geneid | 55183 |
---|---|
ensemblid | ENSG00000080345.18 |
hgncid | 23207 |
symbol | RIF1 |
name | replication timing regulatory factor 1 |
refseq_nuc | NM_018151.5 |
refseq_prot | NP_060621.3 |
ensembl_nuc | ENST00000444746.7 |
ensembl_prot | ENSP00000390181.2 |
mane_status | MANE Select |
chr | chr2 |
start | 151409902 |
end | 151482172 |
strand | + |
ver | v1.2 |
region | chr2:151409902-151482172 |
region5000 | chr2:151404902-151487172 |
regionname0 | RIF1_chr2_151409902_151482172 |
regionname5000 | RIF1_chr2_151404902_151487172 |
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 | 0/1 | 2472 | 206 | 20 | 40 | 113 | 11 | 21 | 88 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002 | 1/0 | 2472 | 109 | 34 | 17 | 37 | 6 | 14 | 30 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0003 | 0/0 | 2472 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0004 | 0/0 | 2472 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0005 | 0/0 | 2472 | 6 | 4 | 0 | 0 | 1 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0006 | 0/0 | 2472 | 4 | 0 | 0 | 4 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0007 | 0/0 | 2472 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0008 | 0/0 | 2472 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0009 | 0/0 | 2472 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0010 | 0/0 | 2472 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0011 | 0/0 | 2472 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0012 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0013 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0014 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0015 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0016 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0017 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0018 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0019 | 0/0 | 2472 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0020 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0021 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0022 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0023 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0024 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0025 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0026 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0027 | 0/0 | 2472 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0028 | 0/0 | 2472 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
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 | 1/0 | 7419 | 106 | 34 | 17 | 34 | 6 | 14 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0002 | 0/0 | 7419 | 81 | 4 | 22 | 44 | 5 | 6 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0003 | 0/1 | 7419 | 75 | 7 | 15 | 39 | 6 | 7 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0004 | 0/0 | 7419 | 36 | 1 | 1 | 30 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0005 | 0/0 | 7419 | 15 | 14 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0006 | 0/0 | 7419 | 7 | 0 | 0 | 7 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0007 | 0/0 | 7419 | 6 | 6 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0008 | 0/0 | 7419 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0009 | 0/0 | 7419 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0010 | 0/0 | 7419 | 4 | 2 | 0 | 0 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0011 | 0/0 | 7419 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0012 | 0/0 | 7419 | 4 | 3 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0013 | 0/0 | 7419 | 3 | 0 | 0 | 3 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0014 | 0/0 | 7419 | 3 | 0 | 3 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0015 | 0/0 | 7419 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0016 | 0/0 | 7419 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0017 | 0/0 | 7419 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0018 | 0/0 | 7419 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0019 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0020 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0021 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0022 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0023 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0024 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0025 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0026 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0027 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0028 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0029 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0030 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0031 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0032 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0033 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0034 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0035 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0036 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0037 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
c0038 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
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 | 7245 | 75 | 0 | 26 | 40 | 5 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0002 | 0/1 | 7245 | 58 | 0 | 15 | 30 | 6 | 6 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0003 | 1/0 | 7244 | 45 | 0 | 8 | 29 | 2 | 5 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0004 | 0/0 | 7244 | 20 | 15 | 0 | 5 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0005 | 0/0 | 7243 | 18 | 0 | 0 | 16 | 0 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0006 | 0/0 | 7243 | 16 | 0 | 1 | 13 | 0 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0007 | 0/0 | 7245 | 16 | 14 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0008 | 0/0 | 7239 | 8 | 0 | 7 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0009 | 0/0 | 7245 | 7 | 0 | 0 | 7 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0010 | 0/0 | 7245 | 5 | 0 | 0 | 3 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0011 | 0/0 | 7241 | 5 | 0 | 0 | 5 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0012 | 0/0 | 7245 | 4 | 0 | 1 | 2 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0013 | 0/0 | 7245 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0014 | 0/0 | 7244 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0015 | 0/0 | 7242 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0016 | 0/0 | 7245 | 4 | 4 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0017 | 0/0 | 7245 | 4 | 2 | 0 | 0 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0018 | 0/0 | 7244 | 3 | 0 | 0 | 0 | 1 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0019 | 0/0 | 7244 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0020 | 0/0 | 7245 | 3 | 0 | 0 | 3 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0021 | 0/0 | 7243 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0022 | 0/0 | 7243 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0023 | 0/0 | 7242 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0024 | 0/0 | 7242 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0025 | 0/0 | 7245 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0026 | 0/0 | 7244 | 3 | 2 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0027 | 0/0 | 7245 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0028 | 0/0 | 7244 | 3 | 2 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0029 | 0/0 | 7241 | 2 | 0 | 0 | 2 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0030 | 0/0 | 7245 | 2 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0031 | 0/0 | 7245 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0032 | 0/0 | 7244 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0033 | 0/0 | 7245 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0034 | 0/0 | 7245 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0035 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0036 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0037 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0038 | 0/0 | 7241 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0039 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0040 | 0/0 | 7245 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0041 | 0/0 | 7245 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0042 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0043 | 0/0 | 7245 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0044 | 0/0 | 7245 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0045 | 0/0 | 7243 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0046 | 0/0 | 7243 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0047 | 0/0 | 7245 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0048 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0049 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0050 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0051 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0052 | 0/0 | 7244 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0053 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0054 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0055 | 0/0 | 7244 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0056 | 0/0 | 7245 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0057 | 0/0 | 7244 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0058 | 0/0 | 7244 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0059 | 0/0 | 7247 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0060 | 0/0 | 7243 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0061 | 0/0 | 7243 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0062 | 0/0 | 7243 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0063 | 0/0 | 7244 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0064 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0065 | 0/0 | 7245 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0066 | 0/0 | 7245 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0067 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0068 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0069 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0070 | 0/0 | 7245 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0071 | 0/0 | 7244 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
t0072 | 0/0 | 7244 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
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 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 7419 | 81 | 4 | 22 | 44 | 5 | 6 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003 | 0/1 | 7419 | 75 | 7 | 15 | 39 | 6 | 7 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0004 | 0/0 | 7419 | 36 | 1 | 1 | 30 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0007 | 0/0 | 7419 | 6 | 6 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0009 | 0/0 | 7419 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0016 | 0/0 | 7419 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0022 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0038 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001 | 1/0 | 7419 | 106 | 34 | 17 | 34 | 6 | 14 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0013 | 0/0 | 7419 | 3 | 0 | 0 | 3 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0003c0005 | 0/0 | 7419 | 15 | 14 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0003c0019 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0004c0006 | 0/0 | 7419 | 7 | 0 | 0 | 7 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0005c0010 | 0/0 | 7419 | 4 | 2 | 0 | 0 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0005c0018 | 0/0 | 7419 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0006c0011 | 0/0 | 7419 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0007c0008 | 0/0 | 7419 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0008c0012 | 0/0 | 7419 | 4 | 3 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0009c0014 | 0/0 | 7419 | 3 | 0 | 3 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0010c0015 | 0/0 | 7419 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0011c0017 | 0/0 | 7419 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0012c0037 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0013c0032 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0014c0033 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0015c0034 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0016c0035 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0017c0029 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0018c0025 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0019c0027 | 0/0 | 7419 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0020c0028 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0021c0023 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0022c0024 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0023c0026 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0024c0021 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0025c0030 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0026c0031 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0027c0020 | 0/0 | 7419 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0028c0036 | 0/0 | 7419 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 14663 | 65 | 0 | 21 | 35 | 5 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0012 | 0/0 | 14663 | 4 | 0 | 1 | 2 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0020 | 0/0 | 14663 | 2 | 0 | 0 | 2 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0027 | 0/0 | 14663 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0035 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0047 | 0/0 | 14663 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0048 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0049 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0050 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0052 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0053 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0002t0054 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0002 | 0/1 | 14663 | 52 | 0 | 10 | 29 | 6 | 6 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0011 | 0/0 | 14659 | 5 | 0 | 0 | 5 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0025 | 0/0 | 14663 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0029 | 0/0 | 14659 | 2 | 0 | 0 | 2 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0030 | 0/0 | 14663 | 2 | 0 | 1 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0039 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0040 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0041 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0042 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0043 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0064 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0065 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0066 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0067 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0068 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0003t0069 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0004t0005 | 0/0 | 14661 | 18 | 0 | 0 | 16 | 0 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0004t0006 | 0/0 | 14661 | 15 | 0 | 1 | 12 | 0 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0004t0038 | 0/0 | 14659 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0004t0045 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0004t0046 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0007t0023 | 0/0 | 14660 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0007t0024 | 0/0 | 14660 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0009t0015 | 0/0 | 14660 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0016t0002 | 0/0 | 14663 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0022t0027 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0001c0038t0033 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0003 | 1/0 | 14662 | 39 | 0 | 8 | 23 | 2 | 5 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0004 | 0/0 | 14662 | 20 | 15 | 0 | 5 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0008 | 0/0 | 14657 | 7 | 0 | 6 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0010 | 0/0 | 14663 | 5 | 0 | 0 | 3 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0014 | 0/0 | 14662 | 4 | 0 | 0 | 0 | 0 | 4 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0018 | 0/0 | 14662 | 3 | 0 | 0 | 0 | 1 | 2 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0019 | 0/0 | 14662 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0021 | 0/0 | 14661 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0022 | 0/0 | 14661 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0026 | 0/0 | 14662 | 3 | 2 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0028 | 0/0 | 14662 | 3 | 2 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0032 | 0/0 | 14662 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0036 | 0/0 | 14662 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0037 | 0/0 | 14662 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0055 | 0/0 | 14662 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0056 | 0/0 | 14663 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0057 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0060 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0061 | 0/0 | 14661 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0062 | 0/0 | 14661 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0063 | 0/0 | 14662 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0071 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0001t0072 | 0/0 | 14662 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0002c0013t0003 | 0/0 | 14662 | 3 | 0 | 0 | 3 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0003c0005t0007 | 0/0 | 14663 | 12 | 11 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0003c0005t0016 | 0/0 | 14663 | 3 | 3 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0003c0019t0070 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0004c0006t0009 | 0/0 | 14663 | 7 | 0 | 0 | 7 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0005c0010t0017 | 0/0 | 14663 | 4 | 2 | 0 | 0 | 1 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0005c0018t0034 | 0/0 | 14663 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0006c0011t0013 | 0/0 | 14663 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0007c0008t0001 | 0/0 | 14663 | 4 | 0 | 0 | 4 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0008c0012t0007 | 0/0 | 14663 | 4 | 3 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0009c0014t0001 | 0/0 | 14663 | 3 | 0 | 3 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0010c0015t0031 | 0/0 | 14663 | 2 | 2 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0011c0017t0002 | 0/0 | 14663 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0012c0037t0020 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0013c0032t0058 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0014c0033t0003 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0015c0034t0059 | 0/0 | 14665 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0016c0035t0003 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0017c0029t0033 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0018c0025t0001 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0019c0027t0016 | 0/0 | 14663 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0020c0028t0002 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0021c0023t0001 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0022c0024t0051 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0023c0026t0044 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0024c0021t0001 | 0/0 | 14663 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0025c0030t0006 | 0/0 | 14661 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0026c0031t0002 | 0/0 | 14663 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0027c0020t0003 | 0/0 | 14662 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
a0028c0036t0008 | 0/0 | 14657 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | copy fasta | chr2 | 151404902 | 151487172 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0012g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0012g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0012g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0020g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0020g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0027g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0027g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0035g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0047g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0048g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0049g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0050g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0052g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0053g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0002t0054g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0025g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0025g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0025g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0029g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0029g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0030g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0030g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0039g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0040g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0041g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0042g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0043g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0064g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0065g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0066g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0067g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0068g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0003t0069g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0038g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0045g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0004t0046g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0023g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0023g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0023g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0024g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0024g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0007t0024g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0009t0015g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0016t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0016t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0022t0027g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0001c0038t0033g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0003g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0008g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0010g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0014g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0014g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0014g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0014g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0018g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0018g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0018g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0019g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0021g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0021g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0021g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0022g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0022g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0022g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0026g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0026g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0026g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0028g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0028g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0028g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0032g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0032g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0036g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0037g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0055g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0056g0373 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0057g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0060g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0061g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0062g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0063g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0071g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0001t0072g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0013t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0013t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0002c0013t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0007g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0016g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0016g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0005t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0003c0019t0070g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0004c0006t0009g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0017g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0017g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0017g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0010t0017g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0018t0034g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0005c0018t0034g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0013g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0013g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0013g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0006c0011t0013g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0008t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0008t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0008t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0007c0008t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0012t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0012t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0012t0007g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0008c0012t0007g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0009c0014t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0009c0014t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0009c0014t0001g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0010c0015t0031g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0010c0015t0031g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0011c0017t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0011c0017t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0012c0037t0020g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0013c0032t0058g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0014c0033t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0015c0034t0059g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0016c0035t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0017c0029t0033g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0018c0025t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0019c0027t0016g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0020c0028t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0021c0023t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0022c0024t0051g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0023c0026t0044g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0024c0021t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0025c0030t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0026c0031t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0027c0020t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
a0028c0036t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0371 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00099 | hp2 | a0001 | c0003 | t0002 | g0129 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00140 | hp1 | a0001 | c0003 | t0002 | g0174 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0304 | EUR | GBR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0336 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00280 | hp2 | a0002 | c0001 | t0055 | g0245 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00323 | hp1 | a0002 | c0001 | t0010 | g0045 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0351 | EUR | FIN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0301 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00423 | hp2 | a0006 | c0011 | t0013 | g0176 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0372 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00438 | hp2 | a0002 | c0001 | t0003 | g0238 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00544 | hp1 | a0002 | c0001 | t0003 | g0206 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00544 | hp2 | a0001 | c0004 | t0006 | g0077 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00558 | hp1 | a0001 | c0002 | t0054 | g0343 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00558 | hp2 | a0001 | c0003 | t0002 | g0112 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00597 | hp1 | a0001 | c0004 | t0005 | g0084 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00597 | hp2 | a0001 | c0003 | t0002 | g0049 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00609 | hp1 | a0006 | c0011 | t0013 | g0092 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00609 | hp2 | a0001 | c0003 | t0002 | g0147 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00621 | hp1 | a0001 | c0003 | t0002 | g0118 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00621 | hp2 | a0022 | c0024 | t0051 | g0337 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00639 | hp1 | a0003 | c0005 | t0007 | g0285 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00639 | hp2 | a0023 | c0026 | t0044 | g0051 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0346 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00642 | hp2 | a0001 | c0003 | t0002 | g0122 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00673 | hp1 | a0001 | c0004 | t0005 | g0079 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00673 | hp2 | a0002 | c0001 | t0003 | g0215 | EAS | CHS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00733 | hp1 | a0001 | c0003 | t0002 | g0131 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00733 | hp2 | a0024 | c0021 | t0001 | g0300 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00738 | hp1 | a0001 | c0003 | t0002 | g0136 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00738 | hp2 | a0002 | c0001 | t0003 | g0240 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00741 | hp1 | a0028 | c0036 | t0008 | g0019 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0108 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01069 | hp1 | a0009 | c0014 | t0001 | g0378 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01069 | hp2 | a0011 | c0017 | t0002 | g0160 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01070 | hp1 | a0009 | c0014 | t0001 | g0377 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01070 | hp2 | a0002 | c0001 | t0003 | g0257 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01071 | hp1 | a0009 | c0014 | t0001 | g0379 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01071 | hp2 | a0011 | c0017 | t0002 | g0159 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01074 | hp1 | a0002 | c0001 | t0003 | g0231 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0324 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01081 | hp1 | a0001 | c0003 | t0002 | g0134 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01081 | hp2 | a0002 | c0001 | t0061 | g0239 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01099 | hp1 | a0002 | c0001 | t0003 | g0221 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0332 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0121 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01106 | hp2 | a0021 | c0023 | t0001 | g0320 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01109 | hp1 | a0002 | c0001 | t0003 | g0274 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01109 | hp2 | a0002 | c0001 | t0026 | g0275 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01169 | hp1 | a0001 | c0003 | t0065 | g0156 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0321 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01175 | hp1 | a0008 | c0012 | t0007 | g0291 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01175 | hp2 | a0001 | c0003 | t0043 | g0096 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0329 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01192 | hp2 | a0002 | c0001 | t0028 | g0015 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01243 | hp1 | a0015 | c0034 | t0059 | g0201 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0130 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0354 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01256 | hp1 | a0001 | c0016 | t0002 | g0100 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0315 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0323 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01258 | hp2 | a0001 | c0016 | t0002 | g0103 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01261 | hp1 | a0001 | c0003 | t0040 | g0148 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0345 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01358 | hp1 | a0001 | c0002 | t0012 | g0173 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01358 | hp2 | a0001 | c0004 | t0006 | g0059 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01433 | hp1 | a0002 | c0001 | t0003 | g0214 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0364 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01496 | hp1 | a0002 | c0001 | t0003 | g0254 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0104 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01515 | hp2 | a0002 | c0001 | t0003 | g0256 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0375 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01516 | hp2 | a0001 | c0003 | t0002 | g0099 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01517 | hp1 | a0002 | c0001 | t0003 | g0255 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01517 | hp2 | a0001 | c0003 | t0002 | g0101 | EUR | IBS | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01884 | hp1 | a0002 | c0001 | t0062 | g0210 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01884 | hp2 | a0001 | c0003 | t0025 | g0268 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01891 | hp1 | a0001 | c0002 | t0027 | g0194 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01891 | hp2 | a0005 | c0010 | t0017 | g0247 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01934 | hp1 | a0001 | c0003 | t0041 | g0133 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0306 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01943 | hp1 | a0002 | c0001 | t0008 | g0033 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0316 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01975 | hp1 | a0002 | c0001 | t0008 | g0035 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0355 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0178 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01993 | hp1 | a0020 | c0028 | t0002 | g0123 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0358 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02004 | hp1 | a0002 | c0001 | t0008 | g0034 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02004 | hp2 | a0001 | c0003 | t0002 | g0137 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02040 | hp1 | a0006 | c0011 | t0013 | g0093 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02040 | hp2 | a0002 | c0001 | t0004 | g0036 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02056 | hp1 | a0014 | c0033 | t0003 | g0202 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02056 | hp2 | a0001 | c0004 | t0005 | g0078 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02071 | hp1 | a0001 | c0004 | t0006 | g0054 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0359 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02074 | hp1 | a0002 | c0001 | t0071 | g0192 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0319 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02080 | hp2 | a0002 | c0001 | t0003 | g0196 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02083 | hp1 | a0013 | c0032 | t0058 | g0226 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02083 | hp2 | a0002 | c0001 | t0003 | g0224 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02132 | hp1 | a0001 | c0003 | t0002 | g0142 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02132 | hp2 | a0001 | c0004 | t0006 | g0076 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0333 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02135 | hp2 | a0001 | c0003 | t0002 | g0143 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02145 | hp1 | a0003 | c0005 | t0007 | g0278 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02145 | hp2 | a0002 | c0001 | t0004 | g0046 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02148 | hp1 | a0002 | c0001 | t0008 | g0038 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02148 | hp2 | a0001 | c0003 | t0002 | g0109 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02155 | hp1 | a0001 | c0002 | t0035 | g0172 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02155 | hp2 | a0001 | c0004 | t0005 | g0082 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02165 | hp1 | a0001 | c0003 | t0039 | g0113 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02165 | hp2 | a0001 | c0004 | t0005 | g0052 | EAS | CDX | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02257 | hp1 | a0002 | c0001 | t0004 | g0017 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02257 | hp2 | a0003 | c0005 | t0007 | g0288 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02258 | hp1 | a0003 | c0005 | t0016 | g0181 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02258 | hp2 | a0001 | c0003 | t0064 | g0259 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02273 | hp1 | a0002 | c0001 | t0008 | g0009 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02280 | hp1 | a0017 | c0029 | t0033 | g0260 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02280 | hp2 | a0002 | c0001 | t0004 | g0023 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0361 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02293 | hp2 | a0002 | c0001 | t0008 | g0018 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02300 | hp1 | a0002 | c0001 | t0003 | g0227 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0144 | AMR | PEL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02451 | hp1 | a0002 | c0001 | t0004 | g0010 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02451 | hp2 | a0010 | c0015 | t0031 | g0004 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02523 | hp1 | a0001 | c0003 | t0002 | g0120 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | KHV | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02572 | hp1 | a0002 | c0001 | t0022 | g0212 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02572 | hp2 | a0019 | c0027 | t0016 | g0282 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02602 | hp1 | a0002 | c0001 | t0018 | g0031 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02602 | hp2 | a0001 | c0003 | t0030 | g0141 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02615 | hp1 | a0003 | c0005 | t0007 | g0296 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02615 | hp2 | a0002 | c0001 | t0004 | g0011 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02630 | hp1 | a0002 | c0001 | t0004 | g0048 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02630 | hp2 | a0001 | c0022 | t0027 | g0193 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02647 | hp1 | a0001 | c0007 | t0024 | g0271 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02647 | hp2 | a0003 | c0005 | t0007 | g0292 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02683 | hp1 | a0001 | c0002 | t0012 | g0175 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02683 | hp2 | a0002 | c0001 | t0010 | g0044 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02735 | hp1 | a0001 | c0004 | t0006 | g0072 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02735 | hp2 | a0002 | c0001 | t0014 | g0218 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02809 | hp1 | a0001 | c0007 | t0024 | g0263 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02809 | hp2 | a0002 | c0001 | t0004 | g0047 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02818 | hp1 | a0002 | c0001 | t0022 | g0232 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02818 | hp2 | a0005 | c0018 | t0034 | g0248 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02886 | hp1 | a0001 | c0002 | t0027 | g0195 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02886 | hp2 | a0010 | c0015 | t0031 | g0005 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02895 | hp1 | a0002 | c0001 | t0022 | g0235 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02895 | hp2 | a0003 | c0005 | t0016 | g0180 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02896 | hp1 | a0002 | c0001 | t0021 | g0208 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02896 | hp2 | a0001 | c0002 | t0048 | g0186 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02897 | hp1 | a0002 | c0001 | t0021 | g0234 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02897 | hp2 | a0003 | c0005 | t0016 | g0182 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02965 | hp1 | a0003 | c0019 | t0070 | g0287 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02965 | hp2 | a0001 | c0007 | t0023 | g0273 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03041 | hp1 | a0002 | c0001 | t0004 | g0022 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03041 | hp2 | a0001 | c0007 | t0023 | g0264 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03098 | hp1 | a0003 | c0005 | t0007 | g0286 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03098 | hp2 | a0001 | c0007 | t0024 | g0270 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03130 | hp1 | a0003 | c0005 | t0007 | g0284 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03130 | hp2 | a0002 | c0001 | t0021 | g0209 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03139 | hp1 | a0002 | c0001 | t0019 | g0006 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03139 | hp2 | a0001 | c0002 | t0050 | g0185 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03195 | hp1 | a0003 | c0005 | t0007 | g0279 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03195 | hp2 | a0005 | c0010 | t0017 | g0246 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03209 | hp1 | a0002 | c0001 | t0004 | g0026 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03209 | hp2 | a0002 | c0001 | t0026 | g0277 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03225 | hp1 | a0002 | c0001 | t0028 | g0043 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03225 | hp2 | a0003 | c0005 | t0007 | g0293 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03239 | hp1 | a0002 | c0001 | t0063 | g0211 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03239 | hp2 | a0001 | c0003 | t0002 | g0138 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03453 | hp1 | a0002 | c0001 | t0028 | g0042 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03453 | hp2 | a0002 | c0001 | t0037 | g0025 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03486 | hp1 | a0001 | c0003 | t0068 | g0261 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03486 | hp2 | a0003 | c0005 | t0007 | g0280 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03491 | hp1 | a0001 | c0009 | t0015 | g0250 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03491 | hp2 | a0002 | c0001 | t0003 | g0188 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03492 | hp1 | a0002 | c0001 | t0003 | g0189 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03492 | hp2 | a0001 | c0004 | t0005 | g0065 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03516 | hp1 | a0002 | c0001 | t0032 | g0021 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03516 | hp2 | a0002 | c0001 | t0004 | g0020 | AFR | ESN | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03540 | hp1 | a0002 | c0001 | t0004 | g0024 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03540 | hp2 | a0008 | c0012 | t0007 | g0294 | AFR | GWD | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03579 | hp1 | a0002 | c0001 | t0019 | g0007 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03579 | hp2 | a0001 | c0003 | t0067 | g0262 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03654 | hp1 | a0005 | c0010 | t0017 | g0184 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0107 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03669 | hp1 | a0002 | c0001 | t0003 | g0241 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03669 | hp2 | a0001 | c0009 | t0015 | g0252 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03688 | hp1 | a0002 | c0001 | t0003 | g0190 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0305 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03704 | hp1 | a0001 | c0009 | t0015 | g0251 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03704 | hp2 | a0002 | c0001 | t0014 | g0229 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0132 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03710 | hp2 | a0001 | c0009 | t0015 | g0253 | SAS | PJL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03831 | hp1 | a0002 | c0001 | t0003 | g0187 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03831 | hp2 | a0001 | c0003 | t0002 | g0111 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03834 | hp1 | a0002 | c0001 | t0014 | g0230 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0356 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03942 | hp1 | a0001 | c0002 | t0047 | g0303 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03942 | hp2 | a0001 | c0004 | t0006 | g0071 | SAS | BEB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04115 | hp1 | a0001 | c0003 | t0002 | g0102 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04115 | hp2 | a0002 | c0001 | t0018 | g0029 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0139 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04204 | hp2 | a0001 | c0004 | t0005 | g0085 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0322 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG04228 | hp2 | a0002 | c0001 | t0014 | g0199 | SAS | STU | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18522 | hp1 | a0002 | c0001 | t0072 | g0003 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18522 | hp2 | a0001 | c0007 | t0023 | g0272 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18906 | hp1 | a0001 | c0003 | t0025 | g0266 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18906 | hp2 | a0002 | c0001 | t0032 | g0014 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0347 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18940 | hp2 | a0001 | c0003 | t0011 | g0150 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18942 | hp1 | a0002 | c0001 | t0057 | g0220 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18943 | hp1 | a0002 | c0001 | t0060 | g0213 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0311 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18945 | hp1 | a0001 | c0003 | t0002 | g0146 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18945 | hp2 | a0001 | c0004 | t0006 | g0075 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0340 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18946 | hp2 | a0002 | c0013 | t0003 | g0242 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18947 | hp1 | a0002 | c0001 | t0003 | g0233 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18947 | hp2 | a0001 | c0003 | t0002 | g0106 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0369 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18948 | hp2 | a0001 | c0004 | t0005 | g0064 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18950 | hp1 | a0001 | c0004 | t0005 | g0083 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18950 | hp2 | a0027 | c0020 | t0003 | g0236 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18951 | hp2 | a0002 | c0001 | t0003 | g0205 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18952 | hp2 | a0002 | c0001 | t0003 | g0222 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18953 | hp1 | a0001 | c0003 | t0042 | g0125 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18953 | hp2 | a0001 | c0004 | t0005 | g0086 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18957 | hp1 | a0002 | c0001 | t0004 | g0037 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18957 | hp2 | a0001 | c0003 | t0029 | g0115 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18960 | hp1 | a0001 | c0003 | t0011 | g0135 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18960 | hp2 | a0002 | c0001 | t0003 | g0219 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18961 | hp1 | a0002 | c0001 | t0003 | g0217 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18961 | hp2 | a0001 | c0003 | t0029 | g0114 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18962 | hp1 | a0002 | c0001 | t0004 | g0040 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18962 | hp2 | a0004 | c0006 | t0009 | g0161 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18963 | hp1 | a0001 | c0002 | t0053 | g0363 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18963 | hp2 | a0002 | c0001 | t0003 | g0225 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18966 | hp1 | a0001 | c0003 | t0002 | g0127 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18966 | hp2 | a0007 | c0008 | t0001 | g0348 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18968 | hp1 | a0001 | c0003 | t0002 | g0149 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18968 | hp2 | a0002 | c0001 | t0010 | g0066 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18970 | hp1 | a0001 | c0002 | t0049 | g0357 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18970 | hp2 | a0002 | c0001 | t0010 | g0068 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18971 | hp1 | a0001 | c0004 | t0006 | g0055 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18971 | hp2 | a0001 | c0003 | t0002 | g0154 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18972 | hp1 | a0006 | c0011 | t0013 | g0177 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18972 | hp2 | a0001 | c0003 | t0002 | g0119 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18973 | hp1 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18973 | hp2 | a0002 | c0001 | t0003 | g0228 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0365 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18977 | hp2 | a0001 | c0003 | t0002 | g0145 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18978 | hp1 | a0002 | c0001 | t0004 | g0039 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18978 | hp2 | a0001 | c0004 | t0005 | g0063 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0362 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18980 | hp2 | a0016 | c0035 | t0003 | g0258 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18981 | hp1 | a0007 | c0008 | t0001 | g0342 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18981 | hp2 | a0001 | c0004 | t0005 | g0080 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18983 | hp1 | a0004 | c0006 | t0009 | g0165 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18984 | hp1 | a0007 | c0008 | t0001 | g0299 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18984 | hp2 | a0001 | c0003 | t0011 | g0116 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18986 | hp1 | a0002 | c0001 | t0003 | g0179 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18986 | hp2 | a0001 | c0003 | t0002 | g0158 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18987 | hp1 | a0001 | c0004 | t0005 | g0081 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18987 | hp2 | a0001 | c0002 | t0052 | g0328 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18989 | hp1 | a0001 | c0004 | t0006 | g0057 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0368 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18990 | hp1 | a0004 | c0006 | t0009 | g0164 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18990 | hp2 | a0001 | c0002 | t0020 | g0325 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18991 | hp1 | a0001 | c0004 | t0005 | g0062 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18991 | hp2 | a0001 | c0002 | t0012 | g0095 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18992 | hp2 | a0001 | c0004 | t0006 | g0067 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0151 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18993 | hp2 | a0002 | c0001 | t0003 | g0237 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18994 | hp1 | a0002 | c0001 | t0003 | g0244 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18994 | hp2 | a0001 | c0003 | t0002 | g0168 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18998 | hp1 | a0001 | c0003 | t0002 | g0105 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18998 | hp2 | a0001 | c0004 | t0006 | g0074 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19000 | hp2 | a0001 | c0003 | t0066 | g0310 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19001 | hp2 | a0001 | c0004 | t0006 | g0056 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0370 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19003 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19005 | hp1 | a0002 | c0013 | t0003 | g0198 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19005 | hp2 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0366 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19007 | hp2 | a0001 | c0004 | t0006 | g0058 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19009 | hp1 | a0001 | c0004 | t0005 | g0094 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0171 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19010 | hp1 | a0001 | c0003 | t0011 | g0152 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19010 | hp2 | a0002 | c0001 | t0004 | g0041 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19011 | hp1 | a0001 | c0004 | t0005 | g0090 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19011 | hp2 | a0002 | c0001 | t0003 | g0203 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19030 | hp1 | a0008 | c0012 | t0007 | g0290 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19030 | hp2 | a0002 | c0001 | t0004 | g0012 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19043 | hp1 | a0001 | c0003 | t0025 | g0267 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19043 | hp2 | a0002 | c0001 | t0019 | g0008 | AFR | LWK | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19056 | hp1 | a0002 | c0001 | t0003 | g0207 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19057 | hp1 | a0001 | c0003 | t0002 | g0126 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19060 | hp1 | a0002 | c0001 | t0003 | g0223 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19060 | hp2 | a0018 | c0025 | t0001 | g0360 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0313 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19062 | hp2 | a0001 | c0003 | t0002 | g0157 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19063 | hp1 | a0001 | c0003 | t0011 | g0155 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19063 | hp2 | a0002 | c0001 | t0003 | g0216 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19064 | hp1 | a0004 | c0006 | t0009 | g0170 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0349 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0344 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19065 | hp2 | a0001 | c0003 | t0002 | g0128 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19066 | hp1 | a0007 | c0008 | t0001 | g0339 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19066 | hp2 | a0026 | c0031 | t0002 | g0167 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19068 | hp1 | a0001 | c0004 | t0045 | g0061 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0374 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19070 | hp1 | a0004 | c0006 | t0009 | g0163 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0334 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0124 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19074 | hp2 | a0001 | c0002 | t0012 | g0091 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19076 | hp2 | a0001 | c0004 | t0006 | g0060 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19077 | hp1 | a0001 | c0003 | t0002 | g0117 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19078 | hp2 | a0001 | c0003 | t0002 | g0153 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19079 | hp1 | a0001 | c0003 | t0002 | g0110 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19079 | hp2 | a0001 | c0004 | t0005 | g0087 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19081 | hp1 | a0002 | c0013 | t0003 | g0197 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19081 | hp2 | a0025 | c0030 | t0006 | g0073 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19084 | hp1 | a0012 | c0037 | t0020 | g0335 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19084 | hp2 | a0002 | c0001 | t0003 | g0243 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19085 | hp1 | a0002 | c0001 | t0003 | g0204 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19085 | hp2 | a0004 | c0006 | t0009 | g0169 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19086 | hp1 | a0002 | c0001 | t0003 | g0200 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19086 | hp2 | a0001 | c0004 | t0046 | g0088 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0353 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19088 | hp2 | a0002 | c0001 | t0010 | g0069 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19090 | hp2 | a0004 | c0006 | t0009 | g0162 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19091 | hp1 | a0001 | c0004 | t0006 | g0070 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19091 | hp2 | a0001 | c0002 | t0020 | g0350 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19240 | hp1 | a0002 | c0001 | t0004 | g0028 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA19240 | hp2 | a0003 | c0005 | t0007 | g0295 | AFR | YRI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20129 | hp1 | a0008 | c0012 | t0007 | g0289 | AFR | ASW | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20129 | hp2 | a0001 | c0038 | t0033 | g0265 | AFR | ASW | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20752 | hp1 | a0002 | c0001 | t0018 | g0030 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0097 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20805 | hp1 | a0002 | c0001 | t0056 | g0373 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20805 | hp2 | a0005 | c0010 | t0017 | g0183 | EUR | TSI | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20905 | hp1 | a0002 | c0001 | t0008 | g0032 | SAS | GIH | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0367 | SAS | GIH | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0318 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG01123 | hp2 | a0001 | c0003 | t0030 | g0140 | AMR | CLM | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02559 | hp1 | a0001 | c0004 | t0038 | g0053 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG02559 | hp2 | a0002 | c0001 | t0026 | g0276 | AFR | ACB | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03471 | hp1 | a0002 | c0001 | t0004 | g0013 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG03471 | hp2 | a0002 | c0001 | t0004 | g0016 | AFR | MSL | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG06807 | hp1 | a0001 | c0003 | t0069 | g0269 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
HG06807 | hp2 | a0003 | c0005 | t0007 | g0281 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18955 | hp1 | a0001 | c0004 | t0005 | g0089 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA18955 | hp2 | a0002 | c0001 | t0003 | g0191 | EAS | JPT | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20300 | hp1 | a0002 | c0001 | t0036 | g0027 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
NA20300 | hp2 | a0005 | c0018 | t0034 | g0249 | AFR | USA | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0002 | g0098 | REF | REF | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0003 | g0283 | REF | REF | RIF1_chr2_151404902_151487172 | RIF1 | chr2 | 151404902 | 151487172 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151420263
|
G | A | 1 | a0010 | 2 | HG02451.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.577G>A | p.Val193Ile | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/36 | 719/14662 | 577/7419 | 193/2472 | chr2 | 151420263 | ||
chr2:151435557
|
A | G | 1 | a0008 | 4 | HG01175.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
missense_variant | MODERATE | c.1172A>G | p.Asn391Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/36 | 1314/14662 | 1172/7419 | 391/2472 | chr2 | 151435557 | ||
chr2:151436856
|
A | G | 1 | a0012 | 1 | NA19084.hp1 | missense_variant | MODERATE | c.1225A>G | p.Thr409Ala | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/36 | 1367/14662 | 1225/7419 | 409/2472 | chr2 | 151436856 | ||
chr2:151441977
|
A | G | 1 | a0028 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1720A>G | p.Met574Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/36 | 1862/14662 | 1720/7419 | 574/2472 | chr2 | 151441977 | ||
chr2:151443629
|
G | A | 1 | a0027 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.1906G>A | p.Ala636Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/36 | 2048/14662 | 1906/7419 | 636/2472 | chr2 | 151443629 | ||
chr2:151455056
|
G | A | 21 | a0001a0003a0004others(18): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
missense_variant | MODERATE | c.2506G>A | p.Gly836Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/36 | 2648/14662 | 2506/7419 | 836/2472 | chr2 | 151455056 | ||
chr2:151455098
|
A | G | 1 | a0005 | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
missense_variant | MODERATE | c.2548A>G | p.Met850Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/36 | 2690/14662 | 2548/7419 | 850/2472 | chr2 | 151455098 | ||
chr2:151455110
|
A | T | 1 | a0026 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.2560A>T | p.Ile854Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/36 | 2702/14662 | 2560/7419 | 854/2472 | chr2 | 151455110 | ||
chr2:151458885
|
A | T | 1 | a0025 | 1 | NA19081.hp2 | missense_variant | MODERATE | c.2930A>T | p.Glu977Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/36 | 3072/14662 | 2930/7419 | 977/2472 | chr2 | 151458885 | ||
chr2:151462304
|
A | G | 1 | a0017 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.3290A>G | p.Tyr1097Cys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 28/36 | 3432/14662 | 3290/7419 | 1097/2472 | chr2 | 151462304 | ||
chr2:151462944
|
G | A | 1 | a0007 | 4 | NA18966.hp2 NA18981.hp1 NA18984.hp1 others(1): Show |
missense_variant | MODERATE | c.3424G>A | p.Ala1142Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 3566/14662 | 3424/7419 | 1142/2472 | chr2 | 151462944 | ||
chr2:151463429
|
G | C | 1 | a0024 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.3909G>C | p.Lys1303Asn | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4051/14662 | 3909/7419 | 1303/2472 | chr2 | 151463429 | ||
chr2:151463604
|
G | A | 22 | a0001a0003a0004others(19): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
missense_variant | MODERATE | c.4084G>A | p.Val1362Met | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4226/14662 | 4084/7419 | 1362/2472 | chr2 | 151463604 | ||
chr2:151463803
|
C | T | 1 | a0018 | 1 | NA19060.hp2 | missense_variant | MODERATE | c.4283C>T | p.Thr1428Ile | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4425/14662 | 4283/7419 | 1428/2472 | chr2 | 151463803 | ||
chr2:151464039
|
G | A | 1 | a0023 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.4519G>A | p.Asp1507Asn | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4661/14662 | 4519/7419 | 1507/2472 | chr2 | 151464039 | ||
chr2:151464056
|
G | T | 1 | a0022 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.4536G>T | p.Lys1512Asn | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4678/14662 | 4536/7419 | 1512/2472 | chr2 | 151464056 | ||
chr2:151464250
|
A | G | 1 | a0011 | 2 | HG01069.hp2 HG01071.hp2 |
missense_variant | MODERATE | c.4730A>G | p.Asn1577Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4872/14662 | 4730/7419 | 1577/2472 | chr2 | 151464250 | ||
chr2:151464378
|
G | A | 1 | a0004 | 7 | NA18962.hp2 NA18983.hp1 NA18990.hp1 others(4): Show |
missense_variant | MODERATE | c.4858G>A | p.Glu1620Lys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5000/14662 | 4858/7419 | 1620/2472 | chr2 | 151464378 | ||
chr2:151464576
|
C | G | 1 | a0006 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
missense_variant | MODERATE | c.5056C>G | p.Arg1686Gly | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5198/14662 | 5056/7419 | 1686/2472 | chr2 | 151464576 | ||
chr2:151464811
|
A | C | 1 | a0016 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.5291A>C | p.Lys1764Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5433/14662 | 5291/7419 | 1764/2472 | chr2 | 151464811 | ||
chr2:151465002
|
C | T | 1 | a0021 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.5482C>T | p.Pro1828Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5624/14662 | 5482/7419 | 1828/2472 | chr2 | 151465002 | ||
chr2:151465104
|
G | A | 3 | a0003a0008a0019 | 21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
missense_variant | MODERATE | c.5584G>A | p.Val1862Ile | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5726/14662 | 5584/7419 | 1862/2472 | chr2 | 151465104 | ||
chr2:151465150
|
T | C | 1 | a0019 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.5630T>C | p.Leu1877Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5772/14662 | 5630/7419 | 1877/2472 | chr2 | 151465150 | ||
chr2:151465581
|
A | T | 23 | a0001a0003a0004others(20): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
missense_variant | MODERATE | c.6061A>T | p.Asn2021Tyr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 6203/14662 | 6061/7419 | 2021/2472 | chr2 | 151465581 | ||
chr2:151465599
|
G | A | 1 | a0020 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.6079G>A | p.Gly2027Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 6221/14662 | 6079/7419 | 2027/2472 | chr2 | 151465599 | ||
chr2:151473973
|
C | T | 1 | a0009 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
missense_variant | MODERATE | c.7105C>T | p.Arg2369Cys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/36 | 7247/14662 | 7105/7419 | 2369/2472 | chr2 | 151473973 | ||
chr2:151474048
|
C | T | 1 | a0014 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.7180C>T | p.Pro2394Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/36 | 7322/14662 | 7180/7419 | 2394/2472 | chr2 | 151474048 | ||
chr2:151474904
|
C | G | 22 | a0001a0003a0004others(19): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
missense_variant | MODERATE | c.7252C>G | p.Leu2418Val | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 7394/14662 | 7252/7419 | 2418/2472 | chr2 | 151474904 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151420361
|
G | A | 1 | a0003c0019 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.675G>A | p.Thr225Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/36 | 817/14662 | 675/7419 | 225/2472 | chr2 | 151420361 | ||
chr2:151435483
|
A | G | 1 | a0001c0038 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1098A>G | p.Gln366Gln | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/36 | 1240/14662 | 1098/7419 | 366/2472 | chr2 | 151435483 | ||
chr2:151436855
|
A | C | 1 | a0009c0014 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.1224A>C | p.Gly408Gly | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/36 | 1366/14662 | 1224/7419 | 408/2472 | chr2 | 151436855 | ||
chr2:151440127
|
G | T | 1 | a0006c0011 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1647G>T | p.Leu549Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/36 | 1789/14662 | 1647/7419 | 549/2472 | chr2 | 151440127 | ||
chr2:151443309
|
A | G | 1 | a0010c0015 | 2 | HG02451.hp2 HG02886.hp2 |
synonymous_variant | LOW | c.1785A>G | p.Glu595Glu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 17/36 | 1927/14662 | 1785/7419 | 595/2472 | chr2 | 151443309 | ||
chr2:151446428
|
C | T | 1 | a0006c0011 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.2097C>T | p.Ala699Ala | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/36 | 2239/14662 | 2097/7419 | 699/2472 | chr2 | 151446428 | ||
chr2:151457871
|
G | A | 12 | a0001c0002a0001c0009a0001c0022others(9): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
synonymous_variant | LOW | c.2763G>A | p.Leu921Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/36 | 2905/14662 | 2763/7419 | 921/2472 | chr2 | 151457871 | ||
chr2:151461155
|
G | A | 2 | a0001c0004a0025c0030 | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
synonymous_variant | LOW | c.3093G>A | p.Ser1031Ser | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/36 | 3235/14662 | 3093/7419 | 1031/2472 | chr2 | 151461155 | ||
chr2:151463450
|
G | A | 1 | a0017c0029 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.3930G>A | p.Pro1310Pro | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4072/14662 | 3930/7419 | 1310/2472 | chr2 | 151463450 | ||
chr2:151463987
|
T | C | 1 | a0001c0007 | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.4467T>C | p.Thr1489Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4609/14662 | 4467/7419 | 1489/2472 | chr2 | 151463987 | ||
chr2:151464017
|
T | G | 1 | a0005c0018 | 2 | HG02818.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.4497T>G | p.Thr1499Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 4639/14662 | 4497/7419 | 1499/2472 | chr2 | 151464017 | ||
chr2:151464596
|
T | C | 1 | a0001c0009 | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
synonymous_variant | LOW | c.5076T>C | p.Cys1692Cys | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5218/14662 | 5076/7419 | 1692/2472 | chr2 | 151464596 | ||
chr2:151464758
|
C | T | 1 | a0006c0011 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
synonymous_variant | LOW | c.5238C>T | p.Leu1746Leu | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 5380/14662 | 5238/7419 | 1746/2472 | chr2 | 151464758 | ||
chr2:151465601
|
C | T | 1 | a0002c0013 | 3 | NA18946.hp2 NA19005.hp1 NA19081.hp1 |
synonymous_variant | LOW | c.6081C>T | p.Gly2027Gly | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/36 | 6223/14662 | 6081/7419 | 2027/2472 | chr2 | 151465601 | ||
chr2:151469756
|
T | C | 1 | a0001c0016 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.6987T>C | p.Thr2329Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/36 | 7129/14662 | 6987/7419 | 2329/2472 | chr2 | 151469756 | ||
chr2:151469798
|
T | C | 1 | a0001c0022 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.7029T>C | p.Thr2343Thr | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/36 | 7171/14662 | 7029/7419 | 2343/2472 | chr2 | 151469798 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151409951
|
G | T | 2 | a0002c0001t0028a0002c0001t0072 | 4 | HG01192.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-93G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/36 | 473 | chr2 | 151409951 | |||||
chr2:151409959
|
T | C | 36 | a0001c0002t0012a0001c0002t0035a0001c0003t0002others(33): Show | 175 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(172): Show |
5_prime_UTR_variant | MODIFIER | c.-85T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/36 | 465 | chr2 | 151409959 | |||||
chr2:151409963
|
A | G | 1 | a0002c0001t0072 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/36 | 461 | chr2 | 151409963 | |||||
chr2:151475231
|
T | G | 18 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(15): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*160T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 160 | chr2 | 151475231 | |||||
chr2:151475255
|
C | CTT | 5 | a0001c0004t0005a0001c0004t0006a0001c0004t0045others(2): Show | 36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*193_*194dupTT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 195 | INFO_REALIGN_3_PRIME | chr2 | 151475255 | ||||
chr2:151475313
|
A | G | 1 | a0002c0001t0071 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 242 | chr2 | 151475313 | |||||
chr2:151475481
|
TGTTG | T | 6 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(3): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*414_*417delGGTT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 414 | INFO_REALIGN_3_PRIME | chr2 | 151475481 | ||||
chr2:151475485
|
G | T | 59 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(56): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 414 | chr2 | 151475485 | |||||
chr2:151475652
|
T | C | 1 | a0001c0002t0047 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*581T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 581 | chr2 | 151475652 | |||||
chr2:151475726
|
CTTA | C | 1 | a0001c0009t0015 | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*657_*659delTAT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 657 | INFO_REALIGN_3_PRIME | chr2 | 151475726 | ||||
chr2:151475811
|
C | A | 1 | a0002c0001t0055 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*740C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 740 | chr2 | 151475811 | |||||
chr2:151475910
|
C | T | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*839C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 839 | chr2 | 151475910 | |||||
chr2:151475913
|
C | T | 1 | a0003c0019t0070 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 842 | chr2 | 151475913 | |||||
chr2:151476308
|
G | A | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1237 | chr2 | 151476308 | |||||
chr2:151476376
|
A | G | 1 | a0023c0026t0044 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1305A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1305 | chr2 | 151476376 | |||||
chr2:151476419
|
A | T | 1 | a0001c0002t0054 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1348 | chr2 | 151476419 | |||||
chr2:151476433
|
T | C | 1 | a0001c0003t0039 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1362T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1362 | chr2 | 151476433 | |||||
chr2:151476583
|
C | A | 2 | a0001c0007t0023a0001c0007t0024 | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1512C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1512 | chr2 | 151476583 | |||||
chr2:151476604
|
C | G | 23 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(20): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1533C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1533 | chr2 | 151476604 | |||||
chr2:151476668
|
T | G | 1 | a0001c0003t0029 | 2 | NA18957.hp2 NA18961.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1597T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1597 | chr2 | 151476668 | |||||
chr2:151476790
|
C | A | 31 | a0001c0003t0002a0001c0003t0011a0001c0003t0025others(28): Show | 119 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1719C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1719 | chr2 | 151476790 | |||||
chr2:151476845
|
A | G | 1 | a0001c0002t0035 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1774A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1774 | chr2 | 151476845 | |||||
chr2:151476930
|
G | A | 1 | a0001c0003t0064 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1859G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1859 | chr2 | 151476930 | |||||
chr2:151476954
|
T | TG | 2 | a0002c0001t0010a0002c0001t0056 | 6 | HG00323.hp1 HG02683.hp2 NA18968.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1883_*1884insG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 1884 | chr2 | 151476954 | |||||
chr2:151477074
|
T | G | 1 | a0001c0004t0045 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2003T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2003 | chr2 | 151477074 | |||||
chr2:151477098
|
T | G | 1 | a0023c0026t0044 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2027T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2027 | chr2 | 151477098 | |||||
chr2:151477258
|
A | G | 2 | a0002c0001t0014a0002c0001t0063 | 5 | HG02735.hp2 HG03239.hp1 HG03704.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2187A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2187 | chr2 | 151477258 | |||||
chr2:151477259
|
C | T | 31 | a0001c0003t0002a0001c0003t0011a0001c0003t0025others(28): Show | 119 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*2188C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2188 | chr2 | 151477259 | |||||
chr2:151477298
|
G | A | 62 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(59): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*2227G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2227 | chr2 | 151477298 | |||||
chr2:151477335
|
A | C | 1 | a0001c0002t0053 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2264A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2264 | chr2 | 151477335 | |||||
chr2:151477404
|
A | G | 1 | a0001c0003t0069 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2333A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2333 | chr2 | 151477404 | |||||
chr2:151477411
|
T | C | 1 | a0005c0018t0034 | 2 | HG02818.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2340T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2340 | chr2 | 151477411 | |||||
chr2:151477471
|
A | C | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2400A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2400 | chr2 | 151477471 | |||||
chr2:151477513
|
T | C | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2442T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2442 | chr2 | 151477513 | |||||
chr2:151477563
|
C | T | 1 | a0023c0026t0044 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2492C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2492 | chr2 | 151477563 | |||||
chr2:151477773
|
G | A | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2702G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2702 | chr2 | 151477773 | |||||
chr2:151477798
|
C | A | 1 | a0002c0001t0071 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2727C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2727 | chr2 | 151477798 | |||||
chr2:151477805
|
G | A | 1 | a0002c0001t0063 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2734G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2734 | chr2 | 151477805 | |||||
chr2:151477819
|
C | T | 1 | a0010c0015t0031 | 2 | HG02451.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2748C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2748 | chr2 | 151477819 | |||||
chr2:151477979
|
C | A | 8 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(5): Show | 42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2908C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2908 | chr2 | 151477979 | |||||
chr2:151478024
|
T | G | 1 | a0002c0001t0036 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2953T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2953 | chr2 | 151478024 | |||||
chr2:151478066
|
A | G | 26 | a0001c0003t0002a0001c0003t0011a0001c0003t0029others(23): Show | 123 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2995A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 2995 | chr2 | 151478066 | |||||
chr2:151478190
|
C | T | 1 | a0001c0003t0030 | 2 | HG01123.hp2 HG02602.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3119C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3119 | chr2 | 151478190 | |||||
chr2:151478355
|
G | A | 6 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(3): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3284G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3284 | chr2 | 151478355 | |||||
chr2:151478450
|
C | T | 1 | a0001c0003t0043 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3379C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3379 | chr2 | 151478450 | |||||
chr2:151478452
|
C | T | 1 | a0001c0003t0068 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3381C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3381 | chr2 | 151478452 | |||||
chr2:151478462
|
AG | A | 4 | a0002c0001t0021a0002c0001t0022a0002c0001t0061others(1): Show | 8 | HG01081.hp2 HG01884.hp1 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3392delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3392 | chr2 | 151478462 | |||||
chr2:151478474
|
G | A | 23 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(20): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3403G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3403 | chr2 | 151478474 | |||||
chr2:151478475
|
CA | C | 3 | a0001c0002t0052a0002c0001t0060a0006c0011t0013 | 6 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3419delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3419 | INFO_REALIGN_3_PRIME | chr2 | 151478475 | ||||
chr2:151478516
|
T | C | 1 | a0002c0001t0021 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3445T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3445 | chr2 | 151478516 | |||||
chr2:151478533
|
A | C | 1 | a0001c0004t0038 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3462A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3462 | chr2 | 151478533 | |||||
chr2:151478547
|
ATAGT | A | 2 | a0001c0003t0011a0001c0003t0029 | 7 | NA18940.hp2 NA18957.hp2 NA18960.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3479_*3482delGTTA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3479 | INFO_REALIGN_3_PRIME | chr2 | 151478547 | ||||
chr2:151478620
|
T | G | 1 | a0001c0002t0048 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3549T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3549 | chr2 | 151478620 | |||||
chr2:151478648
|
A | G | 6 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(3): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3577A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3577 | chr2 | 151478648 | |||||
chr2:151478676
|
T | TA | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3608dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3609 | INFO_REALIGN_3_PRIME | chr2 | 151478676 | ||||
chr2:151478835
|
G | A | 1 | a0001c0003t0040 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3764G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3764 | chr2 | 151478835 | |||||
chr2:151478866
|
T | C | 23 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(20): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*3795T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3795 | chr2 | 151478866 | |||||
chr2:151478920
|
TG | T | 62 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(59): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*3851delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 3851 | INFO_REALIGN_3_PRIME | chr2 | 151478920 | ||||
chr2:151479196
|
A | G | 2 | a0001c0007t0023a0001c0007t0024 | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4125A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4125 | chr2 | 151479196 | |||||
chr2:151479306
|
G | A | 1 | a0002c0001t0057 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4235G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4235 | chr2 | 151479306 | |||||
chr2:151479512
|
A | G | 2 | a0005c0010t0017a0005c0018t0034 | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4441A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4441 | chr2 | 151479512 | |||||
chr2:151479523
|
C | T | 7 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(4): Show | 38 | HG00544.hp2 HG00597.hp1 HG00621.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4452C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4452 | chr2 | 151479523 | |||||
chr2:151479575
|
A | G | 1 | a0001c0002t0050 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4504A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4504 | chr2 | 151479575 | |||||
chr2:151479599
|
T | C | 1 | a0023c0026t0044 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4528T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4528 | chr2 | 151479599 | |||||
chr2:151479665
|
G | A | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4594G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4594 | chr2 | 151479665 | |||||
chr2:151479734
|
G | A | 1 | a0002c0001t0061 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4663G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4663 | chr2 | 151479734 | |||||
chr2:151479914
|
A | G | 64 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(61): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
3_prime_UTR_variant | MODIFIER | c.*4843A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4843 | chr2 | 151479914 | |||||
chr2:151479974
|
A | G | 6 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(3): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*4903A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4903 | chr2 | 151479974 | |||||
chr2:151479989
|
T | C | 1 | a0001c0003t0041 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4918T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4918 | chr2 | 151479989 | |||||
chr2:151480003
|
A | G | 2 | a0001c0003t0025a0001c0003t0069 | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4932A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 4932 | chr2 | 151480003 | |||||
chr2:151480214
|
T | G | 1 | a0002c0001t0019 | 3 | HG03139.hp1 HG03579.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5143T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5143 | chr2 | 151480214 | |||||
chr2:151480284
|
C | A | 2 | a0001c0002t0020a0012c0037t0020 | 3 | NA18990.hp2 NA19084.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5213C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5213 | chr2 | 151480284 | |||||
chr2:151480336
|
A | C | 2 | a0001c0003t0067a0001c0003t0068 | 2 | HG03486.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5265A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5265 | chr2 | 151480336 | |||||
chr2:151480415
|
T | G | 1 | a0004c0006t0009 | 7 | NA18962.hp2 NA18983.hp1 NA18990.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5344T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5344 | chr2 | 151480415 | |||||
chr2:151480491
|
A | G | 1 | a0001c0007t0024 | 3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5420A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5420 | chr2 | 151480491 | |||||
chr2:151480515
|
C | T | 1 | a0002c0001t0062 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5444C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5444 | chr2 | 151480515 | |||||
chr2:151480764
|
ATTTTT | A | 2 | a0002c0001t0008a0028c0036t0008 | 8 | HG00741.hp1 HG01943.hp1 HG01975.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5695_*5699delTTTT others(1): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5695 | INFO_REALIGN_3_PRIME | chr2 | 151480764 | ||||
chr2:151480766
|
T | G | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5695T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5695 | chr2 | 151480766 | |||||
chr2:151480797
|
A | C | 1 | a0002c0001t0018 | 3 | HG02602.hp1 HG04115.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5726A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5726 | chr2 | 151480797 | |||||
chr2:151480861
|
C | G | 1 | a0001c0004t0046 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5790C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5790 | chr2 | 151480861 | |||||
chr2:151480885
|
T | G | 1 | a0001c0003t0065 | 1 | HG01169.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5814T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5814 | chr2 | 151480885 | |||||
chr2:151480950
|
T | C | 3 | a0001c0004t0005a0001c0004t0045a0001c0004t0046 | 20 | HG00597.hp1 HG00673.hp1 HG02056.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*5879T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5879 | chr2 | 151480950 | |||||
chr2:151480969
|
A | AAGG | 6 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(3): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5900_*5901insGAG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5901 | INFO_REALIGN_3_PRIME | chr2 | 151480969 | ||||
chr2:151480972
|
A | AAGG | 55 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(52): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*5903_*5905dupGGA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5906 | INFO_REALIGN_3_PRIME | chr2 | 151480972 | ||||
chr2:151480972
|
A | G | 8 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(5): Show | 43 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*5901A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5901 | chr2 | 151480972 | |||||
chr2:151481041
|
G | A | 2 | a0001c0002t0027a0001c0022t0027 | 3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5970G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 5970 | chr2 | 151481041 | |||||
chr2:151481122
|
C | T | 2 | a0003c0005t0016a0019c0027t0016 | 4 | HG02258.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6051C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6051 | chr2 | 151481122 | |||||
chr2:151481272
|
G | A | 5 | a0003c0005t0007a0003c0005t0016a0003c0019t0070others(2): Show | 21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6201G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6201 | chr2 | 151481272 | |||||
chr2:151481274
|
G | A | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6203G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6203 | chr2 | 151481274 | |||||
chr2:151481282
|
G | A | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6211G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6211 | chr2 | 151481282 | |||||
chr2:151481308
|
G | A | 17 | a0001c0003t0002a0001c0003t0011a0001c0003t0029others(14): Show | 82 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*6237G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6237 | chr2 | 151481308 | |||||
chr2:151481556
|
G | A | 1 | a0001c0002t0049 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6485G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6485 | chr2 | 151481556 | |||||
chr2:151481723
|
A | G | 1 | a0002c0001t0037 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6652A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6652 | chr2 | 151481723 | |||||
chr2:151481889
|
C | G | 1 | a0006c0011t0013 | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6818C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6818 | chr2 | 151481889 | |||||
chr2:151481893
|
A | G | 1 | a0023c0026t0044 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6822A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6822 | chr2 | 151481893 | |||||
chr2:151481903
|
C | T | 6 | a0001c0004t0005a0001c0004t0006a0001c0004t0038others(3): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*6832C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6832 | chr2 | 151481903 | |||||
chr2:151481926
|
C | A | 1 | a0001c0003t0042 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6855C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6855 | chr2 | 151481926 | |||||
chr2:151482024
|
AG | A | 62 | a0001c0002t0001a0001c0002t0012a0001c0002t0020others(59): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*6960delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 36/36 | 6960 | INFO_REALIGN_3_PRIME | chr2 | 151482024 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:151410217
|
T | A | 176 | a0001c0002t0012g0091a0001c0002t0012g0095a0001c0002t0012g0173others(173): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-11+184T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/35 | chr2 | 151410217 | ||||||
chr2:151410226
|
G | A | 1 | a0001c0002t0001g0178 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-10-188G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/35 | chr2 | 151410226 | ||||||
chr2:151410228
|
G | T | 2 | a0006c0011t0013g0176a0006c0011t0013g0177 | 2 | HG00423.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.-10-186G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 1/35 | chr2 | 151410228 | ||||||
chr2:151410547
|
G | A | 47 | a0001c0003t0002g0002a0002c0001t0004g0010a0002c0001t0004g0011others(44): Show | 47 | HG00323.hp1 HG00741.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.104+20G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410547 | ||||||
chr2:151410558
|
T | G | 175 | a0001c0002t0012g0091a0001c0002t0012g0095a0001c0002t0012g0173others(172): Show | 175 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.104+31T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410558 | ||||||
chr2:151410764
|
T | C | 3 | a0003c0005t0016g0180a0003c0005t0016g0181a0003c0005t0016g0182 | 3 | HG02258.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.104+237T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410764 | ||||||
chr2:151410824
|
A | G | 1 | a0002c0001t0004g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104+297A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410824 | ||||||
chr2:151410845
|
G | T | 88 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(85): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.104+318G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410845 | ||||||
chr2:151410865
|
A | AGTT | 260 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(257): Show | 261 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.104+339_104+341dup others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr2 | 151410865 | |||||
chr2:151410969
|
T | G | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.105-291T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410969 | ||||||
chr2:151410998
|
G | T | 1 | a0002c0001t0004g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.105-262G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151410998 | ||||||
chr2:151411065
|
C | T | 3 | a0009c0014t0001g0377a0009c0014t0001g0378a0009c0014t0001g0379 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.105-195C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411065 | ||||||
chr2:151411142
|
G | T | 1 | a0001c0004t0005g0094 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.105-118G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411142 | ||||||
chr2:151411158
|
G | A | 357 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(354): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.105-102G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411158 | ||||||
chr2:151411202
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-58A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411202 | ||||||
chr2:151411207
|
AT | A | 81 | a0001c0002t0012g0095a0001c0003t0002g0002a0001c0003t0002g0049others(78): Show | 81 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.105-42delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr2 | 151411207 | |||||
chr2:151411226
|
A | G | 1 | a0001c0002t0001g0376 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.105-34A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 2/35 | chr2 | 151411226 | ||||||
chr2:151411361
|
G | GTTTTTCA others(17): Show |
1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.183+29_183+52dupCA others(22): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151411361 | |||||
chr2:151411383
|
G | GT | 83 | a0001c0002t0001g0375a0001c0003t0002g0002a0001c0003t0002g0049others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.183+56dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151411383 | |||||
chr2:151411460
|
A | G | 1 | a0001c0002t0001g0374 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.183+122A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411460 | ||||||
chr2:151411472
|
G | A | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.183+134G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411472 | ||||||
chr2:151411632
|
C | G | 4 | a0002c0001t0003g0254a0002c0001t0003g0255a0002c0001t0003g0256others(1): Show | 4 | HG01070.hp2 HG01496.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+294C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411632 | ||||||
chr2:151411814
|
C | G | 10 | a0001c0003t0002g0166a0001c0003t0002g0168a0004c0006t0009g0161others(7): Show | 10 | NA18962.hp2 NA18973.hp1 NA18983.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+476C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411814 | ||||||
chr2:151411827
|
C | A | 2 | a0005c0010t0017g0183a0005c0010t0017g0184 | 2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.183+489C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411827 | ||||||
chr2:151411938
|
G | C | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.183+600G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411938 | ||||||
chr2:151411981
|
C | G | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+643C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411981 | ||||||
chr2:151411996
|
T | G | 1 | a0001c0002t0001g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.183+658T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151411996 | ||||||
chr2:151412043
|
T | C | 40 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(37): Show | 40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.183+705T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412043 | ||||||
chr2:151412050
|
A | G | 45 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(42): Show | 45 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.183+712A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412050 | ||||||
chr2:151412063
|
T | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+725T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412063 | ||||||
chr2:151412200
|
C | A | 2 | a0001c0003t0067g0262a0001c0003t0068g0261 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.183+862C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412200 | ||||||
chr2:151412224
|
T | C | 1 | a0001c0002t0001g0298 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.183+886T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412224 | ||||||
chr2:151412260
|
G | GTTTC | 357 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(354): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.183+925_183+926ins others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151412260 | |||||
chr2:151412291
|
C | T | 261 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(258): Show | 262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.183+953C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412291 | ||||||
chr2:151412309
|
GT | G | 91 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(88): Show | 92 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.183+974delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151412309 | |||||
chr2:151412321
|
TATG | T | 80 | a0001c0003t0002g0049a0001c0003t0002g0050a0001c0003t0002g0097others(77): Show | 80 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.183+985_183+987del others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151412321 | |||||
chr2:151412339
|
C | T | 1 | a0006c0011t0013g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.183+1001C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412339 | ||||||
chr2:151412343
|
T | C | 40 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(37): Show | 40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.183+1005T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412343 | ||||||
chr2:151412389
|
T | C | 4 | a0002c0001t0003g0187a0002c0001t0003g0188a0002c0001t0003g0189others(1): Show | 4 | HG03491.hp2 HG03492.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1051T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412389 | ||||||
chr2:151412498
|
G | A | 10 | a0001c0003t0002g0166a0001c0003t0002g0168a0004c0006t0009g0161others(7): Show | 10 | NA18962.hp2 NA18973.hp1 NA18983.hp1 others(7): Show |
intron_variant | MODIFIER | c.183+1160G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412498 | ||||||
chr2:151412599
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1261C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412599 | ||||||
chr2:151412729
|
C | T | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.183+1391C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412729 | ||||||
chr2:151412744
|
G | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+1406G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412744 | ||||||
chr2:151412823
|
T | G | 1 | a0001c0003t0002g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.183+1485T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151412823 | ||||||
chr2:151413041
|
A | G | 2 | a0002c0001t0026g0276a0002c0001t0026g0277 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.183+1703A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413041 | ||||||
chr2:151413049
|
CT | C | 44 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(41): Show | 44 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.183+1724delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151413049 | |||||
chr2:151413184
|
G | A | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1639G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413184 | ||||||
chr2:151413276
|
G | A | 1 | a0002c0001t0071g0192 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.184-1547G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413276 | ||||||
chr2:151413318
|
A | G | 4 | a0001c0003t0002g0002a0002c0001t0010g0044a0002c0001t0010g0045others(1): Show | 4 | HG00323.hp1 HG02683.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.184-1505A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413318 | ||||||
chr2:151413406
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1417T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413406 | ||||||
chr2:151413488
|
A | G | 2 | a0011c0017t0002g0159a0011c0017t0002g0160 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.184-1335A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413488 | ||||||
chr2:151413534
|
A | T | 1 | a0003c0005t0007g0296 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.184-1289A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413534 | ||||||
chr2:151413560
|
A | G | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-1263A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413560 | ||||||
chr2:151413601
|
A | G | 1 | a0001c0002t0001g0372 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.184-1222A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413601 | ||||||
chr2:151413629
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-1194T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413629 | ||||||
chr2:151413638
|
T | C | 1 | a0001c0007t0024g0263 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.184-1185T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413638 | ||||||
chr2:151413641
|
A | C | 1 | a0001c0003t0002g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.184-1182A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413641 | ||||||
chr2:151413682
|
C | G | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.184-1141C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413682 | ||||||
chr2:151413720
|
C | G | 1 | a0001c0009t0015g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.184-1103C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413720 | ||||||
chr2:151413743
|
C | T | 2 | a0001c0007t0023g0272a0001c0007t0023g0273 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.184-1080C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413743 | ||||||
chr2:151413749
|
G | A | 98 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.184-1074G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413749 | ||||||
chr2:151413785
|
A | G | 1 | a0001c0009t0015g0253 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.184-1038A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413785 | ||||||
chr2:151413833
|
A | G | 5 | a0001c0004t0005g0086a0001c0004t0005g0087a0001c0004t0005g0089others(2): Show | 5 | NA18953.hp2 NA18955.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-990A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151413833 | ||||||
chr2:151414084
|
G | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-739G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414084 | ||||||
chr2:151414286
|
CAAA | C | 112 | a0001c0003t0002g0002a0002c0001t0003g0179a0002c0001t0003g0187others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.184-525_184-523del others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151414286 | |||||
chr2:151414355
|
T | C | 40 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(37): Show | 40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.184-468T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414355 | ||||||
chr2:151414450
|
C | T | 1 | a0001c0009t0015g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.184-373C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414450 | ||||||
chr2:151414507
|
A | G | 3 | a0001c0007t0024g0263a0001c0007t0024g0270a0001c0007t0024g0271 | 3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.184-316A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414507 | ||||||
chr2:151414573
|
T | C | 3 | a0001c0007t0024g0263a0001c0007t0024g0270a0001c0007t0024g0271 | 3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.184-250T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414573 | ||||||
chr2:151414613
|
G | A | 1 | a0002c0001t0026g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.184-210G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | chr2 | 151414613 | ||||||
chr2:151414674
|
GTTTATT | G | 82 | a0001c0003t0002g0049a0001c0003t0002g0050a0001c0003t0002g0097others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.184-133_184-128del others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 3/35 | INFO_REALIGN_3_PRIME | chr2 | 151414674 | |||||
chr2:151414954
|
G | A | 3 | a0002c0001t0019g0006a0002c0001t0019g0007a0002c0001t0019g0008 | 3 | HG03139.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.280+35G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151414954 | ||||||
chr2:151415086
|
G | A | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+167G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415086 | ||||||
chr2:151415196
|
A | G | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.280+277A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415196 | ||||||
chr2:151415290
|
T | C | 1 | a0001c0002t0001g0301 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.280+371T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415290 | ||||||
chr2:151415295
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+376C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415295 | ||||||
chr2:151415302
|
G | A | 1 | a0001c0004t0005g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.280+383G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415302 | ||||||
chr2:151415345
|
C | CA | 113 | a0001c0002t0001g0375a0001c0003t0002g0002a0001c0007t0024g0270others(110): Show | 113 | HG00323.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.280+438dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415345 | |||||
chr2:151415360
|
A | G | 2 | a0002c0001t0028g0042a0002c0001t0028g0043 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.280+441A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415360 | ||||||
chr2:151415393
|
A | G | 112 | a0001c0003t0002g0002a0002c0001t0003g0179a0002c0001t0003g0187others(109): Show | 112 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.280+474A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415393 | ||||||
chr2:151415399
|
G | A | 1 | a0001c0004t0038g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.280+480G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415399 | ||||||
chr2:151415535
|
C | T | 1 | a0002c0001t0003g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.280+616C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415535 | ||||||
chr2:151415563
|
C | CA | 10 | a0001c0002t0027g0195a0001c0003t0002g0157a0001c0003t0025g0267others(7): Show | 10 | HG01069.hp2 HG01109.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+666dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | |||||
chr2:151415563
|
C | CAA | 150 | a0001c0002t0001g0001a0001c0002t0001g0297a0001c0002t0001g0298others(147): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.280+665_280+666dup others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | |||||
chr2:151415563
|
C | CAAA | 29 | a0001c0002t0001g0178a0001c0002t0001g0302a0001c0002t0001g0304others(26): Show | 29 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.280+664_280+666dup others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | |||||
chr2:151415563
|
C | CAAAA | 10 | a0001c0003t0002g0099a0001c0003t0002g0101a0001c0003t0002g0102others(7): Show | 10 | HG01256.hp1 HG01258.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+663_280+666dup others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | |||||
chr2:151415563
|
C | CAAAAA | 36 | a0001c0003t0002g0097a0001c0003t0002g0098a0001c0003t0043g0096others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.280+662_280+666dup others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | |||||
chr2:151415563
|
C | CAAAAAA | 86 | a0001c0003t0002g0002a0001c0004t0005g0062a0001c0004t0005g0063others(83): Show | 86 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.280+661_280+666dup others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | |||||
chr2:151415563
|
C | CAAAAAAA | 24 | a0001c0004t0038g0053a0002c0001t0003g0196a0002c0001t0003g0200others(21): Show | 24 | HG00741.hp1 HG01192.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.280+660_280+666dup others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415563 | |||||
chr2:151415586
|
G | A | 1 | a0002c0001t0026g0275 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.280+667G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415586 | ||||||
chr2:151415590
|
A | AT | 357 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(354): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.280+673dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | INFO_REALIGN_3_PRIME | chr2 | 151415590 | |||||
chr2:151415660
|
G | C | 1 | a0001c0002t0001g0311 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.280+741G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415660 | ||||||
chr2:151415792
|
G | A | 2 | a0001c0002t0001g0312a0001c0002t0001g0313 | 2 | NA18951.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.281-769G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415792 | ||||||
chr2:151415807
|
A | G | 263 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(260): Show | 264 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.281-754A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415807 | ||||||
chr2:151415883
|
T | A | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-678T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151415883 | ||||||
chr2:151416038
|
T | A | 1 | a0001c0003t0002g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.281-523T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416038 | ||||||
chr2:151416139
|
A | G | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.281-422A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416139 | ||||||
chr2:151416166
|
T | G | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281-395T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416166 | ||||||
chr2:151416304
|
T | G | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.281-257T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416304 | ||||||
chr2:151416518
|
G | A | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-43G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 4/35 | chr2 | 151416518 | ||||||
chr2:151416969
|
T | G | 1 | a0001c0003t0039g0113 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.503+68T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151416969 | ||||||
chr2:151416989
|
G | A | 261 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(258): Show | 262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.503+88G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151416989 | ||||||
chr2:151417044
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+143T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417044 | ||||||
chr2:151417135
|
T | C | 1 | a0001c0004t0006g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.503+234T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417135 | ||||||
chr2:151417244
|
G | A | 354 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(351): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.503+343G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417244 | ||||||
chr2:151417303
|
C | T | 5 | a0002c0001t0061g0239a0006c0011t0013g0092a0006c0011t0013g0093others(2): Show | 5 | HG00423.hp2 HG00609.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.503+402C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417303 | ||||||
chr2:151417310
|
A | T | 3 | a0001c0002t0027g0194a0001c0002t0027g0195a0001c0022t0027g0193 | 3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.503+409A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417310 | ||||||
chr2:151417311
|
C | G | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.503+410C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417311 | ||||||
chr2:151417392
|
C | A | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503+491C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417392 | ||||||
chr2:151417719
|
G | A | 2 | a0002c0001t0010g0066a0023c0026t0044g0051 | 2 | HG00639.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.503+818G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417719 | ||||||
chr2:151417892
|
A | G | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.503+991A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151417892 | ||||||
chr2:151418019
|
GTATCTCA others(4): Show |
G | 1 | a0001c0004t0038g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.503+1121_503+1131d others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418019 | |||||
chr2:151418113
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+1212A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418113 | ||||||
chr2:151418330
|
G | A | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.503+1429G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418330 | ||||||
chr2:151418447
|
C | T | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503+1546C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418447 | ||||||
chr2:151418637
|
G | A | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.504-1553G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418637 | ||||||
chr2:151418760
|
G | A | 3 | a0002c0001t0003g0204a0002c0001t0003g0205a0002c0001t0003g0206 | 3 | HG00544.hp1 NA18951.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.504-1430G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418760 | ||||||
chr2:151418790
|
A | G | 262 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(259): Show | 263 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.504-1400A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418790 | ||||||
chr2:151418915
|
A | G | 1 | a0003c0005t0007g0295 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.504-1275A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151418915 | ||||||
chr2:151418968
|
C | CT | 7 | a0001c0007t0024g0263a0001c0007t0024g0270a0001c0007t0024g0271others(4): Show | 7 | HG02280.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.504-1199dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | |||||
chr2:151418968
|
CT | C | 22 | a0001c0003t0002g0104a0001c0003t0002g0110a0001c0003t0002g0111others(19): Show | 22 | HG00438.hp2 HG00558.hp2 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.504-1199delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | |||||
chr2:151418968
|
CTT | C | 298 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.504-1200_504-1199d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | |||||
chr2:151418968
|
CTTT | C | 25 | a0001c0002t0001g0314a0001c0002t0001g0315a0001c0002t0001g0316others(22): Show | 25 | HG00280.hp2 HG00423.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.504-1201_504-1199d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | INFO_REALIGN_3_PRIME | chr2 | 151418968 | |||||
chr2:151419010
|
G | A | 1 | a0001c0003t0002g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.504-1180G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419010 | ||||||
chr2:151419087
|
C | A | 1 | a0001c0009t0015g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.504-1103C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419087 | ||||||
chr2:151419098
|
G | T | 20 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(17): Show | 20 | HG00597.hp1 HG00673.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.504-1092G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419098 | ||||||
chr2:151419388
|
A | T | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.504-802A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419388 | ||||||
chr2:151419542
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.504-648T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419542 | ||||||
chr2:151419619
|
C | G | 97 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.504-571C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419619 | ||||||
chr2:151419703
|
G | A | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.504-487G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419703 | ||||||
chr2:151419935
|
A | G | 1 | a0002c0001t0061g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.504-255A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419935 | ||||||
chr2:151419990
|
G | A | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.504-200G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151419990 | ||||||
chr2:151420181
|
C | G | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.504-9C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 6/35 | chr2 | 151420181 | ||||||
chr2:151420494
|
G | A | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.693+115G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420494 | ||||||
chr2:151420635
|
A | G | 374 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(371): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.693+256A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420635 | ||||||
chr2:151420691
|
C | T | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.693+312C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420691 | ||||||
chr2:151420734
|
C | CA | 96 | a0001c0002t0001g0302a0001c0002t0001g0318a0001c0002t0001g0319others(93): Show | 96 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.693+376dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151420734 | |||||
chr2:151420734
|
C | CAA | 6 | a0002c0001t0003g0187a0002c0001t0003g0196a0002c0001t0004g0048others(3): Show | 6 | HG01884.hp1 HG02080.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+375_693+376dup others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151420734 | |||||
chr2:151420734
|
CA | C | 131 | a0001c0002t0001g0313a0001c0002t0001g0369a0001c0002t0001g0370others(128): Show | 131 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.693+376delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151420734 | |||||
chr2:151420748
|
A | G | 1 | a0001c0002t0001g0371 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.693+369A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420748 | ||||||
chr2:151420776
|
T | G | 1 | a0002c0001t0063g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.693+397T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420776 | ||||||
chr2:151420779
|
T | C | 12 | a0002c0001t0004g0010a0002c0001t0004g0011a0002c0001t0004g0012others(9): Show | 12 | HG02145.hp2 HG02280.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.693+400T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151420779 | ||||||
chr2:151421166
|
T | G | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.693+787T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421166 | ||||||
chr2:151421402
|
C | G | 1 | a0001c0002t0047g0303 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.693+1023C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421402 | ||||||
chr2:151421409
|
A | G | 105 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.693+1030A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421409 | ||||||
chr2:151421588
|
T | C | 111 | a0002c0001t0003g0179a0002c0001t0003g0187a0002c0001t0003g0188others(108): Show | 111 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.693+1209T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421588 | ||||||
chr2:151421629
|
C | T | 2 | a0005c0010t0017g0246a0005c0010t0017g0247 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.693+1250C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421629 | ||||||
chr2:151421649
|
A | G | 8 | a0001c0002t0001g0368a0005c0010t0017g0183a0005c0010t0017g0184others(5): Show | 8 | HG01891.hp2 HG02280.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+1270A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421649 | ||||||
chr2:151421694
|
G | A | 1 | a0002c0001t0004g0047 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.694-1256G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421694 | ||||||
chr2:151421753
|
G | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1197G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421753 | ||||||
chr2:151421837
|
AT | A | 8 | a0001c0002t0001g0298a0001c0003t0002g0174a0001c0004t0006g0071others(5): Show | 8 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-1098delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | INFO_REALIGN_3_PRIME | chr2 | 151421837 | |||||
chr2:151421895
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-1055C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421895 | ||||||
chr2:151421900
|
T | C | 117 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.694-1050T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151421900 | ||||||
chr2:151422081
|
C | T | 2 | a0002c0001t0004g0013a0002c0001t0004g0026 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.694-869C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422081 | ||||||
chr2:151422148
|
C | T | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-802C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422148 | ||||||
chr2:151422644
|
C | T | 2 | a0002c0001t0021g0208a0002c0001t0021g0234 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.694-306C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422644 | ||||||
chr2:151422769
|
A | G | 162 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(159): Show | 162 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.694-181A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 7/35 | chr2 | 151422769 | ||||||
chr2:151423131
|
A | T | 3 | a0002c0001t0003g0240a0002c0001t0003g0241a0002c0001t0003g0274 | 3 | HG00738.hp2 HG01109.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.786+89A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423131 | ||||||
chr2:151423487
|
C | G | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.786+445C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423487 | ||||||
chr2:151423521
|
T | C | 1 | a0002c0001t0004g0020 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.786+479T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423521 | ||||||
chr2:151423581
|
T | G | 2 | a0002c0001t0003g0188a0002c0001t0003g0189 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.786+539T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423581 | ||||||
chr2:151423732
|
A | G | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.786+690A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423732 | ||||||
chr2:151423851
|
G | A | 159 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(156): Show | 159 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.786+809G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151423851 | ||||||
chr2:151424006
|
C | T | 1 | a0014c0033t0003g0202 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.786+964C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424006 | ||||||
chr2:151424012
|
GTC | G | 8 | a0002c0001t0008g0009a0002c0001t0008g0018a0002c0001t0008g0032others(5): Show | 8 | HG00741.hp1 HG01943.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+974_786+975del others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424012 | |||||
chr2:151424125
|
C | T | 1 | a0001c0003t0002g0111 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.786+1083C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424125 | ||||||
chr2:151424126
|
G | A | 1 | a0020c0028t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.786+1084G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424126 | ||||||
chr2:151424147
|
A | T | 40 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(37): Show | 40 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.786+1105A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424147 | ||||||
chr2:151424260
|
T | C | 2 | a0001c0002t0012g0175a0021c0023t0001g0320 | 2 | HG01106.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.786+1218T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424260 | ||||||
chr2:151424265
|
G | A | 1 | a0002c0001t0022g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.786+1223G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424265 | ||||||
chr2:151424706
|
A | G | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.786+1664A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424706 | ||||||
chr2:151424825
|
A | AT | 63 | a0001c0003t0002g0098a0001c0003t0002g0109a0001c0003t0002g0120others(60): Show | 63 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.786+1814dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
A | ATT | 36 | a0001c0003t0002g0049a0001c0003t0002g0050a0001c0003t0002g0121others(33): Show | 36 | HG00544.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.786+1813_786+1814d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
A | ATTT | 7 | a0002c0001t0003g0241a0002c0001t0003g0274a0002c0001t0008g0038others(4): Show | 7 | HG01109.hp1 HG02056.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+1812_786+1814d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
A | ATTTTT | 7 | a0001c0003t0039g0113a0003c0005t0007g0279a0003c0005t0007g0288others(4): Show | 7 | HG02165.hp1 HG02257.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+1810_786+1814d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
A | ATTTTTT | 7 | a0003c0005t0007g0278a0003c0005t0007g0280a0003c0005t0007g0281others(4): Show | 7 | HG01175.hp1 HG02145.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+1809_786+1814d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
AT | A | 12 | a0001c0002t0001g0319a0001c0002t0001g0364a0001c0002t0001g0365others(9): Show | 12 | HG01433.hp2 HG01517.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.786+1814delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATT | A | 40 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0306others(37): Show | 41 | HG00323.hp2 HG00438.hp1 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.786+1813_786+1814d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATTT | A | 52 | a0001c0002t0001g0297a0001c0002t0001g0298a0001c0002t0001g0302others(49): Show | 52 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.786+1812_786+1814d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATTTTTTT others(3): Show |
A | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+1805_786+1814d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATTTTTTT others(4): Show |
A | 2 | a0002c0001t0003g0240a0003c0005t0007g0286 | 2 | HG00738.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.786+1804_786+1814d others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATTTTTTT others(6): Show |
A | 14 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0111others(11): Show | 14 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+1802_786+1814d others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0003t0002g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.786+1801_786+1814d others(16): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATTTTTTT others(8): Show |
A | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.786+1800_786+1814d others(17): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424825
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0003t0002g0124 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.786+1799_786+1814d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151424825 | |||||
chr2:151424840
|
TTTTTTTT others(10): Show |
T | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.786+1799_786+1815d others(19): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424840 | ||||||
chr2:151424841
|
T | C | 1 | a0001c0004t0006g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786+1799T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424841 | ||||||
chr2:151424843
|
TTTTTTTT others(7): Show |
T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+1802_786+1815d others(16): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424843 | ||||||
chr2:151424844
|
TTTTTTTT others(6): Show |
T | 1 | a0001c0004t0006g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786+1803_786+1815d others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424844 | ||||||
chr2:151424850
|
T | C | 38 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(35): Show | 38 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.786+1808T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424850 | ||||||
chr2:151424853
|
TTTTC | T | 39 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(36): Show | 39 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.786+1812_786+1815d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424853 | ||||||
chr2:151424877
|
G | C | 117 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(114): Show | 117 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.786+1835G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424877 | ||||||
chr2:151424895
|
C | G | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.786+1853C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424895 | ||||||
chr2:151424983
|
C | T | 2 | a0002c0001t0028g0042a0002c0001t0028g0043 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.786+1941C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151424983 | ||||||
chr2:151425007
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+1965C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425007 | ||||||
chr2:151425042
|
C | T | 1 | a0001c0004t0006g0070 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.786+2000C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425042 | ||||||
chr2:151425047
|
C | G | 84 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.786+2005C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425047 | ||||||
chr2:151425126
|
T | C | 1 | a0002c0001t0021g0208 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.786+2084T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425126 | ||||||
chr2:151425216
|
C | CT | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+2175dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425216 | |||||
chr2:151425421
|
A | C | 267 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.786+2379A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425421 | ||||||
chr2:151425531
|
A | G | 3 | a0001c0007t0024g0263a0001c0007t0024g0270a0001c0007t0024g0271 | 3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.786+2489A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425531 | ||||||
chr2:151425550
|
T | A | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.786+2508T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425550 | ||||||
chr2:151425647
|
T | A | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.786+2605T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425647 | ||||||
chr2:151425660
|
C | CT | 173 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(170): Show | 173 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.786+2640dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | |||||
chr2:151425660
|
C | CTT | 68 | a0001c0002t0001g0376a0001c0003t0002g0106a0001c0003t0002g0119others(65): Show | 68 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.786+2639_786+2640d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | |||||
chr2:151425660
|
C | CTTT | 83 | a0001c0002t0001g0001a0001c0002t0001g0297a0001c0002t0001g0298others(80): Show | 84 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.786+2638_786+2640d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | |||||
chr2:151425660
|
C | CTTTT | 24 | a0001c0002t0001g0178a0001c0002t0001g0305a0001c0002t0001g0308others(21): Show | 24 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.786+2637_786+2640d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151425660 | |||||
chr2:151425877
|
C | G | 1 | a0001c0002t0050g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.786+2835C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425877 | ||||||
chr2:151425942
|
G | A | 1 | a0001c0003t0043g0096 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.787-2842G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425942 | ||||||
chr2:151425969
|
G | A | 1 | a0018c0025t0001g0360 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.787-2815G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151425969 | ||||||
chr2:151426080
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2704T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426080 | ||||||
chr2:151426167
|
A | ATTTTTTT others(4): Show |
1 | a0001c0004t0038g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.787-2617_787-2616i others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426167 | ||||||
chr2:151426168
|
A | AT | 11 | a0002c0001t0003g0203a0002c0001t0003g0227a0002c0001t0004g0028others(8): Show | 11 | HG00639.hp2 HG02056.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2592dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTT | 89 | a0001c0003t0002g0002a0001c0003t0002g0050a0001c0003t0002g0097others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.787-2594_787-2592d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTT | 37 | a0001c0002t0027g0194a0001c0003t0002g0049a0001c0003t0002g0106others(34): Show | 37 | HG00597.hp2 HG00621.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.787-2595_787-2592d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT | 17 | a0001c0002t0001g0304a0001c0002t0001g0314a0001c0002t0001g0321others(14): Show | 17 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(14): Show |
intron_variant | MODIFIER | c.787-2598_787-2592d others(9): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(1): Show |
34 | a0001c0002t0001g0001a0001c0002t0001g0301a0001c0002t0001g0305others(31): Show | 35 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.787-2599_787-2592d others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(2): Show |
24 | a0001c0002t0001g0178a0001c0002t0001g0297a0001c0002t0001g0302others(21): Show | 24 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.787-2600_787-2592d others(11): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(3): Show |
10 | a0001c0002t0001g0298a0001c0002t0001g0338a0001c0002t0001g0340others(7): Show | 10 | HG01993.hp2 HG02071.hp2 NA18940.hp1 others(7): Show |
intron_variant | MODIFIER | c.787-2601_787-2592d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(4): Show |
5 | a0001c0002t0001g0341a0001c0002t0001g0344a0001c0002t0054g0343others(2): Show | 5 | HG00558.hp1 HG02080.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-2602_787-2592d others(13): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(5): Show |
1 | a0001c0002t0027g0195 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.787-2603_787-2592d others(14): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(6): Show |
1 | a0001c0022t0027g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.787-2604_787-2592d others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0309 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.787-2605_787-2592d others(16): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(8): Show |
14 | a0001c0004t0005g0062a0001c0004t0005g0065a0001c0004t0005g0078others(11): Show | 14 | HG02056.hp2 HG03492.hp2 HG04204.hp2 others(11): Show |
intron_variant | MODIFIER | c.787-2606_787-2592d others(17): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(9): Show |
7 | a0001c0004t0005g0086a0001c0004t0006g0056a0001c0004t0006g0057others(4): Show | 7 | HG03041.hp2 NA18945.hp2 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.787-2607_787-2592d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(10): Show |
4 | a0001c0004t0005g0079a0001c0004t0006g0054a0001c0004t0006g0058others(1): Show | 4 | HG00673.hp1 HG02071.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-2608_787-2592d others(19): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(11): Show |
3 | a0001c0004t0006g0060a0001c0004t0006g0076a0001c0007t0023g0273 | 3 | HG02132.hp2 HG02965.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.787-2609_787-2592d others(20): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(14): Show |
1 | a0001c0004t0006g0077 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.787-2612_787-2592d others(23): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(15): Show |
1 | a0001c0004t0006g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.787-2613_787-2592d others(24): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(21): Show |
1 | a0001c0004t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.787-2592_787-2591i others(30): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | ATTTTTTT others(27): Show |
1 | a0001c0004t0006g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.787-2592_787-2591i others(36): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
A | T | 1 | a0001c0004t0038g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.787-2616A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426168 | ||||||
chr2:151426168
|
AT | A | 11 | a0002c0001t0003g0254a0002c0001t0003g0257a0002c0001t0004g0022others(8): Show | 11 | HG01070.hp2 HG01109.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2592delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426168
|
ATTTT | A | 6 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(3): Show | 6 | HG00609.hp1 HG02040.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-2595_787-2592d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426168 | |||||
chr2:151426219
|
G | A | 1 | a0001c0004t0005g0079 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.787-2565G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426219 | ||||||
chr2:151426223
|
G | A | 1 | a0001c0003t0002g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.787-2561G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426223 | ||||||
chr2:151426323
|
C | T | 105 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.787-2461C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426323 | ||||||
chr2:151426407
|
C | A | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-2377C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426407 | ||||||
chr2:151426659
|
G | GT | 13 | a0001c0003t0002g0143a0001c0003t0025g0266a0001c0003t0025g0267others(10): Show | 13 | HG01109.hp2 HG01884.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.787-2115dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426659 | |||||
chr2:151426660
|
T | G | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-2124T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426660 | ||||||
chr2:151426660
|
T | TTTTTTTT others(3): Show |
1 | a0002c0001t0022g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.787-2114_787-2105d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151426660 | |||||
chr2:151426685
|
C | T | 105 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.787-2099C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426685 | ||||||
chr2:151426841
|
T | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-1943T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426841 | ||||||
chr2:151426946
|
C | G | 1 | a0001c0003t0002g0142 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.787-1838C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151426946 | ||||||
chr2:151427058
|
T | A | 3 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273 | 3 | HG02965.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.787-1726T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427058 | ||||||
chr2:151427102
|
G | A | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-1682G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427102 | ||||||
chr2:151427103
|
C | A | 3 | a0001c0002t0027g0194a0001c0002t0027g0195a0001c0022t0027g0193 | 3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.787-1681C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427103 | ||||||
chr2:151427174
|
C | A | 1 | a0003c0005t0007g0284 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-1610C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427174 | ||||||
chr2:151427259
|
C | T | 17 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(14): Show | 17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.787-1525C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427259 | ||||||
chr2:151427378
|
T | G | 1 | a0001c0002t0001g0341 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.787-1406T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427378 | ||||||
chr2:151427431
|
G | A | 1 | a0002c0001t0022g0235 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.787-1353G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427431 | ||||||
chr2:151427500
|
C | T | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.787-1284C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427500 | ||||||
chr2:151427525
|
A | AT | 115 | a0001c0002t0001g0366a0001c0003t0002g0002a0001c0003t0002g0049others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.787-1248dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151427525 | |||||
chr2:151427746
|
A | G | 1 | a0001c0002t0001g0371 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-1038A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427746 | ||||||
chr2:151427873
|
A | G | 1 | a0002c0001t0004g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787-911A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427873 | ||||||
chr2:151427972
|
G | A | 1 | a0001c0003t0002g0097 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.787-812G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151427972 | ||||||
chr2:151428008
|
G | A | 1 | a0006c0011t0013g0093 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.787-776G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428008 | ||||||
chr2:151428020
|
G | A | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-764G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428020 | ||||||
chr2:151428030
|
C | T | 2 | a0001c0002t0027g0194a0001c0002t0027g0195 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.787-754C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428030 | ||||||
chr2:151428055
|
CAAACA | C | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-710_787-706del others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151428055 | |||||
chr2:151428122
|
G | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-662G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428122 | ||||||
chr2:151428215
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-569C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428215 | ||||||
chr2:151428307
|
T | A | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-477T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428307 | ||||||
chr2:151428446
|
G | A | 1 | a0001c0002t0053g0363 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.787-338G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428446 | ||||||
chr2:151428508
|
CTG | C | 39 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(36): Show | 39 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.787-272_787-271del others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | INFO_REALIGN_3_PRIME | chr2 | 151428508 | |||||
chr2:151428585
|
T | C | 1 | a0002c0001t0021g0208 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.787-199T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428585 | ||||||
chr2:151428630
|
A | G | 2 | a0001c0003t0029g0114a0001c0003t0029g0115 | 2 | NA18957.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.787-154A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428630 | ||||||
chr2:151428681
|
G | A | 3 | a0001c0003t0002g0109a0001c0003t0002g0124a0001c0003t0002g0136 | 3 | HG00738.hp1 HG02148.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.787-103G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428681 | ||||||
chr2:151428776
|
C | A | 1 | a0001c0002t0020g0325 | 1 | NA18990.hp2 | splice_region_variant&intron_variant | LOW | c.787-8C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 8/35 | chr2 | 151428776 | ||||||
chr2:151429034
|
A | C | 1 | a0002c0001t0072g0003 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.925+112A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429034 | ||||||
chr2:151429101
|
G | A | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.925+179G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429101 | ||||||
chr2:151429214
|
G | A | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.925+292G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429214 | ||||||
chr2:151429305
|
C | T | 1 | a0002c0001t0036g0027 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.925+383C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429305 | ||||||
chr2:151429306
|
G | C | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.925+384G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429306 | ||||||
chr2:151429460
|
G | A | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.925+538G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429460 | ||||||
chr2:151429777
|
A | C | 1 | a0001c0003t0002g0134 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.925+855A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429777 | ||||||
chr2:151429863
|
G | A | 2 | a0002c0001t0026g0276a0002c0001t0026g0277 | 2 | HG02559.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.925+941G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151429863 | ||||||
chr2:151430177
|
C | T | 1 | a0001c0003t0040g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.925+1255C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430177 | ||||||
chr2:151430249
|
C | T | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.925+1327C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430249 | ||||||
chr2:151430278
|
CCCAAAGT others(9): Show |
C | 1 | a0002c0001t0018g0030 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.925+1360_925+1375d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151430278 | |||||
chr2:151430320
|
C | CT | 7 | a0001c0004t0006g0057a0005c0010t0017g0183a0005c0010t0017g0184others(4): Show | 7 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.925+1406dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151430320 | |||||
chr2:151430424
|
C | T | 1 | a0001c0004t0038g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.925+1502C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430424 | ||||||
chr2:151430431
|
C | T | 2 | a0005c0010t0017g0183a0005c0010t0017g0184 | 2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.925+1509C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430431 | ||||||
chr2:151430453
|
C | T | 1 | a0001c0002t0012g0095 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.925+1531C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430453 | ||||||
chr2:151430479
|
G | A | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.925+1557G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430479 | ||||||
chr2:151430488
|
A | G | 1 | a0003c0005t0007g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.925+1566A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430488 | ||||||
chr2:151430666
|
T | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.925+1744T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430666 | ||||||
chr2:151430669
|
C | T | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.925+1747C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430669 | ||||||
chr2:151430712
|
G | A | 1 | a0001c0004t0006g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.925+1790G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430712 | ||||||
chr2:151430751
|
C | T | 1 | a0001c0003t0002g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.925+1829C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430751 | ||||||
chr2:151430771
|
GC | G | 264 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.925+1856delC | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151430771 | |||||
chr2:151430866
|
C | G | 3 | a0009c0014t0001g0377a0009c0014t0001g0378a0009c0014t0001g0379 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.925+1944C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151430866 | ||||||
chr2:151431317
|
A | G | 118 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.926-1760A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431317 | ||||||
chr2:151431361
|
C | T | 1 | a0001c0002t0001g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.926-1716C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431361 | ||||||
chr2:151431362
|
G | C | 19 | a0001c0002t0001g0001a0001c0002t0001g0306a0001c0002t0001g0308others(16): Show | 20 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.926-1715G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431362 | ||||||
chr2:151431383
|
A | C | 119 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.926-1694A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431383 | ||||||
chr2:151431579
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-1498C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431579 | ||||||
chr2:151431726
|
C | T | 6 | a0001c0002t0027g0194a0001c0002t0027g0195a0006c0011t0013g0092others(3): Show | 6 | HG00423.hp2 HG00609.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.926-1351C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431726 | ||||||
chr2:151431727
|
G | A | 1 | a0002c0001t0003g0237 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.926-1350G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431727 | ||||||
chr2:151431779
|
C | CTGAA | 51 | a0001c0002t0001g0314a0001c0002t0001g0372a0001c0002t0012g0173others(48): Show | 51 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.926-1265_926-1262d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | |||||
chr2:151431779
|
C | CTGAATGA others(1): Show |
135 | a0001c0002t0001g0178a0001c0002t0001g0297a0001c0002t0001g0298others(132): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.926-1269_926-1262d others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | |||||
chr2:151431779
|
C | CTGAATGA others(5): Show |
52 | a0001c0002t0001g0001a0001c0002t0001g0306a0001c0002t0001g0308others(49): Show | 53 | HG00280.hp1 HG00558.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.926-1273_926-1262d others(14): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | |||||
chr2:151431779
|
C | CTGAATGA others(9): Show |
5 | a0001c0002t0001g0312a0001c0002t0001g0355a0001c0002t0049g0357others(2): Show | 5 | HG00140.hp1 HG00621.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.926-1277_926-1262d others(18): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | |||||
chr2:151431779
|
CTGAA | C | 47 | a0001c0003t0002g0130a0001c0009t0015g0250a0002c0001t0003g0196others(44): Show | 47 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.926-1265_926-1262d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | INFO_REALIGN_3_PRIME | chr2 | 151431779 | |||||
chr2:151431816
|
C | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.926-1261C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431816 | ||||||
chr2:151431822
|
G | A | 1 | a0001c0004t0006g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.926-1255G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151431822 | ||||||
chr2:151432047
|
C | G | 1 | a0001c0004t0005g0065 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.926-1030C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432047 | ||||||
chr2:151432064
|
A | C | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-1013A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432064 | ||||||
chr2:151432100
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-977C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432100 | ||||||
chr2:151432145
|
A | G | 1 | a0001c0002t0001g0344 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.926-932A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432145 | ||||||
chr2:151432154
|
G | T | 1 | a0001c0002t0001g0301 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.926-923G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432154 | ||||||
chr2:151432156
|
C | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.926-921C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432156 | ||||||
chr2:151432220
|
G | A | 4 | a0002c0001t0004g0037a0002c0001t0004g0039a0002c0001t0004g0040others(1): Show | 4 | NA18957.hp1 NA18962.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-857G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432220 | ||||||
chr2:151432265
|
C | T | 1 | a0001c0003t0002g0143 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.926-812C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432265 | ||||||
chr2:151432623
|
G | T | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.926-454G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432623 | ||||||
chr2:151432703
|
G | T | 1 | a0001c0002t0020g0325 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.926-374G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432703 | ||||||
chr2:151432873
|
T | C | 1 | a0001c0002t0001g0327 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.926-204T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151432873 | ||||||
chr2:151433011
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.926-66T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151433011 | ||||||
chr2:151433043
|
C | T | 3 | a0008c0012t0007g0290a0008c0012t0007g0291a0008c0012t0007g0294 | 3 | HG01175.hp1 HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.926-34C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151433043 | ||||||
chr2:151433049
|
T | G | 3 | a0002c0001t0010g0066a0002c0001t0010g0068a0002c0001t0010g0069 | 3 | NA18968.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.926-28T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 9/35 | chr2 | 151433049 | ||||||
chr2:151433253
|
G | A | 83 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1077+25G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433253 | ||||||
chr2:151433256
|
C | T | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1077+28C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433256 | ||||||
chr2:151433313
|
T | C | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1077+85T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433313 | ||||||
chr2:151433318
|
G | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+90G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433318 | ||||||
chr2:151433393
|
A | G | 2 | a0001c0003t0002g0109a0001c0003t0002g0136 | 2 | HG00738.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1077+165A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433393 | ||||||
chr2:151433440
|
T | A | 3 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0002t0001g0362 | 3 | NA18980.hp1 NA19056.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1077+212T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433440 | ||||||
chr2:151433603
|
C | T | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1077+375C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433603 | ||||||
chr2:151433604
|
G | A | 105 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.1077+376G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433604 | ||||||
chr2:151433653
|
C | T | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+425C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433653 | ||||||
chr2:151433675
|
G | A | 1 | a0001c0007t0023g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1077+447G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433675 | ||||||
chr2:151433681
|
C | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1077+453C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433681 | ||||||
chr2:151433747
|
G | A | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1077+519G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433747 | ||||||
chr2:151433859
|
G | A | 1 | a0001c0003t0025g0268 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1077+631G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433859 | ||||||
chr2:151433867
|
C | A | 1 | a0002c0001t0026g0275 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1077+639C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433867 | ||||||
chr2:151433871
|
C | T | 1 | a0001c0002t0001g0326 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1077+643C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433871 | ||||||
chr2:151433874
|
C | T | 1 | a0002c0001t0004g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1077+646C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433874 | ||||||
chr2:151433909
|
T | C | 273 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1077+681T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433909 | ||||||
chr2:151433930
|
G | A | 1 | a0001c0004t0005g0065 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1077+702G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433930 | ||||||
chr2:151433969
|
T | G | 36 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1077+741T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151433969 | ||||||
chr2:151434100
|
G | A | 4 | a0001c0002t0001g0297a0001c0002t0001g0332a0001c0002t0001g0346others(1): Show | 4 | HG00642.hp1 HG01099.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077+872G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434100 | ||||||
chr2:151434167
|
C | CA | 92 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(89): Show | 93 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1077+954dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434167 | |||||
chr2:151434167
|
C | CAA | 7 | a0001c0002t0001g0338a0001c0009t0015g0250a0001c0009t0015g0251others(4): Show | 7 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+953_1077+954d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434167 | |||||
chr2:151434167
|
C | G | 2 | a0001c0004t0006g0059a0001c0004t0006g0071 | 2 | HG01358.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1077+939C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434167 | ||||||
chr2:151434179
|
AAAAG | A | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+953_1077+956d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434179 | |||||
chr2:151434181
|
A | AG | 3 | a0001c0002t0001g0344a0001c0002t0001g0347a0001c0002t0012g0095 | 3 | NA18940.hp1 NA18991.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1077+953_1077+954i others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434181 | ||||||
chr2:151434331
|
C | T | 1 | a0002c0001t0004g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1077+1103C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434331 | ||||||
chr2:151434415
|
T | C | 1 | a0001c0004t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1078-1048T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434415 | ||||||
chr2:151434430
|
T | C | 1 | a0001c0004t0006g0059 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1078-1033T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434430 | ||||||
chr2:151434437
|
A | AT | 41 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(38): Show | 41 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.1078-1005dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | |||||
chr2:151434437
|
A | ATT | 8 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(5): Show | 8 | HG01175.hp1 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1078-1006_1078-100 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | |||||
chr2:151434437
|
A | ATTT | 9 | a0001c0003t0002g0126a0001c0003t0002g0131a0001c0003t0011g0116others(6): Show | 9 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078-1007_1078-100 others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | |||||
chr2:151434437
|
A | ATTTT | 64 | a0001c0003t0002g0050a0001c0003t0002g0097a0001c0003t0002g0098others(61): Show | 64 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.1078-1008_1078-100 others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | |||||
chr2:151434437
|
A | ATTTTT | 13 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0108others(10): Show | 13 | HG00597.hp2 HG00621.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1078-1009_1078-100 others(9): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | |||||
chr2:151434437
|
AT | A | 101 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(98): Show | 102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1078-1005delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | |||||
chr2:151434437
|
ATT | A | 37 | a0001c0002t0001g0369a0001c0004t0005g0052a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1078-1006_1078-100 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | INFO_REALIGN_3_PRIME | chr2 | 151434437 | |||||
chr2:151434586
|
G | A | 2 | a0001c0002t0001g0326a0001c0002t0001g0365 | 2 | NA18977.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.1078-877G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434586 | ||||||
chr2:151434786
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-677C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434786 | ||||||
chr2:151434955
|
A | G | 2 | a0001c0003t0067g0262a0001c0003t0068g0261 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1078-508A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151434955 | ||||||
chr2:151435018
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-445C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435018 | ||||||
chr2:151435085
|
T | C | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-378T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435085 | ||||||
chr2:151435098
|
A | G | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1078-365A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435098 | ||||||
chr2:151435270
|
C | A | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1078-193C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435270 | ||||||
chr2:151435310
|
C | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1078-153C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 10/35 | chr2 | 151435310 | ||||||
chr2:151435601
|
T | G | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1195+21T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435601 | ||||||
chr2:151435609
|
T | C | 1 | a0002c0001t0010g0068 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1195+29T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435609 | ||||||
chr2:151435655
|
GA | G | 118 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(115): Show | 118 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1195+84delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151435655 | |||||
chr2:151435708
|
C | T | 1 | a0001c0003t0002g0126 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1195+128C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435708 | ||||||
chr2:151435722
|
T | C | 2 | a0002c0001t0032g0014a0002c0001t0032g0021 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1195+142T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435722 | ||||||
chr2:151435747
|
A | G | 4 | a0002c0001t0004g0037a0002c0001t0004g0039a0002c0001t0004g0040others(1): Show | 4 | NA18957.hp1 NA18962.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1195+167A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435747 | ||||||
chr2:151435760
|
G | GT | 33 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(30): Show | 33 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.1195+186dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151435760 | |||||
chr2:151435767
|
G | GT | 7 | a0001c0002t0001g0313a0001c0002t0020g0350a0001c0003t0002g0119others(4): Show | 7 | HG00621.hp2 HG01169.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1195+199dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151435767 | |||||
chr2:151435767
|
G | T | 41 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(38): Show | 41 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.1195+187G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435767 | ||||||
chr2:151435768
|
T | G | 8 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(5): Show | 8 | HG01891.hp2 HG02451.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+188T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435768 | ||||||
chr2:151435804
|
C | T | 1 | a0002c0001t0018g0030 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1195+224C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435804 | ||||||
chr2:151435834
|
T | G | 2 | a0001c0002t0012g0175a0021c0023t0001g0320 | 2 | HG01106.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1195+254T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435834 | ||||||
chr2:151435893
|
G | A | 265 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1195+313G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151435893 | ||||||
chr2:151436080
|
C | T | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1195+500C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436080 | ||||||
chr2:151436125
|
T | G | 1 | a0002c0001t0003g0214 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1195+545T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436125 | ||||||
chr2:151436132
|
G | A | 2 | a0005c0010t0017g0183a0005c0010t0017g0184 | 2 | HG03654.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1195+552G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436132 | ||||||
chr2:151436213
|
G | A | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1196-614G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436213 | ||||||
chr2:151436225
|
C | T | 4 | a0001c0004t0006g0055a0001c0004t0006g0056a0001c0004t0006g0067others(1): Show | 4 | NA18945.hp2 NA18971.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196-602C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436225 | ||||||
chr2:151436484
|
T | G | 1 | a0002c0001t0003g0228 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1196-343T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436484 | ||||||
chr2:151436540
|
C | CA | 32 | a0001c0002t0001g0307a0001c0002t0001g0319a0001c0002t0001g0333others(29): Show | 32 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1196-267dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151436540 | |||||
chr2:151436540
|
CA | C | 10 | a0001c0002t0001g0358a0001c0002t0012g0175a0001c0002t0020g0350others(7): Show | 10 | HG01515.hp2 HG01993.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196-267delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151436540 | |||||
chr2:151436578
|
T | C | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1196-249T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436578 | ||||||
chr2:151436683
|
A | G | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-144A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436683 | ||||||
chr2:151436685
|
ATTAATAT others(1): Show |
A | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.1196-140_1196-133d others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | INFO_REALIGN_3_PRIME | chr2 | 151436685 | |||||
chr2:151436741
|
G | C | 1 | a0001c0002t0001g0301 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1196-86G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436741 | ||||||
chr2:151436819
|
T | C | 1 | a0001c0002t0027g0195 | 1 | HG02886.hp1 | splice_region_variant&intron_variant | LOW | c.1196-8T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 11/35 | chr2 | 151436819 | ||||||
chr2:151437039
|
A | C | 17 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(14): Show | 17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1372+36A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/35 | chr2 | 151437039 | ||||||
chr2:151437106
|
C | T | 265 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1372+103C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 12/35 | chr2 | 151437106 | ||||||
chr2:151437592
|
G | A | 1 | a0002c0001t0063g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1483+241G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151437592 | ||||||
chr2:151437927
|
G | T | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1483+576G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151437927 | ||||||
chr2:151438038
|
T | G | 1 | a0001c0004t0006g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1484-646T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438038 | ||||||
chr2:151438237
|
GGA | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-443_1484-442d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr2 | 151438237 | |||||
chr2:151438420
|
A | G | 1 | a0001c0003t0040g0148 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1484-264A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438420 | ||||||
chr2:151438474
|
G | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-210G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438474 | ||||||
chr2:151438518
|
G | A | 1 | a0020c0028t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1484-166G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438518 | ||||||
chr2:151438561
|
AAAATT | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1484-115_1484-111d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | INFO_REALIGN_3_PRIME | chr2 | 151438561 | |||||
chr2:151438627
|
A | G | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1484-57A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 13/35 | chr2 | 151438627 | ||||||
chr2:151438783
|
A | C | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546+37A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438783 | ||||||
chr2:151438791
|
G | A | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546+45G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438791 | ||||||
chr2:151438817
|
C | A | 1 | a0003c0005t0007g0292 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1546+71C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438817 | ||||||
chr2:151438817
|
C | G | 5 | a0001c0002t0001g0336a0001c0002t0001g0340a0001c0002t0001g0344others(2): Show | 5 | HG00280.hp1 NA18940.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+71C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438817 | ||||||
chr2:151438892
|
G | A | 1 | a0002c0001t0004g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1546+146G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438892 | ||||||
chr2:151438937
|
C | T | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546+191C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438937 | ||||||
chr2:151438958
|
A | G | 2 | a0001c0003t0067g0262a0001c0003t0068g0261 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1546+212A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151438958 | ||||||
chr2:151439001
|
A | G | 1 | a0002c0001t0003g0217 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1546+255A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439001 | ||||||
chr2:151439054
|
C | T | 366 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(363): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.1546+308C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439054 | ||||||
chr2:151439108
|
G | T | 1 | a0001c0003t0065g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1546+362G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439108 | ||||||
chr2:151439154
|
C | T | 1 | a0002c0001t0004g0036 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1546+408C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439154 | ||||||
chr2:151439348
|
T | C | 5 | a0001c0003t0002g0121a0001c0003t0002g0122a0001c0003t0002g0174others(2): Show | 5 | HG00140.hp1 HG00642.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546+602T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439348 | ||||||
chr2:151439392
|
C | T | 1 | a0001c0002t0001g0336 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1547-635C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439392 | ||||||
chr2:151439476
|
C | T | 3 | a0002c0001t0004g0016a0002c0001t0004g0020a0002c0001t0036g0027 | 3 | HG03471.hp2 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1547-551C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439476 | ||||||
chr2:151439481
|
A | G | 2 | a0002c0001t0021g0208a0002c0001t0021g0234 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1547-546A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439481 | ||||||
chr2:151439561
|
C | G | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1547-466C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439561 | ||||||
chr2:151439629
|
A | G | 2 | a0001c0003t0002g0120a0001c0003t0002g0151 | 2 | HG02523.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1547-398A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439629 | ||||||
chr2:151439667
|
C | CA | 79 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(76): Show | 79 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1547-343dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439667 | |||||
chr2:151439696
|
A | G | 1 | a0001c0002t0001g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1547-331A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | chr2 | 151439696 | ||||||
chr2:151439972
|
C | CA | 84 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0298others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1547-32dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAA | 17 | a0001c0002t0001g0297a0001c0002t0001g0309a0001c0002t0001g0317others(14): Show | 17 | HG00323.hp2 HG00423.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1547-33_1547-32dup others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAAA | 6 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.1547-34_1547-32dup others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAAAA | 15 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0024g0270others(12): Show | 15 | HG02258.hp1 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1547-35_1547-32dup others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAAAAA | 11 | a0001c0003t0067g0262a0001c0007t0023g0273a0001c0007t0024g0263others(8): Show | 11 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1547-36_1547-32dup others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAAAAAAA | 57 | a0001c0003t0002g0002a0001c0003t0002g0097a0001c0003t0002g0098others(54): Show | 57 | HG00099.hp2 HG00609.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1547-38_1547-32dup others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAAAAAAA others(1): Show |
15 | a0001c0003t0002g0050a0001c0003t0002g0101a0001c0003t0002g0102others(12): Show | 15 | HG00558.hp2 HG01106.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1547-39_1547-32dup others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAAAAAAA others(2): Show |
8 | a0001c0003t0002g0049a0001c0003t0002g0122a0001c0003t0002g0132others(5): Show | 8 | HG00140.hp1 HG00597.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.1547-40_1547-32dup others(9): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
C | CAAAAAAA others(3): Show |
4 | a0001c0003t0002g0168a0001c0003t0030g0140a0001c0003t0030g0141others(1): Show | 4 | HG01123.hp2 HG02602.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1547-41_1547-32dup others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151439972
|
CA | C | 11 | a0001c0004t0005g0086a0001c0022t0027g0193a0002c0001t0003g0221others(8): Show | 11 | HG01081.hp2 HG01099.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1547-32delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 14/35 | INFO_REALIGN_3_PRIME | chr2 | 151439972 | |||||
chr2:151440221
|
CTT | C | 4 | a0002c0001t0028g0015a0002c0001t0028g0042a0002c0001t0028g0043others(1): Show | 4 | HG01192.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+99_1647+100de others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | INFO_REALIGN_3_PRIME | chr2 | 151440221 | |||||
chr2:151440326
|
A | G | 2 | a0003c0005t0007g0284a0003c0005t0007g0285 | 2 | HG00639.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1647+199A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440326 | ||||||
chr2:151440378
|
A | G | 36 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1647+251A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440378 | ||||||
chr2:151440385
|
G | A | 2 | a0001c0003t0002g0111a0001c0003t0002g0153 | 2 | HG03831.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1647+258G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440385 | ||||||
chr2:151440397
|
G | A | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1647+270G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440397 | ||||||
chr2:151440482
|
A | C | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1647+355A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440482 | ||||||
chr2:151440540
|
C | G | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+413C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440540 | ||||||
chr2:151440570
|
G | A | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1647+443G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440570 | ||||||
chr2:151440658
|
T | C | 274 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1647+531T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440658 | ||||||
chr2:151440850
|
A | T | 3 | a0001c0002t0001g0366a0001c0002t0001g0368a0018c0025t0001g0360 | 3 | NA18989.hp2 NA19007.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1647+723A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440850 | ||||||
chr2:151440853
|
C | T | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1647+726C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440853 | ||||||
chr2:151440918
|
G | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1647+791G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151440918 | ||||||
chr2:151441260
|
C | T | 5 | a0002c0001t0003g0227a0002c0001t0003g0254a0002c0001t0003g0255others(2): Show | 5 | HG01070.hp2 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1648-645C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441260 | ||||||
chr2:151441274
|
C | T | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1648-631C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441274 | ||||||
chr2:151441433
|
A | G | 8 | a0002c0001t0003g0191a0002c0001t0003g0200a0002c0001t0003g0207others(5): Show | 8 | HG02056.hp1 HG02083.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.1648-472A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441433 | ||||||
chr2:151441506
|
G | T | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1648-399G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441506 | ||||||
chr2:151441526
|
T | C | 1 | a0003c0005t0007g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1648-379T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441526 | ||||||
chr2:151441737
|
T | C | 1 | a0002c0001t0010g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1648-168T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441737 | ||||||
chr2:151441801
|
G | A | 1 | a0001c0002t0001g0313 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1648-104G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441801 | ||||||
chr2:151441841
|
C | T | 1 | a0002c0001t0062g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1648-64C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 15/35 | chr2 | 151441841 | ||||||
chr2:151442048
|
T | TTTTTA | 97 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1734+91_1734+95dup others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | |||||
chr2:151442048
|
T | TTTTTATT others(3): Show |
110 | a0001c0002t0001g0330a0001c0002t0001g0331a0001c0002t0001g0358others(107): Show | 110 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1734+86_1734+95dup others(10): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | |||||
chr2:151442048
|
T | TTTTTATT others(8): Show |
93 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1734+81_1734+95dup others(15): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | |||||
chr2:151442048
|
T | TTTTTATT others(13): Show |
56 | a0001c0003t0002g0105a0001c0003t0002g0117a0001c0003t0011g0116others(53): Show | 56 | HG00597.hp1 HG00639.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.1734+76_1734+95dup others(20): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | |||||
chr2:151442048
|
T | TTTTTATT others(18): Show |
4 | a0001c0004t0006g0070a0001c0004t0006g0074a0001c0004t0006g0077others(1): Show | 4 | HG00544.hp2 NA18998.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1734+71_1734+95dup others(25): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | |||||
chr2:151442048
|
T | TTTTTGTT others(13): Show |
1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1734+61_1734+62ins others(20): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | |||||
chr2:151442048
|
TTTTTA | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0177others(1): Show | 4 | HG00609.hp1 HG02040.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+91_1734+95del others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442048 | |||||
chr2:151442237
|
G | A | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1734+246G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442237 | ||||||
chr2:151442362
|
T | C | 1 | a0002c0001t0003g0224 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1734+371T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442362 | ||||||
chr2:151442387
|
T | TA | 4 | a0002c0001t0021g0209a0002c0001t0022g0212a0002c0001t0022g0232others(1): Show | 4 | HG01081.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+396_1734+397i others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442387 | ||||||
chr2:151442388
|
T | A | 10 | a0001c0002t0001g0367a0001c0003t0067g0262a0002c0001t0021g0208others(7): Show | 10 | HG00639.hp2 HG01081.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1734+397T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442388 | ||||||
chr2:151442388
|
TA | T | 32 | a0001c0002t0001g0313a0001c0002t0001g0314a0001c0002t0001g0315others(29): Show | 32 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1734+414delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442388 | |||||
chr2:151442389
|
A | T | 10 | a0002c0001t0008g0018a0002c0001t0010g0044a0002c0001t0028g0015others(7): Show | 10 | HG00423.hp2 HG00609.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.1734+398A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442389 | ||||||
chr2:151442390
|
A | T | 1 | a0006c0011t0013g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1734+399A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442390 | ||||||
chr2:151442409
|
A | T | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1734+418A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442409 | ||||||
chr2:151442487
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1734+496A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442487 | ||||||
chr2:151442767
|
A | AT | 106 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(103): Show | 107 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1735-468dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | |||||
chr2:151442767
|
A | ATT | 17 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0327others(14): Show | 17 | HG00621.hp2 HG00639.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.1735-469_1735-468d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | |||||
chr2:151442767
|
ATTT | A | 9 | a0001c0003t0002g0108a0001c0003t0002g0110a0001c0003t0002g0119others(6): Show | 9 | HG00741.hp2 HG02135.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1735-470_1735-468d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | |||||
chr2:151442767
|
ATTTT | A | 77 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(74): Show | 77 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1735-471_1735-468d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | |||||
chr2:151442767
|
ATTTTT | A | 32 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(29): Show | 32 | HG00639.hp1 HG01175.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1735-472_1735-468d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | |||||
chr2:151442767
|
ATTTTTT | A | 7 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(4): Show | 7 | HG02451.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1735-473_1735-468d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151442767 | |||||
chr2:151442813
|
G | A | 19 | a0001c0002t0001g0001a0001c0002t0001g0306a0001c0002t0001g0308others(16): Show | 20 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1735-446G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442813 | ||||||
chr2:151442841
|
G | A | 82 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(79): Show | 82 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.1735-418G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442841 | ||||||
chr2:151442933
|
G | A | 1 | a0001c0004t0005g0086 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1735-326G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151442933 | ||||||
chr2:151443068
|
G | A | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1735-191G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151443068 | ||||||
chr2:151443106
|
AAAT | A | 36 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1735-149_1735-147d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | INFO_REALIGN_3_PRIME | chr2 | 151443106 | |||||
chr2:151443113
|
T | C | 1 | a0001c0009t0015g0250 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1735-146T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151443113 | ||||||
chr2:151443250
|
C | T | 1 | a0002c0001t0062g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1735-9C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 16/35 | chr2 | 151443250 | ||||||
chr2:151443470
|
CATTAA | C | 17 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(14): Show | 17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1806-53_1806-49del others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 17/35 | INFO_REALIGN_3_PRIME | chr2 | 151443470 | |||||
chr2:151443747
|
CCT | C | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986+39_1986+40del others(2): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151443747 | ||||||
chr2:151443783
|
A | G | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1986+74A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151443783 | ||||||
chr2:151443870
|
C | T | 1 | a0001c0003t0002g0108 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1986+161C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151443870 | ||||||
chr2:151444094
|
T | G | 1 | a0001c0004t0005g0081 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1986+385T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444094 | ||||||
chr2:151444310
|
G | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1986+601G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444310 | ||||||
chr2:151444435
|
A | G | 275 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(272): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1986+726A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444435 | ||||||
chr2:151444439
|
G | T | 1 | a0002c0001t0037g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1986+730G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444439 | ||||||
chr2:151444659
|
G | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987-679G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444659 | ||||||
chr2:151444690
|
T | C | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1987-648T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444690 | ||||||
chr2:151444792
|
A | T | 267 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1987-546A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151444792 | ||||||
chr2:151445081
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987-257A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151445081 | ||||||
chr2:151445121
|
T | A | 1 | a0003c0005t0007g0281 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1987-217T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 18/35 | chr2 | 151445121 | ||||||
chr2:151445607
|
G | T | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2094+162G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445607 | ||||||
chr2:151445618
|
G | T | 9 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0117others(6): Show | 9 | HG00621.hp1 NA18947.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+173G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445618 | ||||||
chr2:151445619
|
C | T | 9 | a0001c0003t0002g0105a0001c0003t0002g0106a0001c0003t0002g0117others(6): Show | 9 | HG00621.hp1 NA18947.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.2094+174C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445619 | ||||||
chr2:151445685
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+240T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445685 | ||||||
chr2:151445807
|
G | A | 4 | a0003c0005t0016g0180a0003c0005t0016g0181a0003c0005t0016g0182others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+362G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445807 | ||||||
chr2:151445828
|
T | C | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2094+383T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445828 | ||||||
chr2:151445860
|
ACTT | A | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2094+419_2094+421d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | INFO_REALIGN_3_PRIME | chr2 | 151445860 | |||||
chr2:151445941
|
A | G | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2095-485A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151445941 | ||||||
chr2:151446081
|
A | T | 1 | a0006c0011t0013g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2095-345A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446081 | ||||||
chr2:151446111
|
A | G | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2095-315A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446111 | ||||||
chr2:151446163
|
C | T | 1 | a0001c0022t0027g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2095-263C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446163 | ||||||
chr2:151446205
|
G | T | 1 | a0001c0004t0006g0055 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2095-221G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446205 | ||||||
chr2:151446218
|
C | T | 1 | a0001c0003t0002g0145 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2095-208C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446218 | ||||||
chr2:151446254
|
C | T | 6 | a0001c0002t0001g0302a0001c0002t0001g0307a0001c0002t0001g0309others(3): Show | 6 | HG00438.hp1 NA18952.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2095-172C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446254 | ||||||
chr2:151446296
|
G | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2095-130G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446296 | ||||||
chr2:151446412
|
G | C | 1 | a0001c0003t0002g0002 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2095-14G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 19/35 | chr2 | 151446412 | ||||||
chr2:151446657
|
G | A | 265 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2244+82G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446657 | ||||||
chr2:151446662
|
C | G | 1 | a0002c0001t0004g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2244+87C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446662 | ||||||
chr2:151446761
|
G | T | 4 | a0001c0004t0005g0062a0001c0004t0005g0078a0001c0004t0005g0079others(1): Show | 4 | HG00673.hp1 HG02056.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+186G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446761 | ||||||
chr2:151446792
|
T | C | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2244+217T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446792 | ||||||
chr2:151446945
|
C | CT | 134 | a0001c0002t0027g0194a0001c0002t0027g0195a0001c0003t0002g0002others(131): Show | 134 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(131): Show |
intron_variant | MODIFIER | c.2244+386dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151446945 | |||||
chr2:151446945
|
CTTT | C | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2244+384_2244+386d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151446945 | |||||
chr2:151446947
|
T | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+372T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446947 | ||||||
chr2:151446949
|
T | C | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2244+374T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446949 | ||||||
chr2:151446966
|
C | T | 120 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.2244+391C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446966 | ||||||
chr2:151446982
|
C | T | 1 | a0003c0005t0007g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2244+407C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151446982 | ||||||
chr2:151447015
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+440C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447015 | ||||||
chr2:151447034
|
C | T | 1 | a0001c0004t0006g0056 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2244+459C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447034 | ||||||
chr2:151447037
|
G | A | 103 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(100): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2244+462G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447037 | ||||||
chr2:151447293
|
T | C | 6 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(3): Show | 6 | HG02145.hp1 HG02965.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244+718T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447293 | ||||||
chr2:151447295
|
C | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2244+720C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447295 | ||||||
chr2:151447333
|
C | T | 1 | a0001c0004t0038g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2244+758C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447333 | ||||||
chr2:151447410
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+835A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447410 | ||||||
chr2:151447530
|
T | C | 1 | a0001c0007t0024g0271 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2244+955T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447530 | ||||||
chr2:151447598
|
T | C | 1 | a0001c0003t0068g0261 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2244+1023T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447598 | ||||||
chr2:151447638
|
TG | T | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1066delG | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151447638 | |||||
chr2:151447717
|
G | C | 1 | a0001c0003t0029g0114 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2244+1142G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447717 | ||||||
chr2:151447736
|
G | T | 4 | a0001c0003t0002g0120a0001c0003t0002g0147a0001c0003t0002g0151others(1): Show | 4 | HG00609.hp2 HG02523.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1161G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447736 | ||||||
chr2:151447889
|
A | G | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2244+1314A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151447889 | ||||||
chr2:151448087
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1512A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448087 | ||||||
chr2:151448180
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+1605A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448180 | ||||||
chr2:151448244
|
G | A | 115 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(112): Show | 115 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.2244+1669G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448244 | ||||||
chr2:151448333
|
C | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2244+1758C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448333 | ||||||
chr2:151448336
|
G | C | 1 | a0003c0005t0007g0280 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2244+1761G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448336 | ||||||
chr2:151448568
|
A | G | 1 | a0001c0004t0006g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2244+1993A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448568 | ||||||
chr2:151448649
|
T | C | 1 | a0001c0002t0047g0303 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2244+2074T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448649 | ||||||
chr2:151448677
|
G | GT | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2244+2103dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151448677 | |||||
chr2:151448836
|
T | A | 1 | a0001c0004t0005g0078 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2244+2261T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448836 | ||||||
chr2:151448922
|
A | T | 1 | a0002c0001t0003g0223 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2244+2347A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151448922 | ||||||
chr2:151449292
|
C | T | 1 | a0006c0011t0013g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2245-2314C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449292 | ||||||
chr2:151449396
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-2210A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449396 | ||||||
chr2:151449423
|
CT | C | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-2176delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449423 | |||||
chr2:151449439
|
CTT | C | 3 | a0009c0014t0001g0377a0009c0014t0001g0378a0009c0014t0001g0379 | 3 | HG01069.hp1 HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2245-2163_2245-216 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449439 | |||||
chr2:151449461
|
T | C | 2 | a0002c0001t0028g0042a0002c0001t0028g0043 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2245-2145T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449461 | ||||||
chr2:151449521
|
T | C | 263 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2245-2085T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449521 | ||||||
chr2:151449748
|
A | AC | 163 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(160): Show | 163 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.2245-1858_2245-185 others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449748 | ||||||
chr2:151449842
|
GC | G | 31 | a0001c0004t0005g0052a0001c0004t0005g0063a0001c0004t0005g0064others(28): Show | 31 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.2245-1762delC | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449842 | |||||
chr2:151449843
|
C | A | 3 | a0002c0001t0019g0006a0002c0001t0019g0007a0002c0001t0019g0008 | 3 | HG03139.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2245-1763C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449843 | ||||||
chr2:151449844
|
C | CT | 219 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.2245-1747dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151449844 | |||||
chr2:151449844
|
C | G | 6 | a0001c0004t0005g0062a0001c0004t0005g0086a0001c0004t0006g0054others(3): Show | 6 | HG01358.hp2 HG02071.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.2245-1762C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449844 | ||||||
chr2:151449845
|
T | G | 31 | a0001c0004t0005g0052a0001c0004t0005g0063a0001c0004t0005g0064others(28): Show | 31 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.2245-1761T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449845 | ||||||
chr2:151449912
|
G | A | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2245-1694G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449912 | ||||||
chr2:151449934
|
C | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2245-1672C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151449934 | ||||||
chr2:151450157
|
T | C | 22 | a0001c0003t0068g0261a0003c0005t0007g0278a0003c0005t0007g0279others(19): Show | 22 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.2245-1449T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450157 | ||||||
chr2:151450383
|
T | G | 121 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.2245-1223T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450383 | ||||||
chr2:151450451
|
T | G | 1 | a0002c0001t0008g0038 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2245-1155T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450451 | ||||||
chr2:151450545
|
T | C | 3 | a0001c0002t0001g0307a0001c0002t0001g0372a0001c0002t0053g0363 | 3 | HG00438.hp1 NA18952.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.2245-1061T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450545 | ||||||
chr2:151450577
|
C | A | 97 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(94): Show | 98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.2245-1029C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450577 | ||||||
chr2:151450594
|
C | CT | 6 | a0001c0002t0001g0178a0001c0002t0001g0334a0001c0002t0001g0341others(3): Show | 6 | HG01978.hp1 HG02071.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.2245-1001dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | INFO_REALIGN_3_PRIME | chr2 | 151450594 | |||||
chr2:151450609
|
G | A | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2245-997G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450609 | ||||||
chr2:151450616
|
C | G | 1 | a0001c0003t0069g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2245-990C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450616 | ||||||
chr2:151450662
|
C | T | 1 | a0026c0031t0002g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2245-944C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450662 | ||||||
chr2:151450707
|
C | T | 4 | a0001c0003t0002g0130a0001c0003t0002g0132a0001c0003t0002g0134others(1): Show | 4 | HG01081.hp1 HG01255.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-899C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450707 | ||||||
chr2:151450709
|
G | A | 94 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(91): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.2245-897G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450709 | ||||||
chr2:151450921
|
G | A | 17 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(14): Show | 17 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.2245-685G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450921 | ||||||
chr2:151450979
|
G | A | 2 | a0002c0001t0003g0187a0002c0001t0003g0190 | 2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2245-627G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450979 | ||||||
chr2:151450981
|
A | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-625A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151450981 | ||||||
chr2:151451192
|
C | T | 104 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(101): Show | 105 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.2245-414C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451192 | ||||||
chr2:151451277
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2245-329C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451277 | ||||||
chr2:151451359
|
A | T | 4 | a0001c0003t0025g0266a0001c0003t0025g0267a0001c0003t0025g0268others(1): Show | 4 | HG01884.hp2 HG06807.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-247A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451359 | ||||||
chr2:151451364
|
G | A | 1 | a0001c0002t0001g0362 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2245-242G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 20/35 | chr2 | 151451364 | ||||||
chr2:151452097
|
T | G | 121 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.2344+392T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452097 | ||||||
chr2:151452196
|
A | C | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2344+491A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452196 | ||||||
chr2:151452361
|
T | C | 266 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2344+656T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452361 | ||||||
chr2:151452862
|
A | G | 1 | a0001c0003t0002g0102 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2344+1157A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452862 | ||||||
chr2:151452871
|
C | T | 1 | a0003c0005t0007g0288 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2344+1166C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151452871 | ||||||
chr2:151453002
|
G | A | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2344+1297G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453002 | ||||||
chr2:151453397
|
C | T | 1 | a0002c0001t0063g0211 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2345-1498C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453397 | ||||||
chr2:151453449
|
C | T | 17 | a0001c0002t0001g0001a0001c0002t0001g0306a0001c0002t0001g0308others(14): Show | 18 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2345-1446C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453449 | ||||||
chr2:151453579
|
C | CA | 67 | a0001c0003t0002g0050a0001c0003t0002g0111a0001c0003t0002g0118others(64): Show | 67 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.2345-1293dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | |||||
chr2:151453579
|
C | CAA | 14 | a0001c0003t0002g0134a0001c0003t0002g0139a0001c0004t0005g0062others(11): Show | 14 | HG01081.hp1 HG02145.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.2345-1294_2345-129 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | |||||
chr2:151453579
|
CA | C | 32 | a0001c0002t0001g0306a0001c0002t0001g0312a0001c0002t0001g0322others(29): Show | 32 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.2345-1293delA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | |||||
chr2:151453579
|
CAA | C | 76 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(73): Show | 77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.2345-1294_2345-129 others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | INFO_REALIGN_3_PRIME | chr2 | 151453579 | |||||
chr2:151453609
|
T | A | 21 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(18): Show | 21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2345-1286T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453609 | ||||||
chr2:151453613
|
C | T | 1 | a0001c0003t0002g0143 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2345-1282C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453613 | ||||||
chr2:151453741
|
G | A | 1 | a0002c0001t0037g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2345-1154G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151453741 | ||||||
chr2:151454351
|
A | T | 1 | a0002c0001t0003g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2345-544A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454351 | ||||||
chr2:151454381
|
G | A | 1 | a0002c0001t0062g0210 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2345-514G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454381 | ||||||
chr2:151454414
|
T | G | 120 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.2345-481T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454414 | ||||||
chr2:151454472
|
C | G | 2 | a0002c0001t0032g0014a0002c0001t0032g0021 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2345-423C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454472 | ||||||
chr2:151454736
|
T | C | 1 | a0002c0001t0003g0190 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2345-159T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 21/35 | chr2 | 151454736 | ||||||
chr2:151455173
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609+14A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455173 | ||||||
chr2:151455175
|
T | A | 2 | a0001c0003t0067g0262a0001c0003t0068g0261 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2609+16T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455175 | ||||||
chr2:151455563
|
C | A | 42 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2609+404C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455563 | ||||||
chr2:151455566
|
T | C | 1 | a0002c0001t0037g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2609+407T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455566 | ||||||
chr2:151455661
|
CAT | C | 119 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(116): Show | 119 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.2609+505_2609+506d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr2 | 151455661 | |||||
chr2:151455783
|
C | T | 1 | a0001c0003t0030g0140 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2609+624C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455783 | ||||||
chr2:151455819
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2609+660C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151455819 | ||||||
chr2:151456062
|
C | T | 1 | a0002c0001t0003g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2610-516C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151456062 | ||||||
chr2:151456237
|
G | A | 1 | a0002c0001t0014g0199 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2610-341G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151456237 | ||||||
chr2:151456428
|
G | GT | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2610-144dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | INFO_REALIGN_3_PRIME | chr2 | 151456428 | |||||
chr2:151456548
|
A | C | 1 | a0002c0001t0004g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2610-30A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 22/35 | chr2 | 151456548 | ||||||
chr2:151456802
|
G | A | 36 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.2652+182G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456802 | ||||||
chr2:151456925
|
G | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.2652+305G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456925 | ||||||
chr2:151456953
|
C | T | 16 | a0002c0001t0004g0036a0002c0001t0004g0037a0002c0001t0004g0039others(13): Show | 16 | HG00741.hp1 HG01943.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.2652+333C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456953 | ||||||
chr2:151456971
|
T | G | 1 | a0008c0012t0007g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2652+351T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456971 | ||||||
chr2:151456975
|
T | C | 266 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2652+355T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151456975 | ||||||
chr2:151457025
|
C | T | 98 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(95): Show | 99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.2652+405C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457025 | ||||||
chr2:151457049
|
A | T | 1 | a0001c0004t0038g0053 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2652+429A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457049 | ||||||
chr2:151457084
|
A | G | 1 | a0002c0001t0003g0222 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2652+464A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457084 | ||||||
chr2:151457087
|
G | GT | 31 | a0001c0002t0001g0338a0001c0004t0006g0057a0001c0007t0023g0264others(28): Show | 31 | HG00438.hp2 HG00639.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.2652+480dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr2 | 151457087 | |||||
chr2:151457087
|
G | T | 1 | a0001c0003t0025g0268 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2652+467G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457087 | ||||||
chr2:151457136
|
A | G | 3 | a0002c0001t0010g0066a0002c0001t0010g0068a0002c0001t0010g0069 | 3 | NA18968.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2652+516A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457136 | ||||||
chr2:151457205
|
C | G | 1 | a0001c0003t0066g0310 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2653-556C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457205 | ||||||
chr2:151457223
|
G | A | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2653-538G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457223 | ||||||
chr2:151457234
|
C | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2653-527C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457234 | ||||||
chr2:151457312
|
G | A | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2653-449G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457312 | ||||||
chr2:151457499
|
G | A | 1 | a0008c0012t0007g0290 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2653-262G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457499 | ||||||
chr2:151457583
|
TTAA | T | 21 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(18): Show | 21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.2653-174_2653-172d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | INFO_REALIGN_3_PRIME | chr2 | 151457583 | |||||
chr2:151457585
|
A | G | 2 | a0004c0006t0009g0165a0004c0006t0009g0170 | 2 | NA18983.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2653-176A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457585 | ||||||
chr2:151457658
|
G | T | 5 | a0001c0004t0005g0086a0001c0004t0005g0087a0001c0004t0005g0089others(2): Show | 5 | NA18953.hp2 NA18955.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.2653-103G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 23/35 | chr2 | 151457658 | ||||||
chr2:151458033
|
C | CA | 266 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2855+73dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458033 | |||||
chr2:151458160
|
C | T | 1 | a0020c0028t0002g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2855+197C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458160 | ||||||
chr2:151458225
|
G | GT | 3 | a0003c0005t0007g0288a0008c0012t0007g0289a0019c0027t0016g0282 | 3 | HG02257.hp2 HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2855+262_2855+263i others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458225 | ||||||
chr2:151458226
|
A | AT | 159 | a0001c0002t0001g0001a0001c0002t0001g0298a0001c0002t0001g0304others(156): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.2855+287dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | |||||
chr2:151458226
|
A | ATT | 29 | a0001c0002t0001g0178a0001c0002t0001g0297a0001c0002t0001g0301others(26): Show | 29 | HG00423.hp1 HG00558.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.2855+286_2855+287d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | |||||
chr2:151458226
|
A | ATTT | 6 | a0001c0002t0001g0349a0001c0002t0047g0303a0001c0002t0050g0185others(3): Show | 6 | HG00621.hp1 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2855+285_2855+287d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | |||||
chr2:151458226
|
A | T | 19 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(16): Show | 19 | HG01175.hp1 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2855+263A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458226 | ||||||
chr2:151458226
|
AT | A | 8 | a0001c0002t0027g0194a0001c0038t0033g0265a0002c0001t0003g0179others(5): Show | 8 | HG01515.hp2 HG01891.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.2855+287delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | |||||
chr2:151458226
|
ATTTTTTT others(5): Show |
A | 1 | a0002c0001t0026g0275 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2855+276_2855+287d others(14): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | INFO_REALIGN_3_PRIME | chr2 | 151458226 | |||||
chr2:151458284
|
G | A | 1 | a0001c0002t0047g0303 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2855+321G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458284 | ||||||
chr2:151458325
|
C | T | 2 | a0005c0018t0034g0248a0005c0018t0034g0249 | 2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2855+362C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458325 | ||||||
chr2:151458397
|
T | A | 84 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.2856-414T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458397 | ||||||
chr2:151458540
|
T | A | 1 | a0001c0002t0047g0303 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2856-271T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458540 | ||||||
chr2:151458595
|
C | T | 1 | a0001c0002t0001g0359 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2856-216C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458595 | ||||||
chr2:151458753
|
A | G | 10 | a0002c0001t0003g0196a0002c0001t0003g0203a0002c0001t0003g0216others(7): Show | 10 | HG00438.hp2 HG02080.hp2 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.2856-58A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458753 | ||||||
chr2:151458762
|
C | T | 1 | a0002c0001t0004g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2856-49C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 24/35 | chr2 | 151458762 | ||||||
chr2:151458923
|
G | A | 1 | a0012c0037t0020g0335 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2955+13G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151458923 | ||||||
chr2:151458980
|
G | A | 6 | a0001c0003t0002g0002a0001c0003t0002g0110a0001c0003t0002g0137others(3): Show | 6 | HG01993.hp1 HG02004.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.2955+70G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151458980 | ||||||
chr2:151459035
|
G | T | 265 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(262): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.2955+125G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459035 | ||||||
chr2:151459211
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+301A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459211 | ||||||
chr2:151459302
|
G | C | 267 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(264): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2955+392G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459302 | ||||||
chr2:151459302
|
G | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2955+392G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459302 | ||||||
chr2:151459418
|
T | C | 1 | a0002c0001t0061g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2955+508T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459418 | ||||||
chr2:151459440
|
A | G | 3 | a0001c0007t0024g0263a0001c0007t0024g0270a0001c0007t0024g0271 | 3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2955+530A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459440 | ||||||
chr2:151459554
|
G | T | 42 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2956-446G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459554 | ||||||
chr2:151459588
|
A | G | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.2956-412A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459588 | ||||||
chr2:151459590
|
A | G | 1 | a0001c0002t0001g0366 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2956-410A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459590 | ||||||
chr2:151459604
|
G | A | 1 | a0002c0001t0026g0276 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2956-396G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459604 | ||||||
chr2:151459613
|
C | T | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2956-387C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459613 | ||||||
chr2:151459624
|
A | G | 1 | a0001c0002t0001g0351 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2956-376A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459624 | ||||||
chr2:151459642
|
G | C | 1 | a0002c0001t0003g0191 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2956-358G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459642 | ||||||
chr2:151459830
|
G | A | 42 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.2956-170G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 25/35 | chr2 | 151459830 | ||||||
chr2:151460154
|
A | T | 1 | a0001c0003t0041g0133 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3075+35A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460154 | ||||||
chr2:151460159
|
G | T | 1 | a0017c0029t0033g0260 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3075+40G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460159 | ||||||
chr2:151460226
|
G | A | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3075+107G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460226 | ||||||
chr2:151460526
|
TCTTATCA others(2): Show |
T | 266 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.3075+408_3075+416d others(11): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460526 | ||||||
chr2:151460527
|
C | T | 1 | a0002c0001t0021g0209 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3075+408C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460527 | ||||||
chr2:151460536
|
T | A | 266 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.3075+417T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460536 | ||||||
chr2:151460637
|
GTGAAA | G | 3 | a0001c0007t0024g0263a0001c0007t0024g0270a0001c0007t0024g0271 | 3 | HG02647.hp1 HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.3076-495_3076-491d others(7): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | INFO_REALIGN_3_PRIME | chr2 | 151460637 | |||||
chr2:151460789
|
C | T | 1 | a0001c0004t0006g0074 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.3076-349C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460789 | ||||||
chr2:151460881
|
G | A | 38 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(35): Show | 38 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.3076-257G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460881 | ||||||
chr2:151460924
|
C | G | 1 | a0007c0008t0001g0339 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3076-214C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151460924 | ||||||
chr2:151461007
|
G | A | 1 | a0002c0001t0003g0223 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3076-131G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151461007 | ||||||
chr2:151461017
|
T | C | 122 | a0001c0002t0001g0297a0001c0003t0002g0002a0001c0003t0002g0049others(119): Show | 122 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.3076-121T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151461017 | ||||||
chr2:151461074
|
T | C | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3076-64T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 26/35 | chr2 | 151461074 | ||||||
chr2:151461391
|
A | AT | 48 | a0001c0002t0001g0308a0001c0002t0001g0331a0001c0002t0001g0334others(45): Show | 48 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.3227+120dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr2 | 151461391 | |||||
chr2:151461461
|
G | A | 1 | a0025c0030t0006g0073 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.3227+172G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461461 | ||||||
chr2:151461483
|
C | A | 1 | a0001c0003t0002g0174 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3227+194C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461483 | ||||||
chr2:151461517
|
G | A | 87 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(84): Show | 87 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.3227+228G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461517 | ||||||
chr2:151461814
|
C | T | 1 | a0001c0009t0015g0251 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3228-428C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461814 | ||||||
chr2:151461917
|
A | G | 1 | a0001c0003t0029g0115 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3228-325A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461917 | ||||||
chr2:151461986
|
G | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.3228-256G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461986 | ||||||
chr2:151461999
|
A | T | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3228-243A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151461999 | ||||||
chr2:151462084
|
G | A | 36 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(33): Show | 36 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.3228-158G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151462084 | ||||||
chr2:151462169
|
G | T | 2 | a0001c0002t0001g0345a0024c0021t0001g0300 | 2 | HG00733.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.3228-73G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | chr2 | 151462169 | ||||||
chr2:151462199
|
TATC | T | 103 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(100): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.3228-39_3228-37del others(3): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 27/35 | INFO_REALIGN_3_PRIME | chr2 | 151462199 | |||||
chr2:151462334
|
A | G | 7 | a0001c0003t0011g0116a0001c0003t0011g0135a0001c0003t0011g0150others(4): Show | 7 | NA18940.hp2 NA18957.hp2 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.3308+12A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 28/35 | chr2 | 151462334 | ||||||
chr2:151462399
|
A | G | 1 | a0002c0001t0003g0179 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3309-13A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 28/35 | chr2 | 151462399 | ||||||
chr2:151462471
|
G | A | 6 | a0001c0002t0001g0327a0001c0002t0001g0370a0001c0002t0020g0325others(3): Show | 6 | NA18987.hp2 NA18990.hp2 NA19003.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3363+5G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | chr2 | 151462471 | ||||||
chr2:151462648
|
A | AGT | 191 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(188): Show | 192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.3363+201_3363+202d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | |||||
chr2:151462648
|
A | AGTGT | 8 | a0001c0002t0001g0364a0001c0003t0002g0129a0001c0004t0006g0077others(5): Show | 8 | HG00099.hp2 HG00544.hp2 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.3363+199_3363+202d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | |||||
chr2:151462648
|
A | AGTGTGT | 7 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0018t0034g0248others(4): Show | 7 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.3363+197_3363+202d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | |||||
chr2:151462648
|
A | AGTGTGTG others(3): Show |
2 | a0005c0010t0017g0246a0005c0010t0017g0247 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3363+193_3363+202d others(12): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | |||||
chr2:151462648
|
AGTGT | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.3363+199_3363+202d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | |||||
chr2:151462648
|
AGTGTGT | A | 3 | a0002c0001t0003g0204a0002c0001t0003g0205a0002c0001t0003g0206 | 3 | HG00544.hp1 NA18951.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3363+197_3363+202d others(8): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 29/35 | INFO_REALIGN_3_PRIME | chr2 | 151462648 | |||||
chr2:151466516
|
G | A | 1 | a0001c0004t0005g0084 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.6600+396G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466516 | ||||||
chr2:151466572
|
C | A | 103 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(100): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.6600+452C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466572 | ||||||
chr2:151466724
|
TAAAA | T | 5 | a0001c0007t0024g0263a0001c0009t0015g0250a0001c0009t0015g0251others(2): Show | 5 | HG02809.hp1 HG03491.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.6600+608_6600+611d others(6): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | INFO_REALIGN_3_PRIME | chr2 | 151466724 | |||||
chr2:151466785
|
T | C | 14 | a0001c0002t0001g0001a0001c0002t0001g0308a0001c0002t0001g0315others(11): Show | 15 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.6600+665T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466785 | ||||||
chr2:151466833
|
G | T | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6600+713G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466833 | ||||||
chr2:151466992
|
C | A | 4 | a0001c0004t0005g0062a0001c0004t0005g0078a0001c0004t0005g0079others(1): Show | 4 | HG00673.hp1 HG02056.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.6600+872C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151466992 | ||||||
chr2:151467018
|
C | G | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6600+898C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467018 | ||||||
chr2:151467039
|
A | G | 84 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(81): Show | 84 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.6600+919A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467039 | ||||||
chr2:151467099
|
C | T | 1 | a0001c0002t0001g0334 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.6601-901C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467099 | ||||||
chr2:151467113
|
C | A | 4 | a0001c0009t0015g0250a0001c0009t0015g0251a0001c0009t0015g0252others(1): Show | 4 | HG03491.hp1 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.6601-887C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467113 | ||||||
chr2:151467132
|
G | C | 6 | a0005c0010t0017g0183a0005c0010t0017g0184a0005c0010t0017g0246others(3): Show | 6 | HG01891.hp2 HG02818.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.6601-868G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467132 | ||||||
chr2:151467171
|
G | C | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.6601-829G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467171 | ||||||
chr2:151467206
|
C | T | 90 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(87): Show | 91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.6601-794C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467206 | ||||||
chr2:151467214
|
C | T | 1 | a0001c0038t0033g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.6601-786C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467214 | ||||||
chr2:151467306
|
C | A | 22 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(19): Show | 22 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.6601-694C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467306 | ||||||
chr2:151467385
|
A | G | 1 | a0001c0004t0005g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6601-615A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467385 | ||||||
chr2:151467624
|
C | T | 1 | a0002c0001t0003g0207 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.6601-376C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467624 | ||||||
chr2:151467674
|
G | A | 21 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280others(18): Show | 21 | HG00639.hp1 HG01175.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.6601-326G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467674 | ||||||
chr2:151467695
|
C | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.6601-305C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 30/35 | chr2 | 151467695 | ||||||
chr2:151468221
|
G | C | 1 | a0001c0003t0025g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.6747+75G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 31/35 | chr2 | 151468221 | ||||||
chr2:151468275
|
G | C | 264 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(261): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.6747+129G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 31/35 | chr2 | 151468275 | ||||||
chr2:151468574
|
T | C | 1 | a0002c0001t0004g0036 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.6825+23T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 32/35 | chr2 | 151468574 | ||||||
chr2:151468774
|
C | T | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.6941+18C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151468774 | ||||||
chr2:151468833
|
C | T | 1 | a0001c0004t0006g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6941+77C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151468833 | ||||||
chr2:151469057
|
G | A | 2 | a0001c0002t0027g0194a0001c0002t0027g0195 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.6941+301G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469057 | ||||||
chr2:151469125
|
C | CA | 6 | a0002c0001t0010g0044a0002c0001t0010g0045a0002c0001t0010g0066others(3): Show | 6 | HG00323.hp1 HG02683.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.6941+370dupA | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr2 | 151469125 | |||||
chr2:151469168
|
A | G | 3 | a0003c0005t0016g0180a0003c0005t0016g0181a0003c0005t0016g0182 | 3 | HG02258.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.6941+412A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469168 | ||||||
chr2:151469229
|
C | T | 1 | a0001c0003t0011g0155 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.6941+473C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469229 | ||||||
chr2:151469442
|
G | A | 1 | a0001c0003t0002g0128 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.6942-269G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469442 | ||||||
chr2:151469519
|
C | T | 1 | a0001c0003t0002g0131 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6942-192C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469519 | ||||||
chr2:151469576
|
C | T | 1 | a0002c0001t0018g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6942-135C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 33/35 | chr2 | 151469576 | ||||||
chr2:151470182
|
C | A | 2 | a0003c0005t0007g0284a0003c0005t0007g0285 | 2 | HG00639.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.7095+318C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470182 | ||||||
chr2:151470213
|
C | CT | 88 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(85): Show | 88 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.7095+354dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151470213 | |||||
chr2:151470214
|
T | C | 1 | a0001c0004t0006g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7095+350T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470214 | ||||||
chr2:151470408
|
G | A | 3 | a0003c0005t0007g0281a0003c0005t0007g0286a0003c0019t0070g0287 | 3 | HG02965.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.7095+544G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470408 | ||||||
chr2:151470456
|
T | C | 2 | a0001c0002t0001g0370a0001c0002t0052g0328 | 2 | NA18987.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.7095+592T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470456 | ||||||
chr2:151470638
|
T | C | 1 | a0001c0002t0001g0315 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.7095+774T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470638 | ||||||
chr2:151470961
|
G | T | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.7095+1097G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470961 | ||||||
chr2:151470979
|
T | G | 1 | a0002c0001t0026g0275 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.7095+1115T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151470979 | ||||||
chr2:151471025
|
CT | C | 7 | a0002c0001t0019g0006a0002c0001t0019g0007a0002c0001t0019g0008others(4): Show | 7 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.7095+1170delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151471025 | |||||
chr2:151471236
|
G | A | 1 | a0002c0001t0004g0046 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.7095+1372G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471236 | ||||||
chr2:151471387
|
G | A | 2 | a0010c0015t0031g0004a0010c0015t0031g0005 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.7095+1523G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471387 | ||||||
chr2:151471551
|
G | A | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7095+1687G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471551 | ||||||
chr2:151471660
|
G | T | 1 | a0002c0001t0008g0032 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.7095+1796G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471660 | ||||||
chr2:151471668
|
C | T | 335 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(332): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.7095+1804C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471668 | ||||||
chr2:151471832
|
C | A | 4 | a0006c0011t0013g0092a0006c0011t0013g0093a0006c0011t0013g0176others(1): Show | 4 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.7095+1968C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471832 | ||||||
chr2:151471853
|
G | T | 1 | a0001c0002t0050g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7095+1989G>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471853 | ||||||
chr2:151471945
|
A | G | 1 | a0023c0026t0044g0051 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.7096-2019A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471945 | ||||||
chr2:151471979
|
A | C | 1 | a0002c0001t0004g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.7096-1985A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151471979 | ||||||
chr2:151472065
|
C | T | 1 | a0002c0001t0032g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7096-1899C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472065 | ||||||
chr2:151472067
|
C | A | 1 | a0002c0001t0032g0014 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7096-1897C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472067 | ||||||
chr2:151472067
|
C | T | 1 | a0015c0034t0059g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7096-1897C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472067 | ||||||
chr2:151472085
|
C | T | 1 | a0001c0002t0050g0185 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.7096-1879C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472085 | ||||||
chr2:151472086
|
G | A | 2 | a0002c0001t0032g0014a0002c0001t0032g0021 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.7096-1878G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472086 | ||||||
chr2:151472235
|
T | A | 3 | a0002c0001t0010g0044a0002c0001t0010g0045a0002c0001t0056g0373 | 3 | HG00323.hp1 HG02683.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.7096-1729T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472235 | ||||||
chr2:151472279
|
A | G | 2 | a0001c0003t0011g0150a0001c0003t0011g0155 | 2 | NA18940.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.7096-1685A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472279 | ||||||
chr2:151472431
|
G | C | 1 | a0001c0004t0006g0057 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.7096-1533G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472431 | ||||||
chr2:151472469
|
T | C | 3 | a0001c0002t0027g0194a0001c0002t0027g0195a0001c0022t0027g0193 | 3 | HG01891.hp1 HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.7096-1495T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472469 | ||||||
chr2:151472507
|
T | G | 3 | a0003c0005t0007g0278a0003c0005t0007g0279a0003c0005t0007g0280 | 3 | HG02145.hp1 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.7096-1457T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472507 | ||||||
chr2:151472698
|
G | A | 113 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(110): Show | 113 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.7096-1266G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472698 | ||||||
chr2:151472771
|
G | C | 3 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273 | 3 | HG02965.hp2 HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.7096-1193G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472771 | ||||||
chr2:151472801
|
A | G | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.7096-1163A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472801 | ||||||
chr2:151472827
|
A | T | 1 | a0001c0002t0001g0370 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.7096-1137A>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472827 | ||||||
chr2:151472936
|
A | C | 3 | a0001c0002t0001g0311a0001c0002t0001g0356a0001c0002t0012g0091 | 3 | HG03834.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.7096-1028A>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472936 | ||||||
chr2:151472990
|
T | C | 1 | a0001c0003t0041g0133 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.7096-974T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151472990 | ||||||
chr2:151473003
|
G | C | 5 | a0001c0004t0005g0086a0001c0004t0005g0087a0001c0004t0005g0089others(2): Show | 5 | NA18953.hp2 NA18955.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.7096-961G>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473003 | ||||||
chr2:151473006
|
T | A | 2 | a0001c0002t0001g0323a0001c0002t0001g0329 | 2 | HG01192.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.7096-958T>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473006 | ||||||
chr2:151473292
|
C | CT | 9 | a0002c0001t0003g0187a0002c0001t0003g0190a0002c0001t0004g0012others(6): Show | 9 | HG00639.hp2 HG02280.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.7096-650dupT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | |||||
chr2:151473292
|
CT | C | 119 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(116): Show | 120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.7096-650delT | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | |||||
chr2:151473292
|
CTT | C | 39 | a0001c0002t0001g0375a0001c0002t0020g0350a0001c0002t0053g0363others(36): Show | 39 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.7096-651_7096-650d others(4): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | |||||
chr2:151473292
|
CTTT | C | 8 | a0001c0004t0005g0087a0001c0004t0005g0089a0001c0004t0005g0090others(5): Show | 8 | HG00423.hp2 HG00609.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.7096-652_7096-650d others(5): Show |
RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | INFO_REALIGN_3_PRIME | chr2 | 151473292 | |||||
chr2:151473340
|
C | A | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.7096-624C>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473340 | ||||||
chr2:151473574
|
C | T | 1 | a0001c0004t0005g0062 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.7096-390C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473574 | ||||||
chr2:151473634
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A | G | 103 | a0001c0002t0001g0001a0001c0002t0001g0178a0001c0002t0001g0297others(100): Show | 104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.7096-330A>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473634 | ||||||
chr2:151473644
|
T | C | 1 | a0022c0024t0051g0337 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.7096-320T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473644 | ||||||
chr2:151473759
|
C | G | 3 | a0002c0001t0021g0208a0002c0001t0021g0209a0002c0001t0021g0234 | 3 | HG02896.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.7096-205C>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 34/35 | chr2 | 151473759 | ||||||
chr2:151474133
|
T | C | 6 | a0001c0007t0023g0264a0001c0007t0023g0272a0001c0007t0023g0273others(3): Show | 6 | HG02647.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.7204+61T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474133 | ||||||
chr2:151474346
|
T | G | 1 | a0001c0022t0027g0193 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7204+274T>G | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474346 | ||||||
chr2:151474452
|
G | A | 37 | a0001c0004t0005g0052a0001c0004t0005g0062a0001c0004t0005g0063others(34): Show | 37 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.7204+380G>A | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474452 | ||||||
chr2:151474458
|
C | T | 1 | a0001c0002t0012g0173 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.7204+386C>T | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474458 | ||||||
chr2:151474619
|
T | C | 120 | a0001c0003t0002g0002a0001c0003t0002g0049a0001c0003t0002g0050others(117): Show | 120 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.7205-238T>C | RIF1 | ENSG00000080345.18 | transcript | ENST00000444746.7 | protein_coding | 35/35 | chr2 | 151474619 |