geneid | 51320 |
---|---|
ensemblid | ENSG00000176624.12 |
hgncid | 28040 |
symbol | MEX3C |
name | mex-3 RNA binding family member C |
refseq_nuc | NM_016626.5 |
refseq_prot | NP_057710.3 |
ensembl_nuc | ENST00000406189.4 |
ensembl_prot | ENSP00000385610.3 |
mane_status | MANE Select |
chr | chr18 |
start | 51174550 |
end | 51197681 |
strand | - |
ver | v1.2 |
region | chr18:51174550-51197681 |
region5000 | chr18:51169550-51202681 |
regionname0 | MEX3C_chr18_51174550_51197681 |
regionname5000 | MEX3C_chr18_51169550_51202681 |
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 | 659 | 253 | 58 | 47 | 119 | 9 | 19 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002 | 0/1 | 656 | 95 | 14 | 13 | 48 | 7 | 12 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0003 | 0/0 | 661 | 13 | 0 | 0 | 12 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0004 | 0/0 | 659 | 9 | 9 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0005 | 0/0 | 659 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0006 | 0/0 | 659 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0007 | 0/0 | 659 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0008 | 0/0 | 656 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0009 | 0/0 | 656 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0010 | 0/0 | 659 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | 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 | 0/0 | 1980 | 228 | 41 | 44 | 115 | 9 | 19 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0002 | 0/1 | 1971 | 92 | 14 | 13 | 47 | 7 | 10 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0003 | 1/0 | 1980 | 16 | 15 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0004 | 0/0 | 1986 | 13 | 0 | 0 | 12 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0005 | 0/0 | 1980 | 8 | 8 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0006 | 0/0 | 1980 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0007 | 0/0 | 1980 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0008 | 0/0 | 1971 | 2 | 0 | 0 | 0 | 0 | 2 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0009 | 0/0 | 1980 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0010 | 0/0 | 1980 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0011 | 0/0 | 1980 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0012 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0013 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0014 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0015 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0016 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0017 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0018 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0019 | 0/0 | 1980 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
c0020 | 0/0 | 1980 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | 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 | 2163 | 351 | 71 | 57 | 176 | 16 | 30 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0002 | 0/0 | 2163 | 6 | 3 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0003 | 0/0 | 2163 | 3 | 2 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0004 | 0/0 | 2166 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0005 | 0/0 | 2163 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0006 | 0/0 | 2163 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0007 | 0/0 | 2163 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0008 | 0/0 | 2166 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0009 | 0/0 | 2163 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0010 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0011 | 0/0 | 2163 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0012 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0013 | 0/1 | 2163 | 1 | 0 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0014 | 0/0 | 2163 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
t0015 | 0/0 | 2163 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | 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 | 38 | 1 | 8 | 21 | 1 | 7 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0002 | 0/0 | 37 | 6 | 12 | 13 | 3 | 3 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0003 | 0/0 | 31 | 3 | 6 | 13 | 3 | 6 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0004 | 0/0 | 17 | 3 | 3 | 8 | 1 | 2 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0005 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0012 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
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 | 0/0 | 228 | 41 | 44 | 115 | 9 | 19 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0003 | a0001 | c0003 | 1/0 | 16 | 15 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0007 | a0001 | c0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0011 | a0001 | c0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0014 | a0001 | c0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0015 | a0001 | c0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0020 | a0001 | c0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0002 | a0002 | c0002 | 0/1 | 92 | 14 | 13 | 47 | 7 | 10 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0008 | a0002 | c0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0017 | a0002 | c0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0003c0004 | a0003 | c0004 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0004c0005 | a0004 | c0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0004c0018 | a0004 | c0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0005c0010 | a0005 | c0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0006c0019 | a0006 | c0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0007c0016 | a0007 | c0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0008c0012 | a0008 | c0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0009c0013 | a0009 | c0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0010c0009 | a0010 | c0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | 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 | 0/0 | 209 | 30 | 41 | 111 | 9 | 18 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 6 | 3 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0003t0001 | a0001 | c0003 | t0001 | 1/0 | 15 | 14 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0003t0015 | a0001 | c0003 | t0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0007t0005 | a0001 | c0007 | t0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0011t0001 | a0001 | c0011 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0014t0008 | a0001 | c0014 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0015t0001 | a0001 | c0015 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0001c0020t0001 | a0001 | c0020 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 91 | 14 | 13 | 47 | 7 | 10 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0002t0013 | a0002 | c0002 | t0013 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0008t0001 | a0002 | c0008 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0008t0014 | a0002 | c0008 | t0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0002c0017t0001 | a0002 | c0017 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0003c0004t0001 | a0003 | c0004 | t0001 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0004c0005t0001 | a0004 | c0005 | t0001 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0004c0018t0001 | a0004 | c0018 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0005c0010t0001 | a0005 | c0010 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0006c0019t0001 | a0006 | c0019 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0007c0016t0001 | a0007 | c0016 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0008c0012t0001 | a0008 | c0012 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0009c0013t0001 | a0009 | c0013 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | copy fasta |
a0010c0009t0001 | a0010 | c0009 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C | 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 | 38 | 1 | 8 | 21 | 1 | 7 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 37 | 6 | 12 | 13 | 3 | 3 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 17 | 3 | 3 | 8 | 1 | 2 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0104 | a0001 | c0001 | t0001 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0002g0021 | a0001 | c0001 | t0002 | g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0002g0134 | a0001 | c0001 | t0002 | g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0003g0040 | a0001 | c0001 | t0003 | g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0003g0125 | a0001 | c0001 | t0003 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0004g0026 | a0001 | c0001 | t0004 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0006g0031 | a0001 | c0001 | t0006 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0007g0033 | a0001 | c0001 | t0007 | g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0009g0115 | a0001 | c0001 | t0009 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0010g0116 | a0001 | c0001 | t0010 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0011g0135 | a0001 | c0001 | t0011 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0001t0012g0092 | a0001 | c0001 | t0012 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0024 | a0001 | c0003 | t0001 | g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0025 | a0001 | c0003 | t0001 | g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0045 | a0001 | c0003 | t0001 | g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0046 | a0001 | c0003 | t0001 | g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0047 | a0001 | c0003 | t0001 | g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0140 | a0001 | c0003 | t0001 | g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0141 | a0001 | c0003 | t0001 | g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0001g0142 | a0001 | c0003 | t0001 | g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0003t0015g0143 | a0001 | c0003 | t0015 | g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0006t0001g0048 | a0001 | c0006 | t0001 | g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0006t0001g0151 | a0001 | c0006 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0007t0005g0050 | a0001 | c0007 | t0005 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0007t0005g0051 | a0001 | c0007 | t0005 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0011t0001g0054 | a0001 | c0011 | t0001 | g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0014t0008g0049 | a0001 | c0014 | t0008 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0015t0001g0105 | a0001 | c0015 | t0001 | g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0001c0020t0001g0152 | a0001 | c0020 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0003 | a0002 | c0002 | t0001 | g0003 | 0/0 | 31 | 3 | 6 | 13 | 3 | 6 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0006 | a0002 | c0002 | t0001 | g0006 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0009 | a0002 | c0002 | t0001 | g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0010 | a0002 | c0002 | t0001 | g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0013 | a0002 | c0002 | t0001 | g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0018 | a0002 | c0002 | t0001 | g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0019 | a0002 | c0002 | t0001 | g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0020 | a0002 | c0002 | t0001 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0027 | a0002 | c0002 | t0001 | g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0028 | a0002 | c0002 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0029 | a0002 | c0002 | t0001 | g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0030 | a0002 | c0002 | t0001 | g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0055 | a0002 | c0002 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0056 | a0002 | c0002 | t0001 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0057 | a0002 | c0002 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0058 | a0002 | c0002 | t0001 | g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0059 | a0002 | c0002 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0060 | a0002 | c0002 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0061 | a0002 | c0002 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0062 | a0002 | c0002 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0063 | a0002 | c0002 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0068 | a0002 | c0002 | t0001 | g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0069 | a0002 | c0002 | t0001 | g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0070 | a0002 | c0002 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0071 | a0002 | c0002 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0073 | a0002 | c0002 | t0001 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0074 | a0002 | c0002 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0075 | a0002 | c0002 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0076 | a0002 | c0002 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0077 | a0002 | c0002 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0001g0078 | a0002 | c0002 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0002t0013g0065 | a0002 | c0002 | t0013 | g0065 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0008t0001g0066 | a0002 | c0008 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0008t0014g0067 | a0002 | c0008 | t0014 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0002c0017t0001g0139 | a0002 | c0017 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0003c0004t0001g0005 | a0003 | c0004 | t0001 | g0005 | 0/0 | 11 | 0 | 0 | 10 | 0 | 1 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0003c0004t0001g0148 | a0003 | c0004 | t0001 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0003c0004t0001g0149 | a0003 | c0004 | t0001 | g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0004c0005t0001g0015 | a0004 | c0005 | t0001 | g0015 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0004c0005t0001g0144 | a0004 | c0005 | t0001 | g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0004c0005t0001g0145 | a0004 | c0005 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0004c0005t0001g0146 | a0004 | c0005 | t0001 | g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0004c0018t0001g0147 | a0004 | c0018 | t0001 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0005c0010t0001g0053 | a0005 | c0010 | t0001 | g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0006c0019t0001g0150 | a0006 | c0019 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0007c0016t0001g0117 | a0007 | c0016 | t0001 | g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0008c0012t0001g0064 | a0008 | c0012 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0009c0013t0001g0072 | a0009 | c0013 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
a0010c0009t0001g0052 | a0010 | c0009 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEX3C_chr18_51169550_51202681 | MEX3C |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | GBR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0071 | EUR | FIN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | FIN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | FIN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00408 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00597 | hp2 | a0002 | c0017 | t0001 | g0139 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00639 | hp2 | a0010 | c0009 | t0001 | g0052 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0073 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01168 | hp1 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0033 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01192 | hp2 | a0001 | c0011 | t0001 | g0054 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01255 | hp1 | a0005 | c0010 | t0001 | g0053 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0063 | EUR | IBS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0060 | EUR | IBS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01884 | hp2 | a0009 | c0013 | t0001 | g0072 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01891 | hp2 | a0001 | c0003 | t0015 | g0143 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01978 | hp2 | a0001 | c0007 | t0005 | g0050 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0069 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02027 | hp2 | a0001 | c0006 | t0001 | g0048 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02129 | hp2 | a0003 | c0004 | t0001 | g0005 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | CDX | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | CDX | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02280 | hp1 | a0007 | c0016 | t0001 | g0117 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02523 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02622 | hp1 | a0001 | c0014 | t0008 | g0049 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02717 | hp1 | a0004 | c0005 | t0001 | g0015 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02818 | hp2 | a0001 | c0001 | t0012 | g0092 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02896 | hp1 | a0004 | c0005 | t0001 | g0145 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02965 | hp1 | a0001 | c0001 | t0010 | g0116 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02965 | hp2 | a0006 | c0019 | t0001 | g0150 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03017 | hp1 | a0002 | c0008 | t0014 | g0067 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03017 | hp2 | a0001 | c0001 | t0011 | g0135 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03098 | hp1 | a0004 | c0005 | t0001 | g0015 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03209 | hp2 | a0004 | c0005 | t0001 | g0015 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | GWD | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0025 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | MSL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03669 | hp2 | a0002 | c0008 | t0001 | g0066 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03834 | hp1 | a0003 | c0004 | t0001 | g0005 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MEX3C_chr18_51169550_51202681 | MEX3C |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0057 | SAS | STU | MEX3C_chr18_51169550_51202681 | MEX3C |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | MEX3C_chr18_51169550_51202681 | MEX3C |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | STU | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | YRI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18522 | hp2 | a0004 | c0005 | t0001 | g0015 | AFR | YRI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | CHB | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHB | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18747 | hp2 | a0003 | c0004 | t0001 | g0005 | EAS | CHB | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | YRI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18941 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18941 | hp2 | a0001 | c0020 | t0001 | g0152 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18942 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18966 | hp2 | a0001 | c0006 | t0001 | g0048 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18971 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18972 | hp1 | a0003 | c0004 | t0001 | g0148 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18976 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18976 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18980 | hp1 | a0001 | c0001 | t0009 | g0115 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18982 | hp2 | a0003 | c0004 | t0001 | g0149 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18983 | hp2 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18997 | hp1 | a0008 | c0012 | t0001 | g0064 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19005 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19007 | hp2 | a0001 | c0006 | t0001 | g0151 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19010 | hp2 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19030 | hp1 | a0004 | c0005 | t0001 | g0146 | AFR | LWK | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19030 | hp2 | a0004 | c0005 | t0001 | g0015 | AFR | LWK | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0031 | AFR | LWK | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | LWK | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19059 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19080 | hp1 | a0003 | c0004 | t0001 | g0005 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | YRI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20129 | hp1 | a0004 | c0005 | t0001 | g0144 | AFR | ASW | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ASW | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | TSI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | GIH | MEX3C_chr18_51169550_51202681 | MEX3C |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | GIH | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01123 | hp1 | a0001 | c0007 | t0005 | g0051 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02486 | hp1 | a0004 | c0018 | t0001 | g0147 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | MEX3C_chr18_51169550_51202681 | MEX3C |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | USA | MEX3C_chr18_51169550_51202681 | MEX3C |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0046 | AFR | USA | MEX3C_chr18_51169550_51202681 | MEX3C |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MEX3C_chr18_51169550_51202681 | MEX3C |
NA21309 | hp2 | a0001 | c0015 | t0001 | g0105 | AFR | LWK | MEX3C_chr18_51169550_51202681 | MEX3C |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0013 | g0065 | REF | REF | MEX3C_chr18_51169550_51202681 | MEX3C |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0141 | REF | REF | MEX3C_chr18_51169550_51202681 | MEX3C |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51176535
|
G | T | 1 | a0008 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.1796C>A | p.Pro599His | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 2157/4142 | 1796/1980 | 599/659 | chr18 | 51176535 | ||
chr18:51176710
|
T | G | 1 | a0007 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.1621A>C | p.Thr541Pro | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1982/4142 | 1621/1980 | 541/659 | chr18 | 51176710 | ||
chr18:51176845
|
A | C | 1 | a0006 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1486T>G | p.Ser496Ala | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1847/4142 | 1486/1980 | 496/659 | chr18 | 51176845 | ||
chr18:51177166
|
T | C | 1 | a0009 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1165A>G | p.Met389Val | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1526/4142 | 1165/1980 | 389/659 | chr18 | 51177166 | ||
chr18:51196775
|
CGCCGCCG others(2): Show |
C | 3 | a0002a0008a0009 | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
disruptive_inframe_deletion | MODERATE | c.537_545delCGCGGCGG others(1): Show |
p.Ala180_Ala182del | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 906/4142 | 537/1980 | 179/659 | chr18 | 51196775 | ||
chr18:51196872
|
G | C | 1 | a0004 | 9 | HG02486.hp1 HG02717.hp1 HG02896.hp1 others(6): Show |
missense_variant | MODERATE | c.449C>G | p.Thr150Ser | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 810/4142 | 449/1980 | 150/659 | chr18 | 51196872 | ||
chr18:51197073
|
C | G | 1 | a0005 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.248G>C | p.Arg83Pro | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 609/4142 | 248/1980 | 83/659 | chr18 | 51197073 | ||
chr18:51197099
|
T | TGCCGGG | 1 | a0003 | 13 | HG00408.hp1 HG02129.hp2 HG02523.hp1 others(10): Show |
disruptive_inframe_insertion | MODERATE | c.216_221dupCCCGGC | p.Ala74_Ala75insProA others(2): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 582/4142 | 221/1980 | 74/659 | chr18 | 51197099 | ||
chr18:51197122
|
C | T | 1 | a0010 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.199G>A | p.Ala67Thr | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 560/4142 | 199/1980 | 67/659 | chr18 | 51197122 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51176396
|
T | C | 1 | a0001c0015 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1935A>G | p.Pro645Pro | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 2296/4142 | 1935/1980 | 645/659 | chr18 | 51176396 | ||
chr18:51176444
|
G | A | 1 | a0002c0008 | 2 | HG03017.hp1 HG03669.hp2 |
synonymous_variant | LOW | c.1887C>T | p.Cys629Cys | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 2248/4142 | 1887/1980 | 629/659 | chr18 | 51176444 | ||
chr18:51177308
|
C | T | 1 | a0001c0014 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.1023G>A | p.Val341Val | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1384/4142 | 1023/1980 | 341/659 | chr18 | 51177308 | ||
chr18:51196697
|
G | A | 1 | a0001c0007 | 2 | HG01123.hp1 HG01978.hp2 |
synonymous_variant | LOW | c.624C>T | p.Gly208Gly | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 985/4142 | 624/1980 | 208/659 | chr18 | 51196697 | ||
chr18:51196784
|
G | C | 1 | a0001c0011 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.537C>G | p.Ala179Ala | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 898/4142 | 537/1980 | 179/659 | chr18 | 51196784 | ||
chr18:51196847
|
C | T | 19 | a0001c0001a0001c0006a0001c0007others(16): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
synonymous_variant | LOW | c.474G>A | p.Pro158Pro | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 835/4142 | 474/1980 | 158/659 | chr18 | 51196847 | ||
chr18:51197033
|
G | A | 1 | a0004c0018 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.288C>T | p.Gly96Gly | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 649/4142 | 288/1980 | 96/659 | chr18 | 51197033 | ||
chr18:51197069
|
C | T | 5 | a0001c0011a0002c0002a0002c0008others(2): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
synonymous_variant | LOW | c.252G>A | p.Ala84Ala | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 613/4142 | 252/1980 | 84/659 | chr18 | 51197069 | ||
chr18:51197147
|
G | A | 1 | a0006c0019 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.174C>T | p.Asp58Asp | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 535/4142 | 174/1980 | 58/659 | chr18 | 51197147 | ||
chr18:51197216
|
G | T | 1 | a0001c0007 | 2 | HG01123.hp1 HG01978.hp2 |
synonymous_variant | LOW | c.105C>A | p.Pro35Pro | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 466/4142 | 105/1980 | 35/659 | chr18 | 51197216 | ||
chr18:51197234
|
C | A | 1 | a0001c0006 | 3 | HG02027.hp2 NA18966.hp2 NA19007.hp2 |
synonymous_variant | LOW | c.87G>T | p.Pro29Pro | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 448/4142 | 87/1980 | 29/659 | chr18 | 51197234 | ||
chr18:51197291
|
G | A | 1 | a0001c0020 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.30C>T | p.Ala10Ala | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 391/4142 | 30/1980 | 10/659 | chr18 | 51197291 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51174755
|
G | C | 1 | a0001c0001t0012 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1596C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1596 | chr18 | 51174755 | |||||
chr18:51174849
|
C | T | 1 | a0001c0001t0011 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1502 | chr18 | 51174849 | |||||
chr18:51174855
|
C | G | 1 | a0001c0001t0010 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1496G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1496 | chr18 | 51174855 | |||||
chr18:51175287
|
T | C | 1 | a0002c0002t0013 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1064A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 1064 | chr18 | 51175287 | |||||
chr18:51175412
|
G | A | 1 | a0001c0001t0003 | 3 | HG01192.hp1 HG02622.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*939C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 939 | chr18 | 51175412 | |||||
chr18:51175554
|
C | A | 1 | a0001c0001t0006 | 2 | HG03225.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*797G>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 797 | chr18 | 51175554 | |||||
chr18:51175688
|
T | C | 1 | a0001c0003t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*663A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 663 | chr18 | 51175688 | |||||
chr18:51175721
|
G | A | 1 | a0001c0001t0007 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*630C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 630 | chr18 | 51175721 | |||||
chr18:51175733
|
C | G | 1 | a0001c0001t0009 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*618G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 618 | chr18 | 51175733 | |||||
chr18:51175806
|
T | A | 1 | a0002c0008t0014 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*545A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 545 | chr18 | 51175806 | |||||
chr18:51176160
|
T | C | 1 | a0001c0001t0002 | 6 | HG02559.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*191A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 191 | chr18 | 51176160 | |||||
chr18:51176329
|
G | A | 1 | a0001c0003t0015 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 2/2 | 22 | chr18 | 51176329 | |||||
chr18:51197453
|
G | A | 1 | a0001c0001t0004 | 2 | HG02895.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-133C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 133 | chr18 | 51197453 | |||||
chr18:51197463
|
C | G | 1 | a0001c0007t0005 | 2 | HG01123.hp1 HG01978.hp2 |
5_prime_UTR_variant | MODIFIER | c.-143G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 143 | chr18 | 51197463 | |||||
chr18:51197643
|
C | CGCG | 2 | a0001c0001t0004a0001c0014t0008 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp1 |
5_prime_UTR_variant | MODIFIER | c.-326_-324dupCGC | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/2 | 324 | chr18 | 51197643 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:51177778
|
T | A | 1 | a0008c0012t0001g0064 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.755-202A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51177778 | ||||||
chr18:51177780
|
G | A | 1 | a0002c0002t0001g0028 | 2 | NA18968.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.755-204C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51177780 | ||||||
chr18:51177813
|
C | T | 1 | a0004c0005t0001g0144 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.755-237G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51177813 | ||||||
chr18:51177839
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.755-263G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51177839 | ||||||
chr18:51177894
|
G | A | 1 | a0002c0002t0001g0068 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.755-318C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51177894 | ||||||
chr18:51178012
|
T | A | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-436A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178012 | ||||||
chr18:51178089
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(28): Show | 64 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.755-513G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178089 | ||||||
chr18:51178151
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.755-575A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178151 | ||||||
chr18:51178159
|
T | C | 1 | a0001c0001t0001g0022 | 3 | NA18970.hp2 NA18976.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.755-583A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178159 | ||||||
chr18:51178353
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(147): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.755-777C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178353 | ||||||
chr18:51178374
|
C | CT | 12 | a0001c0001t0001g0037a0001c0001t0001g0081a0001c0001t0001g0086others(9): Show | 13 | HG01106.hp2 HG01123.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.755-799dupA | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178374 | ||||||
chr18:51178374
|
CT | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0082a0001c0001t0001g0113others(5): Show | 12 | HG01169.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.755-799delA | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178374 | ||||||
chr18:51178379
|
T | G | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.755-803A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178379 | ||||||
chr18:51178435
|
G | T | 1 | a0001c0001t0001g0128 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.755-859C>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178435 | ||||||
chr18:51178548
|
A | G | 3 | a0002c0002t0001g0010a0002c0002t0001g0062a0002c0002t0001g0076 | 8 | HG00597.hp1 NA18960.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.755-972T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178548 | ||||||
chr18:51178598
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0001g0113 | 8 | HG00140.hp1 HG00642.hp1 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.755-1022G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178598 | ||||||
chr18:51178605
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.755-1029G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178605 | ||||||
chr18:51178655
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.755-1079T>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178655 | ||||||
chr18:51178718
|
G | A | 1 | a0003c0004t0001g0149 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.755-1142C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178718 | ||||||
chr18:51178747
|
C | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(25): Show | 57 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.755-1171G>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178747 | ||||||
chr18:51178776
|
C | T | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(60): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.755-1200G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178776 | ||||||
chr18:51178789
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.755-1213C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178789 | ||||||
chr18:51178789
|
G | C | 1 | a0001c0003t0015g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.755-1213C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178789 | ||||||
chr18:51178808
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.755-1232G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178808 | ||||||
chr18:51178860
|
C | CA | 13 | a0001c0001t0001g0007a0001c0001t0001g0090a0001c0001t0001g0096others(10): Show | 30 | HG00408.hp1 HG01517.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.755-1285dupT | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178860 | ||||||
chr18:51178860
|
C | CAAA | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-1287_755-1285d others(5): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51178860 | ||||||
chr18:51179008
|
C | CT | 6 | a0001c0001t0001g0100a0001c0001t0001g0110a0002c0002t0001g0062others(3): Show | 6 | HG00438.hp2 HG01516.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.755-1433dupA | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179008 | ||||||
chr18:51179016
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(147): Show | 374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.755-1440G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179016 | ||||||
chr18:51179064
|
T | C | 1 | a0001c0003t0001g0025 | 3 | HG02647.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.755-1488A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179064 | ||||||
chr18:51179117
|
C | T | 1 | a0002c0002t0001g0075 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.755-1541G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179117 | ||||||
chr18:51179206
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.755-1630G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179206 | ||||||
chr18:51179255
|
G | A | 1 | a0002c0002t0001g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.755-1679C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179255 | ||||||
chr18:51179292
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.755-1716C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179292 | ||||||
chr18:51179300
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0091 | 2 | HG02451.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.755-1724G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179300 | ||||||
chr18:51179557
|
A | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.755-1981T>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179557 | ||||||
chr18:51179645
|
C | G | 1 | a0006c0019t0001g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.755-2069G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179645 | ||||||
chr18:51179854
|
T | C | 1 | a0002c0002t0001g0055 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.755-2278A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179854 | ||||||
chr18:51179867
|
T | G | 1 | a0001c0001t0001g0034 | 2 | HG02109.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.755-2291A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179867 | ||||||
chr18:51179896
|
T | C | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(25): Show | 57 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.755-2320A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179896 | ||||||
chr18:51179955
|
C | G | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-2379G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51179955 | ||||||
chr18:51180027
|
C | CT | 63 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(60): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.755-2452dupA | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180027 | ||||||
chr18:51180134
|
A | G | 1 | a0001c0006t0001g0151 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.755-2558T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180134 | ||||||
chr18:51180169
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(25): Show | 57 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.755-2593C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180169 | ||||||
chr18:51180262
|
G | T | 1 | a0001c0001t0006g0031 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.755-2686C>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180262 | ||||||
chr18:51180290
|
T | C | 1 | a0001c0001t0001g0039 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.755-2714A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180290 | ||||||
chr18:51180340
|
G | A | 1 | a0006c0019t0001g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.755-2764C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180340 | ||||||
chr18:51180479
|
T | A | 2 | a0001c0001t0004g0026a0001c0014t0008g0049 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.755-2903A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180479 | ||||||
chr18:51180546
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.755-2970G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180546 | ||||||
chr18:51180558
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.755-2982T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180558 | ||||||
chr18:51180729
|
C | T | 1 | a0001c0003t0001g0047 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.755-3153G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180729 | ||||||
chr18:51180753
|
G | A | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-3177C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180753 | ||||||
chr18:51180762
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.755-3186G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180762 | ||||||
chr18:51180778
|
T | C | 41 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 91 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.755-3202A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180778 | ||||||
chr18:51180935
|
G | A | 28 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(25): Show | 57 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.755-3359C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51180935 | ||||||
chr18:51181307
|
A | C | 1 | a0006c0019t0001g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.755-3731T>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181307 | ||||||
chr18:51181335
|
CAT | C | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.755-3761_755-3760d others(4): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181335 | ||||||
chr18:51181504
|
C | T | 1 | a0001c0015t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755-3928G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181504 | ||||||
chr18:51181505
|
A | C | 2 | a0001c0001t0001g0016a0001c0020t0001g0152 | 5 | HG00558.hp2 NA18941.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.755-3929T>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181505 | ||||||
chr18:51181513
|
TA | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(140): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.755-3938delT | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181513 | ||||||
chr18:51181741
|
A | G | 1 | a0002c0002t0001g0060 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.755-4165T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181741 | ||||||
chr18:51181811
|
T | A | 1 | a0001c0001t0006g0031 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.755-4235A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181811 | ||||||
chr18:51181919
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.755-4343C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51181919 | ||||||
chr18:51182093
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.755-4517G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182093 | ||||||
chr18:51182178
|
A | C | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.755-4602T>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182178 | ||||||
chr18:51182215
|
T | C | 1 | a0002c0002t0001g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.755-4639A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182215 | ||||||
chr18:51182274
|
GAAGGCAT others(13): Show |
G | 2 | a0001c0001t0001g0041a0010c0009t0001g0052 | 3 | HG00639.hp2 HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.755-4718_755-4699d others(22): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182274 | ||||||
chr18:51182308
|
G | A | 2 | a0001c0007t0005g0050a0001c0007t0005g0051 | 2 | HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.755-4732C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182308 | ||||||
chr18:51182478
|
G | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.755-4902C>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182478 | ||||||
chr18:51182598
|
C | G | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG00438.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.755-5022G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182598 | ||||||
chr18:51182734
|
C | T | 53 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(50): Show | 133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.755-5158G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182734 | ||||||
chr18:51182984
|
A | T | 1 | a0001c0003t0001g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.755-5408T>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51182984 | ||||||
chr18:51183284
|
G | T | 21 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(18): Show | 49 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.755-5708C>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51183284 | ||||||
chr18:51183343
|
T | A | 1 | a0006c0019t0001g0150 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.755-5767A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51183343 | ||||||
chr18:51183383
|
A | G | 1 | a0001c0003t0015g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.755-5807T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51183383 | ||||||
chr18:51183556
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.755-5980T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51183556 | ||||||
chr18:51183770
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.755-6194T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51183770 | ||||||
chr18:51183841
|
C | A | 4 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146others(1): Show | 8 | HG02486.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.755-6265G>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51183841 | ||||||
chr18:51184009
|
AT | A | 11 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0120others(8): Show | 28 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.755-6434delA | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184009 | ||||||
chr18:51184010
|
T | A | 2 | a0001c0001t0001g0130a0001c0003t0015g0143 | 2 | HG01891.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.755-6434A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184010 | ||||||
chr18:51184090
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.755-6514C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184090 | ||||||
chr18:51184305
|
AAC | A | 3 | a0002c0002t0001g0013a0002c0002t0001g0058a0002c0002t0001g0059 | 7 | HG00438.hp1 HG00544.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-6731_755-6730d others(4): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184305 | ||||||
chr18:51184446
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.755-6870G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184446 | ||||||
chr18:51184489
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.755-6913T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184489 | ||||||
chr18:51184641
|
G | A | 10 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 11 | HG01123.hp1 HG01978.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.755-7065C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184641 | ||||||
chr18:51184718
|
C | T | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.755-7142G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184718 | ||||||
chr18:51184739
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.755-7163A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184739 | ||||||
chr18:51184800
|
A | G | 22 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(19): Show | 54 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.755-7224T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184800 | ||||||
chr18:51184867
|
G | GA | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.755-7292dupT | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51184867 | ||||||
chr18:51185027
|
C | T | 1 | a0002c0002t0001g0019 | 3 | NA18942.hp2 NA18977.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.755-7451G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51185027 | ||||||
chr18:51185353
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.755-7777T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51185353 | ||||||
chr18:51185704
|
G | A | 1 | a0001c0001t0001g0023 | 3 | HG00621.hp1 NA18969.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.755-8128C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51185704 | ||||||
chr18:51185884
|
A | AC | 38 | a0001c0001t0001g0122a0001c0001t0006g0031a0001c0011t0001g0054others(35): Show | 98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.755-8309dupG | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51185884 | ||||||
chr18:51185892
|
C | G | 15 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(12): Show | 42 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.755-8316G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51185892 | ||||||
chr18:51185892
|
C | T | 10 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 11 | HG01123.hp1 HG01978.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.755-8316G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51185892 | ||||||
chr18:51185893
|
T | C | 1 | a0002c0002t0001g0075 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.755-8317A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51185893 | ||||||
chr18:51186034
|
G | A | 1 | a0001c0001t0001g0042 | 2 | NA18747.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.755-8458C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186034 | ||||||
chr18:51186170
|
T | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(7): Show | 11 | HG01123.hp1 HG01978.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.755-8594A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186170 | ||||||
chr18:51186270
|
C | T | 3 | a0002c0002t0001g0013a0002c0002t0001g0058a0002c0002t0001g0059 | 7 | HG00438.hp1 HG00544.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-8694G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186270 | ||||||
chr18:51186365
|
T | C | 1 | a0001c0003t0015g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.755-8789A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186365 | ||||||
chr18:51186417
|
G | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.755-8841C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186417 | ||||||
chr18:51186569
|
C | T | 1 | a0002c0002t0001g0027 | 2 | HG01496.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.755-8993G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186569 | ||||||
chr18:51186579
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.755-9003C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186579 | ||||||
chr18:51186601
|
TAGAC | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 8 | NA18951.hp1 NA18962.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.755-9029_755-9026d others(6): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186601 | ||||||
chr18:51186670
|
C | T | 8 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 9 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.755-9094G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186670 | ||||||
chr18:51186780
|
CTT | C | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.755-9206_755-9205d others(4): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51186780 | ||||||
chr18:51187025
|
G | C | 1 | a0001c0001t0001g0084 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.755-9449C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51187025 | ||||||
chr18:51187188
|
T | TC | 8 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 9 | HG02257.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.754+9378dupG | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51187188 | ||||||
chr18:51187536
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.754+9031C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51187536 | ||||||
chr18:51187632
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.754+8935G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51187632 | ||||||
chr18:51187696
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0095 | 3 | HG00733.hp2 HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.754+8871C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51187696 | ||||||
chr18:51187703
|
C | T | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+8864G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51187703 | ||||||
chr18:51187784
|
G | T | 45 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(42): Show | 106 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.754+8783C>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51187784 | ||||||
chr18:51188029
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.754+8538C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188029 | ||||||
chr18:51188164
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG02132.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.754+8403C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188164 | ||||||
chr18:51188206
|
T | C | 47 | a0001c0001t0001g0037a0001c0001t0001g0086a0001c0001t0001g0087others(44): Show | 108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.754+8361A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188206 | ||||||
chr18:51188255
|
C | A | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.754+8312G>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188255 | ||||||
chr18:51188257
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.754+8310C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188257 | ||||||
chr18:51188272
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.754+8295C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188272 | ||||||
chr18:51188576
|
C | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(23): Show | 55 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.754+7991G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188576 | ||||||
chr18:51188597
|
C | CA | 2 | a0004c0005t0001g0015a0004c0005t0001g0146 | 6 | HG02717.hp1 HG03098.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.754+7969dupT | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188597 | ||||||
chr18:51188597
|
CA | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.754+7969delT | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188597 | ||||||
chr18:51188614
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.754+7953T>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188614 | ||||||
chr18:51188642
|
G | C | 1 | a0002c0002t0001g0030 | 2 | HG03239.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.754+7925C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188642 | ||||||
chr18:51188644
|
G | A | 1 | a0001c0001t0006g0031 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.754+7923C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188644 | ||||||
chr18:51188902
|
C | A | 2 | a0002c0002t0001g0006a0009c0013t0001g0072 | 8 | HG01884.hp2 HG02257.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.754+7665G>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188902 | ||||||
chr18:51188993
|
A | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(60): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.754+7574T>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188993 | ||||||
chr18:51188993
|
A | T | 2 | a0001c0007t0005g0050a0001c0007t0005g0051 | 2 | HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.754+7574T>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51188993 | ||||||
chr18:51189035
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.754+7532C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51189035 | ||||||
chr18:51189104
|
T | G | 1 | a0004c0005t0001g0146 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.754+7463A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51189104 | ||||||
chr18:51189128
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.754+7439A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51189128 | ||||||
chr18:51189227
|
G | A | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+7340C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51189227 | ||||||
chr18:51189386
|
T | C | 60 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(57): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.754+7181A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51189386 | ||||||
chr18:51189392
|
A | G | 1 | a0001c0003t0015g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.754+7175T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51189392 | ||||||
chr18:51189833
|
T | A | 1 | a0002c0002t0001g0073 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.754+6734A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51189833 | ||||||
chr18:51190048
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.754+6519G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190048 | ||||||
chr18:51190050
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+6517T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190050 | ||||||
chr18:51190188
|
T | A | 1 | a0001c0001t0001g0123 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.754+6379A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190188 | ||||||
chr18:51190397
|
C | T | 18 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(15): Show | 46 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.754+6170G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190397 | ||||||
chr18:51190437
|
T | A | 1 | a0001c0001t0001g0093 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.754+6130A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190437 | ||||||
chr18:51190583
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.754+5984A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190583 | ||||||
chr18:51190590
|
T | C | 2 | a0002c0002t0001g0074a0002c0002t0001g0078 | 2 | HG02080.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.754+5977A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190590 | ||||||
chr18:51190646
|
C | T | 1 | a0001c0003t0001g0047 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.754+5921G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190646 | ||||||
chr18:51190690
|
A | ATTTT | 64 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(61): Show | 170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.754+5876_754+5877i others(6): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190690 | ||||||
chr18:51190733
|
C | T | 1 | a0001c0001t0001g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.754+5834G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190733 | ||||||
chr18:51190839
|
C | T | 1 | a0002c0002t0001g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.754+5728G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190839 | ||||||
chr18:51190900
|
C | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(28): Show | 64 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.754+5667G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190900 | ||||||
chr18:51190993
|
C | T | 79 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(76): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.754+5574G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51190993 | ||||||
chr18:51191301
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0098 | 3 | HG02896.hp2 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.754+5266G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191301 | ||||||
chr18:51191377
|
C | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0089 | 3 | NA18940.hp2 NA18945.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.754+5190G>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191377 | ||||||
chr18:51191405
|
G | A | 1 | a0002c0002t0001g0075 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.754+5162C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191405 | ||||||
chr18:51191556
|
C | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(26): Show | 58 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.754+5011G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191556 | ||||||
chr18:51191638
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.754+4929G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191638 | ||||||
chr18:51191796
|
T | G | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.754+4771A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191796 | ||||||
chr18:51191899
|
A | C | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.754+4668T>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191899 | ||||||
chr18:51191945
|
G | A | 1 | a0001c0003t0001g0047 | 2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.754+4622C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191945 | ||||||
chr18:51191958
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.754+4609T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51191958 | ||||||
chr18:51192116
|
A | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+4451T>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192116 | ||||||
chr18:51192166
|
G | A | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.754+4401C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192166 | ||||||
chr18:51192183
|
T | C | 1 | a0001c0003t0015g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.754+4384A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192183 | ||||||
chr18:51192195
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0126others(7): Show | 27 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(24): Show |
intron_variant | MODIFIER | c.754+4372C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192195 | ||||||
chr18:51192196
|
G | C | 1 | a0001c0001t0003g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.754+4371C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192196 | ||||||
chr18:51192445
|
C | T | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+4122G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192445 | ||||||
chr18:51192490
|
G | A | 79 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0011others(76): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.754+4077C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192490 | ||||||
chr18:51192495
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.754+4072G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192495 | ||||||
chr18:51192576
|
A | G | 1 | a0001c0001t0001g0032 | 2 | HG01261.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.754+3991T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192576 | ||||||
chr18:51192774
|
G | A | 1 | a0002c0002t0001g0076 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.754+3793C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192774 | ||||||
chr18:51192910
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.754+3657C>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51192910 | ||||||
chr18:51193090
|
C | T | 1 | a0001c0007t0005g0050 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.754+3477G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193090 | ||||||
chr18:51193360
|
T | A | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+3207A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193360 | ||||||
chr18:51193541
|
A | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(23): Show | 55 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.754+3026T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193541 | ||||||
chr18:51193592
|
T | C | 1 | a0002c0002t0001g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.754+2975A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193592 | ||||||
chr18:51193683
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0128a0001c0001t0001g0129 | 9 | NA18945.hp2 NA18948.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.754+2884A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193683 | ||||||
chr18:51193771
|
C | T | 1 | a0004c0005t0001g0145 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.754+2796G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193771 | ||||||
chr18:51193916
|
C | T | 2 | a0001c0007t0005g0050a0001c0007t0005g0051 | 2 | HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.754+2651G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193916 | ||||||
chr18:51193967
|
A | T | 1 | a0001c0003t0001g0024 | 3 | HG01891.hp1 HG02486.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.754+2600T>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193967 | ||||||
chr18:51193984
|
T | C | 7 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0045others(4): Show | 14 | HG01891.hp1 HG01891.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.754+2583A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193984 | ||||||
chr18:51193984
|
T | G | 1 | a0001c0001t0001g0130 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.754+2583A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51193984 | ||||||
chr18:51194156
|
T | C | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.754+2411A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194156 | ||||||
chr18:51194326
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.754+2241A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194326 | ||||||
chr18:51194328
|
G | C | 1 | a0001c0001t0001g0132 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.754+2239C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194328 | ||||||
chr18:51194500
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0020 | 6 | HG02165.hp1 NA18942.hp2 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+2067G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194500 | ||||||
chr18:51194511
|
T | A | 1 | a0002c0002t0001g0078 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.754+2056A>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194511 | ||||||
chr18:51194535
|
TAAC | T | 4 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146others(1): Show | 8 | HG02486.hp1 HG02717.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+2029_754+2031d others(5): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194535 | ||||||
chr18:51194630
|
T | G | 3 | a0004c0005t0001g0015a0004c0005t0001g0145a0004c0005t0001g0146 | 7 | HG02717.hp1 HG02896.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+1937A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194630 | ||||||
chr18:51194725
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.754+1842A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194725 | ||||||
chr18:51194922
|
T | G | 1 | a0001c0003t0001g0025 | 3 | HG02647.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.754+1645A>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194922 | ||||||
chr18:51194924
|
C | T | 2 | a0002c0002t0001g0018a0002c0002t0001g0055 | 4 | HG00639.hp1 HG01361.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.754+1643G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194924 | ||||||
chr18:51194931
|
C | T | 1 | a0002c0002t0001g0009 | 6 | NA18952.hp1 NA18993.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+1636G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194931 | ||||||
chr18:51194977
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.754+1590A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51194977 | ||||||
chr18:51195041
|
G | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0090others(1): Show | 10 | HG00408.hp2 HG02027.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.754+1526C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195041 | ||||||
chr18:51195069
|
T | TCTCAA | 29 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(26): Show | 62 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.754+1493_754+1497d others(7): Show |
MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195069 | ||||||
chr18:51195167
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.754+1400A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195167 | ||||||
chr18:51195232
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.754+1335C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195232 | ||||||
chr18:51195248
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0095 | 3 | HG00733.hp2 HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.754+1319G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195248 | ||||||
chr18:51195274
|
A | T | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(23): Show | 55 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.754+1293T>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195274 | ||||||
chr18:51195287
|
A | G | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+1280T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195287 | ||||||
chr18:51195303
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.754+1264A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195303 | ||||||
chr18:51195367
|
T | C | 4 | a0001c0001t0001g0037a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG02258.hp2 HG02451.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+1200A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195367 | ||||||
chr18:51195449
|
C | G | 26 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0032others(23): Show | 55 | HG00099.hp1 HG00408.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.754+1118G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195449 | ||||||
chr18:51195625
|
T | C | 1 | a0001c0001t0001g0017 | 4 | HG01884.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+942A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195625 | ||||||
chr18:51195693
|
G | A | 1 | a0001c0001t0011g0135 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.754+874C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195693 | ||||||
chr18:51195710
|
A | G | 37 | a0001c0011t0001g0054a0002c0002t0001g0003a0002c0002t0001g0006others(34): Show | 97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.754+857T>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195710 | ||||||
chr18:51195797
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.754+770A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195797 | ||||||
chr18:51195884
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.754+683A>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195884 | ||||||
chr18:51195906
|
G | A | 1 | a0001c0003t0015g0143 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.754+661C>T | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195906 | ||||||
chr18:51195982
|
G | C | 2 | a0001c0007t0005g0050a0001c0007t0005g0051 | 2 | HG01123.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.754+585C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51195982 | ||||||
chr18:51196356
|
C | G | 1 | a0001c0001t0001g0079 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.754+211G>C | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51196356 | ||||||
chr18:51196401
|
G | C | 1 | a0001c0001t0001g0138 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.754+166C>G | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51196401 | ||||||
chr18:51196481
|
C | T | 1 | a0001c0001t0006g0031 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.754+86G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51196481 | ||||||
chr18:51196525
|
C | T | 1 | a0001c0003t0001g0045 | 2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.754+42G>A | MEX3C | ENSG00000176624.12 | transcript | ENST00000406189.4 | protein_coding | 1/1 | chr18 | 51196525 |