geneid | 222234 |
---|---|
ensemblid | ENSG00000222011.9 |
hgncid | 22412 |
symbol | FAM185A |
name | family with sequence similarity 185 member A |
refseq_nuc | NM_001145268.2 |
refseq_prot | NP_001138740.2 |
ensembl_nuc | ENST00000413034.3 |
ensembl_prot | ENSP00000395340.2 |
mane_status | MANE Select |
chr | chr7 |
start | 102748999 |
end | 102809225 |
strand | + |
ver | v1.2 |
region | chr7:102748999-102809225 |
region5000 | chr7:102743999-102814225 |
regionname0 | FAM185A_chr7_102748999_102809225 |
regionname5000 | FAM185A_chr7_102743999_102814225 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 392 | 270 | 66 | 38 | 123 | 10 | 33 | 97 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0002 | 0/0 | 392 | 46 | 7 | 4 | 30 | 2 | 3 | 21 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0003 | 0/1 | 392 | 36 | 9 | 20 | 0 | 3 | 3 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0004 | 0/0 | 392 | 18 | 0 | 5 | 9 | 1 | 3 | 6 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0005 | 1/0 | 392 | 5 | 4 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0006 | 0/0 | 392 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0007 | 0/0 | 392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0008 | 0/0 | 392 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1179 | 269 | 66 | 38 | 122 | 10 | 33 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0002 | 0/0 | 1179 | 46 | 7 | 4 | 30 | 2 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0003 | 0/1 | 1179 | 36 | 9 | 20 | 0 | 3 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0004 | 0/0 | 1179 | 18 | 0 | 5 | 9 | 1 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0005 | 1/0 | 1179 | 5 | 4 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0006 | 0/0 | 1179 | 3 | 2 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0007 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0008 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
c0009 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1033 | 293 | 76 | 58 | 109 | 15 | 33 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0002 | 0/0 | 1033 | 37 | 0 | 2 | 26 | 1 | 8 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0003 | 0/0 | 1033 | 35 | 0 | 8 | 26 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0004 | 0/0 | 1033 | 7 | 7 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0005 | 0/0 | 1033 | 3 | 3 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0006 | 0/0 | 1033 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0007 | 0/0 | 1033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0008 | 0/0 | 1033 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
t0009 | 0/0 | 1033 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0002 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0003 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0004 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1179 | 269 | 66 | 38 | 122 | 10 | 33 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0008 | 0/0 | 1179 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0002c0002 | 0/0 | 1179 | 46 | 7 | 4 | 30 | 2 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0003c0003 | 0/1 | 1179 | 36 | 9 | 20 | 0 | 3 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0004c0004 | 0/0 | 1179 | 18 | 0 | 5 | 9 | 1 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0005c0005 | 1/0 | 1179 | 5 | 4 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0006c0006 | 0/0 | 1179 | 3 | 2 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0007c0009 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0008c0007 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2211 | 185 | 54 | 28 | 69 | 9 | 25 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0001t0002 | 0/0 | 2211 | 37 | 0 | 2 | 26 | 1 | 8 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0001t0003 | 0/0 | 2211 | 34 | 0 | 8 | 26 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0001t0004 | 0/0 | 2211 | 6 | 6 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0001t0005 | 0/0 | 2211 | 3 | 3 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0001t0006 | 0/0 | 2211 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0001t0008 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0001t0009 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0001c0008t0001 | 0/0 | 2211 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0002c0002t0001 | 0/0 | 2211 | 45 | 6 | 4 | 30 | 2 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0002c0002t0004 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0003c0003t0001 | 0/1 | 2211 | 35 | 9 | 20 | 0 | 3 | 2 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0003c0003t0003 | 0/0 | 2211 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0004c0004t0001 | 0/0 | 2211 | 18 | 0 | 5 | 9 | 1 | 3 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0005c0005t0001 | 1/0 | 2211 | 5 | 4 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0006c0006t0001 | 0/0 | 2211 | 3 | 2 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0007c0009t0001 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
a0008c0007t0007 | 0/0 | 2211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | copy fasta | chr7 | 102743999 | 102814225 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0001t0009g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0001c0008t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0002c0002t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0002 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0003c0003t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0004c0004t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0005c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0005c0005t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0005c0005t0001g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0006c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0006c0006t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0006c0006t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0007c0009t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
a0008c0007t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00099 | hp2 | a0004 | c0004 | t0001 | g0289 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0244 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00323 | hp1 | a0003 | c0003 | t0001 | g0027 | EUR | FIN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00558 | hp2 | a0004 | c0004 | t0001 | g0285 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00597 | hp2 | a0004 | c0004 | t0001 | g0284 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00642 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0108 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0270 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01070 | hp2 | a0003 | c0003 | t0001 | g0017 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01071 | hp1 | a0003 | c0003 | t0001 | g0017 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01074 | hp2 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0065 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01106 | hp2 | a0003 | c0003 | t0001 | g0083 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0230 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0142 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0018 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0134 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01175 | hp1 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01175 | hp2 | a0004 | c0004 | t0001 | g0294 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01243 | hp1 | a0006 | c0006 | t0001 | g0275 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0049 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01258 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01258 | hp2 | a0003 | c0003 | t0001 | g0151 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0136 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0114 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0144 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0002 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01516 | hp2 | a0003 | c0003 | t0001 | g0002 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01517 | hp2 | a0003 | c0003 | t0001 | g0002 | EUR | IBS | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0158 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0055 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01928 | hp1 | a0004 | c0004 | t0001 | g0005 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01978 | hp1 | a0004 | c0004 | t0001 | g0298 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02055 | hp2 | a0006 | c0006 | t0001 | g0263 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02080 | hp2 | a0001 | c0008 | t0001 | g0156 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02135 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0145 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CDX | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02257 | hp2 | a0007 | c0009 | t0001 | g0025 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02258 | hp2 | a0003 | c0003 | t0001 | g0281 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02273 | hp2 | a0004 | c0004 | t0001 | g0029 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02300 | hp1 | a0004 | c0004 | t0001 | g0029 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02300 | hp2 | a0003 | c0003 | t0001 | g0143 | AMR | PEL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | KHV | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0188 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02717 | hp2 | a0003 | c0003 | t0001 | g0137 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02723 | hp1 | a0005 | c0005 | t0001 | g0028 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0057 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02886 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0146 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02922 | hp2 | a0008 | c0007 | t0007 | g0200 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02970 | hp1 | a0003 | c0003 | t0001 | g0157 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0148 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0237 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0232 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03209 | hp2 | a0006 | c0006 | t0001 | g0038 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0296 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03490 | hp1 | a0003 | c0003 | t0001 | g0130 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0223 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0147 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0234 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0317 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03710 | hp1 | a0004 | c0004 | t0001 | g0287 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03831 | hp2 | a0003 | c0003 | t0003 | g0131 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03942 | hp2 | a0004 | c0004 | t0001 | g0295 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04184 | hp1 | a0004 | c0004 | t0001 | g0297 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | BEB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18522 | hp1 | a0002 | c0002 | t0004 | g0235 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18951 | hp2 | a0004 | c0004 | t0001 | g0290 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18956 | hp2 | a0004 | c0004 | t0001 | g0292 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18960 | hp2 | a0004 | c0004 | t0001 | g0291 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18966 | hp2 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18975 | hp1 | a0001 | c0001 | t0009 | g0205 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18987 | hp1 | a0004 | c0004 | t0001 | g0293 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18993 | hp1 | a0004 | c0004 | t0001 | g0005 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0211 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19043 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19078 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ASW | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | GIH | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01123 | hp1 | a0003 | c0003 | t0001 | g0133 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG02486 | hp2 | a0005 | c0005 | t0001 | g0028 | AFR | ACB | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | USA | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0058 | REF | REF | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
homoSapiens_grch38 | hp1 | a0005 | c0005 | t0001 | g0283 | REF | REF | FAM185A_chr7_102743999_102814225 | FAM185A | chr7 | 102743999 | 102814225 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102749250
|
C | T | 1 | a0004 | 18 | HG00099.hp2 HG00558.hp2 HG00597.hp2 others(15): Show |
missense_variant | MODERATE | c.43C>T | p.Leu15Phe | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 252/2211 | 43/1179 | 15/392 | chr7 | 102749250 | ||
chr7:102749263
|
A | T | 2 | a0002a0007 | 47 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(44): Show |
missense_variant | MODERATE | c.56A>T | p.Gln19Leu | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 265/2211 | 56/1179 | 19/392 | chr7 | 102749263 | ||
chr7:102749386
|
G | C | 7 | a0001a0002a0003others(4): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
missense_variant | MODERATE | c.179G>C | p.Gly60Ala | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 388/2211 | 179/1179 | 60/392 | chr7 | 102749386 | ||
chr7:102751766
|
A | G | 1 | a0007 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.526A>G | p.Thr176Ala | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/8 | 735/2211 | 526/1179 | 176/392 | chr7 | 102751766 | ||
chr7:102757921
|
T | C | 1 | a0008 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.629T>C | p.Ile210Thr | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/8 | 838/2211 | 629/1179 | 210/392 | chr7 | 102757921 | ||
chr7:102787442
|
C | T | 1 | a0003 | 36 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
missense_variant | MODERATE | c.1039C>T | p.Arg347Cys | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/8 | 1248/2211 | 1039/1179 | 347/392 | chr7 | 102787442 | ||
chr7:102808372
|
T | G | 1 | a0006 | 3 | HG01243.hp1 HG02055.hp2 HG03209.hp2 |
missense_variant | MODERATE | c.1149T>G | p.Ser383Arg | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 1358/2211 | 1149/1179 | 383/392 | chr7 | 102808372 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102777257
|
G | A | 1 | a0001c0008 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.840G>A | p.Ser280Ser | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/8 | 1049/2211 | 840/1179 | 280/392 | chr7 | 102777257 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102749077
|
T | A | 1 | a0008c0007t0007 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-131T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 131 | chr7 | 102749077 | |||||
chr7:102749161
|
C | T | 1 | a0001c0001t0009 | 1 | NA18975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-47C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 47 | chr7 | 102749161 | |||||
chr7:102749183
|
T | C | 1 | a0001c0001t0008 | 1 | HG01891.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/8 | 25 | chr7 | 102749183 | |||||
chr7:102808438
|
G | T | 2 | a0001c0001t0003a0003c0003t0003 | 35 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*36G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 36 | chr7 | 102808438 | |||||
chr7:102808475
|
C | G | 1 | a0001c0001t0006 | 2 | HG03471.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*73C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 73 | chr7 | 102808475 | |||||
chr7:102808651
|
C | T | 1 | a0001c0001t0005 | 3 | HG02615.hp2 HG02922.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*249C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 249 | chr7 | 102808651 | |||||
chr7:102808687
|
G | C | 2 | a0001c0001t0004a0002c0002t0004 | 7 | HG02055.hp1 HG02965.hp1 HG03209.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*285G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 285 | chr7 | 102808687 | |||||
chr7:102808971
|
C | A | 1 | a0001c0001t0002 | 37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 8/8 | 569 | chr7 | 102808971 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:102749729
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0323a0001c0001t0002g0324others(1): Show | 5 | HG02015.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+71C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102749729 | ||||||
chr7:102749819
|
G | A | 269 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(266): Show | 311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.451+161G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102749819 | ||||||
chr7:102749960
|
G | A | 2 | a0001c0001t0001g0277a0001c0001t0002g0278 | 2 | NA18949.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.451+302G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102749960 | ||||||
chr7:102750310
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.451+652G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750310 | ||||||
chr7:102750538
|
T | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG02083.hp1 HG02132.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+880T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750538 | ||||||
chr7:102750699
|
C | G | 1 | a0001c0001t0001g0276 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.452-993C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750699 | ||||||
chr7:102750749
|
A | G | 1 | a0006c0006t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.452-943A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750749 | ||||||
chr7:102750782
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-910G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102750782 | ||||||
chr7:102751006
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452-686C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751006 | ||||||
chr7:102751074
|
C | T | 33 | a0001c0001t0001g0277a0001c0001t0001g0300a0001c0001t0001g0307others(30): Show | 38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.452-618C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751074 | ||||||
chr7:102751377
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0006g0045others(1): Show | 4 | HG02109.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-315T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751377 | ||||||
chr7:102751401
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.452-291C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751401 | ||||||
chr7:102751450
|
ATGTTAGT others(4): Show |
A | 1 | a0001c0001t0001g0272 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.452-240_452-230del others(11): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 102751450 | |||||
chr7:102751508
|
C | T | 7 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0271others(4): Show | 8 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.452-184C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751508 | ||||||
chr7:102751527
|
T | A | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 237 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.452-165T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | chr7 | 102751527 | ||||||
chr7:102751540
|
G | GCTGTGGT others(13): Show |
8 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 8 | HG02080.hp1 HG02698.hp1 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-150_452-131dup others(20): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr7 | 102751540 | |||||
chr7:102751817
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+16A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102751817 | ||||||
chr7:102751911
|
C | T | 319 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(316): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.561+110C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102751911 | ||||||
chr7:102752210
|
A | T | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.561+409A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752210 | ||||||
chr7:102752273
|
A | AT | 96 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(93): Show | 115 | HG00733.hp2 HG00738.hp2 HG01070.hp1 others(112): Show |
intron_variant | MODIFIER | c.561+489dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752273 | |||||
chr7:102752273
|
AT | A | 6 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0208others(3): Show | 6 | HG01256.hp1 HG01943.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.561+489delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752273 | |||||
chr7:102752274
|
T | A | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG02258.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.561+473T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752274 | ||||||
chr7:102752295
|
T | C | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+494T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752295 | ||||||
chr7:102752421
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+620A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752421 | ||||||
chr7:102752434
|
G | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(6): Show | 13 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.561+633G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752434 | ||||||
chr7:102752534
|
T | C | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(6): Show | 13 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.561+733T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752534 | ||||||
chr7:102752577
|
A | AT | 22 | a0001c0001t0001g0026a0001c0001t0001g0037a0001c0001t0001g0043others(19): Show | 23 | HG00621.hp1 HG01516.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.561+793dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752577 | |||||
chr7:102752577
|
AT | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.561+793delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102752577 | |||||
chr7:102752578
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.561+777T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752578 | ||||||
chr7:102752617
|
T | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(198): Show | 237 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.561+816T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752617 | ||||||
chr7:102752750
|
A | T | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0004g0256others(5): Show | 8 | HG02055.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+949A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752750 | ||||||
chr7:102752804
|
T | C | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.561+1003T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752804 | ||||||
chr7:102752874
|
A | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0084others(49): Show | 59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.561+1073A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102752874 | ||||||
chr7:102753136
|
A | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.561+1335A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753136 | ||||||
chr7:102753299
|
A | T | 2 | a0001c0001t0006g0045a0001c0001t0006g0046 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.561+1498A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753299 | ||||||
chr7:102753422
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+1621G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753422 | ||||||
chr7:102753584
|
T | C | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.561+1783T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753584 | ||||||
chr7:102753626
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.561+1825C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753626 | ||||||
chr7:102753629
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.561+1828C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753629 | ||||||
chr7:102753638
|
G | T | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0006g0045others(1): Show | 4 | HG02109.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+1837G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753638 | ||||||
chr7:102753741
|
C | CA | 114 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0039others(111): Show | 128 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.561+1951dupA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102753741 | |||||
chr7:102753741
|
C | CAA | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(6): Show | 13 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.561+1950_561+1951d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102753741 | |||||
chr7:102753881
|
T | A | 1 | a0001c0001t0002g0301 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.561+2080T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753881 | ||||||
chr7:102753911
|
C | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.561+2110C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753911 | ||||||
chr7:102753968
|
G | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0023others(66): Show | 78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.561+2167G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102753968 | ||||||
chr7:102754000
|
C | A | 2 | a0001c0001t0002g0302a0001c0001t0002g0303 | 2 | NA18956.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.561+2199C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754000 | ||||||
chr7:102754011
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.561+2210G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754011 | ||||||
chr7:102754204
|
AT | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 207 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.561+2417delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102754204 | |||||
chr7:102754204
|
ATT | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0023others(66): Show | 78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.561+2416_561+2417d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102754204 | |||||
chr7:102754206
|
T | A | 3 | a0001c0001t0001g0064a0003c0003t0001g0017a0003c0003t0001g0130 | 4 | HG01070.hp2 HG01071.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2405T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754206 | ||||||
chr7:102754224
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0006g0045others(1): Show | 4 | HG02109.hp2 HG03471.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+2423G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754224 | ||||||
chr7:102754325
|
C | G | 69 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0023others(66): Show | 78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.561+2524C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754325 | ||||||
chr7:102754604
|
A | G | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0053others(13): Show | 21 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.561+2803A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754604 | ||||||
chr7:102754639
|
C | T | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0053others(13): Show | 21 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.561+2838C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754639 | ||||||
chr7:102754640
|
G | A | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01243.hp1 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.561+2839G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754640 | ||||||
chr7:102754738
|
A | G | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.561+2937A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754738 | ||||||
chr7:102754843
|
T | C | 1 | a0003c0003t0003g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.562-3011T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754843 | ||||||
chr7:102754910
|
T | G | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-2944T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102754910 | ||||||
chr7:102755008
|
C | T | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-2846C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755008 | ||||||
chr7:102755125
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.562-2729G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755125 | ||||||
chr7:102755215
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.562-2639G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755215 | ||||||
chr7:102755252
|
C | T | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0004g0256others(5): Show | 8 | HG02055.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.562-2602C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755252 | ||||||
chr7:102755278
|
A | G | 2 | a0003c0003t0001g0017a0003c0003t0001g0130 | 3 | HG01070.hp2 HG01071.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.562-2576A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755278 | ||||||
chr7:102755382
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.562-2472G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755382 | ||||||
chr7:102755420
|
C | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.562-2434C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755420 | ||||||
chr7:102755476
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 129 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(126): Show |
intron_variant | MODIFIER | c.562-2378A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755476 | ||||||
chr7:102755519
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.562-2335C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755519 | ||||||
chr7:102755596
|
C | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0084others(49): Show | 59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.562-2258C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755596 | ||||||
chr7:102755609
|
T | G | 1 | a0004c0004t0001g0284 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.562-2245T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755609 | ||||||
chr7:102755610
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.562-2244G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755610 | ||||||
chr7:102755804
|
C | T | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-2050C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755804 | ||||||
chr7:102755992
|
TA | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0084others(49): Show | 59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.562-1854delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102755992 | |||||
chr7:102755993
|
A | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0063 | 3 | NA18942.hp2 NA18992.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.562-1861A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102755993 | ||||||
chr7:102756084
|
C | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(6): Show | 13 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.562-1770C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756084 | ||||||
chr7:102756096
|
C | T | 3 | a0002c0002t0001g0243a0002c0002t0001g0244a0002c0002t0001g0245 | 3 | HG00140.hp1 HG01515.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.562-1758C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756096 | ||||||
chr7:102756121
|
A | AT | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-1725dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr7 | 102756121 | |||||
chr7:102756132
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.562-1722C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756132 | ||||||
chr7:102756540
|
C | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 127 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.562-1314C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756540 | ||||||
chr7:102756605
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.562-1249C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756605 | ||||||
chr7:102756635
|
C | T | 1 | a0001c0001t0005g0296 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.562-1219C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756635 | ||||||
chr7:102756691
|
A | C | 1 | a0001c0001t0001g0052 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.562-1163A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756691 | ||||||
chr7:102756780
|
G | A | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.562-1074G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756780 | ||||||
chr7:102756862
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.562-992C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756862 | ||||||
chr7:102756914
|
T | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.562-940T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102756914 | ||||||
chr7:102757052
|
T | C | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.562-802T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757052 | ||||||
chr7:102757297
|
T | C | 1 | a0004c0004t0001g0285 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.562-557T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757297 | ||||||
chr7:102757345
|
A | G | 1 | a0002c0002t0001g0242 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.562-509A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757345 | ||||||
chr7:102757554
|
T | A | 1 | a0003c0003t0001g0133 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.562-300T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757554 | ||||||
chr7:102757813
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0005g0193 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.562-41C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 2/7 | chr7 | 102757813 | ||||||
chr7:102757963
|
C | CT | 85 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 104 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.654+28dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102757963 | |||||
chr7:102757963
|
CT | C | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.654+28delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102757963 | |||||
chr7:102757971
|
T | C | 2 | a0003c0003t0001g0027a0003c0003t0001g0270 | 3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.654+25T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102757971 | ||||||
chr7:102758217
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654+271G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758217 | ||||||
chr7:102758270
|
G | T | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.654+324G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758270 | ||||||
chr7:102758360
|
C | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(6): Show | 13 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.654+414C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758360 | ||||||
chr7:102758426
|
GC | G | 20 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0001t0001g0150others(17): Show | 21 | HG00558.hp1 HG00609.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.654+481delC | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | ||||||
chr7:102758426
|
GCT | G | 39 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0050others(36): Show | 46 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.654+481_654+482del others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | ||||||
chr7:102758426
|
GCTT | G | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(42): Show | 59 | HG00733.hp2 HG01070.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.654+481_654+483del others(3): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | ||||||
chr7:102758426
|
GCTTT | G | 8 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0066others(5): Show | 9 | HG01081.hp1 HG01169.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.654+481_654+484del others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758426 | ||||||
chr7:102758427
|
C | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0207 | 2 | HG06807.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.654+481C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758427 | ||||||
chr7:102758427
|
C | T | 2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | HG02165.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.654+481C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758427 | ||||||
chr7:102758427
|
CT | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0023others(34): Show | 44 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.654+513delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTT | C | 49 | a0001c0001t0001g0039a0001c0001t0001g0052a0001c0001t0001g0060others(46): Show | 55 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.654+512_654+513del others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTTT | C | 51 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0248others(48): Show | 58 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.654+511_654+513del others(3): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTTTT | C | 31 | a0001c0001t0001g0286a0001c0001t0001g0300a0001c0001t0002g0304others(28): Show | 34 | HG00544.hp1 HG00597.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.654+510_654+513del others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0059a0003c0003t0001g0002a0003c0003t0001g0049others(2): Show | 9 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.654+504_654+513del others(10): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(1): Show | 4 | HG01891.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+503_654+513del others(11): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTTTTTTT others(5): Show |
C | 1 | a0003c0003t0001g0027 | 2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.654+502_654+513del others(12): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0271a0001c0001t0006g0045a0001c0001t0006g0046others(1): Show | 4 | HG00741.hp1 HG01516.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+501_654+513del others(13): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758427
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG02109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.654+500_654+513del others(14): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758427 | |||||
chr7:102758428
|
T | A | 11 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0001t0001g0150others(8): Show | 11 | HG00735.hp2 HG01243.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.654+482T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758428 | ||||||
chr7:102758429
|
T | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0050others(34): Show | 44 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.654+483T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758429 | ||||||
chr7:102758430
|
T | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0019others(42): Show | 59 | HG00733.hp2 HG01070.hp1 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.654+484T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758430 | ||||||
chr7:102758431
|
T | A | 8 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0066others(5): Show | 9 | HG01081.hp1 HG01169.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.654+485T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758431 | ||||||
chr7:102758435
|
T | A | 2 | a0001c0001t0001g0192a0003c0003t0001g0151 | 2 | HG01258.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.654+489T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758435 | ||||||
chr7:102758459
|
T | A | 174 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 205 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.654+513T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758459 | ||||||
chr7:102758514
|
C | A | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.654+568C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758514 | ||||||
chr7:102758708
|
T | C | 1 | a0001c0001t0001g0300 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.654+762T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758708 | ||||||
chr7:102758770
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.654+824A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758770 | ||||||
chr7:102758844
|
T | C | 1 | a0004c0004t0001g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.654+898T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758844 | ||||||
chr7:102758868
|
C | CAG | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.654+925_654+926dup others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102758868 | |||||
chr7:102758995
|
C | T | 8 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0004g0256others(5): Show | 8 | HG02055.hp1 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.654+1049C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102758995 | ||||||
chr7:102759092
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.654+1146T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759092 | ||||||
chr7:102759188
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.654+1242T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759188 | ||||||
chr7:102759410
|
C | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0023others(66): Show | 78 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.654+1464C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759410 | ||||||
chr7:102759501
|
CAT | C | 15 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0053others(12): Show | 20 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.654+1557_654+1558d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102759501 | |||||
chr7:102759578
|
A | G | 1 | a0001c0001t0003g0114 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.654+1632A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759578 | ||||||
chr7:102759631
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-1642T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759631 | ||||||
chr7:102759662
|
A | C | 1 | a0001c0001t0001g0274 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.655-1611A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759662 | ||||||
chr7:102759742
|
A | C | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-1531A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759742 | ||||||
chr7:102759836
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0176 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.655-1437C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759836 | ||||||
chr7:102759977
|
G | A | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-1296G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102759977 | ||||||
chr7:102760439
|
A | AC | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-834_655-833ins others(1): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760439 | ||||||
chr7:102760514
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.655-759A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760514 | ||||||
chr7:102760540
|
TCAAA | T | 17 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(14): Show | 19 | HG00621.hp2 HG01106.hp2 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.655-728_655-725del others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr7 | 102760540 | |||||
chr7:102760541
|
C | A | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-732C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760541 | ||||||
chr7:102760685
|
A | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 210 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.655-588A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760685 | ||||||
chr7:102760720
|
C | G | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.655-553C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760720 | ||||||
chr7:102760731
|
C | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.655-542C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760731 | ||||||
chr7:102760806
|
G | A | 105 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 127 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(124): Show |
intron_variant | MODIFIER | c.655-467G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760806 | ||||||
chr7:102760903
|
A | T | 1 | a0001c0001t0002g0304 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.655-370A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760903 | ||||||
chr7:102760966
|
C | T | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(6): Show | 13 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-307C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760966 | ||||||
chr7:102760986
|
A | G | 1 | a0002c0002t0001g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.655-287A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102760986 | ||||||
chr7:102761107
|
C | T | 1 | a0002c0002t0001g0244 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.655-166C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102761107 | ||||||
chr7:102761124
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.655-149G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 3/7 | chr7 | 102761124 | ||||||
chr7:102761537
|
C | CT | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0053others(3): Show | 6 | HG02109.hp2 HG03139.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+131dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102761537 | |||||
chr7:102761542
|
T | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0247 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793+131T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761542 | ||||||
chr7:102761542
|
TA | T | 52 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0084others(49): Show | 59 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.793+142delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102761542 | |||||
chr7:102761543
|
A | T | 10 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0271others(7): Show | 15 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.793+132A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761543 | ||||||
chr7:102761628
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0272 | 3 | NA18990.hp1 NA18994.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.793+217A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761628 | ||||||
chr7:102761678
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.793+267T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761678 | ||||||
chr7:102761800
|
A | T | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+389A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761800 | ||||||
chr7:102761813
|
G | A | 1 | a0002c0002t0001g0210 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.793+402G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761813 | ||||||
chr7:102761939
|
A | G | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+528A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102761939 | ||||||
chr7:102762093
|
T | G | 4 | a0003c0003t0001g0018a0003c0003t0001g0065a0003c0003t0001g0134others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+682T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762093 | ||||||
chr7:102762115
|
G | C | 2 | a0001c0001t0006g0045a0001c0001t0006g0046 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.793+704G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762115 | ||||||
chr7:102762163
|
T | C | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+752T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762163 | ||||||
chr7:102762183
|
T | A | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.793+772T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762183 | ||||||
chr7:102762183
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.793+772T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762183 | ||||||
chr7:102762229
|
T | C | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0053others(13): Show | 21 | HG00323.hp1 HG00642.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.793+818T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762229 | ||||||
chr7:102762339
|
G | A | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+928G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762339 | ||||||
chr7:102762684
|
T | G | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+1273T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762684 | ||||||
chr7:102762810
|
C | T | 243 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 284 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.793+1399C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762810 | ||||||
chr7:102762830
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 208 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.793+1419T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762830 | ||||||
chr7:102762851
|
A | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 208 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.793+1440A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762851 | ||||||
chr7:102762923
|
A | G | 48 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(45): Show | 53 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.793+1512A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102762923 | ||||||
chr7:102763317
|
T | A | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.793+1906T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763317 | ||||||
chr7:102763343
|
T | TG | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 208 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.793+1934dupG | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102763343 | |||||
chr7:102763580
|
G | T | 19 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0068others(16): Show | 27 | HG02040.hp1 HG02071.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.793+2169G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763580 | ||||||
chr7:102763817
|
G | C | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.793+2406G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763817 | ||||||
chr7:102763831
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.793+2420C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763831 | ||||||
chr7:102763906
|
T | C | 49 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(46): Show | 54 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.793+2495T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102763906 | ||||||
chr7:102764004
|
T | C | 1 | a0001c0008t0001g0156 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.793+2593T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764004 | ||||||
chr7:102764141
|
G | C | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.793+2730G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764141 | ||||||
chr7:102764340
|
A | G | 50 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(47): Show | 55 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.793+2929A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764340 | ||||||
chr7:102764407
|
G | T | 2 | a0003c0003t0001g0027a0003c0003t0001g0270 | 3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.793+2996G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764407 | ||||||
chr7:102764621
|
C | T | 9 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 9 | HG02080.hp1 HG02698.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+3210C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764621 | ||||||
chr7:102764665
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0247 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.793+3254A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764665 | ||||||
chr7:102764749
|
G | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0187a0001c0001t0001g0192 | 3 | HG03704.hp1 HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.793+3338G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764749 | ||||||
chr7:102764827
|
GA | G | 7 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0008g0055others(4): Show | 11 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.793+3426delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102764827 | |||||
chr7:102764848
|
A | G | 37 | a0001c0001t0001g0052a0001c0001t0001g0084a0001c0001t0001g0092others(34): Show | 42 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.793+3437A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764848 | ||||||
chr7:102764893
|
T | G | 3 | a0003c0003t0001g0157a0003c0003t0001g0158a0003c0003t0001g0188 | 3 | HG01884.hp2 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.793+3482T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764893 | ||||||
chr7:102764898
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.793+3487T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764898 | ||||||
chr7:102764933
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.793+3522T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102764933 | ||||||
chr7:102765195
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.793+3784C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765195 | ||||||
chr7:102765346
|
G | A | 2 | a0001c0001t0003g0089a0001c0001t0003g0127 | 2 | HG00621.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.793+3935G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765346 | ||||||
chr7:102765395
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.793+3984G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765395 | ||||||
chr7:102765471
|
G | T | 7 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0105others(4): Show | 9 | NA18941.hp2 NA18945.hp2 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.793+4060G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765471 | ||||||
chr7:102765482
|
A | T | 44 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(41): Show | 47 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.793+4071A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765482 | ||||||
chr7:102765829
|
C | T | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+4418C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765829 | ||||||
chr7:102765830
|
G | A | 2 | a0001c0001t0003g0051a0001c0001t0003g0119 | 2 | NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.793+4419G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765830 | ||||||
chr7:102765885
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793+4474T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765885 | ||||||
chr7:102765943
|
A | G | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.793+4532A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765943 | ||||||
chr7:102765947
|
GAAT | G | 4 | a0003c0003t0001g0157a0003c0003t0001g0158a0003c0003t0001g0188others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.793+4541_793+4543d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102765947 | |||||
chr7:102765951
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0184 | 2 | HG01433.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.793+4540A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765951 | ||||||
chr7:102765967
|
C | A | 6 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(3): Show | 6 | HG02055.hp1 HG02965.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+4556C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765967 | ||||||
chr7:102765988
|
T | G | 1 | a0001c0001t0001g0168 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.793+4577T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765988 | ||||||
chr7:102765992
|
C | T | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+4581C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102765992 | ||||||
chr7:102766001
|
C | T | 8 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0059others(5): Show | 9 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.793+4590C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766001 | ||||||
chr7:102766046
|
A | G | 1 | a0001c0001t0002g0318 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.793+4635A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766046 | ||||||
chr7:102766123
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0050a0001c0001t0001g0069others(1): Show | 8 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.793+4712G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766123 | ||||||
chr7:102766230
|
G | A | 5 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(2): Show | 5 | HG02080.hp1 HG02698.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+4819G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766230 | ||||||
chr7:102766554
|
G | C | 1 | a0001c0001t0004g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.793+5143G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766554 | ||||||
chr7:102766619
|
A | AAC | 94 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0039others(91): Show | 100 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.793+5210_793+5211d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766619 | |||||
chr7:102766674
|
T | G | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+5263T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766674 | ||||||
chr7:102766771
|
CTTTGTTT others(2): Show |
C | 3 | a0001c0001t0005g0193a0001c0001t0006g0045a0001c0001t0006g0046 | 3 | HG02922.hp1 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.793+5378_793+5386d others(11): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766771 | |||||
chr7:102766775
|
G | GT | 21 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(18): Show | 23 | HG00544.hp1 HG00621.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.793+5372dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766775 | |||||
chr7:102766784
|
G | GT | 8 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0066others(5): Show | 10 | HG00733.hp2 HG01261.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.793+5381dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102766784 | |||||
chr7:102766789
|
T | G | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+5378T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766789 | ||||||
chr7:102766854
|
G | A | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.793+5443G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766854 | ||||||
chr7:102766940
|
G | A | 23 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0039others(20): Show | 25 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.794-5469G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766940 | ||||||
chr7:102766955
|
T | C | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.794-5454T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766955 | ||||||
chr7:102766986
|
G | T | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.794-5423G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102766986 | ||||||
chr7:102767022
|
C | T | 3 | a0003c0003t0001g0137a0003c0003t0001g0147a0003c0003t0001g0148 | 3 | HG02717.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.794-5387C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767022 | ||||||
chr7:102767038
|
C | T | 1 | a0001c0001t0002g0317 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.794-5371C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767038 | ||||||
chr7:102767041
|
A | G | 1 | a0002c0002t0004g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.794-5368A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767041 | ||||||
chr7:102767042
|
C | T | 39 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0039others(36): Show | 41 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(38): Show |
intron_variant | MODIFIER | c.794-5367C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767042 | ||||||
chr7:102767043
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.794-5366G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767043 | ||||||
chr7:102767073
|
G | C | 46 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(43): Show | 49 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.794-5336G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767073 | ||||||
chr7:102767130
|
A | G | 9 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0264others(6): Show | 10 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.794-5279A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767130 | ||||||
chr7:102767134
|
C | CT | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.794-5261dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102767134 | |||||
chr7:102767134
|
C | CTT | 54 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0099others(51): Show | 57 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.794-5262_794-5261d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102767134 | |||||
chr7:102767134
|
C | CTTT | 37 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0039others(34): Show | 40 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.794-5263_794-5261d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr7 | 102767134 | |||||
chr7:102767431
|
G | T | 23 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(20): Show | 25 | HG00544.hp1 HG00621.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.794-4978G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767431 | ||||||
chr7:102767442
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.794-4967C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767442 | ||||||
chr7:102767560
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.794-4849A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767560 | ||||||
chr7:102767562
|
T | C | 26 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0039others(23): Show | 29 | HG00323.hp1 HG00741.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.794-4847T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767562 | ||||||
chr7:102767576
|
A | C | 48 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0132others(45): Show | 51 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.794-4833A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767576 | ||||||
chr7:102767833
|
C | T | 8 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0178others(5): Show | 8 | HG02109.hp2 HG02886.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-4576C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767833 | ||||||
chr7:102767988
|
T | G | 5 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0149others(2): Show | 5 | HG01106.hp1 HG02717.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-4421T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767988 | ||||||
chr7:102767989
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.794-4420A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102767989 | ||||||
chr7:102768007
|
T | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0261a0001c0001t0001g0262others(4): Show | 8 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.794-4402T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768007 | ||||||
chr7:102768019
|
T | C | 31 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0095others(28): Show | 37 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.794-4390T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768019 | ||||||
chr7:102768119
|
T | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0023others(63): Show | 78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.794-4290T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768119 | ||||||
chr7:102768135
|
C | T | 1 | a0001c0001t0003g0090 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.794-4274C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768135 | ||||||
chr7:102768193
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.794-4216C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768193 | ||||||
chr7:102768451
|
T | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(317): Show | 371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.794-3958T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768451 | ||||||
chr7:102768535
|
T | C | 5 | a0002c0002t0001g0025a0002c0002t0001g0236a0002c0002t0001g0237others(2): Show | 5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.794-3874T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768535 | ||||||
chr7:102768731
|
G | T | 1 | a0003c0003t0001g0136 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.794-3678G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768731 | ||||||
chr7:102768961
|
C | T | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(169): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.794-3448C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102768961 | ||||||
chr7:102769024
|
G | A | 131 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(128): Show | 145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.794-3385G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769024 | ||||||
chr7:102769075
|
G | C | 4 | a0001c0001t0001g0085a0001c0001t0001g0097a0001c0001t0001g0107others(1): Show | 4 | HG02257.hp1 HG03239.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-3334G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769075 | ||||||
chr7:102769437
|
T | A | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.794-2972T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769437 | ||||||
chr7:102769477
|
G | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0138others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.794-2932G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769477 | ||||||
chr7:102769489
|
A | C | 1 | a0003c0003t0001g0146 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.794-2920A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769489 | ||||||
chr7:102769541
|
G | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-2868G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769541 | ||||||
chr7:102769649
|
A | G | 29 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0092others(26): Show | 30 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.794-2760A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769649 | ||||||
chr7:102769765
|
T | C | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.794-2644T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769765 | ||||||
chr7:102769919
|
C | T | 1 | a0002c0002t0001g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.794-2490C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102769919 | ||||||
chr7:102770030
|
C | G | 30 | a0001c0001t0005g0288a0001c0001t0005g0296a0003c0003t0001g0002others(27): Show | 37 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.794-2379C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770030 | ||||||
chr7:102770056
|
G | A | 1 | a0001c0001t0003g0091 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.794-2353G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770056 | ||||||
chr7:102770219
|
T | C | 1 | a0001c0001t0004g0259 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.794-2190T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770219 | ||||||
chr7:102770380
|
G | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.794-2029G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770380 | ||||||
chr7:102770418
|
G | A | 2 | a0001c0001t0006g0045a0001c0001t0006g0046 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.794-1991G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770418 | ||||||
chr7:102770619
|
G | C | 1 | a0001c0001t0003g0123 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.794-1790G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770619 | ||||||
chr7:102770901
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.794-1508T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102770901 | ||||||
chr7:102771024
|
G | A | 60 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(57): Show | 64 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.794-1385G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771024 | ||||||
chr7:102771769
|
C | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.794-640C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771769 | ||||||
chr7:102771853
|
C | T | 1 | a0003c0003t0001g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.794-556C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771853 | ||||||
chr7:102771866
|
A | G | 2 | a0001c0001t0001g0076a0004c0004t0001g0298 | 2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.794-543A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771866 | ||||||
chr7:102771914
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(98): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.794-495C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771914 | ||||||
chr7:102771964
|
T | C | 31 | a0001c0001t0005g0288a0001c0001t0005g0296a0003c0003t0001g0002others(28): Show | 38 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.794-445T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102771964 | ||||||
chr7:102772199
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0252 | 2 | NA18942.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.794-210G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102772199 | ||||||
chr7:102772233
|
C | A | 1 | a0006c0006t0001g0275 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.794-176C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 4/7 | chr7 | 102772233 | ||||||
chr7:102772842
|
A | G | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.835+392A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102772842 | ||||||
chr7:102772953
|
C | A | 1 | a0001c0001t0001g0097 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.835+503C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102772953 | ||||||
chr7:102773100
|
G | C | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.835+650G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773100 | ||||||
chr7:102773259
|
G | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+809G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773259 | ||||||
chr7:102773332
|
A | C | 1 | a0001c0001t0002g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835+882A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773332 | ||||||
chr7:102773426
|
A | G | 61 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0042others(58): Show | 70 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.835+976A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773426 | ||||||
chr7:102773467
|
C | T | 1 | a0002c0002t0001g0226 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.835+1017C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773467 | ||||||
chr7:102773532
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.835+1082T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773532 | ||||||
chr7:102773539
|
G | A | 1 | a0004c0004t0001g0291 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.835+1089G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773539 | ||||||
chr7:102773580
|
G | A | 5 | a0002c0002t0001g0025a0002c0002t0001g0236a0002c0002t0001g0237others(2): Show | 5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.835+1130G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773580 | ||||||
chr7:102773860
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.835+1410G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102773860 | ||||||
chr7:102774151
|
G | A | 150 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0026others(147): Show | 167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.835+1701G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774151 | ||||||
chr7:102774163
|
G | C | 134 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(131): Show | 148 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.835+1713G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774163 | ||||||
chr7:102774258
|
T | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG02970.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.835+1808T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774258 | ||||||
chr7:102774305
|
T | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0266 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.835+1855T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774305 | ||||||
chr7:102774436
|
C | A | 6 | a0001c0001t0001g0011a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.835+1986C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774436 | ||||||
chr7:102774640
|
T | C | 1 | a0001c0001t0004g0257 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.835+2190T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774640 | ||||||
chr7:102774680
|
T | G | 1 | a0001c0001t0002g0299 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.835+2230T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102774680 | ||||||
chr7:102775010
|
G | GT | 50 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0093others(47): Show | 57 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-2231dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102775010 | |||||
chr7:102775016
|
T | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0185 | 2 | HG02165.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.836-2237T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775016 | ||||||
chr7:102775145
|
A | G | 36 | a0001c0001t0001g0036a0001c0001t0001g0115a0001c0001t0001g0196others(33): Show | 41 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.836-2108A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775145 | ||||||
chr7:102775296
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.836-1957T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775296 | ||||||
chr7:102775696
|
CTAA | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.836-1555_836-1553d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102775696 | |||||
chr7:102775780
|
A | G | 4 | a0003c0003t0001g0157a0003c0003t0001g0158a0003c0003t0001g0188others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.836-1473A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775780 | ||||||
chr7:102775807
|
C | T | 153 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0026others(150): Show | 170 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.836-1446C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775807 | ||||||
chr7:102775965
|
G | C | 1 | a0001c0001t0003g0100 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.836-1288G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775965 | ||||||
chr7:102775982
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.836-1271T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102775982 | ||||||
chr7:102776015
|
C | T | 2 | a0002c0002t0001g0224a0002c0002t0001g0225 | 2 | HG00597.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.836-1238C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102776015 | ||||||
chr7:102776046
|
CTCTT | C | 65 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(62): Show | 69 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.836-1205_836-1202d others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776046 | |||||
chr7:102776099
|
T | TACACACA others(21): Show |
1 | a0001c0001t0004g0259 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | |||||
chr7:102776099
|
T | TACACACA others(19): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0004g0256others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(28): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | |||||
chr7:102776099
|
T | TACACACA others(21): Show |
2 | a0002c0002t0001g0234a0002c0002t0004g0235 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | |||||
chr7:102776099
|
T | TACACACA others(23): Show |
1 | a0002c0002t0001g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.836-1137_836-1136i others(32): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | |||||
chr7:102776099
|
T | TACACACA others(17): Show |
51 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(48): Show | 60 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(26): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | |||||
chr7:102776099
|
T | TACACACA others(19): Show |
101 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0026others(98): Show | 115 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(28): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | |||||
chr7:102776099
|
T | TACACACA others(21): Show |
49 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0084others(46): Show | 52 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776099 | |||||
chr7:102776111
|
C | CACACACA others(21): Show |
1 | a0004c0004t0001g0292 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.836-1137_836-1136i others(30): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776111 | |||||
chr7:102776170
|
C | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.836-1083C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102776170 | ||||||
chr7:102776190
|
C | T | 1 | a0003c0003t0001g0148 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.836-1063C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102776190 | ||||||
chr7:102776702
|
T | TAAAAAA | 66 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0115others(63): Show | 76 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.836-539_836-534dup others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776702 | |||||
chr7:102776702
|
T | TAAAAAAA | 50 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(47): Show | 52 | HG00140.hp1 HG00597.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.836-540_836-534dup others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776702 | |||||
chr7:102776702
|
T | TAAAAAAA others(1): Show |
14 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0105others(11): Show | 16 | HG00408.hp1 HG01934.hp1 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.836-541_836-534dup others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102776702 | |||||
chr7:102777034
|
A | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0199 | 2 | NA18989.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.836-219A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102777034 | ||||||
chr7:102777094
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.836-159G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | chr7 | 102777094 | ||||||
chr7:102777218
|
G | GAATTATT others(309): Show |
1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.836-26_836-25insTT others(314): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr7 | 102777218 | |||||
chr7:102777362
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.931+14A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777362 | ||||||
chr7:102777674
|
A | G | 5 | a0001c0001t0001g0208a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.931+326A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777674 | ||||||
chr7:102777724
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.931+376G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777724 | ||||||
chr7:102777770
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.931+422T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777770 | ||||||
chr7:102777978
|
G | T | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.931+630G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102777978 | ||||||
chr7:102778069
|
A | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.931+721A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778069 | ||||||
chr7:102778140
|
G | A | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.931+792G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778140 | ||||||
chr7:102778500
|
CA | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+1155delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102778500 | |||||
chr7:102778509
|
T | C | 34 | a0001c0001t0001g0036a0001c0001t0001g0115a0001c0001t0001g0307others(31): Show | 39 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.931+1161T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778509 | ||||||
chr7:102778609
|
G | A | 34 | a0001c0001t0001g0036a0001c0001t0001g0115a0001c0001t0001g0307others(31): Show | 39 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.931+1261G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778609 | ||||||
chr7:102778857
|
C | A | 214 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(211): Show | 238 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.931+1509C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778857 | ||||||
chr7:102778859
|
C | T | 3 | a0003c0003t0001g0002a0003c0003t0001g0049a0003c0003t0001g0058 | 7 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+1511C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778859 | ||||||
chr7:102778894
|
G | C | 2 | a0001c0001t0001g0152a0001c0001t0001g0176 | 2 | HG02683.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.931+1546G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102778894 | ||||||
chr7:102779172
|
A | G | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+1824A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779172 | ||||||
chr7:102779206
|
T | C | 1 | a0002c0002t0001g0239 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.931+1858T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779206 | ||||||
chr7:102779291
|
G | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.931+1943G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779291 | ||||||
chr7:102779358
|
A | G | 216 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(213): Show | 240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.931+2010A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779358 | ||||||
chr7:102779642
|
T | C | 1 | a0001c0001t0001g0021 | 2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.931+2294T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779642 | ||||||
chr7:102779850
|
C | CT | 7 | a0001c0001t0001g0011a0001c0001t0001g0174a0001c0001t0001g0280others(4): Show | 9 | HG01175.hp2 HG01884.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.931+2531dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | |||||
chr7:102779850
|
CT | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(104): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.931+2531delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | |||||
chr7:102779850
|
CTT | C | 109 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0084others(106): Show | 123 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.931+2530_931+2531d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | |||||
chr7:102779850
|
CTTT | C | 12 | a0001c0001t0001g0064a0001c0001t0001g0082a0001c0001t0001g0140others(9): Show | 12 | HG01975.hp2 HG02015.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.931+2529_931+2531d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | |||||
chr7:102779850
|
CTTTT | C | 15 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0061others(12): Show | 16 | HG01891.hp2 HG02145.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.931+2528_931+2531d others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | |||||
chr7:102779850
|
CTTTTT | C | 54 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0039others(51): Show | 63 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.931+2527_931+2531d others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | |||||
chr7:102779850
|
CTTTTTT | C | 7 | a0001c0001t0004g0256a0001c0001t0004g0257a0001c0001t0004g0258others(4): Show | 7 | HG01256.hp1 HG02055.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.931+2526_931+2531d others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102779850 | |||||
chr7:102779980
|
A | G | 215 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(212): Show | 239 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.931+2632A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102779980 | ||||||
chr7:102780027
|
T | A | 3 | a0001c0001t0005g0193a0001c0001t0005g0288a0001c0001t0005g0296 | 3 | HG02615.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.931+2679T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780027 | ||||||
chr7:102780186
|
C | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+2838C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780186 | ||||||
chr7:102780254
|
A | T | 216 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(213): Show | 240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.931+2906A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780254 | ||||||
chr7:102780277
|
A | G | 2 | a0002c0002t0001g0234a0002c0002t0004g0235 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.931+2929A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780277 | ||||||
chr7:102780358
|
T | G | 218 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(215): Show | 242 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.931+3010T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780358 | ||||||
chr7:102780728
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.931+3380C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780728 | ||||||
chr7:102780826
|
C | A | 65 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0039others(62): Show | 74 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.931+3478C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780826 | ||||||
chr7:102780836
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.931+3488C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780836 | ||||||
chr7:102780858
|
G | A | 1 | a0002c0002t0001g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.931+3510G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780858 | ||||||
chr7:102780901
|
C | A | 49 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(46): Show | 58 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.931+3553C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780901 | ||||||
chr7:102780990
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.931+3642G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102780990 | ||||||
chr7:102781061
|
T | C | 137 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0043others(134): Show | 151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.931+3713T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781061 | ||||||
chr7:102781133
|
G | A | 2 | a0001c0001t0005g0288a0001c0001t0005g0296 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.931+3785G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781133 | ||||||
chr7:102781345
|
G | C | 132 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(129): Show | 146 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.931+3997G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781345 | ||||||
chr7:102781509
|
C | T | 2 | a0003c0003t0001g0027a0003c0003t0001g0270 | 3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.931+4161C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781509 | ||||||
chr7:102781796
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.931+4448A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781796 | ||||||
chr7:102781820
|
C | T | 1 | a0001c0001t0002g0318 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.931+4472C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781820 | ||||||
chr7:102781985
|
G | C | 57 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0042others(54): Show | 66 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.931+4637G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781985 | ||||||
chr7:102781985
|
G | T | 1 | a0001c0001t0001g0080 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.931+4637G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102781985 | ||||||
chr7:102782136
|
A | C | 59 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0042others(56): Show | 68 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.931+4788A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782136 | ||||||
chr7:102782252
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.931+4904C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782252 | ||||||
chr7:102782306
|
A | G | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.931+4958A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782306 | ||||||
chr7:102782318
|
C | T | 1 | a0003c0003t0001g0188 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.931+4970C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782318 | ||||||
chr7:102782430
|
C | A | 2 | a0002c0002t0001g0216a0002c0002t0001g0219 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.932-4905C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782430 | ||||||
chr7:102782499
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.932-4836C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782499 | ||||||
chr7:102782500
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0053 | 2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.932-4835G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782500 | ||||||
chr7:102782567
|
A | G | 218 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(215): Show | 242 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.932-4768A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782567 | ||||||
chr7:102782624
|
C | T | 3 | a0001c0001t0001g0164a0004c0004t0001g0284a0004c0004t0001g0290 | 3 | HG00597.hp2 HG01070.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.932-4711C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782624 | ||||||
chr7:102782673
|
C | T | 1 | a0002c0002t0001g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.932-4662C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782673 | ||||||
chr7:102782810
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.932-4525T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782810 | ||||||
chr7:102782902
|
A | G | 3 | a0003c0003t0001g0137a0003c0003t0001g0147a0003c0003t0001g0148 | 3 | HG02717.hp2 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.932-4433A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782902 | ||||||
chr7:102782912
|
C | T | 136 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0043others(133): Show | 150 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.932-4423C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782912 | ||||||
chr7:102782972
|
A | C | 1 | a0001c0001t0003g0119 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.932-4363A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782972 | ||||||
chr7:102782977
|
A | C | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.932-4358A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102782977 | ||||||
chr7:102783171
|
G | A | 133 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0043others(130): Show | 147 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.932-4164G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783171 | ||||||
chr7:102783192
|
A | G | 1 | a0004c0004t0001g0293 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.932-4143A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783192 | ||||||
chr7:102783229
|
T | C | 137 | a0001c0001t0001g0019a0001c0001t0001g0036a0001c0001t0001g0043others(134): Show | 151 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.932-4106T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783229 | ||||||
chr7:102783241
|
C | T | 2 | a0002c0002t0001g0232a0003c0003t0001g0144 | 2 | HG01433.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.932-4094C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783241 | ||||||
chr7:102783325
|
A | G | 2 | a0002c0002t0001g0025a0007c0009t0001g0025 | 2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.932-4010A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783325 | ||||||
chr7:102783366
|
C | T | 1 | a0003c0003t0001g0146 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.932-3969C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783366 | ||||||
chr7:102783476
|
AG | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.932-3858delG | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783476 | ||||||
chr7:102783600
|
A | C | 31 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0003g0007others(28): Show | 36 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.932-3735A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783600 | ||||||
chr7:102783619
|
C | CATACCAG others(19): Show |
11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-3695_932-3670d others(28): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102783619 | |||||
chr7:102783677
|
G | C | 219 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(216): Show | 243 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.932-3658G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783677 | ||||||
chr7:102783801
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.932-3534A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783801 | ||||||
chr7:102783842
|
A | G | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.932-3493A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783842 | ||||||
chr7:102783889
|
G | C | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-3446G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783889 | ||||||
chr7:102783931
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0192 | 2 | HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.932-3404C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783931 | ||||||
chr7:102783994
|
A | G | 1 | a0001c0001t0002g0322 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.932-3341A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783994 | ||||||
chr7:102783997
|
G | C | 4 | a0001c0001t0002g0032a0001c0001t0002g0323a0001c0001t0002g0324others(1): Show | 5 | HG02015.hp2 NA18955.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-3338G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102783997 | ||||||
chr7:102784009
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.932-3326C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784009 | ||||||
chr7:102784140
|
G | C | 1 | a0002c0002t0001g0217 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.932-3195G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784140 | ||||||
chr7:102784144
|
A | T | 31 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0092others(28): Show | 32 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.932-3191A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784144 | ||||||
chr7:102784211
|
A | G | 6 | a0001c0001t0001g0026a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-3124A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784211 | ||||||
chr7:102784387
|
G | T | 57 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0042others(54): Show | 66 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.932-2948G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784387 | ||||||
chr7:102784405
|
C | G | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.932-2930C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784405 | ||||||
chr7:102784448
|
A | C | 68 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(65): Show | 72 | HG00140.hp1 HG00408.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.932-2887A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784448 | ||||||
chr7:102784457
|
C | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0138others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-2878C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784457 | ||||||
chr7:102784485
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.932-2850A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784485 | ||||||
chr7:102784512
|
T | C | 139 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(136): Show | 153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-2823T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784512 | ||||||
chr7:102784573
|
C | T | 17 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0105others(14): Show | 19 | HG00408.hp1 HG01934.hp1 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.932-2762C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784573 | ||||||
chr7:102784605
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.932-2730C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784605 | ||||||
chr7:102784636
|
T | C | 139 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(136): Show | 153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-2699T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784636 | ||||||
chr7:102784707
|
C | G | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.932-2628C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784707 | ||||||
chr7:102784721
|
A | G | 1 | a0001c0001t0008g0055 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.932-2614A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784721 | ||||||
chr7:102784772
|
C | G | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-2563C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784772 | ||||||
chr7:102784922
|
A | G | 1 | a0001c0001t0003g0106 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.932-2413A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784922 | ||||||
chr7:102784938
|
C | T | 2 | a0001c0001t0001g0162a0001c0001t0002g0311 | 2 | HG02698.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.932-2397C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784938 | ||||||
chr7:102784977
|
C | A | 2 | a0002c0002t0001g0221a0002c0002t0001g0223 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.932-2358C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102784977 | ||||||
chr7:102785031
|
T | C | 139 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(136): Show | 153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-2304T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785031 | ||||||
chr7:102785044
|
CAG | C | 29 | a0003c0003t0001g0002a0003c0003t0001g0017a0003c0003t0001g0018others(26): Show | 36 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.932-2286_932-2285d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr7 | 102785044 | |||||
chr7:102785090
|
G | C | 33 | a0001c0001t0001g0115a0001c0001t0001g0307a0001c0001t0002g0012others(30): Show | 38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.932-2245G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785090 | ||||||
chr7:102785126
|
C | T | 4 | a0003c0003t0001g0018a0003c0003t0001g0065a0003c0003t0001g0134others(1): Show | 5 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-2209C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785126 | ||||||
chr7:102785311
|
C | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0095 | 2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.932-2024C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785311 | ||||||
chr7:102785331
|
T | A | 50 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(47): Show | 59 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.932-2004T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785331 | ||||||
chr7:102785366
|
C | T | 8 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(5): Show | 8 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.932-1969C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785366 | ||||||
chr7:102785375
|
A | G | 140 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(137): Show | 154 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.932-1960A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785375 | ||||||
chr7:102785398
|
C | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG03491.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.932-1937C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785398 | ||||||
chr7:102785410
|
C | T | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.932-1925C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785410 | ||||||
chr7:102785509
|
C | T | 2 | a0002c0002t0001g0216a0002c0002t0001g0219 | 2 | HG02015.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.932-1826C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785509 | ||||||
chr7:102785533
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.932-1802A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785533 | ||||||
chr7:102785589
|
C | G | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.932-1746C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785589 | ||||||
chr7:102785635
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0138others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.932-1700A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785635 | ||||||
chr7:102785659
|
T | C | 220 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(217): Show | 244 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.932-1676T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785659 | ||||||
chr7:102785754
|
C | G | 6 | a0001c0001t0001g0026a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-1581C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785754 | ||||||
chr7:102785783
|
G | T | 2 | a0004c0004t0001g0289a0004c0004t0001g0297 | 2 | HG00099.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.932-1552G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785783 | ||||||
chr7:102785814
|
G | A | 1 | a0002c0002t0001g0245 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.932-1521G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785814 | ||||||
chr7:102785888
|
C | G | 1 | a0001c0001t0001g0277 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.932-1447C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102785888 | ||||||
chr7:102786103
|
G | C | 4 | a0003c0003t0001g0157a0003c0003t0001g0158a0003c0003t0001g0188others(1): Show | 4 | HG01884.hp2 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.932-1232G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786103 | ||||||
chr7:102786157
|
C | T | 31 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0003g0007others(28): Show | 36 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.932-1178C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786157 | ||||||
chr7:102786167
|
A | G | 1 | a0002c0002t0001g0210 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.932-1168A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786167 | ||||||
chr7:102786320
|
C | T | 2 | a0003c0003t0001g0017a0003c0003t0001g0130 | 3 | HG01070.hp2 HG01071.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.932-1015C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786320 | ||||||
chr7:102786407
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 7 | HG01891.hp1 HG02572.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.932-928T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786407 | ||||||
chr7:102786427
|
C | A | 1 | a0001c0001t0001g0204 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.932-908C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786427 | ||||||
chr7:102786439
|
A | C | 4 | a0003c0003t0001g0002a0003c0003t0001g0049a0003c0003t0001g0057others(1): Show | 8 | HG00642.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.932-896A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786439 | ||||||
chr7:102786572
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.932-763G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786572 | ||||||
chr7:102786580
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.932-755A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786580 | ||||||
chr7:102786595
|
A | G | 1 | a0004c0004t0001g0293 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.932-740A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786595 | ||||||
chr7:102786606
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.932-729C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786606 | ||||||
chr7:102786613
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.932-722G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786613 | ||||||
chr7:102786841
|
A | AAG | 133 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(130): Show | 147 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.932-494_932-493ins others(2): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786841 | ||||||
chr7:102786841
|
A | AG | 82 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0026others(79): Show | 92 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.932-494_932-493ins others(1): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102786841 | ||||||
chr7:102787021
|
T | C | 139 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(136): Show | 153 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.932-314T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787021 | ||||||
chr7:102787041
|
T | C | 2 | a0001c0001t0006g0045a0001c0001t0006g0046 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.932-294T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787041 | ||||||
chr7:102787111
|
A | G | 5 | a0002c0002t0001g0025a0002c0002t0001g0236a0002c0002t0001g0237others(2): Show | 5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.932-224A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787111 | ||||||
chr7:102787209
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.932-126A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 6/7 | chr7 | 102787209 | ||||||
chr7:102787519
|
A | G | 31 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0092others(28): Show | 32 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.1066+50A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787519 | ||||||
chr7:102787729
|
C | A | 1 | a0002c0002t0004g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1066+260C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787729 | ||||||
chr7:102787983
|
GAGAC | G | 5 | a0002c0002t0001g0025a0002c0002t0001g0236a0002c0002t0001g0237others(2): Show | 5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+518_1066+521d others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102787983 | |||||
chr7:102787988
|
A | T | 5 | a0002c0002t0001g0025a0002c0002t0001g0236a0002c0002t0001g0237others(2): Show | 5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+519A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787988 | ||||||
chr7:102787998
|
T | A | 6 | a0001c0001t0001g0132a0002c0002t0001g0217a0002c0002t0001g0218others(3): Show | 6 | HG01934.hp1 HG02071.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066+529T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102787998 | ||||||
chr7:102788050
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1066+581C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788050 | ||||||
chr7:102788126
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1066+657G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788126 | ||||||
chr7:102788365
|
C | T | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+896C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788365 | ||||||
chr7:102788657
|
G | C | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1066+1188G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788657 | ||||||
chr7:102788681
|
T | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 11 | HG02109.hp2 HG02572.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.1066+1212T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788681 | ||||||
chr7:102788811
|
C | G | 2 | a0002c0002t0001g0234a0002c0002t0004g0235 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+1342C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788811 | ||||||
chr7:102788822
|
G | T | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1066+1353G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788822 | ||||||
chr7:102788841
|
C | T | 217 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(214): Show | 241 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1066+1372C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102788841 | ||||||
chr7:102788943
|
T | TA | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+1475dupA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102788943 | |||||
chr7:102789008
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1066+1539G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789008 | ||||||
chr7:102789168
|
A | G | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+1699A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789168 | ||||||
chr7:102789257
|
T | C | 221 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0019others(218): Show | 245 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1066+1788T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789257 | ||||||
chr7:102789272
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1066+1803G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789272 | ||||||
chr7:102789274
|
T | G | 222 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0019others(219): Show | 246 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.1066+1805T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789274 | ||||||
chr7:102789276
|
T | C | 221 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0019others(218): Show | 245 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.1066+1807T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789276 | ||||||
chr7:102789453
|
A | C | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+1984A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789453 | ||||||
chr7:102789566
|
G | A | 6 | a0001c0001t0001g0034a0001c0001t0001g0208a0001c0001t0001g0246others(3): Show | 6 | HG02083.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1066+2097G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789566 | ||||||
chr7:102789570
|
G | A | 1 | a0001c0001t0003g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1066+2101G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789570 | ||||||
chr7:102789704
|
C | T | 33 | a0001c0001t0001g0115a0001c0001t0001g0307a0001c0001t0002g0012others(30): Show | 38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1066+2235C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789704 | ||||||
chr7:102789997
|
G | A | 33 | a0001c0001t0001g0115a0001c0001t0001g0307a0001c0001t0002g0012others(30): Show | 38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1066+2528G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102789997 | ||||||
chr7:102790020
|
G | A | 11 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0001g0246others(8): Show | 12 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1066+2551G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790020 | ||||||
chr7:102790075
|
G | T | 132 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(129): Show | 146 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.1066+2606G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790075 | ||||||
chr7:102790316
|
A | T | 2 | a0004c0004t0001g0289a0004c0004t0001g0297 | 2 | HG00099.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1066+2847A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790316 | ||||||
chr7:102790375
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1066+2906C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790375 | ||||||
chr7:102790401
|
G | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0307 | 2 | NA18984.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1066+2932G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102790401 | ||||||
chr7:102791021
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1066+3552A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791021 | ||||||
chr7:102791296
|
AAAC | A | 7 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(4): Show | 7 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1066+3831_1066+383 others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102791296 | |||||
chr7:102791318
|
G | T | 1 | a0001c0001t0001g0135 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1066+3849G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791318 | ||||||
chr7:102791729
|
C | T | 53 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(50): Show | 62 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.1066+4260C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791729 | ||||||
chr7:102791892
|
G | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1066+4423G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102791892 | ||||||
chr7:102792065
|
A | G | 214 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(211): Show | 238 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.1066+4596A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792065 | ||||||
chr7:102792178
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1066+4709A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792178 | ||||||
chr7:102792345
|
T | C | 1 | a0001c0001t0003g0007 | 3 | NA18973.hp1 NA19010.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1066+4876T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792345 | ||||||
chr7:102792556
|
AG | A | 130 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(127): Show | 144 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1066+5089delG | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102792556 | |||||
chr7:102792631
|
A | G | 6 | a0001c0001t0001g0011a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1066+5162A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792631 | ||||||
chr7:102792643
|
C | T | 3 | a0003c0003t0001g0083a0003c0003t0001g0133a0003c0003t0001g0143 | 3 | HG01106.hp2 HG01123.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1066+5174C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792643 | ||||||
chr7:102792925
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG02896.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066+5456A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792925 | ||||||
chr7:102792950
|
G | A | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1066+5481G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102792950 | ||||||
chr7:102793057
|
C | G | 3 | a0001c0001t0001g0208a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1066+5588C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793057 | ||||||
chr7:102793200
|
GT | G | 205 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(202): Show | 229 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.1066+5741delT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102793200 | |||||
chr7:102793208
|
T | G | 100 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(97): Show | 118 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1066+5739T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793208 | ||||||
chr7:102793231
|
A | G | 67 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0039others(64): Show | 76 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.1066+5762A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793231 | ||||||
chr7:102793400
|
C | T | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+5931C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793400 | ||||||
chr7:102793414
|
A | T | 1 | a0001c0001t0001g0197 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1066+5945A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793414 | ||||||
chr7:102793488
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1066+6019C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793488 | ||||||
chr7:102793715
|
A | AT | 4 | a0001c0001t0002g0031a0001c0001t0002g0302a0001c0001t0002g0303others(1): Show | 5 | NA18956.hp1 NA18979.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.1066+6253dupT | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102793715 | |||||
chr7:102793761
|
G | A | 33 | a0001c0001t0001g0115a0001c0001t0001g0307a0001c0001t0002g0012others(30): Show | 38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1066+6292G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793761 | ||||||
chr7:102793771
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1066+6302G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793771 | ||||||
chr7:102793952
|
A | T | 30 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0092others(27): Show | 31 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1066+6483A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102793952 | ||||||
chr7:102794035
|
C | CA | 152 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0034others(149): Show | 167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1066+6590dupA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102794035 | |||||
chr7:102794035
|
C | CAA | 14 | a0001c0001t0001g0040a0001c0001t0001g0084a0001c0001t0001g0092others(11): Show | 14 | HG00544.hp2 HG02148.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1066+6589_1066+659 others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102794035 | |||||
chr7:102794035
|
CA | C | 13 | a0001c0001t0001g0006a0001c0001t0001g0085a0001c0001t0001g0086others(10): Show | 15 | HG00140.hp2 HG00323.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1066+6590delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102794035 | |||||
chr7:102794100
|
C | T | 1 | a0004c0004t0001g0284 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1066+6631C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794100 | ||||||
chr7:102794127
|
A | C | 1 | a0001c0001t0002g0322 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1066+6658A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794127 | ||||||
chr7:102794365
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0053 | 2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1066+6896C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794365 | ||||||
chr7:102794593
|
T | A | 1 | a0003c0003t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1066+7124T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794593 | ||||||
chr7:102794661
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1066+7192G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794661 | ||||||
chr7:102794677
|
A | G | 4 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(1): Show | 4 | HG02896.hp1 HG02970.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1066+7208A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794677 | ||||||
chr7:102794708
|
C | T | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1066+7239C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794708 | ||||||
chr7:102794821
|
C | T | 1 | a0003c0003t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1066+7352C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102794821 | ||||||
chr7:102795001
|
G | A | 131 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(128): Show | 145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1066+7532G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795001 | ||||||
chr7:102795145
|
A | G | 1 | a0001c0001t0002g0322 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1066+7676A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795145 | ||||||
chr7:102795149
|
G | A | 93 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(90): Show | 102 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1066+7680G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795149 | ||||||
chr7:102795557
|
A | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0280 | 2 | HG02809.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1066+8088A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795557 | ||||||
chr7:102795611
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0251 | 3 | NA18942.hp1 NA18962.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1066+8142G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795611 | ||||||
chr7:102795870
|
T | C | 217 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(214): Show | 241 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.1066+8401T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102795870 | ||||||
chr7:102796243
|
A | G | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1066+8774A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796243 | ||||||
chr7:102796404
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1066+8935A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796404 | ||||||
chr7:102796460
|
G | A | 213 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(210): Show | 237 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1066+8991G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796460 | ||||||
chr7:102796818
|
G | A | 212 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(209): Show | 236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1066+9349G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796818 | ||||||
chr7:102796888
|
C | T | 1 | a0002c0002t0001g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1066+9419C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102796888 | ||||||
chr7:102797035
|
T | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG02896.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1066+9566T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797035 | ||||||
chr7:102797134
|
G | A | 16 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0060others(13): Show | 18 | HG00621.hp2 HG01891.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.1066+9665G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797134 | ||||||
chr7:102797448
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG02083.hp1 HG02132.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066+9979C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797448 | ||||||
chr7:102797734
|
A | G | 1 | a0001c0001t0004g0256 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1066+10265A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102797734 | ||||||
chr7:102798150
|
A | G | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-10140A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798150 | ||||||
chr7:102798187
|
CAG | C | 3 | a0003c0003t0001g0144a0003c0003t0001g0145a0003c0003t0001g0151 | 3 | HG01258.hp2 HG01433.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1067-10102_1067-10 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798187 | ||||||
chr7:102798212
|
G | T | 6 | a0001c0001t0001g0011a0001c0001t0001g0279a0001c0001t0001g0280others(3): Show | 8 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067-10078G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798212 | ||||||
chr7:102798242
|
C | A | 3 | a0003c0003t0001g0018a0003c0003t0001g0065a0003c0003t0001g0134 | 4 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-10048C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798242 | ||||||
chr7:102798258
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1067-10032A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798258 | ||||||
chr7:102798360
|
A | G | 1 | a0003c0003t0001g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1067-9930A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798360 | ||||||
chr7:102798415
|
A | G | 1 | a0001c0001t0004g0260 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1067-9875A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798415 | ||||||
chr7:102798439
|
T | C | 1 | a0002c0002t0001g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1067-9851T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798439 | ||||||
chr7:102798458
|
G | T | 213 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(210): Show | 237 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1067-9832G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798458 | ||||||
chr7:102798459
|
C | G | 213 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(210): Show | 237 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1067-9831C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798459 | ||||||
chr7:102798500
|
G | C | 135 | a0001c0001t0001g0019a0001c0001t0001g0043a0001c0001t0001g0044others(132): Show | 149 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1067-9790G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798500 | ||||||
chr7:102798667
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1067-9623G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798667 | ||||||
chr7:102798784
|
G | A | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-9506G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798784 | ||||||
chr7:102798840
|
T | C | 216 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(213): Show | 240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1067-9450T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798840 | ||||||
chr7:102798979
|
G | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-9311G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102798979 | ||||||
chr7:102799037
|
C | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-9253C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799037 | ||||||
chr7:102799100
|
A | C | 212 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(209): Show | 236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-9190A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799100 | ||||||
chr7:102799175
|
G | T | 149 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0039others(146): Show | 164 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1067-9115G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799175 | ||||||
chr7:102799270
|
G | A | 33 | a0001c0001t0001g0115a0001c0001t0001g0307a0001c0001t0002g0012others(30): Show | 38 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1067-9020G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799270 | ||||||
chr7:102799409
|
A | G | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-8881A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799409 | ||||||
chr7:102799594
|
G | A | 147 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0039others(144): Show | 162 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1067-8696G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799594 | ||||||
chr7:102799737
|
T | C | 223 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0020others(220): Show | 249 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1067-8553T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102799737 | ||||||
chr7:102800001
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1067-8289A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800001 | ||||||
chr7:102800149
|
T | C | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1067-8141T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800149 | ||||||
chr7:102800397
|
T | C | 168 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(165): Show | 185 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1067-7893T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800397 | ||||||
chr7:102800467
|
C | T | 44 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0053others(41): Show | 51 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1067-7823C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800467 | ||||||
chr7:102800528
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1067-7762G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800528 | ||||||
chr7:102800549
|
A | G | 1 | a0002c0002t0004g0235 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1067-7741A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800549 | ||||||
chr7:102800644
|
TA | T | 19 | a0001c0001t0001g0084a0001c0001t0001g0104a0001c0001t0001g0105others(16): Show | 21 | HG00408.hp1 HG01934.hp1 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.1067-7644delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102800644 | |||||
chr7:102800653
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041 | 3 | HG02970.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1067-7637G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800653 | ||||||
chr7:102800715
|
C | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1067-7575C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800715 | ||||||
chr7:102800733
|
G | T | 222 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0019others(219): Show | 248 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.1067-7557G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800733 | ||||||
chr7:102800923
|
C | T | 1 | a0003c0003t0001g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1067-7367C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102800923 | ||||||
chr7:102801089
|
C | T | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1067-7201C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801089 | ||||||
chr7:102801124
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1067-7166G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801124 | ||||||
chr7:102801319
|
T | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0009g0205 | 3 | HG01496.hp2 NA18975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1067-6971T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801319 | ||||||
chr7:102801489
|
G | T | 28 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0092others(25): Show | 29 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1067-6801G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801489 | ||||||
chr7:102801497
|
C | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0159a0001c0001t0001g0160 | 3 | HG03491.hp1 HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1067-6793C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801497 | ||||||
chr7:102801726
|
G | A | 213 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(210): Show | 237 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1067-6564G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801726 | ||||||
chr7:102801743
|
G | T | 1 | a0001c0001t0001g0068 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1067-6547G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801743 | ||||||
chr7:102801785
|
C | T | 2 | a0001c0001t0001g0167a0001c0001t0001g0181 | 2 | HG04199.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1067-6505C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801785 | ||||||
chr7:102801818
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0004g0256others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067-6472G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801818 | ||||||
chr7:102801848
|
G | C | 3 | a0003c0003t0001g0018a0003c0003t0001g0065a0003c0003t0001g0134 | 4 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-6442G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801848 | ||||||
chr7:102801853
|
C | G | 1 | a0001c0001t0003g0096 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1067-6437C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102801853 | ||||||
chr7:102801921
|
CA | C | 184 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(181): Show | 207 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.1067-6354delA | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102801921 | |||||
chr7:102801921
|
CAA | C | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-6355_1067-635 others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102801921 | |||||
chr7:102802172
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG02896.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1067-6118A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802172 | ||||||
chr7:102802177
|
T | C | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-6113T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802177 | ||||||
chr7:102802282
|
A | G | 42 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0001g0074others(39): Show | 49 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.1067-6008A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802282 | ||||||
chr7:102802403
|
C | A | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1067-5887C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802403 | ||||||
chr7:102802499
|
A | G | 1 | a0004c0004t0001g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1067-5791A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102802499 | ||||||
chr7:102802721
|
G | GAAAC | 153 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(150): Show | 169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1067-5557_1067-555 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102802721 | |||||
chr7:102803026
|
T | C | 1 | a0003c0003t0001g0151 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1067-5264T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803026 | ||||||
chr7:102803045
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1067-5245T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803045 | ||||||
chr7:102803093
|
AC | A | 2 | a0003c0003t0001g0027a0003c0003t0001g0270 | 3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1067-5195delC | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102803093 | |||||
chr7:102803141
|
G | A | 8 | a0001c0001t0001g0042a0001c0001t0001g0053a0001c0001t0004g0256others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1067-5149G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803141 | ||||||
chr7:102803242
|
A | C | 153 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(150): Show | 169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1067-5048A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803242 | ||||||
chr7:102803248
|
A | G | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-5042A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803248 | ||||||
chr7:102803358
|
G | C | 3 | a0003c0003t0001g0018a0003c0003t0001g0065a0003c0003t0001g0134 | 4 | HG01074.hp2 HG01081.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-4932G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803358 | ||||||
chr7:102803668
|
A | G | 1 | a0001c0001t0004g0257 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1067-4622A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803668 | ||||||
chr7:102803706
|
A | AAAGG | 212 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(209): Show | 236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-4583_1067-458 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102803706 | |||||
chr7:102803726
|
A | C | 1 | a0001c0001t0001g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1067-4564A>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803726 | ||||||
chr7:102803777
|
A | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0138others(1): Show | 4 | HG02622.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1067-4513A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102803777 | ||||||
chr7:102804078
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1067-4212G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804078 | ||||||
chr7:102804095
|
A | G | 150 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(147): Show | 166 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1067-4195A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804095 | ||||||
chr7:102804285
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1067-4005C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804285 | ||||||
chr7:102804376
|
C | T | 27 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0092others(24): Show | 28 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1067-3914C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804376 | ||||||
chr7:102804536
|
G | T | 3 | a0001c0001t0002g0301a0001c0001t0002g0309a0001c0001t0002g0310 | 3 | NA18971.hp1 NA19004.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1067-3754G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804536 | ||||||
chr7:102804611
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1067-3679A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804611 | ||||||
chr7:102804711
|
T | C | 30 | a0001c0001t0003g0007a0001c0001t0003g0014a0001c0001t0003g0015others(27): Show | 35 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1067-3579T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102804711 | ||||||
chr7:102805000
|
G | T | 2 | a0003c0003t0001g0027a0003c0003t0001g0270 | 3 | HG00323.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1067-3290G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805000 | ||||||
chr7:102805151
|
A | G | 2 | a0001c0001t0006g0045a0001c0001t0006g0046 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1067-3139A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805151 | ||||||
chr7:102805324
|
T | C | 1 | a0003c0003t0001g0130 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1067-2966T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805324 | ||||||
chr7:102805345
|
C | T | 1 | a0002c0002t0001g0228 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1067-2945C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805345 | ||||||
chr7:102805381
|
T | G | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-2909T>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805381 | ||||||
chr7:102805383
|
A | G | 151 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(148): Show | 167 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1067-2907A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805383 | ||||||
chr7:102805424
|
T | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-2866T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805424 | ||||||
chr7:102805448
|
T | C | 46 | a0001c0001t0001g0042a0001c0001t0001g0047a0001c0001t0001g0053others(43): Show | 53 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.1067-2842T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805448 | ||||||
chr7:102805536
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1067-2754G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805536 | ||||||
chr7:102805617
|
C | T | 1 | a0001c0001t0005g0193 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1067-2673C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805617 | ||||||
chr7:102805677
|
T | C | 30 | a0001c0001t0003g0007a0001c0001t0003g0014a0001c0001t0003g0015others(27): Show | 35 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.1067-2613T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805677 | ||||||
chr7:102805725
|
G | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-2565G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805725 | ||||||
chr7:102805732
|
G | A | 2 | a0001c0001t0006g0045a0001c0001t0006g0046 | 2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1067-2558G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805732 | ||||||
chr7:102805832
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1067-2458A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102805832 | ||||||
chr7:102806027
|
G | C | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-2263G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806027 | ||||||
chr7:102806122
|
T | C | 212 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(209): Show | 236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-2168T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806122 | ||||||
chr7:102806124
|
ATTGTT | A | 5 | a0001c0001t0001g0013a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 6 | HG00621.hp2 HG02027.hp1 NA18940.hp2 others(3): Show |
intron_variant | MODIFIER | c.1067-2163_1067-215 others(9): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806124 | |||||
chr7:102806142
|
T | TTTG | 211 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(208): Show | 235 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.1067-2130_1067-212 others(7): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806142 | |||||
chr7:102806416
|
C | T | 212 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(209): Show | 236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-1874C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806416 | ||||||
chr7:102806561
|
G | GTTTT | 212 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(209): Show | 236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-1728_1067-172 others(8): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806561 | |||||
chr7:102806577
|
A | G | 1 | a0008c0007t0007g0200 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1067-1713A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806577 | ||||||
chr7:102806609
|
T | C | 212 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(209): Show | 236 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.1067-1681T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806609 | ||||||
chr7:102806625
|
TTC | T | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-1663_1067-166 others(6): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102806625 | |||||
chr7:102806643
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1067-1647G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806643 | ||||||
chr7:102806692
|
C | T | 2 | a0002c0002t0001g0221a0002c0002t0001g0223 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1067-1598C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806692 | ||||||
chr7:102806708
|
T | C | 6 | a0001c0001t0001g0026a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 7 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1067-1582T>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806708 | ||||||
chr7:102806719
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1067-1571C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806719 | ||||||
chr7:102806884
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1067-1406C>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806884 | ||||||
chr7:102806894
|
G | A | 82 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(79): Show | 93 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.1067-1396G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102806894 | ||||||
chr7:102807025
|
C | T | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-1265C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807025 | ||||||
chr7:102807026
|
A | G | 15 | a0001c0001t0001g0026a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 16 | HG02572.hp1 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.1067-1264A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807026 | ||||||
chr7:102807069
|
C | T | 1 | a0001c0001t0003g0120 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1067-1221C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807069 | ||||||
chr7:102807170
|
A | G | 3 | a0001c0001t0001g0048a0002c0002t0001g0234a0002c0002t0004g0235 | 3 | HG03195.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1067-1120A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807170 | ||||||
chr7:102807270
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1067-1020G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807270 | ||||||
chr7:102807339
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1067-951A>G | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807339 | ||||||
chr7:102807544
|
TC | T | 32 | a0001c0001t0002g0012a0001c0001t0002g0030a0001c0001t0002g0031others(29): Show | 37 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1067-745delC | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807544 | ||||||
chr7:102807545
|
C | A | 2 | a0001c0001t0001g0196a0001c0001t0001g0197 | 2 | HG02630.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1067-745C>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807545 | ||||||
chr7:102807710
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0262 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1067-580G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807710 | ||||||
chr7:102807744
|
T | A | 2 | a0001c0001t0001g0048a0002c0002t0001g0234 | 2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1067-546T>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807744 | ||||||
chr7:102807750
|
TAA | T | 117 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(114): Show | 132 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.1067-524_1067-523d others(4): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102807750 | |||||
chr7:102807750
|
TAAA | T | 29 | a0001c0001t0001g0047a0001c0001t0001g0077a0001c0001t0001g0078others(26): Show | 30 | HG00140.hp1 HG00597.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1067-525_1067-523d others(5): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr7 | 102807750 | |||||
chr7:102807751
|
A | T | 34 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0138others(31): Show | 41 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.1067-539A>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807751 | ||||||
chr7:102807781
|
GGGCGTGG others(25): Show |
G | 1 | a0001c0001t0003g0111 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1067-508_1067-477d others(34): Show |
FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807781 | ||||||
chr7:102807830
|
G | T | 5 | a0002c0002t0001g0025a0002c0002t0001g0236a0002c0002t0001g0237others(2): Show | 5 | HG01106.hp1 HG02109.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1067-460G>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807830 | ||||||
chr7:102807932
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1067-358G>A | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102807932 | ||||||
chr7:102808008
|
C | T | 32 | a0001c0001t0001g0074a0001c0001t0001g0135a0001c0001t0001g0138others(29): Show | 39 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.1067-282C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102808008 | ||||||
chr7:102808024
|
G | C | 1 | a0002c0002t0001g0234 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1067-266G>C | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102808024 | ||||||
chr7:102808217
|
C | T | 152 | a0001c0001t0001g0013a0001c0001t0001g0019a0001c0001t0001g0023others(149): Show | 168 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1067-73C>T | FAM185A | ENSG00000222011.9 | transcript | ENST00000413034.3 | protein_coding | 7/7 | chr7 | 102808217 |