geneid | 654346 |
---|---|
ensemblid | ENSG00000171916.17 |
hgncid | 33874 |
symbol | LGALS9C |
name | galectin 9C |
refseq_nuc | NM_001040078.3 |
refseq_prot | NP_001035167.2 |
ensembl_nuc | ENST00000328114.11 |
ensembl_prot | ENSP00000329932.6 |
mane_status | MANE Select |
chr | chr17 |
start | 18476789 |
end | 18494945 |
strand | + |
ver | v1.2 |
region | chr17:18476789-18494945 |
region5000 | chr17:18471789-18499945 |
regionname0 | LGALS9C_chr17_18476789_18494945 |
regionname5000 | LGALS9C_chr17_18471789_18499945 |
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 | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 356 | 196 | 27 | 28 | 122 | 3 | 15 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0002 | 0/0 | 356 | 71 | 11 | 15 | 36 | 2 | 7 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0003 | 0/0 | 356 | 4 | 4 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0004 | 0/0 | 356 | 4 | 3 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0005 | 0/0 | 356 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0006 | 0/0 | 356 | 2 | 0 | 0 | 1 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0007 | 0/0 | 356 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0008 | 0/0 | 356 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0009 | 0/0 | 356 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0010 | 0/0 | 356 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0011 | 0/0 | 356 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0012 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0013 | 0/0 | 356 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1071 | 194 | 26 | 27 | 122 | 3 | 15 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0002 | 0/0 | 1071 | 71 | 11 | 15 | 36 | 2 | 7 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0003 | 0/0 | 1071 | 4 | 4 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0004 | 0/0 | 1071 | 4 | 3 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0005 | 0/0 | 1071 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0006 | 0/0 | 1071 | 2 | 0 | 0 | 1 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0007 | 0/0 | 1071 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0008 | 0/0 | 1071 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0009 | 0/0 | 1071 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0010 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0011 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0012 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0013 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0014 | 0/0 | 1071 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0015 | 0/0 | 1071 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
c0016 | 0/0 | 1071 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 645 | 207 | 35 | 26 | 122 | 4 | 19 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
t0002 | 0/0 | 645 | 78 | 12 | 18 | 37 | 2 | 9 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
t0003 | 0/0 | 645 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
t0004 | 0/0 | 645 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
t0005 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
t0006 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
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 |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 23 | 1 | 3 | 19 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0002 | 0/0 | 21 | 0 | 6 | 13 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0003 | 0/0 | 18 | 0 | 4 | 14 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0004 | 0/0 | 13 | 1 | 3 | 4 | 0 | 5 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0005 | 0/0 | 11 | 2 | 1 | 6 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0006 | 1/0 | 8 | 0 | 1 | 2 | 0 | 4 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/0 | 194 | 26 | 27 | 122 | 3 | 15 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0001c0011 | a0001 | c0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0001c0015 | a0001 | c0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0002c0002 | a0002 | c0002 | 0/0 | 71 | 11 | 15 | 36 | 2 | 7 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0003c0003 | a0003 | c0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0004c0004 | a0004 | c0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0005c0005 | a0005 | c0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0006c0006 | a0006 | c0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0007c0009 | a0007 | c0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0008c0008 | a0008 | c0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0009c0007 | a0009 | c0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0010c0013 | a0010 | c0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0010c0014 | a0010 | c0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0011c0016 | a0011 | c0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0012c0012 | a0012 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0013c0010 | a0013 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
acthapid | ahapid | chapid | thapid | 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 | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 1/0 | 187 | 24 | 24 | 120 | 3 | 15 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0001c0011t0002 | a0001 | c0011 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0001c0015t0001 | a0001 | c0015 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0002c0002t0002 | a0002 | c0002 | t0002 | 0/0 | 71 | 11 | 15 | 36 | 2 | 7 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0003c0003t0001 | a0003 | c0003 | t0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0004c0004t0001 | a0004 | c0004 | t0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0005c0005t0001 | a0005 | c0005 | t0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0006c0006t0001 | a0006 | c0006 | t0001 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0007c0009t0002 | a0007 | c0009 | t0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0008c0008t0001 | a0008 | c0008 | t0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0009c0007t0001 | a0009 | c0007 | t0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0010c0013t0005 | a0010 | c0013 | t0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0010c0014t0003 | a0010 | c0014 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0011c0016t0001 | a0011 | c0016 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0012c0012t0003 | a0012 | c0012 | t0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
a0013c0010t0001 | a0013 | c0010 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C | copy fasta |
actghapid | ahapid | chapid | thapid | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 23 | 1 | 3 | 19 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 18 | 0 | 4 | 14 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 13 | 1 | 3 | 4 | 0 | 5 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 1/0 | 6 | 0 | 1 | 2 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0146 | a0001 | c0001 | t0001 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0002g0022 | a0001 | c0001 | t0002 | g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0002g0130 | a0001 | c0001 | t0002 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0002g0151 | a0001 | c0001 | t0002 | g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0004g0008 | a0001 | c0001 | t0004 | g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0001t0006g0111 | a0001 | c0001 | t0006 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0011t0002g0087 | a0001 | c0011 | t0002 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0001c0015t0001g0142 | a0001 | c0015 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0002 | a0002 | c0002 | t0002 | g0002 | 0/0 | 21 | 0 | 6 | 13 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0005 | a0002 | c0002 | t0002 | g0005 | 0/0 | 11 | 2 | 1 | 6 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0013 | a0002 | c0002 | t0002 | g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0014 | a0002 | c0002 | t0002 | g0014 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0019 | a0002 | c0002 | t0002 | g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0020 | a0002 | c0002 | t0002 | g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0021 | a0002 | c0002 | t0002 | g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0035 | a0002 | c0002 | t0002 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0036 | a0002 | c0002 | t0002 | g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0037 | a0002 | c0002 | t0002 | g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0040 | a0002 | c0002 | t0002 | g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0053 | a0002 | c0002 | t0002 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0054 | a0002 | c0002 | t0002 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0055 | a0002 | c0002 | t0002 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0056 | a0002 | c0002 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0057 | a0002 | c0002 | t0002 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0058 | a0002 | c0002 | t0002 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0059 | a0002 | c0002 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0060 | a0002 | c0002 | t0002 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0061 | a0002 | c0002 | t0002 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0062 | a0002 | c0002 | t0002 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0063 | a0002 | c0002 | t0002 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0064 | a0002 | c0002 | t0002 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0065 | a0002 | c0002 | t0002 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0066 | a0002 | c0002 | t0002 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0119 | a0002 | c0002 | t0002 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0121 | a0002 | c0002 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0122 | a0002 | c0002 | t0002 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0123 | a0002 | c0002 | t0002 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0002c0002t0002g0124 | a0002 | c0002 | t0002 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0003c0003t0001g0011 | a0003 | c0003 | t0001 | g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0003c0003t0001g0043 | a0003 | c0003 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0004c0004t0001g0084 | a0004 | c0004 | t0001 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0004c0004t0001g0127 | a0004 | c0004 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0004c0004t0001g0128 | a0004 | c0004 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0004c0004t0001g0129 | a0004 | c0004 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0005c0005t0001g0041 | a0005 | c0005 | t0001 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0005c0005t0001g0042 | a0005 | c0005 | t0001 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0005c0005t0001g0078 | a0005 | c0005 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0006c0006t0001g0091 | a0006 | c0006 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0006c0006t0001g0137 | a0006 | c0006 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0007c0009t0002g0125 | a0007 | c0009 | t0002 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0007c0009t0002g0126 | a0007 | c0009 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0008c0008t0001g0024 | a0008 | c0008 | t0001 | g0024 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0009c0007t0001g0006 | a0009 | c0007 | t0001 | g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0010c0013t0005g0045 | a0010 | c0013 | t0005 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0010c0014t0003g0150 | a0010 | c0014 | t0003 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0011c0016t0001g0075 | a0011 | c0016 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0012c0012t0003g0149 | a0012 | c0012 | t0003 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
a0013c0010t0001g0031 | a0013 | c0010 | t0001 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LGALS9C_chr17_18471789_18499945 | LGALS9C |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0014 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0005 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00323 | hp2 | a0008 | c0008 | t0001 | g0024 | EUR | FIN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00741 | hp1 | a0004 | c0004 | t0001 | g0084 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01106 | hp1 | a0001 | c0015 | t0001 | g0142 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0036 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01891 | hp1 | a0005 | c0005 | t0001 | g0041 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0123 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02257 | hp2 | a0005 | c0005 | t0001 | g0042 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02273 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02280 | hp1 | a0013 | c0010 | t0001 | g0031 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02451 | hp2 | a0004 | c0004 | t0001 | g0127 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02572 | hp1 | a0010 | c0014 | t0003 | g0150 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02602 | hp1 | a0007 | c0009 | t0002 | g0126 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02630 | hp2 | a0001 | c0011 | t0002 | g0087 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02735 | hp2 | a0007 | c0009 | t0002 | g0125 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02895 | hp1 | a0005 | c0005 | t0001 | g0078 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02922 | hp2 | a0004 | c0004 | t0001 | g0129 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02970 | hp1 | a0003 | c0003 | t0001 | g0043 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03017 | hp1 | a0009 | c0007 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03130 | hp2 | a0004 | c0004 | t0001 | g0128 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03239 | hp1 | a0009 | c0007 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03239 | hp2 | a0008 | c0008 | t0001 | g0024 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03453 | hp1 | a0002 | c0002 | t0002 | g0053 | AFR | MSL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0064 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0054 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0057 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03831 | hp2 | a0006 | c0006 | t0001 | g0137 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0121 | SAS | STU | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | CHB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18957 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18967 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18986 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18990 | hp1 | a0011 | c0016 | t0001 | g0075 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18999 | hp2 | a0006 | c0006 | t0001 | g0091 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0055 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19043 | hp1 | a0012 | c0012 | t0003 | g0149 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19067 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02109 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
HG02559 | hp2 | a0010 | c0013 | t0005 | g0045 | AFR | ACB | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | LGALS9C_chr17_18471789_18499945 | LGALS9C |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | LGALS9C_chr17_18471789_18499945 | LGALS9C |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0006 | REF | REF | LGALS9C_chr17_18471789_18499945 | LGALS9C |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18476871
|
G | C | 1 | a0013 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.17G>C | p.Cys6Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/11 | 83/1715 | 17/1071 | 6/356 | chr17 | 18476871 | ||
chr17:18483878
|
G | A | 1 | a0003 | 4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
missense_variant | MODERATE | c.43G>A | p.Val15Ile | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/11 | 109/1715 | 43/1071 | 15/356 | chr17 | 18483878 | ||
chr17:18483954
|
G | C | 3 | a0005a0010a0012 | 6 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(3): Show |
missense_variant | MODERATE | c.119G>C | p.Cys40Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/11 | 185/1715 | 119/1071 | 40/356 | chr17 | 18483954 | ||
chr17:18485971
|
G | A | 1 | a0005 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
missense_variant | MODERATE | c.169G>A | p.Asp57Asn | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/11 | 235/1715 | 169/1071 | 57/356 | chr17 | 18485971 | ||
chr17:18486044
|
C | G | 4 | a0002a0003a0004others(1): Show | 82 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(79): Show |
missense_variant | MODERATE | c.242C>G | p.Thr81Arg | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/11 | 308/1715 | 242/1071 | 81/356 | chr17 | 18486044 | ||
chr17:18486050
|
G | C | 1 | a0006 | 2 | HG03831.hp2 NA18999.hp2 |
missense_variant | MODERATE | c.248G>C | p.Gly83Ala | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/11 | 314/1715 | 248/1071 | 83/356 | chr17 | 18486050 | ||
chr17:18487689
|
G | A | 3 | a0002a0003a0007 | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
missense_variant | MODERATE | c.376G>A | p.Val126Met | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/11 | 442/1715 | 376/1071 | 126/356 | chr17 | 18487689 | ||
chr17:18488950
|
G | A | 1 | a0004 | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.454G>A | p.Ala152Thr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/11 | 520/1715 | 454/1071 | 152/356 | chr17 | 18488950 | ||
chr17:18488990
|
C | A | 1 | a0009 | 2 | HG03017.hp1 HG03239.hp1 |
missense_variant | MODERATE | c.494C>A | p.Ser165Tyr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/11 | 560/1715 | 494/1071 | 165/356 | chr17 | 18488990 | ||
chr17:18490742
|
G | A | 2 | a0004a0012 | 5 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(2): Show |
missense_variant | MODERATE | c.550G>A | p.Val184Met | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/11 | 616/1715 | 550/1071 | 184/356 | chr17 | 18490742 | ||
chr17:18491954
|
G | C | 1 | a0008 | 2 | HG00323.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.637G>C | p.Ala213Pro | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/11 | 703/1715 | 637/1071 | 213/356 | chr17 | 18491954 | ||
chr17:18494240
|
C | G | 1 | a0011 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.944C>G | p.Ala315Gly | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 1010/1715 | 944/1071 | 315/356 | chr17 | 18494240 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18483931
|
T | C | 1 | a0001c0011 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.96T>C | p.Thr32Thr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/11 | 162/1715 | 96/1071 | 32/356 | chr17 | 18483931 | ||
chr17:18487679
|
C | T | 3 | a0002c0002a0003c0003a0007c0009 | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
synonymous_variant | LOW | c.366C>T | p.Tyr122Tyr | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/11 | 432/1715 | 366/1071 | 122/356 | chr17 | 18487679 | ||
chr17:18488958
|
C | A | 1 | a0005c0005 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
synonymous_variant | LOW | c.462C>A | p.Pro154Pro | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/11 | 528/1715 | 462/1071 | 154/356 | chr17 | 18488958 | ||
chr17:18491302
|
T | C | 5 | a0002c0002a0003c0003a0004c0004others(2): Show | 82 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(79): Show |
synonymous_variant | LOW | c.606T>C | p.Ser202Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/11 | 672/1715 | 606/1071 | 202/356 | chr17 | 18491302 | ||
chr17:18492817
|
T | C | 1 | a0001c0015 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.882T>C | p.Ser294Ser | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/11 | 948/1715 | 882/1071 | 294/356 | chr17 | 18492817 | ||
chr17:18492838
|
C | T | 1 | a0010c0013 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.903C>T | p.Phe301Phe | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/11 | 969/1715 | 903/1071 | 301/356 | chr17 | 18492838 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18476821
|
C | G | 1 | a0001c0001t0006 | 1 | NA18747.hp1 | 5_prime_UTR_variant | MODIFIER | c.-34C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/11 | 34 | chr17 | 18476821 | |||||
chr17:18476830
|
T | C | 1 | a0001c0001t0006 | 1 | NA18747.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/11 | 25 | chr17 | 18476830 | |||||
chr17:18494413
|
T | G | 4 | a0001c0001t0002a0001c0011t0002a0002c0002t0002others(1): Show | 78 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*46T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 46 | chr17 | 18494413 | |||||
chr17:18494415
|
G | A | 1 | a0010c0013t0005 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 48 | chr17 | 18494415 | |||||
chr17:18494771
|
C | T | 1 | a0001c0001t0004 | 2 | HG01891.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*404C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 404 | chr17 | 18494771 | |||||
chr17:18494778
|
C | A | 1 | a0001c0001t0004 | 2 | HG01891.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*411C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 411 | chr17 | 18494778 | |||||
chr17:18494913
|
A | G | 2 | a0010c0014t0003a0012c0012t0003 | 2 | HG02572.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*546A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 11/11 | 546 | chr17 | 18494913 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:18476982
|
G | A | 2 | a0005c0005t0001g0041a0005c0005t0001g0042 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.39+89G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18476982 | ||||||
chr17:18477052
|
G | A | 2 | a0003c0003t0001g0011a0003c0003t0001g0043 | 4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+159G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477052 | ||||||
chr17:18477085
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0002g0151 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.39+192A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477085 | ||||||
chr17:18477102
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0002g0151 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.39+209G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477102 | ||||||
chr17:18477176
|
A | G | 2 | a0010c0014t0003g0150a0012c0012t0003g0149 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+283A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477176 | ||||||
chr17:18477348
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.39+455C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477348 | ||||||
chr17:18477463
|
T | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0044 | 4 | HG00140.hp2 HG00323.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+570T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477463 | ||||||
chr17:18477568
|
G | T | 1 | a0002c0002t0002g0040 | 2 | NA18944.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.39+675G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477568 | ||||||
chr17:18477573
|
G | A | 3 | a0010c0013t0005g0045a0010c0014t0003g0150a0012c0012t0003g0149 | 3 | HG02559.hp2 HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+680G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477573 | ||||||
chr17:18477576
|
G | A | 3 | a0010c0013t0005g0045a0010c0014t0003g0150a0012c0012t0003g0149 | 3 | HG02559.hp2 HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.39+683G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477576 | ||||||
chr17:18477662
|
C | T | 1 | a0010c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.39+769C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477662 | ||||||
chr17:18477774
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(22): Show | 58 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.39+881C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477774 | ||||||
chr17:18477836
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.39+943T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477836 | ||||||
chr17:18477843
|
C | A | 1 | a0012c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.39+950C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477843 | ||||||
chr17:18477861
|
G | A | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.39+968G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477861 | ||||||
chr17:18477940
|
T | C | 35 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0047others(32): Show | 67 | HG00099.hp1 HG00408.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.39+1047T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477940 | ||||||
chr17:18477954
|
C | T | 3 | a0004c0004t0001g0127a0004c0004t0001g0128a0004c0004t0001g0129 | 3 | HG02451.hp2 HG02922.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.39+1061C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18477954 | ||||||
chr17:18478029
|
A | C | 47 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0115others(44): Show | 94 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.39+1136A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478029 | ||||||
chr17:18478035
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.39+1142G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478035 | ||||||
chr17:18478107
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.39+1214C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478107 | ||||||
chr17:18478148
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0068a0001c0001t0001g0069others(1): Show | 5 | HG02055.hp1 HG02486.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+1255T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478148 | ||||||
chr17:18478150
|
G | C | 1 | a0001c0001t0001g0131 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.39+1257G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478150 | ||||||
chr17:18478156
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.39+1263C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478156 | ||||||
chr17:18478156
|
C | T | 10 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0036others(7): Show | 23 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.39+1263C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478156 | ||||||
chr17:18478208
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.39+1315C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478208 | ||||||
chr17:18478209
|
A | G | 4 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0112others(1): Show | 4 | HG01978.hp1 HG02129.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+1316A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478209 | ||||||
chr17:18478233
|
G | T | 2 | a0001c0001t0001g0120a0001c0001t0002g0022 | 3 | HG01069.hp1 HG01099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+1340G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478233 | ||||||
chr17:18478252
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.39+1359A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478252 | ||||||
chr17:18478492
|
T | C | 45 | a0001c0001t0001g0010a0001c0001t0001g0052a0001c0001t0001g0115others(42): Show | 91 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.39+1599T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478492 | ||||||
chr17:18478497
|
C | T | 1 | a0012c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.39+1604C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478497 | ||||||
chr17:18478517
|
T | G | 2 | a0001c0001t0001g0015a0001c0001t0001g0071 | 4 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.39+1624T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478517 | ||||||
chr17:18478621
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.39+1728A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478621 | ||||||
chr17:18478646
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.39+1753G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478646 | ||||||
chr17:18478697
|
A | C | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.39+1804A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478697 | ||||||
chr17:18478782
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0002g0022 | 3 | HG01069.hp1 HG01099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+1889C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478782 | ||||||
chr17:18478783
|
G | A | 13 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0116others(10): Show | 29 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.39+1890G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478783 | ||||||
chr17:18478860
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.39+1967T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478860 | ||||||
chr17:18478914
|
G | C | 5 | a0005c0005t0001g0041a0005c0005t0001g0042a0010c0013t0005g0045others(2): Show | 5 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.39+2021G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18478914 | ||||||
chr17:18479040
|
G | C | 1 | a0001c0001t0001g0072 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.39+2147G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479040 | ||||||
chr17:18479070
|
C | T | 2 | a0003c0003t0001g0011a0003c0003t0001g0043 | 4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+2177C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479070 | ||||||
chr17:18479098
|
C | T | 1 | a0002c0002t0002g0037 | 2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.39+2205C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479098 | ||||||
chr17:18479119
|
C | T | 2 | a0003c0003t0001g0011a0003c0003t0001g0043 | 4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.39+2226C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479119 | ||||||
chr17:18479244
|
C | T | 1 | a0001c0001t0006g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.39+2351C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479244 | ||||||
chr17:18479274
|
T | C | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.39+2381T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479274 | ||||||
chr17:18479317
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.39+2424A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479317 | ||||||
chr17:18479366
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.39+2473G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479366 | ||||||
chr17:18479386
|
G | A | 4 | a0002c0002t0002g0013a0002c0002t0002g0053a0002c0002t0002g0054others(1): Show | 6 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+2493G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479386 | ||||||
chr17:18479439
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0002g0022 | 3 | HG01069.hp1 HG01099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.39+2546C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479439 | ||||||
chr17:18479472
|
T | C | 44 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0116others(41): Show | 90 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.39+2579T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479472 | ||||||
chr17:18479533
|
T | C | 2 | a0005c0005t0001g0041a0005c0005t0001g0042 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.39+2640T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479533 | ||||||
chr17:18479555
|
A | T | 4 | a0002c0002t0002g0013a0002c0002t0002g0053a0002c0002t0002g0054others(1): Show | 6 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.39+2662A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479555 | ||||||
chr17:18479655
|
C | T | 1 | a0001c0001t0006g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.39+2762C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479655 | ||||||
chr17:18479867
|
G | GCTGC | 15 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0116others(12): Show | 31 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.39+2985_39+2988dup others(4): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18479867 | |||||
chr17:18479879
|
C | A | 1 | a0001c0001t0002g0130 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.39+2986C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479879 | ||||||
chr17:18479880
|
C | T | 17 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(14): Show | 43 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.39+2987C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479880 | ||||||
chr17:18479969
|
G | A | 1 | a0008c0008t0001g0024 | 2 | HG00323.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.39+3076G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18479969 | ||||||
chr17:18480112
|
G | A | 1 | a0012c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.39+3219G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480112 | ||||||
chr17:18480156
|
T | C | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.39+3263T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480156 | ||||||
chr17:18480178
|
C | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.39+3285C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480178 | ||||||
chr17:18480208
|
C | CA | 13 | a0001c0001t0001g0012a0001c0001t0001g0025a0001c0001t0001g0073others(10): Show | 19 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(16): Show |
intron_variant | MODIFIER | c.39+3333dupA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18480208 | |||||
chr17:18480208
|
CA | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 7 | HG01069.hp1 HG01099.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.39+3333delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18480208 | |||||
chr17:18480219
|
A | C | 18 | a0001c0001t0001g0010a0001c0001t0001g0116a0001c0001t0001g0117others(15): Show | 36 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.39+3326A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480219 | ||||||
chr17:18480220
|
A | AC | 14 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(11): Show | 40 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.39+3327_39+3328ins others(1): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480220 | ||||||
chr17:18480226
|
A | C | 1 | a0001c0001t0001g0034 | 2 | NA18955.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.39+3333A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480226 | ||||||
chr17:18480322
|
G | A | 21 | a0001c0001t0001g0010a0001c0001t0001g0115a0001c0001t0001g0116others(18): Show | 39 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.39+3429G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480322 | ||||||
chr17:18480554
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0146 | 3 | HG01109.hp2 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.40-3321C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480554 | ||||||
chr17:18480620
|
T | C | 2 | a0001c0001t0001g0080a0001c0001t0001g0081 | 2 | HG00735.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.40-3255T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480620 | ||||||
chr17:18480685
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.40-3190A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480685 | ||||||
chr17:18480812
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.40-3063C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18480812 | ||||||
chr17:18481012
|
T | A | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40-2863T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481012 | ||||||
chr17:18481091
|
A | G | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-2784A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481091 | ||||||
chr17:18481117
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.40-2758G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481117 | ||||||
chr17:18481227
|
G | A | 2 | a0005c0005t0001g0041a0005c0005t0001g0042 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.40-2648G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481227 | ||||||
chr17:18481366
|
G | A | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.40-2509G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481366 | ||||||
chr17:18481383
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.40-2492C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481383 | ||||||
chr17:18481384
|
G | A | 8 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0036others(5): Show | 21 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.40-2491G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481384 | ||||||
chr17:18481485
|
A | G | 12 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(9): Show | 27 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.40-2390A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481485 | ||||||
chr17:18481513
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.40-2362C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481513 | ||||||
chr17:18481515
|
C | T | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-2360C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481515 | ||||||
chr17:18481658
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.40-2217G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481658 | ||||||
chr17:18481666
|
AAGTATTT others(24): Show |
A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-2208_40-2178del others(31): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481666 | ||||||
chr17:18481759
|
C | T | 19 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(16): Show | 47 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.40-2116C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481759 | ||||||
chr17:18481782
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.40-2093G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481782 | ||||||
chr17:18481828
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.40-2047G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481828 | ||||||
chr17:18481925
|
T | C | 37 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(34): Show | 80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.40-1950T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18481925 | ||||||
chr17:18482035
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1840A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482035 | ||||||
chr17:18482081
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.40-1794C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482081 | ||||||
chr17:18482140
|
G | A | 14 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(11): Show | 29 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.40-1735G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482140 | ||||||
chr17:18482158
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1717T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482158 | ||||||
chr17:18482159
|
C | A | 1 | a0002c0002t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40-1716C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482159 | ||||||
chr17:18482159
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1716C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482159 | ||||||
chr17:18482197
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.40-1678G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482197 | ||||||
chr17:18482197
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.40-1678G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482197 | ||||||
chr17:18482204
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0114 | 5 | HG02109.hp1 HG02451.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.40-1671G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482204 | ||||||
chr17:18482213
|
G | A | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-1662G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482213 | ||||||
chr17:18482266
|
C | T | 14 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(11): Show | 29 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.40-1609C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482266 | ||||||
chr17:18482295
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1580A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482295 | ||||||
chr17:18482418
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1457A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482418 | ||||||
chr17:18482478
|
G | A | 16 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(13): Show | 31 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.40-1397G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482478 | ||||||
chr17:18482484
|
C | T | 18 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(15): Show | 45 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.40-1391C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482484 | ||||||
chr17:18482507
|
C | CA | 14 | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0027others(11): Show | 22 | HG00733.hp2 HG00741.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.40-1350dupA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | |||||
chr17:18482507
|
C | CAA | 16 | a0001c0001t0001g0135a0002c0002t0002g0002a0002c0002t0002g0014others(13): Show | 41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.40-1351_40-1350dup others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | |||||
chr17:18482507
|
CA | C | 13 | a0001c0001t0001g0033a0001c0001t0001g0068a0001c0001t0001g0079others(10): Show | 14 | HG00438.hp1 HG00558.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.40-1350delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | |||||
chr17:18482507
|
CAA | C | 8 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0036others(5): Show | 21 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.40-1351_40-1350del others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482507 | |||||
chr17:18482530
|
G | A | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.40-1345G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482530 | ||||||
chr17:18482531
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.40-1344G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482531 | ||||||
chr17:18482568
|
A | C | 2 | a0003c0003t0001g0011a0003c0003t0001g0043 | 4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.40-1307A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482568 | ||||||
chr17:18482582
|
C | T | 1 | a0002c0002t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.40-1293C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482582 | ||||||
chr17:18482606
|
A | T | 13 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(10): Show | 28 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.40-1269A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482606 | ||||||
chr17:18482628
|
G | A | 10 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0036others(7): Show | 23 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.40-1247G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482628 | ||||||
chr17:18482673
|
G | A | 2 | a0005c0005t0001g0041a0005c0005t0001g0042 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.40-1202G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482673 | ||||||
chr17:18482679
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-1196C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482679 | ||||||
chr17:18482853
|
G | A | 1 | a0010c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.40-1022G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482853 | ||||||
chr17:18482868
|
A | G | 15 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(12): Show | 30 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.40-1007A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482868 | ||||||
chr17:18482898
|
C | G | 1 | a0002c0002t0002g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.40-977C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482898 | ||||||
chr17:18482912
|
TG | T | 21 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(18): Show | 49 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.40-957delG | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18482912 | |||||
chr17:18482946
|
T | C | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40-929T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18482946 | ||||||
chr17:18483118
|
G | C | 15 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(12): Show | 30 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.40-757G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483118 | ||||||
chr17:18483175
|
G | A | 2 | a0005c0005t0001g0041a0005c0005t0001g0042 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.40-700G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483175 | ||||||
chr17:18483179
|
AAG | A | 20 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(17): Show | 48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-690_40-689delGA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 18483179 | |||||
chr17:18483204
|
C | T | 16 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0020others(13): Show | 41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.40-671C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483204 | ||||||
chr17:18483228
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-647G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483228 | ||||||
chr17:18483243
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-632C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483243 | ||||||
chr17:18483397
|
C | T | 3 | a0001c0001t0001g0025a0001c0001t0001g0097a0001c0001t0001g0104 | 4 | HG02027.hp1 HG02071.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.40-478C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483397 | ||||||
chr17:18483404
|
G | A | 18 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(15): Show | 44 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.40-471G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483404 | ||||||
chr17:18483407
|
C | T | 38 | a0001c0001t0001g0051a0001c0001t0001g0107a0002c0002t0002g0002others(35): Show | 81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.40-468C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483407 | ||||||
chr17:18483424
|
G | A | 20 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(17): Show | 48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-451G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483424 | ||||||
chr17:18483452
|
G | A | 1 | a0003c0003t0001g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.40-423G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483452 | ||||||
chr17:18483562
|
G | T | 4 | a0002c0002t0002g0013a0002c0002t0002g0053a0002c0002t0002g0054others(1): Show | 6 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.40-313G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483562 | ||||||
chr17:18483571
|
G | A | 1 | a0006c0006t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.40-304G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483571 | ||||||
chr17:18483686
|
T | C | 20 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(17): Show | 48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.40-189T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483686 | ||||||
chr17:18483709
|
C | T | 2 | a0010c0014t0003g0150a0012c0012t0003g0149 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40-166C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483709 | ||||||
chr17:18483777
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40-98A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483777 | ||||||
chr17:18483815
|
C | T | 38 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(35): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.40-60C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483815 | ||||||
chr17:18483817
|
A | G | 17 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0035others(14): Show | 32 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.40-58A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483817 | ||||||
chr17:18483854
|
C | T | 10 | a0002c0002t0002g0005a0002c0002t0002g0035a0002c0002t0002g0036others(7): Show | 23 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.40-21C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 1/10 | chr17 | 18483854 | ||||||
chr17:18483977
|
A | G | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131+11A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18483977 | ||||||
chr17:18484041
|
C | T | 37 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(34): Show | 80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.131+75C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484041 | ||||||
chr17:18484079
|
G | T | 19 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(16): Show | 47 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.131+113G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484079 | ||||||
chr17:18484152
|
T | G | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.131+186T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484152 | ||||||
chr17:18484164
|
G | A | 1 | a0004c0004t0001g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.131+198G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484164 | ||||||
chr17:18484208
|
A | G | 37 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(34): Show | 80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.131+242A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484208 | ||||||
chr17:18484302
|
CA | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.131+337delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484302 | ||||||
chr17:18484312
|
C | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0072 | 5 | HG00558.hp2 HG00597.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.131+346C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484312 | ||||||
chr17:18484456
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.131+490C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484456 | ||||||
chr17:18484509
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.131+543C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484509 | ||||||
chr17:18484538
|
C | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.131+572C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484538 | ||||||
chr17:18484599
|
G | GTGCAGCT others(13): Show |
1 | a0001c0001t0001g0096 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.131+634_131+653dup others(20): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 18484599 | |||||
chr17:18484650
|
G | T | 19 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(16): Show | 46 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.131+684G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484650 | ||||||
chr17:18484775
|
C | G | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(29): Show | 75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.131+809C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484775 | ||||||
chr17:18484799
|
C | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.131+833C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484799 | ||||||
chr17:18484803
|
C | T | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131+837C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484803 | ||||||
chr17:18484868
|
C | T | 3 | a0005c0005t0001g0041a0005c0005t0001g0042a0005c0005t0001g0078 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.131+902C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484868 | ||||||
chr17:18484885
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.131+919C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484885 | ||||||
chr17:18484958
|
T | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.132-976T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484958 | ||||||
chr17:18484959
|
G | T | 11 | a0002c0002t0002g0005a0002c0002t0002g0020a0002c0002t0002g0035others(8): Show | 25 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.132-975G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484959 | ||||||
chr17:18484980
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.132-954C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18484980 | ||||||
chr17:18485012
|
G | A | 20 | a0001c0001t0001g0026a0002c0002t0002g0002a0002c0002t0002g0014others(17): Show | 48 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.132-922G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485012 | ||||||
chr17:18485323
|
G | A | 38 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(35): Show | 81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.132-611G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485323 | ||||||
chr17:18485354
|
A | AAT | 27 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(24): Show | 56 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.132-567_132-566dup others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 18485354 | |||||
chr17:18485354
|
A | AATAT | 11 | a0002c0002t0002g0005a0002c0002t0002g0020a0002c0002t0002g0035others(8): Show | 25 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.132-569_132-566dup others(4): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 18485354 | |||||
chr17:18485360
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.132-574T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485360 | ||||||
chr17:18485439
|
G | A | 15 | a0002c0002t0002g0005a0002c0002t0002g0013a0002c0002t0002g0020others(12): Show | 31 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.132-495G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485439 | ||||||
chr17:18485562
|
G | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.132-372G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485562 | ||||||
chr17:18485604
|
T | C | 2 | a0010c0014t0003g0150a0012c0012t0003g0149 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.132-330T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485604 | ||||||
chr17:18485752
|
C | T | 39 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(36): Show | 82 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.132-182C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485752 | ||||||
chr17:18485792
|
G | C | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-142G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485792 | ||||||
chr17:18485863
|
C | T | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.132-71C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 2/10 | chr17 | 18485863 | ||||||
chr17:18486138
|
A | G | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
splice_region_variant&intron_variant | LOW | c.333+3A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486138 | ||||||
chr17:18486203
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+68G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486203 | ||||||
chr17:18486245
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.333+110C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486245 | ||||||
chr17:18486461
|
A | G | 2 | a0002c0002t0002g0122a0002c0002t0002g0123 | 2 | HG02004.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.333+326A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486461 | ||||||
chr17:18486504
|
C | T | 38 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(35): Show | 81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.333+369C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486504 | ||||||
chr17:18486520
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.333+385T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486520 | ||||||
chr17:18486539
|
G | A | 2 | a0010c0014t0003g0150a0012c0012t0003g0149 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.333+404G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486539 | ||||||
chr17:18486554
|
C | T | 3 | a0005c0005t0001g0041a0005c0005t0001g0042a0005c0005t0001g0078 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.333+419C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486554 | ||||||
chr17:18486645
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+510T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486645 | ||||||
chr17:18486651
|
A | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+516A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486651 | ||||||
chr17:18486705
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0072 | 5 | HG00558.hp2 HG00597.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+570A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486705 | ||||||
chr17:18486734
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.333+599A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486734 | ||||||
chr17:18486747
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.333+612C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486747 | ||||||
chr17:18486765
|
G | T | 1 | a0001c0001t0001g0096 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.333+630G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486765 | ||||||
chr17:18486778
|
G | A | 1 | a0005c0005t0001g0041 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.333+643G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486778 | ||||||
chr17:18486807
|
A | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+672A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486807 | ||||||
chr17:18486839
|
A | G | 3 | a0002c0002t0002g0054a0010c0014t0003g0150a0012c0012t0003g0149 | 3 | HG02572.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.333+704A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486839 | ||||||
chr17:18486857
|
C | A | 1 | a0002c0002t0002g0021 | 2 | NA18953.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.333+722C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486857 | ||||||
chr17:18486857
|
C | T | 6 | a0002c0002t0002g0053a0004c0004t0001g0084a0004c0004t0001g0127others(3): Show | 6 | HG00741.hp1 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+722C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486857 | ||||||
chr17:18486858
|
G | A | 4 | a0002c0002t0002g0055a0005c0005t0001g0041a0005c0005t0001g0042others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+723G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486858 | ||||||
chr17:18486887
|
G | A | 5 | a0002c0002t0002g0013a0005c0005t0001g0041a0005c0005t0001g0042others(2): Show | 7 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.333+752G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486887 | ||||||
chr17:18486887
|
G | C | 7 | a0002c0002t0002g0054a0004c0004t0001g0084a0004c0004t0001g0127others(4): Show | 7 | HG00741.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+752G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486887 | ||||||
chr17:18486953
|
T | C | 24 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(21): Show | 51 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.334-694T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486953 | ||||||
chr17:18486970
|
T | C | 46 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0074others(43): Show | 91 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.334-677T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18486970 | ||||||
chr17:18487007
|
C | A | 1 | a0010c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.334-640C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487007 | ||||||
chr17:18487019
|
C | A | 31 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(28): Show | 74 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.334-628C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487019 | ||||||
chr17:18487023
|
G | T | 16 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(13): Show | 41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.334-624G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487023 | ||||||
chr17:18487100
|
G | A | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-547G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487100 | ||||||
chr17:18487108
|
G | C | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(29): Show | 73 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.334-539G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487108 | ||||||
chr17:18487145
|
A | G | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.334-502A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487145 | ||||||
chr17:18487211
|
C | T | 16 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(13): Show | 41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.334-436C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487211 | ||||||
chr17:18487292
|
CA | C | 29 | a0001c0001t0001g0018a0001c0001t0001g0032a0001c0001t0001g0046others(26): Show | 45 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.334-338delA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 18487292 | |||||
chr17:18487292
|
CAA | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0095a0003c0003t0001g0011others(2): Show | 12 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-339_334-338del others(2): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 18487292 | |||||
chr17:18487319
|
A | AAAAT | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-325_334-322dup others(4): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 18487319 | |||||
chr17:18487435
|
A | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-212A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487435 | ||||||
chr17:18487463
|
C | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.334-184C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487463 | ||||||
chr17:18487488
|
G | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-159G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487488 | ||||||
chr17:18487500
|
C | T | 1 | a0002c0002t0002g0054 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.334-147C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487500 | ||||||
chr17:18487509
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334-138C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487509 | ||||||
chr17:18487527
|
G | A | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-120G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487527 | ||||||
chr17:18487563
|
T | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-84T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487563 | ||||||
chr17:18487614
|
A | G | 33 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0014others(30): Show | 74 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.334-33A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487614 | ||||||
chr17:18487616
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0025others(26): Show | 56 | HG00609.hp2 HG00673.hp2 HG01106.hp2 others(53): Show |
intron_variant | MODIFIER | c.334-31C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487616 | ||||||
chr17:18487621
|
C | T | 4 | a0005c0005t0001g0041a0005c0005t0001g0042a0005c0005t0001g0078others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-26C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487621 | ||||||
chr17:18487630
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.334-17G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 3/10 | chr17 | 18487630 | ||||||
chr17:18487771
|
C | T | 1 | a0010c0013t0005g0045 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.444+14C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18487771 | ||||||
chr17:18487801
|
GGGCCCAG others(14): Show |
G | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+53_444+73delGT others(19): Show |
LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 18487801 | |||||
chr17:18487830
|
C | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+73C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18487830 | ||||||
chr17:18487993
|
G | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.444+236G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18487993 | ||||||
chr17:18488011
|
G | A | 1 | a0002c0002t0002g0053 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.444+254G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488011 | ||||||
chr17:18488160
|
T | C | 14 | a0001c0001t0001g0120a0001c0001t0002g0022a0001c0001t0002g0151others(11): Show | 15 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+403T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488160 | ||||||
chr17:18488193
|
C | G | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+436C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488193 | ||||||
chr17:18488239
|
G | T | 1 | a0001c0011t0002g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.444+482G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488239 | ||||||
chr17:18488435
|
T | A | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.445-506T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488435 | ||||||
chr17:18488493
|
C | A | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-448C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488493 | ||||||
chr17:18488494
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-447T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488494 | ||||||
chr17:18488495
|
A | T | 1 | a0001c0001t0001g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.445-446A>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488495 | ||||||
chr17:18488502
|
G | A | 1 | a0002c0002t0002g0013 | 3 | HG02630.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.445-439G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488502 | ||||||
chr17:18488517
|
C | T | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0014others(29): Show | 73 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.445-424C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488517 | ||||||
chr17:18488614
|
A | G | 38 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(35): Show | 81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.445-327A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488614 | ||||||
chr17:18488615
|
A | G | 18 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(15): Show | 45 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.445-326A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488615 | ||||||
chr17:18488631
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.445-310T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488631 | ||||||
chr17:18488680
|
T | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0032a0001c0001t0001g0051others(4): Show | 13 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.445-261T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488680 | ||||||
chr17:18488756
|
A | G | 1 | a0002c0002t0002g0058 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.445-185A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488756 | ||||||
chr17:18488790
|
C | T | 1 | a0001c0001t0001g0100 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.445-151C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488790 | ||||||
chr17:18488796
|
G | T | 1 | a0002c0002t0002g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.445-145G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488796 | ||||||
chr17:18488800
|
C | T | 27 | a0001c0001t0001g0068a0001c0001t0001g0113a0001c0001t0001g0115others(24): Show | 54 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.445-141C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 4/10 | chr17 | 18488800 | ||||||
chr17:18489049
|
C | A | 16 | a0002c0002t0002g0002a0002c0002t0002g0014a0002c0002t0002g0019others(13): Show | 41 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.540+13C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489049 | ||||||
chr17:18489063
|
G | A | 29 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0014others(26): Show | 68 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.540+27G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489063 | ||||||
chr17:18489106
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.540+70C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489106 | ||||||
chr17:18489224
|
A | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+188A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489224 | ||||||
chr17:18489226
|
C | G | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+190C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489226 | ||||||
chr17:18489228
|
T | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+192T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489228 | ||||||
chr17:18489339
|
C | CA | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+304dupA | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 18489339 | |||||
chr17:18489349
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.540+313C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489349 | ||||||
chr17:18489358
|
A | G | 2 | a0003c0003t0001g0011a0003c0003t0001g0043 | 4 | HG02109.hp2 HG02970.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+322A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489358 | ||||||
chr17:18489429
|
T | C | 44 | a0001c0001t0001g0140a0001c0011t0002g0087a0002c0002t0002g0002others(41): Show | 87 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.540+393T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489429 | ||||||
chr17:18489509
|
A | C | 37 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(34): Show | 80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.540+473A>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489509 | ||||||
chr17:18489512
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.540+476C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489512 | ||||||
chr17:18489577
|
T | C | 1 | a0001c0011t0002g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.540+541T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489577 | ||||||
chr17:18489618
|
T | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+582T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489618 | ||||||
chr17:18489619
|
C | G | 3 | a0002c0002t0002g0013a0002c0002t0002g0053a0002c0002t0002g0054 | 5 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+583C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489619 | ||||||
chr17:18489661
|
G | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.540+625G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489661 | ||||||
chr17:18489683
|
C | T | 1 | a0002c0002t0002g0013 | 3 | HG02630.hp1 HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.540+647C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489683 | ||||||
chr17:18489729
|
A | G | 1 | a0002c0002t0002g0123 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.540+693A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489729 | ||||||
chr17:18489763
|
T | C | 1 | a0001c0001t0001g0141 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.540+727T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18489763 | ||||||
chr17:18489875
|
CT | C | 45 | a0001c0011t0002g0087a0002c0002t0002g0002a0002c0002t0002g0005others(42): Show | 88 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.540+841delT | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 18489875 | |||||
chr17:18490142
|
C | T | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.541-591C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490142 | ||||||
chr17:18490216
|
A | G | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-517A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490216 | ||||||
chr17:18490290
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.541-443C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490290 | ||||||
chr17:18490370
|
C | T | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-363C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490370 | ||||||
chr17:18490379
|
A | G | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.541-354A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490379 | ||||||
chr17:18490382
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0085 | 2 | HG02027.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.541-351G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490382 | ||||||
chr17:18490398
|
C | T | 3 | a0002c0002t0002g0013a0002c0002t0002g0053a0002c0002t0002g0054 | 5 | HG02630.hp1 HG03195.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.541-335C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490398 | ||||||
chr17:18490430
|
G | A | 3 | a0005c0005t0001g0041a0005c0005t0001g0042a0005c0005t0001g0078 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.541-303G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490430 | ||||||
chr17:18490566
|
A | G | 42 | a0001c0001t0001g0033a0001c0001t0001g0079a0001c0001t0001g0098others(39): Show | 86 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.541-167A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490566 | ||||||
chr17:18490695
|
C | T | 1 | a0002c0002t0002g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.541-38C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490695 | ||||||
chr17:18490696
|
G | A | 6 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(3): Show | 6 | HG00741.hp1 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-37G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 5/10 | chr17 | 18490696 | ||||||
chr17:18490787
|
T | C | 1 | a0002c0002t0002g0059 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.576+19T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18490787 | ||||||
chr17:18490893
|
G | A | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+125G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18490893 | ||||||
chr17:18490943
|
C | T | 2 | a0001c0001t0001g0031a0013c0010t0001g0031 | 2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.576+175C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18490943 | ||||||
chr17:18491011
|
C | T | 1 | a0001c0011t0002g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.576+243C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491011 | ||||||
chr17:18491042
|
C | T | 1 | a0012c0012t0003g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.577-231C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491042 | ||||||
chr17:18491087
|
T | C | 2 | a0001c0001t0001g0097a0001c0001t0001g0104 | 2 | NA18973.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.577-186T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491087 | ||||||
chr17:18491104
|
C | T | 38 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(35): Show | 81 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.577-169C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491104 | ||||||
chr17:18491117
|
T | C | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.577-156T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491117 | ||||||
chr17:18491125
|
G | A | 3 | a0005c0005t0001g0041a0005c0005t0001g0042a0005c0005t0001g0078 | 3 | HG01891.hp1 HG02257.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.577-148G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491125 | ||||||
chr17:18491143
|
C | T | 1 | a0001c0001t0001g0032 | 2 | NA18985.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.577-130C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491143 | ||||||
chr17:18491249
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.577-24T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491249 | ||||||
chr17:18491270
|
C | T | 1 | a0001c0001t0001g0038 | 2 | HG03491.hp1 HG03492.hp2 |
splice_region_variant&intron_variant | LOW | c.577-3C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 6/10 | chr17 | 18491270 | ||||||
chr17:18491416
|
C | T | 2 | a0001c0001t0001g0023a0001c0001t0001g0070 | 3 | HG02055.hp1 HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.627+93C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491416 | ||||||
chr17:18491600
|
A | G | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.627+277A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491600 | ||||||
chr17:18491704
|
T | A | 1 | a0001c0001t0001g0012 | 3 | HG00140.hp2 HG00323.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.628-241T>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491704 | ||||||
chr17:18491713
|
T | C | 1 | a0002c0002t0002g0035 | 2 | NA19054.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.628-232T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491713 | ||||||
chr17:18491759
|
T | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0148 | 3 | HG00408.hp1 HG02155.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.628-186T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 7/10 | chr17 | 18491759 | ||||||
chr17:18492084
|
T | C | 1 | a0002c0002t0002g0060 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.672+95T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492084 | ||||||
chr17:18492131
|
G | A | 4 | a0005c0005t0001g0041a0005c0005t0001g0042a0005c0005t0001g0078others(1): Show | 4 | HG01891.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+142G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492131 | ||||||
chr17:18492333
|
G | T | 37 | a0001c0001t0001g0052a0002c0002t0002g0002a0002c0002t0002g0005others(34): Show | 80 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.673-124G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492333 | ||||||
chr17:18492382
|
C | A | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-75C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492382 | ||||||
chr17:18492420
|
A | G | 4 | a0004c0004t0001g0084a0004c0004t0001g0127a0004c0004t0001g0128others(1): Show | 4 | HG00741.hp1 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-37A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 8/10 | chr17 | 18492420 | ||||||
chr17:18492630
|
G | C | 33 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(30): Show | 76 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.762-67G>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 9/10 | chr17 | 18492630 | ||||||
chr17:18492678
|
G | A | 23 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0014others(20): Show | 52 | HG00099.hp1 HG00639.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.762-19G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 9/10 | chr17 | 18492678 | ||||||
chr17:18492693
|
C | G | 1 | a0001c0015t0001g0142 | 1 | HG01106.hp1 | splice_region_variant&intron_variant | LOW | c.762-4C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 9/10 | chr17 | 18492693 | ||||||
chr17:18492905
|
C | CAG | 17 | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0015t0001g0142others(14): Show | 30 | HG00099.hp2 HG01106.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.924+46_924+47insAG | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492905 | ||||||
chr17:18492932
|
T | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0017others(40): Show | 85 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.924+73T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492932 | ||||||
chr17:18492949
|
G | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0134a0001c0001t0001g0140others(5): Show | 25 | HG00408.hp2 HG01975.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.924+90G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492949 | ||||||
chr17:18492997
|
A | G | 31 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(28): Show | 72 | HG00099.hp2 HG00673.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+138A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18492997 | ||||||
chr17:18493011
|
T | C | 31 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(28): Show | 72 | HG00099.hp2 HG00673.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+152T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493011 | ||||||
chr17:18493020
|
T | G | 31 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(28): Show | 72 | HG00099.hp2 HG00673.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+161T>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493020 | ||||||
chr17:18493078
|
A | G | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(29): Show | 75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.924+219A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493078 | ||||||
chr17:18493097
|
T | C | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(29): Show | 75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.924+238T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493097 | ||||||
chr17:18493104
|
C | T | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(29): Show | 75 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.924+245C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493104 | ||||||
chr17:18493176
|
A | G | 12 | a0002c0002t0002g0005a0002c0002t0002g0020a0002c0002t0002g0035others(9): Show | 26 | HG00099.hp2 HG01109.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.924+317A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493176 | ||||||
chr17:18493218
|
A | G | 35 | a0001c0001t0001g0099a0002c0002t0002g0002a0002c0002t0002g0005others(32): Show | 76 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.924+359A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493218 | ||||||
chr17:18493247
|
C | G | 31 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0014others(28): Show | 72 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.924+388C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493247 | ||||||
chr17:18493248
|
G | A | 40 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(37): Show | 83 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.924+389G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493248 | ||||||
chr17:18493260
|
C | A | 1 | a0010c0014t0003g0150 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924+401C>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493260 | ||||||
chr17:18493415
|
T | C | 43 | a0001c0001t0001g0023a0001c0001t0001g0070a0001c0001t0001g0071others(40): Show | 87 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.924+556T>C | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493415 | ||||||
chr17:18493431
|
A | G | 33 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(30): Show | 76 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.924+572A>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493431 | ||||||
chr17:18493454
|
G | A | 1 | a0002c0002t0002g0062 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.924+595G>A | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493454 | ||||||
chr17:18493547
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.925-674C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493547 | ||||||
chr17:18493809
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0146 | 3 | HG01109.hp2 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.925-412C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18493809 | ||||||
chr17:18494014
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.925-207C>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18494014 | ||||||
chr17:18494032
|
C | G | 34 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0013others(31): Show | 77 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.925-189C>G | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18494032 | ||||||
chr17:18494118
|
G | T | 1 | a0002c0002t0002g0055 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.925-103G>T | LGALS9C | ENSG00000171916.17 | transcript | ENST00000328114.11 | protein_coding | 10/10 | chr17 | 18494118 |