geneid | 1687 |
---|---|
ensemblid | ENSG00000105928.16 |
hgncid | 2810 |
symbol | GSDME |
name | gasdermin E |
refseq_nuc | NM_001127453.2 |
refseq_prot | NP_001120925.1 |
ensembl_nuc | ENST00000645220.1 |
ensembl_prot | ENSP00000494186.1 |
mane_status | MANE Select |
chr | chr7 |
start | 24698355 |
end | 24757464 |
strand | - |
ver | v1.2 |
region | chr7:24698355-24757464 |
region5000 | chr7:24693355-24762464 |
regionname0 | GSDME_chr7_24698355_24757464 |
regionname5000 | GSDME_chr7_24693355_24762464 |
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 | 1/1 | 496 | 279 | 74 | 50 | 109 | 17 | 27 | 84 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002 | 0/0 | 496 | 86 | 16 | 6 | 55 | 1 | 8 | 43 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0003 | 0/0 | 496 | 35 | 1 | 7 | 24 | 0 | 3 | 19 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0004 | 0/0 | 496 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0005 | 0/0 | 496 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0006 | 0/0 | 496 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0007 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0008 | 0/0 | 260 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0009 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0010 | 0/0 | 496 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
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 | 1491 | 154 | 58 | 17 | 69 | 1 | 9 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0002 | 0/0 | 1491 | 60 | 1 | 11 | 39 | 4 | 5 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0003 | 0/0 | 1491 | 58 | 10 | 4 | 35 | 1 | 8 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0004 | 1/1 | 1491 | 56 | 12 | 21 | 1 | 10 | 10 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0005 | 0/0 | 1491 | 31 | 1 | 7 | 21 | 0 | 2 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0006 | 0/0 | 1491 | 26 | 6 | 2 | 18 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0007 | 0/0 | 1491 | 7 | 3 | 1 | 0 | 2 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0008 | 0/0 | 1491 | 4 | 0 | 0 | 3 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0009 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0010 | 0/0 | 1491 | 2 | 1 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0011 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0012 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0013 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0014 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0015 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0016 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0017 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
c0018 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
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 | 1/1 | 760 | 267 | 31 | 49 | 137 | 17 | 31 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0002 | 0/0 | 759 | 63 | 16 | 3 | 44 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0003 | 0/0 | 760 | 34 | 16 | 6 | 4 | 1 | 7 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0004 | 0/0 | 760 | 11 | 10 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0005 | 0/0 | 760 | 8 | 5 | 3 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0006 | 0/0 | 760 | 7 | 7 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0007 | 0/0 | 760 | 6 | 4 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0008 | 0/0 | 760 | 4 | 0 | 0 | 4 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0009 | 0/0 | 760 | 3 | 3 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0010 | 0/0 | 759 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0011 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0012 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0013 | 0/0 | 760 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0014 | 0/0 | 760 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
t0015 | 0/0 | 759 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
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 | 7 | 7 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0338 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1491 | 154 | 58 | 17 | 69 | 1 | 9 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0002 | 0/0 | 1491 | 60 | 1 | 11 | 39 | 4 | 5 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0004 | 1/1 | 1491 | 56 | 12 | 21 | 1 | 10 | 10 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0007 | 0/0 | 1491 | 7 | 3 | 1 | 0 | 2 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0016 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0017 | 0/0 | 1491 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0003 | 0/0 | 1491 | 58 | 10 | 4 | 35 | 1 | 8 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0006 | 0/0 | 1491 | 26 | 6 | 2 | 18 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0009 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0003c0005 | 0/0 | 1491 | 31 | 1 | 7 | 21 | 0 | 2 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0003c0008 | 0/0 | 1491 | 4 | 0 | 0 | 3 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0004c0012 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0005c0011 | 0/0 | 1491 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0006c0010 | 0/0 | 1491 | 2 | 1 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0007c0018 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0008c0015 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0009c0013 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0010c0014 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2250 | 39 | 9 | 5 | 22 | 0 | 3 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0002 | 0/0 | 2249 | 61 | 16 | 3 | 42 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0003 | 0/0 | 2250 | 32 | 15 | 6 | 4 | 1 | 6 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0004 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0005 | 0/0 | 2250 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0006 | 0/0 | 2250 | 7 | 7 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0007 | 0/0 | 2250 | 5 | 3 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0009 | 0/0 | 2250 | 3 | 3 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0010 | 0/0 | 2249 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0014 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0001t0015 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0002t0001 | 0/0 | 2250 | 59 | 1 | 11 | 38 | 4 | 5 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0002t0002 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0004t0001 | 1/1 | 2250 | 49 | 6 | 20 | 1 | 10 | 10 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0004t0004 | 0/0 | 2250 | 7 | 6 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0007t0001 | 0/0 | 2250 | 6 | 2 | 1 | 0 | 2 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0007t0013 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0016t0001 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0001c0017t0003 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0003t0001 | 0/0 | 2250 | 53 | 9 | 4 | 31 | 1 | 8 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0003t0007 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0003t0008 | 0/0 | 2250 | 4 | 0 | 0 | 4 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0006t0001 | 0/0 | 2250 | 17 | 0 | 0 | 17 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0006t0003 | 0/0 | 2250 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0006t0005 | 0/0 | 2250 | 7 | 5 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0006t0011 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0002c0009t0001 | 0/0 | 2250 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0003c0005t0001 | 0/0 | 2250 | 31 | 1 | 7 | 21 | 0 | 2 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0003c0008t0001 | 0/0 | 2250 | 4 | 0 | 0 | 3 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0004c0012t0001 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0005c0011t0004 | 0/0 | 2250 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0006c0010t0001 | 0/0 | 2250 | 2 | 1 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0007c0018t0002 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0008c0015t0012 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0009c0013t0001 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
a0010c0014t0001 | 0/0 | 2250 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | copy fasta | chr7 | 24693355 | 24762464 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0006g0001 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0007g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0007g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0007g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0007g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0014g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0001t0015g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0338 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0007t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0007t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0007t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0007t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0007t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0007t0013g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0016t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0001c0017t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0007g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0008g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0003t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0005g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0005g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0006t0011g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0002c0009t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0005t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0008t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0008t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0008t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0003c0008t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0004c0012t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0005c0011t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0005c0011t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0006c0010t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0006c0010t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0007c0018t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0008c0015t0012g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0009c0013t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
a0010c0014t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0183 | EUR | GBR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00099 | hp2 | a0001 | c0004 | t0001 | g0325 | EUR | GBR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0332 | EUR | GBR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00140 | hp2 | a0002 | c0003 | t0001 | g0230 | EUR | GBR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0348 | EUR | FIN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0073 | EUR | FIN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00323 | hp1 | a0001 | c0004 | t0001 | g0334 | EUR | FIN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0072 | EUR | FIN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00544 | hp1 | a0003 | c0005 | t0001 | g0199 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00558 | hp2 | a0002 | c0003 | t0001 | g0151 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00597 | hp1 | a0002 | c0003 | t0001 | g0168 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00621 | hp2 | a0002 | c0003 | t0001 | g0238 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00639 | hp1 | a0001 | c0004 | t0001 | g0313 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00639 | hp2 | a0001 | c0004 | t0001 | g0087 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00642 | hp2 | a0001 | c0004 | t0001 | g0034 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00673 | hp1 | a0002 | c0006 | t0001 | g0257 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CHS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00733 | hp2 | a0001 | c0004 | t0001 | g0319 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0331 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG00735 | hp2 | a0003 | c0005 | t0001 | g0259 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0311 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01069 | hp2 | a0002 | c0003 | t0001 | g0025 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01071 | hp1 | a0002 | c0003 | t0001 | g0025 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01071 | hp2 | a0001 | c0004 | t0001 | g0333 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0356 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01081 | hp2 | a0002 | c0006 | t0005 | g0017 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0050 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01109 | hp1 | a0001 | c0004 | t0001 | g0312 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01168 | hp1 | a0001 | c0004 | t0001 | g0031 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01168 | hp2 | a0002 | c0003 | t0001 | g0195 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01169 | hp1 | a0001 | c0004 | t0001 | g0031 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0096 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0341 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01192 | hp2 | a0001 | c0004 | t0001 | g0034 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01243 | hp1 | a0006 | c0010 | t0001 | g0185 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0352 | AMR | PUR | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01256 | hp1 | a0003 | c0005 | t0001 | g0214 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0324 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01261 | hp1 | a0001 | c0007 | t0001 | g0339 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01261 | hp2 | a0001 | c0004 | t0001 | g0188 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01346 | hp1 | a0002 | c0003 | t0001 | g0043 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01346 | hp2 | a0001 | c0004 | t0001 | g0343 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01358 | hp2 | a0001 | c0004 | t0001 | g0321 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01361 | hp1 | a0001 | c0004 | t0004 | g0153 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01496 | hp2 | a0001 | c0004 | t0001 | g0345 | AMR | CLM | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01515 | hp1 | a0001 | c0004 | t0001 | g0032 | EUR | IBS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0061 | EUR | IBS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01516 | hp1 | a0001 | c0007 | t0001 | g0010 | EUR | IBS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0330 | EUR | IBS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0032 | EUR | IBS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01517 | hp2 | a0001 | c0007 | t0001 | g0010 | EUR | IBS | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01884 | hp1 | a0002 | c0006 | t0005 | g0005 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0327 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0088 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0056 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01928 | hp2 | a0003 | c0005 | t0001 | g0023 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01934 | hp2 | a0003 | c0005 | t0001 | g0227 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01978 | hp1 | a0001 | c0004 | t0001 | g0322 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG01981 | hp2 | a0001 | c0004 | t0001 | g0310 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02015 | hp2 | a0002 | c0006 | t0001 | g0251 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0237 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02027 | hp2 | a0002 | c0006 | t0011 | g0207 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02040 | hp2 | a0003 | c0005 | t0001 | g0247 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0172 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02056 | hp1 | a0001 | c0004 | t0001 | g0346 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02071 | hp1 | a0002 | c0003 | t0001 | g0221 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02080 | hp1 | a0002 | c0003 | t0001 | g0270 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02132 | hp1 | a0002 | c0003 | t0001 | g0079 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0169 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02135 | hp1 | a0003 | c0005 | t0001 | g0234 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02145 | hp1 | a0001 | c0004 | t0001 | g0335 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0049 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02148 | hp2 | a0003 | c0005 | t0001 | g0215 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02155 | hp2 | a0003 | c0005 | t0001 | g0246 | EAS | CDX | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0133 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0109 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02273 | hp2 | a0003 | c0005 | t0001 | g0023 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02280 | hp1 | a0001 | c0004 | t0004 | g0020 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02280 | hp2 | a0005 | c0011 | t0004 | g0142 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0053 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02293 | hp2 | a0002 | c0006 | t0005 | g0005 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02300 | hp1 | a0003 | c0005 | t0001 | g0205 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02451 | hp1 | a0002 | c0006 | t0005 | g0017 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02523 | hp1 | a0003 | c0005 | t0001 | g0159 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0157 | EAS | KHV | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0353 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02572 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0075 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02602 | hp2 | a0002 | c0003 | t0001 | g0228 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02615 | hp1 | a0001 | c0007 | t0001 | g0337 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0271 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0170 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02647 | hp2 | a0002 | c0006 | t0005 | g0005 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0216 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02698 | hp2 | a0003 | c0008 | t0001 | g0208 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0174 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02735 | hp1 | a0003 | c0005 | t0001 | g0262 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02735 | hp2 | a0001 | c0004 | t0001 | g0317 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02738 | hp1 | a0002 | c0003 | t0001 | g0260 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02809 | hp1 | a0003 | c0005 | t0001 | g0200 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02809 | hp2 | a0005 | c0011 | t0004 | g0141 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0354 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0329 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0351 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02922 | hp1 | a0002 | c0003 | t0001 | g0154 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02970 | hp1 | a0004 | c0012 | t0001 | g0016 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02976 | hp1 | a0002 | c0006 | t0005 | g0137 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03041 | hp2 | a0001 | c0004 | t0004 | g0177 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03098 | hp1 | a0001 | c0004 | t0004 | g0178 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03139 | hp1 | a0004 | c0012 | t0001 | g0016 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03209 | hp1 | a0006 | c0010 | t0001 | g0187 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03209 | hp2 | a0001 | c0001 | t0010 | g0092 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03225 | hp1 | a0002 | c0003 | t0007 | g0357 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03239 | hp1 | a0001 | c0004 | t0001 | g0033 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03486 | hp1 | a0001 | c0004 | t0004 | g0020 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03486 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03490 | hp1 | a0001 | c0004 | t0001 | g0315 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03490 | hp2 | a0001 | c0004 | t0001 | g0340 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03491 | hp1 | a0001 | c0004 | t0001 | g0314 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0033 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0097 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03516 | hp2 | a0001 | c0004 | t0004 | g0180 | AFR | ESN | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03540 | hp2 | a0002 | c0006 | t0003 | g0143 | AFR | GWD | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0171 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03669 | hp2 | a0001 | c0017 | t0003 | g0166 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03688 | hp2 | a0002 | c0003 | t0001 | g0222 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03704 | hp2 | a0001 | c0016 | t0001 | g0316 | SAS | PJL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03834 | hp1 | a0003 | c0005 | t0001 | g0347 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03834 | hp2 | a0001 | c0004 | t0001 | g0318 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03927 | hp1 | a0001 | c0007 | t0001 | g0132 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03942 | hp1 | a0002 | c0003 | t0001 | g0229 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04115 | hp1 | a0002 | c0003 | t0001 | g0241 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04184 | hp1 | a0001 | c0004 | t0001 | g0336 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04184 | hp2 | a0002 | c0003 | t0001 | g0217 | SAS | BEB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04199 | hp2 | a0001 | c0004 | t0001 | g0328 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0261 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG04228 | hp2 | a0001 | c0004 | t0001 | g0326 | SAS | STU | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0355 | AFR | YRI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0098 | AFR | YRI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18747 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | CHB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | YRI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18906 | hp2 | a0002 | c0006 | t0005 | g0005 | AFR | YRI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18939 | hp1 | a0002 | c0006 | t0001 | g0255 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18940 | hp1 | a0002 | c0006 | t0001 | g0009 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0028 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18944 | hp1 | a0010 | c0014 | t0001 | g0223 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18944 | hp2 | a0003 | c0005 | t0001 | g0244 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18945 | hp1 | a0002 | c0003 | t0001 | g0219 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18946 | hp1 | a0002 | c0006 | t0001 | g0253 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18948 | hp2 | a0002 | c0003 | t0001 | g0349 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18950 | hp1 | a0002 | c0006 | t0001 | g0256 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18952 | hp1 | a0003 | c0005 | t0001 | g0211 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18952 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18953 | hp1 | a0002 | c0003 | t0001 | g0226 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18954 | hp1 | a0002 | c0006 | t0001 | g0196 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18957 | hp2 | a0003 | c0005 | t0001 | g0350 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18959 | hp2 | a0008 | c0015 | t0012 | g0220 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18960 | hp2 | a0003 | c0008 | t0001 | g0265 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0204 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18965 | hp1 | a0002 | c0006 | t0001 | g0009 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18966 | hp2 | a0002 | c0003 | t0001 | g0232 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18968 | hp2 | a0002 | c0006 | t0001 | g0225 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18970 | hp1 | a0003 | c0005 | t0001 | g0212 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18970 | hp2 | a0002 | c0006 | t0001 | g0248 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18971 | hp1 | a0002 | c0009 | t0001 | g0029 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18973 | hp2 | a0003 | c0005 | t0001 | g0213 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18975 | hp1 | a0003 | c0005 | t0001 | g0218 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18979 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18982 | hp2 | a0009 | c0013 | t0001 | g0190 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18984 | hp1 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18985 | hp2 | a0002 | c0003 | t0008 | g0224 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18986 | hp2 | a0003 | c0005 | t0001 | g0008 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18987 | hp2 | a0002 | c0003 | t0001 | g0028 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18992 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18994 | hp2 | a0002 | c0003 | t0008 | g0022 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18995 | hp2 | a0002 | c0006 | t0001 | g0210 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18997 | hp1 | a0003 | c0005 | t0001 | g0269 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18999 | hp1 | a0003 | c0005 | t0001 | g0209 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19000 | hp2 | a0003 | c0005 | t0001 | g0008 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19001 | hp2 | a0002 | c0006 | t0001 | g0252 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19002 | hp1 | a0001 | c0001 | t0014 | g0191 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19004 | hp2 | a0002 | c0003 | t0001 | g0258 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19007 | hp2 | a0003 | c0005 | t0001 | g0027 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19010 | hp1 | a0002 | c0003 | t0001 | g0243 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19011 | hp1 | a0003 | c0005 | t0001 | g0008 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | LWK | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19055 | hp1 | a0002 | c0006 | t0001 | g0009 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19057 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19058 | hp2 | a0002 | c0006 | t0001 | g0249 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19060 | hp2 | a0002 | c0003 | t0008 | g0022 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19063 | hp1 | a0002 | c0006 | t0001 | g0254 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19064 | hp1 | a0002 | c0009 | t0001 | g0029 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19066 | hp1 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19068 | hp1 | a0007 | c0018 | t0002 | g0189 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19068 | hp2 | a0003 | c0005 | t0001 | g0027 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19070 | hp2 | a0002 | c0003 | t0008 | g0194 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19075 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19075 | hp2 | a0003 | c0005 | t0001 | g0304 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19076 | hp2 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19079 | hp1 | a0003 | c0008 | t0001 | g0206 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19079 | hp2 | a0002 | c0003 | t0001 | g0040 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19081 | hp2 | a0002 | c0006 | t0001 | g0235 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19084 | hp2 | a0003 | c0005 | t0001 | g0242 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19086 | hp2 | a0002 | c0006 | t0001 | g0250 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19087 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19087 | hp2 | a0003 | c0008 | t0001 | g0266 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19090 | hp2 | a0003 | c0005 | t0001 | g0233 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | YRI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | ASW | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ASW | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0080 | EUR | TSI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20752 | hp2 | a0001 | c0004 | t0001 | g0342 | EUR | TSI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0344 | EUR | TSI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0105 | EUR | TSI | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02109 | hp1 | a0001 | c0004 | t0004 | g0179 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02486 | hp2 | a0001 | c0007 | t0013 | g0186 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0175 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ACB | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0192 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0268 | AFR | MSL | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0320 | AFR | USA | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | USA | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18955 | hp1 | a0002 | c0003 | t0001 | g0045 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | USA | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | USA | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | LWK | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
NA21309 | hp2 | a0001 | c0007 | t0001 | g0184 | AFR | LWK | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0001 | g0323 | REF | REF | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0001 | g0338 | REF | REF | GSDME_chr7_24693355_24762464 | GSDME | chr7 | 24693355 | 24762464 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:24699169
|
G | C | 1 | a0010 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1348C>G | p.Arg450Gly | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 1436/2250 | 1348/1491 | 450/496 | chr7 | 24699169 | ||
chr7:24699255
|
C | T | 1 | a0009 | 1 | NA18982.hp2 | missense_variant | MODERATE | c.1262G>A | p.Arg421His | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 1350/2250 | 1262/1491 | 421/496 | chr7 | 24699255 | ||
chr7:24710263
|
T | C | 1 | a0005 | 2 | HG02280.hp2 HG02809.hp2 |
missense_variant | MODERATE | c.823A>G | p.Ile275Val | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/10 | 911/2250 | 823/1491 | 275/496 | chr7 | 24710263 | ||
chr7:24710305
|
G | A | 1 | a0008 | 1 | NA18959.hp2 | stop_gained | HIGH | c.781C>T | p.Arg261* | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/10 | 869/2250 | 781/1491 | 261/496 | chr7 | 24710305 | ||
chr7:24717332
|
C | T | 2 | a0003a0004 | 37 | HG00544.hp1 HG00735.hp2 HG01256.hp1 others(34): Show |
missense_variant | MODERATE | c.619G>A | p.Val207Met | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/10 | 707/2250 | 619/1491 | 207/496 | chr7 | 24717332 | ||
chr7:24719102
|
A | G | 1 | a0006 | 2 | HG01243.hp1 HG03209.hp1 |
missense_variant | MODERATE | c.521T>C | p.Met174Thr | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/10 | 609/2250 | 521/1491 | 174/496 | chr7 | 24719102 | ||
chr7:24719199
|
G | T | 5 | a0002a0003a0008others(2): Show | 124 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(121): Show |
missense_variant | MODERATE | c.424C>A | p.Pro142Thr | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/10 | 512/2250 | 424/1491 | 142/496 | chr7 | 24719199 | ||
chr7:24744694
|
G | A | 1 | a0007 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.272C>T | p.Thr91Ile | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/10 | 360/2250 | 272/1491 | 91/496 | chr7 | 24744694 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:24702817
|
T | C | 7 | a0001c0002a0001c0007a0002c0006others(4): Show | 102 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(99): Show |
synonymous_variant | LOW | c.1200A>G | p.Ala400Ala | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/10 | 1288/2250 | 1200/1491 | 400/496 | chr7 | 24702817 | ||
chr7:24708211
|
C | T | 1 | a0002c0009 | 2 | NA18971.hp1 NA19064.hp1 |
synonymous_variant | LOW | c.906G>A | p.Leu302Leu | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/10 | 994/2250 | 906/1491 | 302/496 | chr7 | 24708211 | ||
chr7:24708253
|
C | T | 1 | a0001c0017 | 1 | HG03669.hp2 | splice_region_variant&synonymous_variant | LOW | c.864G>A | p.Ala288Ala | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/10 | 952/2250 | 864/1491 | 288/496 | chr7 | 24708253 | ||
chr7:24717339
|
G | A | 1 | a0001c0016 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.612C>T | p.Asp204Asp | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/10 | 700/2250 | 612/1491 | 204/496 | chr7 | 24717339 | ||
chr7:24719134
|
C | T | 8 | a0002c0003a0002c0006a0002c0009others(5): Show | 124 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(121): Show |
synonymous_variant | LOW | c.489G>A | p.Thr163Thr | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/10 | 577/2250 | 489/1491 | 163/496 | chr7 | 24719134 | ||
chr7:24719176
|
T | C | 13 | a0001c0001a0001c0002a0001c0017others(10): Show | 342 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(339): Show |
synonymous_variant | LOW | c.447A>G | p.Glu149Glu | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/10 | 535/2250 | 447/1491 | 149/496 | chr7 | 24719176 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:24698427
|
G | A | 1 | a0008c0015t0012 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*599C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 599 | chr7 | 24698427 | |||||
chr7:24698499
|
G | A | 3 | a0001c0001t0004a0001c0004t0004a0005c0011t0004 | 11 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*527C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 527 | chr7 | 24698499 | |||||
chr7:24698520
|
AT | A | 5 | a0001c0001t0002a0001c0001t0010a0001c0001t0015others(2): Show | 66 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*505delA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 505 | chr7 | 24698520 | |||||
chr7:24698545
|
C | G | 4 | a0001c0001t0003a0001c0001t0014a0001c0017t0003others(1): Show | 35 | HG00733.hp1 HG01099.hp1 HG01167.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*481G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 481 | chr7 | 24698545 | |||||
chr7:24698578
|
A | G | 1 | a0001c0001t0009 | 3 | HG02055.hp2 HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*448T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 448 | chr7 | 24698578 | |||||
chr7:24698680
|
C | G | 1 | a0002c0003t0008 | 4 | NA18985.hp2 NA18994.hp2 NA19060.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*346G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 346 | chr7 | 24698680 | |||||
chr7:24698745
|
G | A | 1 | a0001c0007t0013 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*281C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 281 | chr7 | 24698745 | |||||
chr7:24698753
|
G | A | 7 | a0001c0001t0002a0001c0001t0005a0001c0001t0010others(4): Show | 74 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*273C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 273 | chr7 | 24698753 | |||||
chr7:24698883
|
T | A | 1 | a0001c0001t0014 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*143A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 143 | chr7 | 24698883 | |||||
chr7:24698939
|
T | C | 1 | a0001c0001t0006 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*87A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 87 | chr7 | 24698939 | |||||
chr7:24698954
|
G | A | 1 | a0001c0001t0010 | 2 | HG03209.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*72C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 10/10 | 72 | chr7 | 24698954 | |||||
chr7:24749789
|
A | G | 1 | a0002c0006t0011 | 1 | HG02027.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/10 | 15 | chr7 | 24749789 | |||||
chr7:24757405
|
C | A | 3 | a0001c0001t0007a0001c0001t0015a0002c0003t0007 | 7 | HG01081.hp1 HG01243.hp2 HG02572.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-29G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/10 | chr7 | 24757405 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:24699383
|
T | A | 7 | a0002c0003t0001g0079a0002c0003t0001g0168a0002c0003t0001g0226others(4): Show | 7 | HG00597.hp1 HG02080.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.1258-124A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699383 | ||||||
chr7:24699411
|
C | T | 1 | a0001c0002t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1258-152G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699411 | ||||||
chr7:24699468
|
G | A | 2 | a0005c0011t0004g0141a0005c0011t0004g0142 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1258-209C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699468 | ||||||
chr7:24699540
|
G | A | 1 | a0001c0001t0003g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1258-281C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699540 | ||||||
chr7:24699563
|
T | C | 7 | a0001c0001t0004g0146a0001c0004t0004g0020a0001c0004t0004g0153others(4): Show | 8 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258-304A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699563 | ||||||
chr7:24699587
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1258-328T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699587 | ||||||
chr7:24699609
|
T | G | 262 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(259): Show | 307 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(304): Show |
intron_variant | MODIFIER | c.1258-350A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699609 | ||||||
chr7:24699765
|
G | A | 2 | a0005c0011t0004g0141a0005c0011t0004g0142 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1258-506C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699765 | ||||||
chr7:24699860
|
G | A | 4 | a0002c0003t0001g0079a0002c0003t0001g0168a0002c0003t0001g0226others(1): Show | 4 | HG00597.hp1 HG02132.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258-601C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699860 | ||||||
chr7:24699970
|
C | G | 1 | a0001c0001t0004g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1258-711G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24699970 | ||||||
chr7:24700097
|
C | G | 2 | a0001c0001t0002g0303a0001c0001t0002g0309 | 2 | NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1258-838G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700097 | ||||||
chr7:24700100
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1258-841G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700100 | ||||||
chr7:24700201
|
C | T | 2 | a0001c0001t0002g0303a0001c0001t0002g0309 | 2 | NA18988.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1258-942G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700201 | ||||||
chr7:24700226
|
G | A | 17 | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0117others(14): Show | 18 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.1258-967C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700226 | ||||||
chr7:24700234
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1258-975T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700234 | ||||||
chr7:24700261
|
C | T | 1 | a0001c0002t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1258-1002G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700261 | ||||||
chr7:24700290
|
C | A | 3 | a0002c0006t0005g0005a0002c0006t0005g0017a0002c0006t0005g0137 | 7 | HG01081.hp2 HG01884.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-1031G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700290 | ||||||
chr7:24700305
|
A | G | 7 | a0001c0001t0004g0152a0001c0004t0004g0020a0001c0004t0004g0153others(4): Show | 8 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258-1046T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700305 | ||||||
chr7:24700478
|
A | G | 1 | a0001c0002t0001g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1258-1219T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700478 | ||||||
chr7:24700525
|
A | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0136 | 3 | HG01099.hp2 HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1258-1266T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700525 | ||||||
chr7:24700558
|
T | C | 243 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0094others(240): Show | 287 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(284): Show |
intron_variant | MODIFIER | c.1258-1299A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700558 | ||||||
chr7:24700585
|
G | C | 1 | a0001c0007t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1258-1326C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700585 | ||||||
chr7:24700589
|
G | C | 1 | a0001c0004t0001g0340 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1258-1330C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700589 | ||||||
chr7:24700626
|
G | T | 8 | a0001c0001t0004g0146a0001c0001t0004g0152a0001c0004t0004g0020others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1258-1367C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700626 | ||||||
chr7:24700662
|
A | AT | 6 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(3): Show | 7 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1258-1404dupA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700662 | ||||||
chr7:24700688
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1258-1429A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700688 | ||||||
chr7:24700794
|
A | T | 8 | a0001c0001t0004g0146a0001c0001t0004g0152a0001c0004t0004g0020others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1258-1535T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700794 | ||||||
chr7:24700838
|
C | T | 3 | a0001c0007t0013g0186a0006c0010t0001g0185a0006c0010t0001g0187 | 3 | HG01243.hp1 HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1258-1579G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700838 | ||||||
chr7:24700863
|
C | G | 1 | a0001c0001t0002g0296 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1258-1604G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700863 | ||||||
chr7:24700891
|
G | A | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-1632C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700891 | ||||||
chr7:24700956
|
C | T | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1258-1697G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24700956 | ||||||
chr7:24701003
|
C | G | 1 | a0001c0001t0003g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1258-1744G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701003 | ||||||
chr7:24701164
|
A | C | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1257+1596T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701164 | ||||||
chr7:24701166
|
C | G | 3 | a0001c0001t0009g0170a0001c0001t0009g0171a0001c0001t0009g0172 | 3 | HG02055.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1257+1594G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701166 | ||||||
chr7:24701351
|
G | T | 1 | a0002c0006t0003g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1257+1409C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701351 | ||||||
chr7:24701500
|
G | A | 7 | a0001c0001t0004g0152a0001c0004t0004g0020a0001c0004t0004g0153others(4): Show | 8 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1257+1260C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701500 | ||||||
chr7:24701567
|
C | CTT | 3 | a0001c0001t0004g0146a0001c0001t0007g0355a0001c0001t0007g0356 | 3 | HG01081.hp1 NA18522.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1257+1191_1257+119 others(6): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701567 | ||||||
chr7:24701633
|
T | C | 2 | a0001c0001t0007g0355a0001c0001t0007g0356 | 2 | HG01081.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1257+1127A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701633 | ||||||
chr7:24701638
|
A | G | 1 | a0001c0001t0004g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1257+1122T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701638 | ||||||
chr7:24701739
|
T | C | 1 | a0001c0001t0001g0126 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1257+1021A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701739 | ||||||
chr7:24701982
|
C | G | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1257+778G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24701982 | ||||||
chr7:24702067
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1257+693G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702067 | ||||||
chr7:24702240
|
A | G | 4 | a0001c0002t0001g0128a0002c0006t0001g0210a0002c0006t0001g0225others(1): Show | 4 | HG00609.hp2 NA18944.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257+520T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702240 | ||||||
chr7:24702283
|
G | A | 57 | a0001c0001t0002g0006a0001c0001t0002g0015a0001c0001t0002g0021others(54): Show | 64 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1257+477C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702283 | ||||||
chr7:24702326
|
A | C | 9 | a0001c0001t0004g0146a0001c0001t0007g0355a0001c0001t0007g0356others(6): Show | 10 | HG01081.hp1 HG01361.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257+434T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702326 | ||||||
chr7:24702480
|
T | C | 1 | a0001c0001t0004g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1257+280A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702480 | ||||||
chr7:24702491
|
G | A | 1 | a0001c0017t0003g0166 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1257+269C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702491 | ||||||
chr7:24702509
|
G | A | 52 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(49): Show | 61 | HG00733.hp1 HG01081.hp1 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.1257+251C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702509 | ||||||
chr7:24702649
|
A | C | 1 | a0002c0003t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1257+111T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 9/9 | chr7 | 24702649 | ||||||
chr7:24702895
|
C | T | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184-62G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24702895 | ||||||
chr7:24702934
|
G | A | 108 | a0001c0001t0001g0014a0001c0001t0001g0100a0001c0001t0001g0102others(105): Show | 122 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1184-101C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24702934 | ||||||
chr7:24702957
|
C | T | 4 | a0001c0004t0001g0324a0001c0004t0001g0334a0001c0004t0001g0341others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184-124G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24702957 | ||||||
chr7:24702966
|
C | T | 212 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0102others(209): Show | 246 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.1184-133G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24702966 | ||||||
chr7:24702997
|
C | G | 1 | a0002c0006t0001g0235 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1184-164G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24702997 | ||||||
chr7:24702997
|
C | T | 1 | a0002c0003t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1184-164G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24702997 | ||||||
chr7:24703138
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0003g0104 | 6 | HG01109.hp2 HG02559.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184-305C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703138 | ||||||
chr7:24703305
|
C | T | 8 | a0001c0004t0001g0033a0001c0004t0001g0050a0001c0004t0001g0314others(5): Show | 9 | HG01106.hp1 HG01243.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184-472G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703305 | ||||||
chr7:24703310
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1184-477T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703310 | ||||||
chr7:24703450
|
A | T | 1 | a0001c0002t0001g0035 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1184-617T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703450 | ||||||
chr7:24703452
|
G | T | 2 | a0002c0003t0001g0228a0002c0003t0001g0229 | 2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1184-619C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703452 | ||||||
chr7:24703453
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1184-620C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703453 | ||||||
chr7:24703586
|
G | C | 171 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0077others(168): Show | 198 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1184-753C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703586 | ||||||
chr7:24703604
|
G | A | 1 | a0002c0003t0001g0243 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1184-771C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703604 | ||||||
chr7:24703876
|
A | C | 5 | a0001c0001t0002g0006a0001c0001t0002g0021a0001c0001t0002g0201others(2): Show | 9 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184-1043T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703876 | ||||||
chr7:24703887
|
C | T | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1184-1054G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703887 | ||||||
chr7:24703899
|
A | C | 1 | a0001c0002t0001g0065 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1184-1066T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703899 | ||||||
chr7:24703977
|
C | T | 4 | a0002c0006t0003g0143a0002c0006t0005g0005a0002c0006t0005g0017others(1): Show | 8 | HG01081.hp2 HG01884.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184-1144G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703977 | ||||||
chr7:24703984
|
C | T | 1 | a0003c0005t0001g0214 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1184-1151G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24703984 | ||||||
chr7:24704049
|
G | A | 2 | a0005c0011t0004g0141a0005c0011t0004g0142 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1184-1216C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704049 | ||||||
chr7:24704250
|
A | G | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1184-1417T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704250 | ||||||
chr7:24704663
|
A | C | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1183+1521T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704663 | ||||||
chr7:24704690
|
C | A | 306 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(303): Show | 354 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(351): Show |
intron_variant | MODIFIER | c.1183+1494G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704690 | ||||||
chr7:24704723
|
A | AT | 26 | a0001c0001t0001g0018a0001c0001t0001g0115a0001c0001t0001g0116others(23): Show | 27 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1183+1460dupA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704723 | ||||||
chr7:24704723
|
AT | A | 6 | a0001c0002t0001g0074a0002c0006t0001g0249a0002c0006t0003g0143others(3): Show | 10 | HG01081.hp2 HG01884.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+1460delA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704723 | ||||||
chr7:24704723
|
ATT | A | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+1459_1183+146 others(6): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704723 | ||||||
chr7:24704736
|
T | C | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183+1448A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704736 | ||||||
chr7:24704752
|
A | G | 2 | a0002c0003t0001g0097a0002c0003t0001g0175 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1183+1432T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704752 | ||||||
chr7:24704757
|
G | A | 1 | a0002c0003t0001g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1183+1427C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704757 | ||||||
chr7:24704805
|
A | G | 21 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0136others(18): Show | 22 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.1183+1379T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704805 | ||||||
chr7:24704879
|
G | C | 3 | a0002c0003t0001g0195a0002c0003t0001g0230a0002c0003t0001g0260 | 3 | HG00140.hp2 HG01168.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1183+1305C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704879 | ||||||
chr7:24704946
|
C | T | 5 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0084others(2): Show | 6 | HG00423.hp2 NA18948.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183+1238G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704946 | ||||||
chr7:24704953
|
G | A | 2 | a0001c0001t0007g0355a0001c0001t0007g0356 | 2 | HG01081.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1183+1231C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24704953 | ||||||
chr7:24705013
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1183+1171G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705013 | ||||||
chr7:24705076
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1183+1108G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705076 | ||||||
chr7:24705094
|
T | C | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+1090A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705094 | ||||||
chr7:24705140
|
C | T | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1183+1044G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705140 | ||||||
chr7:24705152
|
G | A | 1 | a0002c0003t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1183+1032C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705152 | ||||||
chr7:24705190
|
C | G | 1 | a0002c0003t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1183+994G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705190 | ||||||
chr7:24705296
|
CTA | C | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183+886_1183+887d others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705296 | ||||||
chr7:24705487
|
G | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1183+697C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705487 | ||||||
chr7:24705670
|
G | C | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1183+514C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705670 | ||||||
chr7:24705712
|
T | C | 16 | a0001c0001t0002g0030a0001c0001t0002g0272a0001c0001t0002g0278others(13): Show | 17 | HG00423.hp1 HG00438.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.1183+472A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705712 | ||||||
chr7:24705835
|
G | C | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1183+349C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705835 | ||||||
chr7:24705920
|
C | T | 1 | a0001c0004t0001g0317 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1183+264G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705920 | ||||||
chr7:24705994
|
G | T | 1 | a0001c0002t0001g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1183+190C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705994 | ||||||
chr7:24705995
|
C | CCCCCT | 3 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152 | 4 | HG02896.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183+188_1183+189i others(7): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705995 | ||||||
chr7:24705996
|
A | C | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+188T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705996 | ||||||
chr7:24705996
|
A | T | 3 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152 | 4 | HG02896.hp2 HG02897.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183+188T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705996 | ||||||
chr7:24705997
|
C | CCCTTT | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+186_1183+187i others(7): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705997 | ||||||
chr7:24705998
|
A | G | 11 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152others(8): Show | 13 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183+186T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24705998 | ||||||
chr7:24706000
|
A | T | 11 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152others(8): Show | 13 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183+184T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706000 | ||||||
chr7:24706007
|
A | T | 11 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152others(8): Show | 13 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183+177T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706007 | ||||||
chr7:24706008
|
CCGAAG | C | 11 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152others(8): Show | 13 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183+171_1183+175d others(7): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706008 | ||||||
chr7:24706014
|
G | T | 11 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152others(8): Show | 13 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183+170C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706014 | ||||||
chr7:24706016
|
G | T | 11 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152others(8): Show | 13 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1183+168C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706016 | ||||||
chr7:24706049
|
C | G | 1 | a0003c0005t0001g0205 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1183+135G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706049 | ||||||
chr7:24706095
|
T | C | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1183+89A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706095 | ||||||
chr7:24706098
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1183+86G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706098 | ||||||
chr7:24706109
|
C | T | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1183+75G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706109 | ||||||
chr7:24706167
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0094a0003c0005t0001g0200 | 6 | HG01109.hp2 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183+17A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 8/9 | chr7 | 24706167 | ||||||
chr7:24706403
|
A | G | 61 | a0001c0001t0001g0077a0001c0001t0001g0263a0001c0001t0009g0170others(58): Show | 68 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.991-27T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706403 | ||||||
chr7:24706407
|
C | T | 2 | a0001c0004t0001g0324a0001c0004t0001g0348 | 2 | HG00280.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.991-31G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706407 | ||||||
chr7:24706435
|
G | C | 1 | a0001c0001t0003g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.991-59C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706435 | ||||||
chr7:24706443
|
G | A | 23 | a0001c0001t0001g0018a0001c0001t0001g0115a0001c0001t0001g0116others(20): Show | 24 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.991-67C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706443 | ||||||
chr7:24706483
|
G | A | 1 | a0008c0015t0012g0220 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.991-107C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706483 | ||||||
chr7:24706593
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0155 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.991-217G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706593 | ||||||
chr7:24706628
|
G | A | 7 | a0001c0004t0001g0087a0001c0004t0001g0318a0001c0004t0001g0320others(4): Show | 7 | HG00099.hp2 HG00639.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-252C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706628 | ||||||
chr7:24706707
|
G | A | 2 | a0001c0001t0003g0019a0001c0001t0004g0146 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.991-331C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706707 | ||||||
chr7:24706752
|
G | A | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.991-376C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706752 | ||||||
chr7:24706808
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.991-432C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706808 | ||||||
chr7:24706917
|
G | A | 1 | a0001c0004t0001g0087 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.991-541C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706917 | ||||||
chr7:24706927
|
G | A | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.991-551C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706927 | ||||||
chr7:24706973
|
C | A | 1 | a0003c0005t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.991-597G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24706973 | ||||||
chr7:24707034
|
A | G | 11 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0001t0004g0152others(8): Show | 13 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.991-658T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707034 | ||||||
chr7:24707082
|
C | G | 1 | a0001c0002t0001g0058 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.991-706G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707082 | ||||||
chr7:24707154
|
G | A | 2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | NA19005.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.991-778C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707154 | ||||||
chr7:24707185
|
T | G | 1 | a0001c0001t0003g0104 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.991-809A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707185 | ||||||
chr7:24707273
|
C | A | 64 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0283others(61): Show | 81 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.990+854G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707273 | ||||||
chr7:24707304
|
C | G | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.990+823G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707304 | ||||||
chr7:24707462
|
T | C | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.990+665A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707462 | ||||||
chr7:24707486
|
CTT | C | 4 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0002g0293others(1): Show | 4 | HG01952.hp1 NA18953.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+639_990+640del others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707486 | ||||||
chr7:24707504
|
A | T | 1 | a0001c0002t0001g0078 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.990+623T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707504 | ||||||
chr7:24707658
|
C | G | 35 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0136others(32): Show | 36 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.990+469G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707658 | ||||||
chr7:24707683
|
GAC | G | 301 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(298): Show | 348 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.990+442_990+443del others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707683 | ||||||
chr7:24707694
|
A | C | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.990+433T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707694 | ||||||
chr7:24707753
|
G | C | 3 | a0002c0003t0001g0038a0002c0003t0001g0044a0002c0003t0001g0045 | 3 | NA18955.hp1 NA18971.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.990+374C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707753 | ||||||
chr7:24707862
|
T | C | 1 | a0002c0003t0001g0025 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.990+265A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707862 | ||||||
chr7:24707875
|
CTA | C | 12 | a0001c0001t0003g0156a0001c0001t0003g0157a0001c0001t0003g0158others(9): Show | 12 | HG00733.hp1 HG01099.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.990+250_990+251del others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707875 | ||||||
chr7:24707922
|
G | C | 1 | a0003c0005t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.990+205C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707922 | ||||||
chr7:24707986
|
C | T | 5 | a0001c0001t0002g0275a0001c0001t0002g0279a0001c0001t0002g0280others(2): Show | 5 | HG02074.hp2 NA18959.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.990+141G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24707986 | ||||||
chr7:24708036
|
G | A | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.990+91C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24708036 | ||||||
chr7:24708066
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.990+61G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24708066 | ||||||
chr7:24708081
|
A | G | 1 | a0001c0001t0004g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.990+46T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 7/9 | chr7 | 24708081 | ||||||
chr7:24708291
|
G | A | 296 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(293): Show | 343 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.863-37C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708291 | ||||||
chr7:24708330
|
T | C | 1 | a0004c0012t0001g0016 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.863-76A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708330 | ||||||
chr7:24708426
|
A | G | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | HG02622.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.863-172T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708426 | ||||||
chr7:24708634
|
C | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.863-380G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708634 | ||||||
chr7:24708658
|
C | T | 1 | a0002c0003t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.863-404G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708658 | ||||||
chr7:24708730
|
C | G | 4 | a0001c0004t0001g0324a0001c0004t0001g0334a0001c0004t0001g0341others(1): Show | 4 | HG00280.hp1 HG00323.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-476G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708730 | ||||||
chr7:24708814
|
C | A | 3 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177 | 4 | HG01361.hp1 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.863-560G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708814 | ||||||
chr7:24708831
|
G | A | 44 | a0001c0001t0001g0283a0001c0001t0002g0006a0001c0001t0002g0021others(41): Show | 49 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.863-577C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708831 | ||||||
chr7:24708946
|
T | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(304): Show | 356 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.863-692A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708946 | ||||||
chr7:24708988
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.863-734T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708988 | ||||||
chr7:24708996
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.863-742A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24708996 | ||||||
chr7:24709029
|
G | A | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.863-775C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709029 | ||||||
chr7:24709211
|
C | T | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.863-957G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709211 | ||||||
chr7:24709281
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.862+943C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709281 | ||||||
chr7:24709408
|
G | GA | 91 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(88): Show | 106 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.862+815dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709408 | ||||||
chr7:24709501
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.862+723G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709501 | ||||||
chr7:24709514
|
G | A | 1 | a0001c0001t0003g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.862+710C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709514 | ||||||
chr7:24709525
|
T | C | 1 | a0001c0002t0001g0073 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.862+699A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709525 | ||||||
chr7:24709542
|
A | C | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.862+682T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709542 | ||||||
chr7:24709550
|
G | A | 6 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(3): Show | 7 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.862+674C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709550 | ||||||
chr7:24709551
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.862+673G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709551 | ||||||
chr7:24709580
|
G | T | 51 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0003g0019others(48): Show | 60 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.862+644C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709580 | ||||||
chr7:24709604
|
T | C | 299 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(296): Show | 347 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(344): Show |
intron_variant | MODIFIER | c.862+620A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709604 | ||||||
chr7:24709755
|
C | T | 1 | a0001c0004t0004g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.862+469G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709755 | ||||||
chr7:24709782
|
T | C | 3 | a0001c0001t0002g0015a0001c0001t0007g0351a0001c0001t0007g0353 | 4 | HG02572.hp1 HG02895.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.862+442A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709782 | ||||||
chr7:24709810
|
A | G | 299 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(296): Show | 347 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(344): Show |
intron_variant | MODIFIER | c.862+414T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709810 | ||||||
chr7:24709882
|
G | A | 3 | a0002c0006t0003g0143a0002c0006t0005g0005a0002c0006t0005g0137 | 6 | HG01884.hp1 HG02293.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.862+342C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709882 | ||||||
chr7:24709975
|
G | A | 6 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(3): Show | 7 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.862+249C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24709975 | ||||||
chr7:24710027
|
C | T | 1 | a0001c0001t0003g0157 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.862+197G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24710027 | ||||||
chr7:24710086
|
T | G | 5 | a0001c0001t0002g0129a0001c0001t0002g0273a0001c0001t0002g0274others(2): Show | 5 | NA18942.hp1 NA18967.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.862+138A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24710086 | ||||||
chr7:24710088
|
G | A | 1 | a0001c0001t0007g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.862+136C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24710088 | ||||||
chr7:24710136
|
T | G | 1 | a0002c0006t0001g0250 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.862+88A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24710136 | ||||||
chr7:24710136
|
TC | T | 98 | a0002c0003t0001g0007a0002c0003t0001g0024a0002c0003t0001g0025others(95): Show | 111 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.862+87delG | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24710136 | ||||||
chr7:24710137
|
C | T | 1 | a0002c0006t0001g0250 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.862+87G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 6/9 | chr7 | 24710137 | ||||||
chr7:24710417
|
G | C | 1 | a0001c0001t0003g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.698-29C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24710417 | ||||||
chr7:24710514
|
T | C | 3 | a0001c0001t0009g0170a0001c0001t0009g0171a0001c0001t0009g0172 | 3 | HG02055.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.698-126A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24710514 | ||||||
chr7:24710600
|
TG | T | 52 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0003g0019others(49): Show | 60 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.698-213delC | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24710600 | ||||||
chr7:24710618
|
C | A | 1 | a0001c0001t0002g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.698-230G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24710618 | ||||||
chr7:24710623
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.698-235A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24710623 | ||||||
chr7:24710796
|
C | T | 9 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0153others(6): Show | 10 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.698-408G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24710796 | ||||||
chr7:24710889
|
C | A | 4 | a0001c0004t0001g0033a0001c0004t0001g0314a0001c0004t0001g0315others(1): Show | 5 | HG02056.hp1 HG03239.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-501G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24710889 | ||||||
chr7:24711314
|
C | T | 51 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0003g0019others(48): Show | 59 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.698-926G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711314 | ||||||
chr7:24711315
|
G | A | 1 | a0001c0001t0015g0354 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.698-927C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711315 | ||||||
chr7:24711447
|
GT | G | 52 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0003g0019others(49): Show | 60 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.698-1060delA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711447 | ||||||
chr7:24711578
|
C | T | 1 | a0001c0001t0003g0019 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.698-1190G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711578 | ||||||
chr7:24711643
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.698-1255G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711643 | ||||||
chr7:24711669
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.698-1281C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711669 | ||||||
chr7:24711685
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.698-1297G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711685 | ||||||
chr7:24711815
|
C | CA | 72 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0003g0013others(69): Show | 81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.698-1428dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711815 | ||||||
chr7:24711815
|
C | CAA | 93 | a0001c0001t0001g0197a0001c0001t0001g0263a0001c0001t0001g0264others(90): Show | 106 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.698-1429_698-1428d others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711815 | ||||||
chr7:24711815
|
C | CAAA | 17 | a0002c0003t0001g0226a0002c0003t0001g0229a0002c0003t0001g0239others(14): Show | 19 | HG00544.hp1 HG00735.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.698-1430_698-1428d others(5): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711815 | ||||||
chr7:24711815
|
CA | C | 8 | a0001c0001t0001g0116a0001c0001t0002g0002a0001c0001t0002g0111others(5): Show | 12 | HG02486.hp1 HG02622.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.698-1428delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711815 | ||||||
chr7:24711832
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.698-1444T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711832 | ||||||
chr7:24711964
|
C | A | 2 | a0001c0001t0002g0276a0001c0001t0002g0296 | 2 | HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.698-1576G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24711964 | ||||||
chr7:24712031
|
C | T | 1 | a0001c0002t0001g0068 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.698-1643G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712031 | ||||||
chr7:24712069
|
C | G | 1 | a0001c0002t0001g0085 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.698-1681G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712069 | ||||||
chr7:24712176
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.698-1788T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712176 | ||||||
chr7:24712191
|
A | G | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.698-1803T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712191 | ||||||
chr7:24712228
|
C | T | 60 | a0002c0003t0001g0007a0002c0003t0001g0028a0002c0003t0001g0037others(57): Show | 67 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.698-1840G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712228 | ||||||
chr7:24712231
|
T | G | 1 | a0001c0004t0004g0180 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.698-1843A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712231 | ||||||
chr7:24712339
|
G | C | 50 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0003g0019others(47): Show | 58 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.698-1951C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712339 | ||||||
chr7:24712529
|
T | C | 4 | a0002c0006t0003g0143a0002c0006t0005g0005a0002c0006t0005g0017others(1): Show | 8 | HG01081.hp2 HG01884.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.698-2141A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712529 | ||||||
chr7:24712648
|
C | T | 1 | a0001c0002t0001g0042 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.698-2260G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712648 | ||||||
chr7:24712794
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.698-2406C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712794 | ||||||
chr7:24712808
|
C | T | 1 | a0001c0002t0001g0086 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.698-2420G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712808 | ||||||
chr7:24712847
|
C | T | 1 | a0002c0003t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.698-2459G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712847 | ||||||
chr7:24712855
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.698-2467G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712855 | ||||||
chr7:24712878
|
C | T | 1 | a0001c0002t0001g0051 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.698-2490G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712878 | ||||||
chr7:24712899
|
T | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(125): Show | 149 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.698-2511A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712899 | ||||||
chr7:24712933
|
G | A | 1 | a0003c0008t0001g0208 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.698-2545C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24712933 | ||||||
chr7:24713018
|
C | CA | 110 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0197others(107): Show | 128 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.698-2631dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713018 | ||||||
chr7:24713072
|
G | A | 10 | a0001c0004t0001g0109a0001c0004t0001g0133a0001c0004t0004g0020others(7): Show | 11 | HG01361.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.698-2684C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713072 | ||||||
chr7:24713079
|
A | G | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.698-2691T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713079 | ||||||
chr7:24713088
|
T | A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.698-2700A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713088 | ||||||
chr7:24713178
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.698-2790C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713178 | ||||||
chr7:24713212
|
A | C | 1 | a0002c0003t0001g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.698-2824T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713212 | ||||||
chr7:24713346
|
G | C | 6 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0002g0090others(3): Show | 9 | HG01109.hp2 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.698-2958C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713346 | ||||||
chr7:24713560
|
G | A | 2 | a0001c0001t0007g0355a0001c0001t0007g0356 | 2 | HG01081.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.698-3172C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713560 | ||||||
chr7:24713661
|
C | T | 1 | a0001c0004t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.698-3273G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713661 | ||||||
chr7:24713756
|
C | G | 1 | a0001c0004t0001g0336 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.698-3368G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713756 | ||||||
chr7:24713966
|
G | A | 1 | a0001c0002t0001g0065 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.697+3288C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24713966 | ||||||
chr7:24714010
|
G | A | 1 | a0001c0001t0002g0278 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.697+3244C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714010 | ||||||
chr7:24714051
|
C | T | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.697+3203G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714051 | ||||||
chr7:24714183
|
C | T | 1 | a0006c0010t0001g0187 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.697+3071G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714183 | ||||||
chr7:24714441
|
A | G | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.697+2813T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714441 | ||||||
chr7:24714484
|
C | A | 3 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0164 | 3 | HG01099.hp1 HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.697+2770G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714484 | ||||||
chr7:24714514
|
T | G | 1 | a0001c0001t0002g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.697+2740A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714514 | ||||||
chr7:24714542
|
G | C | 1 | a0001c0004t0001g0312 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.697+2712C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714542 | ||||||
chr7:24714581
|
C | T | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.697+2673G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714581 | ||||||
chr7:24714641
|
T | C | 1 | a0002c0003t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.697+2613A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714641 | ||||||
chr7:24714852
|
G | T | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.697+2402C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714852 | ||||||
chr7:24714890
|
A | G | 254 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(251): Show | 295 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(292): Show |
intron_variant | MODIFIER | c.697+2364T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714890 | ||||||
chr7:24714909
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.697+2345G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714909 | ||||||
chr7:24714910
|
G | A | 16 | a0001c0001t0003g0019a0001c0001t0004g0146a0001c0004t0001g0109others(13): Show | 22 | HG01081.hp2 HG01361.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.697+2344C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24714910 | ||||||
chr7:24715051
|
A | G | 1 | a0003c0005t0001g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.697+2203T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715051 | ||||||
chr7:24715222
|
T | C | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.697+2032A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715222 | ||||||
chr7:24715299
|
T | G | 5 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0311others(2): Show | 7 | HG00639.hp1 HG01069.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.697+1955A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715299 | ||||||
chr7:24715348
|
A | G | 1 | a0001c0001t0003g0162 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.697+1906T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715348 | ||||||
chr7:24715350
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.697+1904G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715350 | ||||||
chr7:24715365
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.697+1889C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715365 | ||||||
chr7:24715745
|
C | T | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.697+1509G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715745 | ||||||
chr7:24715753
|
A | G | 2 | a0001c0002t0001g0041a0001c0002t0001g0046 | 2 | HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.697+1501T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715753 | ||||||
chr7:24715902
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.697+1352C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715902 | ||||||
chr7:24715973
|
C | T | 1 | a0003c0005t0001g0304 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.697+1281G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24715973 | ||||||
chr7:24716244
|
C | G | 1 | a0001c0001t0003g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.697+1010G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716244 | ||||||
chr7:24716291
|
G | A | 1 | a0001c0001t0002g0015 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.697+963C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716291 | ||||||
chr7:24716484
|
C | G | 4 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0001t0002g0277others(1): Show | 4 | NA18942.hp1 NA18967.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.697+770G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716484 | ||||||
chr7:24716504
|
C | A | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.697+750G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716504 | ||||||
chr7:24716504
|
C | T | 20 | a0001c0001t0001g0283a0001c0001t0002g0030a0001c0001t0002g0272others(17): Show | 21 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.697+750G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716504 | ||||||
chr7:24716505
|
G | A | 3 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0006g0001 | 9 | HG01891.hp1 HG02451.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.697+749C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716505 | ||||||
chr7:24716621
|
C | T | 1 | a0002c0003t0001g0245 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.697+633G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716621 | ||||||
chr7:24716643
|
C | T | 1 | a0003c0005t0001g0247 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.697+611G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716643 | ||||||
chr7:24716666
|
G | T | 3 | a0001c0001t0009g0170a0001c0001t0009g0171a0001c0001t0009g0172 | 3 | HG02055.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.697+588C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716666 | ||||||
chr7:24716758
|
G | C | 134 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(131): Show | 155 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.697+496C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716758 | ||||||
chr7:24716763
|
G | C | 1 | a0003c0005t0001g0347 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.697+491C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716763 | ||||||
chr7:24716767
|
TTAA | T | 10 | a0001c0004t0001g0109a0001c0004t0001g0133a0001c0004t0004g0020others(7): Show | 11 | HG01361.hp1 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.697+484_697+486del others(3): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716767 | ||||||
chr7:24716844
|
C | T | 1 | a0001c0004t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.697+410G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24716844 | ||||||
chr7:24717024
|
A | G | 39 | a0002c0003t0001g0024a0002c0003t0001g0025a0002c0003t0001g0097others(36): Show | 46 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.697+230T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24717024 | ||||||
chr7:24717062
|
C | CA | 3 | a0001c0007t0013g0186a0006c0010t0001g0185a0006c0010t0001g0187 | 3 | HG01243.hp1 HG02486.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.697+191dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24717062 | ||||||
chr7:24717191
|
A | AGTCCCTC others(23): Show |
53 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0009g0170others(50): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.697+33_697+62dupCC others(28): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24717191 | ||||||
chr7:24717192
|
G | GTCCCTCT others(23): Show |
1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.697+32_697+61dupTC others(28): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 5/9 | chr7 | 24717192 | ||||||
chr7:24717389
|
G | A | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.577-15C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717389 | ||||||
chr7:24717507
|
G | GAGCC | 3 | a0001c0001t0002g0015a0001c0001t0007g0351a0001c0001t0007g0353 | 4 | HG02572.hp1 HG02895.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-137_577-134dup others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717507 | ||||||
chr7:24717517
|
G | A | 1 | a0002c0003t0001g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.577-143C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717517 | ||||||
chr7:24717576
|
C | T | 44 | a0002c0003t0001g0024a0002c0003t0001g0025a0002c0003t0001g0097others(41): Show | 55 | HG00544.hp1 HG00735.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.577-202G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717576 | ||||||
chr7:24717577
|
G | A | 1 | a0002c0003t0001g0045 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.577-203C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717577 | ||||||
chr7:24717583
|
C | A | 127 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(124): Show | 148 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.577-209G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717583 | ||||||
chr7:24717600
|
G | A | 1 | a0001c0001t0002g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.577-226C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717600 | ||||||
chr7:24717611
|
G | A | 53 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0009g0170others(50): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.577-237C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717611 | ||||||
chr7:24717622
|
A | C | 55 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0002t0001g0003others(52): Show | 63 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.577-248T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717622 | ||||||
chr7:24717624
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.577-250A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717624 | ||||||
chr7:24717864
|
G | A | 1 | a0003c0005t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.577-490C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717864 | ||||||
chr7:24717918
|
A | G | 2 | a0002c0003t0001g0271a0002c0003t0007g0357 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.577-544T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24717918 | ||||||
chr7:24718035
|
C | G | 2 | a0002c0003t0001g0097a0002c0003t0001g0175 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.577-661G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718035 | ||||||
chr7:24718041
|
G | A | 232 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(229): Show | 272 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.577-667C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718041 | ||||||
chr7:24718138
|
C | T | 1 | a0005c0011t0004g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.577-764G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718138 | ||||||
chr7:24718178
|
C | A | 54 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0003g0019others(51): Show | 62 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.577-804G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718178 | ||||||
chr7:24718182
|
G | A | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.577-808C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718182 | ||||||
chr7:24718388
|
C | G | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.576+659G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718388 | ||||||
chr7:24718542
|
T | C | 233 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(230): Show | 273 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(270): Show |
intron_variant | MODIFIER | c.576+505A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718542 | ||||||
chr7:24718563
|
G | C | 1 | a0001c0001t0002g0285 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.576+484C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718563 | ||||||
chr7:24718629
|
A | G | 309 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(306): Show | 357 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(354): Show |
intron_variant | MODIFIER | c.576+418T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718629 | ||||||
chr7:24718684
|
C | T | 3 | a0001c0001t0007g0352a0001c0001t0007g0355a0001c0001t0007g0356 | 3 | HG01081.hp1 HG01243.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.576+363G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718684 | ||||||
chr7:24718819
|
CTA | C | 295 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(292): Show | 342 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.576+226_576+227del others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718819 | ||||||
chr7:24718946
|
G | A | 295 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(292): Show | 342 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.576+101C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24718946 | ||||||
chr7:24719026
|
G | T | 295 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(292): Show | 342 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.576+21C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 4/9 | chr7 | 24719026 | ||||||
chr7:24719233
|
C | T | 107 | a0002c0003t0001g0007a0002c0003t0001g0024a0002c0003t0001g0025others(104): Show | 124 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.405-15G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719233 | ||||||
chr7:24719444
|
G | A | 295 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(292): Show | 342 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(339): Show |
intron_variant | MODIFIER | c.405-226C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719444 | ||||||
chr7:24719477
|
C | T | 1 | a0001c0002t0001g0084 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.405-259G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719477 | ||||||
chr7:24719519
|
G | A | 93 | a0001c0001t0001g0014a0002c0003t0001g0007a0002c0003t0001g0028others(90): Show | 105 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.405-301C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719519 | ||||||
chr7:24719522
|
G | A | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.405-304C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719522 | ||||||
chr7:24719609
|
A | G | 2 | a0001c0001t0003g0019a0001c0001t0004g0146 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.405-391T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719609 | ||||||
chr7:24719653
|
C | T | 3 | a0001c0001t0009g0170a0001c0001t0009g0171a0001c0001t0009g0172 | 3 | HG02055.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.405-435G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719653 | ||||||
chr7:24719655
|
T | C | 1 | a0001c0001t0006g0001 | 7 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-437A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719655 | ||||||
chr7:24719707
|
C | T | 1 | a0001c0001t0003g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.405-489G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719707 | ||||||
chr7:24719758
|
G | A | 101 | a0001c0001t0001g0014a0001c0002t0001g0056a0002c0003t0001g0007others(98): Show | 115 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.405-540C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719758 | ||||||
chr7:24719797
|
A | G | 1 | a0001c0004t0001g0317 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.405-579T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719797 | ||||||
chr7:24719832
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.405-614C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24719832 | ||||||
chr7:24720029
|
A | C | 104 | a0001c0001t0001g0014a0001c0001t0001g0197a0001c0001t0001g0264others(101): Show | 118 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.405-811T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720029 | ||||||
chr7:24720163
|
AC | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0094 | 5 | HG01109.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-946delG | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720163 | ||||||
chr7:24720326
|
G | A | 128 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(125): Show | 150 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.405-1108C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720326 | ||||||
chr7:24720336
|
A | G | 4 | a0002c0006t0003g0143a0002c0006t0005g0005a0002c0006t0005g0017others(1): Show | 8 | HG01081.hp2 HG01884.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-1118T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720336 | ||||||
chr7:24720398
|
G | T | 2 | a0001c0001t0003g0019a0001c0001t0004g0146 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.405-1180C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720398 | ||||||
chr7:24720420
|
A | G | 251 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(248): Show | 294 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(291): Show |
intron_variant | MODIFIER | c.405-1202T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720420 | ||||||
chr7:24720681
|
C | T | 2 | a0001c0001t0002g0095a0001c0001t0005g0096 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.405-1463G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720681 | ||||||
chr7:24720857
|
A | T | 1 | a0001c0002t0001g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.405-1639T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720857 | ||||||
chr7:24720868
|
C | T | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-1650G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720868 | ||||||
chr7:24720869
|
C | T | 8 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(5): Show | 9 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-1651G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720869 | ||||||
chr7:24720884
|
G | A | 1 | a0008c0015t0012g0220 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.405-1666C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720884 | ||||||
chr7:24720907
|
C | CA | 6 | a0001c0002t0001g0012a0001c0002t0001g0083a0001c0002t0001g0084others(3): Show | 7 | HG00423.hp2 NA18948.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-1690dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720907 | ||||||
chr7:24720907
|
CA | C | 126 | a0001c0001t0001g0018a0001c0001t0001g0100a0001c0001t0001g0102others(123): Show | 143 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.405-1690delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720907 | ||||||
chr7:24720907
|
CAA | C | 5 | a0001c0001t0001g0124a0001c0001t0002g0006a0001c0001t0002g0021others(2): Show | 9 | HG00558.hp1 HG00609.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-1691_405-1690d others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720907 | ||||||
chr7:24720955
|
G | T | 1 | a0001c0001t0007g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.405-1737C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720955 | ||||||
chr7:24720970
|
A | G | 2 | a0002c0003t0001g0097a0002c0003t0001g0175 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.405-1752T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24720970 | ||||||
chr7:24721082
|
G | A | 52 | a0001c0001t0001g0077a0001c0001t0001g0094a0001c0001t0009g0170others(49): Show | 58 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.405-1864C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721082 | ||||||
chr7:24721095
|
T | TG | 9 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0153others(6): Show | 10 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-1878_405-1877i others(3): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721095 | ||||||
chr7:24721096
|
T | G | 9 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0153others(6): Show | 10 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-1878A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721096 | ||||||
chr7:24721097
|
C | A | 9 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0153others(6): Show | 10 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-1879G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721097 | ||||||
chr7:24721099
|
C | A | 9 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0153others(6): Show | 10 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-1881G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721099 | ||||||
chr7:24721100
|
T | A | 9 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0153others(6): Show | 10 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-1882A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721100 | ||||||
chr7:24721102
|
C | G | 9 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0153others(6): Show | 10 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-1884G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721102 | ||||||
chr7:24721158
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.405-1940A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721158 | ||||||
chr7:24721443
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.405-2225G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721443 | ||||||
chr7:24721444
|
G | A | 7 | a0002c0006t0001g0009a0002c0006t0001g0196a0002c0006t0001g0249others(4): Show | 9 | HG00673.hp1 NA18939.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-2226C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721444 | ||||||
chr7:24721498
|
A | G | 2 | a0001c0002t0001g0080a0001c0007t0001g0010 | 3 | HG01516.hp1 HG01517.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.405-2280T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721498 | ||||||
chr7:24721509
|
C | G | 2 | a0001c0002t0001g0051a0001c0002t0001g0068 | 2 | HG02083.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.405-2291G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721509 | ||||||
chr7:24721653
|
C | T | 1 | a0003c0005t0001g0234 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.405-2435G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721653 | ||||||
chr7:24721796
|
G | A | 2 | a0001c0002t0001g0041a0001c0002t0001g0046 | 2 | HG02683.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.405-2578C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721796 | ||||||
chr7:24721811
|
C | A | 13 | a0002c0003t0001g0007a0002c0003t0001g0028a0002c0003t0001g0193others(10): Show | 16 | HG00621.hp2 HG02027.hp1 NA18747.hp2 others(13): Show |
intron_variant | MODIFIER | c.405-2593G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721811 | ||||||
chr7:24721836
|
G | A | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.405-2618C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721836 | ||||||
chr7:24721837
|
T | C | 10 | a0002c0006t0001g0248a0003c0005t0001g0008a0003c0005t0001g0159others(7): Show | 12 | HG00544.hp1 HG02135.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.405-2619A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721837 | ||||||
chr7:24721902
|
G | T | 1 | a0002c0003t0001g0228 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.405-2684C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721902 | ||||||
chr7:24721947
|
C | A | 1 | a0001c0001t0003g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.405-2729G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721947 | ||||||
chr7:24721979
|
A | G | 3 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0164 | 3 | HG01099.hp1 HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.405-2761T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24721979 | ||||||
chr7:24722050
|
A | G | 300 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(297): Show | 348 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.405-2832T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722050 | ||||||
chr7:24722231
|
G | T | 189 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0077others(186): Show | 220 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.405-3013C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722231 | ||||||
chr7:24722269
|
G | C | 1 | a0001c0001t0002g0099 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.405-3051C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722269 | ||||||
chr7:24722349
|
G | T | 126 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(123): Show | 147 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.405-3131C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722349 | ||||||
chr7:24722425
|
A | G | 1 | a0001c0001t0003g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.405-3207T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722425 | ||||||
chr7:24722465
|
C | T | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.405-3247G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722465 | ||||||
chr7:24722560
|
C | T | 1 | a0002c0003t0001g0204 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.405-3342G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722560 | ||||||
chr7:24722577
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.405-3359C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722577 | ||||||
chr7:24722673
|
G | T | 298 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(295): Show | 346 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(343): Show |
intron_variant | MODIFIER | c.405-3455C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722673 | ||||||
chr7:24722718
|
T | A | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.405-3500A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722718 | ||||||
chr7:24722731
|
C | T | 98 | a0001c0001t0001g0014a0002c0003t0001g0007a0002c0003t0001g0028others(95): Show | 111 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.405-3513G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722731 | ||||||
chr7:24722943
|
C | T | 6 | a0002c0003t0001g0240a0003c0005t0001g0027a0003c0005t0001g0218others(3): Show | 7 | HG02040.hp2 NA18944.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.405-3725G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24722943 | ||||||
chr7:24723097
|
A | G | 1 | a0002c0003t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.405-3879T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723097 | ||||||
chr7:24723135
|
CT | C | 7 | a0001c0004t0001g0034a0001c0004t0001g0087a0001c0004t0001g0318others(4): Show | 8 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-3918delA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723135 | ||||||
chr7:24723193
|
G | A | 1 | a0001c0004t0001g0340 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.405-3975C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723193 | ||||||
chr7:24723195
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.405-3977C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723195 | ||||||
chr7:24723209
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.405-3991A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723209 | ||||||
chr7:24723211
|
C | T | 2 | a0002c0006t0005g0005a0002c0006t0005g0137 | 5 | HG01884.hp1 HG02293.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-3993G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723211 | ||||||
chr7:24723259
|
C | T | 3 | a0002c0003t0001g0024a0002c0003t0001g0025a0002c0003t0001g0268 | 5 | HG01069.hp2 HG01071.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-4041G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723259 | ||||||
chr7:24723613
|
A | G | 4 | a0001c0001t0001g0197a0001c0001t0001g0264a0001c0001t0003g0019others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-4395T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723613 | ||||||
chr7:24723613
|
A | T | 2 | a0002c0003t0001g0217a0005c0011t0004g0142 | 2 | HG02280.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.405-4395T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723613 | ||||||
chr7:24723622
|
G | A | 1 | a0001c0004t0001g0333 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.405-4404C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723622 | ||||||
chr7:24723624
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.405-4406C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723624 | ||||||
chr7:24723811
|
T | C | 1 | a0001c0001t0004g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.405-4593A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723811 | ||||||
chr7:24723932
|
T | G | 1 | a0002c0003t0001g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.405-4714A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723932 | ||||||
chr7:24723981
|
A | G | 1 | a0001c0001t0002g0287 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.405-4763T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24723981 | ||||||
chr7:24724174
|
C | CA | 13 | a0001c0001t0007g0351a0001c0001t0007g0352a0001c0001t0007g0353others(10): Show | 17 | HG01081.hp2 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.405-4957dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724174 | ||||||
chr7:24724174
|
C | CAA | 100 | a0001c0001t0001g0014a0001c0001t0001g0197a0001c0001t0001g0263others(97): Show | 116 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.405-4958_405-4957d others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724174 | ||||||
chr7:24724174
|
CAA | C | 5 | a0001c0004t0004g0020a0001c0004t0004g0177a0001c0004t0004g0178others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-4958_405-4957d others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724174 | ||||||
chr7:24724211
|
G | A | 3 | a0002c0006t0005g0005a0002c0006t0005g0017a0002c0006t0005g0137 | 7 | HG01081.hp2 HG01884.hp1 HG02293.hp2 others(4): Show |
intron_variant | MODIFIER | c.405-4993C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724211 | ||||||
chr7:24724479
|
C | A | 1 | a0001c0002t0001g0061 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.405-5261G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724479 | ||||||
chr7:24724492
|
G | A | 4 | a0001c0001t0001g0120a0001c0001t0001g0127a0001c0001t0002g0129others(1): Show | 4 | HG00544.hp2 HG00609.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-5274C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724492 | ||||||
chr7:24724528
|
G | A | 3 | a0001c0004t0001g0109a0001c0004t0001g0133a0002c0003t0007g0357 | 3 | HG02257.hp2 HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.405-5310C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724528 | ||||||
chr7:24724607
|
G | C | 5 | a0001c0004t0004g0020a0001c0004t0004g0177a0001c0004t0004g0178others(2): Show | 6 | HG02109.hp1 HG02280.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-5389C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24724607 | ||||||
chr7:24725036
|
C | G | 295 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(292): Show | 338 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(335): Show |
intron_variant | MODIFIER | c.405-5818G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725036 | ||||||
chr7:24725162
|
A | G | 43 | a0001c0001t0001g0283a0001c0001t0002g0006a0001c0001t0002g0021others(40): Show | 49 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.405-5944T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725162 | ||||||
chr7:24725172
|
A | T | 1 | a0002c0003t0001g0219 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.405-5954T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725172 | ||||||
chr7:24725293
|
C | T | 2 | a0005c0011t0004g0141a0005c0011t0004g0142 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.405-6075G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725293 | ||||||
chr7:24725495
|
G | A | 7 | a0001c0004t0004g0020a0001c0004t0004g0177a0001c0004t0004g0178others(4): Show | 8 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-6277C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725495 | ||||||
chr7:24725598
|
C | T | 1 | a0001c0002t0001g0039 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.405-6380G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725598 | ||||||
chr7:24725656
|
A | G | 1 | a0001c0001t0007g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.405-6438T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725656 | ||||||
chr7:24725761
|
A | C | 1 | a0001c0001t0001g0123 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.405-6543T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725761 | ||||||
chr7:24725940
|
G | A | 2 | a0001c0004t0001g0183a0001c0004t0001g0188 | 2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.405-6722C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24725940 | ||||||
chr7:24726013
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.405-6795C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726013 | ||||||
chr7:24726033
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.405-6815C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726033 | ||||||
chr7:24726285
|
A | G | 1 | a0003c0005t0001g0209 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.405-7067T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726285 | ||||||
chr7:24726562
|
G | A | 45 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(42): Show | 47 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.405-7344C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726562 | ||||||
chr7:24726568
|
T | A | 3 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088 | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-7350A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726568 | ||||||
chr7:24726630
|
T | G | 3 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088 | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-7412A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726630 | ||||||
chr7:24726656
|
T | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(77): Show | 95 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.405-7438A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726656 | ||||||
chr7:24726688
|
T | C | 2 | a0001c0001t0004g0152a0001c0004t0004g0153 | 2 | HG01361.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.405-7470A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726688 | ||||||
chr7:24726699
|
C | T | 2 | a0001c0001t0006g0001a0002c0003t0001g0154 | 8 | HG02451.hp2 HG02886.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.405-7481G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726699 | ||||||
chr7:24726775
|
C | A | 2 | a0001c0002t0001g0062a0001c0002t0001g0063 | 2 | HG02015.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.405-7557G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726775 | ||||||
chr7:24726785
|
G | T | 1 | a0002c0003t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.405-7567C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726785 | ||||||
chr7:24726801
|
G | A | 8 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0177others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-7583C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726801 | ||||||
chr7:24726805
|
C | CA | 30 | a0001c0001t0001g0118a0001c0001t0002g0198a0001c0001t0002g0277others(27): Show | 31 | HG00438.hp1 HG01175.hp1 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.405-7588dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726805 | ||||||
chr7:24726805
|
CA | C | 87 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0001g0102others(84): Show | 98 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.405-7588delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726805 | ||||||
chr7:24726805
|
CAAAAA | C | 6 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088others(3): Show | 11 | HG01081.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.405-7592_405-7588d others(7): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726805 | ||||||
chr7:24726835
|
G | A | 1 | a0001c0001t0002g0285 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.405-7617C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726835 | ||||||
chr7:24726888
|
C | G | 32 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(29): Show | 33 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.405-7670G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726888 | ||||||
chr7:24726901
|
T | C | 2 | a0002c0003t0001g0238a0002c0003t0001g0239 | 2 | HG00621.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.405-7683A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726901 | ||||||
chr7:24726995
|
G | T | 309 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(306): Show | 357 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(354): Show |
intron_variant | MODIFIER | c.405-7777C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24726995 | ||||||
chr7:24727141
|
G | A | 1 | a0001c0001t0002g0290 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.405-7923C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727141 | ||||||
chr7:24727156
|
A | C | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.405-7938T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727156 | ||||||
chr7:24727159
|
T | C | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.405-7941A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727159 | ||||||
chr7:24727238
|
T | C | 9 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0004g0152others(6): Show | 9 | HG01081.hp1 HG01243.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.405-8020A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727238 | ||||||
chr7:24727365
|
G | A | 7 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0024others(4): Show | 10 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.405-8147C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727365 | ||||||
chr7:24727777
|
C | T | 56 | a0001c0001t0001g0077a0001c0001t0003g0173a0001c0001t0009g0170others(53): Show | 61 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.405-8559G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727777 | ||||||
chr7:24727864
|
C | T | 33 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(30): Show | 34 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.405-8646G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727864 | ||||||
chr7:24727903
|
C | G | 1 | a0001c0001t0007g0351 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.405-8685G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727903 | ||||||
chr7:24727970
|
G | A | 8 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0177others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-8752C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24727970 | ||||||
chr7:24728021
|
G | A | 3 | a0001c0004t0001g0324a0001c0004t0001g0341a0001c0004t0001g0348 | 3 | HG00280.hp1 HG01175.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.405-8803C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728021 | ||||||
chr7:24728036
|
G | A | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-8818C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728036 | ||||||
chr7:24728071
|
T | C | 8 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0177others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-8853A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728071 | ||||||
chr7:24728150
|
A | G | 3 | a0001c0001t0003g0162a0001c0001t0003g0163a0001c0001t0003g0164 | 3 | HG01099.hp1 HG01978.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.405-8932T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728150 | ||||||
chr7:24728336
|
G | A | 18 | a0001c0004t0001g0031a0001c0004t0001g0032a0001c0004t0001g0311others(15): Show | 20 | HG00140.hp1 HG00639.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.405-9118C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728336 | ||||||
chr7:24728689
|
C | T | 1 | a0001c0001t0003g0148 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.405-9471G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728689 | ||||||
chr7:24728700
|
G | A | 7 | a0001c0004t0004g0020a0001c0004t0004g0177a0001c0004t0004g0178others(4): Show | 8 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-9482C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728700 | ||||||
chr7:24728735
|
A | G | 3 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088 | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-9517T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728735 | ||||||
chr7:24728794
|
C | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(75): Show | 92 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.405-9576G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728794 | ||||||
chr7:24728949
|
G | C | 2 | a0001c0001t0002g0021a0001c0001t0002g0202 | 3 | NA18962.hp2 NA19011.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.405-9731C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24728949 | ||||||
chr7:24729119
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG00438.hp1 NA18954.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.405-9901G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729119 | ||||||
chr7:24729234
|
C | A | 1 | a0001c0016t0001g0316 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.405-10016G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729234 | ||||||
chr7:24729254
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.405-10036A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729254 | ||||||
chr7:24729324
|
T | C | 1 | a0003c0005t0001g0212 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.405-10106A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729324 | ||||||
chr7:24729442
|
G | A | 1 | a0001c0001t0002g0286 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.405-10224C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729442 | ||||||
chr7:24729470
|
G | A | 198 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(195): Show | 229 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.405-10252C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729470 | ||||||
chr7:24729501
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.405-10283C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729501 | ||||||
chr7:24729557
|
C | T | 2 | a0005c0011t0004g0141a0005c0011t0004g0142 | 2 | HG02280.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.405-10339G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729557 | ||||||
chr7:24729612
|
T | C | 242 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(239): Show | 278 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.405-10394A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729612 | ||||||
chr7:24729622
|
C | G | 242 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(239): Show | 278 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.405-10404G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729622 | ||||||
chr7:24729659
|
C | T | 239 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(236): Show | 274 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(271): Show |
intron_variant | MODIFIER | c.405-10441G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729659 | ||||||
chr7:24729742
|
G | T | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.405-10524C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729742 | ||||||
chr7:24729781
|
G | T | 55 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(52): Show | 60 | HG00621.hp2 HG00733.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.405-10563C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729781 | ||||||
chr7:24729896
|
C | T | 2 | a0002c0006t0001g0251a0002c0006t0011g0207 | 2 | HG02015.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.405-10678G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729896 | ||||||
chr7:24729915
|
G | A | 4 | a0001c0001t0002g0002a0001c0001t0002g0111a0001c0001t0002g0112others(1): Show | 8 | HG02486.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.405-10697C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24729915 | ||||||
chr7:24730012
|
A | T | 10 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0273others(7): Show | 10 | HG01361.hp2 HG02004.hp2 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.405-10794T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730012 | ||||||
chr7:24730014
|
G | C | 1 | a0001c0001t0003g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.405-10796C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730014 | ||||||
chr7:24730151
|
G | A | 5 | a0003c0005t0001g0023a0003c0005t0001g0209a0003c0005t0001g0214others(2): Show | 6 | HG01256.hp1 HG01928.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-10933C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730151 | ||||||
chr7:24730168
|
T | C | 8 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0177others(5): Show | 9 | HG02109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.405-10950A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730168 | ||||||
chr7:24730172
|
T | C | 1 | a0001c0002t0001g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.405-10954A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730172 | ||||||
chr7:24730269
|
G | A | 1 | a0001c0016t0001g0316 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.405-11051C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730269 | ||||||
chr7:24730283
|
T | G | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.405-11065A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730283 | ||||||
chr7:24730339
|
T | C | 39 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(36): Show | 40 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.405-11121A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730339 | ||||||
chr7:24730372
|
C | T | 39 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(36): Show | 40 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.405-11154G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730372 | ||||||
chr7:24730602
|
G | A | 4 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088others(1): Show | 5 | HG01891.hp2 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-11384C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730602 | ||||||
chr7:24730644
|
G | A | 4 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088others(1): Show | 5 | HG01891.hp2 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.405-11426C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730644 | ||||||
chr7:24730660
|
C | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(185): Show | 221 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.405-11442G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730660 | ||||||
chr7:24730720
|
C | T | 3 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088 | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.405-11502G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730720 | ||||||
chr7:24730809
|
C | A | 39 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(36): Show | 40 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.405-11591G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24730809 | ||||||
chr7:24731034
|
T | A | 235 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(232): Show | 270 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(267): Show |
intron_variant | MODIFIER | c.405-11816A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731034 | ||||||
chr7:24731075
|
T | C | 39 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(36): Show | 40 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.405-11857A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731075 | ||||||
chr7:24731092
|
G | A | 5 | a0001c0001t0001g0014a0002c0003t0001g0216a0002c0003t0001g0217others(2): Show | 6 | HG02602.hp2 HG02683.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.405-11874C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731092 | ||||||
chr7:24731121
|
C | G | 235 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(232): Show | 270 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(267): Show |
intron_variant | MODIFIER | c.405-11903G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731121 | ||||||
chr7:24731498
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.405-12280C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731498 | ||||||
chr7:24731586
|
G | A | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.405-12368C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731586 | ||||||
chr7:24731613
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.405-12395A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731613 | ||||||
chr7:24731668
|
A | T | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.405-12450T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731668 | ||||||
chr7:24731773
|
C | T | 191 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(188): Show | 224 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.405-12555G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731773 | ||||||
chr7:24731923
|
G | A | 1 | a0002c0003t0001g0268 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.404+12639C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24731923 | ||||||
chr7:24732038
|
C | T | 1 | a0001c0002t0001g0057 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.404+12524G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732038 | ||||||
chr7:24732039
|
G | A | 7 | a0002c0003t0001g0037a0002c0003t0001g0038a0002c0003t0001g0040others(4): Show | 7 | HG01346.hp1 HG02132.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.404+12523C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732039 | ||||||
chr7:24732158
|
T | C | 20 | a0001c0001t0001g0197a0001c0001t0001g0264a0001c0001t0003g0144others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.404+12404A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732158 | ||||||
chr7:24732271
|
G | C | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.404+12291C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732271 | ||||||
chr7:24732286
|
T | C | 1 | a0001c0004t0001g0341 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.404+12276A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732286 | ||||||
chr7:24732310
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.404+12252C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732310 | ||||||
chr7:24732398
|
G | A | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.404+12164C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732398 | ||||||
chr7:24732495
|
T | A | 21 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(18): Show | 22 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.404+12067A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732495 | ||||||
chr7:24732555
|
T | A | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+12007A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732555 | ||||||
chr7:24732668
|
G | C | 1 | a0001c0001t0002g0302 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.404+11894C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732668 | ||||||
chr7:24732790
|
C | T | 38 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(35): Show | 39 | HG00733.hp1 HG01099.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.404+11772G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732790 | ||||||
chr7:24732971
|
C | G | 2 | a0001c0001t0002g0276a0001c0001t0002g0296 | 2 | HG00597.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.404+11591G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24732971 | ||||||
chr7:24733022
|
G | C | 305 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(302): Show | 354 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(351): Show |
intron_variant | MODIFIER | c.404+11540C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733022 | ||||||
chr7:24733067
|
T | G | 22 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(19): Show | 23 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.404+11495A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733067 | ||||||
chr7:24733344
|
C | T | 1 | a0001c0002t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.404+11218G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733344 | ||||||
chr7:24733396
|
A | C | 3 | a0001c0001t0003g0019a0002c0003t0001g0088a0002c0003t0001g0271 | 4 | HG01891.hp2 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+11166T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733396 | ||||||
chr7:24733474
|
C | T | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.404+11088G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733474 | ||||||
chr7:24733545
|
C | G | 1 | a0001c0001t0007g0353 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.404+11017G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733545 | ||||||
chr7:24733688
|
T | C | 3 | a0001c0002t0001g0066a0001c0002t0001g0298a0001c0002t0001g0300 | 3 | NA18986.hp1 NA18998.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.404+10874A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733688 | ||||||
chr7:24733912
|
C | T | 1 | a0002c0006t0005g0017 | 2 | HG01081.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.404+10650G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733912 | ||||||
chr7:24733942
|
G | A | 1 | a0001c0004t0001g0325 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.404+10620C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24733942 | ||||||
chr7:24734079
|
A | G | 1 | a0001c0004t0001g0331 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.404+10483T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734079 | ||||||
chr7:24734282
|
A | G | 1 | a0002c0003t0001g0038 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.404+10280T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734282 | ||||||
chr7:24734321
|
G | A | 1 | a0002c0006t0001g0256 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.404+10241C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734321 | ||||||
chr7:24734351
|
G | T | 1 | a0001c0004t0001g0344 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.404+10211C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734351 | ||||||
chr7:24734395
|
C | G | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.404+10167G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734395 | ||||||
chr7:24734563
|
T | G | 2 | a0002c0003t0001g0097a0002c0003t0001g0175 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404+9999A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734563 | ||||||
chr7:24734680
|
T | C | 23 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0001g0197others(20): Show | 23 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.404+9882A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734680 | ||||||
chr7:24734794
|
A | AATAGAAA others(8): Show |
2 | a0003c0005t0001g0259a0003c0005t0001g0262 | 2 | HG00735.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.404+9767_404+9768i others(17): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734794 | ||||||
chr7:24734796
|
G | A | 2 | a0003c0005t0001g0259a0003c0005t0001g0262 | 2 | HG00735.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.404+9766C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734796 | ||||||
chr7:24734849
|
G | T | 18 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0156others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.404+9713C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24734849 | ||||||
chr7:24735002
|
T | C | 1 | a0001c0004t0001g0341 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.404+9560A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735002 | ||||||
chr7:24735112
|
T | C | 19 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0001g0197others(16): Show | 19 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.404+9450A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735112 | ||||||
chr7:24735231
|
T | G | 2 | a0002c0006t0005g0005a0002c0006t0005g0137 | 5 | HG01884.hp1 HG02293.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+9331A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735231 | ||||||
chr7:24735276
|
C | T | 71 | a0001c0001t0001g0077a0001c0001t0003g0173a0001c0001t0007g0351others(68): Show | 78 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.404+9286G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735276 | ||||||
chr7:24735481
|
G | A | 2 | a0001c0001t0003g0019a0002c0003t0001g0088 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.404+9081C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735481 | ||||||
chr7:24735585
|
C | T | 2 | a0001c0001t0002g0095a0001c0001t0005g0096 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.404+8977G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735585 | ||||||
chr7:24735614
|
C | A | 1 | a0001c0002t0001g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.404+8948G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735614 | ||||||
chr7:24735632
|
C | T | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+8930G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735632 | ||||||
chr7:24735699
|
G | A | 18 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.404+8863C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735699 | ||||||
chr7:24735725
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.404+8837A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735725 | ||||||
chr7:24735760
|
A | AAAAT | 6 | a0001c0001t0003g0104a0001c0001t0003g0148a0001c0002t0001g0052others(3): Show | 6 | HG00423.hp2 HG02559.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+8798_404+8801d others(6): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735760 | ||||||
chr7:24735760
|
AAAAT | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0100others(121): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.404+8798_404+8801d others(6): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735760 | ||||||
chr7:24735760
|
AAAATAAA others(1): Show |
A | 61 | a0001c0001t0001g0018a0001c0001t0001g0115a0001c0001t0001g0120others(58): Show | 68 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.404+8794_404+8801d others(10): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735760 | ||||||
chr7:24735760
|
AAAATAAA others(5): Show |
A | 94 | a0001c0001t0001g0014a0001c0001t0001g0197a0001c0001t0001g0264others(91): Show | 106 | HG00140.hp2 HG00558.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.404+8790_404+8801d others(14): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735760 | ||||||
chr7:24735760
|
AAAATAAA others(9): Show |
A | 5 | a0001c0001t0014g0191a0001c0001t0015g0354a0002c0003t0001g0024others(2): Show | 7 | HG01069.hp2 HG01071.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.404+8786_404+8801d others(18): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735760 | ||||||
chr7:24735760
|
AAAATAAA others(13): Show |
A | 6 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(3): Show | 6 | HG00438.hp1 HG01496.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.404+8782_404+8801d others(22): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735760 | ||||||
chr7:24735893
|
G | A | 1 | a0001c0004t0001g0326 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.404+8669C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735893 | ||||||
chr7:24735895
|
G | A | 20 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.404+8667C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24735895 | ||||||
chr7:24736021
|
A | C | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+8541T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736021 | ||||||
chr7:24736184
|
T | C | 1 | a0001c0001t0002g0113 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.404+8378A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736184 | ||||||
chr7:24736366
|
G | T | 1 | a0001c0001t0002g0093 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.404+8196C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736366 | ||||||
chr7:24736411
|
A | G | 20 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.404+8151T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736411 | ||||||
chr7:24736438
|
A | G | 1 | a0001c0002t0001g0035 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.404+8124T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736438 | ||||||
chr7:24736491
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+8071A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736491 | ||||||
chr7:24736497
|
C | T | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.404+8065G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736497 | ||||||
chr7:24736573
|
G | A | 20 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.404+7989C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736573 | ||||||
chr7:24736786
|
C | A | 97 | a0001c0001t0001g0014a0001c0001t0002g0198a0002c0003t0001g0007others(94): Show | 111 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.404+7776G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736786 | ||||||
chr7:24736883
|
C | T | 1 | a0001c0001t0015g0354 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.404+7679G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736883 | ||||||
chr7:24736910
|
A | G | 1 | a0002c0003t0001g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.404+7652T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736910 | ||||||
chr7:24736957
|
G | A | 2 | a0002c0006t0005g0005a0002c0006t0005g0137 | 5 | HG01884.hp1 HG02293.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.404+7605C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24736957 | ||||||
chr7:24737010
|
C | A | 2 | a0002c0003t0001g0097a0002c0003t0001g0175 | 2 | HG02559.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.404+7552G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737010 | ||||||
chr7:24737052
|
G | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+7510C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737052 | ||||||
chr7:24737127
|
G | T | 4 | a0001c0002t0001g0053a0001c0002t0001g0054a0001c0002t0001g0055others(1): Show | 4 | HG01358.hp1 HG01928.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.404+7435C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737127 | ||||||
chr7:24737142
|
G | A | 19 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(16): Show | 19 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.404+7420C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737142 | ||||||
chr7:24737165
|
T | C | 14 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0156others(11): Show | 14 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.404+7397A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737165 | ||||||
chr7:24737344
|
T | C | 1 | a0001c0001t0007g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.404+7218A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737344 | ||||||
chr7:24737470
|
CA | C | 22 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0019others(19): Show | 23 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.404+7091delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737470 | ||||||
chr7:24737522
|
A | T | 1 | a0001c0001t0002g0289 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.404+7040T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737522 | ||||||
chr7:24737598
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.404+6964G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737598 | ||||||
chr7:24737693
|
CA | C | 278 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(275): Show | 322 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(319): Show |
intron_variant | MODIFIER | c.404+6868delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737693 | ||||||
chr7:24737880
|
A | T | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.404+6682T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737880 | ||||||
chr7:24737889
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+6673A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24737889 | ||||||
chr7:24738252
|
A | G | 236 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(233): Show | 278 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.404+6310T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738252 | ||||||
chr7:24738254
|
G | A | 17 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(14): Show | 17 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.404+6308C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738254 | ||||||
chr7:24738494
|
G | A | 17 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(14): Show | 17 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.404+6068C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738494 | ||||||
chr7:24738633
|
C | G | 1 | a0001c0001t0015g0354 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.404+5929G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738633 | ||||||
chr7:24738653
|
CA | C | 59 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(56): Show | 65 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.404+5908delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738653 | ||||||
chr7:24738702
|
G | A | 2 | a0001c0002t0001g0042a0001c0004t0001g0050 | 2 | HG01106.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.404+5860C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738702 | ||||||
chr7:24738733
|
T | C | 1 | a0001c0007t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.404+5829A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738733 | ||||||
chr7:24738906
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+5656C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738906 | ||||||
chr7:24738998
|
C | T | 60 | a0001c0001t0001g0077a0001c0001t0003g0019a0001c0001t0007g0351others(57): Show | 67 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.404+5564G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24738998 | ||||||
chr7:24739342
|
C | T | 17 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(14): Show | 17 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.404+5220G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24739342 | ||||||
chr7:24739376
|
T | G | 1 | a0001c0001t0003g0105 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.404+5186A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24739376 | ||||||
chr7:24739765
|
A | G | 6 | a0001c0004t0004g0020a0001c0004t0004g0153a0001c0004t0004g0177others(3): Show | 7 | HG01361.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.404+4797T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24739765 | ||||||
chr7:24739821
|
G | A | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.404+4741C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24739821 | ||||||
chr7:24739828
|
C | T | 2 | a0001c0004t0004g0179a0001c0004t0004g0180 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.404+4734G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24739828 | ||||||
chr7:24739832
|
C | T | 1 | a0001c0007t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.404+4730G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24739832 | ||||||
chr7:24739923
|
T | C | 2 | a0002c0006t0001g0255a0002c0006t0001g0256 | 2 | NA18939.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.404+4639A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24739923 | ||||||
chr7:24740092
|
CA | C | 269 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(266): Show | 317 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(314): Show |
intron_variant | MODIFIER | c.404+4469delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740092 | ||||||
chr7:24740115
|
C | T | 1 | a0002c0006t0001g0210 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.404+4447G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740115 | ||||||
chr7:24740126
|
C | T | 1 | a0001c0016t0001g0316 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.404+4436G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740126 | ||||||
chr7:24740300
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+4262C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740300 | ||||||
chr7:24740324
|
A | C | 1 | a0003c0005t0001g0247 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.404+4238T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740324 | ||||||
chr7:24740331
|
C | T | 19 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0001g0197others(16): Show | 19 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.404+4231G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740331 | ||||||
chr7:24740368
|
T | G | 236 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(233): Show | 278 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(275): Show |
intron_variant | MODIFIER | c.404+4194A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740368 | ||||||
chr7:24740434
|
C | T | 230 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(227): Show | 270 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(267): Show |
intron_variant | MODIFIER | c.404+4128G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740434 | ||||||
chr7:24740459
|
AT | A | 19 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0001g0197others(16): Show | 19 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.404+4102delA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740459 | ||||||
chr7:24740697
|
C | T | 306 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(303): Show | 355 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.404+3865G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740697 | ||||||
chr7:24740734
|
G | A | 2 | a0002c0006t0001g0251a0002c0006t0011g0207 | 2 | HG02015.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.404+3828C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740734 | ||||||
chr7:24740969
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.404+3593C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24740969 | ||||||
chr7:24741158
|
C | T | 20 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0001g0197others(17): Show | 20 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.404+3404G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741158 | ||||||
chr7:24741316
|
A | G | 1 | a0003c0008t0001g0265 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.404+3246T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741316 | ||||||
chr7:24741326
|
G | C | 3 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0002g0293 | 3 | HG01952.hp1 NA18953.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.404+3236C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741326 | ||||||
chr7:24741441
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.404+3121G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741441 | ||||||
chr7:24741461
|
A | G | 21 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0001g0197others(18): Show | 21 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.404+3101T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741461 | ||||||
chr7:24741482
|
C | T | 2 | a0001c0002t0001g0080a0001c0007t0001g0010 | 3 | HG01516.hp1 HG01517.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.404+3080G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741482 | ||||||
chr7:24741483
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+3079C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741483 | ||||||
chr7:24741623
|
T | G | 1 | a0002c0003t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.404+2939A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741623 | ||||||
chr7:24741685
|
T | C | 1 | a0001c0004t0001g0321 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.404+2877A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741685 | ||||||
chr7:24741705
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.404+2857G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741705 | ||||||
chr7:24741728
|
G | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+2834C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741728 | ||||||
chr7:24741742
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.404+2820G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741742 | ||||||
chr7:24741743
|
G | C | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.404+2819C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741743 | ||||||
chr7:24741757
|
A | AATG | 3 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113 | 3 | HG02622.hp1 HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.404+2802_404+2804d others(5): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741757 | ||||||
chr7:24741767
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+2795A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741767 | ||||||
chr7:24741824
|
GTAACAAG others(5): Show |
G | 2 | a0001c0001t0003g0089a0001c0001t0006g0001 | 8 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.404+2726_404+2737d others(14): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741824 | ||||||
chr7:24741837
|
T | C | 16 | a0001c0001t0001g0197a0001c0001t0001g0264a0001c0001t0003g0135others(13): Show | 16 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.404+2725A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741837 | ||||||
chr7:24741861
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.404+2701C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741861 | ||||||
chr7:24741913
|
C | T | 307 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(304): Show | 356 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(353): Show |
intron_variant | MODIFIER | c.404+2649G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741913 | ||||||
chr7:24741942
|
G | A | 58 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(55): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.404+2620C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741942 | ||||||
chr7:24741966
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+2596A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24741966 | ||||||
chr7:24742153
|
A | C | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.404+2409T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742153 | ||||||
chr7:24742173
|
A | G | 216 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(213): Show | 258 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(255): Show |
intron_variant | MODIFIER | c.404+2389T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742173 | ||||||
chr7:24742183
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.404+2379G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742183 | ||||||
chr7:24742191
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.404+2371C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742191 | ||||||
chr7:24742205
|
C | T | 19 | a0001c0001t0001g0155a0001c0001t0001g0197a0001c0001t0001g0264others(16): Show | 19 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.404+2357G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742205 | ||||||
chr7:24742424
|
C | T | 45 | a0001c0001t0001g0283a0001c0001t0001g0306a0001c0001t0001g0307others(42): Show | 50 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.404+2138G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742424 | ||||||
chr7:24742448
|
G | A | 1 | a0001c0002t0001g0076 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.404+2114C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742448 | ||||||
chr7:24742473
|
C | A | 1 | a0001c0004t0001g0327 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.404+2089G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742473 | ||||||
chr7:24742488
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.404+2074G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742488 | ||||||
chr7:24742499
|
G | T | 2 | a0001c0004t0001g0183a0001c0004t0001g0188 | 2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.404+2063C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742499 | ||||||
chr7:24742674
|
C | G | 1 | a0001c0001t0002g0291 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.404+1888G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742674 | ||||||
chr7:24742675
|
G | A | 1 | a0001c0001t0002g0291 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.404+1887C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742675 | ||||||
chr7:24742717
|
C | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0091a0001c0001t0003g0110 | 4 | HG02055.hp1 HG02145.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.404+1845G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24742717 | ||||||
chr7:24743035
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.404+1527C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743035 | ||||||
chr7:24743063
|
C | T | 1 | a0001c0002t0001g0114 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.404+1499G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743063 | ||||||
chr7:24743088
|
G | A | 6 | a0001c0002t0001g0039a0001c0002t0001g0065a0001c0002t0001g0066others(3): Show | 6 | NA18939.hp2 NA18950.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.404+1474C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743088 | ||||||
chr7:24743092
|
T | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.404+1470A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743092 | ||||||
chr7:24743142
|
A | T | 13 | a0001c0001t0003g0156a0001c0001t0003g0157a0001c0001t0003g0158others(10): Show | 13 | HG00733.hp1 HG01099.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.404+1420T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743142 | ||||||
chr7:24743162
|
C | T | 15 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0156others(12): Show | 15 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.404+1400G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743162 | ||||||
chr7:24743581
|
T | G | 1 | a0001c0007t0013g0186 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.404+981A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743581 | ||||||
chr7:24743636
|
C | G | 1 | a0002c0006t0003g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.404+926G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743636 | ||||||
chr7:24743650
|
C | T | 3 | a0001c0001t0001g0140a0001c0004t0001g0109a0001c0004t0001g0133 | 3 | HG02257.hp2 HG02258.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.404+912G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743650 | ||||||
chr7:24743684
|
G | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0202 | 3 | NA18962.hp2 NA19011.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.404+878C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743684 | ||||||
chr7:24743908
|
T | A | 2 | a0001c0001t0007g0355a0001c0001t0007g0356 | 2 | HG01081.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.404+654A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743908 | ||||||
chr7:24743969
|
A | G | 1 | a0001c0001t0002g0296 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.404+593T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24743969 | ||||||
chr7:24744037
|
G | A | 18 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.404+525C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744037 | ||||||
chr7:24744074
|
G | A | 17 | a0001c0001t0001g0155a0001c0001t0003g0144a0001c0001t0003g0145others(14): Show | 17 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.404+488C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744074 | ||||||
chr7:24744126
|
C | T | 17 | a0001c0001t0001g0155a0001c0001t0003g0144a0001c0001t0003g0145others(14): Show | 17 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.404+436G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744126 | ||||||
chr7:24744214
|
A | G | 2 | a0001c0002t0001g0012a0001c0002t0001g0083 | 3 | NA18948.hp1 NA18973.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.404+348T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744214 | ||||||
chr7:24744286
|
G | A | 1 | a0001c0004t0001g0034 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.404+276C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744286 | ||||||
chr7:24744362
|
TC | T | 18 | a0001c0001t0001g0140a0001c0001t0001g0155a0001c0001t0003g0144others(15): Show | 18 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.404+199delG | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744362 | ||||||
chr7:24744368
|
C | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(39): Show | 53 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.404+194G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744368 | ||||||
chr7:24744438
|
G | A | 68 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(65): Show | 90 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.404+124C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744438 | ||||||
chr7:24744529
|
T | A | 2 | a0001c0001t0007g0355a0001c0001t0007g0356 | 2 | HG01081.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.404+33A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 3/9 | chr7 | 24744529 | ||||||
chr7:24744771
|
G | A | 1 | a0002c0003t0001g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.212-17C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744771 | ||||||
chr7:24744784
|
C | T | 258 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(255): Show | 302 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.212-30G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744784 | ||||||
chr7:24744787
|
T | C | 5 | a0001c0002t0001g0051a0001c0002t0001g0068a0001c0002t0001g0069others(2): Show | 5 | HG02083.hp2 NA18940.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.212-33A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744787 | ||||||
chr7:24744815
|
G | T | 2 | a0001c0001t0003g0019a0002c0003t0001g0088 | 3 | HG01891.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.212-61C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744815 | ||||||
chr7:24744866
|
A | G | 91 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0094others(88): Show | 112 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.212-112T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744866 | ||||||
chr7:24744871
|
G | T | 1 | a0002c0003t0001g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.212-117C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744871 | ||||||
chr7:24744923
|
C | CGT | 219 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(216): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.212-171_212-170dup others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
C | CGTGT | 35 | a0001c0001t0001g0120a0001c0001t0002g0293a0001c0001t0003g0144others(32): Show | 37 | HG00544.hp2 HG00733.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.212-173_212-170dup others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
C | CGTGTGT | 3 | a0001c0001t0002g0302a0001c0001t0009g0170a0001c0001t0009g0171 | 3 | HG01361.hp2 HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.212-175_212-170dup others(6): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0001g0102 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.212-179_212-170dup others(10): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
C | CGTGTGTG others(5): Show |
1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.212-181_212-170dup others(12): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
C | CGTGTGTG others(9): Show |
2 | a0001c0001t0003g0019a0002c0003t0001g0271 | 3 | HG02622.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.212-185_212-170dup others(16): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
CGT | C | 6 | a0001c0001t0001g0308a0001c0001t0007g0351a0001c0001t0007g0353others(3): Show | 6 | HG02572.hp1 HG02895.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-171_212-170del others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
CGTGT | C | 63 | a0001c0001t0001g0077a0001c0001t0001g0100a0001c0001t0002g0099others(60): Show | 69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.212-173_212-170del others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744923
|
CGTGTGTG others(7): Show |
C | 3 | a0001c0001t0003g0089a0001c0001t0006g0001a0002c0003t0001g0154 | 9 | HG02451.hp2 HG02886.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-183_212-170del others(14): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744923 | ||||||
chr7:24744938
|
G | GTA | 4 | a0003c0005t0001g0027a0003c0005t0001g0218a0003c0005t0001g0244others(1): Show | 5 | NA18944.hp2 NA18975.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-185_212-184ins others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744938 | ||||||
chr7:24744958
|
C | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-204G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744958 | ||||||
chr7:24744966
|
C | G | 1 | a0001c0002t0001g0051 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.212-212G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744966 | ||||||
chr7:24744984
|
C | CGT | 12 | a0001c0001t0007g0352a0001c0002t0001g0298a0001c0004t0001g0188others(9): Show | 12 | HG00140.hp1 HG00735.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.212-232_212-231dup others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
C | CGTGT | 6 | a0001c0004t0001g0183a0001c0004t0001g0320a0001c0004t0001g0328others(3): Show | 6 | HG00099.hp1 HG01516.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-234_212-231dup others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGT | C | 40 | a0001c0001t0001g0283a0001c0001t0001g0306a0001c0001t0001g0307others(37): Show | 42 | HG00280.hp1 HG00423.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.212-232_212-231del others(2): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGT | C | 43 | a0001c0001t0001g0155a0001c0001t0001g0308a0001c0001t0002g0006others(40): Show | 48 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.212-234_212-231del others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGT | C | 34 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(31): Show | 37 | HG00438.hp1 HG01081.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.212-236_212-231del others(6): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(1): Show |
C | 91 | a0001c0001t0001g0014a0001c0001t0001g0077a0001c0001t0001g0119others(88): Show | 110 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.212-238_212-231del others(8): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(3): Show |
C | 62 | a0001c0001t0001g0018a0001c0001t0001g0115a0001c0001t0001g0120others(59): Show | 69 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.212-240_212-231del others(10): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(5): Show |
C | 15 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0001g0136others(12): Show | 22 | HG01099.hp2 HG01109.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.212-242_212-231del others(12): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(7): Show |
C | 14 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(11): Show | 15 | HG02040.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.212-244_212-231del others(14): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(9): Show |
C | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.212-246_212-231del others(16): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(13): Show |
C | 1 | a0002c0003t0001g0193 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.212-250_212-231del others(20): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(15): Show |
C | 2 | a0001c0001t0003g0089a0001c0001t0006g0001 | 8 | HG02451.hp2 HG02886.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.212-252_212-231del others(22): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(17): Show |
C | 3 | a0002c0003t0001g0154a0002c0003t0001g0271a0002c0006t0001g0257 | 3 | HG00673.hp1 HG02622.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.212-254_212-231del others(24): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(19): Show |
C | 1 | a0001c0002t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.212-256_212-231del others(26): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24744984
|
CGTGTGTG others(21): Show |
C | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.212-258_212-231del others(28): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24744984 | ||||||
chr7:24745034
|
T | G | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.212-280A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24745034 | ||||||
chr7:24745040
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-286T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24745040 | ||||||
chr7:24745113
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-359G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24745113 | ||||||
chr7:24745270
|
A | G | 1 | a0002c0006t0003g0143 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.212-516T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24745270 | ||||||
chr7:24745344
|
A | C | 1 | a0001c0001t0002g0275 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.212-590T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24745344 | ||||||
chr7:24745757
|
G | C | 3 | a0001c0001t0003g0019a0001c0001t0004g0146a0002c0003t0001g0088 | 4 | HG01891.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.212-1003C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24745757 | ||||||
chr7:24746263
|
C | G | 15 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0156others(12): Show | 15 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.212-1509G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746263 | ||||||
chr7:24746273
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-1519C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746273 | ||||||
chr7:24746400
|
A | G | 5 | a0001c0001t0007g0351a0001c0001t0007g0352a0001c0001t0007g0353others(2): Show | 5 | HG01081.hp1 HG01243.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-1646T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746400 | ||||||
chr7:24746463
|
TGTAAG | T | 64 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(61): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.212-1714_212-1710d others(7): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746463 | ||||||
chr7:24746738
|
T | C | 1 | a0001c0004t0001g0344 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.212-1984A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746738 | ||||||
chr7:24746808
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2054T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746808 | ||||||
chr7:24746810
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2056G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746810 | ||||||
chr7:24746811
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2057T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746811 | ||||||
chr7:24746812
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2058G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746812 | ||||||
chr7:24746815
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2061C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746815 | ||||||
chr7:24746816
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2062C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746816 | ||||||
chr7:24746817
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2063T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746817 | ||||||
chr7:24746820
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2066C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746820 | ||||||
chr7:24746822
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2068G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746822 | ||||||
chr7:24746823
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2069T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746823 | ||||||
chr7:24746824
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2070T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746824 | ||||||
chr7:24746825
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2071G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746825 | ||||||
chr7:24746826
|
A | C | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2072T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746826 | ||||||
chr7:24746827
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2073G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746827 | ||||||
chr7:24746828
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2074G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746828 | ||||||
chr7:24746829
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2075T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746829 | ||||||
chr7:24746830
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2076C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746830 | ||||||
chr7:24746832
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2078G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746832 | ||||||
chr7:24746833
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2079T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746833 | ||||||
chr7:24746835
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2081G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746835 | ||||||
chr7:24746837
|
C | A | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2083G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746837 | ||||||
chr7:24746838
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2084G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746838 | ||||||
chr7:24746839
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2085G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746839 | ||||||
chr7:24746842
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2088G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746842 | ||||||
chr7:24746843
|
A | G | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.212-2089T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746843 | ||||||
chr7:24746853
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2099C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746853 | ||||||
chr7:24746855
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2101G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746855 | ||||||
chr7:24746856
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2102G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746856 | ||||||
chr7:24746858
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2104C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746858 | ||||||
chr7:24746860
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2106C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746860 | ||||||
chr7:24746862
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2108T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746862 | ||||||
chr7:24746864
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2110G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746864 | ||||||
chr7:24746865
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2111T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746865 | ||||||
chr7:24746867
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2113T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746867 | ||||||
chr7:24746869
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2115T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746869 | ||||||
chr7:24746871
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2117C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746871 | ||||||
chr7:24746872
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2118G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746872 | ||||||
chr7:24746873
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2119G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746873 | ||||||
chr7:24746875
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2121C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746875 | ||||||
chr7:24746877
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2123C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746877 | ||||||
chr7:24746878
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2124T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746878 | ||||||
chr7:24746879
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2125C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746879 | ||||||
chr7:24746880
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2126C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746880 | ||||||
chr7:24746883
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2129C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746883 | ||||||
chr7:24746884
|
C | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2130G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746884 | ||||||
chr7:24746885
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2131C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746885 | ||||||
chr7:24746886
|
A | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2132T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746886 | ||||||
chr7:24746887
|
G | T | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2133C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746887 | ||||||
chr7:24746890
|
G | A | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2136C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746890 | ||||||
chr7:24746894
|
A | G | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2140T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746894 | ||||||
chr7:24746896
|
A | G | 1 | a0001c0004t0001g0315 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.212-2142T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746896 | ||||||
chr7:24746952
|
T | C | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.212-2198A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24746952 | ||||||
chr7:24747020
|
G | A | 3 | a0002c0003t0001g0097a0002c0006t0005g0005a0002c0006t0005g0137 | 6 | HG01884.hp1 HG02293.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-2266C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747020 | ||||||
chr7:24747104
|
G | T | 1 | a0001c0004t0001g0327 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.212-2350C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747104 | ||||||
chr7:24747131
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.212-2377A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747131 | ||||||
chr7:24747238
|
A | G | 6 | a0001c0001t0001g0100a0001c0001t0002g0099a0001c0001t0003g0013others(3): Show | 7 | HG02055.hp1 HG02145.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+2326T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747238 | ||||||
chr7:24747248
|
A | G | 64 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(61): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.211+2316T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747248 | ||||||
chr7:24747337
|
C | T | 6 | a0002c0003t0001g0037a0002c0003t0001g0038a0002c0003t0001g0040others(3): Show | 6 | HG01346.hp1 NA18955.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+2227G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747337 | ||||||
chr7:24747350
|
A | G | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+2214T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747350 | ||||||
chr7:24747414
|
C | T | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+2150G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747414 | ||||||
chr7:24747596
|
C | T | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+1968G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747596 | ||||||
chr7:24747636
|
A | G | 2 | a0001c0001t0004g0152a0001c0004t0004g0153 | 2 | HG01361.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.211+1928T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747636 | ||||||
chr7:24747652
|
C | A | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+1912G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747652 | ||||||
chr7:24747660
|
C | G | 15 | a0001c0001t0003g0144a0001c0001t0003g0145a0001c0001t0003g0156others(12): Show | 15 | HG00733.hp1 HG01099.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.211+1904G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747660 | ||||||
chr7:24747670
|
AT | A | 58 | a0001c0001t0001g0077a0001c0002t0001g0003a0001c0002t0001g0011others(55): Show | 64 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.211+1893delA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747670 | ||||||
chr7:24747696
|
G | C | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.211+1868C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747696 | ||||||
chr7:24747699
|
A | T | 92 | a0001c0001t0001g0077a0001c0001t0001g0155a0001c0001t0003g0144others(89): Show | 99 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.211+1865T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747699 | ||||||
chr7:24747701
|
T | C | 1 | a0002c0003t0001g0154 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.211+1863A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747701 | ||||||
chr7:24747702
|
C | T | 1 | a0001c0001t0010g0192 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.211+1862G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747702 | ||||||
chr7:24747842
|
A | G | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+1722T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747842 | ||||||
chr7:24747968
|
C | T | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+1596G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24747968 | ||||||
chr7:24748122
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.211+1442C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748122 | ||||||
chr7:24748144
|
GTA | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(54): Show | 74 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.211+1418_211+1419d others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748144 | ||||||
chr7:24748159
|
TA | T | 19 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(16): Show | 20 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+1404delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748159 | ||||||
chr7:24748160
|
A | T | 1 | a0001c0001t0003g0105 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.211+1404T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748160 | ||||||
chr7:24748162
|
A | T | 27 | a0001c0001t0001g0100a0001c0001t0001g0102a0001c0001t0001g0103others(24): Show | 28 | HG01099.hp2 HG01167.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.211+1402T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748162 | ||||||
chr7:24748163
|
TA | T | 9 | a0001c0001t0002g0002a0001c0001t0002g0095a0001c0001t0002g0111others(6): Show | 14 | HG01081.hp2 HG01175.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.211+1400delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748163 | ||||||
chr7:24748163
|
TATA | T | 9 | a0001c0001t0001g0155a0001c0001t0015g0354a0001c0002t0001g0041others(6): Show | 10 | HG02280.hp1 HG02683.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+1398_211+1400d others(5): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748163 | ||||||
chr7:24748164
|
A | AT | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+1399dupA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748164 | ||||||
chr7:24748164
|
A | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(63): Show | 83 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.211+1400T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748164 | ||||||
chr7:24748165
|
TA | T | 11 | a0002c0006t0001g0210a0002c0006t0003g0143a0003c0005t0001g0211others(8): Show | 11 | HG00735.hp2 HG02735.hp1 HG03540.hp2 others(8): Show |
intron_variant | MODIFIER | c.211+1398delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748165 | ||||||
chr7:24748165
|
TATA | T | 60 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(57): Show | 66 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.211+1396_211+1398d others(5): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748165 | ||||||
chr7:24748166
|
A | ATT | 3 | a0001c0001t0001g0140a0001c0001t0004g0146a0005c0011t0004g0142 | 3 | HG02280.hp2 HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.211+1397_211+1398i others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748166 | ||||||
chr7:24748166
|
A | T | 107 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(104): Show | 129 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(126): Show |
intron_variant | MODIFIER | c.211+1398T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748166 | ||||||
chr7:24748167
|
TA | T | 59 | a0001c0001t0002g0198a0001c0001t0002g0297a0001c0001t0003g0231others(56): Show | 69 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.211+1396delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748167 | ||||||
chr7:24748168
|
A | AT | 20 | a0001c0001t0001g0263a0001c0001t0002g0299a0001c0002t0001g0076others(17): Show | 23 | HG00673.hp1 HG01168.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.211+1395dupA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748168 | ||||||
chr7:24748168
|
A | T | 183 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(180): Show | 213 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.211+1396T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748168 | ||||||
chr7:24748170
|
T | A | 1 | a0001c0004t0001g0345 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.211+1394A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748170 | ||||||
chr7:24748221
|
G | A | 2 | a0002c0003t0001g0258a0002c0003t0001g0270 | 2 | HG02080.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.211+1343C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748221 | ||||||
chr7:24748242
|
T | C | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+1322A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748242 | ||||||
chr7:24748258
|
C | T | 66 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(63): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.211+1306G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748258 | ||||||
chr7:24748266
|
T | C | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+1298A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748266 | ||||||
chr7:24748303
|
GTGCCTAC others(5): Show |
G | 1 | a0002c0003t0001g0260 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.211+1249_211+1260d others(14): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748303 | ||||||
chr7:24748321
|
G | A | 2 | a0001c0001t0015g0354a0002c0003t0001g0271 | 2 | HG02622.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.211+1243C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748321 | ||||||
chr7:24748348
|
T | C | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+1216A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748348 | ||||||
chr7:24748362
|
G | A | 3 | a0001c0004t0004g0178a0001c0004t0004g0179a0001c0004t0004g0180 | 3 | HG02109.hp1 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+1202C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748362 | ||||||
chr7:24748364
|
T | A | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+1200A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748364 | ||||||
chr7:24748590
|
A | G | 66 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(63): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.211+974T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748590 | ||||||
chr7:24748602
|
G | A | 3 | a0001c0001t0004g0152a0001c0004t0001g0133a0001c0004t0004g0153 | 3 | HG01361.hp1 HG02257.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.211+962C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748602 | ||||||
chr7:24748664
|
A | C | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+900T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748664 | ||||||
chr7:24748692
|
A | G | 66 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(63): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.211+872T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748692 | ||||||
chr7:24748727
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.211+837G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748727 | ||||||
chr7:24748837
|
C | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0111a0001c0001t0002g0112others(1): Show | 8 | HG02486.hp1 HG02622.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+727G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24748837 | ||||||
chr7:24749055
|
C | T | 1 | a0002c0003t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.211+509G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749055 | ||||||
chr7:24749082
|
T | C | 2 | a0003c0005t0001g0259a0003c0005t0001g0262 | 2 | HG00735.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.211+482A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749082 | ||||||
chr7:24749092
|
C | T | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+472G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749092 | ||||||
chr7:24749363
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(43): Show | 63 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.211+201C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749363 | ||||||
chr7:24749447
|
G | A | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.211+117C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749447 | ||||||
chr7:24749463
|
C | T | 320 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(317): Show | 370 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(367): Show |
intron_variant | MODIFIER | c.211+101G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749463 | ||||||
chr7:24749481
|
G | T | 1 | a0002c0003t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.211+83C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749481 | ||||||
chr7:24749491
|
C | A | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+73G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749491 | ||||||
chr7:24749497
|
C | CA | 61 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(58): Show | 78 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.211+66dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749497 | ||||||
chr7:24749497
|
C | CAA | 63 | a0001c0001t0001g0077a0001c0001t0007g0352a0001c0001t0007g0353others(60): Show | 69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.211+65_211+66dupTT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749497 | ||||||
chr7:24749529
|
G | T | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+35C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 2/9 | chr7 | 24749529 | ||||||
chr7:24749830
|
G | A | 65 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(62): Show | 71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19-37C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24749830 | ||||||
chr7:24750089
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-296C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750089 | ||||||
chr7:24750106
|
G | C | 1 | a0002c0003t0001g0174 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19-313C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750106 | ||||||
chr7:24750165
|
C | G | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-372G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750165 | ||||||
chr7:24750171
|
T | A | 5 | a0001c0001t0007g0351a0001c0001t0007g0352a0001c0001t0007g0353others(2): Show | 5 | HG01081.hp1 HG01243.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19-378A>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750171 | ||||||
chr7:24750182
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-389C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750182 | ||||||
chr7:24750220
|
A | G | 1 | a0002c0003t0008g0022 | 2 | NA18994.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-19-427T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750220 | ||||||
chr7:24750345
|
G | C | 1 | a0003c0005t0001g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-19-552C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750345 | ||||||
chr7:24750413
|
T | C | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-620A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750413 | ||||||
chr7:24750434
|
T | C | 1 | a0001c0001t0003g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-19-641A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750434 | ||||||
chr7:24750441
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-19-648T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750441 | ||||||
chr7:24750504
|
T | C | 2 | a0001c0001t0002g0095a0001c0001t0005g0096 | 2 | HG01175.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-19-711A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750504 | ||||||
chr7:24750508
|
G | A | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-715C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750508 | ||||||
chr7:24750569
|
C | T | 4 | a0001c0001t0004g0146a0003c0008t0001g0206a0003c0008t0001g0265others(1): Show | 4 | NA18960.hp2 NA19079.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19-776G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750569 | ||||||
chr7:24750570
|
G | A | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-777C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750570 | ||||||
chr7:24750592
|
G | A | 2 | a0001c0004t0001g0109a0001c0004t0001g0133 | 2 | HG02257.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-19-799C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750592 | ||||||
chr7:24750778
|
C | T | 3 | a0001c0001t0007g0351a0001c0001t0007g0352a0001c0001t0007g0353 | 3 | HG01243.hp2 HG02572.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-19-985G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750778 | ||||||
chr7:24750829
|
T | C | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-1036A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750829 | ||||||
chr7:24750975
|
A | G | 2 | a0001c0001t0001g0140a0002c0003t0001g0271 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-1182T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750975 | ||||||
chr7:24750994
|
T | C | 1 | a0001c0001t0003g0134 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-19-1201A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24750994 | ||||||
chr7:24751259
|
G | A | 1 | a0001c0004t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-19-1466C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751259 | ||||||
chr7:24751278
|
AC | A | 88 | a0001c0001t0002g0198a0001c0001t0003g0231a0001c0002t0001g0026others(85): Show | 102 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19-1486delG | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751278 | ||||||
chr7:24751355
|
T | G | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19-1562A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751355 | ||||||
chr7:24751371
|
C | T | 1 | a0001c0004t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-19-1578G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751371 | ||||||
chr7:24751457
|
C | G | 1 | a0002c0003t0001g0037 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-19-1664G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751457 | ||||||
chr7:24751519
|
G | C | 2 | a0001c0001t0001g0140a0002c0003t0001g0088 | 2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-19-1726C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751519 | ||||||
chr7:24751585
|
C | G | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19-1792G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751585 | ||||||
chr7:24751804
|
C | G | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19-2011G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751804 | ||||||
chr7:24751959
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-19-2166C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751959 | ||||||
chr7:24751959
|
G | C | 1 | a0001c0004t0001g0346 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-19-2166C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24751959 | ||||||
chr7:24752164
|
G | A | 1 | a0002c0003t0001g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-19-2371C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752164 | ||||||
chr7:24752275
|
T | C | 75 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(72): Show | 98 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-19-2482A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752275 | ||||||
chr7:24752379
|
C | T | 168 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(165): Show | 198 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.-19-2586G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752379 | ||||||
chr7:24752482
|
C | T | 16 | a0001c0001t0001g0155a0001c0001t0001g0197a0001c0001t0001g0264others(13): Show | 16 | HG00733.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19-2689G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752482 | ||||||
chr7:24752509
|
G | T | 1 | a0002c0003t0001g0151 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-19-2716C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752509 | ||||||
chr7:24752515
|
A | G | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19-2722T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752515 | ||||||
chr7:24752625
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-19-2832T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752625 | ||||||
chr7:24752630
|
G | A | 1 | a0002c0003t0001g0270 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-19-2837C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752630 | ||||||
chr7:24752638
|
G | C | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-19-2845C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752638 | ||||||
chr7:24752677
|
C | T | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-19-2884G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752677 | ||||||
chr7:24752700
|
C | T | 1 | a0001c0001t0010g0092 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19-2907G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752700 | ||||||
chr7:24752720
|
A | G | 4 | a0002c0003t0001g0097a0002c0006t0005g0005a0002c0006t0005g0017others(1): Show | 8 | HG01081.hp2 HG01884.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19-2927T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752720 | ||||||
chr7:24752822
|
G | A | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19-3029C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752822 | ||||||
chr7:24752956
|
G | T | 1 | a0003c0005t0001g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-19-3163C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752956 | ||||||
chr7:24752992
|
G | GT | 66 | a0001c0001t0001g0077a0001c0001t0001g0140a0001c0001t0007g0351others(63): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-19-3200dupA | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24752992 | ||||||
chr7:24753248
|
G | A | 46 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(43): Show | 63 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-19-3455C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24753248 | ||||||
chr7:24753387
|
A | G | 1 | a0003c0005t0001g0199 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-19-3594T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24753387 | ||||||
chr7:24753591
|
T | C | 30 | a0001c0001t0001g0155a0001c0001t0001g0197a0001c0001t0001g0264others(27): Show | 32 | HG00597.hp1 HG00733.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.-19-3798A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24753591 | ||||||
chr7:24753765
|
A | C | 1 | a0001c0004t0001g0183 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-20+3631T>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24753765 | ||||||
chr7:24754084
|
A | T | 64 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(61): Show | 70 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-20+3312T>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754084 | ||||||
chr7:24754087
|
T | C | 1 | a0001c0001t0004g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-20+3309A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754087 | ||||||
chr7:24754375
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-20+3021G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754375 | ||||||
chr7:24754465
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-20+2931T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754465 | ||||||
chr7:24754485
|
C | CA | 7 | a0002c0003t0001g0267a0002c0003t0001g0268a0002c0003t0001g0270others(4): Show | 7 | HG02080.hp1 HG03471.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+2910dupT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754485 | ||||||
chr7:24754485
|
CA | C | 29 | a0001c0001t0001g0155a0001c0001t0001g0197a0001c0001t0003g0019others(26): Show | 32 | HG00597.hp1 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.-20+2910delT | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754485 | ||||||
chr7:24754485
|
CAA | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(140): Show | 172 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.-20+2909_-20+2910d others(4): Show |
GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754485 | ||||||
chr7:24754567
|
C | T | 1 | a0001c0004t0001g0310 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-20+2829G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754567 | ||||||
chr7:24754695
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-20+2701C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754695 | ||||||
chr7:24754820
|
C | T | 1 | a0002c0003t0001g0193 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-20+2576G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754820 | ||||||
chr7:24754831
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0001t0002g0015others(7): Show | 15 | HG01109.hp2 HG01175.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-20+2565G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24754831 | ||||||
chr7:24755372
|
C | T | 1 | a0001c0001t0001g0014 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-20+2024G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24755372 | ||||||
chr7:24755398
|
G | A | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20+1998C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24755398 | ||||||
chr7:24755400
|
G | C | 100 | a0001c0001t0001g0197a0001c0001t0001g0263a0001c0001t0001g0264others(97): Show | 118 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-20+1996C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24755400 | ||||||
chr7:24755504
|
C | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0091 | 3 | HG02055.hp1 HG02970.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-20+1892G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24755504 | ||||||
chr7:24755644
|
A | G | 1 | a0009c0013t0001g0190 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-20+1752T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24755644 | ||||||
chr7:24755720
|
T | C | 1 | a0002c0006t0005g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-20+1676A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24755720 | ||||||
chr7:24755932
|
C | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA18983.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-20+1464G>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24755932 | ||||||
chr7:24756024
|
A | G | 42 | a0001c0001t0001g0283a0001c0001t0001g0306a0001c0001t0001g0307others(39): Show | 43 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-20+1372T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756024 | ||||||
chr7:24756138
|
C | T | 65 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(62): Show | 87 | HG00438.hp1 HG00544.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-20+1258G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756138 | ||||||
chr7:24756165
|
A | G | 1 | a0002c0003t0001g0271 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-20+1231T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756165 | ||||||
chr7:24756227
|
G | A | 4 | a0001c0001t0003g0173a0001c0001t0009g0170a0001c0001t0009g0171others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20+1169C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756227 | ||||||
chr7:24756233
|
T | G | 66 | a0001c0001t0001g0077a0001c0001t0007g0351a0001c0001t0007g0352others(63): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-20+1163A>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756233 | ||||||
chr7:24756262
|
T | C | 2 | a0001c0001t0003g0148a0001c0001t0003g0149 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-20+1134A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756262 | ||||||
chr7:24756344
|
G | C | 1 | a0001c0002t0001g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-20+1052C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756344 | ||||||
chr7:24756402
|
G | A | 6 | a0001c0001t0003g0176a0001c0004t0004g0020a0001c0004t0004g0177others(3): Show | 7 | HG02109.hp1 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-20+994C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756402 | ||||||
chr7:24756469
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-20+927A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756469 | ||||||
chr7:24756610
|
T | C | 266 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(263): Show | 314 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(311): Show |
intron_variant | MODIFIER | c.-20+786A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756610 | ||||||
chr7:24756701
|
C | T | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-20+695G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756701 | ||||||
chr7:24756705
|
T | C | 1 | a0002c0003t0007g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-20+691A>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756705 | ||||||
chr7:24756788
|
G | A | 2 | a0001c0002t0001g0081a0001c0002t0001g0082 | 2 | NA18993.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.-20+608C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756788 | ||||||
chr7:24756841
|
G | C | 2 | a0001c0001t0004g0152a0001c0004t0004g0153 | 2 | HG01361.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-20+555C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756841 | ||||||
chr7:24756856
|
C | T | 3 | a0001c0001t0003g0089a0001c0001t0006g0001a0002c0003t0001g0154 | 9 | HG02451.hp2 HG02886.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.-20+540G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756856 | ||||||
chr7:24756883
|
A | G | 166 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(163): Show | 196 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.-20+513T>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756883 | ||||||
chr7:24756922
|
C | G | 128 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(125): Show | 156 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-20+474G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24756922 | ||||||
chr7:24757003
|
G | T | 1 | a0002c0003t0001g0088 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-20+393C>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24757003 | ||||||
chr7:24757040
|
G | C | 1 | a0001c0004t0001g0348 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-20+356C>G | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24757040 | ||||||
chr7:24757074
|
C | G | 274 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0018others(271): Show | 322 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(319): Show |
intron_variant | MODIFIER | c.-20+322G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24757074 | ||||||
chr7:24757123
|
G | A | 1 | a0002c0003t0001g0349 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-20+273C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24757123 | ||||||
chr7:24757170
|
C | T | 2 | a0001c0002t0001g0035a0001c0002t0001g0036 | 2 | NA19055.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-20+226G>A | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24757170 | ||||||
chr7:24757386
|
G | A | 1 | a0003c0005t0001g0350 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-20+10C>T | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24757386 | ||||||
chr7:24757387
|
C | G | 57 | a0001c0001t0001g0077a0001c0002t0001g0003a0001c0002t0001g0011others(54): Show | 63 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.-20+9G>C | GSDME | ENSG00000105928.16 | transcript | ENST00000645220.1 | protein_coding | 1/9 | chr7 | 24757387 |