 | t0001 | g0136 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18966 | hp2 | a0003 | c0004 | t0001 | g0107 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18967 | hp1 | a0003 | c0004 | t0001 | g0175 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18967 | hp2 | a0002 | c0003 | t0003 | g0162 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18982 | hp1 | a0001 | c0001 | t0007 | g0094 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18984 | hp1 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19003 | hp2 | a0013 | c0010 | t0001 | g0068 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0198 | AFR | LWK | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | LWK | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0159 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0176 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19065 | hp1 | a0003 | c0004 | t0020 | g0137 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19091 | hp2 | a0002 | c0003 | t0003 | g0037 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0055 | AFR | YRI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0177 | AFR | ASW | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | TSI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | TSI | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | GIH | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0200 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03471 | hp1 | a0004 | c0005 | t0001 | g0015 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG03471 | hp2 | a0001 | c0006 | t0009 | g0052 | AFR | MSL | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG06807 | hp1 | a0001 | c0011 | t0004 | g0112 | AFR | USA | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | USA | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA18955 | hp2 | a0002 | c0003 | t0021 | g0161 | EAS | JPT | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | LWK | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0155 | REF | REF | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0016 | REF | REF | PDIA4_chr7_148998062_149033505 | PDIA4 | chr7 | 148998062 | 149033505 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:149003913 | G | T | 1 | a0009 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1819C>A | p.Pro607Thr | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1916/2767 | 1819/1938 | 607/645 | chr7 | 149003913 | |||
| chr7:149003967 | C | T | 1 | a0010 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1765G>A | p.Asp589Asn | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1862/2767 | 1765/1938 | 589/645 | chr7 | 149003967 | |||
| chr7:149004029 | A | G | 1 | a0007 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1703T>C | p.Leu568Pro | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1800/2767 | 1703/1938 | 568/645 | chr7 | 149004029 | |||
| chr7:149004042 | C | T | 1 | a0006 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.1690G>A | p.Val564Met | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1787/2767 | 1690/1938 | 564/645 | chr7 | 149004042 | |||
| chr7:149004144 | C | T | 1 | a0012 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.1588G>A | p.Val530Met | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1685/2767 | 1588/1938 | 530/645 | chr7 | 149004144 | |||
| chr7:149004153 | C | T | 1 | a0004 | 3 | HG03195.hp1 HG03471.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.1579G>A | p.Val527Ile | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1676/2767 | 1579/1938 | 527/645 | chr7 | 149004153 | |||
| chr7:149012332 | C | T | 1 | a0008 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.643G>A | p.Glu215Lys | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 5/10 | 740/2767 | 643/1938 | 215/645 | chr7 | 149012332 | |||
| chr7:149015000 | G | A | 1 | a0002 | 12 | HG00558.hp1 HG01884.hp1 HG02027.hp1 others(9): Show |
missense_variant | MODERATE | c.518C>T | p.Thr173Met | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/10 | 615/2767 | 518/1938 | 173/645 | chr7 | 149015000 | |||
| chr7:149015021 | T | C | 1 | a0011 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.497A>G | p.Glu166Gly | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/10 | 594/2767 | 497/1938 | 166/645 | chr7 | 149015021 | |||
| chr7:149019045 | T | C | 1 | a0003 | 4 | NA18963.hp2 NA18966.hp2 NA18967.hp1 others(1): Show |
missense_variant | MODERATE | c.422A>G | p.Lys141Arg | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/10 | 519/2767 | 422/1938 | 141/645 | chr7 | 149019045 | |||
| chr7:149019117 | A | G | 1 | a0005 | 2 | HG01167.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.350T>C | p.Val117Ala | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/10 | 447/2767 | 350/1938 | 117/645 | chr7 | 149019117 | |||
| chr7:149021076 | C | G | 1 | a0013 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.160G>C | p.Asp54His | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/10 | 257/2767 | 160/1938 | 54/645 | chr7 | 149021076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:149003956 | G | A | 1 | a0001c0017 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1776C>T | p.Ser592Ser | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1873/2767 | 1776/1938 | 592/645 | chr7 | 149003956 | |||
| chr7:149004034 | G | A | 1 | a0001c0018 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.1698C>T | p.Asn566Asn | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1795/2767 | 1698/1938 | 566/645 | chr7 | 149004034 | |||
| chr7:149004076 | C | T | 1 | a0001c0002 | 28 | HG01069.hp1 HG01071.hp2 HG01346.hp2 others(25): Show |
synonymous_variant | LOW | c.1656G>A | p.Ala552Ala | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 1753/2767 | 1656/1938 | 552/645 | chr7 | 149004076 | |||
| chr7:149005973 | G | A | 1 | a0001c0019 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1212C>T | p.Asn404Asn | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/10 | 1309/2767 | 1212/1938 | 404/645 | chr7 | 149005973 | |||
| chr7:149011898 | G | A | 1 | a0001c0020 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.927C>T | p.Ile309Ile | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/10 | 1024/2767 | 927/1938 | 309/645 | chr7 | 149011898 | |||
| chr7:149011985 | G | A | 1 | a0001c0006 | 3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.840C>T | p.Ile280Ile | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/10 | 937/2767 | 840/1938 | 280/645 | chr7 | 149011985 | |||
| chr7:149019032 | C | T | 1 | a0001c0011 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.435G>A | p.Lys145Lys | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/10 | 532/2767 | 435/1938 | 145/645 | chr7 | 149019032 | |||
| chr7:149028382 | G | T | 1 | a0001c0009 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.27C>A | p.Leu9Leu | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/10 | 124/2767 | 27/1938 | 9/645 | chr7 | 149028382 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:149003077 | G | A | 1 | a0001c0001t0016 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*717C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 717 | chr7 | 149003077 | ||||||
| chr7:149003123 | C | G | 1 | a0001c0001t0010 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*671G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 671 | chr7 | 149003123 | ||||||
| chr7:149003384 | A | T | 1 | a0001c0001t0008 | 2 | HG02258.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*410T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 410 | chr7 | 149003384 | ||||||
| chr7:149003401 | C | A | 2 | a0001c0001t0018 a0001c0020t0017 |
2 | HG03209.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 393 | chr7 | 149003401 | ||||||
| chr7:149003416 | C | T | 2 | a0001c0006t0009 a0001c0006t0015 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*378G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 378 | chr7 | 149003416 | ||||||
| chr7:149003448 | G | A | 1 | a0001c0001t0018 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*346C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 346 | chr7 | 149003448 | ||||||
| chr7:149003450 | A | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
99 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*344T>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 344 | chr7 | 149003450 | ||||||
| chr7:149003498 | G | T | 2 | a0001c0006t0009 a0001c0006t0015 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 296 | chr7 | 149003498 | ||||||
| chr7:149003674 | T | TA | 3 | a0001c0001t0006 a0001c0001t0019 a0001c0019t0013 |
8 | HG00423.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*119dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 119 | chr7 | 149003674 | ||||||
| chr7:149003674 | TA | T | 5 | a0001c0001t0005 a0001c0001t0007 a0001c0002t0011 others(2): Show |
13 | HG00558.hp2 HG01256.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*119delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 119 | chr7 | 149003674 | ||||||
| chr7:149003718 | G | A | 1 | a0001c0002t0012 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 76 | chr7 | 149003718 | ||||||
| chr7:149003724 | G | A | 1 | a0003c0004t0020 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 70 | chr7 | 149003724 | ||||||
| chr7:149003726 | C | G | 4 | a0001c0001t0003 a0001c0017t0003 a0002c0003t0003 others(1): Show |
17 | HG00558.hp1 HG01884.hp1 HG02027.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*68G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 68 | chr7 | 149003726 | ||||||
| chr7:149003728 | T | C | 4 | a0001c0001t0003 a0001c0017t0003 a0002c0003t0003 others(1): Show |
17 | HG00558.hp1 HG01884.hp1 HG02027.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*66A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 66 | chr7 | 149003728 | ||||||
| chr7:149003732 | C | T | 1 | a0001c0001t0014 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 62 | chr7 | 149003732 | ||||||
| chr7:149003738 | G | T | 1 | a0001c0019t0013 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 56 | chr7 | 149003738 | ||||||
| chr7:149003757 | C | T | 6 | a0001c0001t0002 a0001c0001t0008 a0001c0002t0002 others(3): Show |
55 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*37G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 10/10 | 37 | chr7 | 149003757 | ||||||
| chr7:149028427 | C | A | 1 | a0001c0001t0022 | 1 | HG02300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-19G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/10 | 19 | chr7 | 149028427 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:149004255 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1523-46G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004255 | |||||||
| chr7:149004327 | G | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0166 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1523-118C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004327 | |||||||
| chr7:149004369 | ACT | A | 2 | a0001c0006t0009g0052 a0001c0006t0015g0207 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1523-162_1523-161d others(4): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004369 | |||||||
| chr7:149004433 | C | T | 1 | a0001c0001t0016g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1523-224G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004433 | |||||||
| chr7:149004466 | C | T | 8 | a0001c0001t0004g0056 a0001c0001t0004g0183 a0001c0001t0004g0185 others(5): Show |
9 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1523-257G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004466 | |||||||
| chr7:149004554 | G | C | 49 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(46): Show |
72 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1523-345C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004554 | |||||||
| chr7:149004556 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1523-347T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004556 | |||||||
| chr7:149004767 | G | A | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1522+374C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004767 | |||||||
| chr7:149004787 | G | A | 4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+354C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004787 | |||||||
| chr7:149004870 | T | C | 4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+271A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004870 | |||||||
| chr7:149004876 | T | G | 2 | a0001c0001t0008g0061 a0001c0001t0008g0166 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1522+265A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004876 | |||||||
| chr7:149004974 | T | C | 4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522+167A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149004974 | |||||||
| chr7:149005012 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1522+129C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149005012 | |||||||
| chr7:149005048 | G | A | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1522+93C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149005048 | |||||||
| chr7:149005065 | C | T | 49 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(46): Show |
72 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1522+76G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149005065 | |||||||
| chr7:149005120 | C | G | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1522+21G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149005120 | |||||||
| chr7:149005132 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1522+9G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 9/9 | chr7 | 149005132 | |||||||
| chr7:149005394 | A | G | 72 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(69): Show |
99 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1289-20T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/9 | chr7 | 149005394 | |||||||
| chr7:149005404 | C | T | 69 | a0001c0001t0001g0093 a0001c0001t0002g0008 a0001c0001t0002g0014 others(66): Show |
96 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1289-30G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/9 | chr7 | 149005404 | |||||||
| chr7:149005439 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1289-65C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/9 | chr7 | 149005439 | |||||||
| chr7:149005477 | G | A | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1289-103C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/9 | chr7 | 149005477 | |||||||
| chr7:149005594 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1289-220G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/9 | chr7 | 149005594 | |||||||
| chr7:149005866 | AC | A | 49 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(46): Show |
72 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1288+30delG | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/9 | chr7 | 149005866 | |||||||
| chr7:149005883 | T | G | 5 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(2): Show |
7 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1288+14A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 8/9 | chr7 | 149005883 | |||||||
| chr7:149006151 | AG | A | 71 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(68): Show |
98 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.1132-99delC | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006151 | |||||||
| chr7:149006152 | G | A | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1132-99C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006152 | |||||||
| chr7:149006263 | G | A | 1 | a0002c0003t0021g0161 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1132-210C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006263 | |||||||
| chr7:149006365 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0076 |
3 | HG00408.hp2 NA18943.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1132-312C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006365 | |||||||
| chr7:149006400 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
5 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.1132-347A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006400 | |||||||
| chr7:149006574 | G | A | 1 | a0001c0001t0001g0041 | 2 | NA18952.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1132-521C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006574 | |||||||
| chr7:149006691 | G | A | 1 | a0001c0001t0001g0043 | 2 | NA18957.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1132-638C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006691 | |||||||
| chr7:149006757 | G | C | 1 | a0004c0005t0001g0015 | 3 | HG03195.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1132-704C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006757 | |||||||
| chr7:149006796 | A | G | 1 | a0003c0004t0001g0136 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1132-743T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006796 | |||||||
| chr7:149006847 | C | T | 1 | a0001c0001t0016g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1132-794G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006847 | |||||||
| chr7:149006921 | T | C | 1 | a0001c0001t0006g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1132-868A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006921 | |||||||
| chr7:149006946 | C | T | 1 | a0001c0001t0018g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1132-893G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149006946 | |||||||
| chr7:149007068 | G | A | 7 | a0002c0003t0003g0037 a0002c0003t0003g0044 a0002c0003t0003g0159 others(4): Show |
9 | HG00558.hp1 HG02027.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1132-1015C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007068 | |||||||
| chr7:149007108 | A | AGTCCAGG others(4): Show |
4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131+1040_1131+105 others(15): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007108 | |||||||
| chr7:149007137 | C | G | 4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131+1022G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007137 | |||||||
| chr7:149007315 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1131+844G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007315 | |||||||
| chr7:149007433 | G | A | 1 | a0001c0020t0017g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1131+726C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007433 | |||||||
| chr7:149007442 | G | T | 1 | a0004c0005t0001g0015 | 3 | HG03195.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1131+717C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007442 | |||||||
| chr7:149007542 | C | T | 18 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(15): Show |
30 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1131+617G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007542 | |||||||
| chr7:149007720 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1131+439A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007720 | |||||||
| chr7:149007732 | A | G | 7 | a0001c0001t0004g0183 a0001c0001t0004g0185 a0001c0001t0004g0203 others(4): Show |
8 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131+427T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007732 | |||||||
| chr7:149007739 | T | C | 4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1131+420A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007739 | |||||||
| chr7:149007777 | C | T | 69 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(66): Show |
96 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1131+382G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007777 | |||||||
| chr7:149007843 | A | G | 72 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(69): Show |
99 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(96): Show |
intron_variant | MODIFIER | c.1131+316T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007843 | |||||||
| chr7:149007855 | C | T | 1 | a0001c0002t0002g0190 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1131+304G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007855 | |||||||
| chr7:149007889 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0018g0055 a0001c0020t0017g0213 |
3 | HG03209.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1131+270G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007889 | |||||||
| chr7:149007982 | G | A | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1131+177C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149007982 | |||||||
| chr7:149008129 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(182): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.1131+30T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149008129 | |||||||
| chr7:149008152 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA19074.hp1 NA19086.hp1 |
splice_region_variant&intron_variant | LOW | c.1131+7G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 7/9 | chr7 | 149008152 | |||||||
| chr7:149008325 | G | T | 1 | a0011c0021t0001g0129 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.980-15C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008325 | |||||||
| chr7:149008398 | G | A | 69 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(66): Show |
96 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.980-88C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008398 | |||||||
| chr7:149008465 | A | G | 5 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(2): Show |
5 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.980-155T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008465 | |||||||
| chr7:149008535 | T | A | 3 | a0002c0003t0003g0158 a0002c0003t0003g0162 a0002c0003t0003g0215 |
3 | NA18944.hp2 NA18947.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.980-225A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008535 | |||||||
| chr7:149008664 | C | T | 4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.980-354G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008664 | |||||||
| chr7:149008684 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0018g0055 |
2 | NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.980-374G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008684 | |||||||
| chr7:149008709 | TAAAAAGA others(17): Show |
T | 16 | a0001c0001t0001g0179 a0001c0001t0004g0056 a0001c0001t0004g0183 others(13): Show |
18 | HG01891.hp2 HG01952.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.980-423_980-400del others(24): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008709 | |||||||
| chr7:149008715 | GA | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0019 others(26): Show |
40 | HG00140.hp2 HG00741.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.980-406delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008715 | |||||||
| chr7:149008851 | C | G | 73 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(70): Show |
100 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.980-541G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008851 | |||||||
| chr7:149008892 | T | G | 4 | a0001c0001t0006g0059 a0001c0001t0006g0081 a0001c0001t0006g0113 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.980-582A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008892 | |||||||
| chr7:149008905 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG00544.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.980-595G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008905 | |||||||
| chr7:149008942 | T | C | 1 | a0001c0002t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.980-632A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008942 | |||||||
| chr7:149008958 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.980-648G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149008958 | |||||||
| chr7:149009024 | CA | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0041 others(14): Show |
29 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.980-715delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009024 | |||||||
| chr7:149009071 | T | C | 73 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(70): Show |
100 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.980-761A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009071 | |||||||
| chr7:149009080 | G | T | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-770C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009080 | |||||||
| chr7:149009216 | C | A | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.980-906G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009216 | |||||||
| chr7:149009289 | T | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0132 a0001c0001t0001g0145 |
3 | HG00735.hp2 HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.980-979A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009289 | |||||||
| chr7:149009318 | C | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.980-1008G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009318 | |||||||
| chr7:149009479 | C | T | 1 | a0001c0001t0008g0166 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.980-1169G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009479 | |||||||
| chr7:149009618 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.980-1308G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009618 | |||||||
| chr7:149009755 | G | C | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.980-1445C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009755 | |||||||
| chr7:149009775 | C | G | 16 | a0001c0001t0001g0179 a0001c0001t0004g0056 a0001c0001t0004g0183 others(13): Show |
18 | HG01891.hp2 HG01952.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.980-1465G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009775 | |||||||
| chr7:149009779 | T | C | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.980-1469A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009779 | |||||||
| chr7:149009993 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.980-1683C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149009993 | |||||||
| chr7:149010009 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.980-1699C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010009 | |||||||
| chr7:149010021 | T | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0035 others(24): Show |
40 | HG00140.hp2 HG00741.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.980-1711A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010021 | |||||||
| chr7:149010043 | G | T | 1 | a0001c0001t0016g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.980-1733C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010043 | |||||||
| chr7:149010044 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0003g0202 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.980-1734C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010044 | |||||||
| chr7:149010044 | G | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(66): Show |
117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.980-1734C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010044 | |||||||
| chr7:149010125 | C | T | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.979+1721G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010125 | |||||||
| chr7:149010154 | T | C | 1 | a0004c0005t0001g0015 | 3 | HG03195.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.979+1692A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010154 | |||||||
| chr7:149010186 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.979+1660T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010186 | |||||||
| chr7:149010216 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0104 a0001c0001t0001g0105 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.979+1630G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010216 | |||||||
| chr7:149010471 | GCAAT | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(108): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.979+1371_979+1374d others(6): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010471 | |||||||
| chr7:149010488 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.979+1358G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149010488 | |||||||
| chr7:149011111 | G | C | 49 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(46): Show |
72 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.979+735C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149011111 | |||||||
| chr7:149011239 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.979+607C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149011239 | |||||||
| chr7:149011259 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.979+587C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149011259 | |||||||
| chr7:149011762 | T | A | 1 | a0002c0003t0003g0037 | 2 | NA18984.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.979+84A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 6/9 | chr7 | 149011762 | |||||||
| chr7:149012026 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.821-22C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 5/9 | chr7 | 149012026 | |||||||
| chr7:149012415 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0028 others(6): Show |
18 | HG00408.hp2 HG02071.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.615-55A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012415 | |||||||
| chr7:149012442 | C | T | 6 | a0001c0001t0001g0179 a0001c0001t0016g0058 a0001c0001t0018g0055 others(3): Show |
6 | HG01952.hp1 HG02622.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.615-82G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012442 | |||||||
| chr7:149012472 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.615-112C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012472 | |||||||
| chr7:149012485 | T | C | 2 | a0001c0006t0009g0052 a0001c0006t0015g0207 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.615-125A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012485 | |||||||
| chr7:149012524 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.615-164G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012524 | |||||||
| chr7:149012536 | A | T | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.615-176T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012536 | |||||||
| chr7:149012718 | G | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.615-358C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012718 | |||||||
| chr7:149012764 | T | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0111 a0001c0001t0001g0167 others(1): Show |
5 | NA18953.hp2 NA18987.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.615-404A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012764 | |||||||
| chr7:149012784 | T | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0111 a0001c0001t0001g0167 others(1): Show |
5 | NA18953.hp2 NA18987.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.615-424A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012784 | |||||||
| chr7:149012877 | C | T | 3 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 |
5 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.615-517G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012877 | |||||||
| chr7:149012996 | G | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.615-636C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149012996 | |||||||
| chr7:149013051 | C | A | 4 | a0001c0002t0002g0013 a0001c0002t0002g0180 a0001c0002t0002g0198 others(1): Show |
7 | HG01069.hp1 HG01071.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.615-691G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013051 | |||||||
| chr7:149013068 | C | T | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.615-708G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013068 | |||||||
| chr7:149013104 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.615-744A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013104 | |||||||
| chr7:149013124 | T | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0132 |
2 | HG01081.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.615-764A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013124 | |||||||
| chr7:149013428 | G | C | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.615-1068C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013428 | |||||||
| chr7:149013454 | G | C | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.615-1094C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013454 | |||||||
| chr7:149013484 | C | T | 59 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(56): Show |
84 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.615-1124G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013484 | |||||||
| chr7:149013572 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.615-1212C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013572 | |||||||
| chr7:149013616 | G | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0148 |
2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.615-1256C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013616 | |||||||
| chr7:149013746 | C | CA | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.614+1157dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013746 | |||||||
| chr7:149013970 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.614+934G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149013970 | |||||||
| chr7:149014013 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0018g0055 a0001c0020t0017g0213 |
3 | HG03209.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.614+891G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149014013 | |||||||
| chr7:149014200 | G | C | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.614+704C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149014200 | |||||||
| chr7:149014430 | G | A | 1 | a0002c0003t0003g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.614+474C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149014430 | |||||||
| chr7:149014498 | C | T | 39 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(36): Show |
60 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.614+406G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149014498 | |||||||
| chr7:149014700 | A | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0140 a0001c0001t0001g0152 others(1): Show |
5 | HG00423.hp2 HG02056.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.614+204T>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149014700 | |||||||
| chr7:149014841 | T | G | 1 | a0001c0001t0014g0102 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.614+63A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 4/9 | chr7 | 149014841 | |||||||
| chr7:149015201 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.476-159A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015201 | |||||||
| chr7:149015241 | A | T | 1 | a0001c0001t0001g0119 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.476-199T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015241 | |||||||
| chr7:149015247 | T | C | 4 | a0003c0004t0001g0107 a0003c0004t0001g0136 a0003c0004t0001g0175 others(1): Show |
4 | NA18963.hp2 NA18966.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-205A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015247 | |||||||
| chr7:149015492 | C | CA | 23 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(20): Show |
37 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.476-451dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015492 | |||||||
| chr7:149015492 | C | CAA | 14 | a0001c0001t0002g0205 a0001c0001t0004g0056 a0001c0002t0002g0009 others(11): Show |
21 | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.476-452_476-451dup others(2): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015492 | |||||||
| chr7:149015492 | CA | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.476-451delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015492 | |||||||
| chr7:149015521 | T | C | 1 | a0001c0011t0004g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.476-479A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015521 | |||||||
| chr7:149015826 | G | C | 16 | a0001c0001t0001g0179 a0001c0001t0004g0056 a0001c0001t0016g0058 others(13): Show |
18 | HG00558.hp1 HG01884.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.476-784C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015826 | |||||||
| chr7:149015929 | C | A | 1 | a0001c0001t0016g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.476-887G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015929 | |||||||
| chr7:149015937 | T | C | 7 | a0001c0001t0004g0183 a0001c0001t0004g0185 a0001c0001t0004g0203 others(4): Show |
8 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-895A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149015937 | |||||||
| chr7:149016095 | G | A | 1 | a0001c0001t0004g0203 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.476-1053C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016095 | |||||||
| chr7:149016210 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.476-1168G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016210 | |||||||
| chr7:149016218 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0030 |
5 | HG02818.hp2 HG03098.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-1176G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016218 | |||||||
| chr7:149016261 | G | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0133 |
2 | NA18981.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.476-1219C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016261 | |||||||
| chr7:149016526 | C | CT | 7 | a0001c0001t0004g0183 a0001c0001t0004g0185 a0001c0001t0004g0203 others(4): Show |
8 | HG01891.hp2 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-1485dupA | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016526 | |||||||
| chr7:149016532 | T | C | 1 | a0001c0001t0001g0179 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.476-1490A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016532 | |||||||
| chr7:149016619 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.476-1577G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016619 | |||||||
| chr7:149016685 | A | G | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.476-1643T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016685 | |||||||
| chr7:149016746 | C | T | 2 | a0001c0001t0004g0183 a0010c0015t0004g0184 |
2 | HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.476-1704G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016746 | |||||||
| chr7:149016756 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0186 |
3 | HG01256.hp1 HG01257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.476-1714G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016756 | |||||||
| chr7:149016781 | G | T | 3 | a0001c0001t0001g0179 a0001c0001t0018g0055 a0001c0020t0017g0213 |
3 | HG03209.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.476-1739C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016781 | |||||||
| chr7:149016801 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.476-1759C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016801 | |||||||
| chr7:149016944 | C | T | 1 | a0009c0016t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.476-1902G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016944 | |||||||
| chr7:149016985 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0143 |
7 | NA18942.hp1 NA18953.hp1 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.476-1943G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149016985 | |||||||
| chr7:149017045 | T | C | 1 | a0001c0002t0002g0189 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.475+1947A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017045 | |||||||
| chr7:149017095 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.475+1897C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017095 | |||||||
| chr7:149017103 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.475+1889G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017103 | |||||||
| chr7:149017104 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.475+1888C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017104 | |||||||
| chr7:149017107 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.475+1885G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017107 | |||||||
| chr7:149017134 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.475+1858G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017134 | |||||||
| chr7:149017216 | T | C | 1 | a0001c0002t0002g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.475+1776A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017216 | |||||||
| chr7:149017303 | G | T | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.475+1689C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017303 | |||||||
| chr7:149017359 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.475+1633C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017359 | |||||||
| chr7:149017363 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.475+1629G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017363 | |||||||
| chr7:149017411 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.475+1581G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017411 | |||||||
| chr7:149017460 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA18957.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.475+1532A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017460 | |||||||
| chr7:149017515 | T | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.475+1477A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017515 | |||||||
| chr7:149017597 | CATTTTAT others(16): Show |
C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0147 |
2 | HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.475+1372_475+1394d others(25): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017597 | |||||||
| chr7:149017620 | T | TAC | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.475+1371_475+1372i others(4): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017620 | |||||||
| chr7:149017620 | T | TACATTTT others(20): Show |
1 | a0001c0001t0001g0098 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.475+1371_475+1372i others(29): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017620 | |||||||
| chr7:149017633 | T | TAAAATTA others(13): Show |
2 | a0001c0006t0009g0052 a0001c0006t0015g0207 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.475+1339_475+1358d others(22): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017633 | |||||||
| chr7:149017639 | T | TAAATACA others(13): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0088 a0001c0001t0001g0095 |
3 | HG01081.hp1 HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.475+1333_475+1352d others(22): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017639 | |||||||
| chr7:149017639 | TAAATACA others(13): Show |
T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0018 others(12): Show |
19 | HG01891.hp2 HG02080.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.475+1333_475+1352d others(22): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017639 | |||||||
| chr7:149017658 | TAAAATAC others(8): Show |
T | 1 | a0001c0020t0017g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.475+1319_475+1333d others(17): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017658 | |||||||
| chr7:149017679 | A | T | 1 | a0001c0020t0017g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.475+1313T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017679 | |||||||
| chr7:149017694 | AAAATAAA others(18): Show |
A | 1 | a0001c0020t0017g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.475+1273_475+1297d others(27): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017694 | |||||||
| chr7:149017719 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(211): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.475+1273C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149017719 | |||||||
| chr7:149018074 | A | G | 2 | a0002c0003t0003g0163 a0002c0003t0003g0164 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.475+918T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018074 | |||||||
| chr7:149018085 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.475+907G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018085 | |||||||
| chr7:149018090 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.475+902C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018090 | |||||||
| chr7:149018127 | C | T | 8 | a0002c0003t0003g0037 a0002c0003t0003g0044 a0002c0003t0003g0158 others(5): Show |
10 | HG00558.hp1 HG02027.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.475+865G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018127 | |||||||
| chr7:149018160 | C | T | 10 | a0002c0003t0003g0037 a0002c0003t0003g0044 a0002c0003t0003g0158 others(7): Show |
12 | HG00558.hp1 HG01884.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.475+832G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018160 | |||||||
| chr7:149018228 | C | CA | 18 | a0001c0001t0003g0195 a0001c0001t0004g0056 a0001c0001t0004g0183 others(15): Show |
21 | HG00558.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.475+763dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018228 | |||||||
| chr7:149018261 | T | G | 1 | a0002c0003t0003g0160 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.475+731A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018261 | |||||||
| chr7:149018435 | GTTTA | G | 2 | a0001c0001t0001g0032 a0001c0001t0018g0055 |
3 | NA18522.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.475+553_475+556del others(4): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018435 | |||||||
| chr7:149018600 | T | G | 3 | a0001c0001t0001g0179 a0001c0001t0018g0055 a0001c0020t0017g0213 |
3 | HG03209.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.475+392A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018600 | |||||||
| chr7:149018618 | G | A | 1 | a0009c0016t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.475+374C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018618 | |||||||
| chr7:149018659 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475+333A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018659 | |||||||
| chr7:149018709 | G | A | 5 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(2): Show |
7 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.475+283C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018709 | |||||||
| chr7:149018709 | G | C | 39 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(36): Show |
60 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.475+283C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018709 | |||||||
| chr7:149018729 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.475+263C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018729 | |||||||
| chr7:149018899 | C | T | 1 | a0009c0016t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.475+93G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 3/9 | chr7 | 149018899 | |||||||
| chr7:149019227 | C | T | 1 | a0001c0001t0005g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.270-30G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019227 | |||||||
| chr7:149019228 | G | A | 39 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(36): Show |
60 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.270-31C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019228 | |||||||
| chr7:149019382 | T | A | 2 | a0001c0006t0009g0052 a0001c0006t0015g0207 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.270-185A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019382 | |||||||
| chr7:149019393 | T | C | 8 | a0002c0003t0003g0037 a0002c0003t0003g0044 a0002c0003t0003g0158 others(5): Show |
10 | HG00558.hp1 HG02027.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.270-196A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019393 | |||||||
| chr7:149019461 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.270-264A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019461 | |||||||
| chr7:149019540 | C | T | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-343G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019540 | |||||||
| chr7:149019613 | C | T | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-416G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019613 | |||||||
| chr7:149019818 | T | A | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(174): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.270-621A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019818 | |||||||
| chr7:149019819 | T | A | 2 | a0001c0001t0001g0103 a0002c0003t0003g0159 |
2 | NA18969.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.270-622A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019819 | |||||||
| chr7:149019925 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.270-728G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149019925 | |||||||
| chr7:149020026 | T | C | 1 | a0001c0002t0002g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.270-829A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020026 | |||||||
| chr7:149020119 | C | T | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+848G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020119 | |||||||
| chr7:149020252 | T | C | 1 | a0001c0009t0004g0053 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.269+715A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020252 | |||||||
| chr7:149020291 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0139 |
3 | NA18950.hp2 NA18977.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.269+676G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020291 | |||||||
| chr7:149020375 | G | A | 73 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(70): Show |
100 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.269+592C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020375 | |||||||
| chr7:149020533 | C | T | 10 | a0002c0003t0003g0037 a0002c0003t0003g0044 a0002c0003t0003g0158 others(7): Show |
12 | HG00558.hp1 HG01884.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.269+434G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020533 | |||||||
| chr7:149020870 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG01074.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.269+97G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020870 | |||||||
| chr7:149020957 | C | CG | 3 | a0001c0001t0001g0097 a0001c0001t0001g0153 a0001c0002t0002g0211 |
3 | HG00741.hp1 HG02055.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.269+9dupC | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 2/9 | chr7 | 149020957 | |||||||
| chr7:149021213 | G | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0166 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.89-66C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021213 | |||||||
| chr7:149021218 | C | T | 10 | a0002c0003t0003g0037 a0002c0003t0003g0044 a0002c0003t0003g0158 others(7): Show |
12 | HG00558.hp1 HG01884.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.89-71G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021218 | |||||||
| chr7:149021221 | T | C | 2 | a0001c0006t0009g0052 a0001c0006t0015g0207 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-74A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021221 | |||||||
| chr7:149021275 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.89-128C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021275 | |||||||
| chr7:149021346 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
5 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.89-199C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021346 | |||||||
| chr7:149021403 | C | T | 1 | a0009c0016t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.89-256G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021403 | |||||||
| chr7:149021412 | C | T | 1 | a0001c0019t0013g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.89-265G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021412 | |||||||
| chr7:149021488 | C | CA | 37 | a0001c0001t0001g0065 a0001c0001t0001g0076 a0001c0001t0002g0008 others(34): Show |
59 | HG00733.hp1 HG00738.hp1 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.89-342dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021488 | |||||||
| chr7:149021488 | C | CAA | 7 | a0001c0001t0002g0199 a0001c0001t0002g0212 a0001c0001t0005g0054 others(4): Show |
7 | HG00735.hp1 HG00741.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.89-343_89-342dupTT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021488 | |||||||
| chr7:149021488 | CA | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.89-342delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021488 | |||||||
| chr7:149021859 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | HG00621.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.89-712C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021859 | |||||||
| chr7:149021937 | G | A | 2 | a0001c0002t0002g0047 a0001c0002t0002g0177 |
3 | HG02647.hp1 HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.89-790C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021937 | |||||||
| chr7:149021946 | T | A | 39 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(36): Show |
60 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.89-799A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021946 | |||||||
| chr7:149021964 | T | C | 4 | a0001c0001t0005g0024 a0001c0001t0005g0045 a0001c0001t0005g0054 others(1): Show |
6 | HG02257.hp2 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.89-817A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021964 | |||||||
| chr7:149021984 | T | G | 1 | a0001c0001t0006g0025 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-837A>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149021984 | |||||||
| chr7:149022279 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.89-1132T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022279 | |||||||
| chr7:149022403 | TA | T | 2 | a0001c0006t0009g0052 a0001c0006t0015g0207 |
3 | HG02896.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.89-1257delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022403 | |||||||
| chr7:149022472 | T | C | 2 | a0002c0003t0003g0163 a0002c0003t0003g0164 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.89-1325A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022472 | |||||||
| chr7:149022491 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.89-1344A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022491 | |||||||
| chr7:149022520 | C | G | 11 | a0002c0003t0003g0037 a0002c0003t0003g0044 a0002c0003t0003g0158 others(8): Show |
13 | HG00558.hp1 HG01884.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.89-1373G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022520 | |||||||
| chr7:149022547 | G | A | 1 | a0001c0011t0004g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.89-1400C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022547 | |||||||
| chr7:149022564 | T | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(120): Show |
199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.89-1417A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022564 | |||||||
| chr7:149022576 | T | C | 39 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(36): Show |
61 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.89-1429A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022576 | |||||||
| chr7:149022628 | G | A | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG01168.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.89-1481C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022628 | |||||||
| chr7:149022699 | C | T | 42 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(39): Show |
64 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.89-1552G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022699 | |||||||
| chr7:149022700 | G | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0039 others(12): Show |
24 | HG00140.hp2 HG00741.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.89-1553C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022700 | |||||||
| chr7:149022701 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0148 |
2 | HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.89-1554G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022701 | |||||||
| chr7:149022978 | C | T | 1 | a0001c0001t0004g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.89-1831G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022978 | |||||||
| chr7:149022979 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.89-1832A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149022979 | |||||||
| chr7:149023005 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
267 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.89-1858C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023005 | |||||||
| chr7:149023153 | C | A | 5 | a0001c0001t0002g0193 a0001c0001t0003g0049 a0001c0001t0003g0195 others(2): Show |
6 | HG02630.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-2006G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023153 | |||||||
| chr7:149023274 | C | G | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.89-2127G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023274 | |||||||
| chr7:149023379 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0080 a0001c0001t0001g0143 |
8 | NA18942.hp1 NA18953.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.89-2232C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023379 | |||||||
| chr7:149023478 | T | A | 2 | a0001c0001t0005g0024 a0001c0001t0005g0054 |
3 | HG02257.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.89-2331A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023478 | |||||||
| chr7:149023573 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.89-2426G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023573 | |||||||
| chr7:149023613 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
188 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.89-2466A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023613 | |||||||
| chr7:149023664 | C | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0166 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.89-2517G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023664 | |||||||
| chr7:149023814 | C | T | 46 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(43): Show |
70 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.89-2667G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023814 | |||||||
| chr7:149023877 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.89-2730A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023877 | |||||||
| chr7:149023891 | C | G | 1 | a0009c0016t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.89-2744G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023891 | |||||||
| chr7:149023898 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.89-2751C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023898 | |||||||
| chr7:149023958 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.89-2811C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023958 | |||||||
| chr7:149023989 | A | C | 48 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(45): Show |
72 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.89-2842T>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149023989 | |||||||
| chr7:149024022 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.89-2875C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024022 | |||||||
| chr7:149024089 | G | A | 73 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(70): Show |
100 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.89-2942C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024089 | |||||||
| chr7:149024138 | T | C | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.89-2991A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024138 | |||||||
| chr7:149024141 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.89-2994C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024141 | |||||||
| chr7:149024155 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.89-3008C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024155 | |||||||
| chr7:149024180 | G | A | 25 | a0001c0001t0004g0056 a0001c0001t0004g0183 a0001c0001t0004g0185 others(22): Show |
28 | HG00558.hp1 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.89-3033C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024180 | |||||||
| chr7:149024235 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.89-3088T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024235 | |||||||
| chr7:149024272 | T | C | 1 | a0001c0001t0006g0025 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.89-3125A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024272 | |||||||
| chr7:149024339 | AT | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.89-3193delA | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024339 | |||||||
| chr7:149024387 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.89-3240A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024387 | |||||||
| chr7:149024459 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.89-3312A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024459 | |||||||
| chr7:149024689 | A | G | 53 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(50): Show |
77 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.89-3542T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024689 | |||||||
| chr7:149024702 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.89-3555C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024702 | |||||||
| chr7:149024706 | C | A | 5 | a0001c0001t0004g0056 a0001c0001t0008g0061 a0001c0001t0008g0166 others(2): Show |
6 | HG02258.hp1 HG02896.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.89-3559G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024706 | |||||||
| chr7:149024771 | G | A | 46 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(43): Show |
70 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.88+3550C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024771 | |||||||
| chr7:149024797 | C | A | 53 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(50): Show |
77 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.88+3524G>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024797 | |||||||
| chr7:149024812 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.88+3509A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024812 | |||||||
| chr7:149024814 | T | TA | 27 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0030 others(24): Show |
34 | HG00621.hp2 HG00735.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.88+3506dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024814 | |||||||
| chr7:149024814 | TA | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0066 a0001c0001t0018g0055 others(7): Show |
15 | HG00558.hp1 HG02027.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+3506delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024814 | |||||||
| chr7:149024814 | TAA | T | 5 | a0001c0001t0005g0045 a0001c0001t0005g0178 a0001c0001t0006g0059 others(2): Show |
6 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+3505_88+3506del others(2): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024814 | |||||||
| chr7:149024814 | TAAAAAAA | T | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG00735.hp2 HG01433.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+3500_88+3506del others(7): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024814 | |||||||
| chr7:149024814 | TAAAAAAA others(1): Show |
T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.88+3499_88+3506del others(8): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024814 | |||||||
| chr7:149024814 | TAAAAAAA others(2): Show |
T | 6 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(3): Show |
6 | HG00323.hp1 HG02109.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+3498_88+3506del others(9): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024814 | |||||||
| chr7:149024814 | TAAAAAAA others(9): Show |
T | 5 | a0001c0001t0004g0183 a0001c0001t0004g0185 a0001c0001t0004g0203 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.88+3491_88+3506del others(16): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024814 | |||||||
| chr7:149024822 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.88+3499T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149024822 | |||||||
| chr7:149025065 | C | T | 2 | a0001c0001t0005g0024 a0001c0001t0005g0054 |
3 | HG02257.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+3256G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025065 | |||||||
| chr7:149025070 | C | CA | 5 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0074 others(2): Show |
9 | HG00609.hp1 HG02055.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.88+3250dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025070 | |||||||
| chr7:149025083 | AAAATAT | A | 10 | a0001c0001t0005g0178 a0001c0002t0002g0009 a0001c0002t0002g0013 others(7): Show |
14 | HG01433.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.88+3232_88+3237del others(6): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025083 | |||||||
| chr7:149025084 | AAATATAT | A | 5 | a0001c0001t0001g0179 a0001c0001t0002g0046 a0001c0001t0002g0186 others(2): Show |
6 | HG01256.hp1 HG01257.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.88+3230_88+3236del others(7): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025084 | |||||||
| chr7:149025085 | A | AAATATAT others(12): Show |
1 | a0001c0001t0005g0024 | 2 | HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.88+3235_88+3236ins others(19): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025085 | |||||||
| chr7:149025085 | A | AT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0018 others(7): Show |
21 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.88+3235_88+3236ins others(1): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025085 | |||||||
| chr7:149025085 | A | ATAT | 4 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0072 others(1): Show |
6 | HG00673.hp2 NA18943.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.88+3235_88+3236ins others(3): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025085 | |||||||
| chr7:149025085 | A | ATATATAT others(14): Show |
1 | a0001c0001t0005g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.88+3235_88+3236ins others(21): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025085 | |||||||
| chr7:149025085 | A | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0075 |
2 | HG00621.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.88+3236T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025085 | |||||||
| chr7:149025086 | AT | A | 7 | a0001c0001t0001g0084 a0001c0001t0001g0109 a0002c0003t0003g0037 others(4): Show |
8 | HG00558.hp1 HG01884.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.88+3234delA | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025086 | |||||||
| chr7:149025086 | ATAT | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(76): Show |
138 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.88+3232_88+3234del others(3): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025086 | |||||||
| chr7:149025086 | ATATAT | A | 3 | a0001c0001t0001g0082 a0006c0008t0001g0034 a0009c0016t0004g0057 |
3 | HG01952.hp1 HG03491.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.88+3230_88+3234del others(5): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025086 | |||||||
| chr7:149025087 | T | A | 60 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(57): Show |
77 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.88+3234A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025087 | |||||||
| chr7:149025089 | T | A | 47 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
64 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.88+3232A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025089 | |||||||
| chr7:149025091 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.88+3230A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025091 | |||||||
| chr7:149025093 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
131 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.88+3228A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025093 | |||||||
| chr7:149025095 | T | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0148 others(9): Show |
16 | HG00280.hp1 HG00609.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.88+3226A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025095 | |||||||
| chr7:149025100 | ATATATAT others(1): Show |
A | 5 | a0001c0001t0002g0051 a0001c0001t0002g0204 a0001c0001t0002g0205 others(2): Show |
7 | HG00733.hp1 HG00741.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.88+3213_88+3220del others(8): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025100 | |||||||
| chr7:149025102 | ATATATG | A | 22 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0050 others(19): Show |
33 | HG00735.hp1 HG00738.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.88+3213_88+3218del others(6): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025102 | |||||||
| chr7:149025104 | ATATG | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(26): Show |
40 | HG00140.hp2 HG00741.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.88+3213_88+3216del others(4): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025104 | |||||||
| chr7:149025106 | ATG | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0083 others(8): Show |
13 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.88+3213_88+3214del others(2): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025106 | |||||||
| chr7:149025108 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
190 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.88+3213C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025108 | |||||||
| chr7:149025112 | G | A | 2 | a0001c0001t0008g0061 a0001c0001t0008g0166 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.88+3209C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025112 | |||||||
| chr7:149025313 | C | T | 1 | a0001c0001t0018g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+3008G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025313 | |||||||
| chr7:149025416 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+2905T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025416 | |||||||
| chr7:149025463 | T | C | 1 | a0001c0002t0012g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.88+2858A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025463 | |||||||
| chr7:149025521 | C | G | 2 | a0001c0001t0008g0061 a0001c0001t0008g0166 |
2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.88+2800G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025521 | |||||||
| chr7:149025538 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.88+2783A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025538 | |||||||
| chr7:149025555 | C | T | 53 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(50): Show |
77 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.88+2766G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025555 | |||||||
| chr7:149025646 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.88+2675C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025646 | |||||||
| chr7:149025786 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.88+2535C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025786 | |||||||
| chr7:149025816 | G | A | 1 | a0001c0001t0001g0043 | 2 | NA18957.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.88+2505C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149025816 | |||||||
| chr7:149026091 | G | GA | 48 | a0001c0001t0001g0157 a0001c0001t0002g0008 a0001c0001t0002g0014 others(45): Show |
71 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.88+2229dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026091 | |||||||
| chr7:149026177 | A | G | 52 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(49): Show |
76 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.88+2144T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026177 | |||||||
| chr7:149026301 | T | C | 11 | a0001c0001t0001g0080 a0001c0002t0002g0209 a0002c0003t0003g0044 others(8): Show |
12 | HG00558.hp1 HG01884.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.88+2020A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026301 | |||||||
| chr7:149026458 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.88+1863C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026458 | |||||||
| chr7:149026646 | A | G | 1 | a0001c0001t0006g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.88+1675T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026646 | |||||||
| chr7:149026782 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(187): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.88+1539T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026782 | |||||||
| chr7:149026800 | G | GA | 13 | a0001c0001t0001g0023 a0001c0001t0001g0076 a0001c0001t0001g0077 others(10): Show |
15 | HG00544.hp1 HG01255.hp1 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.88+1520dupT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026800 | |||||||
| chr7:149026800 | GA | G | 9 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0216 others(6): Show |
10 | HG00323.hp2 HG00741.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.88+1520delT | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026800 | |||||||
| chr7:149026800 | GAA | G | 51 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(48): Show |
75 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.88+1519_88+1520del others(2): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026800 | |||||||
| chr7:149026801 | A | G | 1 | a0001c0001t0008g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.88+1520T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026801 | |||||||
| chr7:149026803 | A | G | 2 | a0001c0002t0002g0180 a0001c0002t0011g0181 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.88+1518T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026803 | |||||||
| chr7:149026823 | C | T | 1 | a0001c0001t0005g0054 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.88+1498G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026823 | |||||||
| chr7:149026884 | T | C | 187 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.88+1437A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026884 | |||||||
| chr7:149026951 | G | A | 56 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(53): Show |
81 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.88+1370C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026951 | |||||||
| chr7:149026993 | A | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(1): Show |
5 | HG01123.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.88+1328T>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149026993 | |||||||
| chr7:149027144 | A | T | 48 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(45): Show |
70 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.88+1177T>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027144 | |||||||
| chr7:149027295 | G | C | 1 | a0001c0020t0017g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.88+1026C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027295 | |||||||
| chr7:149027317 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.88+1004C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027317 | |||||||
| chr7:149027327 | T | C | 1 | a0001c0001t0007g0176 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.88+994A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027327 | |||||||
| chr7:149027413 | G | A | 56 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0014 others(53): Show |
81 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.88+908C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027413 | |||||||
| chr7:149027446 | T | C | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+875A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027446 | |||||||
| chr7:149027643 | AAGTAGTT others(76): Show |
A | 2 | a0001c0001t0005g0024 a0001c0001t0005g0054 |
3 | HG02257.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+595_88+677delGT others(81): Show |
PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027643 | |||||||
| chr7:149027853 | T | C | 46 | a0001c0001t0002g0008 a0001c0001t0002g0014 a0001c0001t0002g0046 others(43): Show |
68 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.88+468A>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027853 | |||||||
| chr7:149027891 | C | G | 1 | a0001c0001t0006g0059 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.88+430G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027891 | |||||||
| chr7:149027910 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.88+411C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027910 | |||||||
| chr7:149027951 | C | G | 1 | a0001c0001t0016g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.88+370G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027951 | |||||||
| chr7:149027952 | T | A | 1 | a0002c0003t0003g0215 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.88+369A>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027952 | |||||||
| chr7:149027958 | C | G | 1 | a0001c0001t0016g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.88+363G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149027958 | |||||||
| chr7:149028046 | C | T | 1 | a0004c0005t0001g0015 | 3 | HG03195.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.88+275G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028046 | |||||||
| chr7:149028051 | C | T | 1 | a0001c0001t0006g0025 | 2 | HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.88+270G>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028051 | |||||||
| chr7:149028081 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.88+240C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028081 | |||||||
| chr7:149028138 | A | G | 1 | a0009c0016t0004g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.88+183T>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028138 | |||||||
| chr7:149028216 | C | G | 1 | a0001c0001t0004g0056 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.88+105G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028216 | |||||||
| chr7:149028242 | G | C | 2 | a0001c0001t0005g0024 a0001c0001t0005g0054 |
3 | HG02257.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+79C>G | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028242 | |||||||
| chr7:149028242 | G | T | 1 | a0001c0001t0018g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.88+79C>A | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028242 | |||||||
| chr7:149028247 | G | A | 2 | a0001c0001t0005g0024 a0001c0001t0005g0054 |
3 | HG02257.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+74C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028247 | |||||||
| chr7:149028248 | C | G | 2 | a0001c0001t0005g0024 a0001c0001t0005g0054 |
3 | HG02257.hp2 HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.88+73G>C | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028248 | |||||||
| chr7:149028250 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.88+71C>T | PDIA4 | ENSG00000155660.11 | transcript | ENST00000652332.1 | protein_coding | 1/9 | chr7 | 149028250 |