geneid | 5395 |
---|---|
ensemblid | ENSG00000122512.17 |
hgncid | 9122 |
symbol | PMS2 |
name | PMS1 homolog 2, mismatch repair system component |
refseq_nuc | NM_000535.7 |
refseq_prot | NP_000526.2 |
ensembl_nuc | ENST00000265849.12 |
ensembl_prot | ENSP00000265849.7 |
mane_status | MANE Select |
chr | chr7 |
start | 5970925 |
end | 6009049 |
strand | - |
ver | v1.2 |
region | chr7:5970925-6009049 |
region5000 | chr7:5965925-6014049 |
regionname0 | PMS2_chr7_5970925_6009049 |
regionname5000 | PMS2_chr7_5965925_6014049 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 862 | 122 | 24 | 28 | 54 | 8 | 8 | 41 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002 | 0/0 | 862 | 86 | 2 | 2 | 69 | 0 | 13 | 54 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003 | 0/0 | 862 | 55 | 20 | 10 | 14 | 2 | 9 | 11 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004 | 1/0 | 862 | 41 | 8 | 15 | 14 | 1 | 2 | 8 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0005 | 0/1 | 862 | 29 | 8 | 12 | 2 | 2 | 4 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0006 | 0/0 | 862 | 18 | 0 | 2 | 14 | 0 | 2 | 10 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007 | 0/0 | 862 | 13 | 12 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0008 | 0/0 | 862 | 9 | 0 | 0 | 9 | 0 | 0 | 8 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0009 | 0/0 | 862 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0010 | 0/0 | 862 | 6 | 2 | 1 | 3 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0011 | 0/0 | 862 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0012 | 0/0 | 862 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0013 | 0/0 | 862 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0014 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0015 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0016 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0017 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0018 | 0/0 | 862 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0019 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0020 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0021 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0022 | 0/0 | 862 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0023 | 0/0 | 862 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0024 | 0/0 | 862 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0025 | 0/0 | 862 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0026 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0027 | 0/0 | 862 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0028 | 0/0 | 862 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0029 | 0/0 | 862 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2589 | 79 | 1 | 1 | 65 | 0 | 12 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0002 | 0/0 | 2589 | 55 | 3 | 10 | 36 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0003 | 0/0 | 2589 | 47 | 13 | 11 | 13 | 6 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0004 | 0/0 | 2589 | 41 | 7 | 10 | 14 | 2 | 8 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0005 | 1/0 | 2589 | 38 | 6 | 14 | 14 | 1 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0006 | 0/1 | 2589 | 29 | 8 | 12 | 2 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0007 | 0/0 | 2589 | 18 | 0 | 2 | 14 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0008 | 0/0 | 2589 | 11 | 11 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0009 | 0/0 | 2589 | 10 | 10 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0010 | 0/0 | 2589 | 9 | 8 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0011 | 0/0 | 2589 | 9 | 0 | 0 | 9 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0012 | 0/0 | 2589 | 7 | 0 | 3 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0013 | 0/0 | 2589 | 6 | 1 | 1 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0014 | 0/0 | 2589 | 4 | 2 | 1 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0015 | 0/0 | 2589 | 3 | 2 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0016 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0017 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0018 | 0/0 | 2589 | 3 | 0 | 2 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0019 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0020 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0021 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0022 | 0/0 | 2589 | 2 | 0 | 0 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0023 | 0/0 | 2589 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0024 | 0/0 | 2589 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0025 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0026 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0027 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0028 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0029 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0030 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0031 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0032 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0033 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0034 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0035 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0036 | 0/0 | 2552 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0037 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0038 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0039 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0040 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0041 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0042 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0043 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0044 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
c0045 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2501 | 124 | 14 | 15 | 73 | 7 | 15 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0002 | 0/0 | 2506 | 68 | 2 | 10 | 47 | 2 | 7 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0003 | 1/0 | 2505 | 40 | 9 | 14 | 12 | 1 | 3 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0004 | 0/0 | 2504 | 32 | 3 | 7 | 13 | 3 | 6 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0005 | 0/1 | 2504 | 30 | 8 | 12 | 2 | 3 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0006 | 0/0 | 2506 | 15 | 0 | 2 | 11 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0007 | 0/0 | 2504 | 10 | 10 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0008 | 0/0 | 2506 | 9 | 0 | 3 | 3 | 0 | 3 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0009 | 0/0 | 2506 | 9 | 9 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0010 | 0/0 | 2506 | 7 | 6 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0011 | 0/0 | 2505 | 6 | 5 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0012 | 0/0 | 2506 | 4 | 0 | 4 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0013 | 0/0 | 2504 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0014 | 0/0 | 2502 | 3 | 2 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0015 | 0/0 | 2507 | 2 | 0 | 1 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0016 | 0/0 | 2505 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0017 | 0/0 | 2506 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0018 | 0/0 | 2501 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0019 | 0/0 | 2505 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0020 | 0/0 | 2504 | 2 | 1 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0021 | 0/0 | 2501 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0022 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0023 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0024 | 0/0 | 2506 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0025 | 0/0 | 2505 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0026 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0027 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0028 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0029 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0030 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0031 | 0/0 | 2506 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0032 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0033 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0034 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0035 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0036 | 0/0 | 2506 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0037 | 0/0 | 2506 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0038 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0039 | 0/0 | 2505 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0040 | 0/0 | 2508 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0041 | 0/0 | 2505 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0042 | 0/0 | 2505 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0043 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0044 | 0/0 | 2504 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0045 | 0/0 | 2504 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0046 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0047 | 0/0 | 2504 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0048 | 0/0 | 2501 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0049 | 0/0 | 2501 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0050 | 0/0 | 2501 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0051 | 0/0 | 2501 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0052 | 0/0 | 2501 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0053 | 0/0 | 2501 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0054 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
t0055 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0003 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0004 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0290 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 2589 | 55 | 3 | 10 | 36 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003 | 0/0 | 2589 | 47 | 13 | 11 | 13 | 6 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0010 | 0/0 | 2589 | 9 | 8 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0012 | 0/0 | 2589 | 7 | 0 | 3 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0024 | 0/0 | 2589 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0037 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0042 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001 | 0/0 | 2589 | 79 | 1 | 1 | 65 | 0 | 12 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0013 | 0/0 | 2589 | 6 | 1 | 1 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0043 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004 | 0/0 | 2589 | 41 | 7 | 10 | 14 | 2 | 8 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0008 | 0/0 | 2589 | 11 | 11 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0020 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0031 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0005 | 1/0 | 2589 | 38 | 6 | 14 | 14 | 1 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0021 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0029 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0005c0006 | 0/1 | 2589 | 29 | 8 | 12 | 2 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0006c0007 | 0/0 | 2589 | 18 | 0 | 2 | 14 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007c0009 | 0/0 | 2589 | 10 | 10 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007c0015 | 0/0 | 2589 | 3 | 2 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0008c0011 | 0/0 | 2589 | 9 | 0 | 0 | 9 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0009c0016 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0009c0017 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0010c0014 | 0/0 | 2589 | 4 | 2 | 1 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0010c0023 | 0/0 | 2589 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0011c0018 | 0/0 | 2589 | 3 | 0 | 2 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0012c0019 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0013c0022 | 0/0 | 2589 | 2 | 0 | 0 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0014c0025 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0015c0026 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0016c0027 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0017c0044 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0018c0035 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0019c0034 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0020c0030 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0021c0033 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0022c0032 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0023c0039 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0024c0038 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0025c0040 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0026c0036 | 0/0 | 2552 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0027c0041 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0028c0028 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0029c0045 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002 | 0/0 | 5094 | 46 | 2 | 6 | 32 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0008 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0015 | 0/0 | 5095 | 2 | 0 | 1 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0028 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0030 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0031 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0032 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0033 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0002t0036 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0001 | 0/0 | 5089 | 35 | 8 | 10 | 8 | 6 | 3 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0002 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0008 | 0/0 | 5094 | 3 | 0 | 0 | 3 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0014 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0019 | 0/0 | 5093 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0021 | 0/0 | 5089 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0038 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0039 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0003t0050 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0010t0011 | 0/0 | 5093 | 6 | 5 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0010t0014 | 0/0 | 5090 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0010t0029 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0010t0040 | 0/0 | 5096 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0012t0001 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0012t0002 | 0/0 | 5094 | 6 | 0 | 3 | 3 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0024t0008 | 0/0 | 5094 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0037t0002 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0001c0042t0001 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0001 | 0/0 | 5089 | 70 | 0 | 1 | 59 | 0 | 10 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0002 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0014 | 0/0 | 5090 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0018 | 0/0 | 5089 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0048 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0049 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0051 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0052 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0001t0053 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0013t0001 | 0/0 | 5089 | 6 | 1 | 1 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0002c0043t0001 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004t0004 | 0/0 | 5092 | 28 | 3 | 5 | 13 | 2 | 5 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004t0008 | 0/0 | 5094 | 2 | 0 | 0 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004t0012 | 0/0 | 5094 | 4 | 0 | 4 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004t0013 | 0/0 | 5092 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004t0020 | 0/0 | 5092 | 2 | 1 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004t0044 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0004t0045 | 0/0 | 5092 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0008t0007 | 0/0 | 5092 | 10 | 10 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0008t0046 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0020t0054 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0020t0055 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0003c0031t0008 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0005t0001 | 0/0 | 5089 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0005t0003 | 1/0 | 5093 | 35 | 6 | 14 | 11 | 1 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0005t0041 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0005t0047 | 0/0 | 5092 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0021t0003 | 0/0 | 5093 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0004c0029t0035 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0005c0006t0005 | 0/1 | 5092 | 28 | 7 | 12 | 2 | 2 | 4 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0005c0006t0043 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0006c0007t0006 | 0/0 | 5094 | 14 | 0 | 2 | 11 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0006c0007t0022 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0006c0007t0023 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0006c0007t0024 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0006c0007t0025 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007c0009t0009 | 0/0 | 5094 | 8 | 8 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007c0009t0026 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007c0009t0037 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007c0015t0010 | 0/0 | 5094 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0007c0015t0034 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0008c0011t0002 | 0/0 | 5094 | 8 | 0 | 0 | 8 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0008c0011t0016 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0009c0016t0010 | 0/0 | 5094 | 3 | 3 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0009c0017t0001 | 0/0 | 5089 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0009c0017t0003 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0010c0014t0001 | 0/0 | 5089 | 3 | 2 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0010c0014t0042 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0010c0023t0002 | 0/0 | 5094 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0011c0018t0004 | 0/0 | 5092 | 3 | 0 | 2 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0012c0019t0017 | 0/0 | 5094 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0013c0022t0002 | 0/0 | 5094 | 2 | 0 | 0 | 0 | 0 | 2 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0014c0025t0001 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0015c0026t0006 | 0/0 | 5094 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0016c0027t0010 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0017c0044t0001 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0018c0035t0010 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0019c0034t0009 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0020c0030t0003 | 0/0 | 5093 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0021c0033t0005 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0022c0032t0003 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0023c0039t0002 | 0/0 | 5094 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0024c0038t0001 | 0/0 | 5089 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0025c0040t0001 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0026c0036t0027 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0027c0041t0004 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0028c0028t0016 | 0/0 | 5093 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
a0029c0045t0005 | 0/0 | 5092 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | copy fasta | chr7 | 5965925 | 6014049 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0008g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0015g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0015g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0028g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0030g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0031g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0032g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0033g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0002t0036g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0004 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0008g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0008g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0019g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0021g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0021g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0038g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0039g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0003t0050g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0011g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0011g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0011g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0011g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0029g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0010t0040g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0012t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0012t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0012t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0012t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0012t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0012t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0012t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0024t0008g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0024t0008g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0037t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0001c0042t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0014g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0018g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0018g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0048g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0049g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0051g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0052g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0001t0053g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0013t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0013t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0013t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0013t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0013t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0013t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0002c0043t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0003 | 0/0 | 4 | 0 | 0 | 0 | 1 | 3 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0004g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0008g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0008g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0012g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0012g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0012g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0012g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0013g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0013g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0020g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0020g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0044g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0004t0045g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0007g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0008t0046g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0020t0054g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0020t0055g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0003c0031t0008g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0007 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0058 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0041g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0005t0047g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0021t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0021t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0004c0029t0035g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0290 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0005c0006t0043g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0006g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0022g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0023g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0024g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0006c0007t0025g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0026g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0009t0037g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0015t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0015t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0007c0015t0034g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0008c0011t0016g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0009c0016t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0009c0016t0010g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0009c0016t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0009c0017t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0009c0017t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0009c0017t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0010c0014t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0010c0014t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0010c0014t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0010c0014t0042g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0010c0023t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0010c0023t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0011c0018t0004g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0011c0018t0004g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0012c0019t0017g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0012c0019t0017g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0013c0022t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0013c0022t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0014c0025t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0015c0026t0006g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0016c0027t0010g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0017c0044t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0018c0035t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0019c0034t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0020c0030t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0021c0033t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0022c0032t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0023c0039t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0024c0038t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0025c0040t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0026c0036t0027g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0027c0041t0004g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0028c0028t0016g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
a0029c0045t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0115 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00099 | hp2 | a0003 | c0004 | t0004 | g0363 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00140 | hp1 | a0024 | c0038 | t0001 | g0081 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0239 | EUR | GBR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00280 | hp1 | a0029 | c0045 | t0005 | g0301 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0008 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0120 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0092 | EUR | FIN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00423 | hp1 | a0006 | c0007 | t0006 | g0332 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00423 | hp2 | a0002 | c0001 | t0001 | g0146 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00438 | hp1 | a0004 | c0005 | t0001 | g0060 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00438 | hp2 | a0002 | c0001 | t0018 | g0129 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00544 | hp2 | a0001 | c0012 | t0002 | g0190 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00558 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00558 | hp2 | a0002 | c0001 | t0001 | g0123 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00609 | hp1 | a0002 | c0001 | t0001 | g0140 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00609 | hp2 | a0002 | c0013 | t0001 | g0200 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00621 | hp1 | a0002 | c0001 | t0001 | g0157 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00621 | hp2 | a0003 | c0004 | t0004 | g0012 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00639 | hp1 | a0002 | c0013 | t0001 | g0177 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00639 | hp2 | a0004 | c0005 | t0003 | g0061 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00642 | hp1 | a0025 | c0040 | t0001 | g0093 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00642 | hp2 | a0005 | c0006 | t0005 | g0303 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | CHS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00733 | hp1 | a0005 | c0006 | t0005 | g0296 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00733 | hp2 | a0004 | c0005 | t0003 | g0006 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00735 | hp1 | a0001 | c0003 | t0001 | g0071 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00735 | hp2 | a0004 | c0005 | t0003 | g0001 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00738 | hp1 | a0003 | c0004 | t0004 | g0338 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00738 | hp2 | a0006 | c0007 | t0006 | g0374 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00741 | hp1 | a0001 | c0012 | t0002 | g0102 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG00741 | hp2 | a0005 | c0006 | t0005 | g0288 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01069 | hp1 | a0004 | c0005 | t0003 | g0001 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01069 | hp2 | a0011 | c0018 | t0004 | g0013 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01070 | hp1 | a0001 | c0024 | t0008 | g0252 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0118 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01071 | hp1 | a0001 | c0024 | t0008 | g0257 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01071 | hp2 | a0011 | c0018 | t0004 | g0013 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01074 | hp1 | a0001 | c0042 | t0001 | g0117 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01074 | hp2 | a0003 | c0004 | t0004 | g0349 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01081 | hp1 | a0003 | c0004 | t0045 | g0378 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0312 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01106 | hp1 | a0001 | c0002 | t0033 | g0249 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01106 | hp2 | a0003 | c0004 | t0012 | g0111 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01109 | hp1 | a0007 | c0015 | t0034 | g0322 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01109 | hp2 | a0005 | c0006 | t0005 | g0297 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01168 | hp1 | a0003 | c0004 | t0012 | g0203 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01168 | hp2 | a0004 | c0005 | t0003 | g0007 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01175 | hp1 | a0001 | c0003 | t0050 | g0077 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0085 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0119 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0075 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01243 | hp1 | a0001 | c0002 | t0036 | g0098 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01243 | hp2 | a0010 | c0014 | t0001 | g0073 | AMR | PUR | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01255 | hp1 | a0005 | c0006 | t0005 | g0287 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01255 | hp2 | a0002 | c0001 | t0001 | g0178 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01256 | hp1 | a0004 | c0005 | t0003 | g0046 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0076 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01258 | hp1 | a0001 | c0002 | t0008 | g0251 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01258 | hp2 | a0004 | c0005 | t0003 | g0054 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01261 | hp1 | a0003 | c0004 | t0004 | g0351 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01261 | hp2 | a0005 | c0006 | t0005 | g0293 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01346 | hp1 | a0003 | c0004 | t0012 | g0110 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01346 | hp2 | a0018 | c0035 | t0010 | g0108 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01358 | hp1 | a0001 | c0012 | t0002 | g0180 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01358 | hp2 | a0003 | c0004 | t0004 | g0350 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0276 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01361 | hp2 | a0004 | c0005 | t0003 | g0045 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0087 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01433 | hp2 | a0003 | c0004 | t0012 | g0112 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01496 | hp1 | a0006 | c0007 | t0006 | g0375 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01496 | hp2 | a0001 | c0010 | t0011 | g0034 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01515 | hp1 | a0005 | c0006 | t0005 | g0284 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01515 | hp2 | a0003 | c0004 | t0004 | g0003 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0283 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01517 | hp2 | a0005 | c0006 | t0005 | g0286 | EUR | IBS | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01884 | hp1 | a0003 | c0004 | t0013 | g0014 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01884 | hp2 | a0004 | c0005 | t0003 | g0006 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01891 | hp1 | a0012 | c0019 | t0017 | g0376 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0201 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01928 | hp1 | a0004 | c0005 | t0003 | g0051 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01928 | hp2 | a0005 | c0006 | t0005 | g0302 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01934 | hp1 | a0005 | c0006 | t0005 | g0300 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01934 | hp2 | a0001 | c0003 | t0001 | g0094 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01943 | hp1 | a0005 | c0006 | t0005 | g0313 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01943 | hp2 | a0004 | c0005 | t0003 | g0001 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01952 | hp1 | a0004 | c0029 | t0035 | g0057 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01952 | hp2 | a0004 | c0005 | t0003 | g0055 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01978 | hp1 | a0005 | c0006 | t0005 | g0299 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01978 | hp2 | a0023 | c0039 | t0002 | g0279 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01981 | hp1 | a0005 | c0006 | t0005 | g0285 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01981 | hp2 | a0001 | c0002 | t0015 | g0268 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01993 | hp2 | a0004 | c0005 | t0003 | g0056 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02004 | hp1 | a0004 | c0005 | t0003 | g0001 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0267 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0072 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02015 | hp2 | a0004 | c0005 | t0003 | g0063 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02027 | hp2 | a0003 | c0004 | t0004 | g0353 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02040 | hp1 | a0001 | c0002 | t0030 | g0212 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02040 | hp2 | a0002 | c0001 | t0001 | g0141 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02055 | hp1 | a0003 | c0008 | t0007 | g0345 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02055 | hp2 | a0001 | c0010 | t0011 | g0035 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02056 | hp1 | a0004 | c0005 | t0047 | g0062 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02056 | hp2 | a0010 | c0023 | t0002 | g0224 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02071 | hp1 | a0004 | c0005 | t0003 | g0016 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02071 | hp2 | a0002 | c0001 | t0001 | g0134 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0142 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02074 | hp2 | a0002 | c0001 | t0001 | g0188 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02083 | hp1 | a0001 | c0002 | t0002 | g0209 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02083 | hp2 | a0002 | c0001 | t0001 | g0196 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02129 | hp2 | a0006 | c0007 | t0006 | g0369 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02132 | hp1 | a0004 | c0005 | t0003 | g0015 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02132 | hp2 | a0006 | c0007 | t0006 | g0331 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02135 | hp1 | a0006 | c0007 | t0006 | g0320 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02135 | hp2 | a0001 | c0012 | t0002 | g0101 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02145 | hp1 | a0003 | c0008 | t0007 | g0346 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02145 | hp2 | a0005 | c0006 | t0005 | g0298 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0067 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02155 | hp2 | a0008 | c0011 | t0002 | g0247 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02165 | hp1 | a0004 | c0005 | t0003 | g0048 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02165 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | CDX | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02257 | hp1 | a0007 | c0009 | t0009 | g0028 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02257 | hp2 | a0003 | c0004 | t0013 | g0365 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02258 | hp1 | a0007 | c0009 | t0009 | g0029 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02258 | hp2 | a0004 | c0005 | t0003 | g0049 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02273 | hp1 | a0001 | c0012 | t0002 | g0179 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0263 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02280 | hp1 | a0009 | c0017 | t0001 | g0106 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02280 | hp2 | a0001 | c0003 | t0019 | g0091 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0262 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02293 | hp2 | a0001 | c0003 | t0001 | g0088 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02300 | hp1 | a0003 | c0004 | t0004 | g0362 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02300 | hp2 | a0004 | c0005 | t0003 | g0001 | AMR | PEL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02451 | hp1 | a0019 | c0034 | t0009 | g0024 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02451 | hp2 | a0004 | c0005 | t0003 | g0044 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02523 | hp1 | a0005 | c0006 | t0005 | g0305 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02523 | hp2 | a0003 | c0004 | t0004 | g0347 | EAS | KHV | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02602 | hp1 | a0002 | c0001 | t0001 | g0174 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02602 | hp2 | a0002 | c0001 | t0001 | g0153 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0080 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02622 | hp1 | a0009 | c0017 | t0001 | g0109 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0089 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02630 | hp1 | a0007 | c0015 | t0010 | g0039 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02630 | hp2 | a0002 | c0001 | t0049 | g0198 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02698 | hp1 | a0005 | c0006 | t0005 | g0289 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0074 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02717 | hp1 | a0014 | c0025 | t0001 | g0368 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02717 | hp2 | a0003 | c0008 | t0007 | g0342 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02723 | hp1 | a0005 | c0006 | t0005 | g0315 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02723 | hp2 | a0003 | c0008 | t0007 | g0324 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02735 | hp1 | a0015 | c0026 | t0006 | g0371 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02735 | hp2 | a0002 | c0001 | t0001 | g0282 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0319 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02738 | hp2 | a0002 | c0001 | t0001 | g0192 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02809 | hp1 | a0001 | c0010 | t0011 | g0032 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02809 | hp2 | a0007 | c0009 | t0026 | g0027 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02818 | hp1 | a0007 | c0009 | t0009 | g0043 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0068 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02886 | hp2 | a0003 | c0004 | t0004 | g0065 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02895 | hp1 | a0007 | c0015 | t0010 | g0018 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02895 | hp2 | a0001 | c0003 | t0039 | g0277 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02897 | hp1 | a0010 | c0014 | t0001 | g0114 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02897 | hp2 | a0001 | c0003 | t0038 | g0278 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02922 | hp1 | a0003 | c0004 | t0013 | g0014 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02922 | hp2 | a0001 | c0010 | t0011 | g0036 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02965 | hp1 | a0003 | c0004 | t0004 | g0337 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02965 | hp2 | a0003 | c0008 | t0007 | g0340 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02970 | hp1 | a0005 | c0006 | t0005 | g0316 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02970 | hp2 | a0005 | c0006 | t0043 | g0317 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02976 | hp1 | a0003 | c0008 | t0007 | g0339 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02976 | hp2 | a0003 | c0004 | t0004 | g0336 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03017 | hp1 | a0005 | c0006 | t0005 | g0306 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03017 | hp2 | a0006 | c0007 | t0024 | g0096 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03041 | hp2 | a0001 | c0010 | t0040 | g0030 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03098 | hp1 | a0004 | c0005 | t0003 | g0041 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03098 | hp2 | a0007 | c0009 | t0009 | g0021 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03130 | hp1 | a0004 | c0021 | t0003 | g0309 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03130 | hp2 | a0007 | c0009 | t0009 | g0019 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03139 | hp1 | a0005 | c0006 | t0005 | g0311 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03195 | hp1 | a0001 | c0010 | t0011 | g0031 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03195 | hp2 | a0010 | c0014 | t0001 | g0025 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03209 | hp1 | a0009 | c0016 | t0010 | g0103 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03209 | hp2 | a0003 | c0008 | t0007 | g0364 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03239 | hp1 | a0002 | c0001 | t0001 | g0126 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03239 | hp2 | a0006 | c0007 | t0006 | g0370 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03453 | hp1 | a0003 | c0008 | t0007 | g0341 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03453 | hp2 | a0016 | c0027 | t0010 | g0328 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03491 | hp1 | a0001 | c0003 | t0002 | g0250 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03491 | hp2 | a0002 | c0001 | t0001 | g0326 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0327 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03492 | hp2 | a0002 | c0043 | t0001 | g0164 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03516 | hp1 | a0003 | c0008 | t0046 | g0343 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03516 | hp2 | a0009 | c0016 | t0010 | g0107 | AFR | ESN | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0310 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03540 | hp2 | a0007 | c0009 | t0037 | g0026 | AFR | GWD | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03579 | hp1 | a0003 | c0008 | t0007 | g0344 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03579 | hp2 | a0003 | c0008 | t0007 | g0323 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03654 | hp1 | a0003 | c0004 | t0004 | g0003 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03654 | hp2 | a0004 | c0005 | t0003 | g0007 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03669 | hp1 | a0003 | c0004 | t0008 | g0355 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03669 | hp2 | a0002 | c0001 | t0001 | g0191 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03688 | hp1 | a0002 | c0001 | t0053 | g0187 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03688 | hp2 | a0003 | c0004 | t0044 | g0383 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03704 | hp1 | a0020 | c0030 | t0003 | g0053 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03704 | hp2 | a0003 | c0004 | t0004 | g0354 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0182 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03710 | hp2 | a0003 | c0004 | t0008 | g0356 | SAS | PJL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0215 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03831 | hp2 | a0002 | c0001 | t0001 | g0124 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03834 | hp1 | a0005 | c0006 | t0005 | g0295 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03834 | hp2 | a0001 | c0003 | t0001 | g0253 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0244 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03942 | hp2 | a0011 | c0018 | t0004 | g0348 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04115 | hp1 | a0005 | c0006 | t0005 | g0294 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04115 | hp2 | a0003 | c0004 | t0004 | g0384 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04184 | hp1 | a0017 | c0044 | t0001 | g0181 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04184 | hp2 | a0003 | c0031 | t0008 | g0059 | SAS | BEB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04199 | hp1 | a0003 | c0004 | t0004 | g0003 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04199 | hp2 | a0004 | c0005 | t0003 | g0047 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04204 | hp1 | a0013 | c0022 | t0002 | g0260 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04204 | hp2 | a0002 | c0001 | t0051 | g0130 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04228 | hp1 | a0003 | c0004 | t0004 | g0003 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0264 | SAS | STU | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18747 | hp1 | a0002 | c0013 | t0001 | g0259 | EAS | CHB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0082 | EAS | CHB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18906 | hp1 | a0003 | c0020 | t0055 | g0367 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18906 | hp2 | a0007 | c0009 | t0009 | g0020 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18939 | hp2 | a0002 | c0001 | t0002 | g0145 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0245 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18941 | hp2 | a0002 | c0001 | t0001 | g0160 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18942 | hp2 | a0010 | c0023 | t0002 | g0235 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18944 | hp1 | a0003 | c0004 | t0004 | g0385 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18945 | hp1 | a0004 | c0005 | t0003 | g0175 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18945 | hp2 | a0002 | c0001 | t0001 | g0195 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18947 | hp1 | a0006 | c0007 | t0006 | g0335 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18947 | hp2 | a0002 | c0001 | t0001 | g0183 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18948 | hp1 | a0002 | c0001 | t0001 | g0280 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18948 | hp2 | a0003 | c0004 | t0004 | g0381 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18950 | hp1 | a0002 | c0001 | t0001 | g0171 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18950 | hp2 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18951 | hp1 | a0002 | c0001 | t0001 | g0150 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18951 | hp2 | a0002 | c0001 | t0001 | g0139 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18952 | hp1 | a0002 | c0001 | t0001 | g0184 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18953 | hp2 | a0002 | c0001 | t0001 | g0169 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18954 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18954 | hp2 | a0006 | c0007 | t0006 | g0372 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18957 | hp1 | a0004 | c0005 | t0003 | g0002 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18960 | hp1 | a0010 | c0014 | t0042 | g0095 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18960 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18962 | hp1 | a0002 | c0001 | t0001 | g0148 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18962 | hp2 | a0002 | c0001 | t0001 | g0194 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18963 | hp1 | a0004 | c0005 | t0003 | g0050 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18963 | hp2 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18965 | hp1 | a0002 | c0001 | t0001 | g0132 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18965 | hp2 | a0002 | c0001 | t0001 | g0186 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18967 | hp1 | a0002 | c0001 | t0001 | g0159 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18968 | hp1 | a0002 | c0001 | t0001 | g0197 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18969 | hp2 | a0003 | c0004 | t0004 | g0379 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18970 | hp1 | a0002 | c0001 | t0001 | g0147 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18970 | hp2 | a0003 | c0004 | t0004 | g0380 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18971 | hp1 | a0002 | c0001 | t0052 | g0128 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18971 | hp2 | a0008 | c0011 | t0002 | g0255 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18973 | hp1 | a0001 | c0002 | t0031 | g0269 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18973 | hp2 | a0002 | c0001 | t0001 | g0167 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18975 | hp1 | a0002 | c0001 | t0001 | g0133 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18975 | hp2 | a0003 | c0004 | t0004 | g0361 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18977 | hp2 | a0008 | c0011 | t0002 | g0274 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18979 | hp1 | a0001 | c0002 | t0028 | g0226 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18979 | hp2 | a0002 | c0001 | t0001 | g0156 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18980 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0211 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18981 | hp1 | a0006 | c0007 | t0022 | g0329 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18981 | hp2 | a0002 | c0001 | t0014 | g0173 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18983 | hp1 | a0006 | c0007 | t0006 | g0011 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18983 | hp2 | a0002 | c0001 | t0048 | g0143 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18985 | hp1 | a0002 | c0001 | t0001 | g0163 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18985 | hp2 | a0001 | c0003 | t0008 | g0208 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18986 | hp2 | a0006 | c0007 | t0025 | g0321 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18989 | hp2 | a0001 | c0003 | t0021 | g0084 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18990 | hp2 | a0004 | c0005 | t0041 | g0052 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18991 | hp1 | a0006 | c0007 | t0006 | g0330 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18993 | hp1 | a0002 | c0001 | t0001 | g0281 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18994 | hp1 | a0002 | c0001 | t0001 | g0172 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18994 | hp2 | a0026 | c0036 | t0027 | g0230 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18995 | hp2 | a0001 | c0012 | t0002 | g0189 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18998 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18999 | hp1 | a0001 | c0037 | t0002 | g0218 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0154 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19000 | hp1 | a0002 | c0001 | t0001 | g0100 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19001 | hp1 | a0008 | c0011 | t0002 | g0246 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19001 | hp2 | a0003 | c0004 | t0004 | g0382 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19002 | hp1 | a0002 | c0001 | t0001 | g0131 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19002 | hp2 | a0004 | c0005 | t0003 | g0002 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19003 | hp1 | a0006 | c0007 | t0006 | g0333 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19005 | hp1 | a0003 | c0004 | t0004 | g0360 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19005 | hp2 | a0004 | c0005 | t0003 | g0099 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19007 | hp1 | a0005 | c0006 | t0005 | g0307 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0210 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19009 | hp1 | a0001 | c0002 | t0015 | g0220 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19010 | hp2 | a0003 | c0004 | t0004 | g0358 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19011 | hp1 | a0002 | c0013 | t0001 | g0266 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19012 | hp1 | a0006 | c0007 | t0023 | g0334 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19012 | hp2 | a0002 | c0001 | t0018 | g0149 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19030 | hp1 | a0009 | c0017 | t0003 | g0042 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19030 | hp2 | a0012 | c0019 | t0017 | g0377 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19043 | hp1 | a0001 | c0010 | t0011 | g0033 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19043 | hp2 | a0004 | c0021 | t0003 | g0105 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19056 | hp1 | a0002 | c0001 | t0001 | g0166 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19056 | hp2 | a0003 | c0004 | t0004 | g0359 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19057 | hp1 | a0028 | c0028 | t0016 | g0236 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19057 | hp2 | a0022 | c0032 | t0003 | g0325 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19058 | hp1 | a0002 | c0001 | t0001 | g0151 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19058 | hp2 | a0002 | c0001 | t0001 | g0168 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19062 | hp2 | a0002 | c0001 | t0001 | g0135 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0265 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19065 | hp2 | a0006 | c0007 | t0006 | g0373 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19066 | hp1 | a0002 | c0001 | t0001 | g0162 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19066 | hp2 | a0008 | c0011 | t0002 | g0273 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19067 | hp1 | a0008 | c0011 | t0002 | g0237 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19067 | hp2 | a0002 | c0013 | t0001 | g0199 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19068 | hp2 | a0003 | c0004 | t0004 | g0012 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19070 | hp1 | a0008 | c0011 | t0016 | g0254 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19070 | hp2 | a0003 | c0004 | t0020 | g0352 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19074 | hp1 | a0001 | c0003 | t0021 | g0116 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19074 | hp2 | a0001 | c0003 | t0008 | g0225 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0122 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19079 | hp2 | a0002 | c0001 | t0001 | g0165 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19080 | hp1 | a0002 | c0001 | t0001 | g0170 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19080 | hp2 | a0008 | c0011 | t0002 | g0258 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19081 | hp1 | a0002 | c0001 | t0001 | g0158 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19081 | hp2 | a0006 | c0007 | t0006 | g0011 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19082 | hp1 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19084 | hp2 | a0001 | c0012 | t0001 | g0193 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19087 | hp2 | a0002 | c0001 | t0001 | g0161 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19088 | hp2 | a0001 | c0003 | t0008 | g0219 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19091 | hp1 | a0008 | c0011 | t0002 | g0256 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19091 | hp2 | a0004 | c0005 | t0003 | g0002 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19240 | hp1 | a0007 | c0009 | t0009 | g0022 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | YRI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20129 | hp1 | a0001 | c0002 | t0032 | g0064 | AFR | ASW | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20129 | hp2 | a0002 | c0013 | t0001 | g0176 | AFR | ASW | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20752 | hp1 | a0001 | c0003 | t0001 | g0070 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20752 | hp2 | a0027 | c0041 | t0004 | g0357 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20805 | hp1 | a0001 | c0003 | t0001 | g0079 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20805 | hp2 | a0004 | c0005 | t0003 | g0097 | EUR | TSI | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20905 | hp1 | a0013 | c0022 | t0002 | g0261 | SAS | GIH | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0078 | SAS | GIH | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01123 | hp1 | a0005 | c0006 | t0005 | g0291 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02109 | hp1 | a0005 | c0006 | t0005 | g0318 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02109 | hp2 | a0009 | c0016 | t0010 | g0017 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02486 | hp1 | a0003 | c0004 | t0020 | g0308 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02486 | hp2 | a0004 | c0005 | t0003 | g0040 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02559 | hp1 | a0001 | c0003 | t0019 | g0090 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG02559 | hp2 | a0001 | c0010 | t0029 | g0038 | AFR | ACB | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03471 | hp1 | a0001 | c0010 | t0014 | g0037 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG03471 | hp2 | a0003 | c0020 | t0054 | g0366 | AFR | MSL | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG06807 | hp1 | a0005 | c0006 | t0005 | g0292 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
HG06807 | hp2 | a0007 | c0009 | t0009 | g0023 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18955 | hp1 | a0004 | c0005 | t0003 | g0002 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA18955 | hp2 | a0002 | c0001 | t0001 | g0152 | EAS | JPT | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20300 | hp1 | a0005 | c0006 | t0005 | g0304 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA20300 | hp2 | a0021 | c0033 | t0005 | g0314 | AFR | USA | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA21309 | hp1 | a0004 | c0005 | t0003 | g0121 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
NA21309 | hp2 | a0001 | c0003 | t0014 | g0069 | AFR | LWK | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
homoSapiens_chm13v2 | hp1 | a0005 | c0006 | t0005 | g0290 | REF | REF | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
homoSapiens_grch38 | hp1 | a0004 | c0005 | t0003 | g0058 | REF | REF | PMS2_chr7_5965925_6014049 | PMS2 | chr7 | 5965925 | 6014049 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5973418
|
C | G | 4 | a0005a0010a0021others(1): Show | 37 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(34): Show |
missense_variant | MODERATE | c.2570G>C | p.Gly857Ala | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2600/5093 | 2570/2589 | 857/862 | chr7 | 5973418 | ||
chr7:5977677
|
G | T | 1 | a0013 | 2 | HG04204.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.2356C>A | p.Leu786Met | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/15 | 2386/5093 | 2356/2589 | 786/862 | chr7 | 5977677 | ||
chr7:5977709
|
T | C | 7 | a0006a0007a0009others(4): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
missense_variant | MODERATE | c.2324A>G | p.Asn775Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/15 | 2354/5093 | 2324/2589 | 775/862 | chr7 | 5977709 | ||
chr7:5982890
|
G | A | 1 | a0021 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.2108C>T | p.Thr703Met | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/15 | 2138/5093 | 2108/2589 | 703/862 | chr7 | 5982890 | ||
chr7:5986899
|
C | T | 1 | a0020 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.1866G>A | p.Met622Ile | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1896/5093 | 1866/2589 | 622/862 | chr7 | 5986899 | ||
chr7:5986901
|
T | C | 1 | a0015 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.1864A>G | p.Met622Val | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1894/5093 | 1864/2589 | 622/862 | chr7 | 5986901 | ||
chr7:5986976
|
T | A | 1 | a0024 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.1789A>T | p.Thr597Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1819/5093 | 1789/2589 | 597/862 | chr7 | 5986976 | ||
chr7:5987048
|
T | A | 1 | a0017 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.1717A>T | p.Thr573Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1747/5093 | 1717/2589 | 573/862 | chr7 | 5987048 | ||
chr7:5987057
|
T | C | 1 | a0019 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1708A>G | p.Asn570Asp | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1738/5093 | 1708/2589 | 570/862 | chr7 | 5987057 | ||
chr7:5987144
|
T | C | 28 | a0001a0002a0003others(25): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
missense_variant | MODERATE | c.1621A>G | p.Lys541Glu | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1651/5093 | 1621/2589 | 541/862 | chr7 | 5987144 | ||
chr7:5987156
|
C | T | 1 | a0018 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1609G>A | p.Glu537Lys | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1639/5093 | 1609/2589 | 537/862 | chr7 | 5987156 | ||
chr7:5987206
|
G | A | 1 | a0023 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1559C>T | p.Ala520Val | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1589/5093 | 1559/2589 | 520/862 | chr7 | 5987206 | ||
chr7:5987209
|
T | C | 1 | a0023 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1556A>G | p.Tyr519Cys | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1586/5093 | 1556/2589 | 519/862 | chr7 | 5987209 | ||
chr7:5987233
|
G | A | 4 | a0008a0009a0012others(1): Show | 18 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
missense_variant | MODERATE | c.1532C>T | p.Thr511Met | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1562/5093 | 1532/2589 | 511/862 | chr7 | 5987233 | ||
chr7:5987234
|
T | C | 2 | a0011a0027 | 4 | HG01069.hp2 HG01071.hp2 HG03942.hp2 others(1): Show |
missense_variant | MODERATE | c.1531A>G | p.Thr511Ala | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1561/5093 | 1531/2589 | 511/862 | chr7 | 5987234 | ||
chr7:5987291
|
TCTCCACC others(30): Show |
T | 1 | a0026 | 1 | NA18994.hp2 | frameshift_variant | HIGH | c.1437_1473delCGGACC others(31): Show |
p.His479fs | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1503/5093 | 1437/2589 | 479/862 | chr7 | 5987291 | ||
chr7:5987311
|
G | T | 2 | a0002a0017 | 87 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(84): Show |
missense_variant | MODERATE | c.1454C>A | p.Thr485Lys | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1484/5093 | 1454/2589 | 485/862 | chr7 | 5987311 | ||
chr7:5987327
|
C | T | 1 | a0022 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.1438G>A | p.Gly480Arg | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1468/5093 | 1438/2589 | 480/862 | chr7 | 5987327 | ||
chr7:5987328
|
G | C | 2 | a0016a0025 | 2 | HG00642.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.1437C>G | p.His479Gln | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1467/5093 | 1437/2589 | 479/862 | chr7 | 5987328 | ||
chr7:5987357
|
G | A | 9 | a0001a0008a0010others(6): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
missense_variant | MODERATE | c.1408C>T | p.Pro470Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1438/5093 | 1408/2589 | 470/862 | chr7 | 5987357 | ||
chr7:5987554
|
G | C | 1 | a0027 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1211C>G | p.Pro404Arg | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1241/5093 | 1211/2589 | 404/862 | chr7 | 5987554 | ||
chr7:6002611
|
C | T | 1 | a0028 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.379G>A | p.Ala127Thr | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/15 | 409/5093 | 379/2589 | 127/862 | chr7 | 6002611 | ||
chr7:6005996
|
C | T | 5 | a0006a0012a0014others(2): Show | 23 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(20): Show |
missense_variant | MODERATE | c.59G>A | p.Arg20Gln | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/15 | 89/5093 | 59/2589 | 20/862 | chr7 | 6005996 | ||
chr7:6006003
|
T | C | 1 | a0029 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.52A>G | p.Ile18Val | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/15 | 82/5093 | 52/2589 | 18/862 | chr7 | 6006003 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5973450
|
T | C | 1 | a0001c0024 | 2 | HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.2538A>G | p.Gly846Gly | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2568/5093 | 2538/2589 | 846/862 | chr7 | 5973450 | ||
chr7:5973522
|
A | G | 17 | a0001c0002a0001c0024a0001c0037others(14): Show | 104 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(101): Show |
synonymous_variant | LOW | c.2466T>C | p.Leu822Leu | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2496/5093 | 2466/2589 | 822/862 | chr7 | 5973522 | ||
chr7:5977693
|
G | A | 2 | a0006c0007a0015c0026 | 19 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(16): Show |
synonymous_variant | LOW | c.2340C>T | p.Pro780Pro | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/15 | 2370/5093 | 2340/2589 | 780/862 | chr7 | 5977693 | ||
chr7:5978618
|
A | G | 9 | a0006c0007a0007c0009a0007c0015others(6): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
synonymous_variant | LOW | c.2253T>C | p.Phe751Phe | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/15 | 2283/5093 | 2253/2589 | 751/862 | chr7 | 5978618 | ||
chr7:5982871
|
G | A | 1 | a0001c0037 | 1 | NA18999.hp1 | synonymous_variant | LOW | c.2127C>T | p.Phe709Phe | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/15 | 2157/5093 | 2127/2589 | 709/862 | chr7 | 5982871 | ||
chr7:5987208
|
A | G | 1 | a0003c0020 | 2 | HG03471.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1557T>C | p.Tyr519Tyr | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1587/5093 | 1557/2589 | 519/862 | chr7 | 5987208 | ||
chr7:5987277
|
G | A | 1 | a0003c0008 | 11 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(8): Show |
synonymous_variant | LOW | c.1488C>T | p.His496His | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1518/5093 | 1488/2589 | 496/862 | chr7 | 5987277 | ||
chr7:5987499
|
C | T | 1 | a0012c0019 | 2 | HG01891.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1266G>A | p.Glu422Glu | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/15 | 1296/5093 | 1266/2589 | 422/862 | chr7 | 5987499 | ||
chr7:5997349
|
G | C | 40 | a0001c0002a0001c0003a0001c0012others(37): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
synonymous_variant | LOW | c.780C>G | p.Ser260Ser | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/15 | 810/5093 | 780/2589 | 260/862 | chr7 | 5997349 | ||
chr7:5997391
|
G | C | 1 | a0001c0042 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.738C>G | p.Pro246Pro | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/15 | 768/5093 | 738/2589 | 246/862 | chr7 | 5997391 | ||
chr7:6003755
|
G | A | 4 | a0001c0012a0002c0001a0002c0043others(1): Show | 88 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
synonymous_variant | LOW | c.288C>T | p.Ala96Ala | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/15 | 318/5093 | 288/2589 | 96/862 | chr7 | 6003755 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5971011
|
G | C | 26 | a0001c0002t0002a0001c0002t0015a0001c0002t0028others(23): Show | 103 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2388C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2388 | chr7 | 5971011 | |||||
chr7:5971019
|
G | A | 3 | a0001c0003t0038a0001c0003t0039a0001c0010t0011 | 8 | HG01496.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2380C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2380 | chr7 | 5971019 | |||||
chr7:5971074
|
G | C | 1 | a0005c0006t0043 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2325C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2325 | chr7 | 5971074 | |||||
chr7:5971177
|
C | T | 9 | a0001c0002t0032a0001c0003t0021a0001c0010t0040others(6): Show | 37 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2222G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2222 | chr7 | 5971177 | |||||
chr7:5971231
|
G | C | 1 | a0004c0029t0035 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2168C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2168 | chr7 | 5971231 | |||||
chr7:5971305
|
GATC | G | 3 | a0001c0003t0038a0001c0003t0039a0001c0010t0011 | 8 | HG01496.hp2 HG02055.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2091_*2093delGAT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 2091 | chr7 | 5971305 | |||||
chr7:5971503
|
C | A | 1 | a0002c0001t0049 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1896G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1896 | chr7 | 5971503 | |||||
chr7:5971512
|
A | C | 1 | a0012c0019t0017 | 2 | HG01891.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1887T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1887 | chr7 | 5971512 | |||||
chr7:5971540
|
C | T | 1 | a0003c0004t0045 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1859G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1859 | chr7 | 5971540 | |||||
chr7:5971636
|
A | G | 88 | a0001c0002t0002a0001c0002t0008a0001c0002t0015others(85): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*1763T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1763 | chr7 | 5971636 | |||||
chr7:5971721
|
A | C | 1 | a0002c0001t0048 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1678T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1678 | chr7 | 5971721 | |||||
chr7:5971721
|
A | G | 1 | a0001c0002t0036 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1678T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1678 | chr7 | 5971721 | |||||
chr7:5971802
|
G | A | 24 | a0001c0002t0002a0001c0002t0015a0001c0002t0028others(21): Show | 88 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1597C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1597 | chr7 | 5971802 | |||||
chr7:5971805
|
C | G | 1 | a0003c0004t0044 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1594G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1594 | chr7 | 5971805 | |||||
chr7:5971938
|
G | A | 1 | a0001c0002t0033 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1461C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1461 | chr7 | 5971938 | |||||
chr7:5972034
|
GA | G | 30 | a0001c0003t0001a0001c0003t0021a0001c0003t0038others(27): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*1364delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1364 | chr7 | 5972034 | |||||
chr7:5972152
|
T | C | 1 | a0001c0003t0050 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1247A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1247 | chr7 | 5972152 | |||||
chr7:5972202
|
GC | G | 11 | a0003c0004t0004a0003c0004t0013a0003c0004t0020others(8): Show | 52 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1196delG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1196 | chr7 | 5972202 | |||||
chr7:5972260
|
G | A | 24 | a0001c0002t0008a0001c0002t0036a0001c0003t0008others(21): Show | 81 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1139C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1139 | chr7 | 5972260 | |||||
chr7:5972278
|
G | A | 2 | a0003c0008t0007a0003c0008t0046 | 11 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1121C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1121 | chr7 | 5972278 | |||||
chr7:5972285
|
C | T | 1 | a0001c0002t0031 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1114G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1114 | chr7 | 5972285 | |||||
chr7:5972291
|
C | G | 18 | a0001c0002t0002a0001c0002t0015a0001c0002t0028others(15): Show | 78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1108G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1108 | chr7 | 5972291 | |||||
chr7:5972367
|
T | C | 1 | a0002c0001t0051 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1032A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 1032 | chr7 | 5972367 | |||||
chr7:5972498
|
A | C | 1 | a0003c0020t0054 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 901 | chr7 | 5972498 | |||||
chr7:5972550
|
C | A | 1 | a0003c0004t0013 | 3 | HG01884.hp1 HG02257.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*849G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 849 | chr7 | 5972550 | |||||
chr7:5972550
|
C | T | 1 | a0001c0002t0030 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 849 | chr7 | 5972550 | |||||
chr7:5972551
|
G | A | 4 | a0007c0009t0009a0007c0009t0026a0007c0009t0037others(1): Show | 11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*848C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 848 | chr7 | 5972551 | |||||
chr7:5972674
|
C | G | 5 | a0005c0006t0005a0005c0006t0043a0010c0014t0042others(2): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*725G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 725 | chr7 | 5972674 | |||||
chr7:5972694
|
T | C | 25 | a0001c0003t0001a0001c0003t0014a0001c0003t0021others(22): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*705A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 705 | chr7 | 5972694 | |||||
chr7:5972749
|
C | T | 63 | a0001c0002t0002a0001c0002t0008a0001c0002t0015others(60): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*650G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 650 | chr7 | 5972749 | |||||
chr7:5972750
|
A | G | 63 | a0001c0002t0002a0001c0002t0008a0001c0002t0015others(60): Show | 227 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*649T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 649 | chr7 | 5972750 | |||||
chr7:5972824
|
GTTT | G | 24 | a0001c0003t0001a0001c0003t0014a0001c0003t0021others(21): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*572_*574delAAA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 572 | chr7 | 5972824 | |||||
chr7:5972833
|
T | G | 48 | a0001c0002t0002a0001c0002t0008a0001c0002t0028others(45): Show | 172 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*566A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 566 | chr7 | 5972833 | |||||
chr7:5972833
|
T | TG | 2 | a0001c0002t0015a0010c0014t0042 | 3 | HG01981.hp2 NA18960.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*565_*566insC | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 565 | chr7 | 5972833 | |||||
chr7:5972835
|
T | G | 1 | a0003c0008t0046 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 564 | chr7 | 5972835 | |||||
chr7:5972874
|
T | C | 88 | a0001c0002t0002a0001c0002t0008a0001c0002t0015others(85): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
3_prime_UTR_variant | MODIFIER | c.*525A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 525 | chr7 | 5972874 | |||||
chr7:5972876
|
C | CTA | 4 | a0001c0003t0038a0001c0003t0039a0001c0010t0011others(1): Show | 9 | HG01496.hp2 HG02055.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*521_*522dupTA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 522 | chr7 | 5972876 | |||||
chr7:5972896
|
C | T | 11 | a0003c0004t0004a0003c0004t0013a0003c0004t0020others(8): Show | 52 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*503G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 503 | chr7 | 5972896 | |||||
chr7:5972929
|
C | T | 2 | a0001c0003t0038a0001c0003t0039 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*470G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 470 | chr7 | 5972929 | |||||
chr7:5972938
|
G | A | 1 | a0002c0001t0052 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*461C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 461 | chr7 | 5972938 | |||||
chr7:5972993
|
G | A | 2 | a0003c0020t0054a0003c0020t0055 | 2 | HG03471.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*406C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 406 | chr7 | 5972993 | |||||
chr7:5973069
|
C | G | 6 | a0001c0003t0019a0005c0006t0005a0005c0006t0043others(3): Show | 34 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*330G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 330 | chr7 | 5973069 | |||||
chr7:5973085
|
C | T | 43 | a0001c0002t0002a0001c0002t0008a0001c0002t0015others(40): Show | 135 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*314G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 314 | chr7 | 5973085 | |||||
chr7:5973141
|
C | A | 1 | a0002c0001t0053 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*258G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 258 | chr7 | 5973141 | |||||
chr7:5973196
|
C | T | 1 | a0001c0002t0028 | 1 | NA18979.hp1 | 3_prime_UTR_variant | MODIFIER | c.*203G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 203 | chr7 | 5973196 | |||||
chr7:5973225
|
C | T | 1 | a0004c0005t0041 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*174G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 174 | chr7 | 5973225 | |||||
chr7:5973266
|
C | T | 1 | a0026c0036t0027 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*133G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 133 | chr7 | 5973266 | |||||
chr7:5973292
|
T | C | 2 | a0003c0020t0054a0003c0020t0055 | 2 | HG03471.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*107A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 107 | chr7 | 5973292 | |||||
chr7:5973306
|
G | GT | 46 | a0001c0002t0002a0001c0002t0008a0001c0002t0015others(43): Show | 142 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*92dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 92 | chr7 | 5973306 | |||||
chr7:5973306
|
G | T | 1 | a0006c0007t0025 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*93C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 93 | chr7 | 5973306 | |||||
chr7:5973365
|
C | T | 1 | a0007c0009t0026 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*34G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 34 | chr7 | 5973365 | |||||
chr7:5973382
|
C | G | 6 | a0006c0007t0006a0006c0007t0022a0006c0007t0023others(3): Show | 19 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*17G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 15/15 | 17 | chr7 | 5973382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:5973779
|
G | A | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2446-237C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5973779 | ||||||
chr7:5973861
|
C | T | 1 | a0027c0041t0004g0357 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2446-319G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5973861 | ||||||
chr7:5973970
|
G | A | 1 | a0009c0016t0010g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2446-428C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5973970 | ||||||
chr7:5974010
|
C | A | 2 | a0002c0001t0001g0148a0002c0001t0001g0165 | 2 | NA18962.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2446-468G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974010 | ||||||
chr7:5974135
|
C | G | 1 | a0001c0002t0036g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2446-593G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974135 | ||||||
chr7:5974221
|
C | G | 31 | a0005c0006t0005g0284a0005c0006t0005g0285a0005c0006t0005g0286others(28): Show | 31 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2446-679G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974221 | ||||||
chr7:5974397
|
A | AC | 384 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(381): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2446-856dupG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974397 | ||||||
chr7:5974403
|
C | T | 2 | a0007c0015t0010g0018a0007c0015t0010g0039 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2446-861G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974403 | ||||||
chr7:5974513
|
C | T | 1 | a0001c0003t0001g0086 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2446-971G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974513 | ||||||
chr7:5974549
|
C | A | 3 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112 | 3 | HG01106.hp2 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2446-1007G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974549 | ||||||
chr7:5974558
|
G | C | 6 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(3): Show | 6 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2446-1016C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974558 | ||||||
chr7:5974559
|
A | C | 1 | a0003c0020t0054g0366 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2446-1017T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974559 | ||||||
chr7:5974560
|
G | A | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2446-1018C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974560 | ||||||
chr7:5974613
|
G | A | 1 | a0010c0014t0042g0095 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2446-1071C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974613 | ||||||
chr7:5974676
|
C | T | 72 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(69): Show | 72 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.2446-1134G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974676 | ||||||
chr7:5974709
|
A | C | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2446-1167T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974709 | ||||||
chr7:5974718
|
C | T | 3 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112 | 3 | HG01106.hp2 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2446-1176G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974718 | ||||||
chr7:5974719
|
G | A | 1 | a0002c0001t0001g0151 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2446-1177C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974719 | ||||||
chr7:5974848
|
G | A | 1 | a0002c0001t0001g0172 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2446-1306C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974848 | ||||||
chr7:5974881
|
T | C | 33 | a0003c0020t0054g0366a0003c0020t0055g0367a0005c0006t0005g0284others(30): Show | 33 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.2446-1339A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974881 | ||||||
chr7:5974934
|
C | T | 5 | a0002c0001t0018g0129a0002c0001t0018g0149a0002c0001t0052g0128others(2): Show | 5 | HG00438.hp2 HG00609.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2446-1392G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974934 | ||||||
chr7:5974985
|
T | G | 114 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(111): Show | 115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.2446-1443A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5974985 | ||||||
chr7:5975022
|
G | T | 2 | a0003c0020t0054g0366a0003c0020t0055g0367 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2446-1480C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975022 | ||||||
chr7:5975215
|
G | A | 6 | a0003c0008t0007g0340a0003c0008t0007g0341a0003c0008t0007g0344others(3): Show | 6 | HG02055.hp1 HG02965.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2446-1673C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975215 | ||||||
chr7:5975262
|
T | C | 352 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(349): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.2446-1720A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975262 | ||||||
chr7:5975266
|
C | T | 1 | a0001c0003t0001g0086 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2446-1724G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975266 | ||||||
chr7:5975357
|
T | C | 81 | a0001c0003t0001g0004a0001c0003t0001g0008a0001c0003t0001g0009others(78): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2446-1815A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975357 | ||||||
chr7:5975367
|
A | T | 32 | a0005c0006t0005g0284a0005c0006t0005g0285a0005c0006t0005g0286others(29): Show | 32 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.2446-1825T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975367 | ||||||
chr7:5975442
|
C | T | 1 | a0002c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2446-1900G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975442 | ||||||
chr7:5975535
|
C | CT | 40 | a0001c0003t0001g0004a0001c0003t0001g0008a0001c0003t0001g0009others(37): Show | 44 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.2446-1994_2446-199 others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975535 | ||||||
chr7:5975536
|
C | CT | 28 | a0003c0004t0020g0308a0005c0006t0005g0286a0005c0006t0005g0287others(25): Show | 28 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.2446-1995dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | ||||||
chr7:5975536
|
C | T | 42 | a0001c0003t0001g0004a0001c0003t0001g0008a0001c0003t0001g0009others(39): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.2446-1994G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | ||||||
chr7:5975536
|
CT | C | 238 | a0001c0002t0002g0072a0001c0002t0002g0119a0001c0002t0002g0120others(235): Show | 247 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.2446-1995delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | ||||||
chr7:5975536
|
CTT | C | 18 | a0001c0002t0002g0201a0001c0002t0002g0222a0001c0002t0002g0245others(15): Show | 18 | HG00738.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.2446-1996_2446-199 others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975536 | ||||||
chr7:5975556
|
A | C | 1 | a0001c0002t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2446-2014T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975556 | ||||||
chr7:5975598
|
G | A | 3 | a0010c0014t0001g0025a0010c0014t0001g0073a0010c0014t0001g0114 | 3 | HG01243.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2445+1990C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975598 | ||||||
chr7:5975721
|
C | G | 216 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(213): Show | 223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2445+1867G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975721 | ||||||
chr7:5975724
|
A | G | 3 | a0002c0001t0001g0141a0002c0001t0001g0146a0002c0001t0001g0157 | 3 | HG00423.hp2 HG00621.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.2445+1864T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975724 | ||||||
chr7:5975874
|
C | A | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1714G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975874 | ||||||
chr7:5975895
|
A | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1693T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975895 | ||||||
chr7:5975899
|
C | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1689G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975899 | ||||||
chr7:5975918
|
TGTTTTTC others(16): Show |
T | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1647_2445+166 others(27): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975918 | ||||||
chr7:5975938
|
C | A | 1 | a0009c0016t0010g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2445+1650G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975938 | ||||||
chr7:5975944
|
C | T | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1644G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975944 | ||||||
chr7:5975949
|
C | T | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2445+1639G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975949 | ||||||
chr7:5975954
|
T | A | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1634A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975954 | ||||||
chr7:5975956
|
T | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1632A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975956 | ||||||
chr7:5975957
|
T | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1631A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975957 | ||||||
chr7:5975959
|
G | A | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1629C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975959 | ||||||
chr7:5975968
|
C | T | 12 | a0001c0002t0002g0072a0001c0002t0002g0213a0001c0002t0002g0228others(9): Show | 12 | HG00673.hp2 HG02015.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.2445+1620G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5975968 | ||||||
chr7:5976004
|
A | G | 240 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(237): Show | 243 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(240): Show |
intron_variant | MODIFIER | c.2445+1584T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976004 | ||||||
chr7:5976014
|
G | C | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1574C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976014 | ||||||
chr7:5976015
|
C | A | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1573G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976015 | ||||||
chr7:5976016
|
A | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1572T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976016 | ||||||
chr7:5976024
|
AG | A | 96 | a0001c0002t0002g0119a0001c0002t0002g0202a0001c0002t0002g0204others(93): Show | 99 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.2445+1563delC | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976024 | ||||||
chr7:5976038
|
A | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1550T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976038 | ||||||
chr7:5976060
|
G | C | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1528C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976060 | ||||||
chr7:5976062
|
A | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1526T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976062 | ||||||
chr7:5976068
|
A | G | 168 | a0001c0002t0002g0120a0001c0002t0002g0201a0001c0002t0002g0202others(165): Show | 171 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.2445+1520T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976068 | ||||||
chr7:5976076
|
T | C | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1512A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976076 | ||||||
chr7:5976083
|
A | T | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1505T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976083 | ||||||
chr7:5976084
|
T | A | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1504A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976084 | ||||||
chr7:5976088
|
A | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1500T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976088 | ||||||
chr7:5976100
|
G | C | 2 | a0001c0024t0008g0252a0001c0024t0008g0257 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2445+1488C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976100 | ||||||
chr7:5976107
|
G | C | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1481C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976107 | ||||||
chr7:5976108
|
T | C | 138 | a0001c0002t0002g0238a0001c0002t0002g0241a0001c0002t0002g0242others(135): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.2445+1480A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976108 | ||||||
chr7:5976129
|
G | A | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1459C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976129 | ||||||
chr7:5976142
|
A | T | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1446T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976142 | ||||||
chr7:5976145
|
A | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1443T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976145 | ||||||
chr7:5976167
|
C | T | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1421G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976167 | ||||||
chr7:5976168
|
G | C | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1420C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976168 | ||||||
chr7:5976175
|
G | A | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1413C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976175 | ||||||
chr7:5976194
|
T | G | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2445+1394A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976194 | ||||||
chr7:5976337
|
T | C | 8 | a0007c0009t0009g0019a0007c0009t0009g0021a0007c0009t0009g0022others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2445+1251A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976337 | ||||||
chr7:5976478
|
A | G | 250 | a0001c0002t0002g0120a0001c0002t0002g0210a0001c0002t0002g0262others(247): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.2445+1110T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976478 | ||||||
chr7:5976505
|
C | A | 1 | a0006c0007t0006g0332 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2445+1083G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976505 | ||||||
chr7:5976561
|
C | A | 1 | a0009c0016t0010g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2445+1027G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976561 | ||||||
chr7:5976642
|
T | G | 2 | a0003c0008t0007g0323a0009c0017t0003g0042 | 2 | HG03579.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2445+946A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976642 | ||||||
chr7:5976717
|
A | G | 43 | a0001c0002t0002g0267a0001c0003t0019g0090a0001c0003t0019g0091others(40): Show | 44 | HG00423.hp1 HG01346.hp2 HG01496.hp1 others(41): Show |
intron_variant | MODIFIER | c.2445+871T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976717 | ||||||
chr7:5976786
|
G | A | 6 | a0004c0005t0003g0015a0004c0005t0003g0016a0004c0005t0003g0048others(3): Show | 6 | HG02015.hp2 HG02071.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.2445+802C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976786 | ||||||
chr7:5976839
|
C | A | 45 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(42): Show | 51 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.2445+749G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976839 | ||||||
chr7:5976869
|
A | G | 1 | a0002c0001t0001g0170 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2445+719T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5976869 | ||||||
chr7:5977016
|
G | A | 2 | a0005c0006t0005g0285a0005c0006t0005g0291 | 2 | HG01123.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.2445+572C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977016 | ||||||
chr7:5977017
|
G | A | 1 | a0010c0014t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2445+571C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977017 | ||||||
chr7:5977029
|
TA | T | 200 | a0001c0002t0002g0201a0001c0002t0032g0064a0001c0002t0036g0098others(197): Show | 207 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2445+558delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977029 | ||||||
chr7:5977047
|
G | T | 67 | a0001c0002t0002g0201a0001c0003t0001g0265a0001c0010t0011g0031others(64): Show | 67 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2445+541C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977047 | ||||||
chr7:5977056
|
G | T | 4 | a0001c0003t0001g0068a0010c0014t0001g0025a0010c0014t0001g0073others(1): Show | 4 | HG01243.hp2 HG02818.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2445+532C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977056 | ||||||
chr7:5977136
|
G | C | 11 | a0001c0002t0002g0221a0001c0002t0002g0233a0002c0043t0001g0164others(8): Show | 11 | HG00642.hp2 HG01891.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.2445+452C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977136 | ||||||
chr7:5977140
|
C | T | 2 | a0001c0002t0002g0201a0001c0002t0032g0064 | 2 | HG01891.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2445+448G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977140 | ||||||
chr7:5977168
|
C | A | 1 | a0002c0001t0049g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2445+420G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977168 | ||||||
chr7:5977246
|
G | A | 4 | a0001c0002t0002g0239a0001c0002t0002g0248a0001c0002t0033g0249others(1): Show | 4 | HG00140.hp2 HG01106.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2445+342C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977246 | ||||||
chr7:5977258
|
T | C | 175 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(172): Show | 178 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.2445+330A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977258 | ||||||
chr7:5977345
|
A | G | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2445+243T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977345 | ||||||
chr7:5977346
|
T | C | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2445+242A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977346 | ||||||
chr7:5977375
|
G | T | 1 | a0002c0001t0001g0183 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2445+213C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977375 | ||||||
chr7:5977418
|
G | A | 122 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(119): Show | 123 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.2445+170C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977418 | ||||||
chr7:5977465
|
G | A | 1 | a0006c0007t0006g0374 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2445+123C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977465 | ||||||
chr7:5977494
|
G | A | 1 | a0004c0005t0003g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2445+94C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977494 | ||||||
chr7:5977496
|
T | G | 1 | a0003c0004t0020g0308 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2445+92A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977496 | ||||||
chr7:5977499
|
C | T | 1 | a0005c0006t0005g0311 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2445+89G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977499 | ||||||
chr7:5977532
|
C | T | 1 | a0003c0008t0007g0342 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2445+56G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 14/14 | chr7 | 5977532 | ||||||
chr7:5977831
|
C | T | 1 | a0001c0003t0001g0082 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2276-74G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977831 | ||||||
chr7:5977842
|
G | A | 2 | a0009c0017t0001g0106a0009c0017t0001g0109 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2276-85C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977842 | ||||||
chr7:5977843
|
G | C | 1 | a0001c0002t0002g0205 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2276-86C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977843 | ||||||
chr7:5977857
|
C | T | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-100G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977857 | ||||||
chr7:5977862
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-105C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977862 | ||||||
chr7:5977885
|
T | C | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-128A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977885 | ||||||
chr7:5977886
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-129C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977886 | ||||||
chr7:5977891
|
C | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-134G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977891 | ||||||
chr7:5977892
|
A | G | 88 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(85): Show | 89 | HG00280.hp1 HG00423.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.2276-135T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977892 | ||||||
chr7:5977895
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-138C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977895 | ||||||
chr7:5977916
|
C | G | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-159G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977916 | ||||||
chr7:5977956
|
A | G | 1 | a0003c0004t0008g0355 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2276-199T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5977956 | ||||||
chr7:5978028
|
G | A | 9 | a0001c0002t0002g0206a0001c0002t0002g0213a0001c0002t0002g0217others(6): Show | 9 | HG00673.hp2 HG02056.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.2276-271C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978028 | ||||||
chr7:5978033
|
T | C | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-276A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978033 | ||||||
chr7:5978074
|
CG | C | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-318delC | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978074 | ||||||
chr7:5978076
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-319C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978076 | ||||||
chr7:5978085
|
C | T | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-328G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978085 | ||||||
chr7:5978086
|
G | A | 5 | a0008c0011t0002g0256a0008c0011t0002g0258a0008c0011t0002g0274others(2): Show | 5 | HG02717.hp1 NA18977.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.2276-329C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978086 | ||||||
chr7:5978120
|
C | CAA | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-364_2276-363i others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978120 | ||||||
chr7:5978132
|
A | AAAAAAT | 38 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(35): Show | 39 | HG00423.hp1 HG00738.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.2276-376_2276-375i others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978132 | ||||||
chr7:5978141
|
C | T | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-384G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978141 | ||||||
chr7:5978155
|
A | C | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-398T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978155 | ||||||
chr7:5978157
|
C | G | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-400G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978157 | ||||||
chr7:5978176
|
A | G | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2276-419T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978176 | ||||||
chr7:5978180
|
A | AC | 40 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(37): Show | 41 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2275+415dupG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978180 | ||||||
chr7:5978201
|
T | TA | 18 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(15): Show | 19 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2275+394_2275+395i others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978201 | ||||||
chr7:5978202
|
T | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+394A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978202 | ||||||
chr7:5978211
|
C | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+385G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978211 | ||||||
chr7:5978212
|
T | C | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+384A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978212 | ||||||
chr7:5978213
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+383C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978213 | ||||||
chr7:5978253
|
A | G | 1 | a0003c0004t0045g0378 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2275+343T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978253 | ||||||
chr7:5978271
|
G | A | 320 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(317): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2275+325C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978271 | ||||||
chr7:5978272
|
A | AT | 9 | a0001c0002t0028g0226a0001c0003t0001g0086a0001c0003t0008g0208others(6): Show | 9 | HG01361.hp2 HG02717.hp1 NA18977.hp2 others(6): Show |
intron_variant | MODIFIER | c.2275+323dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978272 | ||||||
chr7:5978272
|
A | ATT | 14 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(11): Show | 14 | HG01109.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.2275+322_2275+323d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978272 | ||||||
chr7:5978272
|
A | ATTT | 27 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(24): Show | 28 | HG00423.hp1 HG00738.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.2275+321_2275+323d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978272 | ||||||
chr7:5978273
|
T | A | 1 | a0003c0004t0012g0203 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2275+323A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978273 | ||||||
chr7:5978302
|
C | T | 5 | a0003c0004t0004g0012a0003c0004t0004g0347a0003c0004t0004g0353others(2): Show | 6 | HG00621.hp2 HG02027.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.2275+294G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978302 | ||||||
chr7:5978340
|
G | A | 1 | a0003c0031t0008g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2275+256C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978340 | ||||||
chr7:5978391
|
C | T | 2 | a0007c0015t0010g0018a0007c0015t0010g0039 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2275+205G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978391 | ||||||
chr7:5978426
|
AC | A | 4 | a0004c0005t0003g0001a0004c0005t0003g0047a0004c0005t0003g0051others(1): Show | 8 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.2275+169delG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978426 | ||||||
chr7:5978427
|
C | G | 46 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(43): Show | 47 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2275+169G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978427 | ||||||
chr7:5978459
|
T | C | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2275+137A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978459 | ||||||
chr7:5978470
|
C | G | 2 | a0002c0013t0001g0176a0002c0013t0001g0177 | 2 | HG00639.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2275+126G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978470 | ||||||
chr7:5978479
|
C | G | 43 | a0003c0004t0004g0350a0003c0004t0004g0351a0006c0007t0006g0011others(40): Show | 44 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2275+117G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978479 | ||||||
chr7:5978571
|
G | A | 2 | a0003c0020t0054g0366a0003c0020t0055g0367 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2275+25C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 13/14 | chr7 | 5978571 | ||||||
chr7:5978747
|
C | G | 9 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(6): Show | 9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2175-51G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978747 | ||||||
chr7:5978813
|
A | G | 136 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0265others(133): Show | 141 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.2175-117T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978813 | ||||||
chr7:5978822
|
C | T | 1 | a0002c0001t0049g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2175-126G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978822 | ||||||
chr7:5978824
|
C | T | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-128G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978824 | ||||||
chr7:5978825
|
T | A | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-129A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978825 | ||||||
chr7:5978827
|
C | T | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-131G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978827 | ||||||
chr7:5978882
|
A | G | 8 | a0007c0009t0009g0019a0007c0009t0009g0021a0007c0009t0009g0022others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175-186T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978882 | ||||||
chr7:5978904
|
G | A | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-208C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978904 | ||||||
chr7:5978958
|
C | G | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-262G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978958 | ||||||
chr7:5978960
|
C | T | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-264G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978960 | ||||||
chr7:5978961
|
G | A | 33 | a0002c0001t0001g0005a0002c0001t0001g0010a0002c0001t0001g0104others(30): Show | 36 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.2175-265C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978961 | ||||||
chr7:5978963
|
G | C | 1 | a0005c0006t0005g0296 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2175-267C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978963 | ||||||
chr7:5978983
|
C | T | 1 | a0001c0002t0002g0240 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2175-287G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978983 | ||||||
chr7:5978988
|
A | AGTTTGAG others(8): Show |
1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.2175-307_2175-293d others(17): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978988 | ||||||
chr7:5978997
|
C | T | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-301G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978997 | ||||||
chr7:5978999
|
G | A | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-303C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5978999 | ||||||
chr7:5979013
|
A | G | 42 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(39): Show | 43 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2175-317T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979013 | ||||||
chr7:5979016
|
G | A | 10 | a0002c0001t0014g0173a0009c0016t0010g0017a0009c0016t0010g0103others(7): Show | 10 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2175-320C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979016 | ||||||
chr7:5979021
|
A | C | 48 | a0001c0002t0002g0238a0001c0003t0001g0115a0003c0004t0008g0355others(45): Show | 49 | HG00099.hp1 HG00423.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2175-325T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979021 | ||||||
chr7:5979039
|
A | G | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-343T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979039 | ||||||
chr7:5979103
|
T | G | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-407A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979103 | ||||||
chr7:5979140
|
T | C | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-444A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979140 | ||||||
chr7:5979159
|
G | A | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-463C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979159 | ||||||
chr7:5979165
|
G | A | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-469C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979165 | ||||||
chr7:5979179
|
G | A | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-483C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979179 | ||||||
chr7:5979180
|
C | T | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-484G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979180 | ||||||
chr7:5979181
|
G | A | 1 | a0001c0002t0002g0233 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2175-485C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979181 | ||||||
chr7:5979185
|
C | T | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-489G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979185 | ||||||
chr7:5979186
|
A | G | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-490T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979186 | ||||||
chr7:5979201
|
C | CA | 116 | a0001c0002t0002g0113a0001c0002t0002g0206a0001c0002t0002g0222others(113): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.2175-506dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | ||||||
chr7:5979201
|
C | CAA | 13 | a0001c0003t0001g0085a0001c0003t0001g0087a0001c0003t0050g0077others(10): Show | 13 | HG01175.hp1 HG01175.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.2175-507_2175-506d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | ||||||
chr7:5979201
|
C | CAAA | 58 | a0002c0001t0001g0005a0002c0001t0001g0104a0002c0001t0001g0123others(55): Show | 60 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.2175-508_2175-506d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | ||||||
chr7:5979201
|
C | CAAAA | 34 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0265others(31): Show | 35 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.2175-509_2175-506d others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | ||||||
chr7:5979201
|
C | CAAAAA | 14 | a0002c0001t0001g0161a0002c0001t0001g0192a0006c0007t0006g0375others(11): Show | 14 | HG01109.hp1 HG01496.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2175-510_2175-506d others(7): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | ||||||
chr7:5979201
|
C | CAAAAAA | 17 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0331others(14): Show | 18 | HG00738.hp2 HG01346.hp2 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.2175-511_2175-506d others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979201 | ||||||
chr7:5979217
|
A | C | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-521T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979217 | ||||||
chr7:5979230
|
T | C | 41 | a0004c0029t0035g0057a0006c0007t0006g0011a0006c0007t0006g0320others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-534A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979230 | ||||||
chr7:5979231
|
A | C | 1 | a0018c0035t0010g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2175-535T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979231 | ||||||
chr7:5979236
|
C | G | 1 | a0018c0035t0010g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2175-540G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979236 | ||||||
chr7:5979252
|
G | A | 1 | a0018c0035t0010g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2175-556C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979252 | ||||||
chr7:5979385
|
T | C | 8 | a0001c0003t0001g0066a0001c0003t0001g0067a0002c0001t0001g0183others(5): Show | 8 | HG02074.hp2 HG02155.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.2175-689A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979385 | ||||||
chr7:5979387
|
T | A | 30 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(27): Show | 31 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.2175-691A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979387 | ||||||
chr7:5979390
|
C | CA | 51 | a0001c0003t0001g0088a0001c0003t0050g0077a0002c0001t0001g0158others(48): Show | 52 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.2175-695dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979390 | ||||||
chr7:5979409
|
C | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-713G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979409 | ||||||
chr7:5979410
|
A | T | 1 | a0001c0012t0002g0179 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2175-714T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979410 | ||||||
chr7:5979470
|
T | C | 3 | a0007c0009t0009g0020a0007c0009t0026g0027a0007c0009t0037g0026 | 3 | HG02809.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2175-774A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979470 | ||||||
chr7:5979519
|
C | T | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-823G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979519 | ||||||
chr7:5979532
|
C | G | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-836G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979532 | ||||||
chr7:5979593
|
T | A | 378 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(375): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.2175-897A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979593 | ||||||
chr7:5979622
|
G | C | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-926C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979622 | ||||||
chr7:5979643
|
C | T | 130 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(127): Show | 131 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.2175-947G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979643 | ||||||
chr7:5979665
|
T | A | 128 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(125): Show | 129 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2175-969A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979665 | ||||||
chr7:5979665
|
T | C | 2 | a0001c0002t0002g0240a0014c0025t0001g0368 | 2 | HG02129.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2175-969A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979665 | ||||||
chr7:5979666
|
T | G | 128 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(125): Show | 129 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2175-970A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979666 | ||||||
chr7:5979668
|
G | GCTT | 127 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(124): Show | 128 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.2175-973_2175-972i others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979668 | ||||||
chr7:5979668
|
G | T | 2 | a0001c0002t0002g0240a0014c0025t0001g0368 | 2 | HG02129.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2175-972C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979668 | ||||||
chr7:5979713
|
G | T | 2 | a0012c0019t0017g0376a0012c0019t0017g0377 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2175-1017C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979713 | ||||||
chr7:5979899
|
C | G | 11 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2175-1203G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979899 | ||||||
chr7:5979924
|
G | C | 1 | a0004c0029t0035g0057 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2175-1228C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979924 | ||||||
chr7:5979984
|
G | A | 1 | a0004c0005t0003g0041 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2175-1288C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5979984 | ||||||
chr7:5980320
|
ACAGGGGC others(8): Show |
A | 1 | a0001c0002t0002g0262 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2175-1639_2175-162 others(19): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980320 | ||||||
chr7:5980342
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1646C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980342 | ||||||
chr7:5980435
|
T | C | 44 | a0002c0013t0001g0199a0002c0013t0001g0200a0003c0020t0055g0367others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.2175-1739A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980435 | ||||||
chr7:5980453
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1757C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980453 | ||||||
chr7:5980482
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2175-1786C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980482 | ||||||
chr7:5980498
|
A | G | 319 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(316): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.2175-1802T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980498 | ||||||
chr7:5980534
|
T | C | 1 | a0004c0021t0003g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2175-1838A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980534 | ||||||
chr7:5980552
|
G | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1856C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980552 | ||||||
chr7:5980567
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2175-1871G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980567 | ||||||
chr7:5980705
|
A | C | 5 | a0003c0004t0004g0012a0003c0004t0004g0347a0003c0004t0004g0353others(2): Show | 6 | HG00621.hp2 HG02027.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.2175-2009T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980705 | ||||||
chr7:5980919
|
C | CAAACTAC others(137): Show |
1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1904_2174+190 others(148): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980919 | ||||||
chr7:5980943
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1881A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980943 | ||||||
chr7:5980956
|
A | G | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2174+1868T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980956 | ||||||
chr7:5980967
|
C | T | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2174+1857G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5980967 | ||||||
chr7:5981042
|
G | T | 1 | a0002c0001t0001g0154 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2174+1782C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981042 | ||||||
chr7:5981068
|
T | C | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2174+1756A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981068 | ||||||
chr7:5981080
|
C | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1744G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981080 | ||||||
chr7:5981127
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1697G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981127 | ||||||
chr7:5981142
|
G | C | 1 | a0005c0006t0043g0317 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2174+1682C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981142 | ||||||
chr7:5981143
|
T | C | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2174+1681A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981143 | ||||||
chr7:5981150
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1674C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981150 | ||||||
chr7:5981165
|
T | C | 2 | a0001c0012t0002g0101a0014c0025t0001g0368 | 2 | HG02135.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2174+1659A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981165 | ||||||
chr7:5981172
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1652C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981172 | ||||||
chr7:5981179
|
G | C | 1 | a0003c0004t0004g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2174+1645C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981179 | ||||||
chr7:5981234
|
A | G | 42 | a0002c0013t0001g0199a0002c0013t0001g0200a0006c0007t0006g0011others(39): Show | 43 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2174+1590T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981234 | ||||||
chr7:5981348
|
G | A | 2 | a0003c0004t0008g0355a0003c0004t0008g0356 | 2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.2174+1476C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981348 | ||||||
chr7:5981377
|
T | C | 2 | a0002c0001t0051g0130a0002c0001t0053g0187 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2174+1447A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981377 | ||||||
chr7:5981391
|
C | T | 87 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(84): Show | 87 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.2174+1433G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981391 | ||||||
chr7:5981399
|
C | G | 87 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(84): Show | 87 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.2174+1425G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981399 | ||||||
chr7:5981412
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1412A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981412 | ||||||
chr7:5981719
|
G | A | 4 | a0001c0002t0002g0228a0001c0003t0001g0070a0001c0003t0001g0080others(1): Show | 4 | HG00673.hp2 HG02615.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2174+1105C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981719 | ||||||
chr7:5981725
|
T | G | 3 | a0001c0003t0001g0070a0001c0003t0001g0080a0014c0025t0001g0368 | 3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+1099A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981725 | ||||||
chr7:5981726
|
A | G | 3 | a0001c0003t0001g0070a0001c0003t0001g0080a0014c0025t0001g0368 | 3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+1098T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981726 | ||||||
chr7:5981727
|
C | T | 3 | a0001c0003t0001g0070a0001c0003t0001g0080a0014c0025t0001g0368 | 3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+1097G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981727 | ||||||
chr7:5981762
|
G | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+1062C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981762 | ||||||
chr7:5981838
|
C | T | 3 | a0001c0003t0001g0070a0001c0003t0001g0080a0014c0025t0001g0368 | 3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+986G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981838 | ||||||
chr7:5981839
|
C | G | 3 | a0001c0003t0001g0070a0001c0003t0001g0080a0014c0025t0001g0368 | 3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+985G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981839 | ||||||
chr7:5981841
|
T | C | 3 | a0001c0003t0001g0070a0001c0003t0001g0080a0014c0025t0001g0368 | 3 | HG02615.hp2 HG02717.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2174+983A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981841 | ||||||
chr7:5981865
|
T | A | 1 | a0004c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2174+959A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981865 | ||||||
chr7:5981910
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+914G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981910 | ||||||
chr7:5981912
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+912C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981912 | ||||||
chr7:5981920
|
G | T | 1 | a0001c0003t0001g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2174+904C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981920 | ||||||
chr7:5981973
|
T | C | 2 | a0007c0015t0010g0018a0007c0015t0010g0039 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2174+851A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981973 | ||||||
chr7:5981992
|
A | C | 3 | a0001c0002t0008g0251a0001c0024t0008g0252a0001c0024t0008g0257 | 3 | HG01070.hp1 HG01071.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2174+832T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981992 | ||||||
chr7:5981995
|
T | C | 85 | a0001c0003t0001g0265a0002c0001t0001g0005a0002c0001t0001g0010others(82): Show | 88 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2174+829A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5981995 | ||||||
chr7:5982149
|
G | A | 1 | a0003c0004t0012g0203 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2174+675C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982149 | ||||||
chr7:5982177
|
A | G | 44 | a0002c0013t0001g0199a0002c0013t0001g0200a0006c0007t0006g0011others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.2174+647T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982177 | ||||||
chr7:5982291
|
C | T | 88 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(85): Show | 88 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.2174+533G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982291 | ||||||
chr7:5982299
|
G | A | 1 | a0005c0006t0005g0307 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2174+525C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982299 | ||||||
chr7:5982383
|
T | C | 2 | a0003c0004t0004g0336a0003c0004t0004g0337 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2174+441A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982383 | ||||||
chr7:5982432
|
G | A | 13 | a0002c0001t0001g0100a0002c0001t0001g0122a0002c0001t0001g0147others(10): Show | 13 | NA18941.hp2 NA18948.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.2174+392C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982432 | ||||||
chr7:5982471
|
C | T | 2 | a0002c0001t0014g0173a0014c0025t0001g0368 | 2 | HG02717.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.2174+353G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982471 | ||||||
chr7:5982479
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+345A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982479 | ||||||
chr7:5982483
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+341G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982483 | ||||||
chr7:5982547
|
G | C | 87 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0265others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.2174+277C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982547 | ||||||
chr7:5982629
|
G | A | 9 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(6): Show | 9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2174+195C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982629 | ||||||
chr7:5982712
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+112C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982712 | ||||||
chr7:5982721
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+103C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982721 | ||||||
chr7:5982763
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2174+61A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 12/14 | chr7 | 5982763 | ||||||
chr7:5982995
|
C | T | 83 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(80): Show | 83 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(80): Show |
splice_region_variant&intron_variant | LOW | c.2007-4G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5982995 | ||||||
chr7:5982998
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2007-7C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5982998 | ||||||
chr7:5983118
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-127A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983118 | ||||||
chr7:5983142
|
T | C | 15 | a0006c0007t0006g0370a0006c0007t0006g0375a0007c0009t0009g0019others(12): Show | 15 | HG01496.hp1 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2007-151A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983142 | ||||||
chr7:5983144
|
G | A | 1 | a0003c0020t0054g0366 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2007-153C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983144 | ||||||
chr7:5983154
|
C | T | 6 | a0005c0006t0005g0311a0005c0006t0005g0315a0005c0006t0005g0316others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2007-163G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983154 | ||||||
chr7:5983278
|
T | C | 53 | a0001c0002t0036g0098a0001c0003t0001g0004a0001c0003t0001g0008others(50): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.2007-287A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983278 | ||||||
chr7:5983281
|
T | C | 5 | a0001c0003t0008g0208a0001c0003t0008g0219a0001c0003t0008g0225others(2): Show | 5 | NA18941.hp2 NA18985.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.2007-290A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983281 | ||||||
chr7:5983330
|
C | T | 187 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(184): Show | 191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2007-339G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983330 | ||||||
chr7:5983347
|
G | C | 2 | a0006c0007t0006g0369a0006c0007t0006g0372 | 2 | HG02129.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.2007-356C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983347 | ||||||
chr7:5983349
|
T | A | 1 | a0020c0030t0003g0053 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2007-358A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983349 | ||||||
chr7:5983389
|
G | A | 11 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2007-398C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983389 | ||||||
chr7:5983400
|
C | T | 3 | a0001c0003t0001g0265a0010c0014t0042g0095a0014c0025t0001g0368 | 3 | HG02717.hp1 NA18960.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2007-409G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983400 | ||||||
chr7:5983402
|
T | C | 100 | a0001c0002t0036g0098a0001c0003t0001g0004a0001c0003t0001g0008others(97): Show | 105 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2007-411A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983402 | ||||||
chr7:5983527
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-536G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983527 | ||||||
chr7:5983528
|
A | T | 1 | a0001c0002t0015g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2007-537T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983528 | ||||||
chr7:5983579
|
A | G | 1 | a0002c0001t0052g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2007-588T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983579 | ||||||
chr7:5983591
|
C | T | 1 | a0003c0004t0012g0203 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2007-600G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983591 | ||||||
chr7:5983607
|
C | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-616G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983607 | ||||||
chr7:5983609
|
A | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-618T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983609 | ||||||
chr7:5983615
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-624G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983615 | ||||||
chr7:5983653
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-662A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983653 | ||||||
chr7:5983681
|
A | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-690T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983681 | ||||||
chr7:5983714
|
T | C | 2 | a0001c0002t0030g0212a0014c0025t0001g0368 | 2 | HG02040.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2007-723A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983714 | ||||||
chr7:5983719
|
G | A | 1 | a0002c0001t0049g0198 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2007-728C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983719 | ||||||
chr7:5983745
|
A | G | 2 | a0002c0001t0001g0139a0002c0001t0001g0197 | 2 | NA18951.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2007-754T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983745 | ||||||
chr7:5983754
|
C | T | 1 | a0004c0005t0003g0048 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2007-763G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983754 | ||||||
chr7:5983941
|
C | T | 94 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(91): Show | 94 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.2007-950G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983941 | ||||||
chr7:5983942
|
G | A | 41 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(38): Show | 42 | HG00423.hp1 HG00738.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.2007-951C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983942 | ||||||
chr7:5983947
|
T | C | 44 | a0002c0013t0001g0199a0002c0013t0001g0200a0006c0007t0006g0011others(41): Show | 45 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.2007-956A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983947 | ||||||
chr7:5983949
|
G | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-958C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983949 | ||||||
chr7:5983990
|
C | T | 1 | a0003c0020t0055g0367 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2007-999G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5983990 | ||||||
chr7:5984006
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1015A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984006 | ||||||
chr7:5984025
|
A | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1034T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984025 | ||||||
chr7:5984040
|
A | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1049T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984040 | ||||||
chr7:5984061
|
C | T | 2 | a0004c0005t0003g0041a0014c0025t0001g0368 | 2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2007-1070G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984061 | ||||||
chr7:5984078
|
C | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1087G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984078 | ||||||
chr7:5984088
|
T | C | 1 | a0001c0003t0001g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2007-1097A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984088 | ||||||
chr7:5984138
|
G | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1147C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984138 | ||||||
chr7:5984142
|
G | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1151C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984142 | ||||||
chr7:5984153
|
A | G | 1 | a0001c0002t0002g0222 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2007-1162T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984153 | ||||||
chr7:5984161
|
C | T | 2 | a0002c0001t0053g0187a0014c0025t0001g0368 | 2 | HG02717.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2007-1170G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984161 | ||||||
chr7:5984295
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1304A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984295 | ||||||
chr7:5984320
|
C | T | 9 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(6): Show | 9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2007-1329G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984320 | ||||||
chr7:5984387
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1396G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984387 | ||||||
chr7:5984404
|
G | A | 48 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(45): Show | 54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.2007-1413C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984404 | ||||||
chr7:5984407
|
G | T | 38 | a0006c0007t0006g0011a0006c0007t0006g0320a0006c0007t0006g0330others(35): Show | 39 | HG00423.hp1 HG00738.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.2007-1416C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984407 | ||||||
chr7:5984412
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1421A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984412 | ||||||
chr7:5984433
|
G | A | 2 | a0003c0020t0054g0366a0003c0020t0055g0367 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2007-1442C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984433 | ||||||
chr7:5984440
|
T | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1449A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984440 | ||||||
chr7:5984517
|
C | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1526G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984517 | ||||||
chr7:5984522
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1531C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984522 | ||||||
chr7:5984646
|
A | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1655T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984646 | ||||||
chr7:5984649
|
G | A | 1 | a0005c0006t0005g0304 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2007-1658C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984649 | ||||||
chr7:5984721
|
C | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1730G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984721 | ||||||
chr7:5984727
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1736C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984727 | ||||||
chr7:5984763
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1772G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984763 | ||||||
chr7:5984794
|
A | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1803T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984794 | ||||||
chr7:5984796
|
C | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2007-1805G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984796 | ||||||
chr7:5984852
|
A | G | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2007-1861T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984852 | ||||||
chr7:5984913
|
C | T | 1 | a0003c0004t0004g0363 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2006+1846G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984913 | ||||||
chr7:5984999
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1760C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5984999 | ||||||
chr7:5985039
|
A | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1720T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985039 | ||||||
chr7:5985046
|
G | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1713C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985046 | ||||||
chr7:5985055
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1704C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985055 | ||||||
chr7:5985105
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1654G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985105 | ||||||
chr7:5985147
|
G | A | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1612C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985147 | ||||||
chr7:5985163
|
T | G | 15 | a0003c0004t0004g0012a0003c0004t0004g0347a0003c0004t0004g0353others(12): Show | 16 | HG00621.hp2 HG02027.hp2 HG02300.hp1 others(13): Show |
intron_variant | MODIFIER | c.2006+1596A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985163 | ||||||
chr7:5985179
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+1580G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985179 | ||||||
chr7:5985228
|
C | T | 9 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(6): Show | 9 | HG01346.hp2 HG01891.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2006+1531G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985228 | ||||||
chr7:5985260
|
G | C | 1 | a0001c0002t0002g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2006+1499C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985260 | ||||||
chr7:5985264
|
A | AT | 94 | a0001c0002t0002g0113a0001c0002t0002g0215a0001c0002t0002g0222others(91): Show | 100 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.2006+1494dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985264 | ||||||
chr7:5985264
|
A | ATT | 8 | a0002c0001t0001g0100a0003c0004t0004g0350a0003c0004t0004g0382others(5): Show | 8 | HG01261.hp2 HG01358.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2006+1493_2006+149 others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985264 | ||||||
chr7:5985264
|
AT | A | 8 | a0001c0003t0002g0250a0002c0001t0001g0123a0002c0001t0001g0139others(5): Show | 8 | HG00558.hp2 HG01168.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.2006+1494delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985264 | ||||||
chr7:5985505
|
G | A | 43 | a0002c0013t0001g0199a0002c0013t0001g0200a0006c0007t0006g0011others(40): Show | 44 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.2006+1254C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985505 | ||||||
chr7:5985639
|
C | T | 2 | a0001c0003t0038g0278a0001c0003t0039g0277 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2006+1120G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985639 | ||||||
chr7:5985647
|
G | A | 82 | a0002c0001t0001g0005a0002c0001t0001g0010a0002c0001t0001g0100others(79): Show | 85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2006+1112C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985647 | ||||||
chr7:5985911
|
G | A | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2006+848C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985911 | ||||||
chr7:5985914
|
C | T | 2 | a0007c0015t0010g0018a0007c0015t0010g0039 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.2006+845G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985914 | ||||||
chr7:5985982
|
C | T | 1 | a0002c0001t0001g0194 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2006+777G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5985982 | ||||||
chr7:5986072
|
A | G | 230 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(227): Show | 237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.2006+687T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986072 | ||||||
chr7:5986214
|
C | T | 137 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(134): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2006+545G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986214 | ||||||
chr7:5986263
|
C | T | 33 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(30): Show | 39 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2006+496G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986263 | ||||||
chr7:5986349
|
G | A | 25 | a0005c0006t0005g0284a0005c0006t0005g0285a0005c0006t0005g0286others(22): Show | 25 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.2006+410C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986349 | ||||||
chr7:5986462
|
T | C | 3 | a0006c0007t0006g0370a0006c0007t0006g0375a0015c0026t0006g0371 | 3 | HG01496.hp1 HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2006+297A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986462 | ||||||
chr7:5986490
|
G | A | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.2006+269C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986490 | ||||||
chr7:5986561
|
G | A | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2006+198C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986561 | ||||||
chr7:5986591
|
C | CTGA | 49 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(46): Show | 55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.2006+165_2006+167d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986591 | ||||||
chr7:5986597
|
C | T | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2006+162G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986597 | ||||||
chr7:5986753
|
C | T | 82 | a0002c0001t0001g0005a0002c0001t0001g0010a0002c0001t0001g0100others(79): Show | 85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
splice_region_variant&intron_variant | LOW | c.2006+6G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 11/14 | chr7 | 5986753 | ||||||
chr7:5987736
|
G | A | 6 | a0001c0002t0002g0119a0001c0002t0002g0243a0001c0002t0002g0262others(3): Show | 6 | HG01192.hp1 HG01978.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1145-116C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5987736 | ||||||
chr7:5987818
|
G | A | 2 | a0002c0001t0018g0129a0002c0001t0018g0149 | 2 | HG00438.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1145-198C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5987818 | ||||||
chr7:5988009
|
C | T | 93 | a0001c0002t0002g0113a0001c0002t0002g0119a0001c0002t0002g0120others(90): Show | 93 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1145-389G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988009 | ||||||
chr7:5988052
|
C | CA | 28 | a0001c0002t0002g0113a0001c0002t0002g0204a0001c0002t0002g0205others(25): Show | 28 | HG00673.hp2 HG01071.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.1145-433dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988052 | ||||||
chr7:5988052
|
CA | C | 103 | a0001c0002t0002g0072a0001c0002t0002g0223a0001c0002t0036g0098others(100): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1145-433delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988052 | ||||||
chr7:5988052
|
CAA | C | 109 | a0002c0001t0001g0005a0002c0001t0001g0010a0002c0001t0001g0104others(106): Show | 112 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.1145-434_1145-433d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988052 | ||||||
chr7:5988071
|
A | C | 32 | a0003c0020t0054g0366a0004c0005t0001g0060a0004c0005t0003g0001others(29): Show | 41 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1145-451T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988071 | ||||||
chr7:5988073
|
A | C | 2 | a0003c0004t0013g0014a0003c0004t0013g0365 | 3 | HG01884.hp1 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1145-453T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988073 | ||||||
chr7:5988093
|
A | G | 1 | a0001c0003t0001g0283 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1145-473T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988093 | ||||||
chr7:5988094
|
A | G | 1 | a0002c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1145-474T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988094 | ||||||
chr7:5988293
|
C | T | 2 | a0001c0003t0038g0278a0001c0003t0039g0277 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1145-673G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988293 | ||||||
chr7:5988406
|
A | T | 1 | a0007c0015t0010g0039 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1145-786T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988406 | ||||||
chr7:5988506
|
C | T | 1 | a0001c0003t0001g0310 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1145-886G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988506 | ||||||
chr7:5988548
|
G | C | 2 | a0001c0003t0001g0009a0001c0003t0001g0089 | 3 | HG02622.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1145-928C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988548 | ||||||
chr7:5988556
|
C | T | 1 | a0020c0030t0003g0053 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1145-936G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988556 | ||||||
chr7:5988559
|
T | C | 84 | a0001c0003t0001g0066a0001c0003t0001g0067a0002c0001t0001g0005others(81): Show | 87 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1145-939A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988559 | ||||||
chr7:5988755
|
A | C | 1 | a0003c0004t0045g0378 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1144+1045T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988755 | ||||||
chr7:5988850
|
TTTTG | T | 83 | a0001c0003t0001g0066a0001c0003t0001g0067a0002c0001t0001g0005others(80): Show | 86 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1144+946_1144+949d others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988850 | ||||||
chr7:5988879
|
G | T | 1 | a0002c0001t0001g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1144+921C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988879 | ||||||
chr7:5988946
|
C | G | 4 | a0001c0002t0002g0239a0001c0002t0002g0248a0001c0002t0033g0249others(1): Show | 4 | HG00140.hp2 HG01106.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+854G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988946 | ||||||
chr7:5988969
|
A | C | 1 | a0006c0007t0024g0096 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1144+831T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5988969 | ||||||
chr7:5989005
|
G | A | 2 | a0002c0013t0001g0176a0002c0013t0001g0177 | 2 | HG00639.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1144+795C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989005 | ||||||
chr7:5989016
|
C | T | 136 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(133): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1144+784G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989016 | ||||||
chr7:5989056
|
C | T | 78 | a0001c0002t0002g0113a0001c0002t0002g0119a0001c0002t0002g0120others(75): Show | 78 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1144+744G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989056 | ||||||
chr7:5989065
|
T | C | 23 | a0001c0003t0021g0116a0002c0013t0001g0199a0002c0013t0001g0200others(20): Show | 24 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1144+735A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989065 | ||||||
chr7:5989088
|
G | A | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1144+712C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989088 | ||||||
chr7:5989120
|
G | T | 5 | a0003c0004t0004g0012a0003c0004t0004g0347a0003c0004t0004g0353others(2): Show | 6 | HG00621.hp2 HG02027.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144+680C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989120 | ||||||
chr7:5989130
|
A | G | 3 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112 | 3 | HG01106.hp2 HG01346.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1144+670T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989130 | ||||||
chr7:5989137
|
G | A | 311 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(308): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1144+663C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989137 | ||||||
chr7:5989141
|
C | A | 1 | a0001c0042t0001g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1144+659G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989141 | ||||||
chr7:5989220
|
C | T | 1 | a0001c0002t0032g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1144+580G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989220 | ||||||
chr7:5989274
|
T | C | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+526A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989274 | ||||||
chr7:5989354
|
G | T | 1 | a0001c0003t0001g0078 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1144+446C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989354 | ||||||
chr7:5989381
|
T | C | 307 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(304): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1144+419A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989381 | ||||||
chr7:5989387
|
C | T | 1 | a0009c0016t0010g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1144+413G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989387 | ||||||
chr7:5989514
|
C | T | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144+286G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989514 | ||||||
chr7:5989658
|
C | T | 1 | a0004c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1144+142G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989658 | ||||||
chr7:5989784
|
A | C | 1 | a0007c0015t0010g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1144+16T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 10/14 | chr7 | 5989784 | ||||||
chr7:5990033
|
C | T | 1 | a0002c0001t0001g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.989-78G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990033 | ||||||
chr7:5990059
|
G | GT | 17 | a0001c0003t0001g0008a0001c0003t0001g0070a0001c0003t0001g0071others(14): Show | 18 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.989-105dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990059 | ||||||
chr7:5990117
|
C | T | 131 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(128): Show | 135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.989-162G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990117 | ||||||
chr7:5990211
|
T | A | 82 | a0001c0003t0001g0066a0001c0003t0001g0067a0002c0001t0001g0005others(79): Show | 85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.989-256A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990211 | ||||||
chr7:5990254
|
C | T | 2 | a0001c0010t0011g0033a0001c0010t0011g0034 | 2 | HG01496.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.989-299G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990254 | ||||||
chr7:5990297
|
C | G | 1 | a0006c0007t0006g0370 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.989-342G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990297 | ||||||
chr7:5990327
|
G | T | 1 | a0003c0004t0004g0362 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.989-372C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990327 | ||||||
chr7:5990389
|
C | T | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.989-434G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990389 | ||||||
chr7:5990453
|
A | T | 1 | a0002c0001t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.989-498T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990453 | ||||||
chr7:5990473
|
C | T | 2 | a0001c0002t0036g0098a0002c0001t0001g0153 | 2 | HG01243.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.989-518G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990473 | ||||||
chr7:5990513
|
A | G | 1 | a0006c0007t0006g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.989-558T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990513 | ||||||
chr7:5990656
|
G | A | 129 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.989-701C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990656 | ||||||
chr7:5990757
|
T | A | 1 | a0001c0002t0031g0269 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.989-802A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990757 | ||||||
chr7:5990806
|
G | C | 82 | a0001c0003t0001g0066a0001c0003t0001g0067a0002c0001t0001g0005others(79): Show | 85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.989-851C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990806 | ||||||
chr7:5990834
|
C | T | 7 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(4): Show | 7 | HG00544.hp2 HG00741.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.989-879G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990834 | ||||||
chr7:5990842
|
C | T | 7 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(4): Show | 7 | HG00544.hp2 HG00741.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.989-887G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990842 | ||||||
chr7:5990860
|
A | T | 1 | a0003c0031t0008g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.989-905T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990860 | ||||||
chr7:5990957
|
G | C | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.989-1002C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5990957 | ||||||
chr7:5991011
|
T | C | 3 | a0001c0003t0038g0278a0001c0003t0039g0277a0003c0004t0045g0378 | 3 | HG01081.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.988+962A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991011 | ||||||
chr7:5991091
|
A | G | 37 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(34): Show | 37 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.988+882T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991091 | ||||||
chr7:5991152
|
T | A | 1 | a0004c0021t0003g0309 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.988+821A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991152 | ||||||
chr7:5991347
|
C | T | 2 | a0004c0005t0003g0046a0004c0005t0003g0054 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.988+626G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991347 | ||||||
chr7:5991401
|
AT | A | 6 | a0001c0012t0002g0101a0001c0012t0002g0102a0001c0012t0002g0179others(3): Show | 6 | HG00544.hp2 HG00741.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.988+571delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991401 | ||||||
chr7:5991447
|
C | T | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.988+526G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991447 | ||||||
chr7:5991470
|
TA | T | 129 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.988+502delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991470 | ||||||
chr7:5991524
|
C | T | 1 | a0001c0002t0002g0214 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.988+449G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991524 | ||||||
chr7:5991537
|
TA | T | 47 | a0001c0003t0001g0118a0002c0001t0001g0166a0003c0004t0004g0003others(44): Show | 53 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.988+435delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991537 | ||||||
chr7:5991610
|
C | T | 1 | a0001c0003t0001g0086 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.988+363G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991610 | ||||||
chr7:5991655
|
C | T | 1 | a0004c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.988+318G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991655 | ||||||
chr7:5991664
|
C | A | 2 | a0003c0004t0004g0336a0003c0004t0004g0337 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.988+309G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991664 | ||||||
chr7:5991667
|
G | A | 1 | a0018c0035t0010g0108 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.988+306C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991667 | ||||||
chr7:5991767
|
A | G | 1 | a0002c0001t0001g0127 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.988+206T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991767 | ||||||
chr7:5991787
|
C | T | 8 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(5): Show | 8 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.988+186G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991787 | ||||||
chr7:5991796
|
G | A | 3 | a0001c0003t0001g0066a0001c0003t0001g0067a0002c0001t0001g0186 | 3 | HG02155.hp1 NA18965.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.988+177C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991796 | ||||||
chr7:5991814
|
G | A | 2 | a0002c0013t0001g0176a0002c0013t0001g0177 | 2 | HG00639.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.988+159C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 9/14 | chr7 | 5991814 | ||||||
chr7:5992173
|
G | GT | 21 | a0001c0002t0002g0222a0002c0001t0001g0100a0002c0001t0001g0125others(18): Show | 22 | HG00423.hp1 HG00673.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.904-117dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992173 | ||||||
chr7:5992173
|
G | T | 1 | a0001c0002t0002g0213 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.904-116C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992173 | ||||||
chr7:5992203
|
C | T | 1 | a0001c0002t0030g0212 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.904-146G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992203 | ||||||
chr7:5992269
|
G | T | 1 | a0001c0012t0001g0193 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.904-212C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992269 | ||||||
chr7:5992316
|
A | AT | 9 | a0001c0002t0002g0228a0001c0002t0002g0233a0001c0002t0002g0241others(6): Show | 9 | HG00673.hp2 HG01175.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-260dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992316 | ||||||
chr7:5992326
|
C | T | 129 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0120others(126): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.904-269G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992326 | ||||||
chr7:5992332
|
T | G | 1 | a0003c0004t0012g0111 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.904-275A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992332 | ||||||
chr7:5992333
|
T | C | 3 | a0007c0009t0009g0020a0007c0009t0026g0027a0007c0009t0037g0026 | 3 | HG02809.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.904-276A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992333 | ||||||
chr7:5992412
|
G | A | 1 | a0003c0004t0045g0378 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.904-355C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992412 | ||||||
chr7:5992456
|
A | C | 2 | a0013c0022t0002g0260a0013c0022t0002g0261 | 2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.904-399T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992456 | ||||||
chr7:5992522
|
G | A | 10 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(7): Show | 10 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.904-465C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992522 | ||||||
chr7:5992562
|
C | T | 9 | a0001c0003t0014g0069a0001c0010t0011g0031a0001c0010t0011g0032others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.904-505G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992562 | ||||||
chr7:5992566
|
C | T | 4 | a0002c0001t0001g0154a0002c0001t0001g0155a0002c0001t0001g0156others(1): Show | 4 | HG04184.hp1 NA18979.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.904-509G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992566 | ||||||
chr7:5992567
|
G | A | 1 | a0005c0006t0005g0315 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.904-510C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992567 | ||||||
chr7:5992700
|
A | C | 3 | a0003c0008t0007g0340a0003c0008t0007g0344a0003c0008t0046g0343 | 3 | HG02965.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.904-643T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992700 | ||||||
chr7:5992787
|
A | G | 1 | a0022c0032t0003g0325 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.904-730T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992787 | ||||||
chr7:5992875
|
T | C | 3 | a0007c0009t0009g0020a0007c0009t0026g0027a0007c0009t0037g0026 | 3 | HG02809.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.904-818A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992875 | ||||||
chr7:5992880
|
G | C | 6 | a0001c0002t0002g0119a0001c0002t0002g0243a0001c0002t0002g0262others(3): Show | 6 | HG01192.hp1 HG01978.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-823C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5992880 | ||||||
chr7:5993002
|
T | C | 1 | a0009c0016t0010g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.904-945A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993002 | ||||||
chr7:5993026
|
T | C | 2 | a0013c0022t0002g0260a0013c0022t0002g0261 | 2 | HG04204.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.904-969A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993026 | ||||||
chr7:5993069
|
A | C | 1 | a0001c0010t0040g0030 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.904-1012T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993069 | ||||||
chr7:5993072
|
C | T | 1 | a0002c0001t0001g0138 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.904-1015G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993072 | ||||||
chr7:5993117
|
T | A | 51 | a0001c0003t0038g0278a0001c0003t0039g0277a0003c0004t0004g0003others(48): Show | 57 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.904-1060A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993117 | ||||||
chr7:5993155
|
G | A | 1 | a0001c0002t0032g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.904-1098C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993155 | ||||||
chr7:5993201
|
T | C | 1 | a0009c0017t0003g0042 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.904-1144A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993201 | ||||||
chr7:5993233
|
T | C | 2 | a0001c0003t0038g0278a0001c0003t0039g0277 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.904-1176A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993233 | ||||||
chr7:5993290
|
G | C | 3 | a0002c0001t0001g0191a0002c0001t0001g0192a0002c0001t0001g0282 | 3 | HG02735.hp2 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.904-1233C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993290 | ||||||
chr7:5993370
|
C | CA | 142 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0120others(139): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.904-1314dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993370 | ||||||
chr7:5993370
|
C | CAA | 85 | a0001c0002t0002g0227a0001c0002t0002g0231a0001c0002t0002g0232others(82): Show | 88 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.904-1315_904-1314d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993370 | ||||||
chr7:5993387
|
A | AG | 52 | a0001c0002t0002g0119a0003c0004t0004g0003a0003c0004t0004g0012others(49): Show | 58 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.904-1331_904-1330i others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993387 | ||||||
chr7:5993387
|
A | G | 1 | a0003c0008t0007g0339 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.904-1330T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993387 | ||||||
chr7:5993409
|
C | A | 1 | a0026c0036t0027g0230 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.904-1352G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993409 | ||||||
chr7:5993429
|
A | ATGT | 380 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(377): Show | 402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.904-1375_904-1373d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993429 | ||||||
chr7:5993464
|
T | A | 6 | a0001c0002t0002g0119a0001c0002t0002g0243a0001c0002t0002g0262others(3): Show | 6 | HG01192.hp1 HG01978.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.904-1407A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993464 | ||||||
chr7:5993556
|
A | T | 2 | a0001c0002t0002g0207a0001c0002t0030g0212 | 2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.904-1499T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993556 | ||||||
chr7:5993588
|
C | T | 1 | a0001c0002t0002g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904-1531G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993588 | ||||||
chr7:5993633
|
C | T | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.904-1576G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993633 | ||||||
chr7:5993658
|
C | T | 2 | a0001c0002t0002g0245a0001c0002t0002g0272 | 2 | HG02080.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.904-1601G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993658 | ||||||
chr7:5993720
|
G | C | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.904-1663C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993720 | ||||||
chr7:5993741
|
G | C | 1 | a0002c0001t0001g0151 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.904-1684C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993741 | ||||||
chr7:5993838
|
G | A | 33 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(30): Show | 39 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.903+1696C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993838 | ||||||
chr7:5993849
|
C | T | 5 | a0002c0001t0001g0136a0003c0004t0012g0110a0003c0004t0012g0111others(2): Show | 5 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.903+1685G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993849 | ||||||
chr7:5993862
|
C | CA | 44 | a0001c0010t0011g0035a0002c0001t0001g0132a0002c0001t0001g0133others(41): Show | 49 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.903+1671dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | ||||||
chr7:5993862
|
C | CAA | 13 | a0001c0002t0002g0209a0001c0003t0001g0008a0001c0003t0001g0070others(10): Show | 14 | HG00280.hp2 HG01123.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.903+1670_903+1671d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | ||||||
chr7:5993862
|
C | CAAA | 90 | a0001c0002t0002g0072a0001c0002t0002g0119a0001c0002t0002g0120others(87): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.903+1669_903+1671d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | ||||||
chr7:5993862
|
C | CAAAA | 32 | a0001c0002t0002g0113a0001c0002t0002g0202a0001c0002t0002g0222others(29): Show | 32 | HG00544.hp2 HG00673.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.903+1668_903+1671d others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | ||||||
chr7:5993862
|
CA | C | 21 | a0001c0003t0039g0277a0002c0001t0001g0166a0002c0001t0001g0168others(18): Show | 21 | HG00639.hp1 HG01106.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.903+1671delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5993862 | ||||||
chr7:5994237
|
C | T | 3 | a0001c0002t0002g0120a0001c0002t0002g0275a0001c0002t0002g0276 | 3 | HG00323.hp1 HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.903+1297G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994237 | ||||||
chr7:5994250
|
G | A | 1 | a0001c0012t0002g0101 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.903+1284C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994250 | ||||||
chr7:5994252
|
G | A | 82 | a0001c0003t0001g0066a0001c0003t0001g0067a0002c0001t0001g0005others(79): Show | 85 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.903+1282C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994252 | ||||||
chr7:5994296
|
G | A | 2 | a0003c0004t0004g0336a0003c0004t0004g0337 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.903+1238C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994296 | ||||||
chr7:5994389
|
A | C | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.903+1145T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994389 | ||||||
chr7:5994432
|
G | A | 2 | a0001c0002t0002g0270a0001c0002t0031g0269 | 2 | NA18968.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.903+1102C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994432 | ||||||
chr7:5994486
|
T | C | 2 | a0009c0017t0001g0106a0009c0017t0001g0109 | 2 | HG02280.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.903+1048A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994486 | ||||||
chr7:5994521
|
T | C | 2 | a0001c0003t0038g0278a0001c0003t0039g0277 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.903+1013A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994521 | ||||||
chr7:5994526
|
C | T | 7 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(4): Show | 7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+1008G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994526 | ||||||
chr7:5994539
|
C | T | 12 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(9): Show | 12 | HG01109.hp1 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.903+995G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994539 | ||||||
chr7:5994555
|
C | T | 1 | a0009c0016t0010g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.903+979G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994555 | ||||||
chr7:5994572
|
A | G | 22 | a0002c0013t0001g0199a0002c0013t0001g0200a0006c0007t0006g0011others(19): Show | 23 | HG00423.hp1 HG00609.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.903+962T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994572 | ||||||
chr7:5994589
|
A | C | 384 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(381): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.903+945T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994589 | ||||||
chr7:5994630
|
A | G | 1 | a0001c0042t0001g0117 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.903+904T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994630 | ||||||
chr7:5994662
|
G | C | 87 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.903+872C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994662 | ||||||
chr7:5994693
|
G | A | 8 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(5): Show | 8 | HG02055.hp2 HG02559.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.903+841C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994693 | ||||||
chr7:5994715
|
G | T | 7 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(4): Show | 7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.903+819C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994715 | ||||||
chr7:5994731
|
A | G | 1 | a0008c0011t0002g0273 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.903+803T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994731 | ||||||
chr7:5994769
|
C | T | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+765G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994769 | ||||||
chr7:5994952
|
C | T | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+582G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5994952 | ||||||
chr7:5995039
|
T | A | 49 | a0001c0002t0002g0072a0001c0002t0002g0238a0001c0002t0002g0270others(46): Show | 53 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.903+495A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995039 | ||||||
chr7:5995041
|
T | A | 2 | a0001c0003t0038g0278a0001c0003t0039g0277 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.903+493A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995041 | ||||||
chr7:5995048
|
A | T | 2 | a0001c0002t0036g0098a0002c0001t0001g0167 | 2 | HG01243.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.903+486T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995048 | ||||||
chr7:5995187
|
A | G | 264 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(261): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.903+347T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995187 | ||||||
chr7:5995188
|
A | C | 264 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(261): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.903+346T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995188 | ||||||
chr7:5995236
|
C | A | 1 | a0002c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.903+298G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995236 | ||||||
chr7:5995288
|
C | T | 1 | a0002c0001t0001g0135 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.903+246G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995288 | ||||||
chr7:5995289
|
G | A | 3 | a0001c0010t0011g0036a0001c0010t0014g0037a0001c0010t0029g0038 | 3 | HG02559.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.903+245C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995289 | ||||||
chr7:5995333
|
G | A | 6 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0036others(3): Show | 6 | HG02559.hp2 HG02809.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+201C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995333 | ||||||
chr7:5995390
|
C | A | 48 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(45): Show | 54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.903+144G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995390 | ||||||
chr7:5995434
|
A | C | 87 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.903+100T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995434 | ||||||
chr7:5995450
|
G | A | 87 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.903+84C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 8/14 | chr7 | 5995450 | ||||||
chr7:5995759
|
A | G | 1 | a0001c0002t0028g0226 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.804-126T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995759 | ||||||
chr7:5995797
|
A | C | 123 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(120): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.804-164T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995797 | ||||||
chr7:5995876
|
C | T | 49 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(46): Show | 55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.804-243G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995876 | ||||||
chr7:5995890
|
T | C | 1 | a0010c0014t0042g0095 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.804-257A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995890 | ||||||
chr7:5995905
|
C | T | 7 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0016t0010g0107others(4): Show | 7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.804-272G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995905 | ||||||
chr7:5995910
|
C | T | 1 | a0001c0002t0002g0244 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.804-277G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5995910 | ||||||
chr7:5996055
|
G | A | 1 | a0002c0001t0001g0153 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.804-422C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996055 | ||||||
chr7:5996125
|
G | C | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-492C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996125 | ||||||
chr7:5996140
|
C | T | 1 | a0009c0016t0010g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.804-507G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996140 | ||||||
chr7:5996313
|
A | G | 298 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(295): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.804-680T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996313 | ||||||
chr7:5996317
|
GC | G | 87 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.804-685delG | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996317 | ||||||
chr7:5996368
|
A | G | 1 | a0002c0001t0001g0124 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.804-735T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996368 | ||||||
chr7:5996374
|
C | T | 49 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(46): Show | 55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.804-741G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996374 | ||||||
chr7:5996429
|
C | G | 1 | a0005c0006t0043g0317 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.804-796G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996429 | ||||||
chr7:5996571
|
C | G | 2 | a0003c0004t0004g0384a0003c0004t0044g0383 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.803+755G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996571 | ||||||
chr7:5996575
|
G | A | 49 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(46): Show | 55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.803+751C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996575 | ||||||
chr7:5996577
|
T | TAA | 7 | a0001c0002t0002g0242a0001c0002t0002g0243a0001c0002t0032g0064others(4): Show | 7 | HG00673.hp1 HG02080.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.803+747_803+748dup others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996577 | ||||||
chr7:5996577
|
T | TAAA | 87 | a0001c0002t0002g0113a0001c0002t0002g0119a0001c0002t0002g0202others(84): Show | 90 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.803+746_803+748dup others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996577 | ||||||
chr7:5996585
|
A | C | 11 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(8): Show | 11 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+741T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996585 | ||||||
chr7:5996588
|
A | T | 1 | a0003c0031t0008g0059 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.803+738T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996588 | ||||||
chr7:5996590
|
A | AAAAAT | 6 | a0001c0002t0002g0207a0001c0002t0002g0240a0001c0003t0001g0008others(3): Show | 7 | HG00280.hp2 HG01123.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+735_803+736ins others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | ||||||
chr7:5996590
|
A | AAAATAT | 78 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0012t0001g0193others(75): Show | 81 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.803+735_803+736ins others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | ||||||
chr7:5996590
|
A | AAAATATA others(3): Show |
1 | a0002c0001t0001g0157 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803+735_803+736ins others(10): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | ||||||
chr7:5996590
|
A | AAAT | 7 | a0001c0002t0002g0072a0001c0002t0002g0239a0001c0003t0001g0068others(4): Show | 7 | HG00140.hp2 HG00642.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.803+735_803+736ins others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | ||||||
chr7:5996590
|
A | T | 21 | a0003c0031t0008g0059a0004c0005t0001g0060a0004c0005t0003g0001others(18): Show | 28 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.803+736T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996590 | ||||||
chr7:5996591
|
AT | A | 20 | a0003c0004t0004g0336a0003c0004t0012g0110a0003c0004t0012g0111others(17): Show | 20 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.803+734delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996591 | ||||||
chr7:5996591
|
ATAT | A | 19 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(16): Show | 19 | HG01496.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.803+732_803+734del others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996591 | ||||||
chr7:5996592
|
T | A | 66 | a0001c0002t0002g0270a0002c0013t0001g0199a0002c0013t0001g0200others(63): Show | 73 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.803+734A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996592 | ||||||
chr7:5996594
|
T | A | 39 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0065others(36): Show | 45 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.803+732A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996594 | ||||||
chr7:5996596
|
T | A | 13 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(10): Show | 13 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.803+730A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996596 | ||||||
chr7:5996598
|
T | A | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.803+728A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996598 | ||||||
chr7:5996600
|
T | A | 10 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(7): Show | 10 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.803+726A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996600 | ||||||
chr7:5996606
|
TATATATA others(1): Show |
T | 6 | a0009c0016t0010g0017a0009c0016t0010g0103a0009c0017t0001g0106others(3): Show | 6 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.803+712_803+719del others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996606 | ||||||
chr7:5996612
|
T | C | 2 | a0002c0001t0001g0157a0004c0005t0003g0099 | 2 | HG00621.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.803+714A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996612 | ||||||
chr7:5996612
|
TAC | T | 79 | a0001c0003t0001g0310a0001c0003t0001g0312a0002c0013t0001g0199others(76): Show | 86 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.803+712_803+713del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996612 | ||||||
chr7:5996614
|
C | T | 179 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(176): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.803+712G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996614 | ||||||
chr7:5996616
|
C | T | 1 | a0002c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+710G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996616 | ||||||
chr7:5996620
|
G | C | 1 | a0002c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+706C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996620 | ||||||
chr7:5996622
|
T | C | 1 | a0002c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+704A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996622 | ||||||
chr7:5996638
|
C | T | 1 | a0002c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.803+688G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996638 | ||||||
chr7:5996884
|
C | A | 108 | a0001c0003t0001g0310a0001c0003t0001g0312a0001c0010t0011g0031others(105): Show | 114 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.803+442G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5996884 | ||||||
chr7:5997030
|
C | T | 1 | a0001c0002t0002g0272 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.803+296G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997030 | ||||||
chr7:5997077
|
G | A | 1 | a0001c0002t0002g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803+249C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997077 | ||||||
chr7:5997112
|
G | A | 2 | a0001c0003t0019g0090a0001c0003t0019g0091 | 2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.803+214C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997112 | ||||||
chr7:5997171
|
A | G | 97 | a0001c0003t0001g0310a0001c0003t0001g0312a0001c0003t0038g0278others(94): Show | 103 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.803+155T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 7/14 | chr7 | 5997171 | ||||||
chr7:5997426
|
G | GA | 35 | a0001c0003t0001g0310a0001c0003t0001g0312a0003c0004t0020g0308others(32): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.706-4dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997426 | ||||||
chr7:5997426
|
GA | G | 211 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(208): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
splice_region_variant&intron_variant | LOW | c.706-4delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997426 | ||||||
chr7:5997529
|
A | C | 1 | a0003c0020t0054g0366 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.706-106T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997529 | ||||||
chr7:5997537
|
G | T | 12 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-114C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997537 | ||||||
chr7:5997601
|
A | G | 35 | a0001c0003t0001g0310a0001c0003t0001g0312a0003c0004t0020g0308others(32): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.706-178T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997601 | ||||||
chr7:5997878
|
G | C | 11 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(8): Show | 11 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-455C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5997878 | ||||||
chr7:5998010
|
G | T | 12 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-587C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998010 | ||||||
chr7:5998077
|
G | GT | 12 | a0002c0001t0001g0131a0002c0001t0001g0132a0002c0001t0001g0133others(9): Show | 12 | HG00741.hp2 HG01256.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.706-655dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998077 | ||||||
chr7:5998084
|
T | G | 119 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(116): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.706-661A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998084 | ||||||
chr7:5998092
|
T | G | 119 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(116): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.706-669A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998092 | ||||||
chr7:5998331
|
C | T | 6 | a0003c0004t0004g0003a0003c0004t0004g0363a0003c0004t0012g0110others(3): Show | 9 | HG00099.hp2 HG01106.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.705+777G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998331 | ||||||
chr7:5998359
|
C | T | 1 | a0004c0021t0003g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.705+749G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998359 | ||||||
chr7:5998360
|
G | A | 89 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0012t0001g0193others(86): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.705+748C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998360 | ||||||
chr7:5998376
|
G | A | 1 | a0001c0012t0002g0189 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.705+732C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998376 | ||||||
chr7:5998414
|
T | C | 122 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.705+694A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998414 | ||||||
chr7:5998520
|
C | A | 1 | a0005c0006t0005g0299 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.705+588G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998520 | ||||||
chr7:5998529
|
C | T | 1 | a0003c0004t0012g0203 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.705+579G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998529 | ||||||
chr7:5998548
|
G | C | 46 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(43): Show | 52 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.705+560C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998548 | ||||||
chr7:5998651
|
G | A | 1 | a0001c0002t0002g0271 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.705+457C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998651 | ||||||
chr7:5998664
|
A | C | 36 | a0001c0003t0001g0310a0001c0003t0001g0312a0003c0004t0020g0308others(33): Show | 36 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.705+444T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998664 | ||||||
chr7:5998693
|
C | CA | 55 | a0001c0002t0002g0113a0001c0002t0002g0227a0001c0002t0002g0228others(52): Show | 55 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.705+414dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998693 | ||||||
chr7:5998727
|
C | T | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.705+381G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998727 | ||||||
chr7:5998763
|
T | C | 49 | a0001c0003t0038g0278a0001c0003t0039g0277a0003c0004t0004g0003others(46): Show | 55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.705+345A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998763 | ||||||
chr7:5998819
|
G | A | 12 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.705+289C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998819 | ||||||
chr7:5998852
|
G | A | 48 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(45): Show | 54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.705+256C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998852 | ||||||
chr7:5998989
|
CA | C | 313 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(310): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.705+118delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5998989 | ||||||
chr7:5999072
|
G | A | 3 | a0002c0001t0001g0191a0002c0001t0001g0192a0002c0001t0001g0282 | 3 | HG02735.hp2 HG02738.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.705+36C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5999072 | ||||||
chr7:5999091
|
T | C | 122 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.705+17A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 6/14 | chr7 | 5999091 | ||||||
chr7:5999301
|
T | C | 1 | a0004c0005t0003g0063 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.538-26A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999301 | ||||||
chr7:5999355
|
C | T | 1 | a0002c0001t0001g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.538-80G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999355 | ||||||
chr7:5999448
|
C | T | 1 | a0002c0001t0001g0167 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.538-173G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999448 | ||||||
chr7:5999449
|
G | A | 11 | a0003c0008t0007g0323a0003c0008t0007g0324a0003c0008t0007g0339others(8): Show | 11 | HG02055.hp1 HG02145.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-174C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999449 | ||||||
chr7:5999498
|
T | C | 45 | a0001c0002t0002g0072a0001c0002t0032g0064a0001c0002t0036g0098others(42): Show | 49 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.538-223A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999498 | ||||||
chr7:5999635
|
T | G | 2 | a0001c0003t0001g0118a0025c0040t0001g0093 | 2 | HG00642.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.538-360A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999635 | ||||||
chr7:5999636
|
T | TA | 42 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0338others(39): Show | 48 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.538-362dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999636 | ||||||
chr7:5999697
|
G | A | 1 | a0009c0017t0001g0109 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.538-422C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999697 | ||||||
chr7:5999753
|
A | C | 26 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0012t0001g0193others(23): Show | 26 | HG00544.hp2 HG00741.hp1 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.538-478T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999753 | ||||||
chr7:5999773
|
G | A | 1 | a0001c0002t0036g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.538-498C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999773 | ||||||
chr7:5999857
|
G | T | 1 | a0002c0001t0018g0129 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.538-582C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999857 | ||||||
chr7:5999870
|
G | A | 1 | a0003c0004t0004g0338 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.538-595C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999870 | ||||||
chr7:5999898
|
T | C | 89 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0012t0001g0193others(86): Show | 92 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.538-623A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 5999898 | ||||||
chr7:6000117
|
G | A | 1 | a0007c0009t0009g0029 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.538-842C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000117 | ||||||
chr7:6000163
|
C | G | 1 | a0004c0005t0003g0045 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.538-888G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000163 | ||||||
chr7:6000310
|
G | T | 48 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(45): Show | 54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.538-1035C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000310 | ||||||
chr7:6000321
|
C | T | 1 | a0004c0005t0003g0044 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.538-1046G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000321 | ||||||
chr7:6000377
|
T | TA | 6 | a0005c0006t0005g0304a0005c0006t0005g0315a0005c0006t0005g0316others(3): Show | 6 | HG02109.hp1 HG02723.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.538-1103dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000377 | ||||||
chr7:6000377
|
TA | T | 263 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(260): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.538-1103delT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000377 | ||||||
chr7:6000377
|
TAA | T | 22 | a0001c0002t0002g0206a0001c0002t0002g0238a0001c0003t0001g0070others(19): Show | 22 | HG01106.hp2 HG01168.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.538-1104_538-1103d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000377 | ||||||
chr7:6000455
|
T | C | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.538-1180A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000455 | ||||||
chr7:6000488
|
T | C | 1 | a0003c0004t0004g0338 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.538-1213A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000488 | ||||||
chr7:6000704
|
T | C | 1 | a0003c0004t0004g0362 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.538-1429A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000704 | ||||||
chr7:6000717
|
G | A | 1 | a0003c0020t0054g0366 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.538-1442C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000717 | ||||||
chr7:6000856
|
T | G | 82 | a0001c0002t0002g0113a0001c0002t0002g0119a0001c0002t0002g0120others(79): Show | 82 | HG00140.hp2 HG00323.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.538-1581A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6000856 | ||||||
chr7:6001000
|
A | C | 124 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(121): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.537+1453T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001000 | ||||||
chr7:6001094
|
T | A | 1 | a0001c0002t0002g0204 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.537+1359A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001094 | ||||||
chr7:6001159
|
G | A | 2 | a0007c0015t0010g0018a0007c0015t0010g0039 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.537+1294C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001159 | ||||||
chr7:6001189
|
G | T | 1 | a0006c0007t0006g0320 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.537+1264C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001189 | ||||||
chr7:6001213
|
CTTG | C | 12 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(9): Show | 12 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.537+1237_537+1239d others(5): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001213 | ||||||
chr7:6001373
|
C | CT | 329 | a0001c0002t0002g0072a0001c0002t0002g0119a0001c0002t0002g0120others(326): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.537+1079dupA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001373 | ||||||
chr7:6001373
|
C | CTT | 19 | a0001c0002t0002g0113a0001c0003t0001g0068a0001c0010t0011g0031others(16): Show | 19 | HG01496.hp2 HG01981.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.537+1078_537+1079d others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001373 | ||||||
chr7:6001466
|
A | G | 53 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(50): Show | 59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.537+987T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001466 | ||||||
chr7:6001487
|
C | A | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.537+966G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001487 | ||||||
chr7:6001488
|
A | G | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.537+965T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001488 | ||||||
chr7:6001541
|
T | C | 35 | a0001c0003t0001g0310a0001c0003t0001g0312a0003c0004t0020g0308others(32): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.537+912A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001541 | ||||||
chr7:6001579
|
C | T | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.537+874G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001579 | ||||||
chr7:6001610
|
C | G | 2 | a0003c0004t0004g0384a0003c0004t0044g0383 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.537+843G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001610 | ||||||
chr7:6001668
|
C | T | 1 | a0003c0004t0020g0308 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.537+785G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001668 | ||||||
chr7:6001875
|
T | C | 55 | a0001c0003t0038g0278a0001c0003t0039g0277a0003c0004t0004g0003others(52): Show | 61 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.537+578A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6001875 | ||||||
chr7:6002013
|
A | T | 1 | a0001c0002t0002g0205 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.537+440T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002013 | ||||||
chr7:6002020
|
A | T | 1 | a0016c0027t0010g0328 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.537+433T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002020 | ||||||
chr7:6002022
|
T | A | 11 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.537+431A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002022 | ||||||
chr7:6002156
|
A | G | 1 | a0014c0025t0001g0368 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.537+297T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002156 | ||||||
chr7:6002181
|
C | T | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.537+272G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002181 | ||||||
chr7:6002187
|
G | A | 120 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(117): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.537+266C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002187 | ||||||
chr7:6002204
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.537+249A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002204 | ||||||
chr7:6002205
|
T | A | 122 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.537+248A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002205 | ||||||
chr7:6002266
|
T | C | 49 | a0001c0003t0038g0278a0001c0003t0039g0277a0003c0004t0004g0003others(46): Show | 55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.537+187A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002266 | ||||||
chr7:6002344
|
C | G | 1 | a0002c0001t0014g0173 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.537+109G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002344 | ||||||
chr7:6002384
|
A | G | 1 | a0002c0001t0014g0173 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.537+69T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 5/14 | chr7 | 6002384 | ||||||
chr7:6002891
|
C | T | 122 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(119): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.354-255G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6002891 | ||||||
chr7:6002932
|
C | G | 11 | a0007c0009t0009g0019a0007c0009t0009g0020a0007c0009t0009g0021others(8): Show | 11 | HG02257.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.354-296G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6002932 | ||||||
chr7:6003004
|
A | G | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-368T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003004 | ||||||
chr7:6003020
|
G | A | 87 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.354-384C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003020 | ||||||
chr7:6003234
|
C | T | 1 | a0003c0004t0004g0065 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.353+456G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003234 | ||||||
chr7:6003299
|
A | G | 42 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0338others(39): Show | 48 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.353+391T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003299 | ||||||
chr7:6003306
|
G | GAT | 60 | a0001c0002t0002g0113a0001c0002t0002g0202a0001c0002t0002g0205others(57): Show | 60 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.353+382_353+383dup others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | ||||||
chr7:6003306
|
G | GATAT | 7 | a0001c0010t0011g0033a0001c0010t0011g0034a0001c0010t0011g0035others(4): Show | 7 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.353+380_353+383dup others(4): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | ||||||
chr7:6003306
|
G | GATATAT | 3 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0040g0030 | 3 | HG02809.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.353+378_353+383dup others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | ||||||
chr7:6003306
|
G | T | 1 | a0005c0006t0005g0307 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.353+384C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | ||||||
chr7:6003306
|
GAT | G | 53 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(50): Show | 59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.353+382_353+383del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003306 | ||||||
chr7:6003308
|
T | G | 3 | a0001c0003t0038g0278a0001c0003t0039g0277a0006c0007t0024g0096 | 3 | HG02895.hp2 HG02897.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.353+382A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003308 | ||||||
chr7:6003324
|
T | A | 1 | a0002c0001t0001g0281 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.353+366A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | ||||||
chr7:6003324
|
T | TATATATA others(1): Show |
80 | a0001c0012t0002g0101a0001c0012t0002g0102a0001c0012t0002g0179others(77): Show | 83 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.353+365_353+366ins others(8): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | ||||||
chr7:6003324
|
T | TATATATA others(3): Show |
5 | a0002c0001t0001g0123a0002c0001t0001g0125a0002c0001t0001g0126others(2): Show | 5 | HG00558.hp2 HG00673.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+365_353+366ins others(10): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | ||||||
chr7:6003324
|
T | TATATATA others(9): Show |
1 | a0001c0012t0001g0193 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.353+365_353+366ins others(16): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003324 | ||||||
chr7:6003369
|
C | T | 1 | a0005c0006t0005g0302 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.353+321G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003369 | ||||||
chr7:6003426
|
A | G | 53 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(50): Show | 59 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.353+264T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003426 | ||||||
chr7:6003434
|
C | T | 87 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.353+256G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003434 | ||||||
chr7:6003481
|
C | T | 264 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(261): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.353+209G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 4/14 | chr7 | 6003481 | ||||||
chr7:6003836
|
A | G | 1 | a0001c0002t0032g0064 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.251-44T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 3/14 | chr7 | 6003836 | ||||||
chr7:6003864
|
T | C | 4 | a0003c0004t0012g0110a0003c0004t0012g0111a0003c0004t0012g0112others(1): Show | 4 | HG01106.hp2 HG01168.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-72A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 3/14 | chr7 | 6003864 | ||||||
chr7:6004120
|
T | C | 3 | a0001c0010t0011g0036a0001c0010t0014g0037a0001c0010t0029g0038 | 3 | HG02559.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.164-62A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004120 | ||||||
chr7:6004166
|
C | G | 87 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(84): Show | 90 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.164-108G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004166 | ||||||
chr7:6004290
|
T | C | 2 | a0003c0020t0054g0366a0003c0020t0055g0367 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.164-232A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004290 | ||||||
chr7:6004333
|
CTG | C | 75 | a0002c0013t0001g0199a0002c0013t0001g0200a0003c0004t0004g0003others(72): Show | 82 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.164-277_164-276del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004333 | ||||||
chr7:6004468
|
C | A | 1 | a0001c0010t0029g0038 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.164-410G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004468 | ||||||
chr7:6004490
|
C | T | 1 | a0003c0020t0054g0366 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-432G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004490 | ||||||
chr7:6004620
|
C | T | 1 | a0001c0002t0002g0204 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.164-562G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004620 | ||||||
chr7:6004693
|
C | T | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-635G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004693 | ||||||
chr7:6004715
|
C | CA | 33 | a0001c0003t0038g0278a0001c0003t0039g0277a0003c0004t0004g0336others(30): Show | 33 | HG00280.hp1 HG00733.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.164-658dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004715 | ||||||
chr7:6004715
|
C | CAA | 32 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0338others(29): Show | 38 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.164-659_164-658dup others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004715 | ||||||
chr7:6004797
|
G | A | 2 | a0003c0004t0004g0003a0003c0004t0004g0363 | 5 | HG00099.hp2 HG01515.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-739C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004797 | ||||||
chr7:6004884
|
C | T | 287 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(284): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.164-826G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004884 | ||||||
chr7:6004889
|
G | T | 1 | a0007c0009t0009g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-831C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004889 | ||||||
chr7:6004890
|
T | G | 76 | a0002c0013t0001g0199a0002c0013t0001g0200a0003c0004t0004g0003others(73): Show | 83 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-832A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004890 | ||||||
chr7:6004897
|
T | A | 4 | a0001c0002t0002g0120a0001c0002t0002g0275a0001c0002t0002g0276others(1): Show | 4 | HG00323.hp1 HG01361.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-839A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6004897 | ||||||
chr7:6005019
|
T | C | 344 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(341): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.163+873A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005019 | ||||||
chr7:6005268
|
G | A | 6 | a0002c0001t0001g0167a0002c0001t0001g0168a0002c0001t0001g0169others(3): Show | 6 | NA18950.hp1 NA18953.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+624C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005268 | ||||||
chr7:6005361
|
G | C | 1 | a0002c0001t0014g0173 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.163+531C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005361 | ||||||
chr7:6005561
|
T | C | 7 | a0004c0021t0003g0105a0009c0016t0010g0017a0009c0016t0010g0103others(4): Show | 7 | HG01346.hp2 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+331A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005561 | ||||||
chr7:6005589
|
G | A | 2 | a0003c0004t0004g0003a0003c0004t0004g0363 | 5 | HG00099.hp2 HG01515.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+303C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005589 | ||||||
chr7:6005754
|
T | C | 124 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(121): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.163+138A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005754 | ||||||
chr7:6005760
|
C | G | 1 | a0007c0009t0009g0019 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.163+132G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005760 | ||||||
chr7:6005884
|
A | C | 1 | a0002c0001t0001g0174 | 1 | HG02602.hp1 | splice_region_variant&intron_variant | LOW | c.163+8T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 2/14 | chr7 | 6005884 | ||||||
chr7:6006152
|
T | C | 1 | a0010c0014t0042g0095 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.24-121A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006152 | ||||||
chr7:6006189
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-158T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006189 | ||||||
chr7:6006191
|
C | CTTAGTCT others(4): Show |
1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-161_24-160insTG others(9): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006191 | ||||||
chr7:6006192
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-161T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006192 | ||||||
chr7:6006197
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-166A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006197 | ||||||
chr7:6006199
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-168A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006199 | ||||||
chr7:6006200
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-169T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006200 | ||||||
chr7:6006203
|
A | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-172T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006203 | ||||||
chr7:6006205
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-174G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006205 | ||||||
chr7:6006209
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-178T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006209 | ||||||
chr7:6006210
|
A | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-179T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006210 | ||||||
chr7:6006211
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-180T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006211 | ||||||
chr7:6006212
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-181G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006212 | ||||||
chr7:6006213
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-182T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006213 | ||||||
chr7:6006214
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-183A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006214 | ||||||
chr7:6006217
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-186T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006217 | ||||||
chr7:6006220
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-189G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006220 | ||||||
chr7:6006221
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-190T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006221 | ||||||
chr7:6006225
|
T | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-194A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006225 | ||||||
chr7:6006229
|
T | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-198A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006229 | ||||||
chr7:6006230
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-199G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006230 | ||||||
chr7:6006231
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-200A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006231 | ||||||
chr7:6006232
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-201C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006232 | ||||||
chr7:6006238
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-207T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006238 | ||||||
chr7:6006242
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-211A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006242 | ||||||
chr7:6006246
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-215T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006246 | ||||||
chr7:6006247
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-216T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006247 | ||||||
chr7:6006250
|
C | T | 48 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(45): Show | 54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.24-219G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006250 | ||||||
chr7:6006251
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-220T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006251 | ||||||
chr7:6006255
|
G | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-224C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006255 | ||||||
chr7:6006258
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-227G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006258 | ||||||
chr7:6006262
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-231T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006262 | ||||||
chr7:6006271
|
T | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-240A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006271 | ||||||
chr7:6006272
|
T | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-241A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006272 | ||||||
chr7:6006273
|
A | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-242T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006273 | ||||||
chr7:6006276
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-245G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006276 | ||||||
chr7:6006277
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-246A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006277 | ||||||
chr7:6006279
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-248T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006279 | ||||||
chr7:6006292
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-261C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006292 | ||||||
chr7:6006294
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-263T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006294 | ||||||
chr7:6006297
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-266G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006297 | ||||||
chr7:6006302
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-271T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006302 | ||||||
chr7:6006303
|
T | C | 49 | a0001c0003t0038g0278a0001c0003t0039g0277a0003c0004t0004g0003others(46): Show | 55 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.24-272A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006303 | ||||||
chr7:6006307
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-276T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006307 | ||||||
chr7:6006321
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-290G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006321 | ||||||
chr7:6006322
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-291T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006322 | ||||||
chr7:6006323
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-292T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006323 | ||||||
chr7:6006324
|
A | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-293T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006324 | ||||||
chr7:6006325
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-294T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006325 | ||||||
chr7:6006327
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-296G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006327 | ||||||
chr7:6006333
|
C | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-302G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006333 | ||||||
chr7:6006335
|
A | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-304T>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006335 | ||||||
chr7:6006337
|
A | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-306T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006337 | ||||||
chr7:6006338
|
A | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-307T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006338 | ||||||
chr7:6006339
|
T | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-308A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006339 | ||||||
chr7:6006350
|
T | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-319A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006350 | ||||||
chr7:6006352
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-321G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006352 | ||||||
chr7:6006355
|
G | C | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-324C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006355 | ||||||
chr7:6006361
|
T | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-330A>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006361 | ||||||
chr7:6006362
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-331C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006362 | ||||||
chr7:6006366
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-335C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006366 | ||||||
chr7:6006367
|
C | G | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-336G>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006367 | ||||||
chr7:6006374
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-343C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006374 | ||||||
chr7:6006376
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-345G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006376 | ||||||
chr7:6006377
|
T | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-346A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006377 | ||||||
chr7:6006378
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-347C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006378 | ||||||
chr7:6006380
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-349C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006380 | ||||||
chr7:6006384
|
G | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-353C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006384 | ||||||
chr7:6006385
|
C | A | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-354G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006385 | ||||||
chr7:6006394
|
G | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-363C>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006394 | ||||||
chr7:6006399
|
C | T | 1 | a0001c0002t0002g0202 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.24-368G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006399 | ||||||
chr7:6006431
|
A | G | 1 | a0007c0015t0034g0322 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.24-400T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006431 | ||||||
chr7:6006511
|
G | C | 1 | a0001c0002t0002g0120 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.24-480C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006511 | ||||||
chr7:6006610
|
G | A | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.24-579C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006610 | ||||||
chr7:6006638
|
C | CA | 24 | a0005c0006t0005g0318a0006c0007t0006g0011a0006c0007t0006g0320others(21): Show | 25 | HG00423.hp1 HG00738.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.24-608dupT | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006638 | ||||||
chr7:6006666
|
T | A | 2 | a0003c0020t0054g0366a0003c0020t0055g0367 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.24-635A>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006666 | ||||||
chr7:6006846
|
G | A | 4 | a0002c0001t0001g0104a0002c0001t0001g0194a0002c0001t0001g0195others(1): Show | 4 | HG02083.hp2 HG02165.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.24-815C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006846 | ||||||
chr7:6006899
|
A | C | 1 | a0002c0001t0001g0124 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.24-868T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006899 | ||||||
chr7:6006996
|
C | A | 9 | a0001c0010t0011g0031a0001c0010t0011g0032a0001c0010t0011g0033others(6): Show | 9 | HG01496.hp2 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.24-965G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006996 | ||||||
chr7:6006998
|
A | G | 1 | a0003c0004t0004g0338 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.24-967T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6006998 | ||||||
chr7:6007083
|
C | T | 1 | a0002c0001t0001g0282 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.24-1052G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007083 | ||||||
chr7:6007087
|
C | CATT | 30 | a0001c0012t0001g0193a0001c0012t0002g0101a0001c0012t0002g0102others(27): Show | 30 | HG00544.hp2 HG00639.hp1 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.24-1059_24-1057dup others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | ||||||
chr7:6007087
|
C | CATTATT | 56 | a0002c0001t0001g0005a0002c0001t0001g0010a0002c0001t0001g0100others(53): Show | 59 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.24-1062_24-1057dup others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | ||||||
chr7:6007087
|
C | CATTATTA others(5): Show |
1 | a0002c0001t0001g0123 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.24-1068_24-1057dup others(12): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | ||||||
chr7:6007087
|
CATT | C | 245 | a0001c0002t0002g0072a0001c0002t0002g0113a0001c0002t0002g0119others(242): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.24-1059_24-1057del others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | ||||||
chr7:6007087
|
CATTATT | C | 3 | a0004c0005t0003g0097a0004c0005t0003g0121a0007c0015t0010g0039 | 3 | HG02630.hp1 NA20805.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.24-1062_24-1057del others(6): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | ||||||
chr7:6007087
|
CATTATTA others(2): Show |
C | 3 | a0003c0004t0013g0014a0003c0004t0013g0365a0003c0008t0007g0364 | 4 | HG01884.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.24-1065_24-1057del others(9): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007087 | ||||||
chr7:6007103
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ATTATTAT others(5): Show |
A | 1 | a0001c0002t0036g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.24-1084_24-1073del others(12): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007103 | ||||||
chr7:6007152
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G | A | 69 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(66): Show | 76 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.24-1121C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007152 | ||||||
chr7:6007175
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G | A | 2 | a0003c0020t0054g0366a0003c0020t0055g0367 | 2 | HG03471.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.24-1144C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007175 | ||||||
chr7:6007302
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G | A | 1 | a0004c0005t0003g0099 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.24-1271C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007302 | ||||||
chr7:6007359
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G | A | 57 | a0001c0003t0001g0310a0001c0003t0001g0312a0001c0010t0011g0031others(54): Show | 57 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.24-1328C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007359 | ||||||
chr7:6007403
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A | G | 2 | a0003c0004t0004g0336a0003c0004t0004g0337 | 2 | HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.24-1372T>C | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007403 | ||||||
chr7:6007442
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C | T | 1 | a0002c0001t0001g0122 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.24-1411G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007442 | ||||||
chr7:6007500
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C | T | 48 | a0003c0004t0004g0003a0003c0004t0004g0012a0003c0004t0004g0336others(45): Show | 54 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.24-1469G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007500 | ||||||
chr7:6007551
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C | T | 1 | a0007c0015t0010g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.23+1446G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007551 | ||||||
chr7:6007672
|
G | C | 1 | a0003c0004t0045g0378 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.23+1325C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007672 | ||||||
chr7:6007856
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AT | A | 44 | a0001c0002t0002g0113a0001c0002t0002g0119a0001c0002t0002g0120others(41): Show | 44 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.23+1140delA | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007856 | ||||||
chr7:6007856
|
ATT | A | 208 | a0001c0002t0002g0201a0001c0002t0002g0202a0001c0002t0002g0204others(205): Show | 212 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.23+1139_23+1140del others(2): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007856 | ||||||
chr7:6007856
|
ATTT | A | 63 | a0002c0001t0001g0280a0002c0001t0001g0281a0002c0001t0001g0282others(60): Show | 69 | HG00099.hp2 HG00621.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.23+1138_23+1140del others(3): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007856 | ||||||
chr7:6007945
|
C | T | 57 | a0001c0003t0001g0310a0001c0003t0001g0312a0001c0010t0011g0031others(54): Show | 57 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.23+1052G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6007945 | ||||||
chr7:6008134
|
G | A | 1 | a0001c0003t0001g0283 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.23+863C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008134 | ||||||
chr7:6008336
|
T | C | 4 | a0003c0004t0004g0379a0003c0004t0004g0380a0003c0004t0004g0381others(1): Show | 4 | NA18948.hp2 NA18969.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+661A>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008336 | ||||||
chr7:6008504
|
C | A | 2 | a0003c0004t0004g0384a0003c0004t0044g0383 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.23+493G>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008504 | ||||||
chr7:6008555
|
G | C | 71 | a0002c0001t0001g0326a0002c0001t0001g0327a0003c0004t0004g0003others(68): Show | 78 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.23+442C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008555 | ||||||
chr7:6008649
|
G | A | 1 | a0003c0004t0004g0385 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.23+348C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008649 | ||||||
chr7:6008728
|
C | T | 71 | a0002c0001t0001g0326a0002c0001t0001g0327a0003c0004t0004g0003others(68): Show | 78 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.23+269G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008728 | ||||||
chr7:6008731
|
GTCT | G | 35 | a0001c0003t0001g0310a0001c0003t0001g0312a0003c0004t0020g0308others(32): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.23+263_23+265delAG others(1): Show |
PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008731 | ||||||
chr7:6008735
|
G | C | 35 | a0001c0003t0001g0310a0001c0003t0001g0312a0003c0004t0020g0308others(32): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.23+262C>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008735 | ||||||
chr7:6008736
|
G | A | 35 | a0001c0003t0001g0310a0001c0003t0001g0312a0003c0004t0020g0308others(32): Show | 35 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.23+261C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008736 | ||||||
chr7:6008741
|
G | A | 1 | a0001c0002t0002g0319 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.23+256C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008741 | ||||||
chr7:6008796
|
A | C | 1 | a0009c0016t0010g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.23+201T>G | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008796 | ||||||
chr7:6008891
|
C | T | 2 | a0004c0005t0003g0015a0004c0005t0003g0016 | 2 | HG02071.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.23+106G>A | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008891 | ||||||
chr7:6008925
|
G | A | 71 | a0002c0001t0001g0326a0002c0001t0001g0327a0003c0004t0004g0003others(68): Show | 78 | HG00099.hp2 HG00423.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.23+72C>T | PMS2 | ENSG00000122512.17 | transcript | ENST00000265849.12 | protein_coding | 1/14 | chr7 | 6008925 |