geneid | 150864 |
---|---|
ensemblid | ENSG00000138439.12 |
hgncid | 14440 |
symbol | FAM117B |
name | family with sequence similarity 117 member B |
refseq_nuc | NM_173511.4 |
refseq_prot | NP_775782.2 |
ensembl_nuc | ENST00000392238.3 |
ensembl_prot | ENSP00000376071.2 |
mane_status | MANE Select |
chr | chr2 |
start | 202634969 |
end | 202769757 |
strand | + |
ver | v1.2 |
region | chr2:202634969-202769757 |
region5000 | chr2:202629969-202774757 |
regionname0 | FAM117B_chr2_202634969_202769757 |
regionname5000 | FAM117B_chr2_202629969_202774757 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 589 | 279 | 48 | 59 | 124 | 6 | 40 | 90 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002 | 0/0 | 590 | 30 | 25 | 5 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0003 | 0/0 | 591 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1770 | 272 | 46 | 55 | 123 | 6 | 40 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
c0002 | 0/0 | 1773 | 29 | 24 | 5 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
c0003 | 0/0 | 1776 | 9 | 9 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
c0004 | 0/0 | 1770 | 4 | 0 | 4 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
c0005 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
c0006 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
c0007 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
c0008 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4213 | 33 | 2 | 9 | 17 | 1 | 4 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0002 | 0/0 | 4212 | 17 | 0 | 3 | 12 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0003 | 0/0 | 4200 | 9 | 5 | 4 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0004 | 1/0 | 4213 | 9 | 0 | 1 | 4 | 0 | 3 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0005 | 0/0 | 4215 | 8 | 1 | 3 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0006 | 0/0 | 4212 | 6 | 4 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0007 | 0/0 | 4211 | 6 | 1 | 1 | 3 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0008 | 0/0 | 4209 | 6 | 1 | 3 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0009 | 0/0 | 4211 | 5 | 3 | 0 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0010 | 0/0 | 4207 | 5 | 5 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0011 | 0/0 | 4209 | 5 | 0 | 1 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0012 | 0/0 | 4214 | 5 | 0 | 0 | 3 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0013 | 0/1 | 4209 | 5 | 0 | 2 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0014 | 0/0 | 4215 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0015 | 0/0 | 4210 | 4 | 0 | 2 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0016 | 0/0 | 4210 | 4 | 3 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0017 | 0/0 | 4214 | 4 | 0 | 3 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0018 | 0/0 | 4215 | 4 | 0 | 2 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0019 | 0/0 | 4212 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0020 | 0/0 | 4215 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0021 | 0/0 | 4213 | 4 | 0 | 0 | 2 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0022 | 0/0 | 4211 | 4 | 0 | 1 | 1 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0023 | 0/0 | 4211 | 4 | 0 | 2 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0024 | 0/0 | 4204 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0025 | 0/0 | 4222 | 3 | 1 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0026 | 0/0 | 4214 | 3 | 0 | 0 | 1 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0027 | 0/0 | 4212 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0028 | 0/0 | 4209 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0029 | 0/0 | 4204 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0030 | 0/0 | 4203 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0031 | 0/0 | 4229 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0032 | 0/0 | 4213 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0033 | 0/0 | 4192 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0034 | 0/0 | 4219 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0035 | 0/0 | 4216 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0036 | 0/0 | 4214 | 2 | 1 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0037 | 0/0 | 4226 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0038 | 0/0 | 4220 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0039 | 0/0 | 4211 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0040 | 0/0 | 4212 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0041 | 0/0 | 4211 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0042 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0043 | 0/0 | 4216 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0044 | 0/0 | 4214 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0045 | 0/0 | 4209 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0046 | 0/0 | 4209 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0047 | 0/0 | 4203 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0048 | 0/0 | 4207 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0049 | 0/0 | 4205 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0050 | 0/0 | 4208 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0051 | 0/0 | 4186 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0052 | 0/0 | 4221 | 2 | 0 | 0 | 1 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0053 | 0/0 | 4216 | 2 | 0 | 1 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0054 | 0/0 | 4211 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0055 | 0/0 | 4207 | 2 | 0 | 1 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0056 | 0/0 | 4215 | 2 | 0 | 1 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0057 | 0/0 | 4229 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0058 | 0/0 | 4227 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0059 | 0/0 | 4223 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0060 | 0/0 | 4203 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0061 | 0/0 | 4216 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0062 | 0/0 | 4217 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0063 | 0/0 | 4205 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0064 | 0/0 | 4229 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0065 | 0/0 | 4230 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0066 | 0/0 | 4228 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0067 | 0/0 | 4224 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0068 | 0/0 | 4225 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0069 | 0/0 | 4221 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0070 | 0/0 | 4223 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0071 | 0/0 | 4216 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0072 | 0/0 | 4219 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0073 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0074 | 0/0 | 4217 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0075 | 0/0 | 4218 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0076 | 0/0 | 4213 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0077 | 0/0 | 4212 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0078 | 0/0 | 4213 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0079 | 0/0 | 4214 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0080 | 0/0 | 4215 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0081 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0082 | 0/0 | 4215 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0083 | 0/0 | 4214 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0084 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0085 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0086 | 0/0 | 4213 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0087 | 0/0 | 4206 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0088 | 0/0 | 4204 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0089 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0090 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0091 | 0/0 | 4221 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0092 | 0/0 | 4213 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0093 | 0/0 | 4216 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0094 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0095 | 0/0 | 4207 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0096 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0097 | 0/0 | 4210 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0098 | 0/0 | 4211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0099 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0100 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0101 | 0/0 | 4208 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0102 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0103 | 0/0 | 4210 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0104 | 0/0 | 4205 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0105 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0106 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0107 | 0/0 | 4200 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0108 | 0/0 | 4211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0109 | 0/0 | 4563 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0110 | 0/0 | 4211 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0111 | 0/0 | 4223 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0112 | 0/0 | 4217 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0113 | 0/0 | 4219 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0114 | 0/0 | 4213 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0115 | 0/0 | 4214 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0116 | 0/0 | 4214 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0117 | 0/0 | 4214 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0118 | 0/0 | 4210 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0119 | 0/0 | 4211 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0120 | 0/0 | 4218 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0121 | 0/0 | 4209 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0122 | 0/0 | 4211 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0123 | 0/0 | 4203 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0124 | 0/0 | 4207 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0125 | 0/0 | 4197 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0126 | 0/0 | 4194 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0127 | 0/0 | 4191 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0128 | 0/0 | 4232 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0129 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0130 | 0/0 | 4215 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0131 | 0/0 | 4218 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0132 | 0/0 | 4214 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0133 | 0/0 | 4210 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0134 | 0/0 | 4207 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0135 | 0/0 | 4207 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0136 | 0/0 | 4205 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0137 | 0/0 | 4211 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0138 | 0/0 | 4215 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
t0139 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
g0318 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1770 | 272 | 46 | 55 | 123 | 6 | 40 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0004 | 0/0 | 1770 | 4 | 0 | 4 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0006 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0007 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0008 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002 | 0/0 | 1773 | 29 | 24 | 5 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0005 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0003c0003 | 0/0 | 1776 | 9 | 9 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5982 | 33 | 2 | 9 | 17 | 1 | 4 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0002 | 0/0 | 5981 | 17 | 0 | 3 | 12 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0004 | 1/0 | 5982 | 9 | 0 | 1 | 4 | 0 | 3 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0005 | 0/0 | 5984 | 8 | 1 | 3 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0006 | 0/0 | 5981 | 5 | 3 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0007 | 0/0 | 5980 | 6 | 1 | 1 | 3 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0008 | 0/0 | 5978 | 6 | 1 | 3 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0009 | 0/0 | 5980 | 5 | 3 | 0 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0011 | 0/0 | 5978 | 5 | 0 | 1 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0012 | 0/0 | 5983 | 5 | 0 | 0 | 3 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0013 | 0/1 | 5978 | 5 | 0 | 2 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0014 | 0/0 | 5984 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0015 | 0/0 | 5979 | 4 | 0 | 2 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0017 | 0/0 | 5983 | 4 | 0 | 3 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0018 | 0/0 | 5984 | 4 | 0 | 2 | 0 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0019 | 0/0 | 5981 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0020 | 0/0 | 5984 | 4 | 0 | 0 | 4 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0021 | 0/0 | 5982 | 4 | 0 | 0 | 2 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0022 | 0/0 | 5980 | 4 | 0 | 1 | 1 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0023 | 0/0 | 5980 | 4 | 0 | 2 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0025 | 0/0 | 5991 | 3 | 1 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0026 | 0/0 | 5983 | 3 | 0 | 0 | 1 | 0 | 2 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0027 | 0/0 | 5981 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0028 | 0/0 | 5978 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0029 | 0/0 | 5973 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0030 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0031 | 0/0 | 5998 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0032 | 0/0 | 5982 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0033 | 0/0 | 5961 | 3 | 0 | 0 | 3 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0034 | 0/0 | 5988 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0035 | 0/0 | 5985 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0036 | 0/0 | 5983 | 2 | 1 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0038 | 0/0 | 5989 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0039 | 0/0 | 5980 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0040 | 0/0 | 5981 | 2 | 0 | 0 | 0 | 1 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0041 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0042 | 0/0 | 5982 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0043 | 0/0 | 5985 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0044 | 0/0 | 5983 | 2 | 0 | 0 | 1 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0045 | 0/0 | 5978 | 2 | 1 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0046 | 0/0 | 5978 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0047 | 0/0 | 5972 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0048 | 0/0 | 5976 | 2 | 0 | 0 | 2 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0049 | 0/0 | 5974 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0050 | 0/0 | 5977 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0052 | 0/0 | 5990 | 2 | 0 | 0 | 1 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0053 | 0/0 | 5985 | 2 | 0 | 1 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0054 | 0/0 | 5980 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0055 | 0/0 | 5976 | 2 | 0 | 1 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0056 | 0/0 | 5984 | 2 | 0 | 1 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0057 | 0/0 | 5998 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0058 | 0/0 | 5996 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0059 | 0/0 | 5992 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0060 | 0/0 | 5972 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0061 | 0/0 | 5985 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0062 | 0/0 | 5986 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0067 | 0/0 | 5993 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0068 | 0/0 | 5994 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0069 | 0/0 | 5990 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0070 | 0/0 | 5992 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0071 | 0/0 | 5985 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0072 | 0/0 | 5988 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0073 | 0/0 | 5982 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0074 | 0/0 | 5986 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0075 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0076 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0077 | 0/0 | 5981 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0078 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0079 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0080 | 0/0 | 5984 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0081 | 0/0 | 5984 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0082 | 0/0 | 5984 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0083 | 0/0 | 5983 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0084 | 0/0 | 5982 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0085 | 0/0 | 5982 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0086 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0087 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0088 | 0/0 | 5973 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0089 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0090 | 0/0 | 5961 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0091 | 0/0 | 5990 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0092 | 0/0 | 5982 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0093 | 0/0 | 5985 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0095 | 0/0 | 5976 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0101 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0102 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0103 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0110 | 0/0 | 5980 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0111 | 0/0 | 5992 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0112 | 0/0 | 5986 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0113 | 0/0 | 5988 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0114 | 0/0 | 5982 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0115 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0116 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0117 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0118 | 0/0 | 5979 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0119 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0120 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0121 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0122 | 0/0 | 5980 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0123 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0124 | 0/0 | 5976 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0125 | 0/0 | 5966 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0126 | 0/0 | 5963 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0127 | 0/0 | 5960 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0128 | 0/0 | 6001 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0130 | 0/0 | 5984 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0131 | 0/0 | 5987 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0132 | 0/0 | 5983 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0133 | 0/0 | 5979 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0134 | 0/0 | 5976 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0135 | 0/0 | 5976 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0136 | 0/0 | 5974 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0137 | 0/0 | 5980 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0138 | 0/0 | 5984 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0001t0139 | 0/0 | 5981 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0004t0037 | 0/0 | 5995 | 2 | 0 | 2 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0004t0065 | 0/0 | 5999 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0004t0066 | 0/0 | 5997 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0006t0129 | 0/0 | 5984 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0007t0106 | 0/0 | 5969 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0001c0008t0064 | 0/0 | 5998 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0003 | 0/0 | 5972 | 9 | 5 | 4 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0016 | 0/0 | 5982 | 3 | 2 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0024 | 0/0 | 5976 | 3 | 3 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0030 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0051 | 0/0 | 5958 | 2 | 2 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0063 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0096 | 0/0 | 5975 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0097 | 0/0 | 5982 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0098 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0099 | 0/0 | 5981 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0100 | 0/0 | 5980 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0104 | 0/0 | 5977 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0105 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0107 | 0/0 | 5972 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0108 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0002t0109 | 0/0 | 6335 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0002c0005t0016 | 0/0 | 5982 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0003c0003t0006 | 0/0 | 5987 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0003c0003t0010 | 0/0 | 5982 | 5 | 5 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0003c0003t0030 | 0/0 | 5978 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0003c0003t0041 | 0/0 | 5986 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
a0003c0003t0094 | 0/0 | 5983 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | copy fasta | chr2 | 202629969 | 202774757 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0004g0318 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0006g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0008g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0009g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0011g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0012g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0012g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0033 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0013g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0015g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0017g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0018g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0019g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0020g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0021g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0021g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0021g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0021g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0022g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0022g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0022g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0022g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0023g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0023g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0023g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0023g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0025g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0025g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0025g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0026g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0026g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0026g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0027g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0027g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0027g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0028g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0028g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0028g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0029g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0029g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0029g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0030g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0031g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0031g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0031g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0032g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0032g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0032g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0033g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0033g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0033g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0034g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0034g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0035g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0035g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0036g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0036g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0038g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0038g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0039g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0039g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0040g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0040g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0041g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0042g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0042g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0043g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0043g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0044g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0044g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0045g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0045g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0046g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0046g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0047g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0047g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0048g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0048g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0049g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0049g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0050g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0050g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0052g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0052g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0053g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0053g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0054g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0054g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0055g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0055g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0056g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0056g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0057g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0058g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0059g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0060g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0061g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0062g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0067g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0068g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0069g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0070g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0071g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0072g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0073g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0074g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0075g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0076g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0077g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0078g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0079g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0080g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0081g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0082g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0083g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0084g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0085g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0086g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0087g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0088g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0089g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0090g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0091g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0092g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0093g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0095g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0101g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0102g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0103g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0110g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0111g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0112g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0113g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0114g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0115g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0116g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0117g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0118g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0119g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0120g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0121g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0122g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0123g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0124g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0125g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0126g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0127g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0128g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0130g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0131g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0132g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0133g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0134g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0135g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0136g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0137g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0138g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0001t0139g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0037g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0037g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0065g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0004t0066g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0006t0129g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0007t0106g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0001c0008t0064g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0016g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0016g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0016g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0024g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0024g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0024g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0030g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0051g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0051g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0063g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0096g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0097g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0098g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0099g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0100g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0104g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0105g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0107g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0108g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0002t0109g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0002c0005t0016g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0010g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0030g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0041g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
a0003c0003t0094g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0038 | g0025 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00099 | hp2 | a0001 | c0001 | t0052 | g0159 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00140 | hp1 | a0001 | c0001 | t0056 | g0170 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00140 | hp2 | a0001 | c0001 | t0023 | g0049 | EUR | GBR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00323 | hp2 | a0001 | c0001 | t0040 | g0263 | EUR | FIN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00408 | hp1 | a0001 | c0001 | t0111 | g0122 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00544 | hp1 | a0001 | c0001 | t0117 | g0123 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00544 | hp2 | a0001 | c0001 | t0139 | g0028 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00558 | hp1 | a0001 | c0001 | t0007 | g0014 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00558 | hp2 | a0001 | c0001 | t0014 | g0275 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00597 | hp1 | a0001 | c0001 | t0074 | g0094 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00597 | hp2 | a0001 | c0001 | t0036 | g0271 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00609 | hp1 | a0001 | c0001 | t0138 | g0040 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00609 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00639 | hp1 | a0001 | c0001 | t0136 | g0037 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00639 | hp2 | a0001 | c0001 | t0095 | g0262 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00642 | hp1 | a0001 | c0001 | t0137 | g0032 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00673 | hp2 | a0001 | c0001 | t0017 | g0218 | EAS | CHS | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00733 | hp1 | a0002 | c0002 | t0003 | g0303 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00733 | hp2 | a0001 | c0001 | t0076 | g0264 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0043 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00738 | hp2 | a0001 | c0001 | t0018 | g0017 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG00741 | hp2 | a0001 | c0001 | t0013 | g0030 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01081 | hp2 | a0001 | c0001 | t0018 | g0016 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0042 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01099 | hp2 | a0001 | c0001 | t0092 | g0257 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01106 | hp1 | a0001 | c0001 | t0013 | g0046 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01106 | hp2 | a0001 | c0004 | t0066 | g0179 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0189 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0304 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01167 | hp1 | a0001 | c0001 | t0023 | g0044 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01167 | hp2 | a0001 | c0004 | t0037 | g0022 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01168 | hp1 | a0002 | c0002 | t0003 | g0301 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0010 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01169 | hp1 | a0002 | c0002 | t0003 | g0302 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01169 | hp2 | a0001 | c0004 | t0037 | g0023 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0074 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01192 | hp1 | a0001 | c0001 | t0022 | g0130 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0114 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01243 | hp1 | a0002 | c0002 | t0016 | g0295 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0096 | AMR | PUR | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01255 | hp1 | a0001 | c0001 | t0086 | g0142 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01256 | hp1 | a0001 | c0001 | t0054 | g0118 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01261 | hp1 | a0001 | c0001 | t0039 | g0260 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01261 | hp2 | a0001 | c0001 | t0110 | g0036 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01346 | hp1 | a0001 | c0001 | t0056 | g0169 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01346 | hp2 | a0001 | c0001 | t0078 | g0259 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01358 | hp1 | a0001 | c0001 | t0083 | g0156 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01358 | hp2 | a0001 | c0004 | t0065 | g0172 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01361 | hp1 | a0001 | c0001 | t0017 | g0206 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01433 | hp1 | a0001 | c0001 | t0023 | g0048 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01433 | hp2 | a0001 | c0001 | t0015 | g0180 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01496 | hp1 | a0001 | c0001 | t0082 | g0101 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0045 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01884 | hp1 | a0001 | c0001 | t0091 | g0265 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01884 | hp2 | a0002 | c0002 | t0024 | g0288 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01891 | hp1 | a0001 | c0001 | t0049 | g0269 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01891 | hp2 | a0001 | c0001 | t0025 | g0211 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01943 | hp1 | a0001 | c0001 | t0054 | g0008 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0019 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01952 | hp2 | a0001 | c0001 | t0045 | g0149 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0086 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01981 | hp1 | a0001 | c0001 | t0128 | g0099 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02055 | hp2 | a0001 | c0001 | t0041 | g0266 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02056 | hp1 | a0001 | c0001 | t0022 | g0031 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02071 | hp1 | a0001 | c0001 | t0011 | g0093 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02080 | hp1 | a0001 | c0001 | t0060 | g0278 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02080 | hp2 | a0001 | c0001 | t0075 | g0052 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02083 | hp1 | a0001 | c0001 | t0034 | g0277 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02083 | hp2 | a0001 | c0001 | t0031 | g0178 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02132 | hp1 | a0001 | c0001 | t0131 | g0041 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02132 | hp2 | a0001 | c0001 | t0032 | g0071 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02145 | hp1 | a0003 | c0003 | t0094 | g0248 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02145 | hp2 | a0001 | c0001 | t0062 | g0056 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02155 | hp1 | a0001 | c0001 | t0031 | g0063 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02165 | hp1 | a0001 | c0001 | t0072 | g0173 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CDX | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02257 | hp1 | a0001 | c0001 | t0035 | g0055 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02257 | hp2 | a0001 | c0001 | t0042 | g0003 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02258 | hp1 | a0002 | c0002 | t0099 | g0312 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02258 | hp2 | a0001 | c0001 | t0027 | g0252 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02273 | hp1 | a0001 | c0001 | t0017 | g0024 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02293 | hp1 | a0001 | c0001 | t0069 | g0089 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02293 | hp2 | a0001 | c0001 | t0055 | g0148 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02300 | hp1 | a0001 | c0001 | t0017 | g0198 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02300 | hp2 | a0001 | c0001 | t0053 | g0146 | AMR | PEL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02451 | hp1 | a0003 | c0003 | t0010 | g0246 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02451 | hp2 | a0002 | c0002 | t0105 | g0314 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02523 | hp1 | a0001 | c0001 | t0116 | g0100 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02523 | hp2 | a0001 | c0001 | t0025 | g0082 | EAS | KHV | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02572 | hp1 | a0002 | c0002 | t0003 | g0307 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0085 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02602 | hp2 | a0001 | c0001 | t0093 | g0243 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0070 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02615 | hp2 | a0002 | c0002 | t0109 | g0299 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02622 | hp1 | a0001 | c0001 | t0036 | g0147 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0002 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02683 | hp1 | a0001 | c0001 | t0022 | g0029 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02683 | hp2 | a0001 | c0001 | t0071 | g0212 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02698 | hp2 | a0001 | c0001 | t0040 | g0256 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02717 | hp1 | a0002 | c0002 | t0003 | g0310 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02717 | hp2 | a0003 | c0003 | t0010 | g0247 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02723 | hp1 | a0002 | c0002 | t0016 | g0300 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02723 | hp2 | a0001 | c0001 | t0102 | g0283 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02738 | hp1 | a0001 | c0001 | t0023 | g0047 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02818 | hp1 | a0002 | c0002 | t0107 | g0305 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02818 | hp2 | a0001 | c0001 | t0029 | g0137 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02886 | hp1 | a0002 | c0002 | t0100 | g0306 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02886 | hp2 | a0003 | c0003 | t0006 | g0072 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02895 | hp1 | a0002 | c0002 | t0051 | g0293 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02895 | hp2 | a0003 | c0003 | t0041 | g0227 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0309 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02896 | hp2 | a0003 | c0003 | t0010 | g0244 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02897 | hp1 | a0002 | c0002 | t0051 | g0313 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02897 | hp2 | a0003 | c0003 | t0010 | g0196 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02965 | hp1 | a0001 | c0001 | t0028 | g0076 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0250 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02970 | hp1 | a0002 | c0005 | t0016 | g0297 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02970 | hp2 | a0001 | c0008 | t0064 | g0134 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02976 | hp1 | a0001 | c0001 | t0087 | g0117 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02976 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03017 | hp1 | a0001 | c0001 | t0022 | g0035 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03017 | hp2 | a0001 | c0001 | t0122 | g0209 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03041 | hp1 | a0002 | c0002 | t0030 | g0292 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03041 | hp2 | a0001 | c0001 | t0029 | g0004 | AFR | GWD | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03098 | hp1 | a0001 | c0001 | t0030 | g0005 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03098 | hp2 | a0002 | c0002 | t0098 | g0316 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03130 | hp1 | a0001 | c0001 | t0119 | g0225 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03130 | hp2 | a0002 | c0002 | t0024 | g0289 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03139 | hp1 | a0001 | c0001 | t0045 | g0006 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03139 | hp2 | a0001 | c0001 | t0050 | g0285 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03195 | hp1 | a0001 | c0001 | t0047 | g0268 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03195 | hp2 | a0001 | c0001 | t0121 | g0226 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03209 | hp1 | a0002 | c0002 | t0108 | g0294 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03209 | hp2 | a0001 | c0001 | t0089 | g0107 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03225 | hp1 | a0001 | c0001 | t0073 | g0229 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03225 | hp2 | a0002 | c0002 | t0096 | g0317 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03453 | hp1 | a0001 | c0007 | t0106 | g0286 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0034 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03490 | hp2 | a0001 | c0001 | t0088 | g0261 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03491 | hp1 | a0001 | c0001 | t0021 | g0067 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03491 | hp2 | a0001 | c0001 | t0013 | g0050 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03492 | hp2 | a0001 | c0001 | t0013 | g0051 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03516 | hp1 | a0003 | c0003 | t0030 | g0245 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03516 | hp2 | a0002 | c0002 | t0063 | g0291 | AFR | ESN | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03579 | hp1 | a0003 | c0003 | t0010 | g0249 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0064 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03654 | hp1 | a0001 | c0001 | t0012 | g0223 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03654 | hp2 | a0001 | c0001 | t0021 | g0027 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03669 | hp1 | a0001 | c0001 | t0124 | g0208 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03669 | hp2 | a0001 | c0001 | t0009 | g0165 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0207 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03688 | hp2 | a0001 | c0001 | t0070 | g0231 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03704 | hp1 | a0001 | c0001 | t0009 | g0060 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03704 | hp2 | a0001 | c0001 | t0077 | g0026 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0106 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03710 | hp2 | a0001 | c0001 | t0012 | g0066 | SAS | PJL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03831 | hp1 | a0001 | c0001 | t0055 | g0161 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0115 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03927 | hp1 | a0001 | c0001 | t0130 | g0230 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03927 | hp2 | a0001 | c0001 | t0026 | g0168 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03942 | hp2 | a0001 | c0001 | t0018 | g0143 | SAS | BEB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04115 | hp1 | a0001 | c0001 | t0026 | g0186 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04115 | hp2 | a0001 | c0001 | t0114 | g0121 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04199 | hp1 | a0001 | c0001 | t0043 | g0109 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04199 | hp2 | a0001 | c0001 | t0038 | g0238 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04204 | hp2 | a0001 | c0001 | t0044 | g0098 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04228 | hp1 | a0001 | c0001 | t0018 | g0120 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG04228 | hp2 | a0001 | c0001 | t0080 | g0111 | SAS | STU | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18522 | hp1 | a0001 | c0001 | t0028 | g0001 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18747 | hp1 | a0001 | c0001 | t0115 | g0221 | EAS | CHB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18747 | hp2 | a0001 | c0001 | t0031 | g0084 | EAS | CHB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18906 | hp1 | a0002 | c0002 | t0016 | g0296 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18906 | hp2 | a0001 | c0001 | t0027 | g0136 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18939 | hp2 | a0001 | c0001 | t0014 | g0270 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18940 | hp1 | a0001 | c0001 | t0044 | g0110 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18940 | hp2 | a0001 | c0001 | t0015 | g0129 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18945 | hp1 | a0001 | c0001 | t0015 | g0282 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18946 | hp2 | a0001 | c0001 | t0021 | g0183 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18949 | hp1 | a0001 | c0006 | t0129 | g0187 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18949 | hp2 | a0001 | c0001 | t0020 | g0160 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18950 | hp1 | a0001 | c0001 | t0048 | g0233 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18950 | hp2 | a0001 | c0001 | t0120 | g0144 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18951 | hp1 | a0001 | c0001 | t0025 | g0113 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18952 | hp1 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18952 | hp2 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18954 | hp2 | a0001 | c0001 | t0079 | g0200 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18962 | hp2 | a0001 | c0001 | t0052 | g0077 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0073 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18964 | hp2 | a0001 | c0001 | t0020 | g0234 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18965 | hp1 | a0001 | c0001 | t0067 | g0219 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18965 | hp2 | a0001 | c0001 | t0019 | g0215 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18966 | hp2 | a0001 | c0001 | t0008 | g0150 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18969 | hp1 | a0001 | c0001 | t0125 | g0079 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18969 | hp2 | a0001 | c0001 | t0085 | g0013 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18970 | hp1 | a0001 | c0001 | t0046 | g0138 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18970 | hp2 | a0001 | c0001 | t0133 | g0039 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18972 | hp1 | a0001 | c0001 | t0032 | g0090 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18972 | hp2 | a0001 | c0001 | t0011 | g0177 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18974 | hp1 | a0001 | c0001 | t0058 | g0280 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18974 | hp2 | a0001 | c0001 | t0084 | g0018 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18977 | hp1 | a0001 | c0001 | t0019 | g0197 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18980 | hp1 | a0001 | c0001 | t0033 | g0083 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18981 | hp1 | a0001 | c0001 | t0068 | g0239 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18981 | hp2 | a0001 | c0001 | t0061 | g0276 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18983 | hp1 | a0001 | c0001 | t0014 | g0272 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18985 | hp1 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18985 | hp2 | a0001 | c0001 | t0020 | g0214 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18986 | hp2 | a0001 | c0001 | t0132 | g0237 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18988 | hp1 | a0001 | c0001 | t0112 | g0091 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18991 | hp1 | a0001 | c0001 | t0026 | g0192 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18991 | hp2 | a0001 | c0001 | t0043 | g0141 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18993 | hp1 | a0001 | c0001 | t0019 | g0188 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18993 | hp2 | a0001 | c0001 | t0021 | g0145 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18994 | hp1 | a0001 | c0001 | t0081 | g0128 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18999 | hp1 | a0001 | c0001 | t0090 | g0059 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19003 | hp1 | a0001 | c0001 | t0059 | g0279 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19004 | hp1 | a0001 | c0001 | t0057 | g0281 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19004 | hp2 | a0001 | c0001 | t0103 | g0133 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19009 | hp1 | a0001 | c0001 | t0126 | g0242 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19009 | hp2 | a0001 | c0001 | t0046 | g0139 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19010 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19010 | hp2 | a0001 | c0001 | t0033 | g0163 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19011 | hp1 | a0001 | c0001 | t0113 | g0125 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19030 | hp1 | a0002 | c0002 | t0104 | g0298 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19030 | hp2 | a0002 | c0002 | t0003 | g0311 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19043 | hp1 | a0001 | c0001 | t0035 | g0054 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19043 | hp2 | a0001 | c0001 | t0047 | g0267 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19058 | hp2 | a0001 | c0001 | t0048 | g0068 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19064 | hp1 | a0001 | c0001 | t0032 | g0241 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19064 | hp2 | a0001 | c0001 | t0012 | g0222 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19065 | hp1 | a0001 | c0001 | t0053 | g0119 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19070 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19070 | hp2 | a0001 | c0001 | t0019 | g0190 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19078 | hp1 | a0001 | c0001 | t0012 | g0164 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19078 | hp2 | a0001 | c0001 | t0127 | g0124 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19082 | hp1 | a0001 | c0001 | t0034 | g0274 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19082 | hp2 | a0001 | c0001 | t0134 | g0102 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19083 | hp1 | a0001 | c0001 | t0014 | g0273 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19083 | hp2 | a0001 | c0001 | t0020 | g0015 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19085 | hp1 | a0001 | c0001 | t0135 | g0235 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19085 | hp2 | a0001 | c0001 | t0011 | g0007 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19088 | hp1 | a0001 | c0001 | t0033 | g0078 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19240 | hp1 | a0001 | c0001 | t0049 | g0053 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | YRI | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG01123 | hp2 | a0001 | c0001 | t0118 | g0205 | AMR | CLM | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02109 | hp1 | a0001 | c0001 | t0101 | g0287 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02109 | hp2 | a0001 | c0001 | t0042 | g0153 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02559 | hp1 | a0001 | c0001 | t0123 | g0151 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG02559 | hp2 | a0002 | c0002 | t0003 | g0308 | AFR | ACB | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03471 | hp1 | a0002 | c0002 | t0097 | g0315 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG03471 | hp2 | a0001 | c0001 | t0027 | g0254 | AFR | MSL | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG06807 | hp1 | a0001 | c0001 | t0029 | g0112 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
HG06807 | hp2 | a0002 | c0002 | t0024 | g0290 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA20300 | hp1 | a0001 | c0001 | t0050 | g0284 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | USA | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA21309 | hp1 | a0001 | c0001 | t0039 | g0258 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
NA21309 | hp2 | a0001 | c0001 | t0009 | g0105 | AFR | LWK | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0013 | g0033 | REF | REF | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0318 | REF | REF | FAM117B_chr2_202629969_202774757 | FAM117B | chr2 | 202629969 | 202774757 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202635418
|
A | AGGC | 1 | a0002 | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
disruptive_inframe_insertion | MODERATE | c.246_248dupCGG | p.Gly83dup | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 468/5982 | 249/1770 | 83/589 | INFO_REALIGN_3_PRIME | chr2 | 202635418 | |
chr2:202635418
|
A | AGGCGGC | 1 | a0003 | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
disruptive_inframe_insertion | MODERATE | c.243_248dupCGGCGG | p.Gly82_Gly83dup | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 468/5982 | 249/1770 | 83/589 | INFO_REALIGN_3_PRIME | chr2 | 202635418 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202635226
|
G | A | 1 | a0001c0004 | 4 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
synonymous_variant | LOW | c.39G>A | p.Pro13Pro | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 258/5982 | 39/1770 | 13/589 | chr2 | 202635226 | ||
chr2:202695900
|
T | C | 1 | a0001c0006 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.621T>C | p.Pro207Pro | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/8 | 840/5982 | 621/1770 | 207/589 | chr2 | 202695900 | ||
chr2:202757305
|
G | A | 1 | a0001c0007 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1197G>A | p.Gly399Gly | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/8 | 1416/5982 | 1197/1770 | 399/589 | chr2 | 202757305 | ||
chr2:202757383
|
T | C | 1 | a0002c0005 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.1275T>C | p.Gly425Gly | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/8 | 1494/5982 | 1275/1770 | 425/589 | chr2 | 202757383 | ||
chr2:202759294
|
T | C | 1 | a0001c0008 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.1392T>C | p.Tyr464Tyr | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/8 | 1611/5982 | 1392/1770 | 464/589 | chr2 | 202759294 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202634993
|
G | GAGC | 10 | a0001c0001t0014a0001c0001t0034a0001c0001t0035others(7): Show | 16 | HG00558.hp2 HG00597.hp2 HG02080.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-194_-192dupAGC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 191 | INFO_REALIGN_3_PRIME | chr2 | 202634993 | ||||
chr2:202634994
|
AGCG | A | 19 | a0001c0001t0050a0001c0001t0101a0001c0001t0102others(16): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-173_-171delGGC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 171 | INFO_REALIGN_3_PRIME | chr2 | 202634994 | ||||
chr2:202634994
|
AGCGGCG | A | 14 | a0001c0001t0008a0001c0001t0013a0001c0001t0022others(11): Show | 29 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-176_-171delGGCGGC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 171 | INFO_REALIGN_3_PRIME | chr2 | 202634994 | ||||
chr2:202634997
|
G | A | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(64): Show | 174 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
5_prime_UTR_variant | MODIFIER | c.-191G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 191 | chr2 | 202634997 | |||||
chr2:202635000
|
G | A | 19 | a0001c0001t0050a0001c0001t0101a0001c0001t0102others(16): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-188G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 188 | chr2 | 202635000 | |||||
chr2:202635003
|
G | A | 1 | a0001c0001t0110 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-185G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 185 | chr2 | 202635003 | |||||
chr2:202635108
|
C | T | 1 | a0001c0001t0130 | 1 | HG03927.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-80C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | chr2 | 202635108 | ||||||
chr2:202635123
|
T | TC | 3 | a0002c0002t0024a0002c0002t0063a0002c0002t0096 | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-60dupC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 59 | INFO_REALIGN_3_PRIME | chr2 | 202635123 | ||||
chr2:202635160
|
C | A | 2 | a0002c0002t0097a0002c0002t0098 | 2 | HG03098.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-28C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 28 | chr2 | 202635160 | |||||
chr2:202635176
|
A | AG | 14 | a0001c0001t0012a0001c0001t0061a0001c0001t0062others(11): Show | 18 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-4dupG | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/8 | 3 | INFO_REALIGN_3_PRIME | chr2 | 202635176 | ||||
chr2:202765839
|
C | T | 2 | a0001c0001t0013a0001c0001t0056 | 7 | HG00140.hp1 HG00741.hp2 HG01106.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*75C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 75 | chr2 | 202765839 | |||||
chr2:202765975
|
A | G | 1 | a0001c0001t0091 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*211A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 211 | chr2 | 202765975 | |||||
chr2:202766025
|
A | G | 1 | a0001c0001t0137 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*261A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 261 | chr2 | 202766025 | |||||
chr2:202766061
|
A | AAC | 7 | a0001c0001t0017a0001c0001t0018a0001c0001t0026others(4): Show | 15 | HG00597.hp1 HG00673.hp2 HG00738.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*342_*343dupAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
A | AACAC | 7 | a0001c0001t0034a0001c0001t0053a0001c0001t0071others(4): Show | 9 | HG02083.hp1 HG02165.hp1 HG02300.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*340_*343dupACAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
A | AACACACA others(1): Show |
7 | a0001c0001t0038a0001c0001t0052a0001c0001t0059others(4): Show | 9 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*336_*343dupACACAC others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
A | AACACACA others(3): Show |
6 | a0001c0001t0025a0001c0001t0067a0001c0001t0068others(3): Show | 8 | HG00408.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*334_*343dupACACAC others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
A | AACACACA others(5): Show |
1 | a0001c0001t0058 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332_*343dupACACAC others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
A | AACACACA others(7): Show |
2 | a0001c0001t0057a0001c0004t0037 | 3 | HG01167.hp2 HG01169.hp2 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*330_*343dupACACAC others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
A | AACACACA others(9): Show |
2 | a0001c0001t0031a0001c0004t0066 | 4 | HG01106.hp2 HG02083.hp2 HG02155.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*328_*343dupACACAC others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
A | AACACACA others(11): Show |
3 | a0001c0001t0128a0001c0004t0065a0001c0008t0064 | 3 | HG01358.hp2 HG01981.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326_*343dupACACAC others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 344 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AAC | A | 21 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(18): Show | 74 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*342_*343delAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 342 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACAC | A | 7 | a0001c0001t0007a0001c0001t0028a0001c0001t0045others(4): Show | 19 | HG00558.hp1 HG01243.hp2 HG01952.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*340_*343delACAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 340 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACAC | A | 7 | a0001c0001t0011a0001c0001t0046a0001c0001t0055others(4): Show | 13 | HG00609.hp2 HG00639.hp2 HG01192.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*338_*343delACACAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 338 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACACA others(1): Show |
A | 12 | a0001c0001t0029a0001c0001t0047a0001c0001t0048others(9): Show | 18 | HG01884.hp2 HG02451.hp2 HG02559.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*336_*343delACACAC others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 336 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACACA others(3): Show |
A | 5 | a0001c0001t0030a0001c0001t0049a0002c0002t0003others(2): Show | 14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*334_*343delACACAC others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 334 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACACA others(5): Show |
A | 1 | a0001c0001t0060 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*332_*343delACACAC others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 332 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACACA others(9): Show |
A | 1 | a0001c0001t0125 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328_*343delACACAC others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 328 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACACA others(11): Show |
A | 1 | a0001c0001t0126 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326_*343delACACAC others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 326 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACACA others(13): Show |
A | 3 | a0001c0001t0033a0001c0001t0090a0001c0001t0127 | 5 | NA18980.hp1 NA18999.hp1 NA19010.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*324_*343delACACAC others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 324 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766061
|
AACACACA others(17): Show |
A | 1 | a0002c0002t0051 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*320_*343delACACAC others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 320 | INFO_REALIGN_3_PRIME | chr2 | 202766061 | ||||
chr2:202766102
|
A | ACACACC | 4 | a0001c0001t0022a0001c0001t0110a0001c0001t0137others(1): Show | 7 | HG00544.hp2 HG00642.hp1 HG01192.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*340_*345dupACACCC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 346 | INFO_REALIGN_3_PRIME | chr2 | 202766102 | ||||
chr2:202766102
|
A | ACACC | 4 | a0001c0001t0008a0001c0001t0013a0001c0001t0056others(1): Show | 14 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*341_*342insCCAC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 342 | INFO_REALIGN_3_PRIME | chr2 | 202766102 | ||||
chr2:202766102
|
A | ACC | 3 | a0001c0001t0023a0001c0001t0120a0001c0001t0135 | 6 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*339_*340insCC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 340 | INFO_REALIGN_3_PRIME | chr2 | 202766102 | ||||
chr2:202766102
|
A | C | 1 | a0001c0001t0136 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*338A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 338 | chr2 | 202766102 | |||||
chr2:202766180
|
A | T | 1 | a0001c0001t0086 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*416A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 416 | chr2 | 202766180 | |||||
chr2:202766636
|
G | A | 65 | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(62): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*872G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 872 | chr2 | 202766636 | |||||
chr2:202766645
|
C | T | 10 | a0001c0001t0041a0001c0001t0047a0001c0001t0073others(7): Show | 17 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*881C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 881 | chr2 | 202766645 | |||||
chr2:202766646
|
G | A | 1 | a0001c0001t0028 | 3 | HG02965.hp1 HG03579.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*882G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 882 | chr2 | 202766646 | |||||
chr2:202766722
|
T | C | 66 | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(63): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*958T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 958 | chr2 | 202766722 | |||||
chr2:202766724
|
C | T | 37 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(34): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*960C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 960 | chr2 | 202766724 | |||||
chr2:202766744
|
T | G | 1 | a0001c0008t0064 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 980 | chr2 | 202766744 | |||||
chr2:202766833
|
G | A | 37 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(34): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*1069G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1069 | chr2 | 202766833 | |||||
chr2:202766860
|
G | A | 1 | a0001c0001t0114 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1096G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1096 | chr2 | 202766860 | |||||
chr2:202766898
|
G | A | 1 | a0001c0001t0046 | 2 | NA18970.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1134G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1134 | chr2 | 202766898 | |||||
chr2:202766972
|
A | T | 1 | a0001c0001t0085 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1208A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1208 | chr2 | 202766972 | |||||
chr2:202767085
|
A | G | 1 | a0001c0001t0081 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1321A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1321 | chr2 | 202767085 | |||||
chr2:202767157
|
C | CT | 8 | a0001c0001t0006a0001c0001t0067a0001c0001t0102others(5): Show | 12 | HG00544.hp1 HG01168.hp2 HG01943.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1413dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1414 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | ||||
chr2:202767157
|
C | CTT | 27 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(24): Show | 91 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1412_*1413dupTT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1414 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | ||||
chr2:202767157
|
C | CTTT | 4 | a0001c0001t0043a0001c0001t0044a0001c0001t0075others(1): Show | 6 | HG02080.hp2 HG04199.hp1 HG04204.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1411_*1413dupTTT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1414 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | ||||
chr2:202767157
|
CT | C | 7 | a0001c0001t0027a0001c0001t0029a0001c0001t0053others(4): Show | 12 | HG01346.hp2 HG02258.hp1 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1413delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1413 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | ||||
chr2:202767157
|
CTT | C | 59 | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(56): Show | 119 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1412_*1413delTT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1412 | INFO_REALIGN_3_PRIME | chr2 | 202767157 | ||||
chr2:202767182
|
C | T | 1 | a0003c0003t0094 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1418C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1418 | chr2 | 202767182 | |||||
chr2:202767217
|
A | G | 1 | a0001c0001t0084 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1453A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1453 | chr2 | 202767217 | |||||
chr2:202767344
|
T | G | 99 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(96): Show | 229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
3_prime_UTR_variant | MODIFIER | c.*1580T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1580 | chr2 | 202767344 | |||||
chr2:202767461
|
G | GGAGCAGC others(345): Show |
1 | a0002c0002t0109 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1713_*1714insTTTT others(348): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1714 | INFO_REALIGN_3_PRIME | chr2 | 202767461 | ||||
chr2:202767543
|
A | T | 1 | a0001c0001t0101 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1779A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1779 | chr2 | 202767543 | |||||
chr2:202767564
|
C | T | 2 | a0001c0001t0091a0001c0008t0064 | 2 | HG01884.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1800C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1800 | chr2 | 202767564 | |||||
chr2:202767730
|
C | A | 1 | a0001c0001t0117 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1966C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 1966 | chr2 | 202767730 | |||||
chr2:202767787
|
T | C | 67 | a0001c0001t0002a0001c0001t0008a0001c0001t0013others(64): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2023T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2023 | chr2 | 202767787 | |||||
chr2:202767882
|
A | T | 2 | a0001c0001t0032a0001c0001t0125 | 4 | HG02132.hp2 NA18969.hp1 NA18972.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2118A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2118 | chr2 | 202767882 | |||||
chr2:202768067
|
G | A | 1 | a0001c0001t0127 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2303G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2303 | chr2 | 202768067 | |||||
chr2:202768069
|
A | G | 1 | a0001c0001t0127 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2305A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2305 | chr2 | 202768069 | |||||
chr2:202768070
|
G | GT | 37 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(34): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2308dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2309 | INFO_REALIGN_3_PRIME | chr2 | 202768070 | ||||
chr2:202768070
|
G | T | 1 | a0001c0001t0127 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2306G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2306 | chr2 | 202768070 | |||||
chr2:202768522
|
A | C | 5 | a0001c0001t0040a0001c0001t0078a0001c0001t0088others(2): Show | 6 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2758A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2758 | chr2 | 202768522 | |||||
chr2:202768565
|
T | C | 2 | a0001c0001t0119a0001c0001t0121 | 2 | HG03130.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2801T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 2801 | chr2 | 202768565 | |||||
chr2:202769222
|
T | G | 1 | a0001c0001t0080 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3458T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3458 | chr2 | 202769222 | |||||
chr2:202769497
|
A | G | 1 | a0001c0001t0077 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3733A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3733 | chr2 | 202769497 | |||||
chr2:202769650
|
A | G | 1 | a0001c0007t0106 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3886A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3886 | chr2 | 202769650 | |||||
chr2:202769714
|
G | A | 1 | a0001c0007t0106 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3950G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 3950 | chr2 | 202769714 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202635928
|
TG | T | 317 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.601+145delG | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202635928 | |||||
chr2:202635937
|
C | G | 35 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(32): Show | 35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+149C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202635937 | ||||||
chr2:202636002
|
C | T | 1 | a0001c0001t0015g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.601+214C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636002 | ||||||
chr2:202636256
|
A | G | 12 | a0001c0001t0014g0270a0001c0001t0014g0272a0001c0001t0014g0273others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.601+468A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636256 | ||||||
chr2:202636277
|
A | T | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.601+489A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636277 | ||||||
chr2:202636455
|
A | G | 1 | a0001c0001t0049g0269 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.601+667A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636455 | ||||||
chr2:202636716
|
C | T | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601+928C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636716 | ||||||
chr2:202636968
|
C | T | 30 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.601+1180C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202636968 | ||||||
chr2:202637041
|
C | T | 3 | a0001c0001t0041g0266a0001c0001t0047g0267a0001c0001t0047g0268 | 3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+1253C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637041 | ||||||
chr2:202637123
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+1335C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637123 | ||||||
chr2:202637139
|
C | T | 9 | a0001c0001t0039g0258a0001c0001t0039g0260a0001c0001t0040g0256others(6): Show | 9 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+1351C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637139 | ||||||
chr2:202637148
|
T | C | 41 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0029g0004others(38): Show | 41 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.601+1360T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637148 | ||||||
chr2:202637184
|
A | C | 6 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0006g0250others(3): Show | 6 | HG02027.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+1396A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637184 | ||||||
chr2:202637445
|
T | C | 35 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(32): Show | 35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+1657T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637445 | ||||||
chr2:202637670
|
T | C | 1 | a0001c0001t0011g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.601+1882T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637670 | ||||||
chr2:202637738
|
A | G | 35 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(32): Show | 35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+1950A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637738 | ||||||
chr2:202637873
|
C | CT | 13 | a0001c0001t0049g0269a0001c0001t0050g0284a0001c0001t0050g0285others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.601+2106dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202637873 | |||||
chr2:202637873
|
CT | C | 57 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(54): Show | 57 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.601+2106delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202637873 | |||||
chr2:202637970
|
G | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+2182G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637970 | ||||||
chr2:202637981
|
A | T | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+2193A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202637981 | ||||||
chr2:202638127
|
C | T | 1 | a0001c0001t0093g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.601+2339C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638127 | ||||||
chr2:202638164
|
A | G | 1 | a0001c0001t0126g0242 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.601+2376A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638164 | ||||||
chr2:202638168
|
C | T | 1 | a0001c0001t0032g0241 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.601+2380C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638168 | ||||||
chr2:202638369
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.601+2581A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638369 | ||||||
chr2:202638401
|
T | A | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+2613T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638401 | ||||||
chr2:202638572
|
AAAAT | A | 35 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(32): Show | 35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+2805_601+2808d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202638572 | |||||
chr2:202638740
|
G | A | 1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+2952G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638740 | ||||||
chr2:202638889
|
A | C | 35 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(32): Show | 35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.601+3101A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638889 | ||||||
chr2:202638911
|
C | T | 15 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(12): Show | 15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+3123C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202638911 | ||||||
chr2:202639072
|
T | C | 1 | a0001c0001t0075g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.601+3284T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639072 | ||||||
chr2:202639146
|
A | G | 1 | a0001c0001t0068g0239 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.601+3358A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639146 | ||||||
chr2:202639231
|
T | C | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+3443T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639231 | ||||||
chr2:202639301
|
T | G | 7 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0016g0300others(4): Show | 7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+3513T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639301 | ||||||
chr2:202639375
|
A | G | 1 | a0001c0001t0038g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.601+3587A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639375 | ||||||
chr2:202639378
|
C | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+3590C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639378 | ||||||
chr2:202639438
|
C | T | 15 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(12): Show | 15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+3650C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639438 | ||||||
chr2:202639665
|
G | A | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601+3877G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639665 | ||||||
chr2:202639786
|
T | G | 1 | a0001c0001t0047g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.601+3998T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639786 | ||||||
chr2:202639992
|
G | A | 5 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+4204G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202639992 | ||||||
chr2:202640293
|
A | AATATATA others(3): Show |
1 | a0001c0001t0137g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.601+4506_601+4507i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640293
|
A | AATATATA others(5): Show |
1 | a0001c0001t0022g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+4506_601+4507i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640293
|
A | AATATATA others(7): Show |
2 | a0001c0001t0013g0030a0001c0001t0022g0029 | 2 | HG00741.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.601+4506_601+4507i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640293
|
AAAATAT | A | 8 | a0001c0001t0005g0236a0001c0001t0008g0038a0001c0001t0131g0041others(5): Show | 8 | HG00609.hp1 HG00639.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+4507_601+4512d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640293
|
AAAATATA others(1): Show |
A | 3 | a0001c0001t0008g0042a0001c0001t0008g0043a0001c0001t0023g0044 | 3 | HG00738.hp1 HG01099.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4514d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640293
|
AAAATATA others(3): Show |
A | 3 | a0001c0001t0008g0045a0001c0001t0013g0046a0001c0001t0023g0047 | 3 | HG01106.hp1 HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4516d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640293
|
AAAATATA others(5): Show |
A | 2 | a0001c0001t0023g0048a0001c0001t0023g0049 | 2 | HG00140.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4518d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640293
|
AAAATATA others(13): Show |
A | 2 | a0001c0001t0013g0050a0001c0001t0013g0051 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.601+4507_601+4526d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640293 | |||||
chr2:202640295
|
A | AAT | 28 | a0001c0001t0001g0116a0001c0001t0001g0127a0001c0001t0001g0240others(25): Show | 28 | HG00408.hp1 HG00544.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.601+4554_601+4555d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATAT | 17 | a0001c0001t0001g0092a0001c0001t0001g0095a0001c0001t0001g0097others(14): Show | 17 | HG00558.hp1 HG00597.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.601+4552_601+4555d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATAT | 16 | a0001c0001t0001g0080a0001c0001t0001g0088a0001c0001t0002g0087others(13): Show | 16 | HG01975.hp2 HG02027.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.601+4550_601+4555d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(1): Show |
14 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0075others(11): Show | 14 | HG00673.hp1 HG01168.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.601+4548_601+4555d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(3): Show |
10 | a0001c0001t0001g0069a0001c0001t0004g0009a0001c0001t0009g0070others(7): Show | 10 | HG01943.hp1 HG02132.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+4546_601+4555d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(5): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0028g0064others(1): Show | 4 | HG00323.hp1 HG02155.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4544_601+4555d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(7): Show |
1 | a0001c0001t0075g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.601+4542_601+4555d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(11): Show |
1 | a0002c0002t0003g0303 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.601+4522_601+4523i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(13): Show |
2 | a0002c0002t0003g0301a0002c0002t0003g0302 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601+4522_601+4523i others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601+4540_601+4555d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(11): Show |
5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0009g0060others(2): Show | 5 | HG03098.hp1 HG03704.hp1 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+4538_601+4555d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | AATATATA others(15): Show |
1 | a0001c0001t0006g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.601+4534_601+4555d others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
A | ATATATAT | 3 | a0001c0001t0004g0232a0001c0001t0048g0233a0002c0002t0016g0300 | 3 | HG02723.hp1 NA18950.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.601+4507_601+4508i others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640295 | ||||||
chr2:202640295
|
A | T | 10 | a0001c0001t0008g0034a0001c0001t0013g0030a0001c0001t0013g0033others(7): Show | 10 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+4507A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640295 | ||||||
chr2:202640295
|
AAT | A | 19 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(16): Show | 19 | HG00099.hp2 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.601+4554_601+4555d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATAT | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0027g0254 | 3 | HG01975.hp1 HG02155.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601+4552_601+4555d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATAT | A | 6 | a0001c0001t0004g0171a0001c0001t0007g0255a0001c0001t0026g0168others(3): Show | 6 | HG00140.hp1 HG01346.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+4550_601+4555d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(1): Show |
A | 9 | a0001c0001t0001g0175a0001c0001t0005g0174a0001c0001t0005g0176others(6): Show | 9 | HG01081.hp1 HG01358.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+4548_601+4555d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(3): Show |
A | 12 | a0001c0001t0001g0020a0001c0001t0001g0182a0001c0001t0001g0184others(9): Show | 12 | HG00609.hp2 HG00621.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+4546_601+4555d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(5): Show |
A | 17 | a0001c0001t0001g0194a0001c0001t0002g0191a0001c0001t0002g0193others(14): Show | 17 | HG00408.hp2 HG00597.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.601+4544_601+4555d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(7): Show |
A | 52 | a0001c0001t0001g0224a0001c0001t0002g0195a0001c0001t0002g0199others(49): Show | 52 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.601+4542_601+4555d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(9): Show |
A | 8 | a0001c0001t0014g0270a0001c0001t0057g0281a0001c0001t0058g0280others(5): Show | 8 | HG02615.hp2 HG03130.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+4540_601+4555d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(11): Show |
A | 6 | a0001c0001t0005g0228a0003c0003t0010g0246a0003c0003t0010g0247others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+4538_601+4555d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(13): Show |
A | 3 | a0001c0001t0047g0267a0001c0001t0073g0229a0001c0001t0101g0287 | 3 | HG02109.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+4536_601+4555d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(17): Show |
A | 1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+4532_601+4555d others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(25): Show |
A | 1 | a0001c0001t0130g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.601+4524_601+4555d others(34): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640295
|
AATATATA others(29): Show |
A | 1 | a0001c0001t0070g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.601+4520_601+4555d others(38): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640295 | |||||
chr2:202640299
|
T | TATATATA others(5): Show |
1 | a0002c0002t0030g0292 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.601+4522_601+4523i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640299 | |||||
chr2:202640329
|
T | C | 1 | a0001c0001t0139g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601+4541T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640329 | ||||||
chr2:202640340
|
A | ATATATAT others(7): Show |
1 | a0002c0002t0003g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+4555_601+4556i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | |||||
chr2:202640340
|
A | ATATATAT others(5): Show |
1 | a0002c0002t0107g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+4555_601+4556i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | |||||
chr2:202640340
|
A | ATATATAT others(3): Show |
2 | a0002c0002t0003g0307a0002c0002t0100g0306 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.601+4555_601+4556i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | |||||
chr2:202640340
|
A | ATATATG | 3 | a0002c0002t0003g0308a0002c0002t0003g0309a0002c0002t0003g0310 | 3 | HG02559.hp2 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.601+4555_601+4556i others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | |||||
chr2:202640340
|
A | ATATG | 8 | a0002c0002t0003g0311a0002c0002t0016g0295a0002c0002t0016g0296others(5): Show | 8 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+4553_601+4556d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | |||||
chr2:202640340
|
A | ATG | 4 | a0002c0002t0024g0289a0002c0002t0024g0290a0002c0002t0063g0291others(1): Show | 4 | HG02970.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+4553_601+4554i others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202640340 | |||||
chr2:202640340
|
A | G | 10 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(7): Show | 10 | HG00733.hp1 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+4552A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640340 | ||||||
chr2:202640344
|
G | A | 3 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0062g0056 | 3 | HG02145.hp2 HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.601+4556G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640344 | ||||||
chr2:202640402
|
A | G | 12 | a0001c0001t0004g0009a0001c0001t0004g0106a0001c0001t0004g0171others(9): Show | 12 | HG00738.hp2 HG01943.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+4614A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640402 | ||||||
chr2:202640447
|
G | A | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+4659G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640447 | ||||||
chr2:202640462
|
G | A | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+4674G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640462 | ||||||
chr2:202640470
|
G | A | 3 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303 | 3 | HG00733.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601+4682G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640470 | ||||||
chr2:202640803
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0102g0283others(1): Show | 4 | HG02723.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+5015G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640803 | ||||||
chr2:202640874
|
G | T | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+5086G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640874 | ||||||
chr2:202640907
|
C | G | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0102g0283others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+5119C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202640907 | ||||||
chr2:202641266
|
T | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0102g0283others(1): Show | 4 | HG02723.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+5478T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641266 | ||||||
chr2:202641315
|
A | T | 1 | a0001c0001t0081g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.601+5527A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641315 | ||||||
chr2:202641442
|
A | G | 6 | a0001c0001t0008g0038a0001c0001t0008g0150a0001c0001t0131g0041others(3): Show | 6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+5654A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641442 | ||||||
chr2:202641475
|
C | T | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0102g0283others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+5687C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641475 | ||||||
chr2:202641550
|
T | G | 1 | a0003c0003t0030g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.601+5762T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641550 | ||||||
chr2:202641554
|
A | G | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601+5766A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641554 | ||||||
chr2:202641641
|
CT | C | 125 | a0001c0001t0001g0062a0001c0001t0001g0080a0001c0001t0002g0181others(122): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.601+5868delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202641641 | |||||
chr2:202641641
|
CTT | C | 34 | a0001c0001t0002g0195a0001c0001t0050g0284a0001c0001t0050g0285others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+5867_601+5868d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202641641 | |||||
chr2:202641891
|
G | C | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0102g0283others(1): Show | 4 | HG02723.hp2 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+6103G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641891 | ||||||
chr2:202641947
|
C | CT | 10 | a0001c0001t0001g0167a0001c0001t0009g0060a0001c0001t0009g0070others(7): Show | 10 | HG01952.hp2 HG02155.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.601+6174dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202641947 | |||||
chr2:202641965
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0088a0001c0001t0001g0127others(2): Show | 5 | HG02080.hp2 NA18962.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+6177C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202641965 | ||||||
chr2:202642117
|
C | CT | 8 | a0001c0001t0008g0038a0001c0001t0008g0150a0001c0001t0131g0041others(5): Show | 8 | HG00609.hp1 HG02132.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+6346dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642117 | |||||
chr2:202642344
|
A | AAT | 11 | a0001c0001t0001g0185a0001c0001t0002g0104a0001c0001t0006g0010others(8): Show | 11 | HG01168.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.601+6576_601+6577d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642344
|
A | AATAT | 18 | a0001c0001t0008g0034a0001c0001t0013g0033a0001c0001t0013g0050others(15): Show | 18 | HG00544.hp2 HG00642.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.601+6574_601+6577d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642344
|
A | AATATAT | 19 | a0001c0001t0008g0038a0001c0001t0008g0042a0001c0001t0008g0043others(16): Show | 19 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.601+6572_601+6577d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642344
|
A | AATATATA others(3): Show |
18 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(15): Show | 18 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.601+6568_601+6577d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642344
|
A | AATATATA others(5): Show |
4 | a0002c0002t0003g0310a0002c0002t0016g0296a0002c0002t0051g0293others(1): Show | 4 | HG02717.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+6566_601+6577d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642344
|
A | AATATATA others(11): Show |
4 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(1): Show | 4 | HG01884.hp2 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+6560_601+6577d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642344
|
A | AATATATA others(15): Show |
1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+6577_601+6578i others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642344
|
A | AATATATA others(21): Show |
1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.601+6577_601+6578i others(30): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202642344 | |||||
chr2:202642541
|
G | C | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.601+6753G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642541 | ||||||
chr2:202642666
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.601+6878A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642666 | ||||||
chr2:202642701
|
A | G | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+6913A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642701 | ||||||
chr2:202642759
|
G | C | 3 | a0001c0001t0006g0103a0001c0001t0006g0131a0003c0003t0006g0072 | 3 | HG02572.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.601+6971G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642759 | ||||||
chr2:202642837
|
A | C | 1 | a0001c0001t0009g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.601+7049A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642837 | ||||||
chr2:202642940
|
C | T | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.601+7152C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202642940 | ||||||
chr2:202643157
|
A | G | 4 | a0001c0001t0023g0044a0001c0001t0023g0047a0001c0001t0023g0048others(1): Show | 4 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+7369A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643157 | ||||||
chr2:202643263
|
G | T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+7475G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643263 | ||||||
chr2:202643344
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0182 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.601+7556G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643344 | ||||||
chr2:202643555
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601+7767G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643555 | ||||||
chr2:202643910
|
G | A | 12 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0016g0300others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+8122G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202643910 | ||||||
chr2:202644030
|
G | A | 1 | a0002c0002t0003g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+8242G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644030 | ||||||
chr2:202644053
|
G | GT | 24 | a0001c0001t0002g0193a0001c0001t0002g0199a0001c0001t0002g0202others(21): Show | 24 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+8275dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTT | 23 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0207others(20): Show | 23 | HG00558.hp2 HG01109.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.601+8274_601+8275d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTTT | 9 | a0001c0001t0002g0181a0001c0001t0002g0216a0001c0001t0002g0217others(6): Show | 9 | HG00673.hp2 HG01884.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+8273_601+8275d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTTTTT | 8 | a0001c0001t0002g0220a0002c0002t0016g0295a0002c0002t0016g0296others(5): Show | 8 | HG00621.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+8271_601+8275d others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTTTTTTT others(3): Show |
4 | a0002c0002t0003g0307a0002c0002t0030g0292a0002c0002t0051g0293others(1): Show | 4 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+8266_601+8275d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTTTTTTT others(4): Show |
1 | a0002c0002t0107g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+8275_601+8276i others(13): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0030g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601+8275_601+8276i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTTTTTTT others(6): Show |
1 | a0002c0002t0003g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+8275_601+8276i others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644053
|
G | GTTTTTTT others(9): Show |
1 | a0002c0002t0003g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.601+8275_601+8276i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644053 | |||||
chr2:202644056
|
T | TTTTTTTT others(6): Show |
1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.601+8275_601+8276i others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644056 | |||||
chr2:202644060
|
T | TTTTTTTT others(6): Show |
3 | a0001c0001t0028g0001a0001c0001t0042g0003a0001c0001t0045g0006 | 3 | HG02257.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+8275_601+8276i others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644060 | |||||
chr2:202644064
|
G | GT | 25 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(22): Show | 25 | HG00558.hp1 HG01975.hp2 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.601+8296dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644064 | |||||
chr2:202644064
|
G | T | 101 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(98): Show | 101 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.601+8276G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644064 | ||||||
chr2:202644064
|
GT | G | 7 | a0001c0001t0004g0009a0001c0001t0004g0108a0001c0001t0023g0047others(4): Show | 7 | HG01891.hp1 HG02738.hp1 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+8296delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644064 | |||||
chr2:202644064
|
GTT | G | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.601+8295_601+8296d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202644064 | |||||
chr2:202644065
|
T | G | 1 | a0002c0002t0100g0306 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.601+8277T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644065 | ||||||
chr2:202644074
|
T | G | 4 | a0001c0001t0001g0011a0001c0001t0007g0132a0001c0001t0012g0073others(1): Show | 4 | NA18948.hp2 NA18964.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+8286T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644074 | ||||||
chr2:202644075
|
T | G | 1 | a0001c0001t0089g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601+8287T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644075 | ||||||
chr2:202644514
|
T | C | 1 | a0001c0001t0031g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.601+8726T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644514 | ||||||
chr2:202644521
|
G | A | 1 | a0001c0001t0056g0169 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.601+8733G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644521 | ||||||
chr2:202644722
|
T | C | 7 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0016g0300others(4): Show | 7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+8934T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644722 | ||||||
chr2:202644835
|
C | T | 14 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(11): Show | 14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+9047C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644835 | ||||||
chr2:202644898
|
A | G | 6 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0029g0004others(3): Show | 6 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+9110A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202644898 | ||||||
chr2:202645147
|
T | G | 1 | a0003c0003t0010g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601+9359T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645147 | ||||||
chr2:202645283
|
C | CT | 8 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(5): Show | 8 | HG01952.hp2 HG02293.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+9506dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202645283 | |||||
chr2:202645349
|
C | T | 1 | a0001c0001t0082g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+9561C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645349 | ||||||
chr2:202645359
|
G | A | 68 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.601+9571G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645359 | ||||||
chr2:202645479
|
C | T | 1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+9691C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645479 | ||||||
chr2:202645493
|
G | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+9705G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645493 | ||||||
chr2:202645493
|
G | T | 1 | a0001c0001t0004g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.601+9705G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645493 | ||||||
chr2:202645533
|
C | T | 1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.601+9745C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645533 | ||||||
chr2:202645609
|
GATTTATT others(1): Show |
G | 6 | a0001c0001t0001g0012a0001c0001t0001g0088a0001c0001t0001g0127others(3): Show | 6 | HG02080.hp2 NA18962.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+9826_601+9833d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202645609 | |||||
chr2:202645701
|
T | G | 1 | a0001c0001t0112g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.601+9913T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645701 | ||||||
chr2:202645780
|
A | G | 1 | a0001c0001t0030g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601+9992A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645780 | ||||||
chr2:202645837
|
C | T | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601+10049C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202645837 | ||||||
chr2:202646031
|
G | GT | 6 | a0001c0001t0001g0251a0001c0001t0006g0250a0001c0001t0007g0255others(3): Show | 6 | HG02895.hp2 HG02965.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+10256dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202646031 | |||||
chr2:202646034
|
T | G | 1 | a0002c0002t0003g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.601+10246T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646034 | ||||||
chr2:202646050
|
G | GA | 102 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(99): Show | 102 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.601+10262_601+1026 others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646050 | ||||||
chr2:202646119
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.601+10331C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646119 | ||||||
chr2:202646122
|
G | A | 1 | a0001c0001t0027g0254 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.601+10334G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646122 | ||||||
chr2:202646137
|
C | G | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+10349C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646137 | ||||||
chr2:202646254
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0127 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.601+10466G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646254 | ||||||
chr2:202646288
|
A | G | 317 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.601+10500A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646288 | ||||||
chr2:202646453
|
C | A | 1 | a0001c0001t0043g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.601+10665C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646453 | ||||||
chr2:202646622
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.601+10834C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646622 | ||||||
chr2:202646691
|
T | A | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+10903T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646691 | ||||||
chr2:202646809
|
C | T | 1 | a0001c0001t0022g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.601+11021C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646809 | ||||||
chr2:202646825
|
A | G | 5 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11037A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646825 | ||||||
chr2:202646840
|
CTTGT | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11055_601+1105 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202646840 | |||||
chr2:202646848
|
A | C | 79 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(76): Show | 79 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.601+11060A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646848 | ||||||
chr2:202646917
|
G | A | 2 | a0001c0004t0037g0022a0001c0004t0037g0023 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.601+11129G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202646917 | ||||||
chr2:202647023
|
T | G | 3 | a0001c0001t0041g0266a0001c0001t0047g0267a0001c0001t0047g0268 | 3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+11235T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647023 | ||||||
chr2:202647415
|
C | A | 27 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(24): Show | 27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+11627C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647415 | ||||||
chr2:202647420
|
A | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+11632A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647420 | ||||||
chr2:202647434
|
A | T | 1 | a0001c0001t0087g0117 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.601+11646A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647434 | ||||||
chr2:202647436
|
T | A | 1 | a0001c0001t0052g0159 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.601+11648T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647436 | ||||||
chr2:202647759
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+11971G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647759 | ||||||
chr2:202647843
|
A | AT | 6 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0213others(3): Show | 6 | HG00099.hp1 HG01071.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+12062dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202647843 | |||||
chr2:202647967
|
C | T | 1 | a0001c0001t0112g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.601+12179C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202647967 | ||||||
chr2:202648244
|
T | C | 1 | a0001c0001t0005g0152 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.601+12456T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648244 | ||||||
chr2:202648518
|
A | AC | 156 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(153): Show | 156 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.601+12740dupC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648518 | |||||
chr2:202648518
|
A | ACC | 38 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0116others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.601+12739_601+1274 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648518 | |||||
chr2:202648518
|
A | C | 2 | a0001c0001t0009g0165a0001c0001t0045g0149 | 2 | HG01952.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.601+12730A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648518 | ||||||
chr2:202648518
|
AC | A | 31 | a0001c0001t0027g0252a0001c0001t0027g0254a0002c0002t0003g0301others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.601+12740delC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648518 | |||||
chr2:202648529
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601+12741A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648529 | ||||||
chr2:202648542
|
C | CAT | 3 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0102g0283 | 3 | HG02723.hp2 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601+12765_601+1276 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648542 | |||||
chr2:202648542
|
C | CATAT | 31 | a0001c0001t0101g0287a0001c0007t0106g0286a0002c0002t0003g0301others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.601+12763_601+1276 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202648542 | |||||
chr2:202648820
|
T | G | 317 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.601+13032T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648820 | ||||||
chr2:202648953
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.601+13165C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648953 | ||||||
chr2:202648973
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.601+13185C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648973 | ||||||
chr2:202648987
|
C | T | 1 | a0001c0001t0112g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.601+13199C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202648987 | ||||||
chr2:202649008
|
C | CCT | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+13222_601+1322 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202649008 | |||||
chr2:202649106
|
G | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+13318G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649106 | ||||||
chr2:202649297
|
C | G | 3 | a0001c0001t0021g0027a0001c0001t0122g0209a0001c0001t0124g0208 | 3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.601+13509C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649297 | ||||||
chr2:202649303
|
T | C | 1 | a0001c0001t0056g0170 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.601+13515T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649303 | ||||||
chr2:202649535
|
GTTAT | G | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+13762_601+1376 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202649535 | |||||
chr2:202649760
|
C | G | 2 | a0001c0001t0028g0064a0001c0001t0028g0076 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.601+13972C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649760 | ||||||
chr2:202649858
|
ATTTG | A | 9 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+14086_601+1408 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202649858 | |||||
chr2:202649913
|
G | A | 1 | a0001c0001t0124g0208 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.601+14125G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649913 | ||||||
chr2:202649930
|
C | T | 3 | a0001c0001t0002g0202a0001c0001t0005g0201a0001c0001t0079g0200 | 3 | HG02165.hp2 NA18954.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.601+14142C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202649930 | ||||||
chr2:202650898
|
C | T | 3 | a0001c0001t0041g0266a0001c0001t0047g0267a0001c0001t0047g0268 | 3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+15110C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202650898 | ||||||
chr2:202650929
|
T | C | 3 | a0001c0001t0006g0103a0001c0001t0006g0131a0003c0003t0006g0072 | 3 | HG02572.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.601+15141T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202650929 | ||||||
chr2:202651013
|
G | A | 2 | a0001c0001t0042g0153a0001c0001t0087g0117 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+15225G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651013 | ||||||
chr2:202651060
|
CT | C | 138 | a0001c0001t0001g0065a0001c0001t0002g0181a0001c0001t0002g0191others(135): Show | 138 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.601+15292delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202651060 | |||||
chr2:202651060
|
CTT | C | 7 | a0001c0001t0014g0270a0001c0001t0059g0279a0001c0004t0037g0022others(4): Show | 7 | HG01167.hp2 HG01168.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+15291_601+1529 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202651060 | |||||
chr2:202651080
|
T | A | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.601+15292T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651080 | ||||||
chr2:202651218
|
C | T | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+15430C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651218 | ||||||
chr2:202651264
|
G | A | 4 | a0001c0001t0023g0044a0001c0001t0023g0048a0001c0001t0023g0049others(1): Show | 4 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+15476G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651264 | ||||||
chr2:202651376
|
C | T | 146 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(143): Show | 146 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.601+15588C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651376 | ||||||
chr2:202651409
|
G | T | 1 | a0001c0001t0060g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.601+15621G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651409 | ||||||
chr2:202651512
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.601+15724A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651512 | ||||||
chr2:202651523
|
C | T | 1 | a0001c0001t0121g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.601+15735C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651523 | ||||||
chr2:202651588
|
G | A | 1 | a0001c0001t0092g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.601+15800G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651588 | ||||||
chr2:202651769
|
A | G | 1 | a0002c0002t0107g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601+15981A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651769 | ||||||
chr2:202651829
|
G | A | 14 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(11): Show | 14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+16041G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651829 | ||||||
chr2:202651834
|
A | G | 5 | a0001c0001t0001g0251a0001c0001t0006g0250a0001c0001t0007g0255others(2): Show | 5 | HG02258.hp2 HG02965.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+16046A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651834 | ||||||
chr2:202651839
|
A | G | 1 | a0001c0001t0017g0024 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.601+16051A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651839 | ||||||
chr2:202651909
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0025g0082 | 2 | HG00673.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.601+16121C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651909 | ||||||
chr2:202651947
|
G | A | 1 | a0001c0001t0118g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.601+16159G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202651947 | ||||||
chr2:202652034
|
C | A | 1 | a0001c0001t0004g0171 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.601+16246C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652034 | ||||||
chr2:202652052
|
T | TA | 9 | a0001c0001t0009g0002a0001c0001t0022g0029a0001c0001t0028g0001others(6): Show | 9 | HG00544.hp2 HG01981.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+16284dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202652052 | |||||
chr2:202652052
|
TA | T | 46 | a0001c0001t0001g0116a0001c0001t0001g0135a0001c0001t0001g0167others(43): Show | 46 | HG00733.hp1 HG00741.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.601+16284delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202652052 | |||||
chr2:202652086
|
G | A | 2 | a0001c0001t0033g0083a0001c0001t0090g0059 | 2 | NA18980.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.601+16298G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652086 | ||||||
chr2:202652183
|
C | T | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+16395C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652183 | ||||||
chr2:202652210
|
C | T | 1 | a0001c0001t0127g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.601+16422C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652210 | ||||||
chr2:202652245
|
C | A | 1 | a0001c0001t0085g0013 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.601+16457C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652245 | ||||||
chr2:202652328
|
T | C | 2 | a0001c0001t0019g0188a0001c0006t0129g0187 | 2 | NA18949.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.601+16540T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652328 | ||||||
chr2:202652488
|
A | G | 1 | a0001c0001t0095g0262 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.601+16700A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652488 | ||||||
chr2:202652572
|
T | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+16784T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652572 | ||||||
chr2:202652723
|
G | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.601+16935G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652723 | ||||||
chr2:202652864
|
G | A | 2 | a0001c0001t0008g0042a0001c0001t0008g0045 | 2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.601+17076G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652864 | ||||||
chr2:202652878
|
C | A | 1 | a0001c0001t0007g0081 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.601+17090C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202652878 | ||||||
chr2:202653171
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+17383G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653171 | ||||||
chr2:202653318
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+17530G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653318 | ||||||
chr2:202653400
|
C | T | 3 | a0001c0001t0041g0266a0001c0001t0047g0267a0001c0001t0047g0268 | 3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+17612C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653400 | ||||||
chr2:202653406
|
G | A | 1 | a0001c0001t0025g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.601+17618G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653406 | ||||||
chr2:202653550
|
A | G | 2 | a0001c0001t0007g0081a0001c0001t0048g0068 | 2 | NA18952.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.601+17762A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653550 | ||||||
chr2:202653723
|
G | A | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+17935G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653723 | ||||||
chr2:202653774
|
G | A | 2 | a0001c0001t0052g0159a0002c0002t0105g0314 | 2 | HG00099.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.601+17986G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653774 | ||||||
chr2:202653997
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.601+18209C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202653997 | ||||||
chr2:202654062
|
T | A | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.601+18274T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654062 | ||||||
chr2:202654062
|
T | TGA | 64 | a0001c0001t0001g0185a0001c0001t0002g0210a0001c0001t0004g0085others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.601+18308_601+1830 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
T | TGAGA | 15 | a0001c0001t0007g0132a0001c0001t0013g0046a0001c0001t0017g0218others(12): Show | 15 | HG00673.hp2 HG01106.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.601+18306_601+1830 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
T | TGAGTGAG others(1): Show |
5 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0029g0004others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+18277_601+1827 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
T | TGAGTGAG others(3): Show |
1 | a0001c0001t0045g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.601+18277_601+1827 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
TGA | T | 4 | a0001c0001t0001g0184a0001c0001t0013g0030a0001c0001t0031g0063others(1): Show | 4 | HG00621.hp2 HG00741.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+18308_601+1830 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
TGAGA | T | 29 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0216others(26): Show | 29 | HG00621.hp1 HG00738.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+18306_601+1830 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
TGAGAGAG others(1): Show |
T | 31 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.601+18302_601+1830 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
TGAGAGAG others(3): Show |
T | 2 | a0001c0001t0042g0153a0001c0001t0087g0117 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.601+18300_601+1830 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
TGAGAGAG others(5): Show |
T | 5 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+18298_601+1830 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654062
|
TGAGAGAG others(7): Show |
T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+18296_601+1830 others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654062 | |||||
chr2:202654066
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.601+18278A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654066 | ||||||
chr2:202654161
|
AAGAC | A | 33 | a0001c0001t0001g0166a0001c0001t0001g0175a0001c0001t0005g0174others(30): Show | 33 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.601+18376_601+1837 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654161 | |||||
chr2:202654262
|
C | CA | 71 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(68): Show | 71 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.601+18486dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654262 | |||||
chr2:202654263
|
A | C | 1 | a0001c0001t0035g0055 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.601+18475A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654263 | ||||||
chr2:202654527
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+18739G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654527 | ||||||
chr2:202654541
|
G | T | 27 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(24): Show | 27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.601+18753G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654541 | ||||||
chr2:202654632
|
T | G | 1 | a0001c0001t0023g0048 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.601+18844T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654632 | ||||||
chr2:202654665
|
CT | C | 10 | a0001c0001t0002g0203a0001c0001t0002g0204a0001c0001t0002g0213others(7): Show | 10 | HG00099.hp1 HG01071.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+18891delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202654665 | |||||
chr2:202654772
|
C | T | 1 | a0001c0001t0048g0233 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.601+18984C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654772 | ||||||
chr2:202654870
|
C | A | 5 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19082C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202654870 | ||||||
chr2:202655060
|
T | G | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.601+19272T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655060 | ||||||
chr2:202655077
|
A | AAATT | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+19291_601+1929 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655077 | |||||
chr2:202655099
|
T | C | 1 | a0001c0001t0032g0241 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.601+19311T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655099 | ||||||
chr2:202655122
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+19334G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655122 | ||||||
chr2:202655250
|
G | C | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+19462G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655250 | ||||||
chr2:202655317
|
A | C | 1 | a0001c0001t0022g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+19529A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655317 | ||||||
chr2:202655549
|
A | G | 248 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(245): Show | 248 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.601+19761A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655549 | ||||||
chr2:202655552
|
T | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19764T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655552 | ||||||
chr2:202655625
|
T | G | 1 | a0001c0001t0032g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.601+19837T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655625 | ||||||
chr2:202655697
|
G | A | 29 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(26): Show | 29 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+19909G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655697 | ||||||
chr2:202655707
|
T | TGA | 5 | a0001c0001t0004g0106a0001c0001t0054g0118a0001c0001t0119g0225others(2): Show | 5 | HG01256.hp1 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19973_601+1997 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
T | TGAGA | 4 | a0001c0001t0006g0250a0001c0001t0018g0143a0001c0001t0020g0160others(1): Show | 4 | HG02523.hp1 HG02965.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19971_601+1997 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
T | TGAGAGAC others(1): Show |
8 | a0001c0001t0008g0038a0001c0001t0013g0050a0001c0001t0013g0051others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
T | TGAGAGAC others(3): Show |
4 | a0001c0001t0008g0034a0001c0001t0022g0031a0001c0001t0023g0047others(1): Show | 4 | HG02056.hp1 HG02738.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
T | TGAGAGAC others(5): Show |
3 | a0001c0001t0008g0150a0001c0001t0013g0033a0001c0001t0023g0048 | 3 | HG01433.hp1 NA18966.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.601+19925_601+1992 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
T | TGAGAGAC others(7): Show |
1 | a0001c0001t0139g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601+19925_601+1992 others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGA | T | 51 | a0001c0001t0001g0224a0001c0001t0002g0181a0001c0001t0002g0193others(48): Show | 51 | HG00099.hp1 HG00408.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.601+19973_601+1997 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGA | T | 65 | a0001c0001t0001g0057a0001c0001t0002g0191a0001c0001t0002g0195others(62): Show | 65 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.601+19971_601+1997 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGA | T | 51 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(48): Show | 51 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.601+19969_601+1997 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGAG others(1): Show |
T | 24 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0092others(21): Show | 24 | HG00741.hp1 HG01123.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+19967_601+1997 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGAG others(3): Show |
T | 8 | a0001c0001t0004g0086a0001c0001t0005g0176a0001c0001t0006g0103others(5): Show | 8 | HG01081.hp1 HG01975.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+19965_601+1997 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGAG others(5): Show |
T | 6 | a0001c0001t0002g0104a0001c0001t0007g0096a0001c0001t0070g0231others(3): Show | 6 | HG00544.hp1 HG01243.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.601+19963_601+1997 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGAG others(7): Show |
T | 12 | a0001c0001t0062g0056a0002c0002t0016g0295a0002c0002t0016g0300others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+19961_601+1997 others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGAG others(9): Show |
T | 3 | a0001c0001t0055g0161a0002c0002t0097g0315a0002c0002t0098g0316 | 3 | HG03098.hp2 HG03471.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.601+19959_601+1997 others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGAG others(11): Show |
T | 15 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(12): Show | 15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+19957_601+1997 others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655707
|
TGAGAGAG others(15): Show |
T | 1 | a0001c0001t0027g0252 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.601+19953_601+1997 others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655707 | |||||
chr2:202655708
|
G | GAGAGAC | 5 | a0001c0001t0008g0042a0001c0001t0008g0045a0001c0001t0022g0130others(2): Show | 5 | HG00609.hp1 HG00639.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655708 | |||||
chr2:202655710
|
G | GAGAC | 5 | a0001c0001t0022g0029a0001c0001t0040g0256a0001c0001t0091g0265others(2): Show | 5 | HG01261.hp2 HG01884.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655710 | |||||
chr2:202655712
|
G | GAC | 4 | a0001c0001t0008g0043a0001c0001t0027g0136a0001c0001t0088g0261others(1): Show | 4 | HG00738.hp1 HG02723.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19925_601+1992 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655712 | |||||
chr2:202655714
|
G | C | 24 | a0001c0001t0009g0002a0001c0001t0013g0030a0001c0001t0013g0046others(21): Show | 24 | HG00558.hp2 HG00673.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.601+19926G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655714 | ||||||
chr2:202655716
|
G | C | 38 | a0001c0001t0001g0224a0001c0001t0002g0181a0001c0001t0002g0193others(35): Show | 38 | HG00099.hp1 HG00408.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.601+19928G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655716 | ||||||
chr2:202655718
|
G | C | 53 | a0001c0001t0001g0057a0001c0001t0002g0191a0001c0001t0002g0195others(50): Show | 53 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.601+19930G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655718 | ||||||
chr2:202655720
|
G | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0058others(38): Show | 41 | HG00323.hp1 HG00558.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.601+19932G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655720 | ||||||
chr2:202655722
|
G | C | 22 | a0001c0001t0001g0020a0001c0001t0001g0061a0001c0001t0001g0092others(19): Show | 22 | HG00741.hp1 HG01123.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.601+19934G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655722 | ||||||
chr2:202655724
|
G | C | 8 | a0001c0001t0005g0176a0001c0001t0006g0103a0001c0001t0006g0131others(5): Show | 8 | HG01081.hp1 HG02572.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+19936G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655724 | ||||||
chr2:202655726
|
G | C | 7 | a0001c0001t0001g0061a0001c0001t0002g0104a0001c0001t0007g0096others(4): Show | 7 | HG01243.hp2 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.601+19938G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655726 | ||||||
chr2:202655728
|
G | C | 11 | a0002c0002t0016g0295a0002c0002t0016g0300a0002c0002t0024g0288others(8): Show | 11 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.601+19940G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655728 | ||||||
chr2:202655730
|
G | C | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601+19942G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655730 | ||||||
chr2:202655732
|
G | C | 15 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(12): Show | 15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.601+19944G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655732 | ||||||
chr2:202655741
|
A | T | 1 | a0001c0001t0044g0110 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.601+19953A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655741 | ||||||
chr2:202655747
|
A | T | 2 | a0001c0001t0050g0284a0001c0001t0102g0283 | 2 | HG02723.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601+19959A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655747 | ||||||
chr2:202655749
|
A | T | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+19961A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655749 | ||||||
chr2:202655751
|
A | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+19963A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655751 | ||||||
chr2:202655753
|
A | T | 6 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(3): Show | 6 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+19965A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655753 | ||||||
chr2:202655753
|
AGAGAGAG others(3): Show |
A | 2 | a0001c0001t0028g0001a0001c0001t0045g0006 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.601+19967_601+1997 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655753 | |||||
chr2:202655755
|
A | T | 12 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(9): Show | 12 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+19967A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655755 | ||||||
chr2:202655755
|
AGAGAGAG others(1): Show |
A | 3 | a0001c0001t0013g0046a0003c0003t0010g0196a0003c0003t0010g0244 | 3 | HG01106.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.601+19969_601+1997 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655755 | |||||
chr2:202655755
|
AGAGAGAG others(3): Show |
A | 1 | a0001c0001t0030g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601+19969_601+1997 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202655755 | |||||
chr2:202655757
|
A | T | 12 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(9): Show | 12 | HG01243.hp1 HG02109.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.601+19969A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655757 | ||||||
chr2:202655759
|
A | T | 30 | a0001c0001t0043g0109a0001c0001t0050g0284a0001c0001t0050g0285others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.601+19971A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655759 | ||||||
chr2:202655761
|
A | T | 48 | a0001c0001t0004g0009a0001c0001t0007g0014a0001c0001t0009g0060others(45): Show | 48 | HG00558.hp1 HG00733.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.601+19973A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655761 | ||||||
chr2:202655763
|
T | A | 6 | a0001c0001t0008g0043a0001c0001t0013g0033a0001c0001t0013g0050others(3): Show | 6 | HG00738.hp1 HG01884.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+19975T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655763 | ||||||
chr2:202655765
|
T | A | 1 | a0003c0003t0030g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.601+19977T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655765 | ||||||
chr2:202655994
|
C | A | 1 | a0001c0001t0012g0164 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.601+20206C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202655994 | ||||||
chr2:202656001
|
G | T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601+20213G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656001 | ||||||
chr2:202656106
|
A | G | 1 | a0001c0001t0022g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.601+20318A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656106 | ||||||
chr2:202656262
|
G | A | 1 | a0001c0001t0053g0119 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.601+20474G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656262 | ||||||
chr2:202656274
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.601+20486C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656274 | ||||||
chr2:202656444
|
T | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+20656T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656444 | ||||||
chr2:202656468
|
G | A | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+20680G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656468 | ||||||
chr2:202656623
|
G | C | 1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+20835G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656623 | ||||||
chr2:202656755
|
A | T | 1 | a0001c0001t0022g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+20967A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656755 | ||||||
chr2:202656762
|
T | A | 1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+20974T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656762 | ||||||
chr2:202656851
|
G | A | 1 | a0001c0001t0031g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.601+21063G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656851 | ||||||
chr2:202656910
|
A | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+21122A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656910 | ||||||
chr2:202656989
|
A | C | 1 | a0001c0001t0022g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.601+21201A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202656989 | ||||||
chr2:202657007
|
A | G | 1 | a0001c0001t0123g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.601+21219A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657007 | ||||||
chr2:202657055
|
ATTG | A | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+21271_601+2127 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202657055 | |||||
chr2:202657087
|
T | A | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+21299T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657087 | ||||||
chr2:202657484
|
T | C | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601+21696T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657484 | ||||||
chr2:202657561
|
C | T | 14 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(11): Show | 14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.601+21773C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657561 | ||||||
chr2:202657607
|
G | A | 1 | a0001c0001t0048g0068 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.601+21819G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657607 | ||||||
chr2:202657626
|
C | T | 149 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.601+21838C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657626 | ||||||
chr2:202657819
|
A | C | 1 | a0001c0001t0027g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.601+22031A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657819 | ||||||
chr2:202657832
|
C | T | 9 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.601+22044C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202657832 | ||||||
chr2:202658319
|
A | G | 67 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.601+22531A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202658319 | ||||||
chr2:202658720
|
C | T | 1 | a0001c0001t0060g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.601+22932C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202658720 | ||||||
chr2:202658805
|
A | G | 1 | a0001c0001t0130g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.601+23017A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202658805 | ||||||
chr2:202659297
|
C | T | 7 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(4): Show | 7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.601+23509C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659297 | ||||||
chr2:202659341
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.601+23553G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659341 | ||||||
chr2:202659558
|
C | A | 317 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.601+23770C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659558 | ||||||
chr2:202659591
|
G | A | 2 | a0001c0001t0019g0188a0001c0006t0129g0187 | 2 | NA18949.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.601+23803G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659591 | ||||||
chr2:202659604
|
C | CT | 77 | a0001c0001t0001g0012a0001c0001t0001g0069a0001c0001t0001g0075others(74): Show | 77 | HG00140.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.601+23846dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
C | CTT | 31 | a0001c0001t0001g0020a0001c0001t0001g0057a0001c0001t0001g0058others(28): Show | 31 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.601+23845_601+2384 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
C | CTTT | 8 | a0001c0001t0001g0065a0001c0001t0001g0080a0001c0001t0005g0074others(5): Show | 8 | HG01175.hp2 HG01884.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+23844_601+2384 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
CTTTTTT | C | 6 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0217others(3): Show | 6 | NA18940.hp2 NA18946.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+23841_601+2384 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
CTTTTTTT | C | 62 | a0001c0001t0002g0181a0001c0001t0002g0193a0001c0001t0002g0199others(59): Show | 62 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.601+23840_601+2384 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.601+23839_601+2384 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0011g0114 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.601+23836_601+2384 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0004g0086a0001c0001t0047g0267a0001c0001t0047g0268 | 3 | HG01975.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+23835_601+2384 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0036g0147others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+23834_601+2384 others(17): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659604
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0040g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.601+23826_601+2384 others(25): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202659604 | |||||
chr2:202659911
|
G | A | 3 | a0001c0001t0005g0236a0001c0001t0019g0197a0001c0001t0072g0173 | 3 | HG02165.hp1 NA18977.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.601+24123G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659911 | ||||||
chr2:202659918
|
C | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+24130C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202659918 | ||||||
chr2:202660287
|
A | G | 1 | a0001c0001t0008g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601+24499A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660287 | ||||||
chr2:202660383
|
C | T | 1 | a0001c0001t0136g0037 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.601+24595C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660383 | ||||||
chr2:202660699
|
A | G | 3 | a0001c0001t0023g0044a0001c0001t0023g0047a0001c0001t0023g0048 | 3 | HG01167.hp1 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.601+24911A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660699 | ||||||
chr2:202660711
|
A | G | 1 | a0001c0001t0135g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.601+24923A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660711 | ||||||
chr2:202660790
|
C | G | 1 | a0001c0001t0035g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.601+25002C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202660790 | ||||||
chr2:202661057
|
G | A | 2 | a0003c0003t0010g0196a0003c0003t0010g0244 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.601+25269G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661057 | ||||||
chr2:202661245
|
A | G | 69 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(66): Show | 69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.601+25457A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661245 | ||||||
chr2:202661251
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.601+25463G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661251 | ||||||
chr2:202661457
|
G | A | 1 | a0001c0001t0012g0164 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.601+25669G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661457 | ||||||
chr2:202661586
|
C | T | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.601+25798C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661586 | ||||||
chr2:202661661
|
A | G | 1 | a0001c0001t0055g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.601+25873A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661661 | ||||||
chr2:202661744
|
C | T | 1 | a0001c0001t0082g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.601+25956C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661744 | ||||||
chr2:202661751
|
C | T | 1 | a0001c0001t0136g0037 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.601+25963C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661751 | ||||||
chr2:202661777
|
A | G | 2 | a0001c0001t0019g0190a0001c0001t0115g0221 | 2 | NA18747.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.601+25989A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661777 | ||||||
chr2:202661780
|
G | A | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.601+25992G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661780 | ||||||
chr2:202661864
|
C | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+26076C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202661864 | ||||||
chr2:202661919
|
T | TA | 34 | a0001c0001t0014g0273a0001c0001t0017g0198a0001c0001t0020g0160others(31): Show | 34 | HG00544.hp2 HG00733.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.601+26150dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202661919 | |||||
chr2:202661919
|
TA | T | 6 | a0001c0001t0001g0167a0001c0001t0002g0140a0001c0001t0006g0103others(3): Show | 6 | HG01891.hp1 HG02155.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+26150delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202661919 | |||||
chr2:202662036
|
C | G | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+26248C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662036 | ||||||
chr2:202662089
|
C | T | 1 | a0001c0001t0006g0019 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.601+26301C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662089 | ||||||
chr2:202662119
|
G | GGT | 100 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(97): Show | 100 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.601+26350_601+2635 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202662119 | |||||
chr2:202662119
|
GGT | G | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.601+26350_601+2635 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202662119 | |||||
chr2:202662136
|
G | A | 1 | a0001c0001t0092g0257 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.601+26348G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662136 | ||||||
chr2:202662252
|
G | T | 6 | a0001c0001t0001g0057a0001c0001t0001g0069a0001c0001t0002g0087others(3): Show | 6 | HG02027.hp2 NA18951.hp1 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.601+26464G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662252 | ||||||
chr2:202662428
|
T | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+26640T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662428 | ||||||
chr2:202662583
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601+26795C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662583 | ||||||
chr2:202662592
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.601+26804C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662592 | ||||||
chr2:202662758
|
T | C | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+26970T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202662758 | ||||||
chr2:202663256
|
T | C | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(174): Show | 177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.601+27468T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663256 | ||||||
chr2:202663580
|
C | CT | 167 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0058others(164): Show | 167 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.601+27807dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202663580 | |||||
chr2:202663604
|
A | G | 4 | a0001c0001t0053g0119a0001c0001t0053g0146a0001c0001t0068g0239others(1): Show | 4 | HG02293.hp1 HG02300.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.601+27816A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663604 | ||||||
chr2:202663767
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.601+27979G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663767 | ||||||
chr2:202663773
|
G | A | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601+27985G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663773 | ||||||
chr2:202663836
|
G | A | 1 | a0001c0001t0009g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.601+28048G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663836 | ||||||
chr2:202663995
|
T | C | 1 | a0003c0003t0010g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601+28207T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202663995 | ||||||
chr2:202664104
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0127 | 2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.601+28316T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664104 | ||||||
chr2:202664159
|
T | G | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+28371T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664159 | ||||||
chr2:202664346
|
CAT | C | 10 | a0001c0001t0002g0203a0001c0001t0017g0024a0001c0001t0017g0198others(7): Show | 10 | HG00673.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+28560_601+2856 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202664346 | |||||
chr2:202664447
|
G | A | 1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.601+28659G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664447 | ||||||
chr2:202664463
|
A | G | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.601+28675A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664463 | ||||||
chr2:202664738
|
C | T | 4 | a0001c0001t0007g0096a0001c0001t0007g0115a0001c0001t0070g0231others(1): Show | 4 | HG01243.hp2 HG01255.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.601+28950C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664738 | ||||||
chr2:202664787
|
T | A | 1 | a0003c0003t0010g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601+28999T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664787 | ||||||
chr2:202664838
|
A | G | 1 | a0001c0001t0022g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.601+29050A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664838 | ||||||
chr2:202664940
|
A | G | 1 | a0001c0001t0081g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.601+29152A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202664940 | ||||||
chr2:202665558
|
T | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.601+29770T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665558 | ||||||
chr2:202665609
|
T | C | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.601+29821T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665609 | ||||||
chr2:202665815
|
G | A | 10 | a0001c0001t0002g0203a0001c0001t0017g0024a0001c0001t0017g0198others(7): Show | 10 | HG00673.hp2 HG01071.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.601+30027G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665815 | ||||||
chr2:202665864
|
G | A | 1 | a0001c0001t0113g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.602-30017G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202665864 | ||||||
chr2:202666403
|
C | T | 7 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(4): Show | 7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-29478C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666403 | ||||||
chr2:202666500
|
T | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-29381T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666500 | ||||||
chr2:202666614
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.602-29267C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666614 | ||||||
chr2:202666668
|
C | CT | 31 | a0001c0001t0001g0116a0001c0001t0009g0070a0001c0001t0009g0105others(28): Show | 31 | HG00408.hp1 HG00741.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.602-29195dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202666668 | |||||
chr2:202666668
|
C | CTT | 17 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(14): Show | 17 | HG00733.hp1 HG01109.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.602-29196_602-2919 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202666668 | |||||
chr2:202666690
|
A | G | 1 | a0001c0001t0004g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.602-29191A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666690 | ||||||
chr2:202666699
|
C | T | 30 | a0001c0001t0004g0126a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-29182C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666699 | ||||||
chr2:202666923
|
G | A | 1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.602-28958G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666923 | ||||||
chr2:202666974
|
A | T | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-28907A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666974 | ||||||
chr2:202666987
|
G | C | 8 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0216others(5): Show | 8 | HG00621.hp1 NA18940.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.602-28894G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202666987 | ||||||
chr2:202667163
|
C | T | 1 | a0001c0001t0007g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-28718C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667163 | ||||||
chr2:202667173
|
T | G | 1 | a0001c0001t0028g0001 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.602-28708T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667173 | ||||||
chr2:202667212
|
T | A | 70 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(67): Show | 70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.602-28669T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667212 | ||||||
chr2:202667347
|
C | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-28534C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667347 | ||||||
chr2:202667392
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.602-28489C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667392 | ||||||
chr2:202667446
|
A | G | 33 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(30): Show | 33 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.602-28435A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667446 | ||||||
chr2:202667454
|
C | G | 1 | a0002c0002t0099g0312 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.602-28427C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667454 | ||||||
chr2:202667492
|
G | A | 1 | a0001c0001t0019g0197 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.602-28389G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667492 | ||||||
chr2:202667581
|
A | G | 70 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(67): Show | 70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.602-28300A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667581 | ||||||
chr2:202667846
|
G | T | 1 | a0001c0001t0073g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-28035G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202667846 | ||||||
chr2:202668004
|
C | T | 6 | a0001c0001t0008g0038a0001c0001t0008g0150a0001c0001t0131g0041others(3): Show | 6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-27877C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668004 | ||||||
chr2:202668069
|
A | G | 1 | a0001c0001t0073g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-27812A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668069 | ||||||
chr2:202668075
|
A | G | 99 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(96): Show | 99 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.602-27806A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668075 | ||||||
chr2:202668094
|
A | AATATATT | 27 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(24): Show | 27 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.602-27786_602-2778 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668094 | |||||
chr2:202668101
|
T | TA | 6 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-27780_602-2777 others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668101 | ||||||
chr2:202668106
|
T | TTTATA | 6 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-27775_602-2777 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668106 | ||||||
chr2:202668107
|
A | T | 6 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-27774A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668107 | ||||||
chr2:202668155
|
TA | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-27724delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668155 | |||||
chr2:202668172
|
CATATT | C | 28 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(25): Show | 28 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.602-27699_602-2769 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668172 | |||||
chr2:202668202
|
ATTT | A | 9 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-27676_602-2767 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668202 | |||||
chr2:202668233
|
T | G | 1 | a0001c0001t0070g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.602-27648T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668233 | ||||||
chr2:202668281
|
A | G | 1 | a0001c0001t0031g0084 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.602-27600A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668281 | ||||||
chr2:202668412
|
C | T | 1 | a0001c0001t0006g0103 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.602-27469C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668412 | ||||||
chr2:202668514
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.602-27367C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668514 | ||||||
chr2:202668527
|
C | CA | 77 | a0001c0001t0001g0116a0001c0001t0002g0181a0001c0001t0002g0191others(74): Show | 77 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.602-27335dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668527 | |||||
chr2:202668527
|
C | CAA | 25 | a0001c0001t0019g0190a0001c0006t0129g0187a0002c0002t0003g0301others(22): Show | 25 | HG00733.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.602-27336_602-2733 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668527 | |||||
chr2:202668527
|
CA | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0240a0001c0001t0020g0015others(5): Show | 8 | HG00140.hp2 HG02698.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-27335delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668527 | |||||
chr2:202668539
|
A | G | 3 | a0001c0001t0041g0266a0001c0001t0047g0267a0001c0001t0047g0268 | 3 | HG02055.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-27342A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668539 | ||||||
chr2:202668542
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.602-27339A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668542 | ||||||
chr2:202668543
|
A | G | 3 | a0001c0001t0001g0224a0001c0001t0012g0222a0001c0001t0083g0156 | 3 | HG01358.hp1 HG02056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.602-27338A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668543 | ||||||
chr2:202668578
|
T | C | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-27303T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668578 | ||||||
chr2:202668620
|
T | A | 1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.602-27261T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202668620 | ||||||
chr2:202668620
|
T | TAATA | 49 | a0001c0001t0004g0085a0001c0001t0004g0108a0001c0001t0004g0126others(46): Show | 49 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.602-27230_602-2722 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668620 | |||||
chr2:202668620
|
TAATA | T | 108 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(105): Show | 108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.602-27230_602-2722 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202668620 | |||||
chr2:202669198
|
A | G | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-26683A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202669198 | ||||||
chr2:202669517
|
C | T | 4 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0036g0147others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-26364C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202669517 | ||||||
chr2:202669809
|
T | G | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-26072T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202669809 | ||||||
chr2:202670062
|
T | G | 1 | a0001c0001t0040g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.602-25819T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670062 | ||||||
chr2:202670176
|
G | T | 1 | a0001c0001t0004g0171 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.602-25705G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670176 | ||||||
chr2:202670237
|
A | C | 6 | a0001c0001t0004g0171a0001c0001t0032g0071a0001c0001t0032g0090others(3): Show | 6 | HG02132.hp2 NA18966.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-25644A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670237 | ||||||
chr2:202670257
|
C | G | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-25624C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670257 | ||||||
chr2:202670298
|
TC | T | 32 | a0001c0001t0101g0287a0001c0001t0102g0283a0001c0007t0106g0286others(29): Show | 32 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.602-25582delC | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670298 | ||||||
chr2:202670299
|
C | T | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-25582C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670299 | ||||||
chr2:202670352
|
C | T | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.602-25529C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670352 | ||||||
chr2:202670427
|
T | A | 1 | a0001c0001t0082g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.602-25454T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670427 | ||||||
chr2:202670634
|
A | G | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-25247A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670634 | ||||||
chr2:202670763
|
T | C | 2 | a0001c0001t0001g0097a0001c0001t0021g0067 | 2 | HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.602-25118T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202670763 | ||||||
chr2:202671025
|
A | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-24856A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671025 | ||||||
chr2:202671092
|
C | T | 147 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(144): Show | 147 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.602-24789C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671092 | ||||||
chr2:202671158
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.602-24723G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671158 | ||||||
chr2:202671177
|
A | G | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-24704A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671177 | ||||||
chr2:202671224
|
A | T | 2 | a0001c0001t0018g0017a0001c0001t0054g0008 | 2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.602-24657A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671224 | ||||||
chr2:202671362
|
C | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-24519C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671362 | ||||||
chr2:202671597
|
C | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-24284C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671597 | ||||||
chr2:202671738
|
A | G | 1 | a0002c0002t0104g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602-24143A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671738 | ||||||
chr2:202671798
|
C | T | 1 | a0001c0001t0008g0042 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.602-24083C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671798 | ||||||
chr2:202671944
|
T | G | 1 | a0001c0001t0012g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.602-23937T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202671944 | ||||||
chr2:202672251
|
C | A | 5 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-23630C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672251 | ||||||
chr2:202672258
|
G | A | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-23623G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672258 | ||||||
chr2:202672281
|
C | T | 1 | a0001c0001t0047g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.602-23600C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672281 | ||||||
chr2:202672282
|
G | A | 3 | a0001c0001t0011g0007a0001c0001t0011g0021a0001c0001t0011g0114 | 3 | HG00609.hp2 HG01192.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.602-23599G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672282 | ||||||
chr2:202672340
|
G | A | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-23541G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672340 | ||||||
chr2:202672420
|
C | T | 1 | a0001c0001t0119g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.602-23461C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672420 | ||||||
chr2:202672570
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-23311G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672570 | ||||||
chr2:202672817
|
T | A | 1 | a0001c0001t0112g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.602-23064T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672817 | ||||||
chr2:202672921
|
A | T | 7 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(4): Show | 7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-22960A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672921 | ||||||
chr2:202672948
|
T | C | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-22933T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672948 | ||||||
chr2:202672980
|
C | T | 1 | a0001c0001t0006g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.602-22901C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202672980 | ||||||
chr2:202673433
|
G | GT | 30 | a0001c0001t0001g0167a0001c0001t0004g0085a0001c0001t0004g0108others(27): Show | 30 | HG01256.hp1 HG01952.hp2 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-22416dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
G | GTT | 12 | a0001c0001t0009g0165a0001c0001t0018g0016a0001c0001t0018g0120others(9): Show | 12 | HG01081.hp2 HG02293.hp2 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.602-22417_602-2241 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
G | GTTTT | 6 | a0001c0001t0004g0106a0001c0001t0004g0171a0001c0001t0018g0017others(3): Show | 6 | HG00738.hp2 HG01943.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-22419_602-2241 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
G | GTTTTT | 8 | a0001c0001t0004g0009a0001c0001t0032g0071a0001c0001t0032g0090others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-22420_602-2241 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
G | GTTTTTTT | 9 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0030g0292others(6): Show | 9 | HG01168.hp1 HG01169.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.602-22422_602-2241 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
G | GTTTTTTT others(1): Show |
10 | a0002c0002t0003g0303a0002c0002t0003g0308a0002c0002t0003g0309others(7): Show | 10 | HG00733.hp1 HG01243.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.602-22423_602-2241 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0102g0283a0002c0002t0096g0317 | 2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.602-22425_602-2241 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
GT | G | 73 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0062others(70): Show | 73 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.602-22416delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
GTT | G | 12 | a0001c0001t0001g0057a0001c0001t0001g0166a0001c0001t0001g0194others(9): Show | 12 | HG00544.hp2 HG01975.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.602-22417_602-2241 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
GTTTT | G | 8 | a0001c0001t0002g0210a0001c0001t0002g0213a0001c0001t0014g0273others(5): Show | 8 | HG01099.hp2 HG01175.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.602-22419_602-2241 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
GTTTTT | G | 74 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.602-22420_602-2241 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0116g0100 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.602-22425_602-2241 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673433
|
GTTTTTTT others(6): Show |
G | 1 | a0002c0002t0104g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602-22428_602-2241 others(17): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202673433 | |||||
chr2:202673444
|
T | G | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-22437T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673444 | ||||||
chr2:202673568
|
C | G | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.602-22313C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673568 | ||||||
chr2:202673605
|
A | G | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-22276A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673605 | ||||||
chr2:202673608
|
C | T | 8 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(5): Show | 8 | HG02257.hp2 HG02559.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-22273C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673608 | ||||||
chr2:202673651
|
T | G | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-22230T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673651 | ||||||
chr2:202673784
|
T | A | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.602-22097T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673784 | ||||||
chr2:202673893
|
A | T | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-21988A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202673893 | ||||||
chr2:202674027
|
C | G | 1 | a0001c0001t0068g0239 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.602-21854C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674027 | ||||||
chr2:202674033
|
C | G | 26 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(23): Show | 26 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.602-21848C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674033 | ||||||
chr2:202674343
|
C | T | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-21538C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674343 | ||||||
chr2:202674580
|
C | T | 1 | a0001c0001t0071g0212 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602-21301C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674580 | ||||||
chr2:202674957
|
G | A | 1 | a0001c0001t0002g0217 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.602-20924G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202674957 | ||||||
chr2:202675090
|
C | G | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-20791C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675090 | ||||||
chr2:202675101
|
G | A | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.602-20780G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675101 | ||||||
chr2:202675180
|
A | C | 21 | a0001c0001t0001g0075a0001c0001t0001g0166a0001c0001t0001g0175others(18): Show | 21 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-20701A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675180 | ||||||
chr2:202675237
|
A | C | 98 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(95): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.602-20644A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675237 | ||||||
chr2:202675445
|
C | CA | 13 | a0001c0001t0001g0253a0001c0001t0018g0143a0001c0001t0020g0160others(10): Show | 13 | HG02027.hp1 HG02451.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.602-20413dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | |||||
chr2:202675445
|
C | CAA | 46 | a0001c0001t0008g0038a0001c0001t0008g0042a0001c0001t0008g0043others(43): Show | 46 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.602-20414_602-2041 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | |||||
chr2:202675445
|
C | CAAA | 159 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(156): Show | 159 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.602-20415_602-2041 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | |||||
chr2:202675445
|
C | CAAAA | 29 | a0001c0001t0001g0058a0001c0001t0001g0154a0001c0001t0001g0155others(26): Show | 29 | HG00597.hp1 HG00642.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.602-20416_602-2041 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675445 | |||||
chr2:202675526
|
C | T | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.602-20355C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675526 | ||||||
chr2:202675547
|
T | C | 1 | a0001c0001t0070g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.602-20334T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675547 | ||||||
chr2:202675630
|
G | T | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-20251G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675630 | ||||||
chr2:202675712
|
T | C | 248 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(245): Show | 248 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.602-20169T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675712 | ||||||
chr2:202675733
|
C | G | 3 | a0001c0001t0011g0093a0001c0001t0046g0138a0001c0001t0046g0139 | 3 | HG02071.hp1 NA18970.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.602-20148C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675733 | ||||||
chr2:202675737
|
A | C | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-20144A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675737 | ||||||
chr2:202675741
|
C | T | 39 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(36): Show | 39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.602-20140C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675741 | ||||||
chr2:202675940
|
G | A | 1 | a0001c0001t0071g0212 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602-19941G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202675940 | ||||||
chr2:202675984
|
C | CA | 17 | a0001c0001t0001g0062a0001c0001t0001g0116a0001c0001t0002g0220others(14): Show | 17 | HG00323.hp1 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.602-19876dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675984 | |||||
chr2:202675984
|
C | CAA | 27 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(24): Show | 27 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.602-19877_602-1987 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675984 | |||||
chr2:202675984
|
CA | C | 13 | a0001c0001t0004g0009a0001c0001t0018g0016a0001c0001t0026g0186others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.602-19876delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202675984 | |||||
chr2:202676109
|
A | G | 28 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(25): Show | 28 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.602-19772A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676109 | ||||||
chr2:202676180
|
A | G | 1 | a0001c0001t0040g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.602-19701A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676180 | ||||||
chr2:202676375
|
GT | G | 222 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(219): Show | 222 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.602-19490delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202676375 | |||||
chr2:202676441
|
G | A | 1 | a0001c0001t0005g0228 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.602-19440G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676441 | ||||||
chr2:202676831
|
C | T | 2 | a0001c0001t0018g0017a0001c0001t0054g0008 | 2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.602-19050C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676831 | ||||||
chr2:202676931
|
T | C | 70 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(67): Show | 70 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.602-18950T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676931 | ||||||
chr2:202676946
|
G | T | 20 | a0001c0001t0002g0191a0001c0001t0002g0195a0001c0001t0002g0216others(17): Show | 20 | HG00558.hp2 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.602-18935G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202676946 | ||||||
chr2:202677027
|
T | C | 98 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(95): Show | 98 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.602-18854T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677027 | ||||||
chr2:202677063
|
C | CT | 30 | a0001c0001t0017g0198a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-18803dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202677063 | |||||
chr2:202677073
|
T | G | 3 | a0001c0001t0039g0258a0001c0001t0039g0260a0001c0001t0076g0264 | 3 | HG00733.hp2 HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.602-18808T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677073 | ||||||
chr2:202677093
|
C | T | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-18788C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677093 | ||||||
chr2:202677163
|
G | A | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18718G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677163 | ||||||
chr2:202677192
|
C | T | 2 | a0001c0001t0009g0165a0001c0001t0045g0149 | 2 | HG01952.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.602-18689C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677192 | ||||||
chr2:202677302
|
G | A | 1 | a0001c0001t0082g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.602-18579G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677302 | ||||||
chr2:202677308
|
C | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18573C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677308 | ||||||
chr2:202677433
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.602-18448G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677433 | ||||||
chr2:202677533
|
G | A | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18348G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677533 | ||||||
chr2:202677566
|
C | T | 1 | a0001c0001t0139g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.602-18315C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677566 | ||||||
chr2:202677781
|
A | G | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18100A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677781 | ||||||
chr2:202677862
|
A | G | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-18019A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202677862 | ||||||
chr2:202678009
|
T | G | 1 | a0001c0001t0001g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.602-17872T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678009 | ||||||
chr2:202678139
|
A | G | 3 | a0001c0001t0006g0103a0001c0001t0006g0131a0003c0003t0006g0072 | 3 | HG02572.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.602-17742A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678139 | ||||||
chr2:202678472
|
C | T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-17409C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678472 | ||||||
chr2:202678581
|
C | T | 1 | a0001c0001t0030g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.602-17300C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678581 | ||||||
chr2:202678746
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-17135C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678746 | ||||||
chr2:202678767
|
A | C | 1 | a0001c0001t0007g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.602-17114A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202678767 | ||||||
chr2:202679029
|
C | G | 1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.602-16852C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679029 | ||||||
chr2:202679151
|
A | G | 12 | a0001c0001t0004g0009a0001c0001t0004g0106a0001c0001t0004g0171others(9): Show | 12 | HG00738.hp2 HG01943.hp1 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.602-16730A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679151 | ||||||
chr2:202679406
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-16475G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679406 | ||||||
chr2:202679479
|
T | C | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-16402T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679479 | ||||||
chr2:202679627
|
G | A | 5 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-16254G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679627 | ||||||
chr2:202679723
|
A | T | 1 | a0001c0001t0119g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.602-16158A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202679723 | ||||||
chr2:202680010
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-15871G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680010 | ||||||
chr2:202680221
|
C | T | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-15660C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680221 | ||||||
chr2:202680266
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.602-15615A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680266 | ||||||
chr2:202680271
|
G | T | 1 | a0001c0001t0005g0228 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.602-15610G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680271 | ||||||
chr2:202680286
|
G | T | 1 | a0001c0001t0042g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.602-15595G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680286 | ||||||
chr2:202680404
|
A | T | 26 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(23): Show | 26 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.602-15477A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680404 | ||||||
chr2:202680421
|
T | A | 230 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(227): Show | 230 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.602-15460T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680421 | ||||||
chr2:202680475
|
C | T | 149 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(146): Show | 149 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.602-15406C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680475 | ||||||
chr2:202680543
|
C | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-15338C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680543 | ||||||
chr2:202680608
|
C | T | 1 | a0001c0001t0119g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.602-15273C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680608 | ||||||
chr2:202680642
|
A | G | 1 | a0001c0001t0008g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.602-15239A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202680642 | ||||||
chr2:202681021
|
T | C | 1 | a0001c0001t0081g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.602-14860T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681021 | ||||||
chr2:202681476
|
C | T | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-14405C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681476 | ||||||
chr2:202681531
|
A | G | 9 | a0001c0001t0004g0106a0001c0001t0004g0171a0001c0001t0018g0017others(6): Show | 9 | HG00738.hp2 HG01943.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-14350A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681531 | ||||||
chr2:202681586
|
T | A | 3 | a0002c0002t0024g0289a0002c0002t0024g0290a0002c0002t0063g0291 | 3 | HG03130.hp2 HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.602-14295T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681586 | ||||||
chr2:202681814
|
C | A | 3 | a0001c0001t0021g0027a0001c0001t0122g0209a0001c0001t0124g0208 | 3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.602-14067C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681814 | ||||||
chr2:202681980
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.602-13901G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202681980 | ||||||
chr2:202682027
|
T | C | 1 | a0001c0001t0007g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.602-13854T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682027 | ||||||
chr2:202682037
|
C | T | 8 | a0001c0001t0028g0064a0001c0001t0028g0076a0001c0001t0029g0004others(5): Show | 8 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.602-13844C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682037 | ||||||
chr2:202682050
|
C | T | 1 | a0001c0001t0075g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.602-13831C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682050 | ||||||
chr2:202682150
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(75): Show | 78 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.602-13731C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682150 | ||||||
chr2:202682166
|
C | T | 3 | a0001c0001t0021g0027a0001c0001t0122g0209a0001c0001t0124g0208 | 3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.602-13715C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682166 | ||||||
chr2:202682383
|
C | T | 26 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(23): Show | 26 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.602-13498C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682383 | ||||||
chr2:202682739
|
G | A | 2 | a0001c0001t0101g0287a0001c0007t0106g0286 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.602-13142G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682739 | ||||||
chr2:202682890
|
G | T | 1 | a0001c0001t0122g0209 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.602-12991G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202682890 | ||||||
chr2:202682902
|
TATA | T | 6 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0006g0250others(3): Show | 6 | HG02027.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-12977_602-1297 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202682902 | |||||
chr2:202683093
|
C | T | 27 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(24): Show | 27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.602-12788C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683093 | ||||||
chr2:202683098
|
C | T | 9 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-12783C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683098 | ||||||
chr2:202683114
|
G | C | 9 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.602-12767G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683114 | ||||||
chr2:202683147
|
G | A | 1 | a0001c0001t0009g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.602-12734G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683147 | ||||||
chr2:202683164
|
C | G | 6 | a0001c0001t0008g0038a0001c0001t0008g0150a0001c0001t0131g0041others(3): Show | 6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-12717C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683164 | ||||||
chr2:202683184
|
C | T | 68 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.602-12697C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683184 | ||||||
chr2:202683198
|
T | C | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-12683T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683198 | ||||||
chr2:202683278
|
G | A | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-12603G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683278 | ||||||
chr2:202683336
|
CAAAA | C | 21 | a0001c0001t0001g0075a0001c0001t0001g0166a0001c0001t0001g0175others(18): Show | 21 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.602-12542_602-1253 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202683336 | |||||
chr2:202683612
|
C | A | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.602-12269C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683612 | ||||||
chr2:202683630
|
T | C | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-12251T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683630 | ||||||
chr2:202683696
|
C | G | 1 | a0001c0001t0020g0015 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.602-12185C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683696 | ||||||
chr2:202683812
|
T | G | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-12069T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683812 | ||||||
chr2:202683929
|
C | T | 1 | a0001c0001t0015g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.602-11952C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202683929 | ||||||
chr2:202684015
|
C | T | 1 | a0001c0001t0060g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.602-11866C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684015 | ||||||
chr2:202684087
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.602-11794G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684087 | ||||||
chr2:202684288
|
A | G | 261 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(258): Show | 261 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.602-11593A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684288 | ||||||
chr2:202684302
|
CTTA | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-11573_602-1157 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202684302 | |||||
chr2:202684328
|
C | T | 2 | a0001c0001t0012g0066a0001c0001t0044g0098 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.602-11553C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684328 | ||||||
chr2:202684363
|
C | T | 1 | a0001c0004t0037g0023 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.602-11518C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684363 | ||||||
chr2:202684437
|
T | C | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-11444T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684437 | ||||||
chr2:202684465
|
C | T | 3 | a0001c0001t0039g0258a0001c0001t0039g0260a0001c0001t0076g0264 | 3 | HG00733.hp2 HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.602-11416C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684465 | ||||||
chr2:202684492
|
G | A | 1 | a0001c0001t0018g0017 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.602-11389G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684492 | ||||||
chr2:202684494
|
G | A | 34 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-11387G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684494 | ||||||
chr2:202684521
|
C | T | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.602-11360C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684521 | ||||||
chr2:202684663
|
G | A | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-11218G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684663 | ||||||
chr2:202684685
|
T | TTA | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-11193_602-1119 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202684685 | |||||
chr2:202684879
|
T | C | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.602-11002T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684879 | ||||||
chr2:202684917
|
A | C | 1 | a0001c0001t0011g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.602-10964A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684917 | ||||||
chr2:202684990
|
A | AT | 14 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(11): Show | 14 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.602-10879dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202684990 | |||||
chr2:202684990
|
A | T | 6 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0006g0250others(3): Show | 6 | HG02027.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-10891A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684990 | ||||||
chr2:202684991
|
T | A | 5 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-10890T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202684991 | ||||||
chr2:202685017
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.602-10864C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685017 | ||||||
chr2:202685149
|
A | T | 1 | a0001c0001t0011g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.602-10732A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685149 | ||||||
chr2:202685234
|
C | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-10647C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685234 | ||||||
chr2:202685302
|
C | T | 69 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(66): Show | 69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.602-10579C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685302 | ||||||
chr2:202685475
|
G | A | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-10406G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685475 | ||||||
chr2:202685658
|
A | G | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-10223A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685658 | ||||||
chr2:202685751
|
C | T | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-10130C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685751 | ||||||
chr2:202685779
|
A | C | 29 | a0002c0002t0003g0301a0002c0002t0003g0302a0002c0002t0003g0303others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-10102A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685779 | ||||||
chr2:202685847
|
G | A | 1 | a0001c0001t0055g0148 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.602-10034G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202685847 | ||||||
chr2:202686018
|
T | C | 156 | a0001c0001t0001g0251a0001c0001t0001g0253a0001c0001t0002g0181others(153): Show | 156 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.602-9863T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686018 | ||||||
chr2:202686049
|
C | A | 6 | a0001c0001t0008g0038a0001c0001t0008g0150a0001c0001t0131g0041others(3): Show | 6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-9832C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686049 | ||||||
chr2:202686100
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.602-9781A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686100 | ||||||
chr2:202686117
|
T | G | 1 | a0001c0001t0013g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.602-9764T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686117 | ||||||
chr2:202686163
|
T | C | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-9718T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686163 | ||||||
chr2:202686584
|
G | A | 1 | a0001c0001t0084g0018 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.602-9297G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686584 | ||||||
chr2:202686637
|
C | T | 2 | a0002c0002t0016g0300a0002c0002t0108g0294 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.602-9244C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686637 | ||||||
chr2:202686805
|
C | CA | 71 | a0001c0001t0001g0116a0001c0001t0002g0181a0001c0001t0002g0191others(68): Show | 71 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.602-9063dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202686805 | |||||
chr2:202686822
|
G | T | 68 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.602-9059G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686822 | ||||||
chr2:202686825
|
T | C | 1 | a0001c0001t0078g0259 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.602-9056T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686825 | ||||||
chr2:202686869
|
G | A | 1 | a0001c0001t0134g0102 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.602-9012G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686869 | ||||||
chr2:202686899
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.602-8982A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202686899 | ||||||
chr2:202687149
|
A | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-8732A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687149 | ||||||
chr2:202687375
|
A | G | 1 | a0002c0005t0016g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.602-8506A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687375 | ||||||
chr2:202687617
|
C | T | 1 | a0001c0001t0139g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.602-8264C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687617 | ||||||
chr2:202687618
|
C | T | 1 | a0001c0001t0020g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.602-8263C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687618 | ||||||
chr2:202687684
|
T | G | 1 | a0001c0001t0022g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.602-8197T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687684 | ||||||
chr2:202687687
|
A | T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602-8194A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687687 | ||||||
chr2:202687710
|
C | G | 1 | a0001c0001t0022g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.602-8171C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687710 | ||||||
chr2:202687820
|
T | C | 1 | a0001c0001t0077g0026 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.602-8061T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687820 | ||||||
chr2:202687860
|
G | T | 1 | a0001c0001t0086g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.602-8021G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202687860 | ||||||
chr2:202688469
|
T | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0167a0001c0001t0005g0228others(3): Show | 6 | HG02155.hp2 NA18940.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-7412T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688469 | ||||||
chr2:202688531
|
T | G | 1 | a0002c0002t0107g0305 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.602-7350T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688531 | ||||||
chr2:202688652
|
T | G | 1 | a0001c0001t0031g0178 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.602-7229T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688652 | ||||||
chr2:202688904
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-6977C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202688904 | ||||||
chr2:202689113
|
G | A | 78 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(75): Show | 78 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.602-6768G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689113 | ||||||
chr2:202689191
|
A | C | 1 | a0001c0001t0007g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-6690A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689191 | ||||||
chr2:202689601
|
A | C | 16 | a0001c0001t0008g0038a0001c0001t0008g0042a0001c0001t0008g0043others(13): Show | 16 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.602-6280A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689601 | ||||||
chr2:202689911
|
C | T | 3 | a0001c0001t0021g0027a0001c0001t0122g0209a0001c0001t0124g0208 | 3 | HG03017.hp2 HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.602-5970C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689911 | ||||||
chr2:202689912
|
G | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.602-5969G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202689912 | ||||||
chr2:202690484
|
C | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-5397C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202690484 | ||||||
chr2:202690620
|
G | T | 175 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(172): Show | 175 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.602-5261G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202690620 | ||||||
chr2:202690796
|
A | T | 1 | a0001c0001t0001g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.602-5085A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202690796 | ||||||
chr2:202690981
|
CT | C | 34 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(31): Show | 34 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-4895delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202690981 | |||||
chr2:202691043
|
A | C | 1 | a0001c0001t0030g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.602-4838A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691043 | ||||||
chr2:202691105
|
C | T | 63 | a0001c0001t0004g0009a0001c0001t0004g0085a0001c0001t0004g0086others(60): Show | 63 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.602-4776C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691105 | ||||||
chr2:202691452
|
T | A | 1 | a0001c0001t0071g0212 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602-4429T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691452 | ||||||
chr2:202691501
|
T | TA | 13 | a0001c0001t0004g0085a0001c0001t0050g0284a0001c0001t0050g0285others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.602-4369dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691501 | |||||
chr2:202691501
|
TA | T | 175 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(172): Show | 175 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.602-4369delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691501 | |||||
chr2:202691503
|
A | T | 5 | a0001c0001t0002g0204a0001c0001t0002g0213a0001c0001t0025g0211others(2): Show | 5 | HG00099.hp1 HG01071.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-4378A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691503 | ||||||
chr2:202691581
|
A | G | 1 | a0001c0001t0055g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.602-4300A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691581 | ||||||
chr2:202691581
|
ATAGT | A | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-4296_602-4293d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691581 | |||||
chr2:202691649
|
T | TTG | 4 | a0001c0001t0055g0161a0001c0001t0073g0229a0002c0002t0024g0290others(1): Show | 4 | HG03225.hp1 HG03516.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.602-4183_602-4182d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
T | TTGTG | 5 | a0001c0001t0009g0105a0001c0001t0035g0055a0001c0001t0045g0149others(2): Show | 5 | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-4185_602-4182d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0013g0046 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.602-4217_602-4216i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
TTG | T | 43 | a0001c0001t0001g0065a0001c0001t0001g0253a0001c0001t0002g0210others(40): Show | 43 | HG00408.hp1 HG01109.hp2 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.602-4183_602-4182d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
TTGTG | T | 50 | a0001c0001t0001g0080a0001c0001t0001g0157a0001c0001t0001g0251others(47): Show | 50 | HG00099.hp1 HG00544.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.602-4185_602-4182d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
TTGTGTG | T | 61 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(58): Show | 61 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.602-4187_602-4182d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
TTGTGTGT others(1): Show |
T | 26 | a0001c0001t0001g0057a0001c0001t0002g0087a0001c0001t0002g0104others(23): Show | 26 | HG00140.hp1 HG01346.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.602-4189_602-4182d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0069a0001c0001t0005g0228a0001c0001t0012g0164others(2): Show | 5 | HG02818.hp2 NA18988.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-4191_602-4182d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691649
|
TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0077g0026 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.602-4195_602-4182d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691649 | |||||
chr2:202691651
|
G | GTGTGTGT others(7): Show |
2 | a0001c0001t0008g0034a0001c0001t0013g0033 | 2 | HG03453.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.602-4217_602-4216i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691651 | |||||
chr2:202691653
|
G | GTGTGTGT others(5): Show |
2 | a0001c0001t0013g0030a0001c0001t0023g0048 | 2 | HG00741.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.602-4217_602-4216i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691653 | |||||
chr2:202691655
|
G | GTGTGTGT others(3): Show |
7 | a0001c0001t0008g0042a0001c0001t0008g0043a0001c0001t0013g0050others(4): Show | 7 | HG00140.hp2 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-4217_602-4216i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691655 | |||||
chr2:202691657
|
G | GTGTGTGT others(1): Show |
4 | a0001c0001t0008g0045a0001c0001t0023g0047a0001c0001t0110g0036others(1): Show | 4 | HG00639.hp1 HG01261.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.602-4217_602-4216i others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691657 | |||||
chr2:202691657
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0022g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.602-4215_602-4214i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691657 | |||||
chr2:202691659
|
G | GTGTGTA | 3 | a0001c0001t0022g0130a0001c0001t0137g0032a0001c0001t0139g0028 | 3 | HG00544.hp2 HG00642.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.602-4217_602-4216i others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691659 | |||||
chr2:202691663
|
G | GTA | 5 | a0001c0001t0008g0038a0001c0001t0008g0150a0001c0001t0131g0041others(2): Show | 5 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.602-4217_602-4216i others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691663 | |||||
chr2:202691667
|
G | A | 1 | a0001c0001t0133g0039 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.602-4214G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691667 | ||||||
chr2:202691682
|
TGTGTGTG others(11): Show |
T | 1 | a0002c0002t0097g0315 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.602-4197_602-4180d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691682 | |||||
chr2:202691690
|
TGTGTGTG others(3): Show |
T | 1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.602-4189_602-4180d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691690 | |||||
chr2:202691692
|
TGTGTGTG others(1): Show |
T | 5 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0045g0006others(2): Show | 5 | HG02622.hp2 HG03139.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-4187_602-4180d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691692 | |||||
chr2:202691694
|
T | C | 1 | a0001c0001t0007g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-4187T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691694 | ||||||
chr2:202691696
|
T | C | 15 | a0001c0001t0002g0181a0001c0001t0002g0202a0001c0001t0002g0203others(12): Show | 15 | HG00673.hp2 HG01071.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.602-4185T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691696 | ||||||
chr2:202691696
|
T | TGC | 7 | a0001c0001t0002g0193a0001c0001t0002g0199a0001c0001t0017g0024others(4): Show | 7 | HG00408.hp2 HG01361.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.602-4184_602-4183i others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691696 | |||||
chr2:202691696
|
TGTGC | T | 3 | a0001c0001t0042g0003a0001c0007t0106g0286a0002c0002t0098g0316 | 3 | HG02257.hp2 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.602-4183_602-4180d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691696 | |||||
chr2:202691698
|
T | C | 134 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(131): Show | 134 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.602-4183T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691698 | ||||||
chr2:202691698
|
T | TGC | 15 | a0001c0001t0001g0155a0001c0001t0001g0240a0001c0001t0002g0204others(12): Show | 15 | HG00642.hp2 HG01071.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-4174_602-4173d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | |||||
chr2:202691698
|
T | TGTGC | 12 | a0001c0001t0001g0158a0001c0001t0002g0213a0001c0001t0014g0270others(9): Show | 12 | HG00597.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.602-4182_602-4181i others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | |||||
chr2:202691698
|
T | TGTGTGCG others(3): Show |
1 | a0001c0001t0026g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.602-4182_602-4181i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | |||||
chr2:202691698
|
T | TGTGTGTG others(5): Show |
1 | a0001c0001t0122g0209 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.602-4182_602-4181i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202691698 | |||||
chr2:202691700
|
C | T | 2 | a0001c0001t0009g0060a0001c0001t0073g0229 | 2 | HG03225.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.602-4181C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691700 | ||||||
chr2:202691744
|
G | A | 6 | a0001c0001t0008g0038a0001c0001t0008g0150a0001c0001t0131g0041others(3): Show | 6 | HG00609.hp1 HG02132.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.602-4137G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691744 | ||||||
chr2:202691803
|
T | C | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.602-4078T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202691803 | ||||||
chr2:202692149
|
A | C | 1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.602-3732A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692149 | ||||||
chr2:202692277
|
A | G | 1 | a0001c0001t0045g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.602-3604A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692277 | ||||||
chr2:202692428
|
T | C | 29 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(26): Show | 29 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.602-3453T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692428 | ||||||
chr2:202692716
|
C | T | 1 | a0001c0001t0038g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.602-3165C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692716 | ||||||
chr2:202692746
|
G | A | 8 | a0003c0003t0010g0196a0003c0003t0010g0244a0003c0003t0010g0246others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.602-3135G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692746 | ||||||
chr2:202692785
|
A | G | 6 | a0001c0001t0001g0020a0001c0001t0001g0062a0001c0001t0001g0182others(3): Show | 6 | HG00323.hp1 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.602-3096A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692785 | ||||||
chr2:202692887
|
G | C | 1 | a0001c0001t0007g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.602-2994G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692887 | ||||||
chr2:202692963
|
A | C | 2 | a0001c0001t0027g0252a0001c0001t0027g0254 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.602-2918A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202692963 | ||||||
chr2:202693196
|
G | A | 1 | a0001c0001t0015g0129 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.602-2685G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693196 | ||||||
chr2:202693334
|
T | TGTG | 34 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-2543_602-2541d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202693334 | |||||
chr2:202693442
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.602-2439C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693442 | ||||||
chr2:202693582
|
C | T | 1 | a0001c0001t0055g0148 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.602-2299C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693582 | ||||||
chr2:202693596
|
AAAAAC | A | 3 | a0001c0001t0031g0063a0001c0001t0031g0084a0001c0001t0067g0219 | 3 | HG02155.hp1 NA18747.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.602-2271_602-2267d others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202693596 | |||||
chr2:202693718
|
G | C | 39 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(36): Show | 39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.602-2163G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693718 | ||||||
chr2:202693800
|
G | A | 39 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(36): Show | 39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.602-2081G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693800 | ||||||
chr2:202693808
|
A | G | 69 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(66): Show | 69 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.602-2073A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202693808 | ||||||
chr2:202694177
|
A | C | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.602-1704A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694177 | ||||||
chr2:202694188
|
C | CT | 40 | a0001c0001t0001g0194a0001c0001t0008g0034a0001c0001t0008g0038others(37): Show | 40 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.602-1672dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0009g0002a0001c0001t0045g0006 | 2 | HG02622.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.602-1681_602-1672d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.602-1682_602-1672d others(13): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.602-1683_602-1672d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(6): Show |
1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.602-1684_602-1672d others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0102g0283 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.602-1685_602-1672d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(11): Show |
2 | a0002c0002t0016g0300a0002c0002t0108g0294 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.602-1689_602-1672d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(12): Show |
5 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0105g0314others(2): Show | 5 | HG01243.hp1 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-1690_602-1672d others(21): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
C | CTTTTTTT others(13): Show |
1 | a0002c0002t0104g0298 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602-1691_602-1672d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694188
|
CTTTTTT | C | 15 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(12): Show | 15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-1677_602-1672d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 202694188 | |||||
chr2:202694282
|
T | C | 251 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(248): Show | 251 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.602-1599T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694282 | ||||||
chr2:202694387
|
C | T | 1 | a0001c0001t0007g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.602-1494C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694387 | ||||||
chr2:202694506
|
A | G | 2 | a0001c0001t0119g0225a0001c0001t0121g0226 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.602-1375A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694506 | ||||||
chr2:202694528
|
C | G | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.602-1353C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694528 | ||||||
chr2:202694627
|
G | A | 1 | a0001c0001t0081g0128 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.602-1254G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694627 | ||||||
chr2:202694718
|
G | C | 34 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(31): Show | 34 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.602-1163G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694718 | ||||||
chr2:202694721
|
C | T | 1 | a0001c0001t0005g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.602-1160C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694721 | ||||||
chr2:202694837
|
A | T | 1 | a0001c0001t0017g0198 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.602-1044A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202694837 | ||||||
chr2:202695055
|
G | A | 15 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(12): Show | 15 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.602-826G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695055 | ||||||
chr2:202695416
|
C | G | 1 | a0001c0001t0073g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.602-465C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695416 | ||||||
chr2:202695489
|
C | A | 1 | a0001c0001t0007g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.602-392C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695489 | ||||||
chr2:202695510
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.602-371T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | chr2 | 202695510 | ||||||
chr2:202696062
|
T | G | 1 | a0001c0001t0047g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.753+30T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696062 | ||||||
chr2:202696353
|
C | T | 29 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(26): Show | 29 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.753+321C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696353 | ||||||
chr2:202696507
|
C | T | 3 | a0001c0001t0018g0016a0001c0001t0056g0169a0001c0001t0056g0170 | 3 | HG00140.hp1 HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.753+475C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696507 | ||||||
chr2:202696592
|
G | C | 1 | a0001c0001t0070g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.753+560G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696592 | ||||||
chr2:202696811
|
G | A | 1 | a0001c0001t0007g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.753+779G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696811 | ||||||
chr2:202696832
|
G | A | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+800G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202696832 | ||||||
chr2:202697099
|
A | G | 2 | a0001c0001t0015g0180a0001c0001t0015g0189 | 2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.753+1067A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697099 | ||||||
chr2:202697532
|
A | T | 1 | a0001c0001t0030g0005 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.753+1500A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697532 | ||||||
chr2:202697562
|
T | C | 4 | a0001c0001t0014g0270a0001c0001t0057g0281a0001c0001t0058g0280others(1): Show | 4 | NA18939.hp2 NA18974.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+1530T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697562 | ||||||
chr2:202697573
|
T | G | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+1541T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697573 | ||||||
chr2:202697590
|
G | A | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+1558G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697590 | ||||||
chr2:202697694
|
C | T | 1 | a0001c0001t0112g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.753+1662C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202697694 | ||||||
chr2:202698000
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.753+1968G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698000 | ||||||
chr2:202698017
|
A | G | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.753+1985A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698017 | ||||||
chr2:202698144
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.753+2112C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698144 | ||||||
chr2:202698323
|
G | A | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+2291G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698323 | ||||||
chr2:202698384
|
C | T | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.753+2352C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698384 | ||||||
chr2:202698549
|
A | G | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+2517A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698549 | ||||||
chr2:202698571
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0059g0279 | 2 | NA18999.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.753+2539C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698571 | ||||||
chr2:202698572
|
G | A | 3 | a0001c0001t0001g0135a0001c0001t0043g0141a0001c0001t0044g0110 | 3 | NA18940.hp1 NA18977.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.753+2540G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698572 | ||||||
chr2:202698665
|
C | T | 2 | a0001c0004t0037g0022a0001c0004t0037g0023 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.753+2633C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698665 | ||||||
chr2:202698669
|
C | T | 4 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0036g0147others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+2637C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698669 | ||||||
chr2:202698713
|
G | A | 5 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+2681G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698713 | ||||||
chr2:202698778
|
C | G | 1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.753+2746C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202698778 | ||||||
chr2:202699369
|
G | A | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+3337G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699369 | ||||||
chr2:202699426
|
C | CA | 12 | a0001c0001t0001g0065a0001c0001t0007g0132a0001c0001t0012g0073others(9): Show | 12 | HG01192.hp1 HG01358.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.753+3416dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699426 | |||||
chr2:202699426
|
CA | C | 9 | a0001c0001t0006g0010a0001c0001t0006g0250a0001c0001t0021g0067others(6): Show | 9 | HG01168.hp2 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.753+3416delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699426 | |||||
chr2:202699445
|
A | G | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.753+3413A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699445 | ||||||
chr2:202699449
|
G | A | 14 | a0001c0001t0002g0220a0001c0001t0009g0002a0001c0001t0028g0001others(11): Show | 14 | HG00621.hp1 HG01109.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.753+3417G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699449 | ||||||
chr2:202699449
|
GA | G | 98 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(95): Show | 98 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.753+3432delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699449 | |||||
chr2:202699449
|
GAA | G | 7 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(4): Show | 7 | HG01884.hp2 HG03098.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+3431_753+3432d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202699449 | |||||
chr2:202699450
|
A | AG | 8 | a0001c0001t0028g0001a0001c0001t0045g0006a0001c0001t0050g0284others(5): Show | 8 | HG02109.hp1 HG02723.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+3418_753+3419i others(3): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699450 | ||||||
chr2:202699450
|
A | G | 7 | a0001c0001t0002g0220a0001c0001t0009g0002a0001c0001t0042g0003others(4): Show | 7 | HG00621.hp1 HG01109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.753+3418A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699450 | ||||||
chr2:202699580
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.753+3548C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699580 | ||||||
chr2:202699604
|
A | T | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+3572A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699604 | ||||||
chr2:202699752
|
C | A | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+3720C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699752 | ||||||
chr2:202699959
|
C | A | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+3927C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202699959 | ||||||
chr2:202700001
|
G | T | 1 | a0001c0001t0133g0039 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.753+3969G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700001 | ||||||
chr2:202700276
|
CAGCT | C | 9 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+4248_753+4251d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202700276 | |||||
chr2:202700399
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.753+4367G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700399 | ||||||
chr2:202700685
|
A | AT | 58 | a0001c0001t0002g0217a0001c0001t0009g0002a0001c0001t0027g0136others(55): Show | 58 | HG00733.hp1 HG01109.hp2 HG01169.hp1 others(55): Show |
intron_variant | MODIFIER | c.753+4672dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202700685 | |||||
chr2:202700713
|
G | A | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+4681G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700713 | ||||||
chr2:202700761
|
G | A | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+4729G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202700761 | ||||||
chr2:202701106
|
T | C | 1 | a0003c0003t0006g0072 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.753+5074T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701106 | ||||||
chr2:202701254
|
T | C | 2 | a0001c0001t0014g0272a0001c0001t0061g0276 | 2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.753+5222T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701254 | ||||||
chr2:202701355
|
C | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0092a0001c0001t0001g0116others(15): Show | 18 | HG00642.hp2 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.753+5323C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701355 | ||||||
chr2:202701582
|
T | C | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.753+5550T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701582 | ||||||
chr2:202701634
|
C | G | 1 | a0001c0001t0127g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.753+5602C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701634 | ||||||
chr2:202701753
|
G | A | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.753+5721G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701753 | ||||||
chr2:202701998
|
A | G | 9 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(6): Show | 9 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.753+5966A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202701998 | ||||||
chr2:202702001
|
G | C | 76 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(73): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.753+5969G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702001 | ||||||
chr2:202702055
|
G | T | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+6023G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702055 | ||||||
chr2:202702114
|
C | T | 2 | a0003c0003t0010g0196a0003c0003t0010g0244 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.753+6082C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702114 | ||||||
chr2:202702121
|
G | A | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+6089G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702121 | ||||||
chr2:202702198
|
C | T | 7 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(4): Show | 7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+6166C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702198 | ||||||
chr2:202702227
|
T | C | 40 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(37): Show | 40 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.753+6195T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702227 | ||||||
chr2:202702242
|
T | G | 1 | a0001c0001t0004g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.753+6210T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702242 | ||||||
chr2:202702288
|
G | T | 1 | a0001c0001t0004g0086 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.753+6256G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702288 | ||||||
chr2:202702313
|
C | T | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+6281C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702313 | ||||||
chr2:202702414
|
T | G | 12 | a0001c0001t0009g0105a0001c0001t0039g0258a0001c0001t0039g0260others(9): Show | 12 | HG00323.hp2 HG00639.hp2 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.753+6382T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702414 | ||||||
chr2:202702703
|
G | A | 1 | a0001c0001t0073g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.753+6671G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702703 | ||||||
chr2:202702743
|
C | T | 2 | a0003c0003t0010g0196a0003c0003t0010g0244 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.753+6711C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702743 | ||||||
chr2:202702775
|
G | A | 1 | a0001c0001t0045g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.753+6743G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702775 | ||||||
chr2:202702821
|
G | A | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+6789G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702821 | ||||||
chr2:202702956
|
A | G | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.753+6924A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202702956 | ||||||
chr2:202703219
|
A | G | 2 | a0002c0002t0051g0293a0002c0002t0051g0313 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.753+7187A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703219 | ||||||
chr2:202703225
|
C | G | 2 | a0001c0001t0091g0265a0002c0002t0105g0314 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.753+7193C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703225 | ||||||
chr2:202703359
|
A | G | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.753+7327A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703359 | ||||||
chr2:202703468
|
G | T | 1 | a0001c0001t0068g0239 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.753+7436G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202703468 | ||||||
chr2:202703510
|
A | ATG | 5 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(2): Show | 5 | HG02109.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+7479_753+7480d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202703510 | |||||
chr2:202704235
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.753+8203T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704235 | ||||||
chr2:202704237
|
T | C | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.753+8205T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704237 | ||||||
chr2:202704365
|
A | G | 3 | a0001c0001t0001g0253a0001c0001t0027g0252a0001c0001t0027g0254 | 3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.753+8333A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704365 | ||||||
chr2:202704564
|
T | C | 19 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(16): Show | 19 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.753+8532T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704564 | ||||||
chr2:202704626
|
A | G | 1 | a0001c0001t0002g0216 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.753+8594A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704626 | ||||||
chr2:202704788
|
A | G | 3 | a0001c0001t0002g0202a0001c0001t0005g0201a0001c0001t0079g0200 | 3 | HG02165.hp2 NA18954.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.753+8756A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704788 | ||||||
chr2:202704843
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.753+8811C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704843 | ||||||
chr2:202704907
|
T | A | 3 | a0002c0002t0016g0296a0002c0002t0109g0299a0002c0005t0016g0297 | 3 | HG02615.hp2 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.753+8875T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202704907 | ||||||
chr2:202705165
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+9133G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705165 | ||||||
chr2:202705174
|
C | T | 1 | a0001c0001t0014g0270 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.753+9142C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705174 | ||||||
chr2:202705175
|
G | A | 2 | a0001c0001t0002g0216a0001c0001t0002g0220 | 2 | HG00621.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.753+9143G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705175 | ||||||
chr2:202705293
|
T | TGAAA | 7 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0016g0300others(4): Show | 7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+9262_753+9265d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202705293 | |||||
chr2:202705537
|
C | CTGAG | 5 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.753+9506_753+9509d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202705537 | |||||
chr2:202705719
|
C | T | 1 | a0001c0001t0047g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.753+9687C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705719 | ||||||
chr2:202705764
|
A | G | 250 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(247): Show | 250 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.753+9732A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705764 | ||||||
chr2:202705848
|
G | A | 1 | a0001c0001t0005g0176 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.753+9816G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202705848 | ||||||
chr2:202706038
|
G | C | 27 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(24): Show | 27 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.753+10006G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706038 | ||||||
chr2:202706082
|
G | A | 1 | a0001c0001t0011g0007 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.753+10050G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706082 | ||||||
chr2:202706098
|
A | T | 1 | a0001c0001t0004g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.753+10066A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706098 | ||||||
chr2:202706170
|
C | T | 1 | a0001c0001t0047g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.753+10138C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706170 | ||||||
chr2:202706456
|
A | G | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.753+10424A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706456 | ||||||
chr2:202706530
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0012g0073a0001c0001t0020g0214 | 3 | NA18948.hp2 NA18964.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.753+10498G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706530 | ||||||
chr2:202706724
|
T | C | 1 | a0001c0001t0075g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.753+10692T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706724 | ||||||
chr2:202706772
|
G | A | 16 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0016g0300others(13): Show | 16 | HG01243.hp1 HG01884.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.753+10740G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706772 | ||||||
chr2:202706848
|
G | A | 2 | a0001c0001t0014g0272a0001c0001t0061g0276 | 2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.753+10816G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706848 | ||||||
chr2:202706919
|
C | T | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+10887C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202706919 | ||||||
chr2:202706928
|
TGA | T | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+10899_753+1090 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202706928 | |||||
chr2:202707017
|
G | C | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+10985G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707017 | ||||||
chr2:202707100
|
G | T | 4 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0036g0147others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+11068G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707100 | ||||||
chr2:202707215
|
AT | A | 75 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(72): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.753+11197delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202707215 | |||||
chr2:202707230
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.753+11198G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707230 | ||||||
chr2:202707236
|
A | G | 1 | a0001c0001t0130g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.753+11204A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707236 | ||||||
chr2:202707239
|
C | G | 260 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(257): Show | 260 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.753+11207C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707239 | ||||||
chr2:202707364
|
G | A | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.753+11332G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707364 | ||||||
chr2:202707471
|
C | T | 2 | a0001c0001t0015g0180a0001c0001t0015g0189 | 2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.753+11439C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707471 | ||||||
chr2:202707484
|
A | C | 2 | a0001c0001t0018g0017a0001c0001t0054g0008 | 2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.753+11452A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707484 | ||||||
chr2:202707672
|
A | G | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+11640A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202707672 | ||||||
chr2:202707772
|
AT | A | 41 | a0001c0001t0009g0002a0001c0001t0011g0007a0001c0001t0011g0021others(38): Show | 41 | HG00609.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.753+11754delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202707772 | |||||
chr2:202708119
|
C | T | 35 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(32): Show | 35 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.753+12087C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708119 | ||||||
chr2:202708239
|
A | G | 1 | a0003c0003t0094g0248 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.753+12207A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708239 | ||||||
chr2:202708264
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.753+12232T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708264 | ||||||
chr2:202708432
|
T | A | 66 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(63): Show | 66 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.753+12400T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708432 | ||||||
chr2:202708562
|
A | C | 1 | a0001c0001t0054g0008 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.753+12530A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708562 | ||||||
chr2:202708665
|
G | A | 75 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(72): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.753+12633G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708665 | ||||||
chr2:202708667
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.753+12635G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708667 | ||||||
chr2:202708901
|
C | T | 7 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(4): Show | 7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+12869C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202708901 | ||||||
chr2:202709273
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.753+13241A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202709273 | ||||||
chr2:202709902
|
C | A | 1 | a0001c0001t0023g0044 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.753+13870C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202709902 | ||||||
chr2:202709907
|
A | G | 1 | a0001c0001t0015g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.753+13875A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202709907 | ||||||
chr2:202710209
|
G | T | 1 | a0001c0001t0080g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.753+14177G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710209 | ||||||
chr2:202710383
|
A | G | 68 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.753+14351A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710383 | ||||||
chr2:202710424
|
A | C | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.753+14392A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710424 | ||||||
chr2:202710715
|
G | A | 39 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(36): Show | 39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.754-14202G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710715 | ||||||
chr2:202710847
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG00621.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.754-14070A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202710847 | ||||||
chr2:202711229
|
C | T | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-13688C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711229 | ||||||
chr2:202711276
|
A | G | 31 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.754-13641A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711276 | ||||||
chr2:202711857
|
G | A | 11 | a0001c0001t0014g0270a0001c0001t0014g0272a0001c0001t0014g0273others(8): Show | 11 | HG00558.hp2 HG02080.hp1 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.754-13060G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711857 | ||||||
chr2:202711927
|
A | G | 1 | a0001c0001t0082g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.754-12990A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202711927 | ||||||
chr2:202712166
|
A | C | 9 | a0001c0001t0027g0136a0001c0001t0028g0064a0001c0001t0028g0076others(6): Show | 9 | HG02109.hp2 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.754-12751A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712166 | ||||||
chr2:202712199
|
T | C | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-12718T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712199 | ||||||
chr2:202712419
|
C | CT | 28 | a0001c0001t0001g0116a0001c0001t0001g0158a0001c0001t0004g0086others(25): Show | 28 | HG00741.hp1 HG01243.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.754-12476dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202712419 | |||||
chr2:202712419
|
C | CTT | 17 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(14): Show | 17 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.754-12477_754-1247 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202712419 | |||||
chr2:202712419
|
CT | C | 101 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0253others(98): Show | 101 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.754-12476delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202712419 | |||||
chr2:202712445
|
C | T | 1 | a0001c0001t0048g0068 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.754-12472C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712445 | ||||||
chr2:202712665
|
A | G | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.754-12252A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712665 | ||||||
chr2:202712729
|
A | G | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-12188A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202712729 | ||||||
chr2:202713173
|
C | T | 1 | a0001c0001t0047g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.754-11744C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713173 | ||||||
chr2:202713285
|
A | G | 29 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(26): Show | 29 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.754-11632A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713285 | ||||||
chr2:202713287
|
T | C | 3 | a0001c0001t0004g0009a0001c0001t0036g0271a0001c0001t0112g0091 | 3 | HG00597.hp2 NA18948.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.754-11630T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713287 | ||||||
chr2:202713305
|
C | T | 1 | a0001c0001t0079g0200 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.754-11612C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713305 | ||||||
chr2:202713467
|
C | A | 16 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(13): Show | 16 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.754-11450C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713467 | ||||||
chr2:202713583
|
C | G | 168 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(165): Show | 168 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.754-11334C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713583 | ||||||
chr2:202713700
|
A | T | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-11217A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713700 | ||||||
chr2:202713860
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0012g0222 | 2 | HG02056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.754-11057C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713860 | ||||||
chr2:202713967
|
C | T | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10950C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202713967 | ||||||
chr2:202714187
|
G | C | 1 | a0001c0001t0123g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-10730G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714187 | ||||||
chr2:202714225
|
A | G | 1 | a0001c0001t0043g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.754-10692A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714225 | ||||||
chr2:202714312
|
A | G | 2 | a0001c0001t0101g0287a0001c0007t0106g0286 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.754-10605A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714312 | ||||||
chr2:202714367
|
T | G | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10550T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714367 | ||||||
chr2:202714443
|
CTATT | C | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10471_754-1046 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714443 | |||||
chr2:202714474
|
A | G | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10443A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714474 | ||||||
chr2:202714497
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0012g0164 | 3 | NA18962.hp1 NA18986.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.754-10420G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714497 | ||||||
chr2:202714520
|
ATCTTTTT others(4): Show |
A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10384_754-1037 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714520 | |||||
chr2:202714522
|
CT | C | 38 | a0001c0001t0002g0193a0001c0001t0009g0002a0001c0001t0028g0001others(35): Show | 38 | HG00408.hp2 HG00733.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.754-10385delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714522 | |||||
chr2:202714527
|
T | C | 1 | a0001c0001t0131g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.754-10390T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714527 | ||||||
chr2:202714532
|
T | C | 65 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0195others(62): Show | 65 | HG00099.hp1 HG00323.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.754-10385T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714532 | ||||||
chr2:202714533
|
C | CT | 37 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(34): Show | 37 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.754-10367dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202714533 | |||||
chr2:202714534
|
T | C | 3 | a0001c0001t0002g0193a0001c0001t0079g0200a0001c0001t0091g0265 | 3 | HG00408.hp2 HG01884.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.754-10383T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714534 | ||||||
chr2:202714537
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.754-10380T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714537 | ||||||
chr2:202714543
|
T | C | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10374T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714543 | ||||||
chr2:202714676
|
C | T | 2 | a0001c0001t0007g0014a0001c0001t0025g0211 | 2 | HG00558.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.754-10241C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714676 | ||||||
chr2:202714899
|
C | G | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-10018C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202714899 | ||||||
chr2:202715073
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-9844G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715073 | ||||||
chr2:202715135
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.754-9782G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715135 | ||||||
chr2:202715138
|
C | T | 15 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(12): Show | 15 | HG01952.hp2 HG02145.hp1 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.754-9779C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715138 | ||||||
chr2:202715139
|
G | A | 101 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(98): Show | 101 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.754-9778G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715139 | ||||||
chr2:202715143
|
C | T | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.754-9774C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715143 | ||||||
chr2:202715182
|
G | A | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.754-9735G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715182 | ||||||
chr2:202715190
|
C | T | 4 | a0001c0001t0006g0103a0001c0001t0006g0131a0001c0001t0102g0283others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-9727C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715190 | ||||||
chr2:202715229
|
G | A | 1 | a0001c0001t0130g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.754-9688G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715229 | ||||||
chr2:202715250
|
G | A | 1 | a0001c0001t0123g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-9667G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715250 | ||||||
chr2:202715337
|
C | T | 1 | a0001c0001t0086g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.754-9580C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715337 | ||||||
chr2:202715347
|
C | T | 1 | a0001c0001t0049g0053 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.754-9570C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715347 | ||||||
chr2:202715365
|
C | T | 4 | a0001c0001t0006g0103a0001c0001t0006g0131a0001c0001t0102g0283others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.754-9552C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715365 | ||||||
chr2:202715381
|
C | T | 1 | a0003c0003t0030g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.754-9536C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715381 | ||||||
chr2:202715443
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-9474G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715443 | ||||||
chr2:202715495
|
C | T | 1 | a0001c0001t0038g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.754-9422C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715495 | ||||||
chr2:202715527
|
G | A | 1 | a0001c0001t0007g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.754-9390G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715527 | ||||||
chr2:202715562
|
A | G | 1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.754-9355A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715562 | ||||||
chr2:202715610
|
G | A | 2 | a0001c0001t0042g0153a0001c0001t0087g0117 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.754-9307G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715610 | ||||||
chr2:202715836
|
T | C | 1 | a0001c0001t0121g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754-9081T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715836 | ||||||
chr2:202715839
|
GGAGGCCG others(12): Show |
G | 1 | a0001c0001t0121g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.754-9077_754-9059d others(21): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715839 | ||||||
chr2:202715854
|
C | T | 1 | a0001c0001t0022g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.754-9063C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715854 | ||||||
chr2:202715889
|
G | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.754-9028G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715889 | ||||||
chr2:202715949
|
G | A | 2 | a0001c0001t0015g0180a0001c0001t0015g0189 | 2 | HG01109.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.754-8968G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715949 | ||||||
chr2:202715951
|
G | A | 1 | a0002c0002t0003g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.754-8966G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715951 | ||||||
chr2:202715961
|
A | T | 1 | a0001c0001t0007g0081 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.754-8956A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202715961 | ||||||
chr2:202716541
|
CTGT | C | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-8369_754-8367d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202716541 | |||||
chr2:202716655
|
T | C | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-8262T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716655 | ||||||
chr2:202716722
|
C | G | 1 | a0002c0002t0016g0300 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.754-8195C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716722 | ||||||
chr2:202716731
|
G | A | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-8186G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716731 | ||||||
chr2:202716759
|
A | G | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.754-8158A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202716759 | ||||||
chr2:202717016
|
C | T | 1 | a0001c0001t0013g0046 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.754-7901C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717016 | ||||||
chr2:202717017
|
G | A | 2 | a0001c0001t0009g0070a0002c0002t0100g0306 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.754-7900G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717017 | ||||||
chr2:202717086
|
A | G | 1 | a0001c0001t0040g0263 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.754-7831A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717086 | ||||||
chr2:202717147
|
C | A | 1 | a0002c0005t0016g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.754-7770C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717147 | ||||||
chr2:202717424
|
A | G | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.754-7493A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717424 | ||||||
chr2:202717466
|
T | C | 101 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(98): Show | 101 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.754-7451T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717466 | ||||||
chr2:202717487
|
G | A | 1 | a0001c0001t0123g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-7430G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717487 | ||||||
chr2:202717607
|
T | C | 1 | a0001c0001t0007g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.754-7310T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717607 | ||||||
chr2:202717608
|
C | T | 1 | a0001c0001t0007g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.754-7309C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717608 | ||||||
chr2:202717714
|
A | C | 1 | a0001c0001t0007g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.754-7203A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202717714 | ||||||
chr2:202717831
|
T | TG | 37 | a0001c0001t0030g0005a0001c0001t0041g0266a0001c0001t0050g0284others(34): Show | 37 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.754-7083dupG | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202717831 | |||||
chr2:202718012
|
A | T | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-6905A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718012 | ||||||
chr2:202718124
|
G | C | 1 | a0001c0001t0043g0141 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.754-6793G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718124 | ||||||
chr2:202718152
|
G | A | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.754-6765G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718152 | ||||||
chr2:202718159
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-6758G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718159 | ||||||
chr2:202718192
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.754-6725T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718192 | ||||||
chr2:202718476
|
A | AT | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-6437dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202718476 | |||||
chr2:202718531
|
G | A | 144 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(141): Show | 144 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.754-6386G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718531 | ||||||
chr2:202718578
|
A | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-6339A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718578 | ||||||
chr2:202718673
|
T | G | 68 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.754-6244T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202718673 | ||||||
chr2:202719319
|
G | A | 1 | a0001c0004t0066g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.754-5598G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719319 | ||||||
chr2:202719391
|
TTTTTA | T | 80 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(77): Show | 80 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.754-5521_754-5517d others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202719391 | |||||
chr2:202719478
|
A | G | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.754-5439A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719478 | ||||||
chr2:202719542
|
G | A | 1 | a0001c0001t0123g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.754-5375G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719542 | ||||||
chr2:202719733
|
G | A | 31 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.754-5184G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719733 | ||||||
chr2:202719782
|
C | G | 3 | a0001c0001t0001g0253a0001c0001t0027g0252a0001c0001t0027g0254 | 3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.754-5135C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202719782 | ||||||
chr2:202720014
|
T | C | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-4903T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720014 | ||||||
chr2:202720225
|
A | G | 67 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(64): Show | 67 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.754-4692A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720225 | ||||||
chr2:202720241
|
T | C | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.754-4676T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720241 | ||||||
chr2:202720400
|
C | CGT | 28 | a0001c0001t0001g0127a0001c0001t0001g0154a0001c0001t0007g0014others(25): Show | 28 | HG00558.hp1 HG00733.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.754-4491_754-4490d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720400 | |||||
chr2:202720400
|
CGTGT | C | 3 | a0001c0001t0001g0253a0001c0001t0027g0252a0001c0001t0027g0254 | 3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.754-4493_754-4490d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720400 | |||||
chr2:202720426
|
TGC | T | 37 | a0001c0001t0008g0034a0001c0001t0008g0042a0001c0001t0008g0043others(34): Show | 37 | HG00140.hp2 HG00544.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.754-4488_754-4487d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720426 | |||||
chr2:202720428
|
C | T | 111 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(108): Show | 111 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.754-4489C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720428 | ||||||
chr2:202720604
|
CT | C | 68 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.754-4301delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202720604 | |||||
chr2:202720722
|
A | G | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.754-4195A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720722 | ||||||
chr2:202720863
|
T | C | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-4054T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720863 | ||||||
chr2:202720890
|
C | T | 1 | a0001c0001t0017g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.754-4027C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720890 | ||||||
chr2:202720985
|
T | G | 5 | a0001c0001t0013g0030a0001c0001t0013g0033a0001c0001t0013g0046others(2): Show | 5 | HG00741.hp2 HG01106.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.754-3932T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202720985 | ||||||
chr2:202721036
|
A | T | 80 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(77): Show | 80 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.754-3881A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721036 | ||||||
chr2:202721127
|
A | T | 101 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(98): Show | 101 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.754-3790A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721127 | ||||||
chr2:202721140
|
C | CT | 12 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0016g0300others(9): Show | 12 | HG01243.hp1 HG01884.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.754-3768dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202721140 | |||||
chr2:202721313
|
A | G | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-3604A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721313 | ||||||
chr2:202721321
|
A | T | 33 | a0001c0001t0030g0005a0001c0001t0041g0266a0001c0001t0091g0265others(30): Show | 33 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.754-3596A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721321 | ||||||
chr2:202721616
|
A | G | 1 | a0001c0001t0022g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.754-3301A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721616 | ||||||
chr2:202721779
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0006g0250a0001c0001t0007g0255 | 3 | HG02965.hp2 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.754-3138G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721779 | ||||||
chr2:202721810
|
T | A | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-3107T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721810 | ||||||
chr2:202721881
|
G | C | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.754-3036G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202721881 | ||||||
chr2:202722007
|
A | AT | 50 | a0001c0001t0001g0092a0001c0001t0001g0184a0001c0001t0001g0185others(47): Show | 50 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.754-2890dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202722007 | |||||
chr2:202722007
|
A | ATT | 6 | a0001c0001t0006g0131a0001c0001t0023g0047a0001c0001t0050g0284others(3): Show | 6 | HG02109.hp1 HG02572.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-2891_754-2890d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202722007 | |||||
chr2:202722071
|
C | T | 1 | a0001c0001t0007g0255 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.754-2846C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722071 | ||||||
chr2:202722113
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-2804C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722113 | ||||||
chr2:202722154
|
G | C | 1 | a0001c0001t0022g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.754-2763G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722154 | ||||||
chr2:202722200
|
C | T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.754-2717C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722200 | ||||||
chr2:202722776
|
C | T | 1 | a0001c0001t0004g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.754-2141C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202722776 | ||||||
chr2:202723428
|
A | G | 1 | a0001c0001t0012g0073 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.754-1489A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723428 | ||||||
chr2:202723441
|
C | T | 2 | a0002c0002t0016g0300a0002c0002t0108g0294 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.754-1476C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723441 | ||||||
chr2:202723474
|
A | G | 7 | a0001c0001t0009g0060a0001c0001t0009g0070a0001c0001t0009g0105others(4): Show | 7 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-1443A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723474 | ||||||
chr2:202723776
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.754-1141G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202723776 | ||||||
chr2:202724051
|
C | CT | 253 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.754-842dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724051 | |||||
chr2:202724051
|
C | CTT | 32 | a0001c0001t0001g0253a0001c0001t0002g0191a0001c0001t0002g0195others(29): Show | 32 | HG00621.hp1 HG00738.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.754-843_754-842dup others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724051 | |||||
chr2:202724051
|
C | CTTT | 11 | a0001c0001t0005g0236a0001c0001t0035g0055a0001c0001t0049g0053others(8): Show | 11 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.754-844_754-842dup others(3): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724051 | |||||
chr2:202724089
|
CCT | C | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.754-825_754-824del others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724089 | |||||
chr2:202724168
|
C | T | 1 | a0001c0001t0053g0146 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.754-749C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724168 | ||||||
chr2:202724264
|
C | T | 1 | a0003c0003t0010g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.754-653C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724264 | ||||||
chr2:202724334
|
C | T | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.754-583C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724334 | ||||||
chr2:202724338
|
C | T | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.754-579C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724338 | ||||||
chr2:202724584
|
A | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.754-333A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724584 | ||||||
chr2:202724634
|
A | C | 31 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.754-283A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | chr2 | 202724634 | ||||||
chr2:202724667
|
T | TGTAGTAT others(18): Show |
1 | a0001c0001t0011g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.754-249_754-225dup others(25): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 202724667 | |||||
chr2:202725229
|
A | C | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.846+220A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202725229 | ||||||
chr2:202725299
|
C | CT | 228 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(225): Show | 228 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.846+306dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 202725299 | |||||
chr2:202725299
|
C | CTT | 6 | a0001c0001t0012g0164a0001c0001t0047g0267a0001c0001t0047g0268others(3): Show | 6 | HG03139.hp2 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.846+305_846+306dup others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 202725299 | |||||
chr2:202725299
|
CTTTT | C | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.846+303_846+306del others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 202725299 | |||||
chr2:202725597
|
G | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.846+588G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202725597 | ||||||
chr2:202726066
|
A | G | 1 | a0001c0001t0015g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.847-184A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202726066 | ||||||
chr2:202726173
|
G | C | 1 | a0001c0001t0004g0086 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.847-77G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 3/7 | chr2 | 202726173 | ||||||
chr2:202726505
|
A | T | 1 | a0001c0001t0093g0243 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.960+142A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726505 | ||||||
chr2:202726538
|
T | C | 1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.960+175T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726538 | ||||||
chr2:202726802
|
A | C | 1 | a0001c0001t0055g0161 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.960+439A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726802 | ||||||
chr2:202726817
|
G | A | 2 | a0001c0001t0008g0042a0001c0001t0008g0045 | 2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.960+454G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726817 | ||||||
chr2:202726893
|
C | T | 1 | a0001c0001t0002g0191 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.960+530C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726893 | ||||||
chr2:202726946
|
T | TA | 6 | a0001c0001t0001g0020a0001c0001t0001g0182a0001c0001t0031g0063others(3): Show | 6 | HG01167.hp2 HG02155.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+594dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202726946 | |||||
chr2:202726957
|
A | T | 1 | a0001c0001t0120g0144 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.960+594A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202726957 | ||||||
chr2:202727062
|
C | CT | 29 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(26): Show | 29 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.960+707dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202727062 | |||||
chr2:202727094
|
C | T | 1 | a0001c0001t0040g0263 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.960+731C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727094 | ||||||
chr2:202727244
|
A | G | 37 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(34): Show | 37 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.960+881A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727244 | ||||||
chr2:202727265
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+902G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727265 | ||||||
chr2:202727423
|
C | T | 1 | a0001c0001t0022g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.960+1060C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727423 | ||||||
chr2:202727457
|
A | G | 177 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(174): Show | 177 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.960+1094A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727457 | ||||||
chr2:202727487
|
A | G | 1 | a0001c0001t0055g0148 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.960+1124A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727487 | ||||||
chr2:202727806
|
C | A | 2 | a0001c0001t0008g0042a0001c0001t0008g0045 | 2 | HG01099.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.960+1443C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727806 | ||||||
chr2:202727966
|
A | G | 1 | a0001c0001t0135g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+1603A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727966 | ||||||
chr2:202727997
|
G | A | 3 | a0001c0001t0030g0005a0002c0002t0003g0307a0002c0002t0003g0309 | 3 | HG02572.hp1 HG02896.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.960+1634G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202727997 | ||||||
chr2:202728049
|
GA | G | 39 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(36): Show | 39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.960+1687delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202728049 | ||||||
chr2:202728051
|
T | C | 39 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0030g0005others(36): Show | 39 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.960+1688T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202728051 | ||||||
chr2:202728135
|
A | G | 1 | a0002c0002t0003g0304 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.960+1772A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202728135 | ||||||
chr2:202729052
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.960+2689C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729052 | ||||||
chr2:202729266
|
G | A | 1 | a0001c0001t0015g0282 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.960+2903G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729266 | ||||||
chr2:202729333
|
CA | C | 100 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(97): Show | 100 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.960+2983delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202729333 | |||||
chr2:202729510
|
C | T | 1 | a0001c0001t0082g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.960+3147C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729510 | ||||||
chr2:202729669
|
A | G | 31 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.960+3306A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729669 | ||||||
chr2:202729693
|
C | T | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+3330C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729693 | ||||||
chr2:202729724
|
T | C | 145 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(142): Show | 145 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.960+3361T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729724 | ||||||
chr2:202729836
|
A | G | 28 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(25): Show | 28 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.960+3473A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202729836 | ||||||
chr2:202730002
|
T | G | 1 | a0001c0001t0025g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.960+3639T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730002 | ||||||
chr2:202730435
|
C | T | 2 | a0001c0001t0002g0204a0001c0001t0071g0212 | 2 | HG01071.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.960+4072C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730435 | ||||||
chr2:202730647
|
G | A | 68 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(65): Show | 68 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.960+4284G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730647 | ||||||
chr2:202730675
|
A | G | 2 | a0001c0001t0007g0081a0001c0001t0048g0068 | 2 | NA18952.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.960+4312A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730675 | ||||||
chr2:202730704
|
G | A | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.960+4341G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730704 | ||||||
chr2:202730722
|
A | G | 1 | a0001c0001t0019g0197 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.960+4359A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730722 | ||||||
chr2:202730736
|
C | T | 50 | a0001c0001t0004g0009a0001c0001t0004g0085a0001c0001t0004g0106others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.960+4373C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202730736 | ||||||
chr2:202731087
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.960+4724C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731087 | ||||||
chr2:202731136
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.960+4773G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731136 | ||||||
chr2:202731151
|
C | T | 2 | a0001c0004t0037g0022a0001c0004t0037g0023 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.960+4788C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731151 | ||||||
chr2:202731246
|
C | A | 1 | a0001c0001t0044g0098 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.960+4883C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731246 | ||||||
chr2:202731332
|
A | AAAAAATA others(3): Show |
1 | a0001c0001t0022g0035 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.960+4970_960+4971i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(1): Show |
3 | a0001c0001t0013g0033a0001c0001t0013g0050a0001c0001t0013g0051 | 3 | HG03491.hp2 HG03492.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(3): Show |
4 | a0001c0001t0013g0046a0001c0001t0023g0049a0001c0001t0110g0036others(1): Show | 4 | HG00140.hp2 HG00642.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+4970_960+4971i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(5): Show |
4 | a0001c0001t0022g0031a0001c0001t0023g0044a0001c0001t0023g0047others(1): Show | 4 | HG00639.hp1 HG01167.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+4970_960+4971i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(7): Show |
1 | a0001c0001t0008g0034 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(9): Show |
1 | a0001c0001t0013g0030 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(11): Show |
2 | a0001c0001t0008g0043a0001c0001t0023g0048 | 2 | HG00738.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(13): Show |
2 | a0001c0001t0008g0038a0001c0001t0138g0040 | 2 | HG00609.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(15): Show |
2 | a0001c0001t0008g0045a0001c0001t0008g0150 | 2 | HG01496.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(17): Show |
2 | a0001c0001t0022g0130a0001c0001t0133g0039 | 2 | HG01192.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.960+4970_960+4971i others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(19): Show |
1 | a0001c0001t0008g0042 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.960+4970_960+4971i others(28): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(21): Show |
1 | a0001c0001t0132g0237 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(30): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(25): Show |
1 | a0001c0001t0139g0028 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(34): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AAAATATA others(27): Show |
1 | a0001c0001t0131g0041 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.960+4970_960+4971i others(36): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AACATATA others(19): Show |
1 | a0001c0001t0001g0095 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.960+4970_960+4971i others(28): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATAT | 8 | a0001c0001t0009g0002a0001c0001t0020g0234a0001c0001t0021g0145others(5): Show | 8 | HG02622.hp2 NA18950.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+5002_960+5005d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATAT | 14 | a0001c0001t0004g0106a0001c0001t0017g0206a0001c0001t0019g0215others(11): Show | 14 | HG00140.hp1 HG00733.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.960+5000_960+5005d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(1): Show |
17 | a0001c0001t0002g0217a0001c0001t0015g0282a0001c0001t0021g0027others(14): Show | 17 | HG02083.hp1 HG02132.hp2 HG02818.hp2 others(14): Show |
intron_variant | MODIFIER | c.960+4998_960+5005d others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(3): Show |
20 | a0001c0001t0001g0092a0001c0001t0002g0191a0001c0001t0002g0203others(17): Show | 20 | HG00099.hp2 HG00621.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.960+4996_960+5005d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(5): Show |
23 | a0001c0001t0001g0116a0001c0001t0001g0155a0001c0001t0002g0202others(20): Show | 23 | HG00099.hp1 HG00673.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.960+4994_960+5005d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(7): Show |
16 | a0001c0001t0002g0193a0001c0001t0005g0152a0001c0001t0014g0272others(13): Show | 16 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.960+4992_960+5005d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(9): Show |
21 | a0001c0001t0001g0253a0001c0001t0002g0181a0001c0001t0002g0195others(18): Show | 21 | HG00323.hp2 HG01071.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.960+4990_960+5005d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(11): Show |
11 | a0001c0001t0001g0061a0001c0001t0001g0154a0001c0001t0002g0207others(8): Show | 11 | HG00558.hp2 HG01099.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+4988_960+5005d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(13): Show |
4 | a0001c0001t0002g0199a0001c0001t0117g0123a0003c0003t0010g0196others(1): Show | 4 | HG00544.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+4986_960+5005d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(15): Show |
2 | a0001c0001t0004g0232a0001c0001t0018g0120 | 2 | HG04228.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.960+4984_960+5005d others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
A | AATATATA others(17): Show |
1 | a0001c0001t0015g0180 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.960+4982_960+5005d others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AAT | A | 6 | a0001c0001t0049g0053a0001c0001t0049g0269a0001c0001t0060g0278others(3): Show | 6 | HG01891.hp1 HG02080.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+5004_960+5005d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AATAT | A | 8 | a0001c0001t0018g0017a0001c0001t0047g0268a0001c0001t0054g0008others(5): Show | 8 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.960+5002_960+5005d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AATATAT | A | 17 | a0001c0001t0030g0005a0001c0007t0106g0286a0002c0002t0003g0301others(14): Show | 17 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.960+5000_960+5005d others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AATATATA others(3): Show |
A | 3 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287 | 3 | HG02109.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.960+4996_960+5005d others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0111g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.960+4994_960+5005d others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AATATATA others(7): Show |
A | 1 | a0001c0001t0121g0226 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.960+4992_960+5005d others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AATATATA others(11): Show |
A | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960+4988_960+5005d others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731332
|
AATATATA others(13): Show |
A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+4986_960+5005d others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731332 | |||||
chr2:202731334
|
T | A | 1 | a0001c0001t0135g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+4971T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731334 | ||||||
chr2:202731345
|
A | G | 1 | a0001c0001t0055g0148 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.960+4982A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731345 | ||||||
chr2:202731362
|
T | TATATATA others(11): Show |
1 | a0001c0001t0068g0239 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | |||||
chr2:202731362
|
T | TATATATA others(15): Show |
1 | a0001c0001t0053g0119 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(24): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | |||||
chr2:202731362
|
T | TATATATA others(17): Show |
1 | a0001c0001t0053g0146 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.960+5005_960+5006i others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | |||||
chr2:202731362
|
T | TATATATA others(19): Show |
1 | a0001c0001t0069g0089 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(28): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202731362 | |||||
chr2:202731368
|
T | G | 64 | a0001c0001t0001g0095a0001c0001t0005g0174a0001c0001t0008g0034others(61): Show | 64 | HG00140.hp2 HG00609.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.960+5005T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATAG | 6 | a0001c0001t0001g0069a0001c0001t0001g0167a0001c0001t0009g0105others(3): Show | 6 | HG01952.hp2 HG02155.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATAG | 5 | a0001c0001t0007g0014a0001c0001t0021g0183a0001c0001t0027g0136others(2): Show | 5 | HG00558.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(1): Show |
28 | a0001c0001t0001g0020a0001c0001t0001g0057a0001c0001t0001g0062others(25): Show | 28 | HG00323.hp1 HG01081.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(3): Show |
24 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0075others(21): Show | 24 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(5): Show |
11 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0185others(8): Show | 11 | HG02165.hp1 HG02723.hp2 HG03942.hp1 others(8): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(7): Show |
10 | a0001c0001t0001g0135a0001c0001t0001g0157a0001c0001t0011g0021others(7): Show | 10 | HG00609.hp2 HG02080.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(9): Show |
4 | a0001c0001t0001g0058a0001c0001t0006g0131a0001c0001t0043g0141others(1): Show | 4 | HG02572.hp2 HG02970.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+5005_960+5006i others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(11): Show |
2 | a0001c0001t0007g0132a0001c0001t0043g0109 | 2 | HG04199.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.960+5005_960+5006i others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(13): Show |
1 | a0001c0001t0035g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(22): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731368
|
T | TATATATA others(17): Show |
1 | a0001c0001t0112g0091 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.960+5005_960+5006i others(26): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731368 | ||||||
chr2:202731523
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960+5160C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731523 | ||||||
chr2:202731602
|
T | C | 1 | a0002c0002t0003g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.960+5239T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731602 | ||||||
chr2:202731722
|
A | G | 1 | a0001c0001t0025g0082 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.960+5359A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731722 | ||||||
chr2:202731761
|
G | A | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.960+5398G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202731761 | ||||||
chr2:202732046
|
C | CT | 16 | a0001c0001t0001g0011a0001c0001t0001g0253a0001c0001t0002g0210others(13): Show | 16 | HG00140.hp2 HG00597.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.960+5699dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732046 | |||||
chr2:202732105
|
G | A | 2 | a0002c0002t0097g0315a0002c0002t0098g0316 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.960+5742G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732105 | ||||||
chr2:202732180
|
C | T | 1 | a0001c0001t0060g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.960+5817C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732180 | ||||||
chr2:202732202
|
A | G | 1 | a0001c0001t0084g0018 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.960+5839A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732202 | ||||||
chr2:202732275
|
T | C | 1 | a0001c0001t0020g0234 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.960+5912T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732275 | ||||||
chr2:202732376
|
A | G | 1 | a0003c0003t0010g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.960+6013A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732376 | ||||||
chr2:202732546
|
C | T | 29 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(26): Show | 29 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.960+6183C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732546 | ||||||
chr2:202732686
|
C | T | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+6323C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732686 | ||||||
chr2:202732691
|
C | T | 100 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(97): Show | 100 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.960+6328C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732691 | ||||||
chr2:202732723
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.960+6360C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732723 | ||||||
chr2:202732725
|
G | A | 1 | a0001c0001t0040g0256 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.960+6362G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732725 | ||||||
chr2:202732752
|
C | T | 5 | a0002c0002t0024g0288a0002c0002t0024g0289a0002c0002t0024g0290others(2): Show | 5 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+6389C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732752 | ||||||
chr2:202732763
|
C | G | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+6400C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732763 | ||||||
chr2:202732777
|
C | G | 1 | a0001c0001t0135g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+6414C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732777 | ||||||
chr2:202732815
|
C | T | 1 | a0001c0001t0020g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.960+6452C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732815 | ||||||
chr2:202732826
|
G | GTAAA | 7 | a0001c0001t0001g0057a0001c0001t0005g0176a0001c0001t0007g0096others(4): Show | 7 | HG01081.hp1 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+6492_960+6495d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732826 | |||||
chr2:202732826
|
GTAAA | G | 121 | a0001c0001t0001g0061a0001c0001t0002g0181a0001c0001t0002g0191others(118): Show | 121 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.960+6492_960+6495d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732826 | |||||
chr2:202732834
|
A | G | 73 | a0001c0001t0001g0061a0001c0001t0002g0181a0001c0001t0002g0191others(70): Show | 73 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.960+6471A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732834 | ||||||
chr2:202732873
|
TA | T | 121 | a0001c0001t0001g0061a0001c0001t0002g0181a0001c0001t0002g0191others(118): Show | 121 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.960+6524delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202732873 | |||||
chr2:202732939
|
T | C | 2 | a0001c0001t0101g0287a0001c0007t0106g0286 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.960+6576T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202732939 | ||||||
chr2:202733177
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.960+6814G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733177 | ||||||
chr2:202733204
|
G | C | 1 | a0001c0001t0009g0070 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.960+6841G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733204 | ||||||
chr2:202733278
|
T | A | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.960+6915T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733278 | ||||||
chr2:202733396
|
A | G | 1 | a0001c0001t0005g0174 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.960+7033A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733396 | ||||||
chr2:202733556
|
A | G | 31 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.960+7193A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733556 | ||||||
chr2:202733602
|
G | A | 1 | a0001c0001t0135g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.960+7239G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733602 | ||||||
chr2:202733606
|
A | G | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+7243A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733606 | ||||||
chr2:202733651
|
C | T | 6 | a0002c0002t0016g0295a0002c0002t0016g0300a0002c0002t0104g0298others(3): Show | 6 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+7288C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733651 | ||||||
chr2:202733739
|
C | T | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.960+7376C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733739 | ||||||
chr2:202733744
|
T | G | 1 | a0001c0001t0130g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.960+7381T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733744 | ||||||
chr2:202733835
|
C | T | 1 | a0001c0001t0123g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.960+7472C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733835 | ||||||
chr2:202733936
|
T | A | 76 | a0001c0001t0001g0061a0001c0001t0002g0181a0001c0001t0002g0191others(73): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.960+7573T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202733936 | ||||||
chr2:202734054
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+7691G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734054 | ||||||
chr2:202734077
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.960+7714G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734077 | ||||||
chr2:202734113
|
G | A | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.960+7750G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734113 | ||||||
chr2:202734124
|
A | C | 1 | a0003c0003t0030g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.960+7761A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734124 | ||||||
chr2:202734221
|
A | G | 1 | a0001c0001t0086g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.960+7858A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734221 | ||||||
chr2:202734274
|
C | G | 4 | a0001c0001t0014g0270a0001c0001t0057g0281a0001c0001t0058g0280others(1): Show | 4 | NA18939.hp2 NA18974.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+7911C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734274 | ||||||
chr2:202734422
|
A | G | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.960+8059A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734422 | ||||||
chr2:202734643
|
G | T | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+8280G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734643 | ||||||
chr2:202734672
|
G | A | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.960+8309G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734672 | ||||||
chr2:202734902
|
G | A | 4 | a0001c0001t0006g0103a0001c0001t0006g0131a0001c0001t0102g0283others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.960+8539G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202734902 | ||||||
chr2:202735145
|
T | C | 31 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(28): Show | 31 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.960+8782T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735145 | ||||||
chr2:202735269
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.960+8906G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735269 | ||||||
chr2:202735366
|
A | G | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+9003A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735366 | ||||||
chr2:202735789
|
T | G | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+9426T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735789 | ||||||
chr2:202735934
|
C | T | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+9571C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735934 | ||||||
chr2:202735999
|
C | T | 1 | a0001c0001t0070g0231 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.960+9636C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202735999 | ||||||
chr2:202736076
|
A | G | 2 | a0001c0001t0041g0266a0001c0001t0091g0265 | 2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.960+9713A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736076 | ||||||
chr2:202736508
|
C | T | 1 | a0001c0001t0073g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.960+10145C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736508 | ||||||
chr2:202736526
|
C | T | 1 | a0003c0003t0010g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.960+10163C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736526 | ||||||
chr2:202736586
|
C | T | 37 | a0001c0001t0004g0085a0001c0001t0004g0108a0001c0001t0004g0126others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.960+10223C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736586 | ||||||
chr2:202736711
|
G | C | 2 | a0001c0001t0047g0267a0001c0001t0047g0268 | 2 | HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.960+10348G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736711 | ||||||
chr2:202736873
|
C | T | 4 | a0001c0001t0009g0002a0001c0001t0028g0001a0001c0001t0042g0003others(1): Show | 4 | HG02257.hp2 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+10510C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736873 | ||||||
chr2:202736911
|
TA | T | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+10559delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202736911 | |||||
chr2:202736931
|
A | G | 1 | a0001c0001t0033g0163 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.960+10568A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202736931 | ||||||
chr2:202737158
|
C | T | 1 | a0001c0001t0005g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.960+10795C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737158 | ||||||
chr2:202737170
|
TA | T | 7 | a0001c0001t0001g0182a0001c0001t0002g0210a0001c0001t0004g0232others(4): Show | 7 | HG02738.hp2 HG03017.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+10819delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202737170 | |||||
chr2:202737319
|
G | T | 1 | a0001c0001t0074g0094 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.960+10956G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737319 | ||||||
chr2:202737338
|
A | G | 3 | a0001c0001t0039g0258a0001c0001t0039g0260a0001c0001t0076g0264 | 3 | HG00733.hp2 HG01261.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.960+10975A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737338 | ||||||
chr2:202737444
|
C | G | 1 | a0001c0001t0130g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.960+11081C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737444 | ||||||
chr2:202737484
|
C | A | 148 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(145): Show | 148 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.960+11121C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737484 | ||||||
chr2:202737495
|
A | C | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+11132A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737495 | ||||||
chr2:202737607
|
CT | C | 6 | a0002c0002t0003g0302a0002c0002t0024g0288a0002c0002t0024g0289others(3): Show | 6 | HG01169.hp1 HG01884.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.960+11256delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202737607 | |||||
chr2:202737633
|
G | T | 2 | a0001c0001t0119g0225a0001c0001t0121g0226 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.960+11270G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737633 | ||||||
chr2:202737767
|
A | C | 1 | a0001c0001t0014g0273 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.960+11404A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737767 | ||||||
chr2:202737781
|
T | C | 1 | a0001c0001t0004g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.960+11418T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737781 | ||||||
chr2:202737826
|
G | T | 148 | a0001c0001t0002g0181a0001c0001t0002g0191a0001c0001t0002g0193others(145): Show | 148 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.960+11463G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737826 | ||||||
chr2:202737894
|
G | A | 1 | a0002c0002t0099g0312 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.960+11531G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737894 | ||||||
chr2:202737927
|
A | G | 1 | a0001c0001t0007g0132 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.960+11564A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737927 | ||||||
chr2:202737956
|
G | A | 1 | a0001c0001t0074g0094 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.960+11593G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202737956 | ||||||
chr2:202738458
|
G | A | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+12095G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738458 | ||||||
chr2:202738512
|
T | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+12149T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738512 | ||||||
chr2:202738732
|
A | G | 15 | a0001c0001t0008g0034a0001c0001t0013g0030a0001c0001t0013g0033others(12): Show | 15 | HG00544.hp2 HG00642.hp1 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.960+12369A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738732 | ||||||
chr2:202738872
|
A | G | 1 | a0001c0001t0074g0094 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.960+12509A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738872 | ||||||
chr2:202738908
|
G | A | 7 | a0002c0002t0016g0295a0002c0002t0016g0296a0002c0002t0016g0300others(4): Show | 7 | HG01243.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.960+12545G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738908 | ||||||
chr2:202738991
|
C | G | 3 | a0001c0001t0018g0016a0001c0001t0056g0169a0001c0001t0056g0170 | 3 | HG00140.hp1 HG01081.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.960+12628C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202738991 | ||||||
chr2:202739235
|
G | C | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.960+12872G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739235 | ||||||
chr2:202739257
|
A | G | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.960+12894A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739257 | ||||||
chr2:202739307
|
G | A | 4 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0036g0147others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+12944G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739307 | ||||||
chr2:202739317
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0025g0113 | 2 | NA18951.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.960+12954A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739317 | ||||||
chr2:202739356
|
T | A | 1 | a0001c0001t0022g0130 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.960+12993T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739356 | ||||||
chr2:202739392
|
CGTCTGTC others(5): Show |
C | 5 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0007g0132others(2): Show | 5 | HG02080.hp2 NA18962.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+13039_960+1305 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202739392 | |||||
chr2:202739554
|
C | T | 1 | a0001c0001t0120g0144 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.960+13191C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739554 | ||||||
chr2:202739601
|
G | A | 3 | a0001c0001t0002g0181a0001c0001t0002g0193a0001c0001t0026g0168 | 3 | HG00408.hp2 HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.960+13238G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739601 | ||||||
chr2:202739645
|
C | T | 30 | a0001c0001t0030g0005a0002c0002t0003g0301a0002c0002t0003g0302others(27): Show | 30 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.960+13282C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202739645 | ||||||
chr2:202740166
|
T | C | 4 | a0001c0001t0050g0284a0001c0001t0050g0285a0001c0001t0101g0287others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.960+13803T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740166 | ||||||
chr2:202740173
|
C | CA | 6 | a0001c0001t0007g0132a0001c0001t0009g0002a0001c0001t0019g0197others(3): Show | 6 | HG02055.hp2 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAA | 23 | a0001c0001t0002g0191a0001c0001t0002g0193a0001c0001t0002g0195others(20): Show | 23 | HG00099.hp1 HG00408.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAA | 31 | a0001c0001t0002g0181a0001c0001t0002g0199a0001c0001t0002g0203others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAA | 28 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0158others(25): Show | 28 | HG00544.hp2 HG00639.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAAA | 50 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0062others(47): Show | 50 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAAAA | 43 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0095others(40): Show | 43 | HG00609.hp1 HG00609.hp2 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(11): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAAAA others(1): Show |
29 | a0001c0001t0001g0057a0001c0001t0001g0075a0001c0001t0001g0251others(26): Show | 29 | HG00673.hp1 HG00733.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(12): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAAAA others(2): Show |
12 | a0001c0001t0001g0012a0001c0001t0001g0116a0001c0001t0001g0127others(9): Show | 12 | HG00741.hp1 HG01081.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(13): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAAAA others(3): Show |
8 | a0001c0001t0006g0131a0001c0001t0028g0064a0001c0001t0029g0137others(5): Show | 8 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+13810_960+1381 others(14): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0011a0001c0001t0029g0112a0001c0001t0042g0153 | 3 | HG02109.hp2 HG06807.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.960+13810_960+1381 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
C | CAAAAAAA others(6): Show |
2 | a0001c0001t0020g0214a0001c0001t0044g0098 | 2 | HG04204.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.960+13810_960+1381 others(17): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
CCAAAAAA others(4): Show |
C | 2 | a0001c0001t0101g0287a0001c0007t0106g0286 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.960+13811_960+1382 others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740173
|
CCAAAAAA others(5): Show |
C | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.960+13811_960+1382 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740173 | ||||||
chr2:202740174
|
C | A | 238 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(235): Show | 238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.960+13811C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740174 | ||||||
chr2:202740174
|
C | CA | 17 | a0001c0001t0004g0009a0001c0001t0004g0086a0001c0001t0004g0126others(14): Show | 17 | HG00544.hp1 HG00597.hp2 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.960+13839dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740174 | |||||
chr2:202740175
|
A | C | 2 | a0001c0001t0001g0253a0001c0001t0116g0100 | 2 | HG02027.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.960+13812A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740175 | ||||||
chr2:202740176
|
A | C | 3 | a0001c0001t0001g0253a0001c0001t0027g0252a0001c0001t0027g0254 | 3 | HG02027.hp1 HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.960+13813A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740176 | ||||||
chr2:202740261
|
G | A | 2 | a0001c0001t0042g0153a0001c0001t0087g0117 | 2 | HG02109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.960+13898G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740261 | ||||||
chr2:202740279
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.960+13916G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740279 | ||||||
chr2:202740292
|
G | A | 1 | a0001c0001t0086g0142 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.960+13929G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740292 | ||||||
chr2:202740359
|
C | CA | 92 | a0001c0001t0001g0224a0001c0001t0002g0181a0001c0001t0002g0191others(89): Show | 92 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.960+14017dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | |||||
chr2:202740359
|
C | CAA | 7 | a0001c0001t0014g0270a0001c0001t0019g0215a0001c0001t0137g0032others(4): Show | 7 | HG00642.hp1 HG03130.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.960+14016_960+1401 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | |||||
chr2:202740359
|
CA | C | 14 | a0001c0001t0004g0232a0001c0001t0020g0015a0001c0001t0020g0234others(11): Show | 14 | HG02258.hp2 HG02523.hp1 HG03471.hp2 others(11): Show |
intron_variant | MODIFIER | c.960+14017delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | |||||
chr2:202740359
|
CAA | C | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.960+14016_960+1401 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740359 | |||||
chr2:202740388
|
A | G | 1 | a0001c0001t0114g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.960+14025A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740388 | ||||||
chr2:202740436
|
T | G | 1 | a0001c0001t0034g0274 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.960+14073T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202740436 | ||||||
chr2:202740863
|
C | CA | 5 | a0001c0001t0007g0014a0001c0001t0007g0096a0001c0001t0007g0115others(2): Show | 5 | HG00558.hp1 HG01243.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.960+14509dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740863 | |||||
chr2:202740994
|
T | TG | 8 | a0001c0001t0047g0267a0001c0001t0047g0268a0001c0001t0123g0151others(5): Show | 8 | HG01884.hp2 HG02559.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-14540dupG | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202740994 | |||||
chr2:202741191
|
G | A | 2 | a0001c0001t0101g0287a0001c0007t0106g0286 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.961-14347G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741191 | ||||||
chr2:202741231
|
T | G | 6 | a0001c0001t0047g0268a0002c0002t0024g0288a0002c0002t0024g0289others(3): Show | 6 | HG01884.hp2 HG03130.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.961-14307T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741231 | ||||||
chr2:202741344
|
G | A | 1 | a0001c0001t0136g0037 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.961-14194G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741344 | ||||||
chr2:202741416
|
C | CA | 27 | a0001c0001t0001g0135a0001c0001t0001g0157a0001c0001t0004g0085others(24): Show | 27 | HG00099.hp2 HG01109.hp2 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.961-14092dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
C | CAAA | 10 | a0001c0001t0004g0009a0001c0001t0004g0106a0001c0001t0004g0171others(7): Show | 10 | HG00597.hp2 HG00738.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-14094_961-1409 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
CA | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0062others(59): Show | 62 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.961-14092delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
CAA | C | 17 | a0001c0001t0001g0057a0001c0001t0001g0075a0001c0001t0001g0166others(14): Show | 17 | HG00673.hp1 HG01081.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.961-14093_961-1409 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
CAAAA | C | 13 | a0001c0001t0001g0253a0001c0001t0008g0034a0001c0001t0013g0030others(10): Show | 13 | HG00741.hp2 HG01884.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.961-14095_961-1409 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
CAAAAA | C | 51 | a0001c0001t0001g0061a0001c0001t0002g0087a0001c0001t0002g0181others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.961-14096_961-1409 others(9): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
CAAAAAA | C | 62 | a0001c0001t0001g0069a0001c0001t0002g0104a0001c0001t0002g0140others(59): Show | 62 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.961-14097_961-1409 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-14103_961-1409 others(16): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741416
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0137g0032 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.961-14107_961-1409 others(20): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741416 | |||||
chr2:202741492
|
G | A | 130 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.961-14046G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741492 | ||||||
chr2:202741542
|
A | T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-13996A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741542 | ||||||
chr2:202741542
|
AT | A | 8 | a0001c0001t0004g0232a0001c0001t0009g0060a0001c0001t0009g0070others(5): Show | 8 | HG01952.hp2 HG02293.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.961-13984delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741542 | |||||
chr2:202741542
|
ATTTTTT | A | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13989_961-1398 others(10): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741542 | |||||
chr2:202741552
|
T | C | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13986T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741552 | ||||||
chr2:202741553
|
T | A | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13985T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741553 | ||||||
chr2:202741555
|
G | A | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13983G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741555 | ||||||
chr2:202741557
|
G | A | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-13981G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741557 | ||||||
chr2:202741600
|
G | A | 1 | a0001c0001t0028g0001 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.961-13938G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741600 | ||||||
chr2:202741605
|
C | T | 130 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.961-13933C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741605 | ||||||
chr2:202741682
|
G | A | 1 | a0001c0001t0026g0168 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.961-13856G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741682 | ||||||
chr2:202741693
|
C | T | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-13845C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741693 | ||||||
chr2:202741871
|
CA | C | 3 | a0001c0001t0031g0063a0001c0001t0031g0084a0001c0001t0067g0219 | 3 | HG02155.hp1 NA18747.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.961-13665delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202741871 | |||||
chr2:202741886
|
A | G | 1 | a0001c0001t0019g0215 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.961-13652A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202741886 | ||||||
chr2:202742031
|
T | C | 133 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.961-13507T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742031 | ||||||
chr2:202742132
|
A | C | 24 | a0001c0001t0001g0057a0001c0001t0001g0075a0001c0001t0001g0116others(21): Show | 24 | HG00609.hp2 HG00621.hp2 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.961-13406A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742132 | ||||||
chr2:202742278
|
C | T | 1 | a0003c0003t0010g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.961-13260C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742278 | ||||||
chr2:202742530
|
C | T | 1 | a0001c0001t0009g0002 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.961-13008C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742530 | ||||||
chr2:202742566
|
C | T | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-12972C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742566 | ||||||
chr2:202742599
|
T | A | 129 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.961-12939T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742599 | ||||||
chr2:202742600
|
C | A | 129 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.961-12938C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742600 | ||||||
chr2:202742664
|
A | G | 1 | a0001c0001t0043g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.961-12874A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742664 | ||||||
chr2:202742732
|
CAG | C | 8 | a0001c0001t0047g0267a0001c0001t0047g0268a0001c0001t0123g0151others(5): Show | 8 | HG01884.hp2 HG02559.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-12804_961-1280 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202742732 | |||||
chr2:202742752
|
T | C | 1 | a0001c0001t0004g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.961-12786T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742752 | ||||||
chr2:202742850
|
A | C | 1 | a0001c0001t0021g0067 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.961-12688A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202742850 | ||||||
chr2:202743050
|
C | T | 1 | a0001c0001t0053g0119 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.961-12488C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743050 | ||||||
chr2:202743307
|
A | G | 1 | a0001c0001t0118g0205 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.961-12231A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743307 | ||||||
chr2:202743385
|
A | G | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-12153A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743385 | ||||||
chr2:202743442
|
T | C | 1 | a0001c0001t0032g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.961-12096T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743442 | ||||||
chr2:202743450
|
G | A | 1 | a0001c0001t0041g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.961-12088G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743450 | ||||||
chr2:202743467
|
A | G | 116 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.961-12071A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743467 | ||||||
chr2:202743595
|
T | C | 2 | a0001c0001t0101g0287a0001c0007t0106g0286 | 2 | HG02109.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.961-11943T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743595 | ||||||
chr2:202743621
|
G | T | 1 | a0001c0001t0005g0228 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.961-11917G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743621 | ||||||
chr2:202743626
|
C | CAAAT | 56 | a0001c0001t0001g0253a0001c0001t0008g0034a0001c0001t0008g0038others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.961-11909_961-1190 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202743626 | |||||
chr2:202743630
|
C | T | 76 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0002g0087others(73): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.961-11908C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743630 | ||||||
chr2:202743699
|
A | C | 4 | a0001c0001t0053g0119a0001c0001t0053g0146a0001c0001t0068g0239others(1): Show | 4 | HG02293.hp1 HG02300.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-11839A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743699 | ||||||
chr2:202743834
|
C | T | 1 | a0001c0001t0135g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.961-11704C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202743834 | ||||||
chr2:202744019
|
T | C | 132 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.961-11519T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744019 | ||||||
chr2:202744047
|
A | G | 8 | a0001c0001t0042g0153a0002c0002t0016g0295a0002c0002t0016g0296others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-11491A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744047 | ||||||
chr2:202744053
|
G | T | 1 | a0001c0001t0080g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.961-11485G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744053 | ||||||
chr2:202744155
|
T | TCTTA | 78 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(75): Show | 78 | HG00323.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.961-11382_961-1137 others(8): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744155 | |||||
chr2:202744250
|
A | G | 2 | a0001c0001t0050g0284a0001c0001t0050g0285 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.961-11288A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744250 | ||||||
chr2:202744403
|
C | T | 2 | a0001c0001t0027g0252a0001c0001t0027g0254 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.961-11135C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744403 | ||||||
chr2:202744461
|
A | G | 2 | a0001c0001t0014g0272a0001c0001t0061g0276 | 2 | NA18981.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.961-11077A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744461 | ||||||
chr2:202744590
|
G | A | 1 | a0001c0001t0043g0141 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.961-10948G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744590 | ||||||
chr2:202744706
|
C | T | 4 | a0001c0001t0021g0027a0001c0001t0021g0067a0001c0001t0122g0209others(1): Show | 4 | HG03017.hp2 HG03491.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-10832C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744706 | ||||||
chr2:202744960
|
G | C | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-10578G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202744960 | ||||||
chr2:202744976
|
C | CA | 17 | a0001c0001t0001g0092a0001c0001t0001g0184a0001c0001t0001g0224others(14): Show | 17 | HG00597.hp1 HG00621.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.961-10539dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | |||||
chr2:202744976
|
CA | C | 18 | a0001c0001t0001g0012a0001c0001t0001g0061a0001c0001t0001g0127others(15): Show | 18 | HG00558.hp2 HG00609.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-10539delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | |||||
chr2:202744976
|
CAA | C | 95 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(92): Show | 95 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.961-10540_961-1053 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | |||||
chr2:202744976
|
CAAA | C | 26 | a0001c0001t0001g0253a0001c0001t0008g0038a0001c0001t0008g0042others(23): Show | 26 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.961-10541_961-1053 others(7): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202744976 | |||||
chr2:202745000
|
G | T | 1 | a0001c0001t0038g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961-10538G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745000 | ||||||
chr2:202745053
|
A | G | 1 | a0001c0001t0022g0031 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.961-10485A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745053 | ||||||
chr2:202745060
|
T | TCA | 132 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.961-10477_961-1047 others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202745060 | |||||
chr2:202745279
|
CA | C | 30 | a0001c0001t0012g0073a0001c0001t0020g0234a0001c0001t0021g0145others(27): Show | 30 | HG00597.hp1 HG00733.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.961-10245delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202745279 | |||||
chr2:202745295
|
G | A | 1 | a0002c0002t0098g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.961-10243G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745295 | ||||||
chr2:202745649
|
A | G | 1 | a0002c0002t0003g0303 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.961-9889A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745649 | ||||||
chr2:202745682
|
T | C | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-9856T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745682 | ||||||
chr2:202745741
|
G | T | 1 | a0001c0001t0004g0009 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.961-9797G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745741 | ||||||
chr2:202745967
|
A | T | 1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.961-9571A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202745967 | ||||||
chr2:202746107
|
A | G | 31 | a0001c0001t0001g0253a0001c0001t0008g0034a0001c0001t0008g0038others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.961-9431A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746107 | ||||||
chr2:202746217
|
A | C | 76 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0002g0087others(73): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.961-9321A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746217 | ||||||
chr2:202746379
|
A | T | 236 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(233): Show | 236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.961-9159A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746379 | ||||||
chr2:202746498
|
TA | T | 132 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.961-9031delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746498 | |||||
chr2:202746946
|
C | T | 1 | a0001c0001t0113g0125 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.961-8592C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746946 | ||||||
chr2:202746948
|
GA | G | 129 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.961-8581delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746948 | |||||
chr2:202746948
|
GAAAAAAA others(9): Show |
G | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.961-8581_961-8566d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746948 | |||||
chr2:202746957
|
ACAAAACA others(9): Show |
A | 1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.961-8580_961-8565d others(18): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746957 | ||||||
chr2:202746960
|
AAAC | A | 74 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0002g0087others(71): Show | 74 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.961-8575_961-8573d others(5): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746960 | |||||
chr2:202746961
|
AAC | A | 51 | a0001c0001t0001g0253a0001c0001t0008g0034a0001c0001t0008g0038others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.961-8575_961-8574d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202746961 | |||||
chr2:202746962
|
A | C | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-8576A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746962 | ||||||
chr2:202746963
|
C | A | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-8575C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202746963 | ||||||
chr2:202747001
|
C | G | 18 | a0001c0001t0030g0005a0001c0007t0106g0286a0001c0008t0064g0134others(15): Show | 18 | HG00733.hp1 HG01109.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.961-8537C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747001 | ||||||
chr2:202747078
|
G | A | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-8460G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747078 | ||||||
chr2:202747160
|
A | G | 1 | a0001c0001t0114g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.961-8378A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747160 | ||||||
chr2:202747374
|
G | A | 4 | a0001c0001t0023g0044a0001c0001t0023g0047a0001c0001t0023g0048others(1): Show | 4 | HG00140.hp2 HG01167.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-8164G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747374 | ||||||
chr2:202747530
|
A | G | 1 | a0001c0001t0123g0151 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.961-8008A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747530 | ||||||
chr2:202747681
|
A | C | 235 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(232): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.961-7857A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747681 | ||||||
chr2:202747706
|
G | A | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-7832G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747706 | ||||||
chr2:202747718
|
C | G | 1 | a0001c0001t0033g0163 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.961-7820C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747718 | ||||||
chr2:202747766
|
A | G | 2 | a0001c0007t0106g0286a0001c0008t0064g0134 | 2 | HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.961-7772A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747766 | ||||||
chr2:202747916
|
G | C | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.961-7622G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202747916 | ||||||
chr2:202748016
|
C | T | 1 | a0001c0001t0115g0221 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.961-7522C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202748016 | ||||||
chr2:202748543
|
A | T | 7 | a0001c0001t0027g0136a0001c0001t0028g0064a0001c0001t0029g0004others(4): Show | 7 | HG02818.hp2 HG02976.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.961-6995A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202748543 | ||||||
chr2:202748860
|
C | A | 1 | a0001c0001t0075g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.961-6678C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202748860 | ||||||
chr2:202749054
|
AAAAT | A | 5 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0036g0147others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.961-6479_961-6476d others(6): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202749054 | |||||
chr2:202749139
|
A | G | 1 | a0003c0003t0010g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.961-6399A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749139 | ||||||
chr2:202749400
|
C | T | 1 | a0001c0001t0055g0148 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.961-6138C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749400 | ||||||
chr2:202749442
|
TA | T | 155 | a0001c0001t0001g0069a0001c0001t0001g0253a0001c0001t0002g0087others(152): Show | 155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.961-6084delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202749442 | |||||
chr2:202749827
|
C | G | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-5711C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749827 | ||||||
chr2:202749921
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.961-5617G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202749921 | ||||||
chr2:202750231
|
G | C | 235 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(232): Show | 235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.961-5307G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202750231 | ||||||
chr2:202750577
|
A | G | 1 | a0001c0001t0011g0177 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.961-4961A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202750577 | ||||||
chr2:202750728
|
T | C | 1 | a0001c0001t0047g0267 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.961-4810T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202750728 | ||||||
chr2:202751374
|
G | T | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.961-4164G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751374 | ||||||
chr2:202751771
|
CA | C | 162 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(159): Show | 162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.961-3744delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202751771 | |||||
chr2:202751771
|
CAA | C | 94 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0080others(91): Show | 94 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.961-3745_961-3744d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202751771 | |||||
chr2:202751771
|
CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0006g0103a0001c0001t0006g0131a0001c0001t0102g0283others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-3756_961-3744d others(15): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202751771 | |||||
chr2:202751793
|
A | T | 2 | a0001c0001t0006g0250a0001c0001t0028g0076 | 2 | HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.961-3745A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751793 | ||||||
chr2:202751881
|
T | C | 1 | a0001c0001t0002g0140 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.961-3657T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751881 | ||||||
chr2:202751911
|
A | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-3627A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751911 | ||||||
chr2:202751920
|
C | G | 2 | a0001c0001t0028g0001a0001c0001t0045g0006 | 2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.961-3618C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202751920 | ||||||
chr2:202752206
|
C | T | 1 | a0001c0001t0008g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.961-3332C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752206 | ||||||
chr2:202752316
|
T | C | 2 | a0001c0001t0091g0265a0002c0002t0105g0314 | 2 | HG01884.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.961-3222T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752316 | ||||||
chr2:202752317
|
C | G | 10 | a0001c0001t0047g0267a0001c0001t0047g0268a0001c0001t0049g0053others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.961-3221C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752317 | ||||||
chr2:202752416
|
C | CT | 86 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0002g0087others(83): Show | 86 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.961-3106dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202752416 | |||||
chr2:202752416
|
CT | C | 14 | a0001c0001t0009g0070a0001c0001t0042g0153a0001c0001t0046g0138others(11): Show | 14 | HG01168.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.961-3106delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202752416 | |||||
chr2:202752718
|
G | A | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-2820G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752718 | ||||||
chr2:202752736
|
G | A | 1 | a0001c0001t0125g0079 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.961-2802G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752736 | ||||||
chr2:202752999
|
C | T | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.961-2539C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202752999 | ||||||
chr2:202753240
|
A | G | 4 | a0001c0001t0006g0103a0001c0001t0006g0131a0001c0001t0102g0283others(1): Show | 4 | HG02572.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.961-2298A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753240 | ||||||
chr2:202753408
|
A | G | 3 | a0001c0001t0002g0213a0001c0001t0025g0211a0001c0001t0038g0025 | 3 | HG00099.hp1 HG01175.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.961-2130A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753408 | ||||||
chr2:202753548
|
A | C | 1 | a0001c0008t0064g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.961-1990A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753548 | ||||||
chr2:202753558
|
A | T | 1 | a0001c0001t0110g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.961-1980A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753558 | ||||||
chr2:202753753
|
T | TA | 22 | a0001c0001t0001g0061a0001c0001t0008g0150a0001c0001t0013g0050others(19): Show | 22 | HG00558.hp2 HG00609.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.961-1772dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202753753 | |||||
chr2:202753753
|
TA | T | 6 | a0001c0001t0070g0231a0002c0002t0024g0288a0002c0002t0024g0289others(3): Show | 6 | HG01884.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.961-1772delA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202753753 | |||||
chr2:202753784
|
C | G | 1 | a0001c0001t0047g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.961-1754C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753784 | ||||||
chr2:202753784
|
C | T | 1 | a0001c0001t0073g0229 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.961-1754C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753784 | ||||||
chr2:202753986
|
G | C | 134 | a0001c0001t0001g0061a0001c0001t0001g0069a0001c0001t0001g0253others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.961-1552G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202753986 | ||||||
chr2:202754056
|
A | G | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.961-1482A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754056 | ||||||
chr2:202754360
|
C | T | 1 | a0001c0001t0038g0238 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.961-1178C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754360 | ||||||
chr2:202754385
|
A | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.961-1153A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754385 | ||||||
chr2:202754465
|
G | T | 1 | a0002c0002t0003g0310 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.961-1073G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754465 | ||||||
chr2:202754503
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.961-1035A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754503 | ||||||
chr2:202754519
|
C | A | 1 | a0002c0002t0098g0316 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.961-1019C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754519 | ||||||
chr2:202754664
|
G | A | 1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.961-874G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754664 | ||||||
chr2:202754732
|
C | A | 11 | a0001c0001t0004g0009a0001c0001t0004g0106a0001c0001t0004g0171others(8): Show | 11 | HG00597.hp2 HG00738.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.961-806C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754732 | ||||||
chr2:202754868
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.961-670T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754868 | ||||||
chr2:202754888
|
C | CA | 15 | a0001c0001t0004g0126a0001c0001t0009g0070a0001c0001t0018g0017others(12): Show | 15 | HG00738.hp2 HG01243.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.961-631dupA | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | |||||
chr2:202754888
|
C | CAA | 24 | a0001c0001t0001g0012a0001c0001t0001g0154a0001c0001t0001g0251others(21): Show | 24 | HG01081.hp1 HG01192.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.961-632_961-631dup others(2): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | |||||
chr2:202754888
|
C | CAAA | 192 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0057others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.961-633_961-631dup others(3): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | |||||
chr2:202754888
|
C | CAAAA | 13 | a0001c0001t0006g0103a0001c0001t0011g0177a0001c0001t0020g0234others(10): Show | 13 | HG02055.hp2 HG02165.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.961-634_961-631dup others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 202754888 | |||||
chr2:202754954
|
C | T | 35 | a0001c0001t0001g0116a0001c0001t0001g0166a0001c0001t0001g0175others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.961-584C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202754954 | ||||||
chr2:202755100
|
G | A | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-438G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755100 | ||||||
chr2:202755245
|
C | T | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.961-293C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755245 | ||||||
chr2:202755311
|
G | A | 2 | a0001c0001t0002g0204a0001c0001t0101g0287 | 2 | HG01071.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.961-227G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755311 | ||||||
chr2:202755510
|
C | T | 5 | a0001c0001t0035g0054a0001c0001t0035g0055a0001c0001t0036g0147others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.961-28C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | 202755510 | ||||||
chr2:202755723
|
A | C | 1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1104+42A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202755723 | ||||||
chr2:202755862
|
T | G | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1104+181T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202755862 | ||||||
chr2:202756234
|
T | C | 2 | a0001c0001t0006g0131a0003c0003t0006g0072 | 2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1104+553T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202756234 | ||||||
chr2:202756391
|
A | G | 1 | a0001c0001t0020g0234 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1104+710A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202756391 | ||||||
chr2:202756500
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1105-713G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202756500 | ||||||
chr2:202757033
|
C | T | 127 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1105-180C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202757033 | ||||||
chr2:202757077
|
A | C | 76 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(73): Show | 76 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1105-136A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202757077 | ||||||
chr2:202757179
|
T | C | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1105-34T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 5/7 | chr2 | 202757179 | ||||||
chr2:202757468
|
T | C | 1 | a0001c0001t0002g0203 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1330+30T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202757468 | ||||||
chr2:202757698
|
A | G | 8 | a0001c0001t0073g0229a0003c0003t0010g0196a0003c0003t0010g0244others(5): Show | 8 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1330+260A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202757698 | ||||||
chr2:202757927
|
A | G | 2 | a0001c0001t0047g0267a0001c0001t0123g0151 | 2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1330+489A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202757927 | ||||||
chr2:202758543
|
T | C | 3 | a0001c0001t0091g0265a0001c0007t0106g0286a0001c0008t0064g0134 | 3 | HG01884.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1331-690T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202758543 | ||||||
chr2:202758563
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1331-670A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202758563 | ||||||
chr2:202758954
|
A | C | 2 | a0002c0002t0016g0300a0002c0002t0108g0294 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1331-279A>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 6/7 | chr2 | 202758954 | ||||||
chr2:202759364
|
C | T | 1 | a0001c0001t0116g0100 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1451+11C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759364 | ||||||
chr2:202759374
|
C | T | 1 | a0002c0002t0096g0317 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1451+21C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759374 | ||||||
chr2:202759543
|
C | A | 2 | a0001c0001t0049g0053a0001c0001t0049g0269 | 2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1451+190C>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759543 | ||||||
chr2:202759557
|
AT | A | 95 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(92): Show | 95 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1451+222delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202759557 | |||||
chr2:202759557
|
ATT | A | 32 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.1451+221_1451+222d others(4): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202759557 | |||||
chr2:202759786
|
T | A | 1 | a0001c0001t0075g0052 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1451+433T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759786 | ||||||
chr2:202759860
|
C | T | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1451+507C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759860 | ||||||
chr2:202759880
|
T | G | 1 | a0001c0001t0038g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1451+527T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202759880 | ||||||
chr2:202760182
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1451+829C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760182 | ||||||
chr2:202760279
|
G | C | 132 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1451+926G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760279 | ||||||
chr2:202760401
|
G | A | 1 | a0001c0001t0074g0094 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1451+1048G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760401 | ||||||
chr2:202760528
|
A | G | 1 | a0001c0001t0032g0090 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1451+1175A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760528 | ||||||
chr2:202760567
|
T | C | 1 | a0001c0001t0091g0265 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1451+1214T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760567 | ||||||
chr2:202760760
|
G | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0062a0001c0001t0001g0182others(3): Show | 6 | HG00323.hp1 HG01168.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451+1407G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760760 | ||||||
chr2:202760779
|
T | G | 1 | a0001c0001t0116g0100 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1451+1426T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202760779 | ||||||
chr2:202761143
|
T | C | 133 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(130): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1451+1790T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761143 | ||||||
chr2:202761160
|
A | G | 317 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.1451+1807A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761160 | ||||||
chr2:202761572
|
G | C | 1 | a0001c0001t0101g0287 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1451+2219G>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761572 | ||||||
chr2:202761596
|
G | T | 1 | a0001c0001t0130g0230 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1451+2243G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761596 | ||||||
chr2:202761878
|
CT | C | 7 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0080others(4): Show | 7 | HG03130.hp1 HG03195.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.1451+2537delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202761878 | |||||
chr2:202761890
|
T | A | 6 | a0001c0001t0012g0073a0001c0001t0020g0015a0001c0001t0020g0160others(3): Show | 6 | HG02523.hp1 NA18949.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.1451+2537T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761890 | ||||||
chr2:202761956
|
C | T | 1 | a0001c0001t0035g0054 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1451+2603C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202761956 | ||||||
chr2:202762105
|
C | T | 1 | a0001c0001t0046g0139 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1451+2752C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762105 | ||||||
chr2:202762114
|
C | T | 129 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(126): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1451+2761C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762114 | ||||||
chr2:202762442
|
C | G | 128 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1452-3004C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762442 | ||||||
chr2:202762522
|
T | C | 1 | a0001c0001t0011g0114 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1452-2924T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762522 | ||||||
chr2:202762588
|
G | A | 128 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(125): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1452-2858G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762588 | ||||||
chr2:202762688
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1452-2758C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762688 | ||||||
chr2:202762689
|
C | T | 108 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.1452-2757C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762689 | ||||||
chr2:202762716
|
A | G | 1 | a0001c0001t0045g0149 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1452-2730A>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202762716 | ||||||
chr2:202763070
|
C | CT | 6 | a0001c0001t0023g0047a0001c0001t0041g0266a0001c0001t0091g0265others(3): Show | 6 | HG00639.hp1 HG01884.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1452-2357dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202763070 | |||||
chr2:202763070
|
CT | C | 179 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0020others(176): Show | 179 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1452-2357delT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202763070 | |||||
chr2:202763073
|
T | C | 1 | a0001c0001t0004g0171 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1452-2373T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763073 | ||||||
chr2:202763164
|
C | T | 31 | a0001c0001t0008g0034a0001c0001t0008g0038a0001c0001t0008g0042others(28): Show | 31 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.1452-2282C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763164 | ||||||
chr2:202763167
|
G | T | 1 | a0001c0001t0020g0214 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1452-2279G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763167 | ||||||
chr2:202763220
|
C | T | 75 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(72): Show | 75 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.1452-2226C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763220 | ||||||
chr2:202763309
|
T | C | 1 | a0002c0002t0105g0314 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1452-2137T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763309 | ||||||
chr2:202763364
|
G | A | 1 | a0001c0001t0054g0118 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1452-2082G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202763364 | ||||||
chr2:202764004
|
G | A | 1 | a0001c0001t0007g0096 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1452-1442G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764004 | ||||||
chr2:202764034
|
G | A | 127 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(124): Show | 127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1452-1412G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764034 | ||||||
chr2:202764128
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1452-1318T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764128 | ||||||
chr2:202764254
|
G | A | 9 | a0001c0001t0041g0266a0001c0001t0047g0267a0001c0001t0047g0268others(6): Show | 9 | HG01884.hp2 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1452-1192G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764254 | ||||||
chr2:202764273
|
G | T | 1 | a0001c0001t0080g0111 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1452-1173G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764273 | ||||||
chr2:202764328
|
G | A | 1 | a0003c0003t0030g0245 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1452-1118G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764328 | ||||||
chr2:202764430
|
A | T | 7 | a0001c0001t0002g0181a0001c0001t0002g0193a0001c0001t0002g0199others(4): Show | 7 | HG00408.hp2 HG02071.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1452-1016A>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764430 | ||||||
chr2:202764464
|
C | G | 1 | a0001c0001t0082g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1452-982C>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202764464 | ||||||
chr2:202765121
|
C | T | 126 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1452-325C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765121 | ||||||
chr2:202765149
|
G | A | 1 | a0003c0003t0010g0246 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1452-297G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765149 | ||||||
chr2:202765181
|
T | C | 2 | a0001c0001t0091g0265a0001c0008t0064g0134 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1452-265T>C | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765181 | ||||||
chr2:202765210
|
G | A | 1 | a0001c0001t0022g0029 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1452-236G>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765210 | ||||||
chr2:202765296
|
T | G | 126 | a0001c0001t0001g0069a0001c0001t0002g0087a0001c0001t0002g0104others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.1452-150T>G | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765296 | ||||||
chr2:202765375
|
C | T | 3 | a0001c0001t0091g0265a0001c0007t0106g0286a0001c0008t0064g0134 | 3 | HG01884.hp1 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1452-71C>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765375 | ||||||
chr2:202765379
|
C | CT | 11 | a0001c0001t0002g0181a0001c0001t0002g0193a0001c0001t0002g0199others(8): Show | 11 | HG00408.hp2 HG02071.hp2 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.1452-53dupT | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 202765379 | |||||
chr2:202765387
|
T | A | 1 | a0001c0007t0106g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1452-59T>A | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765387 | ||||||
chr2:202765408
|
G | T | 1 | a0001c0001t0038g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1452-38G>T | FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 7/7 | chr2 | 202765408 |