geneid | 57096 |
---|---|
ensemblid | ENSG00000092200.13 |
hgncid | 13436 |
symbol | RPGRIP1 |
name | RPGR interacting protein 1 |
refseq_nuc | NM_020366.4 |
refseq_prot | NP_065099.3 |
ensembl_nuc | ENST00000400017.7 |
ensembl_prot | ENSP00000382895.2 |
mane_status | MANE Select |
chr | chr14 |
start | 21280083 |
end | 21351301 |
strand | + |
ver | v1.2 |
region | chr14:21280083-21351301 |
region5000 | chr14:21275083-21356301 |
regionname0 | RPGRIP1_chr14_21280083_21351301 |
regionname5000 | RPGRIP1_chr14_21275083_21356301 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1286 | 141 | 28 | 23 | 67 | 7 | 14 | 47 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0002 | 0/0 | 1286 | 55 | 1 | 11 | 32 | 1 | 10 | 25 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003 | 0/0 | 1286 | 38 | 15 | 6 | 10 | 1 | 6 | 7 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004 | 0/0 | 1286 | 20 | 0 | 0 | 16 | 0 | 4 | 10 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0005 | 0/0 | 1286 | 17 | 14 | 2 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0006 | 0/0 | 1286 | 12 | 2 | 8 | 1 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0007 | 0/0 | 1286 | 11 | 1 | 2 | 0 | 2 | 6 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0008 | 0/0 | 1286 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0009 | 0/0 | 1286 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0010 | 0/0 | 1286 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0011 | 0/0 | 1286 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0012 | 0/0 | 1286 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0013 | 0/0 | 1286 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0014 | 0/0 | 1286 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0015 | 0/0 | 1286 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0016 | 0/0 | 1286 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0017 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0018 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0019 | 0/0 | 1286 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0020 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0021 | 0/0 | 1286 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0022 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0023 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0024 | 0/0 | 1286 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0025 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0026 | 0/0 | 1286 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0027 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0028 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0029 | 0/0 | 1286 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0030 | 0/0 | 1286 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0031 | 0/0 | 1286 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
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 | 3861 | 105 | 21 | 14 | 54 | 5 | 10 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0002 | 0/0 | 3861 | 52 | 1 | 9 | 32 | 1 | 9 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0003 | 0/0 | 3861 | 35 | 15 | 6 | 9 | 1 | 4 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0004 | 0/1 | 3861 | 30 | 5 | 8 | 11 | 2 | 3 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0005 | 0/0 | 3861 | 16 | 13 | 2 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0006 | 0/0 | 3861 | 12 | 2 | 8 | 1 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0007 | 0/0 | 3861 | 12 | 0 | 0 | 12 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0008 | 0/0 | 3861 | 8 | 1 | 2 | 0 | 1 | 4 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0009 | 0/0 | 3861 | 4 | 4 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0010 | 0/0 | 3861 | 4 | 0 | 0 | 3 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0011 | 0/0 | 3861 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0012 | 0/0 | 3861 | 3 | 0 | 0 | 1 | 0 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0013 | 0/0 | 3861 | 3 | 0 | 0 | 0 | 1 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0014 | 0/0 | 3861 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0015 | 0/0 | 3861 | 3 | 0 | 0 | 1 | 0 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0016 | 0/0 | 3861 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0017 | 0/0 | 3861 | 3 | 1 | 2 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0018 | 0/0 | 3861 | 2 | 0 | 2 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0019 | 0/0 | 3861 | 2 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0020 | 0/0 | 3861 | 2 | 0 | 0 | 2 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0021 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0022 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0023 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0024 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0025 | 0/0 | 3861 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0026 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0027 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0028 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0029 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0030 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0031 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0032 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0033 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0034 | 0/0 | 3861 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0035 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0036 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0037 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0038 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0039 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0040 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0041 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0042 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0043 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0044 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0045 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0046 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
c0047 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
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 | 1/1 | 201 | 313 | 72 | 55 | 128 | 14 | 42 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
t0002 | 0/0 | 201 | 7 | 7 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
t0003 | 0/0 | 201 | 6 | 5 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
t0004 | 0/0 | 201 | 4 | 4 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
t0005 | 0/0 | 201 | 2 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 3861 | 105 | 21 | 14 | 54 | 5 | 10 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0004 | 0/1 | 3861 | 30 | 5 | 8 | 11 | 2 | 3 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0020 | 0/0 | 3861 | 2 | 0 | 0 | 2 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0026 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0027 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0031 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0037 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0002c0002 | 0/0 | 3861 | 52 | 1 | 9 | 32 | 1 | 9 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0002c0018 | 0/0 | 3861 | 2 | 0 | 2 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0002c0039 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003c0003 | 0/0 | 3861 | 35 | 15 | 6 | 9 | 1 | 4 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003c0012 | 0/0 | 3861 | 3 | 0 | 0 | 1 | 0 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0007 | 0/0 | 3861 | 12 | 0 | 0 | 12 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0010 | 0/0 | 3861 | 4 | 0 | 0 | 3 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0015 | 0/0 | 3861 | 3 | 0 | 0 | 1 | 0 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0036 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0005c0005 | 0/0 | 3861 | 16 | 13 | 2 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0005c0046 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0006c0006 | 0/0 | 3861 | 12 | 2 | 8 | 1 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0007c0008 | 0/0 | 3861 | 8 | 1 | 2 | 0 | 1 | 4 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0007c0013 | 0/0 | 3861 | 3 | 0 | 0 | 0 | 1 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0008c0009 | 0/0 | 3861 | 4 | 4 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0009c0016 | 0/0 | 3861 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0010c0014 | 0/0 | 3861 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0011c0011 | 0/0 | 3861 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0012c0017 | 0/0 | 3861 | 3 | 1 | 2 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0013c0043 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0013c0044 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0014c0029 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0014c0047 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0015c0019 | 0/0 | 3861 | 2 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0016c0021 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0017c0038 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0018c0042 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0019c0041 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0020c0040 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0021c0045 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0022c0033 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0023c0028 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0024c0030 | 0/0 | 3861 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0025c0032 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0026c0034 | 0/0 | 3861 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0027c0035 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0028c0022 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0029c0023 | 0/0 | 3861 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0030c0025 | 0/0 | 3861 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0031c0024 | 0/0 | 3861 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4061 | 102 | 18 | 14 | 54 | 5 | 10 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0001t0002 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0001t0004 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0004t0001 | 0/1 | 4061 | 29 | 4 | 8 | 11 | 2 | 3 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0004t0002 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0020t0001 | 0/0 | 4061 | 2 | 0 | 0 | 2 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0026t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0027t0004 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0031t0001 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0001c0037t0001 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0002c0002t0001 | 0/0 | 4061 | 52 | 1 | 9 | 32 | 1 | 9 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0002c0018t0001 | 0/0 | 4061 | 2 | 0 | 2 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0002c0039t0001 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003c0003t0001 | 0/0 | 4061 | 26 | 7 | 5 | 9 | 1 | 4 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003c0003t0002 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003c0003t0003 | 0/0 | 4061 | 5 | 4 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003c0003t0005 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0003c0012t0001 | 0/0 | 4061 | 3 | 0 | 0 | 1 | 0 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0007t0001 | 0/0 | 4061 | 12 | 0 | 0 | 12 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0010t0001 | 0/0 | 4061 | 4 | 0 | 0 | 3 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0015t0001 | 0/0 | 4061 | 3 | 0 | 0 | 1 | 0 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0004c0036t0001 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0005c0005t0001 | 0/0 | 4061 | 15 | 12 | 2 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0005c0005t0002 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0005c0046t0002 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0006c0006t0001 | 0/0 | 4061 | 12 | 2 | 8 | 1 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0007c0008t0001 | 0/0 | 4061 | 8 | 1 | 2 | 0 | 1 | 4 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0007c0013t0001 | 0/0 | 4061 | 3 | 0 | 0 | 0 | 1 | 2 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0008c0009t0001 | 0/0 | 4061 | 4 | 4 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0009c0016t0001 | 0/0 | 4061 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0010c0014t0001 | 0/0 | 4061 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0011c0011t0001 | 0/0 | 4061 | 3 | 3 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0012c0017t0001 | 0/0 | 4061 | 3 | 1 | 2 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0013c0043t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0013c0044t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0014c0029t0004 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0014c0047t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0015c0019t0001 | 0/0 | 4061 | 2 | 2 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0016c0021t0001 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0017c0038t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0018c0042t0003 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0019c0041t0001 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0020c0040t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0021c0045t0001 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0022c0033t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0023c0028t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0024c0030t0001 | 0/0 | 4061 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0025c0032t0002 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0026c0034t0001 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0027c0035t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0028c0022t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0029c0023t0001 | 0/0 | 4061 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0030c0025t0001 | 0/0 | 4061 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
a0031c0024t0001 | 0/0 | 4061 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | copy fasta | chr14 | 21275083 | 21356301 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0223 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0004t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0020t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0020t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0026t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0027t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0031t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0001c0037t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0018t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0018t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0002c0039t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0003t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0012t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0012t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0003c0012t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0007t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0010t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0010t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0010t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0010t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0015t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0015t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0015t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0004c0036t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0005t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0005c0046t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0006c0006t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0008t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0013t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0013t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0007c0013t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0008c0009t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0008c0009t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0008c0009t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0008c0009t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0009c0016t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0009c0016t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0009c0016t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0010c0014t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0010c0014t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0010c0014t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0011c0011t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0011c0011t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0011c0011t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0012c0017t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0012c0017t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0012c0017t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0013c0043t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0013c0044t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0014c0029t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0014c0047t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0015c0019t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0015c0019t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0016c0021t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0017c0038t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0018c0042t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0019c0041t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0020c0040t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0021c0045t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0022c0033t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0023c0028t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0024c0030t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0025c0032t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0026c0034t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0027c0035t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0028c0022t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0029c0023t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0030c0025t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
a0031c0024t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0005 | t0001 | g0162 | EUR | GBR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00099 | hp2 | a0016 | c0021 | t0001 | g0045 | EUR | GBR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00140 | hp1 | a0006 | c0006 | t0001 | g0036 | EUR | GBR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0106 | EUR | GBR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00280 | hp1 | a0003 | c0003 | t0001 | g0164 | EUR | FIN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00323 | hp1 | a0001 | c0004 | t0001 | g0213 | EUR | FIN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | FIN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00408 | hp2 | a0001 | c0020 | t0001 | g0230 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00438 | hp1 | a0006 | c0006 | t0001 | g0035 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00544 | hp1 | a0001 | c0004 | t0001 | g0219 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00639 | hp2 | a0012 | c0017 | t0001 | g0323 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0222 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00673 | hp1 | a0001 | c0004 | t0001 | g0198 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00733 | hp2 | a0007 | c0008 | t0001 | g0157 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0260 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00738 | hp2 | a0001 | c0004 | t0001 | g0215 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0147 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG00741 | hp2 | a0021 | c0045 | t0001 | g0111 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01070 | hp2 | a0002 | c0018 | t0001 | g0030 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01071 | hp2 | a0002 | c0018 | t0001 | g0029 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01074 | hp1 | a0001 | c0004 | t0001 | g0242 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0071 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01099 | hp1 | a0001 | c0004 | t0001 | g0258 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01099 | hp2 | a0005 | c0005 | t0001 | g0167 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01109 | hp1 | a0003 | c0003 | t0003 | g0008 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01109 | hp2 | a0012 | c0017 | t0001 | g0320 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0098 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0221 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01257 | hp1 | a0006 | c0006 | t0001 | g0142 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01261 | hp2 | a0006 | c0006 | t0001 | g0182 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01346 | hp1 | a0006 | c0006 | t0001 | g0017 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01358 | hp1 | a0005 | c0005 | t0001 | g0306 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01433 | hp1 | a0006 | c0006 | t0001 | g0042 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01433 | hp2 | a0001 | c0031 | t0001 | g0274 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01496 | hp1 | a0003 | c0003 | t0001 | g0097 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01496 | hp2 | a0003 | c0003 | t0001 | g0039 | AMR | CLM | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01516 | hp1 | a0007 | c0008 | t0001 | g0165 | EUR | IBS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0211 | EUR | IBS | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01928 | hp2 | a0003 | c0003 | t0001 | g0108 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01975 | hp2 | a0001 | c0004 | t0001 | g0327 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG01993 | hp2 | a0007 | c0008 | t0001 | g0178 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02004 | hp1 | a0006 | c0006 | t0001 | g0041 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0259 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02027 | hp2 | a0030 | c0025 | t0001 | g0037 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02040 | hp1 | a0001 | c0004 | t0001 | g0200 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02055 | hp1 | a0028 | c0022 | t0001 | g0301 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02055 | hp2 | a0003 | c0003 | t0005 | g0015 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02074 | hp2 | a0003 | c0012 | t0001 | g0019 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02080 | hp1 | a0003 | c0003 | t0001 | g0224 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02083 | hp1 | a0004 | c0007 | t0001 | g0263 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02129 | hp1 | a0004 | c0010 | t0001 | g0202 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02135 | hp1 | a0004 | c0007 | t0001 | g0205 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02145 | hp1 | a0003 | c0003 | t0001 | g0176 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02145 | hp2 | a0005 | c0005 | t0001 | g0302 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02148 | hp1 | a0006 | c0006 | t0001 | g0038 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02148 | hp2 | a0006 | c0006 | t0001 | g0031 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02155 | hp1 | a0004 | c0010 | t0001 | g0238 | EAS | CDX | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | CDX | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02165 | hp1 | a0001 | c0004 | t0001 | g0212 | EAS | CDX | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02165 | hp2 | a0001 | c0020 | t0001 | g0229 | EAS | CDX | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02257 | hp1 | a0003 | c0003 | t0003 | g0011 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02258 | hp1 | a0013 | c0043 | t0001 | g0117 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02273 | hp2 | a0006 | c0006 | t0001 | g0048 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02280 | hp1 | a0005 | c0005 | t0001 | g0021 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02300 | hp1 | a0031 | c0024 | t0001 | g0040 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02300 | hp2 | a0003 | c0003 | t0001 | g0068 | AMR | PEL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02451 | hp1 | a0003 | c0003 | t0001 | g0307 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02523 | hp1 | a0004 | c0007 | t0001 | g0328 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02523 | hp2 | a0001 | c0004 | t0001 | g0254 | EAS | KHV | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02572 | hp2 | a0011 | c0011 | t0001 | g0128 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0085 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02615 | hp2 | a0003 | c0003 | t0001 | g0046 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02630 | hp1 | a0018 | c0042 | t0003 | g0012 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02630 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02683 | hp1 | a0003 | c0003 | t0001 | g0180 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02717 | hp1 | a0022 | c0033 | t0001 | g0001 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02723 | hp1 | a0005 | c0005 | t0001 | g0109 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02723 | hp2 | a0005 | c0005 | t0001 | g0300 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02809 | hp1 | a0020 | c0040 | t0001 | g0264 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02818 | hp1 | a0005 | c0005 | t0001 | g0044 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02818 | hp2 | a0008 | c0009 | t0001 | g0298 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02886 | hp1 | a0011 | c0011 | t0001 | g0126 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0188 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02895 | hp1 | a0009 | c0016 | t0001 | g0247 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02895 | hp2 | a0011 | c0011 | t0001 | g0005 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02896 | hp2 | a0009 | c0016 | t0001 | g0311 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02922 | hp1 | a0005 | c0005 | t0001 | g0020 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02922 | hp2 | a0010 | c0014 | t0001 | g0175 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02965 | hp1 | a0005 | c0005 | t0002 | g0303 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02965 | hp2 | a0003 | c0003 | t0003 | g0013 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02970 | hp1 | a0008 | c0009 | t0001 | g0110 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02970 | hp2 | a0003 | c0003 | t0003 | g0009 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0249 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02976 | hp2 | a0014 | c0029 | t0004 | g0172 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03041 | hp1 | a0010 | c0014 | t0001 | g0250 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03041 | hp2 | a0007 | c0008 | t0001 | g0113 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03098 | hp1 | a0014 | c0047 | t0001 | g0317 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03098 | hp2 | a0025 | c0032 | t0002 | g0183 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03139 | hp2 | a0005 | c0005 | t0001 | g0119 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0193 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03195 | hp2 | a0015 | c0019 | t0001 | g0192 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03209 | hp1 | a0005 | c0005 | t0001 | g0112 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03209 | hp2 | a0001 | c0004 | t0002 | g0244 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03225 | hp1 | a0005 | c0046 | t0002 | g0140 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0057 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03239 | hp2 | a0004 | c0010 | t0001 | g0237 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03453 | hp2 | a0006 | c0006 | t0001 | g0174 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0129 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03486 | hp2 | a0003 | c0003 | t0001 | g0308 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03490 | hp1 | a0003 | c0003 | t0001 | g0076 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03491 | hp1 | a0001 | c0004 | t0001 | g0201 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03491 | hp2 | a0007 | c0008 | t0001 | g0166 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0074 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0214 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03516 | hp1 | a0017 | c0038 | t0001 | g0121 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03516 | hp2 | a0003 | c0003 | t0002 | g0184 | AFR | ESN | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03540 | hp1 | a0001 | c0026 | t0001 | g0194 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0006 | AFR | GWD | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03579 | hp1 | a0023 | c0028 | t0001 | g0169 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0083 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03669 | hp1 | a0004 | c0015 | t0001 | g0225 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03669 | hp2 | a0003 | c0012 | t0001 | g0133 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03688 | hp2 | a0001 | c0037 | t0001 | g0270 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03704 | hp1 | a0007 | c0008 | t0001 | g0160 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03704 | hp2 | a0007 | c0013 | t0001 | g0155 | SAS | PJL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03831 | hp2 | a0003 | c0003 | t0001 | g0054 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03927 | hp2 | a0007 | c0008 | t0001 | g0163 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03942 | hp1 | a0002 | c0039 | t0001 | g0018 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0159 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04115 | hp2 | a0004 | c0036 | t0001 | g0280 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04199 | hp1 | a0019 | c0041 | t0001 | g0330 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04199 | hp2 | a0024 | c0030 | t0001 | g0313 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04204 | hp1 | a0001 | c0004 | t0001 | g0196 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0103 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04228 | hp1 | a0004 | c0015 | t0001 | g0236 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG04228 | hp2 | a0003 | c0012 | t0001 | g0161 | SAS | STU | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18522 | hp2 | a0005 | c0005 | t0001 | g0127 | AFR | YRI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18612 | hp1 | a0003 | c0003 | t0001 | g0027 | EAS | CHB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18612 | hp2 | a0004 | c0007 | t0001 | g0197 | EAS | CHB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18906 | hp1 | a0003 | c0003 | t0005 | g0014 | AFR | YRI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18946 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18947 | hp2 | a0001 | c0004 | t0001 | g0216 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18950 | hp2 | a0004 | c0007 | t0001 | g0322 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18959 | hp1 | a0004 | c0007 | t0001 | g0226 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18963 | hp2 | a0004 | c0007 | t0001 | g0285 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18965 | hp2 | a0001 | c0004 | t0001 | g0326 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18970 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18970 | hp2 | a0001 | c0004 | t0001 | g0208 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18978 | hp1 | a0004 | c0007 | t0001 | g0315 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18980 | hp1 | a0004 | c0007 | t0001 | g0268 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18981 | hp2 | a0001 | c0004 | t0001 | g0217 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18987 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18991 | hp2 | a0003 | c0003 | t0001 | g0084 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18993 | hp1 | a0004 | c0007 | t0001 | g0316 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19000 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19007 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19009 | hp1 | a0003 | c0003 | t0001 | g0082 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19009 | hp2 | a0026 | c0034 | t0001 | g0286 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19030 | hp1 | a0005 | c0005 | t0001 | g0116 | AFR | LWK | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19030 | hp2 | a0012 | c0017 | t0001 | g0022 | AFR | LWK | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19043 | hp1 | a0003 | c0003 | t0002 | g0185 | AFR | LWK | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19043 | hp2 | a0005 | c0005 | t0001 | g0120 | AFR | LWK | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19055 | hp1 | a0004 | c0015 | t0001 | g0218 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19058 | hp1 | a0001 | c0004 | t0001 | g0210 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19064 | hp1 | a0004 | c0007 | t0001 | g0321 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19084 | hp2 | a0004 | c0007 | t0001 | g0284 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19091 | hp1 | a0001 | c0004 | t0001 | g0209 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19091 | hp2 | a0004 | c0010 | t0001 | g0227 | EAS | JPT | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19240 | hp1 | a0027 | c0035 | t0001 | g0131 | AFR | YRI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA19240 | hp2 | a0013 | c0044 | t0001 | g0034 | AFR | YRI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20129 | hp1 | a0008 | c0009 | t0001 | g0253 | AFR | ASW | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ASW | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | TSI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20805 | hp2 | a0007 | c0013 | t0001 | g0158 | EUR | TSI | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20905 | hp1 | a0007 | c0013 | t0001 | g0154 | SAS | GIH | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20905 | hp2 | a0007 | c0008 | t0001 | g0100 | SAS | GIH | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02109 | hp1 | a0010 | c0014 | t0001 | g0276 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02559 | hp1 | a0006 | c0006 | t0001 | g0115 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG02559 | hp2 | a0015 | c0019 | t0001 | g0191 | AFR | ACB | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03471 | hp1 | a0009 | c0016 | t0001 | g0248 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG03471 | hp2 | a0001 | c0027 | t0004 | g0171 | AFR | MSL | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG06807 | hp1 | a0003 | c0003 | t0001 | g0186 | AFR | USA | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
HG06807 | hp2 | a0005 | c0005 | t0001 | g0118 | AFR | USA | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20300 | hp1 | a0008 | c0009 | t0001 | g0114 | AFR | USA | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | USA | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | LWK | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
NA21309 | hp2 | a0029 | c0023 | t0001 | g0299 | AFR | LWK | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0001 | g0223 | REF | REF | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0136 | REF | REF | RPGRIP1_chr14_21275083_21356301 | RPGRIP1 | chr14 | 21275083 | 21356301 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:21294686
|
T | A | 1 | a0016 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.95T>A | p.Met32Lys | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/25 | 210/4061 | 95/3861 | 32/1286 | chr14 | 21294686 | ||
chr14:21301003
|
C | T | 1 | a0012 | 3 | HG00639.hp2 HG01109.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.256C>T | p.Arg86Trp | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/25 | 371/4061 | 256/3861 | 86/1286 | chr14 | 21301003 | ||
chr14:21301034
|
C | A | 6 | a0006a0016a0028others(3): Show | 17 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(14): Show |
missense_variant | MODERATE | c.287C>A | p.Pro96Gln | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/25 | 402/4061 | 287/3861 | 96/1286 | chr14 | 21301034 | ||
chr14:21302571
|
A | G | 17 | a0002a0003a0005others(14): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
missense_variant | MODERATE | c.574A>G | p.Lys192Glu | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/25 | 689/4061 | 574/3861 | 192/1286 | chr14 | 21302571 | ||
chr14:21321881
|
G | T | 6 | a0005a0007a0011others(3): Show | 35 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(32): Show |
missense_variant | MODERATE | c.1639G>T | p.Ala547Ser | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/25 | 1754/4061 | 1639/3861 | 547/1286 | chr14 | 21321881 | ||
chr14:21324648
|
G | A | 4 | a0008a0017a0028others(1): Show | 7 | HG02055.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
missense_variant | MODERATE | c.1793G>A | p.Arg598Gln | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 15/25 | 1908/4061 | 1793/3861 | 598/1286 | chr14 | 21324648 | ||
chr14:21324651
|
C | T | 1 | a0018 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.1796C>T | p.Pro599Leu | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 15/25 | 1911/4061 | 1796/3861 | 599/1286 | chr14 | 21324651 | ||
chr14:21324657
|
C | G | 1 | a0026 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.1802C>G | p.Ser601Trp | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 15/25 | 1917/4061 | 1802/3861 | 601/1286 | chr14 | 21324657 | ||
chr14:21325880
|
C | T | 3 | a0009a0018a0022 | 5 | HG02630.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
missense_variant | MODERATE | c.2417C>T | p.Thr806Ile | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/25 | 2532/4061 | 2417/3861 | 806/1286 | chr14 | 21325880 | ||
chr14:21325898
|
G | A | 1 | a0019 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2435G>A | p.Arg812Gln | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/25 | 2550/4061 | 2435/3861 | 812/1286 | chr14 | 21325898 | ||
chr14:21326062
|
C | T | 1 | a0025 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.2599C>T | p.Arg867Trp | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/25 | 2714/4061 | 2599/3861 | 867/1286 | chr14 | 21326062 | ||
chr14:21326114
|
C | T | 1 | a0023 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.2651C>T | p.Ser884Leu | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/25 | 2766/4061 | 2651/3861 | 884/1286 | chr14 | 21326114 | ||
chr14:21327790
|
G | C | 1 | a0010 | 3 | HG02109.hp1 HG02922.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.2878G>C | p.Ala960Pro | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/25 | 2993/4061 | 2878/3861 | 960/1286 | chr14 | 21327790 | ||
chr14:21328473
|
C | G | 1 | a0024 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.2945C>G | p.Ser982Cys | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/25 | 3060/4061 | 2945/3861 | 982/1286 | chr14 | 21328473 | ||
chr14:21328625
|
G | C | 4 | a0002a0004a0007others(1): Show | 87 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
missense_variant&splice_region_variant | MODERATE | c.3097G>C | p.Glu1033Gln | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/25 | 3212/4061 | 3097/3861 | 1033/1286 | chr14 | 21328625 | ||
chr14:21343037
|
A | G | 3 | a0015a0021a0023 | 4 | HG00741.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
missense_variant&splice_region_variant | MODERATE | c.3341A>G | p.Asp1114Gly | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/25 | 3456/4061 | 3341/3861 | 1114/1286 | chr14 | 21343037 | ||
chr14:21348273
|
G | A | 7 | a0008a0011a0013others(4): Show | 14 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(11): Show |
missense_variant | MODERATE | c.3719G>A | p.Gly1240Glu | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/25 | 3834/4061 | 3719/3861 | 1240/1286 | chr14 | 21348273 | ||
chr14:21351179
|
C | G | 1 | a0030 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.3824C>G | p.Ala1275Gly | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 25/25 | 3939/4061 | 3824/3861 | 1275/1286 | chr14 | 21351179 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:21301197
|
C | G | 2 | a0001c0020a0004c0010 | 6 | HG00408.hp2 HG02129.hp1 HG02155.hp1 others(3): Show |
synonymous_variant | LOW | c.450C>G | p.Leu150Leu | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/25 | 565/4061 | 450/3861 | 150/1286 | chr14 | 21301197 | ||
chr14:21302522
|
A | G | 6 | a0001c0004a0004c0015a0009c0016others(3): Show | 42 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(39): Show |
synonymous_variant | LOW | c.525A>G | p.Pro175Pro | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/25 | 640/4061 | 525/3861 | 175/1286 | chr14 | 21302522 | ||
chr14:21317741
|
C | T | 2 | a0001c0037a0004c0036 | 2 | HG03688.hp2 HG04115.hp2 |
synonymous_variant | LOW | c.1197C>T | p.Asn399Asn | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/25 | 1312/4061 | 1197/3861 | 399/1286 | chr14 | 21317741 | ||
chr14:21322003
|
T | C | 1 | a0002c0018 | 2 | HG01070.hp2 HG01071.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1761T>C | p.Ser587Ser | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/25 | 1876/4061 | 1761/3861 | 587/1286 | chr14 | 21322003 | ||
chr14:21324652
|
G | A | 11 | a0001c0026a0002c0039a0003c0012others(8): Show | 37 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(34): Show |
synonymous_variant | LOW | c.1797G>A | p.Pro599Pro | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 15/25 | 1912/4061 | 1797/3861 | 599/1286 | chr14 | 21324652 | ||
chr14:21325308
|
G | A | 2 | a0001c0027a0023c0028 | 2 | HG03471.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.2292G>A | p.Ala764Ala | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 16/25 | 2407/4061 | 2292/3861 | 764/1286 | chr14 | 21325308 | ||
chr14:21327780
|
A | G | 1 | a0001c0031 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.2868A>G | p.Glu956Glu | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/25 | 2983/4061 | 2868/3861 | 956/1286 | chr14 | 21327780 | ||
chr14:21343143
|
C | T | 1 | a0013c0044 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.3447C>T | p.Tyr1149Tyr | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/25 | 3562/4061 | 3447/3861 | 1149/1286 | chr14 | 21343143 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:21280111
|
A | G | 3 | a0001c0001t0004a0001c0027t0004a0014c0029t0004 | 4 | HG02258.hp2 HG02622.hp1 HG02976.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-87A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/25 | 7866 | chr14 | 21280111 | |||||
chr14:21280145
|
G | T | 3 | a0003c0003t0003a0003c0003t0005a0018c0042t0003 | 8 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-53G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/25 | 7832 | chr14 | 21280145 | |||||
chr14:21351226
|
T | C | 7 | a0001c0001t0002a0001c0004t0002a0003c0003t0002others(4): Show | 9 | HG02055.hp2 HG02109.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 25/25 | 10 | chr14 | 21351226 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:21280195
|
A | G | 1 | a0001c0001t0001g0332 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-39+36A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280195 | ||||||
chr14:21280241
|
C | CT | 145 | a0001c0001t0001g0189a0001c0001t0001g0195a0001c0001t0001g0199others(142): Show | 145 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.-39+102dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21280241 | |||||
chr14:21280241
|
CT | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-39+102delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21280241 | |||||
chr14:21280266
|
CAG | C | 10 | a0001c0001t0001g0187a0003c0003t0001g0186a0003c0003t0002g0184others(7): Show | 10 | HG00741.hp2 HG01261.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-39+110_-39+111del others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21280266 | |||||
chr14:21280283
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-39+124G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280283 | ||||||
chr14:21280301
|
C | T | 112 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0043others(109): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-39+142C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280301 | ||||||
chr14:21280325
|
C | T | 3 | a0002c0002t0001g0107a0002c0002t0001g0181a0003c0003t0001g0108 | 3 | HG00639.hp1 HG01928.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-39+166C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280325 | ||||||
chr14:21280376
|
TG | T | 45 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0043others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-39+221delG | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21280376 | |||||
chr14:21280487
|
T | C | 51 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0043others(48): Show | 51 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-39+328T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280487 | ||||||
chr14:21280648
|
C | T | 1 | a0006c0006t0001g0048 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-39+489C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280648 | ||||||
chr14:21280937
|
T | A | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-39+778T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280937 | ||||||
chr14:21280988
|
T | G | 10 | a0001c0001t0001g0189a0001c0004t0001g0188a0001c0004t0001g0190others(7): Show | 10 | HG00741.hp2 HG02257.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+829T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280988 | ||||||
chr14:21280997
|
T | G | 1 | a0001c0004t0001g0193 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-39+838T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21280997 | ||||||
chr14:21281016
|
GCTTTT | G | 6 | a0001c0001t0001g0187a0003c0003t0001g0186a0003c0003t0002g0184others(3): Show | 6 | HG01261.hp2 HG03098.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+863_-39+867del others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281016 | |||||
chr14:21281030
|
T | C | 46 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0043others(43): Show | 46 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.-39+871T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281030 | ||||||
chr14:21281057
|
C | T | 8 | a0003c0003t0003g0008a0003c0003t0003g0009a0003c0003t0003g0010others(5): Show | 8 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39+898C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281057 | ||||||
chr14:21281112
|
G | A | 4 | a0003c0003t0003g0008a0003c0003t0003g0009a0003c0003t0003g0010others(1): Show | 4 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+953G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281112 | ||||||
chr14:21281136
|
A | T | 62 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0099others(59): Show | 62 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.-39+977A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281136 | ||||||
chr14:21281164
|
C | T | 6 | a0003c0003t0003g0011a0005c0005t0001g0109a0005c0005t0001g0112others(3): Show | 6 | HG00741.hp2 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+1005C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281164 | ||||||
chr14:21281228
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-39+1069C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281228 | ||||||
chr14:21281229
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-39+1070G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281229 | ||||||
chr14:21281254
|
T | G | 1 | a0001c0026t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-39+1095T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281254 | ||||||
chr14:21281301
|
C | T | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-39+1142C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281301 | ||||||
chr14:21281314
|
A | G | 62 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0043others(59): Show | 62 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(59): Show |
intron_variant | MODIFIER | c.-39+1155A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281314 | ||||||
chr14:21281407
|
GC | G | 9 | a0005c0005t0001g0116a0005c0005t0001g0118a0005c0005t0001g0119others(6): Show | 9 | HG02258.hp1 HG02559.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39+1251delC | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281407 | |||||
chr14:21281595
|
A | G | 1 | a0002c0002t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-39+1436A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281595 | ||||||
chr14:21281670
|
C | T | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-39+1511C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281670 | ||||||
chr14:21281698
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39+1539A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281698 | ||||||
chr14:21281699
|
A | T | 58 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0047others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(55): Show |
intron_variant | MODIFIER | c.-39+1540A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281699 | ||||||
chr14:21281700
|
AAAT | A | 11 | a0001c0001t0001g0016a0001c0001t0004g0170a0001c0001t0004g0177others(8): Show | 11 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39+1544_-39+1546d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281700 | |||||
chr14:21281701
|
A | T | 1 | a0001c0001t0001g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-39+1542A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281701 | ||||||
chr14:21281703
|
T | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0195others(12): Show | 15 | HG00642.hp2 HG01884.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-39+1544T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281703 | ||||||
chr14:21281704
|
A | AAAT | 151 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0099others(148): Show | 151 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-39+1576_-39+1578d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281704 | |||||
chr14:21281704
|
A | AAATAAT | 34 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(31): Show | 34 | HG00408.hp2 HG01074.hp1 HG02074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-39+1573_-39+1578d others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281704 | |||||
chr14:21281704
|
A | AAATAATA others(2): Show |
32 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0206others(29): Show | 32 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-39+1570_-39+1578d others(11): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281704 | |||||
chr14:21281704
|
A | AAATAATA others(5): Show |
2 | a0001c0001t0001g0199a0001c0004t0001g0198 | 2 | HG00673.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-39+1567_-39+1578d others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281704 | |||||
chr14:21281704
|
A | AAATAATA others(8): Show |
2 | a0001c0004t0001g0196a0004c0007t0001g0197 | 2 | HG04204.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-39+1564_-39+1578d others(17): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281704 | |||||
chr14:21281704
|
A | AAT | 3 | a0001c0001t0001g0329a0001c0004t0001g0327a0004c0007t0001g0328 | 3 | HG01975.hp2 HG02523.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-39+1546_-39+1547i others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281704 | |||||
chr14:21281704
|
A | T | 2 | a0001c0001t0001g0003a0003c0003t0001g0050 | 2 | HG02809.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-39+1545A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281704 | ||||||
chr14:21281704
|
AAAT | A | 4 | a0003c0003t0003g0013a0003c0003t0005g0014a0003c0003t0005g0015others(1): Show | 4 | HG01261.hp2 HG02055.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+1576_-39+1578d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281704 | |||||
chr14:21281707
|
T | A | 8 | a0001c0001t0004g0170a0001c0001t0004g0177a0001c0027t0004g0171others(5): Show | 8 | HG01109.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+1548T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281707 | ||||||
chr14:21281710
|
T | A | 2 | a0001c0001t0004g0177a0023c0028t0001g0169 | 2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-39+1551T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281710 | ||||||
chr14:21281801
|
GA | G | 5 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(2): Show | 5 | HG00741.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+1650delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21281801 | |||||
chr14:21281803
|
A | C | 4 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(1): Show | 4 | HG03098.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+1644A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281803 | ||||||
chr14:21281850
|
G | A | 56 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0047others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(53): Show |
intron_variant | MODIFIER | c.-39+1691G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281850 | ||||||
chr14:21281884
|
G | A | 1 | a0002c0002t0001g0053 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-39+1725G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281884 | ||||||
chr14:21281891
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(8): Show | 11 | HG01884.hp2 HG02258.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-39+1732G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281891 | ||||||
chr14:21281917
|
A | C | 4 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(1): Show | 4 | HG03098.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+1758A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281917 | ||||||
chr14:21281927
|
T | C | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-39+1768T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21281927 | ||||||
chr14:21282149
|
C | T | 55 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0047others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.-39+1990C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282149 | ||||||
chr14:21282198
|
T | C | 61 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0047others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(58): Show |
intron_variant | MODIFIER | c.-39+2039T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282198 | ||||||
chr14:21282215
|
T | C | 1 | a0001c0001t0001g0243 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-39+2056T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282215 | ||||||
chr14:21282255
|
T | C | 1 | a0003c0003t0001g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-39+2096T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282255 | ||||||
chr14:21282261
|
G | A | 3 | a0003c0003t0003g0013a0003c0003t0005g0014a0003c0003t0005g0015 | 3 | HG02055.hp2 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-39+2102G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282261 | ||||||
chr14:21282403
|
A | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-39+2244A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282403 | ||||||
chr14:21282447
|
A | G | 4 | a0001c0004t0001g0221a0001c0004t0001g0222a0001c0004t0001g0223others(1): Show | 4 | HG00642.hp1 HG01074.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+2288A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282447 | ||||||
chr14:21282530
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-39+2371C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282530 | ||||||
chr14:21282605
|
A | AT | 36 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0102others(33): Show | 36 | HG00423.hp2 HG00741.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.-39+2468dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21282605 | |||||
chr14:21282605
|
AT | A | 9 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0002g0004others(6): Show | 9 | HG00099.hp2 HG01993.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39+2468delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21282605 | |||||
chr14:21282605
|
ATT | A | 52 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0047others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(49): Show |
intron_variant | MODIFIER | c.-39+2467_-39+2468d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21282605 | |||||
chr14:21282678
|
C | T | 2 | a0001c0001t0001g0309a0001c0001t0001g0319 | 2 | NA18990.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-39+2519C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282678 | ||||||
chr14:21282755
|
G | A | 4 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(1): Show | 4 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+2596G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282755 | ||||||
chr14:21282770
|
C | T | 60 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0099others(57): Show | 60 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.-39+2611C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282770 | ||||||
chr14:21282774
|
T | C | 2 | a0001c0001t0001g0134a0002c0002t0001g0310 | 2 | NA18968.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.-39+2615T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282774 | ||||||
chr14:21282875
|
G | T | 4 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(1): Show | 4 | HG03098.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+2716G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282875 | ||||||
chr14:21282878
|
G | A | 1 | a0002c0002t0001g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-39+2719G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282878 | ||||||
chr14:21282901
|
T | C | 55 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0047others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.-39+2742T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282901 | ||||||
chr14:21282925
|
C | T | 55 | a0001c0001t0001g0025a0001c0001t0001g0043a0001c0001t0001g0047others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.-39+2766C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282925 | ||||||
chr14:21282961
|
A | G | 61 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0099others(58): Show | 61 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-39+2802A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282961 | ||||||
chr14:21282988
|
G | A | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-39+2829G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21282988 | ||||||
chr14:21283039
|
T | C | 6 | a0001c0001t0001g0187a0003c0003t0001g0186a0003c0003t0002g0184others(3): Show | 6 | HG01261.hp2 HG03098.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+2880T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283039 | ||||||
chr14:21283067
|
A | G | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-39+2908A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283067 | ||||||
chr14:21283098
|
G | A | 2 | a0001c0001t0001g0199a0001c0004t0001g0196 | 2 | HG04204.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-39+2939G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283098 | ||||||
chr14:21283101
|
C | T | 1 | a0001c0001t0001g0168 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-39+2942C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283101 | ||||||
chr14:21283184
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-39+3025A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283184 | ||||||
chr14:21283322
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0005c0005t0001g0109others(5): Show | 8 | HG00741.hp2 HG01884.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39+3163A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283322 | ||||||
chr14:21283552
|
C | T | 25 | a0001c0001t0001g0043a0003c0003t0001g0159a0003c0003t0001g0164others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.-39+3393C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283552 | ||||||
chr14:21283554
|
G | T | 1 | a0016c0021t0001g0045 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-39+3395G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283554 | ||||||
chr14:21283643
|
A | G | 1 | a0001c0001t0001g0305 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-39+3484A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283643 | ||||||
chr14:21283653
|
A | C | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-39+3494A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283653 | ||||||
chr14:21283782
|
C | A | 2 | a0001c0001t0001g0199a0001c0004t0001g0196 | 2 | HG04204.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-39+3623C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283782 | ||||||
chr14:21283782
|
C | T | 1 | a0002c0002t0001g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-39+3623C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283782 | ||||||
chr14:21283838
|
C | G | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-39+3679C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21283838 | ||||||
chr14:21284051
|
A | G | 40 | a0001c0001t0002g0004a0002c0039t0001g0018a0003c0003t0001g0039others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(37): Show |
intron_variant | MODIFIER | c.-38-3888A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284051 | ||||||
chr14:21284141
|
G | A | 3 | a0009c0016t0001g0247a0009c0016t0001g0248a0009c0016t0001g0311 | 3 | HG02895.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-38-3798G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284141 | ||||||
chr14:21284218
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-38-3721A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284218 | ||||||
chr14:21284364
|
G | A | 120 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.-38-3575G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284364 | ||||||
chr14:21284402
|
ACTGGTAA others(15): Show |
A | 5 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(2): Show | 5 | HG00741.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-3534_-38-3513d others(24): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21284402 | |||||
chr14:21284540
|
A | AT | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(234): Show | 237 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-38-3379dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21284540 | |||||
chr14:21284540
|
A | ATT | 68 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(65): Show | 68 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-38-3380_-38-3379d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21284540 | |||||
chr14:21284540
|
A | ATTT | 6 | a0001c0001t0001g0099a0002c0002t0001g0105a0003c0003t0001g0097others(3): Show | 6 | HG01256.hp1 HG01496.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38-3381_-38-3379d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21284540 | |||||
chr14:21284566
|
T | C | 75 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(72): Show | 75 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-38-3373T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284566 | ||||||
chr14:21284685
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-38-3254C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284685 | ||||||
chr14:21284957
|
G | T | 1 | a0005c0005t0001g0306 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-38-2982G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284957 | ||||||
chr14:21284957
|
GTTCGTTC others(1536): Show |
G | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-38-2981_-38-1439d others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21284957 | ||||||
chr14:21285027
|
C | T | 1 | a0005c0005t0001g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-38-2912C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21285027 | ||||||
chr14:21285302
|
G | A | 1 | a0013c0044t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-38-2637G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21285302 | ||||||
chr14:21285364
|
G | A | 1 | a0003c0003t0001g0062 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-38-2575G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21285364 | ||||||
chr14:21285394
|
A | G | 3 | a0005c0005t0001g0120a0008c0009t0001g0114a0017c0038t0001g0121 | 3 | HG03516.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-38-2545A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21285394 | ||||||
chr14:21285489
|
G | C | 140 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0025others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-38-2450G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21285489 | ||||||
chr14:21285605
|
C | CA | 131 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.-38-2320dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21285605 | |||||
chr14:21286027
|
T | C | 3 | a0007c0013t0001g0154a0007c0013t0001g0155a0007c0013t0001g0158 | 3 | HG03704.hp2 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-38-1912T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286027 | ||||||
chr14:21286033
|
A | G | 1 | a0002c0002t0001g0096 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-38-1906A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286033 | ||||||
chr14:21286146
|
C | T | 1 | a0017c0038t0001g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-38-1793C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286146 | ||||||
chr14:21286151
|
G | A | 1 | a0001c0004t0001g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-38-1788G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286151 | ||||||
chr14:21286172
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257others(1): Show | 4 | HG00544.hp2 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38-1767G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286172 | ||||||
chr14:21286206
|
G | T | 79 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(76): Show | 79 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-38-1733G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286206 | ||||||
chr14:21286451
|
G | A | 6 | a0005c0005t0001g0109a0005c0005t0001g0112a0006c0006t0001g0182others(3): Show | 6 | HG00741.hp2 HG01261.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-1488G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286451 | ||||||
chr14:21286499
|
A | C | 2 | a0004c0010t0001g0237a0004c0010t0001g0238 | 2 | HG02155.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-38-1440A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286499 | ||||||
chr14:21286877
|
T | A | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-38-1062T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21286877 | ||||||
chr14:21287015
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0043 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-38-924C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287015 | ||||||
chr14:21287049
|
G | GAGGA | 10 | a0001c0001t0001g0016a0001c0001t0004g0170a0001c0027t0004g0171others(7): Show | 10 | HG00741.hp2 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38-872_-38-869dup others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21287049 | |||||
chr14:21287100
|
GA | G | 9 | a0003c0003t0001g0006a0003c0003t0003g0008a0003c0003t0003g0009others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38-832delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr14 | 21287100 | |||||
chr14:21287160
|
G | A | 6 | a0002c0002t0001g0063a0002c0002t0001g0064a0002c0002t0001g0065others(3): Show | 6 | HG02080.hp1 HG02083.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-779G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287160 | ||||||
chr14:21287213
|
C | A | 9 | a0003c0003t0001g0006a0003c0003t0003g0008a0003c0003t0003g0009others(6): Show | 9 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38-726C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287213 | ||||||
chr14:21287224
|
C | G | 1 | a0002c0002t0001g0107 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-38-715C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287224 | ||||||
chr14:21287499
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0004g0170a0001c0027t0004g0171others(2): Show | 5 | HG02258.hp2 HG02976.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-440C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287499 | ||||||
chr14:21287568
|
G | A | 4 | a0001c0004t0001g0258a0001c0004t0001g0259a0001c0004t0001g0260others(1): Show | 4 | HG00735.hp2 HG01099.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-371G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287568 | ||||||
chr14:21287575
|
A | G | 54 | a0001c0001t0002g0004a0001c0001t0004g0177a0002c0039t0001g0018others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.-38-364A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287575 | ||||||
chr14:21287612
|
A | T | 1 | a0001c0004t0001g0254 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-38-327A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287612 | ||||||
chr14:21287695
|
A | T | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-38-244A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 1/24 | chr14 | 21287695 | ||||||
chr14:21288180
|
C | CT | 86 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(83): Show | 86 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.85+137dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21288180 | |||||
chr14:21288180
|
CT | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0199others(5): Show | 8 | HG01884.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+137delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21288180 | |||||
chr14:21288195
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.85+134T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288195 | ||||||
chr14:21288247
|
C | T | 1 | a0002c0002t0001g0095 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.85+186C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288247 | ||||||
chr14:21288433
|
G | A | 1 | a0006c0006t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.85+372G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288433 | ||||||
chr14:21288451
|
T | A | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.85+390T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288451 | ||||||
chr14:21288451
|
T | G | 144 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0043others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.85+390T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288451 | ||||||
chr14:21288706
|
G | T | 1 | a0018c0042t0003g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.85+645G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288706 | ||||||
chr14:21288756
|
C | T | 1 | a0001c0004t0001g0219 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.85+695C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288756 | ||||||
chr14:21288767
|
G | T | 2 | a0005c0005t0002g0303a0014c0047t0001g0317 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.85+706G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288767 | ||||||
chr14:21288776
|
C | A | 4 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(1): Show | 4 | HG03098.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+715C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288776 | ||||||
chr14:21288804
|
T | C | 89 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(86): Show | 89 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.85+743T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288804 | ||||||
chr14:21288869
|
A | C | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.85+808A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288869 | ||||||
chr14:21288885
|
A | G | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.85+824A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288885 | ||||||
chr14:21288913
|
A | G | 54 | a0001c0001t0002g0004a0001c0001t0004g0177a0002c0039t0001g0018others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.85+852A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288913 | ||||||
chr14:21288933
|
C | T | 1 | a0001c0004t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.85+872C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21288933 | ||||||
chr14:21289041
|
T | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0043 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.85+980T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21289041 | ||||||
chr14:21289053
|
C | T | 31 | a0001c0001t0001g0199a0001c0001t0001g0207a0001c0001t0001g0332others(28): Show | 31 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.85+992C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21289053 | ||||||
chr14:21289189
|
G | A | 20 | a0003c0003t0001g0006a0003c0003t0001g0039a0003c0003t0003g0008others(17): Show | 20 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.85+1128G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21289189 | ||||||
chr14:21289339
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.85+1278C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21289339 | ||||||
chr14:21289462
|
C | T | 1 | a0002c0002t0001g0033 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.85+1401C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21289462 | ||||||
chr14:21289683
|
G | A | 5 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(2): Show | 5 | HG01261.hp2 HG03098.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.85+1622G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21289683 | ||||||
chr14:21289766
|
G | A | 3 | a0001c0001t0001g0239a0004c0007t0001g0226a0004c0007t0001g0321 | 3 | NA18959.hp1 NA19002.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.85+1705G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21289766 | ||||||
chr14:21289865
|
A | AT | 11 | a0002c0039t0001g0018a0003c0003t0001g0006a0003c0003t0003g0008others(8): Show | 11 | HG01109.hp1 HG02055.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.85+1813dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21289865 | |||||
chr14:21289865
|
A | ATT | 52 | a0001c0001t0002g0004a0001c0001t0004g0177a0003c0003t0001g0039others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.85+1812_85+1813dup others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21289865 | |||||
chr14:21290000
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.85+1939G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290000 | ||||||
chr14:21290265
|
G | T | 1 | a0001c0004t0001g0260 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.85+2204G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290265 | ||||||
chr14:21290289
|
A | G | 2 | a0001c0004t0001g0258a0001c0004t0001g0259 | 2 | HG01099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.85+2228A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290289 | ||||||
chr14:21290372
|
A | T | 4 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(1): Show | 4 | HG03098.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+2311A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290372 | ||||||
chr14:21290399
|
C | G | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.85+2338C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290399 | ||||||
chr14:21290582
|
C | T | 7 | a0003c0003t0001g0249a0005c0005t0001g0300a0005c0005t0001g0302others(4): Show | 7 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.85+2521C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290582 | ||||||
chr14:21290696
|
G | A | 48 | a0001c0001t0004g0177a0002c0039t0001g0018a0003c0003t0001g0039others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.85+2635G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290696 | ||||||
chr14:21290774
|
G | A | 80 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(77): Show | 80 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.85+2713G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290774 | ||||||
chr14:21290797
|
C | T | 1 | a0009c0016t0001g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.85+2736C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290797 | ||||||
chr14:21290800
|
C | T | 80 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(77): Show | 80 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.85+2739C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290800 | ||||||
chr14:21290818
|
C | CA | 57 | a0001c0001t0001g0067a0001c0001t0001g0262a0001c0001t0002g0004others(54): Show | 57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.85+2771dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21290818 | |||||
chr14:21290818
|
CA | C | 11 | a0001c0001t0001g0329a0002c0002t0001g0032a0003c0003t0001g0006others(8): Show | 11 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.85+2771delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21290818 | |||||
chr14:21290994
|
C | G | 1 | a0006c0006t0001g0017 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.85+2933C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21290994 | ||||||
chr14:21291000
|
C | CA | 78 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(75): Show | 78 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.85+2955dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21291000 | |||||
chr14:21291068
|
A | G | 1 | a0002c0002t0001g0093 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.85+3007A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21291068 | ||||||
chr14:21291105
|
A | G | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.85+3044A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21291105 | ||||||
chr14:21291206
|
T | A | 4 | a0001c0001t0004g0170a0001c0027t0004g0171a0014c0029t0004g0172others(1): Show | 4 | HG02258.hp2 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.85+3145T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21291206 | ||||||
chr14:21291364
|
T | A | 1 | a0004c0007t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85+3303T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21291364 | ||||||
chr14:21291542
|
T | G | 54 | a0001c0001t0002g0004a0001c0001t0004g0177a0002c0039t0001g0018others(51): Show | 54 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(51): Show |
intron_variant | MODIFIER | c.86-3135T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21291542 | ||||||
chr14:21291606
|
G | A | 1 | a0020c0040t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.86-3071G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21291606 | ||||||
chr14:21291642
|
G | A | 1 | a0001c0004t0001g0327 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.86-3035G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21291642 | ||||||
chr14:21292003
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.86-2674C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292003 | ||||||
chr14:21292021
|
G | A | 5 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(2): Show | 5 | HG00741.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-2656G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292021 | ||||||
chr14:21292143
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.86-2534T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292143 | ||||||
chr14:21292183
|
C | T | 7 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0240others(4): Show | 7 | HG02083.hp1 HG02129.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.86-2494C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292183 | ||||||
chr14:21292320
|
A | AT | 55 | a0001c0001t0001g0153a0001c0001t0002g0004a0001c0001t0004g0177others(52): Show | 55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.86-2346dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21292320 | |||||
chr14:21292379
|
G | A | 2 | a0001c0001t0001g0007a0001c0001t0001g0043 | 2 | HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.86-2298G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292379 | ||||||
chr14:21292526
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.86-2151G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292526 | ||||||
chr14:21292573
|
G | T | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-2104G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292573 | ||||||
chr14:21292714
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.86-1963T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292714 | ||||||
chr14:21292873
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.86-1804G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292873 | ||||||
chr14:21292918
|
G | A | 1 | a0001c0004t0001g0219 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.86-1759G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21292918 | ||||||
chr14:21293101
|
G | A | 5 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(2): Show | 5 | HG00741.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-1576G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293101 | ||||||
chr14:21293165
|
C | T | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-1512C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293165 | ||||||
chr14:21293451
|
T | C | 2 | a0001c0001t0001g0267a0024c0030t0001g0313 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.86-1226T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293451 | ||||||
chr14:21293476
|
C | T | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-1201C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293476 | ||||||
chr14:21293548
|
G | A | 5 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(2): Show | 5 | HG00741.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.86-1129G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293548 | ||||||
chr14:21293645
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.86-1032G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293645 | ||||||
chr14:21293674
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.86-1003C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293674 | ||||||
chr14:21293866
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.86-811G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293866 | ||||||
chr14:21293874
|
G | A | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-803G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21293874 | ||||||
chr14:21294052
|
C | CA | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.86-606dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21294052 | |||||
chr14:21294052
|
C | CAA | 15 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0001t0001g0318others(12): Show | 15 | HG00438.hp1 HG00597.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.86-607_86-606dupAA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21294052 | |||||
chr14:21294069
|
A | AG | 5 | a0001c0001t0001g0016a0001c0001t0004g0170a0001c0027t0004g0171others(2): Show | 5 | HG02258.hp2 HG02976.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-608_86-607insG | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21294069 | ||||||
chr14:21294184
|
T | A | 1 | a0013c0044t0001g0034 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.86-493T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21294184 | ||||||
chr14:21294233
|
G | GT | 6 | a0001c0001t0001g0125a0001c0001t0001g0265a0001c0001t0001g0314others(3): Show | 6 | HG00438.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.86-431dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21294233 | |||||
chr14:21294233
|
GT | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0043others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.86-431delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr14 | 21294233 | |||||
chr14:21294412
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0004g0170a0001c0027t0004g0171others(2): Show | 5 | HG02258.hp2 HG02976.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-265T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21294412 | ||||||
chr14:21294613
|
C | G | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.86-64C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 2/24 | chr14 | 21294613 | ||||||
chr14:21294830
|
A | AT | 27 | a0001c0001t0001g0132a0001c0001t0001g0139a0001c0001t0001g0148others(24): Show | 27 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(24): Show |
intron_variant | MODIFIER | c.218+53dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
A | ATT | 39 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(36): Show | 39 | HG00323.hp1 HG00642.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.218+52_218+53dupTT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
A | ATTT | 38 | a0001c0001t0001g0125a0001c0001t0001g0152a0001c0001t0001g0168others(35): Show | 38 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.218+51_218+53dupTT others(1): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
A | ATTTT | 28 | a0001c0001t0001g0016a0001c0001t0001g0156a0001c0001t0001g0189others(25): Show | 28 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.218+50_218+53dupTT others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
A | T | 1 | a0009c0016t0001g0247 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.218+21A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21294830 | ||||||
chr14:21294830
|
AT | A | 7 | a0001c0001t0001g0173a0001c0001t0001g0331a0001c0001t0004g0170others(4): Show | 7 | HG01257.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+53delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(1): Show |
A | 45 | a0001c0001t0004g0177a0002c0039t0001g0018a0003c0003t0001g0039others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.218+46_218+53delTT others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(2): Show |
A | 9 | a0001c0001t0001g0099a0002c0002t0001g0023a0002c0002t0001g0085others(6): Show | 9 | HG02080.hp1 HG02135.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.218+45_218+53delTT others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(3): Show |
A | 63 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(60): Show | 63 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.218+44_218+53delTT others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(4): Show |
A | 8 | a0001c0001t0001g0187a0002c0002t0001g0070a0003c0003t0001g0050others(5): Show | 8 | HG01109.hp1 HG03516.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.218+43_218+53delTT others(9): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(5): Show |
A | 10 | a0001c0001t0001g0007a0001c0001t0001g0043a0003c0003t0001g0006others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.218+42_218+53delTT others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(7): Show |
A | 1 | a0014c0047t0001g0317 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+40_218+53delTT others(12): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(9): Show |
A | 1 | a0001c0004t0001g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.218+38_218+53delTT others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294830
|
ATTTTTTT others(10): Show |
A | 2 | a0001c0026t0001g0194a0005c0005t0002g0303 | 2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.218+37_218+53delTT others(15): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21294830 | |||||
chr14:21294836
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.218+27T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21294836 | ||||||
chr14:21294984
|
T | G | 1 | a0001c0004t0001g0129 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.218+175T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21294984 | ||||||
chr14:21295014
|
A | T | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.218+205A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295014 | ||||||
chr14:21295053
|
A | C | 4 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(1): Show | 4 | HG03098.hp2 HG03516.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+244A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295053 | ||||||
chr14:21295096
|
G | A | 1 | a0014c0047t0001g0317 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+287G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295096 | ||||||
chr14:21295139
|
C | T | 1 | a0014c0029t0004g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218+330C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295139 | ||||||
chr14:21295170
|
C | T | 1 | a0001c0004t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.218+361C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295170 | ||||||
chr14:21295194
|
A | T | 1 | a0001c0001t0001g0282 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.218+385A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295194 | ||||||
chr14:21295198
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0279 | 2 | NA19056.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.218+389C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295198 | ||||||
chr14:21295237
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.218+428G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295237 | ||||||
chr14:21295249
|
A | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.218+440A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295249 | ||||||
chr14:21295282
|
G | T | 50 | a0001c0001t0002g0004a0001c0001t0004g0177a0002c0039t0001g0018others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.218+473G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295282 | ||||||
chr14:21295302
|
T | A | 1 | a0001c0001t0001g0252 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.218+493T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295302 | ||||||
chr14:21295337
|
C | G | 1 | a0001c0001t0001g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218+528C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295337 | ||||||
chr14:21295444
|
CATTTATT others(1): Show |
C | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.218+656_218+663del others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21295444 | |||||
chr14:21295478
|
AT | A | 127 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0122others(124): Show | 127 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.218+691delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21295478 | |||||
chr14:21295478
|
ATT | A | 10 | a0001c0001t0001g0168a0001c0001t0001g0199a0001c0001t0001g0243others(7): Show | 10 | HG00280.hp2 HG01261.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+690_218+691del others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21295478 | |||||
chr14:21295478
|
ATTTTTTT | A | 18 | a0002c0002t0001g0083a0003c0003t0001g0006a0003c0003t0003g0008others(15): Show | 18 | HG00741.hp2 HG01109.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.218+685_218+691del others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21295478 | |||||
chr14:21295478
|
ATTTTTTT others(1): Show |
A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.218+684_218+691del others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21295478 | |||||
chr14:21295536
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.218+727C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295536 | ||||||
chr14:21295633
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.218+824G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295633 | ||||||
chr14:21295642
|
C | T | 1 | a0001c0001t0001g0319 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.218+833C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295642 | ||||||
chr14:21295665
|
G | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.218+856G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295665 | ||||||
chr14:21295677
|
T | A | 1 | a0003c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.218+868T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295677 | ||||||
chr14:21295815
|
G | A | 9 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(6): Show | 9 | HG01884.hp2 HG02622.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+1006G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295815 | ||||||
chr14:21295980
|
A | G | 4 | a0001c0001t0001g0016a0001c0027t0004g0171a0014c0029t0004g0172others(1): Show | 4 | HG02976.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.218+1171A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295980 | ||||||
chr14:21295997
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.218+1188G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21295997 | ||||||
chr14:21296005
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.218+1196G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296005 | ||||||
chr14:21296099
|
C | A | 21 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0240others(18): Show | 21 | HG02027.hp1 HG02083.hp1 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.218+1290C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296099 | ||||||
chr14:21296102
|
A | AT | 6 | a0001c0001t0001g0252a0001c0001t0001g0314a0001c0001t0001g0324others(3): Show | 6 | HG02895.hp1 HG03927.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+1309dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21296102 | |||||
chr14:21296124
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.218+1315C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296124 | ||||||
chr14:21296286
|
C | T | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.218+1477C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296286 | ||||||
chr14:21296378
|
A | AT | 7 | a0001c0001t0001g0149a0001c0001t0001g0220a0002c0002t0001g0086others(4): Show | 7 | HG02738.hp2 HG03098.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+1584dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21296378 | |||||
chr14:21296479
|
G | A | 2 | a0012c0017t0001g0022a0012c0017t0001g0320 | 2 | HG01109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.218+1670G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296479 | ||||||
chr14:21296506
|
G | T | 1 | a0003c0003t0001g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218+1697G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296506 | ||||||
chr14:21296536
|
A | T | 1 | a0003c0003t0001g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218+1727A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296536 | ||||||
chr14:21296598
|
A | G | 68 | a0001c0001t0002g0004a0001c0001t0004g0177a0002c0039t0001g0018others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(65): Show |
intron_variant | MODIFIER | c.218+1789A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296598 | ||||||
chr14:21296653
|
T | C | 1 | a0004c0010t0001g0237 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.218+1844T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296653 | ||||||
chr14:21296688
|
G | A | 73 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(70): Show | 73 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.218+1879G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296688 | ||||||
chr14:21296725
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.218+1916G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296725 | ||||||
chr14:21296780
|
C | A | 6 | a0001c0001t0001g0199a0001c0004t0001g0196a0001c0004t0001g0221others(3): Show | 6 | HG00642.hp1 HG01074.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.218+1971C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296780 | ||||||
chr14:21296847
|
C | T | 1 | a0003c0003t0002g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.218+2038C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296847 | ||||||
chr14:21296930
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.218+2121C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296930 | ||||||
chr14:21296951
|
TA | T | 29 | a0001c0001t0001g0016a0001c0027t0004g0171a0002c0002t0001g0061others(26): Show | 29 | HG00741.hp2 HG01070.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.218+2159delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21296951 | |||||
chr14:21296978
|
C | A | 1 | a0001c0001t0004g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.218+2169C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21296978 | ||||||
chr14:21297195
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.218+2386A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297195 | ||||||
chr14:21297234
|
A | G | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.218+2425A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297234 | ||||||
chr14:21297305
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.218+2496C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297305 | ||||||
chr14:21297337
|
C | T | 59 | a0001c0001t0002g0004a0001c0001t0004g0177a0002c0039t0001g0018others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.218+2528C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297337 | ||||||
chr14:21297338
|
G | A | 2 | a0003c0003t0001g0097a0003c0003t0001g0098 | 2 | HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.218+2529G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297338 | ||||||
chr14:21297387
|
G | A | 74 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(71): Show | 74 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.218+2578G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297387 | ||||||
chr14:21297622
|
T | C | 1 | a0001c0004t0001g0222 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.218+2813T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297622 | ||||||
chr14:21297758
|
G | C | 2 | a0001c0001t0001g0067a0001c0001t0001g0102 | 2 | HG00423.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.218+2949G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297758 | ||||||
chr14:21297804
|
C | T | 1 | a0003c0003t0001g0186 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.218+2995C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297804 | ||||||
chr14:21297834
|
A | ATTCT | 29 | a0001c0001t0001g0047a0001c0001t0001g0132a0001c0001t0001g0134others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.218+3068_218+3071d others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTCTTTC others(1): Show |
37 | a0001c0001t0001g0016a0001c0001t0001g0130a0001c0001t0001g0141others(34): Show | 37 | HG00280.hp2 HG00735.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.218+3064_218+3071d others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTCTTTC others(5): Show |
46 | a0001c0001t0001g0173a0001c0001t0001g0228a0001c0001t0001g0235others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.218+3060_218+3071d others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTCTTTC others(9): Show |
68 | a0001c0001t0001g0099a0001c0001t0001g0123a0001c0001t0001g0125others(65): Show | 68 | HG00544.hp2 HG00597.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.218+3056_218+3071d others(18): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTCTTTC others(13): Show |
31 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0152others(28): Show | 31 | HG00544.hp1 HG01071.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.218+3052_218+3071d others(22): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTCTTTC others(17): Show |
15 | a0001c0001t0001g0294a0001c0004t0001g0188a0001c0004t0001g0223others(12): Show | 15 | HG00140.hp1 HG01109.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.218+3048_218+3071d others(26): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTCTTTC others(21): Show |
2 | a0001c0004t0001g0196a0003c0003t0003g0013 | 2 | HG02965.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.218+3044_218+3071d others(30): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTTTTTC others(1): Show |
3 | a0001c0001t0001g0043a0002c0002t0001g0066a0002c0002t0001g0094 | 3 | HG02738.hp1 HG03579.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.218+3027_218+3028i others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTTTTTC others(5): Show |
11 | a0001c0001t0001g0007a0002c0002t0001g0049a0002c0002t0001g0080others(8): Show | 11 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.218+3027_218+3028i others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTTTTTC others(9): Show |
22 | a0001c0001t0001g0025a0002c0002t0001g0024a0002c0002t0001g0032others(19): Show | 22 | HG00140.hp2 HG00597.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.218+3027_218+3028i others(18): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTTTTTC others(13): Show |
27 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0102others(24): Show | 27 | HG00408.hp1 HG00423.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.218+3027_218+3028i others(22): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTTTTTC others(17): Show |
4 | a0002c0002t0001g0057a0002c0002t0001g0063a0002c0002t0001g0071others(1): Show | 4 | HG01074.hp2 HG02083.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+3027_218+3028i others(26): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297834
|
A | ATTTTTTC others(21): Show |
1 | a0002c0002t0001g0089 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.218+3027_218+3028i others(30): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297834 | |||||
chr14:21297837
|
C | T | 10 | a0001c0001t0001g0002a0001c0001t0001g0003a0002c0002t0001g0058others(7): Show | 10 | HG01361.hp2 HG01884.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+3028C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297837 | ||||||
chr14:21297841
|
C | T | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.218+3032C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297841 | ||||||
chr14:21297845
|
C | CTTCTTTC others(8): Show |
1 | a0009c0016t0001g0247 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.218+3038_218+3039i others(17): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297845 | |||||
chr14:21297877
|
C | CTTTCTTT others(6): Show |
1 | a0008c0009t0001g0110 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.218+3071_218+3072i others(15): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297877 | |||||
chr14:21297877
|
C | CTTTCTTT others(10): Show |
2 | a0006c0006t0001g0035a0011c0011t0001g0005 | 2 | HG00438.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.218+3071_218+3072i others(19): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297877 | |||||
chr14:21297877
|
C | CTTTCTTT others(14): Show |
1 | a0003c0003t0001g0051 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.218+3071_218+3072i others(23): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297877 | |||||
chr14:21297878
|
T | TTTCTTTC others(8): Show |
2 | a0002c0002t0001g0077a0003c0003t0001g0076 | 2 | HG03490.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.218+3071_218+3072i others(17): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297878 | |||||
chr14:21297878
|
T | TTTCTTTC others(12): Show |
3 | a0001c0001t0001g0292a0002c0002t0001g0093a0028c0022t0001g0301 | 3 | HG02055.hp1 HG02071.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.218+3071_218+3072i others(21): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297878 | |||||
chr14:21297878
|
T | TTTCTTTC others(16): Show |
3 | a0001c0001t0001g0204a0001c0004t0001g0193a0015c0019t0001g0192 | 3 | HG03195.hp1 HG03195.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.218+3071_218+3072i others(25): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297878 | |||||
chr14:21297878
|
T | TTTCTTTC others(20): Show |
1 | a0004c0007t0001g0268 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.218+3071_218+3072i others(29): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297878 | |||||
chr14:21297879
|
T | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.218+3070T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297879 | ||||||
chr14:21297879
|
T | TTCTTTCT others(7): Show |
2 | a0006c0006t0001g0182a0021c0045t0001g0111 | 2 | HG00741.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.218+3071_218+3072i others(16): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297879 | |||||
chr14:21297879
|
T | TTCTTTCT others(11): Show |
2 | a0001c0001t0001g0287a0001c0001t0001g0319 | 2 | NA18990.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.218+3071_218+3072i others(20): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297879 | |||||
chr14:21297879
|
T | TTCTTTCT others(14): Show |
1 | a0003c0003t0001g0180 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.218+3071_218+3072i others(23): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297879 | |||||
chr14:21297879
|
T | TTCTTTCT others(19): Show |
1 | a0002c0002t0001g0088 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.218+3071_218+3072i others(28): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297879 | |||||
chr14:21297879
|
T | TTCTTTCT others(23): Show |
1 | a0002c0002t0001g0087 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.218+3071_218+3072i others(32): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21297879 | |||||
chr14:21297880
|
T | TCTTTCTT others(10): Show |
1 | a0002c0002t0001g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.218+3071_218+3072i others(19): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297880 | ||||||
chr14:21297881
|
T | C | 14 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(11): Show | 14 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.218+3072T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297881 | ||||||
chr14:21297890
|
T | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0043a0020c0040t0001g0264 | 3 | HG02622.hp2 HG02809.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.219-3076T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297890 | ||||||
chr14:21297931
|
A | T | 5 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(2): Show | 5 | HG00741.hp2 HG02723.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-3035A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297931 | ||||||
chr14:21297966
|
C | G | 25 | a0002c0039t0001g0018a0003c0003t0001g0159a0003c0003t0001g0164others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.219-3000C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21297966 | ||||||
chr14:21298186
|
T | C | 1 | a0003c0003t0001g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.219-2780T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21298186 | ||||||
chr14:21298320
|
T | C | 1 | a0018c0042t0003g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.219-2646T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21298320 | ||||||
chr14:21298652
|
G | A | 3 | a0001c0027t0004g0171a0014c0029t0004g0172a0023c0028t0001g0169 | 3 | HG02976.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.219-2314G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21298652 | ||||||
chr14:21298808
|
T | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.219-2158T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21298808 | ||||||
chr14:21298941
|
T | TA | 47 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(44): Show | 47 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.219-2002dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21298941 | |||||
chr14:21298941
|
TA | T | 7 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0004t0001g0201others(4): Show | 7 | HG02027.hp2 HG02055.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.219-2002delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21298941 | |||||
chr14:21298941
|
TAA | T | 15 | a0003c0003t0001g0046a0003c0003t0001g0159a0003c0003t0001g0176others(12): Show | 15 | HG00140.hp1 HG00438.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-2003_219-2002d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21298941 | |||||
chr14:21298941
|
TAAA | T | 46 | a0001c0001t0002g0004a0001c0001t0004g0177a0002c0039t0001g0018others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(43): Show |
intron_variant | MODIFIER | c.219-2004_219-2002d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21298941 | |||||
chr14:21298951
|
A | G | 2 | a0005c0005t0002g0303a0013c0044t0001g0034 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.219-2015A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21298951 | ||||||
chr14:21299019
|
A | AT | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(85): Show | 88 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.219-1935dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21299019 | |||||
chr14:21299019
|
AT | A | 6 | a0001c0001t0001g0203a0001c0001t0001g0246a0001c0001t0001g0251others(3): Show | 6 | HG00438.hp2 HG02132.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.219-1935delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21299019 | |||||
chr14:21299036
|
T | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.219-1930T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299036 | ||||||
chr14:21299039
|
G | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(80): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.219-1927G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299039 | ||||||
chr14:21299040
|
A | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(80): Show | 83 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.219-1926A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299040 | ||||||
chr14:21299194
|
G | T | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.219-1772G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299194 | ||||||
chr14:21299198
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.219-1768C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299198 | ||||||
chr14:21299321
|
G | A | 1 | a0003c0003t0001g0249 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.219-1645G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299321 | ||||||
chr14:21299532
|
C | T | 3 | a0003c0003t0001g0026a0003c0003t0001g0027a0003c0003t0001g0028 | 3 | NA18612.hp1 NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.219-1434C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299532 | ||||||
chr14:21299777
|
G | A | 319 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.219-1189G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299777 | ||||||
chr14:21299890
|
CT | C | 22 | a0003c0003t0001g0039a0005c0005t0001g0020a0005c0005t0001g0021others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.219-1075delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21299890 | ||||||
chr14:21300067
|
G | A | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.219-899G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300067 | ||||||
chr14:21300249
|
G | A | 1 | a0002c0002t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.219-717G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300249 | ||||||
chr14:21300283
|
A | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.219-683A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300283 | ||||||
chr14:21300301
|
G | A | 118 | a0001c0001t0001g0025a0001c0001t0001g0067a0001c0001t0001g0075others(115): Show | 118 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.219-665G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300301 | ||||||
chr14:21300305
|
C | CA | 147 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0043others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.219-645dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21300305 | |||||
chr14:21300305
|
C | CAA | 6 | a0001c0001t0001g0331a0002c0002t0001g0087a0003c0003t0001g0054others(3): Show | 6 | HG01261.hp2 HG01361.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.219-646_219-645dup others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21300305 | |||||
chr14:21300678
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.219-288A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300678 | ||||||
chr14:21300705
|
C | CA | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.219-261_219-260ins others(1): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300705 | ||||||
chr14:21300705
|
C | CT | 135 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0067others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.219-234dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21300705 | |||||
chr14:21300705
|
C | CTT | 33 | a0001c0001t0001g0007a0001c0001t0001g0187a0001c0001t0001g0220others(30): Show | 33 | HG00140.hp1 HG01261.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.219-235_219-234dup others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21300705 | |||||
chr14:21300705
|
C | CTTT | 16 | a0001c0001t0001g0016a0001c0001t0001g0314a0001c0001t0001g0324others(13): Show | 16 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.219-236_219-234dup others(3): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21300705 | |||||
chr14:21300705
|
CT | C | 16 | a0001c0001t0001g0132a0001c0001t0001g0173a0001c0001t0001g0199others(13): Show | 16 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.219-234delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21300705 | |||||
chr14:21300732
|
T | TA | 9 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0139others(6): Show | 9 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-233dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr14 | 21300732 | |||||
chr14:21300733
|
A | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.219-233A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300733 | ||||||
chr14:21300734
|
C | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.219-232C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300734 | ||||||
chr14:21300736
|
A | T | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.219-230A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300736 | ||||||
chr14:21300837
|
A | C | 1 | a0006c0006t0001g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.219-129A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300837 | ||||||
chr14:21300912
|
G | A | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.219-54G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300912 | ||||||
chr14:21300913
|
T | A | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.219-53T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 3/24 | chr14 | 21300913 | ||||||
chr14:21301621
|
G | A | 10 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(7): Show | 10 | HG02109.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.490+384G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | chr14 | 21301621 | ||||||
chr14:21301676
|
AAAATAAT others(6): Show |
A | 1 | a0009c0016t0001g0247 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.490+442_490+454del others(13): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301676 | |||||
chr14:21301677
|
A | AAAT | 59 | a0001c0001t0001g0075a0001c0001t0001g0132a0001c0001t0001g0134others(56): Show | 59 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.490+485_490+487dup others(3): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301677 | |||||
chr14:21301677
|
A | AAATAAT | 7 | a0001c0001t0001g0189a0001c0001t0001g0265a0001c0001t0001g0279others(4): Show | 7 | HG00438.hp2 HG02738.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+482_490+487dup others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301677 | |||||
chr14:21301677
|
AAATAATA others(2): Show |
A | 8 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0139others(5): Show | 8 | HG01167.hp1 HG01192.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.490+479_490+487del others(9): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301677 | |||||
chr14:21301677
|
AAATAATA others(8): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.490+473_490+487del others(15): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301677 | |||||
chr14:21301701
|
TAATAATA others(17): Show |
T | 5 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(2): Show | 5 | HG02976.hp1 HG03516.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.490+467_490+490del others(24): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301701 | |||||
chr14:21301710
|
TAATAATA others(8): Show |
T | 42 | a0001c0001t0001g0102a0001c0001t0001g0135a0001c0001t0001g0204others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.490+476_490+490del others(15): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301710 | |||||
chr14:21301713
|
TAATAATA others(5): Show |
T | 13 | a0001c0001t0001g0067a0001c0001t0001g0138a0001c0001t0001g0267others(10): Show | 13 | HG02027.hp1 HG02165.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.490+479_490+490del others(12): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301713 | |||||
chr14:21301716
|
TAATAATA others(2): Show |
T | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0003c0003t0001g0164others(16): Show | 19 | HG00099.hp1 HG00280.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+482_490+490del others(9): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301716 | |||||
chr14:21301719
|
TAATAAA | T | 38 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0241others(35): Show | 38 | HG00544.hp1 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.490+485_490+490del others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301719 | |||||
chr14:21301722
|
TAAA | T | 44 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0099others(41): Show | 44 | HG00140.hp1 HG00423.hp1 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.490+489_490+491del others(3): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21301722 | |||||
chr14:21301725
|
A | T | 157 | a0001c0001t0001g0075a0001c0001t0001g0122a0001c0001t0001g0123others(154): Show | 157 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.490+488A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | chr14 | 21301725 | ||||||
chr14:21302029
|
G | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.491-459G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | chr14 | 21302029 | ||||||
chr14:21302206
|
G | T | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.491-282G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | chr14 | 21302206 | ||||||
chr14:21302227
|
A | G | 1 | a0001c0001t0001g0067 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.491-261A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | chr14 | 21302227 | ||||||
chr14:21302334
|
TA | T | 103 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.491-144delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr14 | 21302334 | |||||
chr14:21302442
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0002g0004 | 3 | HG02109.hp2 HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.491-46G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 4/24 | chr14 | 21302442 | ||||||
chr14:21302696
|
G | A | 1 | a0001c0001t0001g0332 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.587+112G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | chr14 | 21302696 | ||||||
chr14:21302755
|
G | A | 44 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0002g0004others(41): Show | 44 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.587+171G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | chr14 | 21302755 | ||||||
chr14:21302831
|
T | C | 47 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(44): Show | 47 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.587+247T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | chr14 | 21302831 | ||||||
chr14:21302854
|
TC | T | 93 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.587+272delC | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr14 | 21302854 | |||||
chr14:21302861
|
T | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0138a0001c0001t0001g0187others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.587+277T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | chr14 | 21302861 | ||||||
chr14:21302865
|
G | GT | 153 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0067others(150): Show | 153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.587+303dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr14 | 21302865 | |||||
chr14:21302865
|
G | GTT | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0135others(46): Show | 49 | HG00140.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.587+302_587+303dup others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr14 | 21302865 | |||||
chr14:21302865
|
GT | G | 32 | a0001c0001t0001g0016a0001c0001t0001g0199a0001c0004t0001g0196others(29): Show | 32 | HG00323.hp1 HG00544.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.587+303delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr14 | 21302865 | |||||
chr14:21302962
|
C | T | 4 | a0003c0003t0003g0008a0003c0003t0003g0009a0003c0003t0003g0010others(1): Show | 4 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.588-369C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | chr14 | 21302962 | ||||||
chr14:21303176
|
C | T | 40 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.588-155C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 5/24 | chr14 | 21303176 | ||||||
chr14:21303579
|
G | A | 1 | a0001c0004t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.800+36G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303579 | ||||||
chr14:21303684
|
T | C | 2 | a0005c0005t0001g0300a0005c0005t0001g0302 | 2 | HG02145.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.800+141T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303684 | ||||||
chr14:21303706
|
T | C | 1 | a0004c0036t0001g0280 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.800+163T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303706 | ||||||
chr14:21303707
|
G | T | 40 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.800+164G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303707 | ||||||
chr14:21303708
|
C | T | 48 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(45): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.800+165C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303708 | ||||||
chr14:21303763
|
G | A | 42 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.800+220G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303763 | ||||||
chr14:21303794
|
C | T | 5 | a0005c0005t0001g0116a0005c0005t0001g0118a0005c0005t0001g0119others(2): Show | 5 | HG02258.hp1 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+251C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303794 | ||||||
chr14:21303905
|
T | C | 1 | a0003c0003t0001g0176 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.800+362T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303905 | ||||||
chr14:21303908
|
A | C | 1 | a0004c0007t0001g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.800+365A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303908 | ||||||
chr14:21303944
|
C | T | 51 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(48): Show | 51 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.800+401C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303944 | ||||||
chr14:21303968
|
A | T | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.800+425A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303968 | ||||||
chr14:21303988
|
C | CA | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(60): Show | 63 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.800+458dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21303988 | |||||
chr14:21303988
|
CA | C | 15 | a0001c0001t0001g0304a0003c0003t0001g0006a0003c0003t0001g0186others(12): Show | 15 | HG01109.hp1 HG01257.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.800+458delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21303988 | |||||
chr14:21303997
|
A | AG | 42 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.800+454_800+455ins others(1): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21303997 | ||||||
chr14:21304039
|
G | T | 1 | a0005c0005t0001g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.800+496G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304039 | ||||||
chr14:21304298
|
A | G | 106 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.800+755A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304298 | ||||||
chr14:21304320
|
A | T | 1 | a0003c0003t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.800+777A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304320 | ||||||
chr14:21304387
|
G | C | 3 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0002g0004 | 3 | HG02109.hp2 HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.800+844G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304387 | ||||||
chr14:21304389
|
G | A | 1 | a0020c0040t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.800+846G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304389 | ||||||
chr14:21304389
|
G | GAAAGAAA others(7): Show |
1 | a0004c0007t0001g0315 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.800+847_800+848ins others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
G | GAGAA | 35 | a0001c0001t0001g0025a0001c0001t0001g0124a0001c0001t0001g0138others(32): Show | 35 | HG00140.hp1 HG00423.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.800+900_800+903dup others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
G | GAGAAAA | 5 | a0005c0005t0001g0116a0005c0005t0001g0120a0005c0005t0002g0303others(2): Show | 5 | HG02965.hp1 HG03704.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.800+851_800+852ins others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
G | GAGAAAGA others(1): Show |
5 | a0001c0001t0001g0206a0002c0002t0001g0093a0003c0003t0003g0010others(2): Show | 5 | HG00639.hp2 HG01070.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+896_800+903dup others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
G | GAGAAAGA others(5): Show |
2 | a0002c0002t0001g0096a0002c0002t0001g0101 | 2 | NA18966.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.800+892_800+903dup others(12): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
G | GAGAAAGA others(13): Show |
1 | a0001c0001t0001g0271 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.800+884_800+903dup others(20): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
G | GAGAGAAA others(15): Show |
1 | a0001c0001t0001g0292 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.800+849_800+850ins others(22): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
GAGAA | G | 64 | a0001c0001t0001g0016a0001c0001t0001g0047a0001c0001t0001g0067others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.800+900_800+903del others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
GAGAAAGA others(1): Show |
G | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0099others(54): Show | 57 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.800+896_800+903del others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
GAGAAAGA others(5): Show |
G | 16 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(13): Show | 16 | HG01192.hp2 HG01516.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.800+892_800+903del others(12): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
GAGAAAGA others(9): Show |
G | 11 | a0001c0001t0001g0233a0001c0001t0004g0177a0001c0004t0001g0215others(8): Show | 11 | HG00738.hp2 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.800+888_800+903del others(16): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304389
|
GAGAAAGA others(17): Show |
G | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.800+880_800+903del others(24): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304389 | |||||
chr14:21304391
|
G | GAA | 3 | a0003c0012t0001g0133a0003c0012t0001g0161a0007c0008t0001g0165 | 3 | HG01516.hp1 HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.800+850_800+851dup others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304391 | |||||
chr14:21304393
|
AAG | A | 13 | a0002c0039t0001g0018a0003c0003t0001g0176a0005c0005t0001g0021others(10): Show | 13 | HG00741.hp2 HG01358.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.800+852_800+853del others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304393 | |||||
chr14:21304393
|
AAGAAAG | A | 15 | a0003c0003t0001g0046a0003c0003t0001g0159a0003c0003t0001g0164others(12): Show | 15 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.800+852_800+857del others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304393 | |||||
chr14:21304393
|
AAGAAAGA others(3): Show |
A | 6 | a0005c0005t0001g0044a0005c0005t0001g0167a0005c0046t0002g0140others(3): Show | 6 | HG01099.hp2 HG02818.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.800+852_800+861del others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304393 | |||||
chr14:21304416
|
A | AAAGAAAG others(33): Show |
1 | a0001c0001t0001g0290 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.800+903_800+904ins others(40): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304416 | |||||
chr14:21304416
|
A | AAAGAAAG others(25): Show |
1 | a0001c0001t0001g0294 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.800+903_800+904ins others(32): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304416 | |||||
chr14:21304420
|
A | AAAGAAAG others(12): Show |
1 | a0004c0007t0001g0205 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.800+880_800+898dup others(19): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(25): Show |
1 | a0001c0001t0001g0289 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.800+903_800+904ins others(32): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(17): Show |
3 | a0001c0001t0001g0288a0004c0007t0001g0285a0026c0034t0001g0286 | 3 | NA18963.hp2 NA19009.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.800+900_800+901ins others(24): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(13): Show |
3 | a0001c0001t0001g0243a0001c0001t0001g0283a0001c0001t0001g0319 | 3 | NA18957.hp2 NA18959.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.800+896_800+897ins others(20): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(9): Show |
10 | a0001c0001t0001g0204a0001c0001t0001g0234a0001c0001t0001g0240others(7): Show | 10 | HG00544.hp2 NA18939.hp1 NA18943.hp1 others(7): Show |
intron_variant | MODIFIER | c.800+892_800+893ins others(16): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(7): Show |
1 | a0001c0001t0001g0269 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.800+890_800+891ins others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(6): Show |
1 | a0001c0001t0001g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.800+889_800+890ins others(13): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(5): Show |
18 | a0001c0001t0001g0220a0001c0001t0001g0235a0001c0001t0001g0245others(15): Show | 18 | HG01071.hp1 HG02027.hp1 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.800+888_800+889ins others(12): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | AAAGAAAG others(9): Show |
1 | a0001c0001t0001g0135 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.800+888_800+889ins others(16): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304420 | |||||
chr14:21304420
|
A | G | 4 | a0001c0001t0001g0292a0004c0007t0001g0315a0022c0033t0001g0001others(1): Show | 4 | HG02071.hp2 HG02717.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+877A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304420 | ||||||
chr14:21304424
|
A | AAAGAAAG others(17): Show |
1 | a0001c0001t0001g0102 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.800+903_800+904ins others(24): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21304424 | |||||
chr14:21304443
|
G | T | 1 | a0003c0003t0001g0006 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.800+900G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304443 | ||||||
chr14:21304582
|
A | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(59): Show | 62 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.800+1039A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304582 | ||||||
chr14:21304587
|
T | C | 1 | a0005c0005t0001g0127 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.800+1044T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304587 | ||||||
chr14:21304620
|
A | C | 47 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(44): Show | 47 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.800+1077A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304620 | ||||||
chr14:21304621
|
A | C | 1 | a0005c0005t0001g0306 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.800+1078A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304621 | ||||||
chr14:21304682
|
A | G | 3 | a0007c0013t0001g0154a0007c0013t0001g0155a0007c0013t0001g0158 | 3 | HG03704.hp2 NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.800+1139A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304682 | ||||||
chr14:21304826
|
G | A | 4 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(1): Show | 4 | HG00741.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+1283G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304826 | ||||||
chr14:21304864
|
T | C | 148 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.800+1321T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21304864 | ||||||
chr14:21305004
|
A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.800+1461A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305004 | ||||||
chr14:21305006
|
G | A | 42 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.800+1463G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305006 | ||||||
chr14:21305304
|
A | G | 93 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.800+1761A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305304 | ||||||
chr14:21305321
|
A | G | 4 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(1): Show | 4 | HG00741.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+1778A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305321 | ||||||
chr14:21305348
|
C | T | 4 | a0011c0011t0001g0005a0011c0011t0001g0126a0011c0011t0001g0128others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.800+1805C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305348 | ||||||
chr14:21305453
|
A | C | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.800+1910A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305453 | ||||||
chr14:21305456
|
G | A | 1 | a0002c0039t0001g0018 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.800+1913G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305456 | ||||||
chr14:21305582
|
C | T | 3 | a0003c0003t0001g0046a0003c0003t0001g0176a0005c0005t0001g0116 | 3 | HG02145.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.800+2039C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305582 | ||||||
chr14:21305588
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.800+2045C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305588 | ||||||
chr14:21305718
|
G | A | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.801-2013G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305718 | ||||||
chr14:21305845
|
A | G | 2 | a0003c0003t0005g0014a0003c0003t0005g0015 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.801-1886A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305845 | ||||||
chr14:21305973
|
T | C | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(58): Show | 61 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.801-1758T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21305973 | ||||||
chr14:21306102
|
G | C | 1 | a0003c0003t0003g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.801-1629G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306102 | ||||||
chr14:21306105
|
T | A | 1 | a0001c0001t0001g0137 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.801-1626T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306105 | ||||||
chr14:21306112
|
C | CT | 37 | a0001c0001t0001g0025a0001c0001t0001g0130a0001c0001t0001g0134others(34): Show | 37 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.801-1582dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
C | CTT | 10 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0156others(7): Show | 10 | HG00738.hp1 HG01192.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.801-1583_801-1582d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CT | C | 16 | a0001c0001t0001g0002a0001c0001t0001g0150a0001c0001t0001g0151others(13): Show | 16 | HG00323.hp1 HG01074.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.801-1582delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTT | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0152a0001c0004t0001g0258others(4): Show | 7 | HG01099.hp1 HG02809.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.801-1583_801-1582d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTT | C | 8 | a0003c0003t0001g0006a0003c0003t0001g0249a0003c0003t0003g0008others(5): Show | 8 | HG00438.hp1 HG01109.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-1586_801-1582d others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTT | C | 30 | a0002c0002t0001g0049a0002c0002t0001g0053a0002c0002t0001g0066others(27): Show | 30 | HG00642.hp2 HG01261.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.801-1587_801-1582d others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT | C | 61 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0004g0170others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.801-1588_801-1582d others(9): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0122a0001c0001t0001g0123a0002c0002t0001g0091others(5): Show | 8 | HG02451.hp2 HG02717.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.801-1589_801-1582d others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(3): Show |
C | 3 | a0003c0003t0001g0176a0004c0007t0001g0205a0023c0028t0001g0169 | 3 | HG02135.hp1 HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.801-1591_801-1582d others(12): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(4): Show |
C | 15 | a0001c0001t0001g0256a0001c0001t0001g0269a0001c0001t0001g0271others(12): Show | 15 | HG00544.hp2 HG00597.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.801-1592_801-1582d others(13): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(5): Show |
C | 67 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.801-1593_801-1582d others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(6): Show |
C | 8 | a0001c0001t0001g0243a0001c0004t0001g0259a0005c0005t0001g0109others(5): Show | 8 | HG02004.hp2 HG02145.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.801-1594_801-1582d others(15): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(7): Show |
C | 1 | a0005c0046t0002g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.801-1595_801-1582d others(16): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(8): Show |
C | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.801-1596_801-1582d others(17): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0026t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.801-1600_801-1582d others(21): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306112
|
CTTTTTTT others(17): Show |
C | 1 | a0006c0006t0001g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.801-1605_801-1582d others(26): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr14 | 21306112 | |||||
chr14:21306163
|
A | G | 47 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0099others(44): Show | 47 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.801-1568A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306163 | ||||||
chr14:21306225
|
G | A | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.801-1506G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306225 | ||||||
chr14:21306419
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.801-1312C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306419 | ||||||
chr14:21306608
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0122others(4): Show | 7 | HG01884.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.801-1123G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306608 | ||||||
chr14:21306750
|
C | G | 1 | a0003c0003t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.801-981C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306750 | ||||||
chr14:21306752
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0278 | 2 | NA18522.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.801-979G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306752 | ||||||
chr14:21306752
|
G | C | 1 | a0003c0003t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.801-979G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306752 | ||||||
chr14:21306815
|
C | T | 42 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.801-916C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306815 | ||||||
chr14:21306856
|
A | C | 1 | a0004c0007t0001g0285 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.801-875A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306856 | ||||||
chr14:21306876
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.801-855A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306876 | ||||||
chr14:21306931
|
A | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0138a0001c0001t0001g0187others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.801-800A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306931 | ||||||
chr14:21306967
|
G | A | 42 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.801-764G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21306967 | ||||||
chr14:21307010
|
G | A | 48 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(45): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.801-721G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21307010 | ||||||
chr14:21307179
|
C | G | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.801-552C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21307179 | ||||||
chr14:21307414
|
G | A | 1 | a0003c0003t0001g0249 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.801-317G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21307414 | ||||||
chr14:21307542
|
G | A | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.801-189G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21307542 | ||||||
chr14:21307577
|
G | A | 1 | a0030c0025t0001g0037 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.801-154G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21307577 | ||||||
chr14:21307657
|
G | C | 43 | a0002c0039t0001g0018a0003c0003t0001g0046a0003c0003t0001g0159others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.801-74G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 6/24 | chr14 | 21307657 | ||||||
chr14:21307860
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.906+24C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21307860 | ||||||
chr14:21307933
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.906+97T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21307933 | ||||||
chr14:21308002
|
C | T | 3 | a0003c0003t0001g0068a0003c0003t0001g0097a0003c0003t0001g0098 | 3 | HG01256.hp1 HG01496.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.906+166C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308002 | ||||||
chr14:21308361
|
A | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.906+525A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308361 | ||||||
chr14:21308432
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.906+596G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308432 | ||||||
chr14:21308446
|
A | AC | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.906+610_906+611ins others(1): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308446 | ||||||
chr14:21308478
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.906+642A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308478 | ||||||
chr14:21308489
|
C | A | 1 | a0001c0001t0001g0294 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.906+653C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308489 | ||||||
chr14:21308509
|
A | C | 1 | a0007c0008t0001g0178 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.906+673A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308509 | ||||||
chr14:21308751
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.906+915G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308751 | ||||||
chr14:21308758
|
C | T | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.906+922C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308758 | ||||||
chr14:21308767
|
C | T | 1 | a0003c0003t0005g0015 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.906+931C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308767 | ||||||
chr14:21308772
|
A | G | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.906+936A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308772 | ||||||
chr14:21308776
|
T | C | 1 | a0006c0006t0001g0038 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.906+940T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308776 | ||||||
chr14:21308892
|
C | G | 93 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.906+1056C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308892 | ||||||
chr14:21308956
|
G | T | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.906+1120G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21308956 | ||||||
chr14:21309074
|
C | T | 49 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(46): Show | 49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.906+1238C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309074 | ||||||
chr14:21309302
|
A | G | 2 | a0003c0003t0001g0307a0003c0003t0001g0308 | 2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.907-1282A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309302 | ||||||
chr14:21309342
|
T | C | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.907-1242T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309342 | ||||||
chr14:21309394
|
C | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(7): Show | 10 | HG02109.hp2 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.907-1190C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309394 | ||||||
chr14:21309442
|
C | T | 73 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(70): Show | 73 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.907-1142C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309442 | ||||||
chr14:21309481
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-1103C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309481 | ||||||
chr14:21309487
|
C | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.907-1097C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309487 | ||||||
chr14:21309513
|
A | G | 49 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(46): Show | 49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.907-1071A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309513 | ||||||
chr14:21309553
|
G | A | 83 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(80): Show | 83 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.907-1031G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309553 | ||||||
chr14:21309742
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.907-842A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309742 | ||||||
chr14:21309834
|
T | TA | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.907-741dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 21309834 | |||||
chr14:21309845
|
T | A | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.907-739T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309845 | ||||||
chr14:21309846
|
T | G | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.907-738T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309846 | ||||||
chr14:21309919
|
G | A | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.907-665G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21309919 | ||||||
chr14:21309940
|
T | TTATC | 302 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.907-642_907-641ins others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 21309940 | |||||
chr14:21310027
|
GTGAGCCA others(208): Show |
G | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.907-555_907-341del | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 21310027 | |||||
chr14:21310045
|
G | A | 6 | a0009c0016t0001g0247a0009c0016t0001g0248a0009c0016t0001g0311others(3): Show | 6 | HG02109.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-539G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21310045 | ||||||
chr14:21310192
|
T | C | 2 | a0004c0015t0001g0225a0004c0015t0001g0236 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.907-392T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21310192 | ||||||
chr14:21310240
|
CTT | C | 50 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0099others(47): Show | 50 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.907-335_907-334del others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 21310240 | |||||
chr14:21310266
|
A | T | 3 | a0001c0001t0001g0255a0001c0001t0001g0257a0001c0001t0001g0312 | 3 | NA18943.hp1 NA18947.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.907-318A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21310266 | ||||||
chr14:21310312
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.907-272C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21310312 | ||||||
chr14:21310385
|
G | T | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG03927.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.907-199G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21310385 | ||||||
chr14:21310429
|
G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.907-155G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21310429 | ||||||
chr14:21310440
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.907-144C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | chr14 | 21310440 | ||||||
chr14:21310558
|
AAAT | A | 93 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.907-16_907-14delAA others(1): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr14 | 21310558 | |||||
chr14:21310633
|
T | C | 170 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(167): Show | 170 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.930+26T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21310633 | ||||||
chr14:21310935
|
A | G | 4 | a0004c0007t0001g0197a0004c0007t0001g0205a0004c0007t0001g0315others(1): Show | 4 | HG02135.hp1 HG02523.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+328A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21310935 | ||||||
chr14:21311099
|
C | T | 4 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(1): Show | 4 | HG00741.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.930+492C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21311099 | ||||||
chr14:21311264
|
C | T | 1 | a0018c0042t0003g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.931-560C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21311264 | ||||||
chr14:21311289
|
C | T | 1 | a0005c0046t0002g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.931-535C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21311289 | ||||||
chr14:21311336
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.931-488A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21311336 | ||||||
chr14:21311357
|
G | A | 1 | a0001c0001t0001g0290 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.931-467G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21311357 | ||||||
chr14:21311545
|
C | CAATA | 3 | a0001c0004t0001g0217a0001c0020t0001g0229a0001c0020t0001g0230 | 3 | HG00408.hp2 HG02165.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.931-258_931-255dup others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr14 | 21311545 | |||||
chr14:21311545
|
CAATA | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.931-258_931-255del others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr14 | 21311545 | |||||
chr14:21311744
|
A | C | 1 | a0002c0002t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.931-80A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 8/24 | chr14 | 21311744 | ||||||
chr14:21312078
|
G | A | 1 | a0001c0001t0001g0331 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1077+108G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 9/24 | chr14 | 21312078 | ||||||
chr14:21312086
|
G | A | 26 | a0003c0003t0001g0164a0005c0005t0001g0044a0005c0005t0001g0116others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1077+116G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 9/24 | chr14 | 21312086 | ||||||
chr14:21312157
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1077+187T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 9/24 | chr14 | 21312157 | ||||||
chr14:21312160
|
A | G | 1 | a0002c0002t0001g0060 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1077+190A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 9/24 | chr14 | 21312160 | ||||||
chr14:21312362
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1078-71A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 9/24 | chr14 | 21312362 | ||||||
chr14:21312556
|
T | G | 4 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(1): Show | 4 | HG00741.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151+50T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21312556 | ||||||
chr14:21312692
|
CT | C | 53 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(50): Show | 53 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1151+200delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21312692 | |||||
chr14:21312741
|
T | C | 1 | a0001c0004t0001g0210 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1151+235T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21312741 | ||||||
chr14:21312954
|
T | TCC | 50 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(47): Show | 50 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1151+451_1151+452d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21312954 | |||||
chr14:21312986
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1151+480C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21312986 | ||||||
chr14:21313155
|
T | TG | 96 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.1151+655dupG | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21313155 | |||||
chr14:21313159
|
G | A | 3 | a0001c0004t0001g0258a0001c0004t0001g0259a0001c0004t0001g0260 | 3 | HG00735.hp2 HG01099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1151+653G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313159 | ||||||
chr14:21313184
|
T | G | 96 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(93): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.1151+678T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313184 | ||||||
chr14:21313234
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0002g0004 | 3 | HG02109.hp2 HG02622.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1151+728G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313234 | ||||||
chr14:21313280
|
T | C | 1 | a0003c0003t0001g0051 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1151+774T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313280 | ||||||
chr14:21313318
|
A | C | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1151+812A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313318 | ||||||
chr14:21313321
|
G | C | 1 | a0012c0017t0001g0320 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1151+815G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313321 | ||||||
chr14:21313345
|
G | GA | 11 | a0001c0001t0001g0025a0001c0001t0001g0075a0001c0001t0001g0137others(8): Show | 11 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1151+853dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21313345 | |||||
chr14:21313345
|
GA | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1151+853delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21313345 | |||||
chr14:21313518
|
G | A | 48 | a0001c0001t0001g0067a0001c0001t0001g0102a0001c0001t0001g0135others(45): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1151+1012G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313518 | ||||||
chr14:21313521
|
G | A | 1 | a0003c0003t0001g0054 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1151+1015G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313521 | ||||||
chr14:21313555
|
C | T | 11 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(8): Show | 11 | HG01884.hp1 HG02109.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1151+1049C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313555 | ||||||
chr14:21313616
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.1151+1110T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313616 | ||||||
chr14:21313643
|
C | T | 4 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(1): Show | 4 | HG00741.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151+1137C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313643 | ||||||
chr14:21313656
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1151+1150C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21313656 | ||||||
chr14:21313787
|
G | GA | 42 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1151+1295dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21313787 | |||||
chr14:21313787
|
GA | G | 16 | a0001c0001t0001g0002a0001c0001t0001g0003a0002c0002t0001g0056others(13): Show | 16 | HG00597.hp2 HG01109.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1151+1295delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21313787 | |||||
chr14:21313944
|
CT | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0002c0002t0001g0085others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1151+1454delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21313944 | |||||
chr14:21314054
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1151+1548C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314054 | ||||||
chr14:21314082
|
G | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1151+1576G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314082 | ||||||
chr14:21314232
|
G | A | 23 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(20): Show | 23 | HG01109.hp1 HG02055.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1151+1726G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314232 | ||||||
chr14:21314244
|
G | A | 1 | a0003c0012t0001g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1151+1738G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314244 | ||||||
chr14:21314366
|
G | A | 1 | a0007c0008t0001g0166 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1151+1860G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314366 | ||||||
chr14:21314541
|
C | A | 2 | a0005c0005t0002g0303a0013c0044t0001g0034 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1151+2035C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314541 | ||||||
chr14:21314562
|
G | T | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1151+2056G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314562 | ||||||
chr14:21314714
|
G | GA | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1151+2224dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21314714 | |||||
chr14:21314736
|
G | A | 2 | a0002c0002t0001g0057a0003c0003t0001g0076 | 2 | HG03239.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1151+2230G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314736 | ||||||
chr14:21314920
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1151+2414G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21314920 | ||||||
chr14:21315121
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1152-2575T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315121 | ||||||
chr14:21315186
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1152-2510G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315186 | ||||||
chr14:21315234
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1152-2462G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315234 | ||||||
chr14:21315278
|
T | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1152-2418T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315278 | ||||||
chr14:21315292
|
G | C | 4 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(1): Show | 4 | HG00741.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152-2404G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315292 | ||||||
chr14:21315400
|
G | A | 1 | a0024c0030t0001g0313 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1152-2296G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315400 | ||||||
chr14:21315424
|
G | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1152-2272G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315424 | ||||||
chr14:21315455
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1152-2241C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315455 | ||||||
chr14:21315506
|
C | CAA | 54 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(51): Show | 54 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1152-2177_1152-217 others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315506 | |||||
chr14:21315521
|
C | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0003a0022c0033t0001g0001 | 3 | HG01884.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1152-2175C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315521 | ||||||
chr14:21315539
|
C | CT | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1152-2154dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315539 | |||||
chr14:21315571
|
T | G | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1152-2125T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315571 | ||||||
chr14:21315725
|
G | A | 95 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0099others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1152-1971G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315725 | ||||||
chr14:21315800
|
A | ATTT | 7 | a0003c0003t0001g0186a0003c0003t0002g0184a0003c0003t0002g0185others(4): Show | 7 | HG01109.hp1 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1152-1894_1152-189 others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315800 | |||||
chr14:21315803
|
A | AT | 35 | a0001c0001t0001g0199a0001c0004t0001g0129a0001c0004t0001g0188others(32): Show | 35 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1152-1891dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315803 | |||||
chr14:21315803
|
A | ATTT | 4 | a0003c0003t0001g0006a0003c0003t0001g0249a0003c0003t0005g0014others(1): Show | 4 | HG02055.hp2 HG02976.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152-1891_1152-189 others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315803 | |||||
chr14:21315803
|
A | T | 14 | a0001c0004t0001g0190a0001c0026t0001g0194a0002c0039t0001g0018others(11): Show | 14 | HG01109.hp1 HG02074.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1152-1893A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315803 | ||||||
chr14:21315806
|
A | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(130): Show | 133 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1152-1890A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315806 | ||||||
chr14:21315809
|
T | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0002g0004others(2): Show | 5 | HG02109.hp2 HG02622.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152-1887T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315809 | ||||||
chr14:21315816
|
T | G | 5 | a0001c0001t0001g0003a0002c0002t0001g0060a0002c0002t0001g0088others(2): Show | 5 | HG01257.hp2 HG01261.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1152-1880T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315816 | ||||||
chr14:21315818
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(97): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.1152-1878A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21315818 | ||||||
chr14:21315974
|
G | GT | 33 | a0001c0001t0001g0007a0001c0001t0001g0124a0001c0001t0001g0149others(30): Show | 33 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.1152-1703dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315974 | |||||
chr14:21315974
|
G | GTT | 30 | a0003c0003t0001g0164a0003c0003t0001g0307a0003c0003t0001g0308others(27): Show | 30 | HG00099.hp1 HG00280.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.1152-1704_1152-170 others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315974 | |||||
chr14:21315974
|
G | GTTT | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0003c0003t0001g0159others(5): Show | 8 | HG00741.hp2 HG01884.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1152-1705_1152-170 others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315974 | |||||
chr14:21315974
|
GT | G | 88 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0099others(85): Show | 88 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.1152-1703delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21315974 | |||||
chr14:21316038
|
G | A | 1 | a0001c0031t0001g0274 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1152-1658G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316038 | ||||||
chr14:21316125
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1152-1571C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316125 | ||||||
chr14:21316299
|
A | T | 92 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(89): Show | 92 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1152-1397A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316299 | ||||||
chr14:21316479
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1152-1217C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316479 | ||||||
chr14:21316575
|
C | A | 2 | a0001c0001t0001g0267a0024c0030t0001g0313 | 2 | HG03017.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1152-1121C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316575 | ||||||
chr14:21316638
|
G | A | 4 | a0005c0005t0001g0109a0005c0005t0001g0112a0007c0008t0001g0113others(1): Show | 4 | HG00741.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152-1058G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316638 | ||||||
chr14:21316776
|
G | A | 1 | a0001c0001t0001g0329 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1152-920G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316776 | ||||||
chr14:21316860
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1152-836C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316860 | ||||||
chr14:21316885
|
C | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1152-811C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316885 | ||||||
chr14:21316974
|
G | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1152-722G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316974 | ||||||
chr14:21316989
|
G | A | 1 | a0004c0007t0001g0284 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1152-707G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21316989 | ||||||
chr14:21317137
|
G | GA | 6 | a0001c0001t0001g0329a0005c0005t0001g0118a0005c0005t0001g0119others(3): Show | 6 | HG02258.hp1 HG02809.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1152-550dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr14 | 21317137 | |||||
chr14:21317162
|
T | C | 4 | a0001c0001t0004g0177a0001c0027t0004g0171a0014c0029t0004g0172others(1): Show | 4 | HG02622.hp1 HG02976.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1152-534T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21317162 | ||||||
chr14:21317197
|
T | G | 1 | a0001c0001t0001g0141 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1152-499T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21317197 | ||||||
chr14:21317277
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0168 | 2 | HG00280.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1152-419A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21317277 | ||||||
chr14:21317286
|
T | G | 1 | a0002c0002t0001g0078 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1152-410T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21317286 | ||||||
chr14:21317457
|
G | A | 2 | a0003c0003t0001g0026a0003c0003t0001g0028 | 2 | NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1152-239G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21317457 | ||||||
chr14:21317631
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1152-65G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 10/24 | chr14 | 21317631 | ||||||
chr14:21317908
|
A | T | 1 | a0004c0007t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1306+58A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21317908 | ||||||
chr14:21318053
|
T | C | 11 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(8): Show | 11 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306+203T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318053 | ||||||
chr14:21318186
|
AACCTTCA others(197): Show |
A | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1306+337_1306+540d others(2): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318186 | ||||||
chr14:21318241
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1306+391G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318241 | ||||||
chr14:21318253
|
T | C | 1 | a0003c0012t0001g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1306+403T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318253 | ||||||
chr14:21318272
|
A | AT | 8 | a0001c0001t0001g0003a0001c0001t0001g0025a0003c0003t0001g0046others(5): Show | 8 | HG00639.hp2 HG01109.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306+435dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr14 | 21318272 | |||||
chr14:21318272
|
AT | A | 193 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.1306+435delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr14 | 21318272 | |||||
chr14:21318313
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1306+463T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318313 | ||||||
chr14:21318313
|
TGTTA | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1306+469_1306+472d others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr14 | 21318313 | |||||
chr14:21318343
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1306+493C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318343 | ||||||
chr14:21318393
|
T | G | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1306+543T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318393 | ||||||
chr14:21318395
|
C | T | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1306+545C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318395 | ||||||
chr14:21318400
|
C | A | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1306+550C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318400 | ||||||
chr14:21318401
|
T | G | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1306+551T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318401 | ||||||
chr14:21318408
|
G | A | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1306+558G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318408 | ||||||
chr14:21318465
|
C | G | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1306+615C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318465 | ||||||
chr14:21318489
|
T | G | 2 | a0001c0001t0001g0273a0001c0001t0001g0324 | 2 | HG03017.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1306+639T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318489 | ||||||
chr14:21318533
|
T | G | 1 | a0002c0002t0001g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1306+683T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318533 | ||||||
chr14:21318621
|
G | T | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(95): Show | 98 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1306+771G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318621 | ||||||
chr14:21318638
|
A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(95): Show | 98 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1306+788A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318638 | ||||||
chr14:21318658
|
A | C | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1306+808A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318658 | ||||||
chr14:21318697
|
G | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1306+847G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318697 | ||||||
chr14:21318723
|
C | A | 1 | a0002c0002t0001g0053 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1306+873C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318723 | ||||||
chr14:21318759
|
G | T | 5 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306+909G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318759 | ||||||
chr14:21318783
|
T | C | 22 | a0003c0003t0001g0159a0003c0003t0001g0307a0003c0003t0001g0308others(19): Show | 22 | HG00099.hp1 HG00733.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.1306+933T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318783 | ||||||
chr14:21318840
|
C | CT | 6 | a0001c0001t0001g0124a0001c0001t0001g0199a0001c0001t0001g0293others(3): Show | 6 | HG02027.hp1 HG02572.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306+1004dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr14 | 21318840 | |||||
chr14:21318859
|
T | C | 1 | a0005c0005t0001g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1306+1009T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318859 | ||||||
chr14:21318976
|
A | C | 2 | a0002c0002t0001g0074a0002c0002t0001g0077 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1307-1041A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21318976 | ||||||
chr14:21319124
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1307-893T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21319124 | ||||||
chr14:21319206
|
C | T | 1 | a0001c0001t0001g0329 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1307-811C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21319206 | ||||||
chr14:21319207
|
T | C | 1 | a0001c0001t0001g0329 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1307-810T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21319207 | ||||||
chr14:21319247
|
C | T | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1307-770C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21319247 | ||||||
chr14:21319328
|
G | A | 2 | a0001c0004t0001g0258a0001c0004t0001g0259 | 2 | HG01099.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1307-689G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21319328 | ||||||
chr14:21319673
|
G | T | 1 | a0002c0002t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1307-344G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21319673 | ||||||
chr14:21319681
|
G | T | 1 | a0002c0002t0001g0106 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1307-336G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 11/24 | chr14 | 21319681 | ||||||
chr14:21320345
|
A | C | 3 | a0001c0001t0001g0047a0001c0001t0001g0261a0001c0001t0001g0318 | 3 | NA18991.hp1 NA18998.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1467+168A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320345 | ||||||
chr14:21320347
|
T | TG | 3 | a0007c0008t0001g0157a0007c0008t0001g0163a0007c0008t0001g0166 | 3 | HG00733.hp2 HG03491.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1467+172dupG | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr14 | 21320347 | |||||
chr14:21320571
|
G | A | 1 | a0006c0006t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1467+394G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320571 | ||||||
chr14:21320581
|
G | A | 19 | a0005c0005t0001g0044a0005c0005t0001g0127a0005c0005t0001g0162others(16): Show | 19 | HG00099.hp1 HG00733.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1467+404G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320581 | ||||||
chr14:21320582
|
C | A | 19 | a0005c0005t0001g0044a0005c0005t0001g0127a0005c0005t0001g0162others(16): Show | 19 | HG00099.hp1 HG00733.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.1467+405C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320582 | ||||||
chr14:21320587
|
G | C | 1 | a0001c0001t0001g0329 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1467+410G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320587 | ||||||
chr14:21320595
|
C | CT | 21 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(18): Show | 21 | HG01167.hp1 HG01256.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.1467+439dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr14 | 21320595 | |||||
chr14:21320595
|
C | CTT | 89 | a0001c0001t0001g0151a0002c0002t0001g0023a0002c0002t0001g0032others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.1467+438_1467+439d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr14 | 21320595 | |||||
chr14:21320595
|
CT | C | 9 | a0001c0001t0001g0290a0001c0001t0001g0305a0001c0004t0001g0188others(6): Show | 9 | HG00741.hp2 HG01256.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1467+439delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr14 | 21320595 | |||||
chr14:21320636
|
G | T | 1 | a0001c0001t0001g0329 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1467+459G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320636 | ||||||
chr14:21320662
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0228 | 2 | HG02135.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1467+485C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320662 | ||||||
chr14:21320663
|
G | A | 10 | a0003c0003t0001g0307a0003c0003t0001g0308a0006c0006t0001g0115others(7): Show | 10 | HG02055.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1467+486G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320663 | ||||||
chr14:21320672
|
T | G | 1 | a0004c0007t0001g0197 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1467+495T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320672 | ||||||
chr14:21320745
|
G | A | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1468-514G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320745 | ||||||
chr14:21320815
|
G | T | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1468-444G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320815 | ||||||
chr14:21320821
|
G | A | 2 | a0001c0001t0001g0002a0001c0001t0001g0003 | 2 | HG01884.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1468-438G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320821 | ||||||
chr14:21320933
|
A | T | 199 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.1468-326A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21320933 | ||||||
chr14:21321245
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1468-14G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 12/24 | chr14 | 21321245 | ||||||
chr14:21321635
|
G | A | 95 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0099others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.1612-219G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 13/24 | chr14 | 21321635 | ||||||
chr14:21321669
|
C | T | 103 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(100): Show | 103 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1612-185C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 13/24 | chr14 | 21321669 | ||||||
chr14:21321761
|
A | G | 1 | a0011c0011t0001g0005 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1612-93A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 13/24 | chr14 | 21321761 | ||||||
chr14:21321764
|
A | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1612-90A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 13/24 | chr14 | 21321764 | ||||||
chr14:21322031
|
ACTTCGGG others(3): Show |
A | 1 | a0002c0002t0001g0060 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1762+32_1762+41del others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 21322031 | |||||
chr14:21322301
|
T | A | 204 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(201): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1762+297T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322301 | ||||||
chr14:21322403
|
C | T | 1 | a0006c0006t0001g0048 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1762+399C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322403 | ||||||
chr14:21322441
|
G | A | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1762+437G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322441 | ||||||
chr14:21322457
|
C | G | 1 | a0001c0001t0001g0329 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1762+453C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322457 | ||||||
chr14:21322459
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1762+455C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322459 | ||||||
chr14:21322469
|
G | A | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1762+465G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322469 | ||||||
chr14:21322752
|
C | T | 3 | a0003c0003t0001g0046a0003c0003t0001g0176a0025c0032t0002g0183 | 3 | HG02145.hp1 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1762+748C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322752 | ||||||
chr14:21322824
|
G | T | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1762+820G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322824 | ||||||
chr14:21322841
|
A | T | 95 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(92): Show | 95 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.1762+837A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322841 | ||||||
chr14:21322847
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1762+843A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322847 | ||||||
chr14:21322956
|
T | G | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1762+952T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322956 | ||||||
chr14:21322963
|
C | T | 96 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0099others(93): Show | 96 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1762+959C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21322963 | ||||||
chr14:21323019
|
A | G | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1762+1015A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323019 | ||||||
chr14:21323113
|
T | C | 97 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0099others(94): Show | 97 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.1762+1109T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323113 | ||||||
chr14:21323192
|
C | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0047others(95): Show | 98 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1762+1188C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323192 | ||||||
chr14:21323192
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1762+1188C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323192 | ||||||
chr14:21323250
|
C | A | 1 | a0001c0001t0001g0329 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1762+1246C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323250 | ||||||
chr14:21323296
|
C | T | 1 | a0015c0019t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1762+1292C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323296 | ||||||
chr14:21323315
|
A | G | 303 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0016others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1763-1303A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323315 | ||||||
chr14:21323336
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1763-1282C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323336 | ||||||
chr14:21323347
|
G | A | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1763-1271G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323347 | ||||||
chr14:21323427
|
G | GA | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0004g0177others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1763-1179dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 21323427 | |||||
chr14:21323487
|
C | G | 205 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1763-1131C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323487 | ||||||
chr14:21323548
|
A | G | 205 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1763-1070A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323548 | ||||||
chr14:21323623
|
T | C | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1763-995T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323623 | ||||||
chr14:21323635
|
A | G | 1 | a0001c0001t0001g0332 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1763-983A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323635 | ||||||
chr14:21323708
|
C | A | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1763-910C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323708 | ||||||
chr14:21323786
|
C | CGT | 32 | a0003c0003t0001g0046a0003c0003t0001g0159a0003c0003t0001g0176others(29): Show | 32 | HG00099.hp1 HG00733.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.1763-815_1763-814d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 21323786 | |||||
chr14:21323786
|
C | CGTGT | 4 | a0011c0011t0001g0005a0011c0011t0001g0126a0011c0011t0001g0128others(1): Show | 4 | HG02572.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1763-817_1763-814d others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr14 | 21323786 | |||||
chr14:21323789
|
G | A | 91 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(88): Show | 91 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.1763-829G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323789 | ||||||
chr14:21323791
|
G | A | 2 | a0003c0003t0001g0026a0003c0003t0001g0028 | 2 | NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1763-827G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21323791 | ||||||
chr14:21324004
|
G | A | 2 | a0013c0043t0001g0117a0020c0040t0001g0264 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1763-614G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324004 | ||||||
chr14:21324128
|
T | G | 1 | a0001c0001t0001g0138 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1763-490T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324128 | ||||||
chr14:21324177
|
A | G | 7 | a0001c0001t0001g0016a0001c0001t0001g0138a0001c0001t0001g0187others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1763-441A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324177 | ||||||
chr14:21324209
|
G | C | 1 | a0002c0002t0001g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1763-409G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324209 | ||||||
chr14:21324215
|
A | T | 1 | a0002c0002t0001g0073 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1763-403A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324215 | ||||||
chr14:21324226
|
C | T | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1763-392C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324226 | ||||||
chr14:21324307
|
C | T | 93 | a0002c0002t0001g0023a0002c0002t0001g0024a0002c0002t0001g0032others(90): Show | 93 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1763-311C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324307 | ||||||
chr14:21324308
|
A | G | 208 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0102others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1763-310A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324308 | ||||||
chr14:21324351
|
C | A | 1 | a0006c0006t0001g0038 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1763-267C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324351 | ||||||
chr14:21324352
|
C | T | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1763-266C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324352 | ||||||
chr14:21324552
|
C | T | 13 | a0003c0003t0001g0006a0003c0003t0001g0186a0003c0003t0001g0249others(10): Show | 13 | HG01109.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1763-66C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 14/24 | chr14 | 21324552 | ||||||
chr14:21325077
|
G | A | 27 | a0005c0005t0001g0044a0005c0005t0001g0116a0005c0005t0001g0118others(24): Show | 27 | HG00099.hp1 HG00733.hp2 HG01099.hp2 others(24): Show |
splice_region_variant&intron_variant | LOW | c.2215+7G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 15/24 | chr14 | 21325077 | ||||||
chr14:21325160
|
T | G | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2216-72T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 15/24 | chr14 | 21325160 | ||||||
chr14:21325444
|
C | A | 1 | a0002c0002t0001g0091 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2367+61C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 16/24 | chr14 | 21325444 | ||||||
chr14:21325818
|
A | C | 1 | a0007c0008t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2368-13A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 16/24 | chr14 | 21325818 | ||||||
chr14:21326333
|
G | C | 1 | a0002c0002t0001g0070 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2710+160G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21326333 | ||||||
chr14:21326430
|
A | C | 1 | a0003c0003t0001g0050 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2710+257A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21326430 | ||||||
chr14:21326491
|
A | G | 32 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(29): Show | 32 | HG00408.hp2 HG01071.hp1 HG02027.hp1 others(29): Show |
intron_variant | MODIFIER | c.2710+318A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21326491 | ||||||
chr14:21326498
|
TAGCTGGG others(5): Show |
T | 1 | a0001c0001t0001g0132 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2710+328_2710+339d others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr14 | 21326498 | |||||
chr14:21326515
|
A | T | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2710+342A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21326515 | ||||||
chr14:21326559
|
G | A | 3 | a0005c0005t0001g0116a0005c0005t0001g0118a0005c0005t0001g0119 | 3 | HG03139.hp2 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2710+386G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21326559 | ||||||
chr14:21326649
|
C | T | 1 | a0003c0003t0003g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2710+476C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21326649 | ||||||
chr14:21326750
|
A | T | 1 | a0002c0002t0001g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2710+577A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21326750 | ||||||
chr14:21327029
|
T | C | 1 | a0006c0006t0001g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2711-594T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21327029 | ||||||
chr14:21327170
|
A | G | 1 | a0023c0028t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2711-453A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21327170 | ||||||
chr14:21327511
|
C | T | 2 | a0005c0005t0001g0109a0021c0045t0001g0111 | 2 | HG00741.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2711-112C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 17/24 | chr14 | 21327511 | ||||||
chr14:21327918
|
C | A | 2 | a0005c0005t0001g0109a0021c0045t0001g0111 | 2 | HG00741.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2895+111C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/24 | chr14 | 21327918 | ||||||
chr14:21328031
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2895+224G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/24 | chr14 | 21328031 | ||||||
chr14:21328034
|
G | A | 1 | a0023c0028t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2895+227G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/24 | chr14 | 21328034 | ||||||
chr14:21328066
|
G | T | 1 | a0002c0002t0001g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2895+259G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/24 | chr14 | 21328066 | ||||||
chr14:21328109
|
C | T | 1 | a0001c0001t0004g0170 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2895+302C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/24 | chr14 | 21328109 | ||||||
chr14:21328169
|
CA | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0123others(82): Show | 85 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.2896-244delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr14 | 21328169 | |||||
chr14:21328222
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2896-202C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 18/24 | chr14 | 21328222 | ||||||
chr14:21328658
|
T | C | 7 | a0001c0001t0001g0002a0003c0003t0001g0046a0003c0003t0001g0176others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.3099+31T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21328658 | ||||||
chr14:21328681
|
T | C | 1 | a0006c0006t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3099+54T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21328681 | ||||||
chr14:21328759
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3099+132C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21328759 | ||||||
chr14:21328801
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3099+174T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21328801 | ||||||
chr14:21328870
|
G | A | 73 | a0001c0001t0001g0016a0001c0001t0001g0123a0001c0001t0001g0138others(70): Show | 73 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.3099+243G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21328870 | ||||||
chr14:21328915
|
G | C | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3099+288G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21328915 | ||||||
chr14:21329147
|
C | CA | 57 | a0001c0001t0001g0002a0001c0001t0001g0123a0001c0001t0001g0204others(54): Show | 57 | HG00408.hp2 HG01071.hp1 HG01261.hp2 others(54): Show |
intron_variant | MODIFIER | c.3099+538dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr14 | 21329147 | |||||
chr14:21329307
|
A | G | 1 | a0023c0028t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3099+680A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329307 | ||||||
chr14:21329337
|
T | C | 1 | a0006c0006t0001g0036 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3099+710T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329337 | ||||||
chr14:21329356
|
A | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0123others(80): Show | 83 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.3099+729A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329356 | ||||||
chr14:21329357
|
T | A | 1 | a0022c0033t0001g0001 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3099+730T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329357 | ||||||
chr14:21329366
|
G | C | 2 | a0005c0005t0001g0109a0021c0045t0001g0111 | 2 | HG00741.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3099+739G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329366 | ||||||
chr14:21329463
|
T | G | 2 | a0005c0005t0001g0109a0021c0045t0001g0111 | 2 | HG00741.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3100-786T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329463 | ||||||
chr14:21329567
|
C | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0123others(82): Show | 85 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.3100-682C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329567 | ||||||
chr14:21329625
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3100-624C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329625 | ||||||
chr14:21329738
|
C | G | 1 | a0002c0002t0001g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.3100-511C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329738 | ||||||
chr14:21329775
|
C | T | 6 | a0003c0003t0001g0046a0003c0003t0001g0176a0005c0005t0001g0020others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3100-474C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329775 | ||||||
chr14:21329799
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0123others(82): Show | 85 | HG00280.hp2 HG00408.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.3100-450G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329799 | ||||||
chr14:21329856
|
G | A | 1 | a0003c0012t0001g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3100-393G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329856 | ||||||
chr14:21329866
|
C | G | 1 | a0005c0046t0002g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3100-383C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21329866 | ||||||
chr14:21330043
|
A | G | 2 | a0005c0005t0001g0109a0021c0045t0001g0111 | 2 | HG00741.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3100-206A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21330043 | ||||||
chr14:21330187
|
G | A | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3100-62G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 19/24 | chr14 | 21330187 | ||||||
chr14:21330434
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3238+47C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21330434 | ||||||
chr14:21330557
|
G | A | 1 | a0001c0037t0001g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3238+170G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21330557 | ||||||
chr14:21330611
|
A | G | 1 | a0001c0004t0001g0200 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3238+224A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21330611 | ||||||
chr14:21330614
|
C | T | 1 | a0012c0017t0001g0022 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3238+227C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21330614 | ||||||
chr14:21330685
|
T | C | 1 | a0007c0013t0001g0158 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3238+298T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21330685 | ||||||
chr14:21330973
|
G | A | 1 | a0018c0042t0003g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3238+586G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21330973 | ||||||
chr14:21331051
|
A | G | 2 | a0004c0007t0001g0226a0004c0007t0001g0321 | 2 | NA18959.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.3238+664A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331051 | ||||||
chr14:21331134
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0138others(73): Show | 76 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.3238+747T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331134 | ||||||
chr14:21331151
|
C | T | 7 | a0008c0009t0001g0110a0008c0009t0001g0114a0008c0009t0001g0253others(4): Show | 7 | HG02055.hp1 HG02818.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.3238+764C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331151 | ||||||
chr14:21331312
|
C | T | 23 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(20): Show | 23 | HG00280.hp2 HG00642.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.3238+925C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331312 | ||||||
chr14:21331414
|
G | C | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3238+1027G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331414 | ||||||
chr14:21331559
|
A | G | 1 | a0001c0004t0001g0327 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3238+1172A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331559 | ||||||
chr14:21331578
|
C | A | 5 | a0003c0003t0003g0009a0003c0003t0003g0010a0003c0003t0003g0011others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3238+1191C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331578 | ||||||
chr14:21331625
|
A | G | 3 | a0009c0016t0001g0247a0009c0016t0001g0248a0009c0016t0001g0311 | 3 | HG02895.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3238+1238A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331625 | ||||||
chr14:21331627
|
TTCTGACA others(4): Show |
T | 1 | a0025c0032t0002g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3238+1243_3238+125 others(15): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 21331627 | |||||
chr14:21331740
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0243others(1): Show | 4 | NA18959.hp2 NA18963.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.3238+1353C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21331740 | ||||||
chr14:21331936
|
A | AT | 13 | a0001c0001t0001g0149a0001c0001t0001g0234a0001c0001t0001g0269others(10): Show | 13 | HG01361.hp2 HG02004.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.3238+1569dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 21331936 | |||||
chr14:21331936
|
AT | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0123others(32): Show | 35 | HG01071.hp1 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.3238+1569delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 21331936 | |||||
chr14:21331936
|
ATT | A | 14 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(11): Show | 14 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.3238+1568_3238+156 others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 21331936 | |||||
chr14:21331936
|
ATTT | A | 14 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0006others(11): Show | 14 | HG01261.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3238+1567_3238+156 others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 21331936 | |||||
chr14:21332125
|
G | T | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.3238+1738G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332125 | ||||||
chr14:21332247
|
T | C | 1 | a0003c0003t0001g0249 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3238+1860T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332247 | ||||||
chr14:21332337
|
T | C | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3238+1950T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332337 | ||||||
chr14:21332574
|
G | C | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.3239-2031G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332574 | ||||||
chr14:21332932
|
C | T | 14 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0006others(11): Show | 14 | HG01261.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.3239-1673C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332932 | ||||||
chr14:21332956
|
T | C | 25 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(22): Show | 25 | HG01071.hp1 HG02027.hp1 HG02074.hp2 others(22): Show |
intron_variant | MODIFIER | c.3239-1649T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332956 | ||||||
chr14:21332977
|
G | A | 4 | a0002c0002t0001g0087a0007c0008t0001g0157a0007c0008t0001g0163others(1): Show | 4 | HG00733.hp2 HG01361.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.3239-1628G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332977 | ||||||
chr14:21332986
|
C | T | 1 | a0003c0003t0001g0039 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3239-1619C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21332986 | ||||||
chr14:21333115
|
A | G | 1 | a0001c0001t0001g0016 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3239-1490A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333115 | ||||||
chr14:21333122
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3239-1483C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333122 | ||||||
chr14:21333361
|
CG | C | 40 | a0001c0001t0001g0123a0001c0001t0001g0138a0001c0001t0004g0177others(37): Show | 40 | HG00741.hp2 HG01261.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.3239-1243delG | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333361 | ||||||
chr14:21333375
|
C | G | 27 | a0001c0001t0001g0123a0001c0001t0001g0138a0001c0001t0004g0177others(24): Show | 27 | HG00741.hp2 HG02055.hp1 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.3239-1230C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333375 | ||||||
chr14:21333525
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3239-1080G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333525 | ||||||
chr14:21333569
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3239-1036T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333569 | ||||||
chr14:21333575
|
T | C | 5 | a0001c0001t0001g0278a0003c0003t0003g0008a0005c0005t0001g0044others(2): Show | 5 | HG01109.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3239-1030T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333575 | ||||||
chr14:21333576
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3239-1029G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333576 | ||||||
chr14:21333577
|
G | C | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3239-1028G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333577 | ||||||
chr14:21333833
|
G | A | 1 | a0001c0001t0001g0278 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3239-772G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333833 | ||||||
chr14:21333924
|
C | CT | 31 | a0001c0001t0001g0002a0001c0001t0001g0102a0001c0001t0001g0123others(28): Show | 31 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.3239-662dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 21333924 | |||||
chr14:21333924
|
C | CTT | 43 | a0001c0001t0001g0138a0001c0001t0001g0204a0001c0001t0001g0233others(40): Show | 43 | HG01071.hp1 HG01261.hp2 HG02027.hp1 others(40): Show |
intron_variant | MODIFIER | c.3239-663_3239-662d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr14 | 21333924 | |||||
chr14:21333930
|
T | TC | 5 | a0015c0019t0001g0191a0015c0019t0001g0192a0018c0042t0003g0012others(2): Show | 5 | HG00741.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3239-675_3239-674i others(3): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333930 | ||||||
chr14:21333931
|
T | C | 12 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0249others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3239-674T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333931 | ||||||
chr14:21333951
|
A | C | 3 | a0001c0001t0001g0144a0001c0031t0001g0274a0005c0005t0001g0306 | 3 | HG01358.hp1 HG01433.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.3239-654A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333951 | ||||||
chr14:21333972
|
G | C | 11 | a0001c0004t0002g0244a0003c0003t0001g0249a0003c0003t0002g0184others(8): Show | 11 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.3239-633G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21333972 | ||||||
chr14:21334032
|
C | T | 1 | a0008c0009t0001g0298 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3239-573C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334032 | ||||||
chr14:21334058
|
G | A | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3239-547G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334058 | ||||||
chr14:21334109
|
A | G | 5 | a0003c0003t0003g0009a0003c0003t0003g0010a0003c0003t0003g0011others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3239-496A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334109 | ||||||
chr14:21334110
|
C | T | 30 | a0001c0001t0001g0002a0001c0001t0001g0173a0001c0001t0001g0187others(27): Show | 30 | HG01071.hp1 HG01261.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3239-495C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334110 | ||||||
chr14:21334114
|
G | A | 1 | a0006c0006t0001g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3239-491G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334114 | ||||||
chr14:21334420
|
A | T | 4 | a0015c0019t0001g0191a0015c0019t0001g0192a0021c0045t0001g0111others(1): Show | 4 | HG00741.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3239-185A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334420 | ||||||
chr14:21334471
|
C | T | 2 | a0001c0001t0001g0003a0018c0042t0003g0012 | 2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.3239-134C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334471 | ||||||
chr14:21334502
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3239-103G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 20/24 | chr14 | 21334502 | ||||||
chr14:21334744
|
C | T | 1 | a0003c0003t0003g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3339+39C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21334744 | ||||||
chr14:21334971
|
G | A | 1 | a0002c0002t0001g0052 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3339+266G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21334971 | ||||||
chr14:21335002
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+297C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335002 | ||||||
chr14:21335009
|
G | C | 1 | a0006c0006t0001g0035 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3339+304G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335009 | ||||||
chr14:21335046
|
C | CA | 46 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0146others(43): Show | 46 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3339+366dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21335046 | |||||
chr14:21335046
|
CA | C | 15 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0039others(12): Show | 15 | HG00280.hp1 HG01496.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.3339+366delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21335046 | |||||
chr14:21335111
|
G | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+406G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335111 | ||||||
chr14:21335125
|
A | G | 3 | a0001c0001t0002g0004a0005c0005t0001g0020a0005c0005t0001g0021 | 3 | HG02109.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3339+420A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335125 | ||||||
chr14:21335165
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3339+460A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335165 | ||||||
chr14:21335192
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(4): Show | 7 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3339+487G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335192 | ||||||
chr14:21335196
|
A | G | 6 | a0003c0003t0001g0046a0003c0003t0001g0176a0015c0019t0001g0191others(3): Show | 6 | HG00741.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3339+491A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335196 | ||||||
chr14:21335257
|
G | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+552G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335257 | ||||||
chr14:21335305
|
C | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+600C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335305 | ||||||
chr14:21335359
|
A | G | 316 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.3339+654A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335359 | ||||||
chr14:21335426
|
A | G | 1 | a0005c0046t0002g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3339+721A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335426 | ||||||
chr14:21335443
|
C | A | 6 | a0003c0003t0001g0046a0003c0003t0001g0176a0015c0019t0001g0191others(3): Show | 6 | HG00741.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3339+738C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335443 | ||||||
chr14:21335484
|
G | T | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3339+779G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335484 | ||||||
chr14:21335520
|
G | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+815G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335520 | ||||||
chr14:21335579
|
C | T | 3 | a0001c0001t0002g0004a0005c0005t0001g0020a0005c0005t0001g0021 | 3 | HG02109.hp2 HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3339+874C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335579 | ||||||
chr14:21335602
|
G | A | 1 | a0018c0042t0003g0012 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3339+897G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335602 | ||||||
chr14:21335657
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.3339+952C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335657 | ||||||
chr14:21335700
|
T | A | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+995T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335700 | ||||||
chr14:21335704
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+999A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335704 | ||||||
chr14:21335785
|
C | T | 6 | a0003c0003t0001g0046a0003c0003t0001g0176a0015c0019t0001g0191others(3): Show | 6 | HG00741.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3339+1080C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335785 | ||||||
chr14:21335800
|
A | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+1095A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335800 | ||||||
chr14:21335806
|
C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0003a0001c0001t0001g0173a0017c0038t0001g0121others(1): Show | 4 | HG01884.hp1 HG02630.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3339+1109_3339+111 others(17): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21335806 | |||||
chr14:21335806
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3339+1109_3339+111 others(18): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21335806 | |||||
chr14:21335806
|
C | CAAAAAAA others(8): Show |
12 | a0001c0001t0001g0187a0001c0026t0001g0194a0003c0003t0001g0249others(9): Show | 12 | HG01261.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3339+1109_3339+111 others(19): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21335806 | |||||
chr14:21335806
|
C | CAAAAAAA others(9): Show |
2 | a0001c0004t0002g0244a0003c0003t0005g0015 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3339+1109_3339+111 others(20): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21335806 | |||||
chr14:21335895
|
A | G | 1 | a0003c0003t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3339+1190A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335895 | ||||||
chr14:21335915
|
T | C | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(42): Show | 45 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.3339+1210T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335915 | ||||||
chr14:21335916
|
C | T | 2 | a0001c0004t0001g0198a0001c0004t0001g0219 | 2 | HG00544.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.3339+1211C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335916 | ||||||
chr14:21335917
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3339+1212G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335917 | ||||||
chr14:21335945
|
C | CAGTT | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+1241_3339+124 others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21335945 | |||||
chr14:21335972
|
A | G | 12 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0249others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3339+1267A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335972 | ||||||
chr14:21335973
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+1268A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335973 | ||||||
chr14:21335983
|
A | G | 1 | a0005c0046t0002g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3339+1278A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21335983 | ||||||
chr14:21336052
|
G | A | 1 | a0004c0007t0001g0284 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3339+1347G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336052 | ||||||
chr14:21336076
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3339+1371G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336076 | ||||||
chr14:21336158
|
T | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(42): Show | 45 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.3339+1453T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336158 | ||||||
chr14:21336201
|
A | C | 5 | a0001c0001t0001g0130a0002c0002t0001g0087a0007c0008t0001g0157others(2): Show | 5 | HG00733.hp2 HG00735.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.3339+1496A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336201 | ||||||
chr14:21336349
|
C | T | 1 | a0007c0008t0001g0113 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3339+1644C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336349 | ||||||
chr14:21336351
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(42): Show | 45 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.3339+1646C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336351 | ||||||
chr14:21336399
|
T | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(42): Show | 45 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.3339+1694T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336399 | ||||||
chr14:21336405
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0173others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+1700C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336405 | ||||||
chr14:21336436
|
G | C | 1 | a0001c0001t0001g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3339+1731G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336436 | ||||||
chr14:21336504
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3339+1799T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336504 | ||||||
chr14:21336591
|
A | G | 6 | a0003c0003t0001g0046a0003c0003t0001g0176a0015c0019t0001g0191others(3): Show | 6 | HG00741.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3339+1886A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336591 | ||||||
chr14:21336678
|
C | T | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(42): Show | 45 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.3339+1973C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336678 | ||||||
chr14:21336691
|
A | C | 1 | a0001c0004t0001g0217 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3339+1986A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336691 | ||||||
chr14:21336890
|
A | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(43): Show | 46 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3339+2185A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336890 | ||||||
chr14:21336998
|
G | A | 4 | a0015c0019t0001g0191a0015c0019t0001g0192a0021c0045t0001g0111others(1): Show | 4 | HG00741.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3339+2293G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21336998 | ||||||
chr14:21337007
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(45): Show | 48 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.3339+2302A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337007 | ||||||
chr14:21337085
|
C | G | 20 | a0001c0001t0001g0003a0001c0001t0001g0138a0005c0005t0002g0303others(17): Show | 20 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.3339+2380C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337085 | ||||||
chr14:21337155
|
G | GT | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0138others(43): Show | 46 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.3339+2453dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21337155 | |||||
chr14:21337161
|
G | A | 6 | a0003c0003t0001g0046a0003c0003t0001g0176a0015c0019t0001g0191others(3): Show | 6 | HG00741.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3339+2456G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337161 | ||||||
chr14:21337395
|
A | C | 12 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0249others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3339+2690A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337395 | ||||||
chr14:21337438
|
C | CT | 7 | a0001c0001t0001g0228a0001c0001t0001g0291a0002c0002t0001g0066others(4): Show | 7 | HG02145.hp2 HG02280.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.3339+2750dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21337438 | |||||
chr14:21337438
|
C | CTTT | 10 | a0001c0026t0001g0194a0003c0003t0001g0249a0003c0003t0002g0184others(7): Show | 10 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3339+2748_3339+275 others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21337438 | |||||
chr14:21337438
|
C | CTTTTTT | 27 | a0001c0001t0001g0003a0001c0001t0001g0150a0001c0001t0001g0151others(24): Show | 27 | HG00280.hp2 HG01099.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.3339+2745_3339+275 others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21337438 | |||||
chr14:21337503
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3339+2798G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337503 | ||||||
chr14:21337685
|
A | G | 1 | a0003c0003t0001g0224 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3339+2980A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337685 | ||||||
chr14:21337745
|
G | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(40): Show | 43 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.3339+3040G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337745 | ||||||
chr14:21337753
|
A | AT | 70 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0124others(67): Show | 70 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.3339+3073dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21337753 | |||||
chr14:21337753
|
AT | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0173a0005c0005t0001g0120others(16): Show | 19 | HG01884.hp1 HG02630.hp1 HG02717.hp1 others(16): Show |
intron_variant | MODIFIER | c.3339+3073delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21337753 | |||||
chr14:21337753
|
ATTT | A | 6 | a0001c0001t0001g0150a0001c0001t0001g0168a0001c0004t0001g0196others(3): Show | 6 | HG00280.hp2 HG01099.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.3339+3071_3339+307 others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21337753 | |||||
chr14:21337819
|
C | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(40): Show | 43 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.3339+3114C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337819 | ||||||
chr14:21337834
|
C | A | 1 | a0003c0003t0001g0159 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3339+3129C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337834 | ||||||
chr14:21337868
|
G | A | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(6): Show | 9 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.3339+3163G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337868 | ||||||
chr14:21337977
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(39): Show | 42 | HG00280.hp2 HG01192.hp2 HG01256.hp2 others(39): Show |
intron_variant | MODIFIER | c.3339+3272T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21337977 | ||||||
chr14:21338041
|
C | T | 1 | a0001c0001t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3339+3336C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338041 | ||||||
chr14:21338106
|
T | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(40): Show | 43 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.3339+3401T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338106 | ||||||
chr14:21338107
|
G | A | 43 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(40): Show | 43 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.3339+3402G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338107 | ||||||
chr14:21338152
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3339+3447G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338152 | ||||||
chr14:21338163
|
G | T | 43 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(40): Show | 43 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.3339+3458G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338163 | ||||||
chr14:21338186
|
G | C | 1 | a0004c0007t0001g0285 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3339+3481G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338186 | ||||||
chr14:21338196
|
G | A | 1 | a0006c0006t0001g0042 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3339+3491G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338196 | ||||||
chr14:21338199
|
A | G | 19 | a0001c0001t0001g0102a0002c0002t0001g0056a0002c0002t0001g0061others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.3339+3494A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338199 | ||||||
chr14:21338240
|
G | A | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(6): Show | 9 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.3339+3535G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338240 | ||||||
chr14:21338263
|
T | C | 12 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0249others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3339+3558T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338263 | ||||||
chr14:21338271
|
T | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(63): Show | 66 | HG00280.hp2 HG01071.hp1 HG01099.hp1 others(63): Show |
intron_variant | MODIFIER | c.3339+3566T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338271 | ||||||
chr14:21338341
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(51): Show | 54 | HG00280.hp2 HG00741.hp2 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.3339+3636C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338341 | ||||||
chr14:21338342
|
A | T | 1 | a0001c0001t0001g0275 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3339+3637A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338342 | ||||||
chr14:21338474
|
G | C | 3 | a0009c0016t0001g0247a0009c0016t0001g0248a0009c0016t0001g0311 | 3 | HG02895.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3339+3769G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338474 | ||||||
chr14:21338626
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0138a0001c0001t0001g0150others(28): Show | 31 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(28): Show |
intron_variant | MODIFIER | c.3339+3921T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338626 | ||||||
chr14:21338876
|
C | T | 23 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(20): Show | 23 | HG01071.hp1 HG02027.hp1 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.3340-4160C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338876 | ||||||
chr14:21338877
|
G | A | 12 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0249others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3340-4159G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338877 | ||||||
chr14:21338913
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3340-4123C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338913 | ||||||
chr14:21338957
|
G | C | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3340-4079G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338957 | ||||||
chr14:21338996
|
C | A | 2 | a0002c0002t0001g0074a0002c0002t0001g0077 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3340-4040C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338996 | ||||||
chr14:21338997
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0004g0177 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.3340-4039G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21338997 | ||||||
chr14:21339018
|
C | A | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(7): Show | 10 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.3340-4018C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339018 | ||||||
chr14:21339035
|
T | C | 1 | a0001c0027t0004g0171 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3340-4001T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339035 | ||||||
chr14:21339136
|
A | G | 24 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(21): Show | 24 | HG01071.hp1 HG02027.hp1 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.3340-3900A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339136 | ||||||
chr14:21339217
|
G | A | 1 | a0006c0006t0001g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3340-3819G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339217 | ||||||
chr14:21339243
|
C | G | 2 | a0005c0005t0001g0020a0005c0005t0001g0021 | 2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3340-3793C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339243 | ||||||
chr14:21339271
|
C | A | 12 | a0001c0004t0002g0244a0001c0026t0001g0194a0003c0003t0001g0249others(9): Show | 12 | HG02055.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.3340-3765C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339271 | ||||||
chr14:21339306
|
C | T | 11 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(8): Show | 11 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.3340-3730C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339306 | ||||||
chr14:21339315
|
G | A | 1 | a0001c0004t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3340-3721G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339315 | ||||||
chr14:21339377
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3340-3659C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339377 | ||||||
chr14:21339378
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0187a0006c0006t0001g0182 | 3 | HG01261.hp2 HG01884.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3340-3658G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339378 | ||||||
chr14:21339412
|
C | T | 1 | a0003c0003t0003g0008 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3340-3624C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339412 | ||||||
chr14:21339431
|
C | T | 1 | a0005c0005t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3340-3605C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339431 | ||||||
chr14:21339448
|
A | C | 1 | a0005c0046t0002g0140 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3340-3588A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339448 | ||||||
chr14:21339463
|
A | G | 2 | a0001c0004t0001g0215a0001c0004t0001g0222 | 2 | HG00642.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.3340-3573A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339463 | ||||||
chr14:21339467
|
A | G | 1 | a0005c0005t0002g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3340-3569A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339467 | ||||||
chr14:21339640
|
T | C | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(6): Show | 9 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.3340-3396T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339640 | ||||||
chr14:21339779
|
A | G | 1 | a0024c0030t0001g0313 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3340-3257A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339779 | ||||||
chr14:21339886
|
G | A | 2 | a0001c0001t0001g0187a0006c0006t0001g0182 | 2 | HG01261.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3340-3150G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339886 | ||||||
chr14:21339983
|
G | T | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3340-3053G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21339983 | ||||||
chr14:21340084
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3340-2952G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340084 | ||||||
chr14:21340114
|
A | G | 31 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0220others(28): Show | 31 | HG00741.hp2 HG01071.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.3340-2922A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340114 | ||||||
chr14:21340292
|
T | C | 1 | a0002c0002t0001g0023 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3340-2744T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340292 | ||||||
chr14:21340375
|
C | T | 1 | a0005c0005t0002g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3340-2661C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340375 | ||||||
chr14:21340392
|
C | T | 3 | a0003c0003t0001g0046a0003c0003t0001g0176a0006c0006t0001g0041 | 3 | HG02004.hp1 HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3340-2644C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340392 | ||||||
chr14:21340479
|
A | G | 2 | a0003c0003t0005g0014a0003c0003t0005g0015 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3340-2557A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340479 | ||||||
chr14:21340540
|
A | G | 6 | a0001c0001t0001g0003a0003c0003t0001g0006a0003c0003t0001g0186others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3340-2496A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340540 | ||||||
chr14:21340570
|
G | T | 1 | a0029c0023t0001g0299 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3340-2466G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340570 | ||||||
chr14:21340606
|
C | G | 33 | a0001c0001t0001g0123a0001c0001t0001g0138a0001c0001t0001g0187others(30): Show | 33 | HG01261.hp2 HG02055.hp1 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.3340-2430C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340606 | ||||||
chr14:21340609
|
C | T | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3340-2427C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340609 | ||||||
chr14:21340729
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3340-2307T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340729 | ||||||
chr14:21340786
|
C | CA | 7 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0004g0177others(4): Show | 7 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3340-2248dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21340786 | |||||
chr14:21340907
|
G | A | 1 | a0001c0001t0002g0004 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3340-2129G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21340907 | ||||||
chr14:21340930
|
C | CA | 6 | a0003c0003t0001g0249a0003c0003t0002g0184a0003c0003t0002g0185others(3): Show | 6 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.3340-2097dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21340930 | |||||
chr14:21340930
|
CA | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0150a0001c0001t0001g0151others(12): Show | 15 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.3340-2097delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21340930 | |||||
chr14:21341027
|
A | G | 5 | a0001c0001t0001g0187a0003c0003t0001g0046a0003c0003t0001g0176others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3340-2009A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341027 | ||||||
chr14:21341041
|
T | TTTTG | 10 | a0001c0001t0001g0002a0001c0001t0001g0150a0001c0001t0001g0151others(7): Show | 10 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.3340-1979_3340-197 others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21341041 | |||||
chr14:21341049
|
G | A | 6 | a0001c0001t0001g0003a0003c0003t0001g0006a0003c0003t0001g0186others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3340-1987G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341049 | ||||||
chr14:21341250
|
T | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(75): Show | 78 | HG00280.hp2 HG00741.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.3340-1786T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341250 | ||||||
chr14:21341309
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0004t0001g0193others(3): Show | 6 | HG02109.hp1 HG02622.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3340-1727G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341309 | ||||||
chr14:21341313
|
G | T | 1 | a0002c0002t0001g0083 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3340-1723G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341313 | ||||||
chr14:21341328
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3340-1708G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341328 | ||||||
chr14:21341409
|
A | G | 1 | a0005c0005t0002g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3340-1627A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341409 | ||||||
chr14:21341468
|
G | A | 5 | a0001c0001t0001g0187a0003c0003t0001g0046a0003c0003t0001g0176others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3340-1568G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341468 | ||||||
chr14:21341545
|
G | A | 1 | a0006c0006t0001g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3340-1491G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341545 | ||||||
chr14:21341749
|
T | C | 2 | a0003c0003t0001g0308a0005c0005t0001g0120 | 2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3340-1287T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341749 | ||||||
chr14:21341751
|
G | A | 1 | a0002c0002t0001g0071 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3340-1285G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341751 | ||||||
chr14:21341787
|
G | T | 1 | a0012c0017t0001g0323 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3340-1249G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341787 | ||||||
chr14:21341794
|
G | A | 6 | a0001c0001t0001g0257a0002c0002t0001g0058a0002c0002t0001g0310others(3): Show | 6 | HG02083.hp1 HG02129.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.3340-1242G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341794 | ||||||
chr14:21341827
|
G | A | 1 | a0003c0003t0001g0308 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3340-1209G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341827 | ||||||
chr14:21341907
|
G | A | 5 | a0001c0001t0001g0187a0003c0003t0001g0046a0003c0003t0001g0176others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3340-1129G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341907 | ||||||
chr14:21341942
|
C | T | 5 | a0001c0001t0001g0187a0003c0003t0001g0046a0003c0003t0001g0176others(2): Show | 5 | HG01261.hp2 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.3340-1094C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341942 | ||||||
chr14:21341981
|
A | G | 2 | a0001c0001t0002g0004a0005c0005t0002g0303 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3340-1055A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341981 | ||||||
chr14:21341996
|
G | A | 6 | a0001c0001t0001g0003a0003c0003t0001g0006a0003c0003t0001g0186others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3340-1040G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21341996 | ||||||
chr14:21342005
|
G | A | 1 | a0002c0002t0001g0094 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3340-1031G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342005 | ||||||
chr14:21342007
|
G | A | 23 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(20): Show | 23 | HG01071.hp1 HG02027.hp1 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.3340-1029G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342007 | ||||||
chr14:21342049
|
C | CA | 21 | a0001c0001t0001g0138a0001c0004t0002g0244a0003c0003t0001g0307others(18): Show | 21 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.3340-972dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21342049 | |||||
chr14:21342049
|
C | CAA | 8 | a0003c0003t0001g0249a0003c0003t0002g0184a0003c0003t0002g0185others(5): Show | 8 | HG02055.hp2 HG02717.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.3340-973_3340-972d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21342049 | |||||
chr14:21342065
|
G | A | 5 | a0003c0003t0001g0006a0003c0003t0001g0186a0005c0005t0001g0044others(2): Show | 5 | HG02630.hp1 HG02818.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3340-971G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342065 | ||||||
chr14:21342199
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3340-837G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342199 | ||||||
chr14:21342331
|
C | T | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3340-705C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342331 | ||||||
chr14:21342349
|
C | T | 10 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(7): Show | 10 | HG00280.hp2 HG00733.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.3340-687C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342349 | ||||||
chr14:21342543
|
C | CA | 28 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0220others(25): Show | 28 | HG01071.hp1 HG01109.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.3340-477dupA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21342543 | |||||
chr14:21342543
|
CA | C | 14 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(11): Show | 14 | HG00280.hp2 HG00733.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.3340-477delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr14 | 21342543 | |||||
chr14:21342572
|
C | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0187a0003c0003t0001g0046others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3340-464C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342572 | ||||||
chr14:21342607
|
G | A | 6 | a0001c0001t0001g0123a0001c0001t0001g0187a0003c0003t0001g0046others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3340-429G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342607 | ||||||
chr14:21342633
|
T | G | 18 | a0001c0001t0001g0123a0001c0001t0001g0150a0001c0001t0001g0151others(15): Show | 18 | HG00280.hp2 HG00733.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.3340-403T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342633 | ||||||
chr14:21342666
|
G | A | 12 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0187others(9): Show | 12 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.3340-370G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342666 | ||||||
chr14:21342693
|
C | G | 1 | a0002c0002t0001g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3340-343C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342693 | ||||||
chr14:21342710
|
G | C | 6 | a0001c0001t0001g0123a0001c0001t0001g0187a0003c0003t0001g0046others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3340-326G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342710 | ||||||
chr14:21342712
|
C | T | 6 | a0001c0001t0001g0123a0001c0001t0001g0187a0003c0003t0001g0046others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3340-324C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342712 | ||||||
chr14:21342736
|
T | A | 23 | a0001c0001t0001g0002a0001c0001t0001g0204a0001c0001t0001g0220others(20): Show | 23 | HG01071.hp1 HG01884.hp2 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.3340-300T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342736 | ||||||
chr14:21342785
|
G | T | 1 | a0002c0002t0001g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3340-251G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342785 | ||||||
chr14:21342839
|
A | G | 6 | a0001c0001t0001g0123a0001c0001t0001g0187a0003c0003t0001g0046others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3340-197A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342839 | ||||||
chr14:21342959
|
A | G | 4 | a0015c0019t0001g0191a0015c0019t0001g0192a0021c0045t0001g0111others(1): Show | 4 | HG00741.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3340-77A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342959 | ||||||
chr14:21342984
|
C | T | 1 | a0017c0038t0001g0121 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3340-52C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342984 | ||||||
chr14:21342985
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3340-51A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21342985 | ||||||
chr14:21343021
|
C | T | 25 | a0001c0004t0002g0244a0003c0003t0001g0249a0003c0003t0002g0184others(22): Show | 25 | HG02055.hp1 HG02055.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.3340-15C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 21/24 | chr14 | 21343021 | ||||||
chr14:21343371
|
T | C | 3 | a0001c0001t0001g0123a0005c0005t0002g0303a0006c0006t0001g0182 | 3 | HG01261.hp2 HG02451.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3532+143T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343371 | ||||||
chr14:21343378
|
A | G | 1 | a0002c0002t0001g0033 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3532+150A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343378 | ||||||
chr14:21343453
|
C | T | 1 | a0005c0005t0002g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3532+225C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343453 | ||||||
chr14:21343471
|
G | C | 59 | a0001c0001t0001g0123a0001c0001t0001g0187a0001c0001t0001g0204others(56): Show | 59 | HG00741.hp2 HG01071.hp1 HG01261.hp2 others(56): Show |
intron_variant | MODIFIER | c.3532+243G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343471 | ||||||
chr14:21343471
|
G | T | 6 | a0001c0001t0001g0003a0003c0003t0001g0006a0003c0003t0001g0186others(3): Show | 6 | HG02630.hp1 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3532+243G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343471 | ||||||
chr14:21343536
|
G | A | 7 | a0001c0001t0001g0003a0003c0003t0001g0006a0003c0003t0001g0186others(4): Show | 7 | HG01261.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.3532+308G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343536 | ||||||
chr14:21343601
|
G | T | 2 | a0008c0009t0001g0110a0028c0022t0001g0301 | 2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3532+373G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343601 | ||||||
chr14:21343646
|
G | A | 65 | a0001c0001t0001g0003a0001c0001t0001g0123a0001c0001t0001g0187others(62): Show | 65 | HG00741.hp2 HG01071.hp1 HG01261.hp2 others(62): Show |
intron_variant | MODIFIER | c.3532+418G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343646 | ||||||
chr14:21343677
|
A | G | 1 | a0001c0001t0001g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3532+449A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343677 | ||||||
chr14:21343725
|
C | T | 37 | a0001c0001t0001g0187a0001c0001t0001g0204a0001c0001t0001g0220others(34): Show | 37 | HG01071.hp1 HG02027.hp1 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.3532+497C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343725 | ||||||
chr14:21343739
|
G | A | 25 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(22): Show | 25 | HG01071.hp1 HG02027.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.3532+511G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343739 | ||||||
chr14:21343814
|
A | G | 25 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(22): Show | 25 | HG01071.hp1 HG02027.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.3532+586A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343814 | ||||||
chr14:21343866
|
G | GT | 20 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(17): Show | 20 | HG00544.hp1 HG00544.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.3532+679dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GT | G | 38 | a0001c0001t0001g0043a0001c0001t0001g0102a0001c0001t0001g0138others(35): Show | 38 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.3532+679delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTT | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0075others(70): Show | 73 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.3532+678_3532+679d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTT | G | 68 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0099others(65): Show | 68 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.3532+677_3532+679d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTT | G | 12 | a0001c0001t0001g0134a0001c0001t0001g0204a0001c0001t0001g0255others(9): Show | 12 | HG01256.hp1 HG01496.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.3532+676_3532+679d others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTT | G | 13 | a0001c0001t0001g0220a0001c0001t0001g0233a0001c0001t0001g0293others(10): Show | 13 | HG01109.hp1 HG02027.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3532+675_3532+679d others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTT | G | 8 | a0001c0001t0001g0243a0001c0001t0001g0266a0001c0001t0001g0309others(5): Show | 8 | HG01071.hp1 HG02027.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.3532+674_3532+679d others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(1): Show |
G | 11 | a0001c0001t0001g0324a0001c0001t0002g0004a0001c0004t0002g0244others(8): Show | 11 | HG02055.hp2 HG02109.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.3532+672_3532+679d others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(2): Show |
G | 11 | a0001c0001t0001g0187a0003c0003t0001g0176a0003c0003t0002g0185others(8): Show | 11 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3532+671_3532+679d others(11): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(3): Show |
G | 3 | a0002c0002t0001g0059a0003c0003t0001g0046a0025c0032t0002g0183 | 3 | HG01167.hp2 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3532+670_3532+679d others(12): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(4): Show |
G | 4 | a0006c0006t0001g0048a0015c0019t0001g0191a0015c0019t0001g0192others(1): Show | 4 | HG02273.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3532+669_3532+679d others(13): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0146a0001c0004t0001g0190a0006c0006t0001g0038 | 3 | HG01192.hp1 HG02148.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.3532+668_3532+679d others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(6): Show |
G | 10 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0141others(7): Show | 10 | HG00738.hp1 HG01167.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.3532+667_3532+679d others(15): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0004g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3532+666_3532+679d others(16): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(8): Show |
G | 4 | a0001c0001t0001g0267a0003c0003t0001g0307a0007c0008t0001g0113others(1): Show | 4 | HG00099.hp2 HG02451.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.3532+665_3532+679d others(17): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(11): Show |
G | 3 | a0001c0001t0001g0003a0007c0008t0001g0157a0021c0045t0001g0111 | 3 | HG00733.hp2 HG00741.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.3532+662_3532+679d others(20): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(12): Show |
G | 3 | a0001c0001t0001g0130a0002c0002t0001g0087a0007c0008t0001g0163 | 3 | HG00735.hp1 HG01361.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.3532+661_3532+679d others(21): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(13): Show |
G | 2 | a0005c0005t0002g0303a0018c0042t0003g0012 | 2 | HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3532+660_3532+679d others(22): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(14): Show |
G | 4 | a0003c0003t0001g0006a0003c0003t0001g0186a0005c0005t0001g0044others(1): Show | 4 | HG02818.hp1 HG03516.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.3532+659_3532+679d others(23): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(15): Show |
G | 2 | a0001c0001t0001g0132a0006c0006t0001g0182 | 2 | HG00323.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.3532+658_3532+679d others(24): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(19): Show |
G | 1 | a0004c0007t0001g0284 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3532+654_3532+679d others(28): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343866
|
GTTTTTTT others(20): Show |
G | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(6): Show | 9 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.3532+653_3532+679d others(29): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr14 | 21343866 | |||||
chr14:21343870
|
T | G | 1 | a0007c0008t0001g0178 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3532+642T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343870 | ||||||
chr14:21343891
|
T | G | 3 | a0015c0019t0001g0191a0015c0019t0001g0192a0023c0028t0001g0169 | 3 | HG02559.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3532+663T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343891 | ||||||
chr14:21343898
|
T | G | 4 | a0015c0019t0001g0191a0015c0019t0001g0192a0021c0045t0001g0111others(1): Show | 4 | HG00741.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3532+670T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21343898 | ||||||
chr14:21344132
|
A | G | 3 | a0015c0019t0001g0191a0015c0019t0001g0192a0023c0028t0001g0169 | 3 | HG02559.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3532+904A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344132 | ||||||
chr14:21344135
|
G | A | 1 | a0001c0037t0001g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3532+907G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344135 | ||||||
chr14:21344175
|
G | A | 105 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0102others(102): Show | 105 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.3533-938G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344175 | ||||||
chr14:21344250
|
G | A | 1 | a0019c0041t0001g0330 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3533-863G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344250 | ||||||
chr14:21344266
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3533-847T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344266 | ||||||
chr14:21344277
|
C | A | 1 | a0003c0012t0001g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3533-836C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344277 | ||||||
chr14:21344311
|
G | A | 3 | a0015c0019t0001g0191a0015c0019t0001g0192a0023c0028t0001g0169 | 3 | HG02559.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3533-802G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344311 | ||||||
chr14:21344366
|
A | G | 1 | a0002c0002t0001g0089 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3533-747A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344366 | ||||||
chr14:21344421
|
C | T | 8 | a0001c0001t0001g0139a0002c0002t0001g0147a0003c0003t0001g0068others(5): Show | 8 | HG00741.hp1 HG01257.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.3533-692C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344421 | ||||||
chr14:21344716
|
C | T | 1 | a0012c0017t0001g0320 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3533-397C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344716 | ||||||
chr14:21344860
|
C | T | 1 | a0002c0002t0001g0088 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3533-253C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344860 | ||||||
chr14:21344914
|
C | G | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(6): Show | 9 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.3533-199C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344914 | ||||||
chr14:21344949
|
C | T | 1 | a0001c0004t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3533-164C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344949 | ||||||
chr14:21344959
|
T | C | 3 | a0015c0019t0001g0191a0015c0019t0001g0192a0023c0028t0001g0169 | 3 | HG02559.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3533-154T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344959 | ||||||
chr14:21344965
|
T | G | 3 | a0001c0001t0001g0239a0001c0001t0001g0332a0001c0004t0001g0210 | 3 | NA18969.hp1 NA19002.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.3533-148T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344965 | ||||||
chr14:21344978
|
T | C | 1 | a0001c0004t0001g0242 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3533-135T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21344978 | ||||||
chr14:21345086
|
T | A | 1 | a0001c0001t0001g0282 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3533-27T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 22/24 | chr14 | 21345086 | ||||||
chr14:21345351
|
A | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(64): Show | 67 | HG01071.hp1 HG01261.hp2 HG01884.hp1 others(64): Show |
intron_variant | MODIFIER | c.3617+154A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21345351 | ||||||
chr14:21345387
|
G | GTTAT | 35 | a0001c0001t0001g0123a0001c0001t0001g0150a0001c0001t0001g0151others(32): Show | 35 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(32): Show |
intron_variant | MODIFIER | c.3617+217_3617+220d others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 21345387 | |||||
chr14:21345387
|
G | GTTATTTA others(1): Show |
9 | a0001c0001t0002g0004a0001c0004t0001g0196a0001c0004t0002g0244others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.3617+213_3617+220d others(10): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 21345387 | |||||
chr14:21345387
|
G | GTTATTTA others(5): Show |
25 | a0001c0001t0001g0204a0001c0001t0001g0220a0001c0001t0001g0233others(22): Show | 25 | HG01071.hp1 HG02027.hp1 HG02027.hp2 others(22): Show |
intron_variant | MODIFIER | c.3617+209_3617+220d others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 21345387 | |||||
chr14:21345387
|
GTTATTTA others(5): Show |
G | 1 | a0007c0008t0001g0178 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3617+209_3617+220d others(14): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 21345387 | |||||
chr14:21345435
|
T | C | 2 | a0001c0001t0001g0148a0003c0003t0001g0224 | 2 | HG00738.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.3617+238T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21345435 | ||||||
chr14:21345543
|
TA | T | 7 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(4): Show | 7 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.3617+347delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21345543 | ||||||
chr14:21345619
|
G | C | 7 | a0011c0011t0001g0005a0011c0011t0001g0126a0011c0011t0001g0128others(4): Show | 7 | HG02258.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3617+422G>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21345619 | ||||||
chr14:21345684
|
C | T | 1 | a0023c0028t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3617+487C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21345684 | ||||||
chr14:21345767
|
G | A | 8 | a0001c0001t0002g0004a0001c0004t0002g0244a0003c0003t0002g0184others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3617+570G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21345767 | ||||||
chr14:21345883
|
A | C | 1 | a0012c0017t0001g0320 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3617+686A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21345883 | ||||||
chr14:21346021
|
G | A | 1 | a0001c0004t0001g0221 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3617+824G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21346021 | ||||||
chr14:21346247
|
A | ATACT | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(72): Show | 75 | HG00280.hp2 HG01071.hp1 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.3617+1053_3617+105 others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 21346247 | |||||
chr14:21346363
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.3617+1166G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21346363 | ||||||
chr14:21346365
|
C | T | 1 | a0001c0004t0001g0327 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3617+1168C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21346365 | ||||||
chr14:21346392
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3617+1195A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21346392 | ||||||
chr14:21346555
|
GA | G | 8 | a0003c0003t0001g0006a0003c0003t0001g0046a0003c0003t0001g0176others(5): Show | 8 | HG01261.hp2 HG02145.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.3617+1368delA | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr14 | 21346555 | |||||
chr14:21346645
|
G | A | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3617+1448G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21346645 | ||||||
chr14:21347040
|
T | TAAA | 8 | a0001c0001t0002g0004a0001c0004t0002g0244a0003c0003t0002g0184others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3618-1132_3618-113 others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347040 | ||||||
chr14:21347049
|
C | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.3618-1123C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347049 | ||||||
chr14:21347147
|
G | T | 1 | a0005c0005t0002g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3618-1025G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347147 | ||||||
chr14:21347418
|
C | T | 1 | a0005c0005t0002g0303 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3618-754C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347418 | ||||||
chr14:21347484
|
G | T | 3 | a0001c0001t0001g0199a0002c0002t0001g0066a0003c0003t0001g0076 | 3 | HG02738.hp1 HG03490.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3618-688G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347484 | ||||||
chr14:21347722
|
G | A | 8 | a0001c0001t0002g0004a0001c0004t0002g0244a0003c0003t0002g0184others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3618-450G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347722 | ||||||
chr14:21347753
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3618-419G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347753 | ||||||
chr14:21347893
|
T | C | 21 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0156others(18): Show | 21 | HG00280.hp2 HG01099.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.3618-279T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347893 | ||||||
chr14:21347916
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3618-256G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21347916 | ||||||
chr14:21348048
|
A | G | 6 | a0003c0003t0001g0006a0003c0003t0001g0186a0005c0005t0001g0044others(3): Show | 6 | HG01261.hp2 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.3618-124A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21348048 | ||||||
chr14:21348054
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3618-118G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 23/24 | chr14 | 21348054 | ||||||
chr14:21348617
|
C | T | 1 | a0027c0035t0001g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3748+315C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21348617 | ||||||
chr14:21348663
|
CT | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.3748+381delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21348663 | |||||
chr14:21348692
|
G | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0137a0001c0001t0001g0141others(6): Show | 9 | HG00738.hp1 HG01167.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.3748+390G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21348692 | ||||||
chr14:21348708
|
C | T | 3 | a0006c0006t0001g0036a0016c0021t0001g0045a0031c0024t0001g0040 | 3 | HG00099.hp2 HG00140.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.3748+406C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21348708 | ||||||
chr14:21348850
|
C | T | 3 | a0010c0014t0001g0250a0015c0019t0001g0191a0015c0019t0001g0192 | 3 | HG02559.hp2 HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3748+548C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21348850 | ||||||
chr14:21348874
|
T | G | 1 | a0006c0006t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3748+572T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21348874 | ||||||
chr14:21349068
|
A | AT | 252 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3748+786dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21349068 | |||||
chr14:21349068
|
A | ATT | 31 | a0001c0001t0001g0139a0001c0001t0001g0150a0001c0001t0001g0151others(28): Show | 31 | HG00140.hp2 HG00741.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.3748+785_3748+786d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21349068 | |||||
chr14:21349139
|
C | T | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3748+837C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349139 | ||||||
chr14:21349152
|
C | G | 1 | a0001c0001t0001g0239 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3748+850C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349152 | ||||||
chr14:21349293
|
C | T | 4 | a0010c0014t0001g0250a0015c0019t0001g0191a0015c0019t0001g0192others(1): Show | 4 | HG02559.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3748+991C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349293 | ||||||
chr14:21349329
|
C | T | 2 | a0003c0003t0001g0046a0003c0003t0001g0176 | 2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3748+1027C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349329 | ||||||
chr14:21349366
|
G | A | 1 | a0006c0006t0001g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3748+1064G>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349366 | ||||||
chr14:21349399
|
CT | C | 253 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3748+1115delT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21349399 | |||||
chr14:21349404
|
T | C | 1 | a0003c0003t0001g0307 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3748+1102T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349404 | ||||||
chr14:21349421
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3748+1119A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349421 | ||||||
chr14:21349462
|
C | A | 4 | a0001c0001t0001g0152a0003c0003t0003g0013a0012c0017t0001g0022others(1): Show | 4 | HG02896.hp1 HG02965.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3748+1160C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349462 | ||||||
chr14:21349519
|
C | T | 1 | a0021c0045t0001g0111 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3748+1217C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349519 | ||||||
chr14:21349554
|
C | T | 6 | a0008c0009t0001g0110a0008c0009t0001g0114a0008c0009t0001g0253others(3): Show | 6 | HG02055.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3748+1252C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349554 | ||||||
chr14:21349578
|
A | T | 264 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.3748+1276A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349578 | ||||||
chr14:21349596
|
TTCTTCAT others(26): Show |
T | 1 | a0001c0004t0001g0200 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3748+1295_3748+132 others(37): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349596 | ||||||
chr14:21349683
|
C | T | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0003c0003t0001g0046others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3748+1381C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349683 | ||||||
chr14:21349700
|
A | G | 264 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.3748+1398A>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349700 | ||||||
chr14:21349766
|
G | T | 19 | a0001c0001t0001g0047a0001c0001t0001g0173a0001c0001t0001g0195others(16): Show | 19 | HG00438.hp1 HG01884.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.3749-1338G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21349766 | ||||||
chr14:21350063
|
C | G | 4 | a0010c0014t0001g0250a0015c0019t0001g0191a0015c0019t0001g0192others(1): Show | 4 | HG02559.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3749-1041C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350063 | ||||||
chr14:21350271
|
C | T | 4 | a0010c0014t0001g0250a0015c0019t0001g0191a0015c0019t0001g0192others(1): Show | 4 | HG02559.hp2 HG03041.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.3749-833C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350271 | ||||||
chr14:21350357
|
C | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(26): Show | 29 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.3749-747C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350357 | ||||||
chr14:21350366
|
ACT | A | 23 | a0001c0001t0002g0004a0001c0004t0002g0244a0003c0003t0002g0184others(20): Show | 23 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.3749-735_3749-734d others(4): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350366 | |||||
chr14:21350391
|
A | AAAAAAAC | 15 | a0001c0001t0002g0004a0003c0003t0002g0184a0003c0003t0002g0185others(12): Show | 15 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.3749-708_3749-707i others(9): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350391 | |||||
chr14:21350391
|
A | AAAAAAC | 6 | a0001c0004t0002g0244a0003c0003t0005g0014a0003c0003t0005g0015others(3): Show | 6 | HG02055.hp2 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.3749-708_3749-707i others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350391 | |||||
chr14:21350391
|
A | AAAAC | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3749-710_3749-709i others(6): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350391 | |||||
chr14:21350391
|
A | AACAAAC | 6 | a0001c0001t0001g0294a0002c0002t0001g0053a0003c0003t0001g0050others(3): Show | 6 | NA18978.hp1 NA18983.hp1 NA18987.hp1 others(3): Show |
intron_variant | MODIFIER | c.3749-712_3749-711i others(8): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350391 | |||||
chr14:21350391
|
A | ACAAAC | 255 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0043others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.3749-713_3749-712i others(7): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350391 | ||||||
chr14:21350391
|
A | C | 2 | a0003c0003t0001g0046a0003c0003t0001g0307 | 2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.3749-713A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350391 | ||||||
chr14:21350395
|
A | T | 1 | a0007c0008t0001g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3749-709A>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350395 | ||||||
chr14:21350477
|
AATT | A | 18 | a0002c0002t0001g0033a0002c0002t0001g0056a0002c0002t0001g0058others(15): Show | 18 | HG00423.hp1 HG00597.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.3749-623_3749-621d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350477 | |||||
chr14:21350490
|
GATC | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0134a0001c0004t0001g0200 | 3 | HG02040.hp1 HG02135.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.3749-611_3749-609d others(5): Show |
RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350490 | |||||
chr14:21350575
|
C | A | 16 | a0001c0001t0001g0099a0001c0001t0001g0134a0001c0001t0001g0203others(13): Show | 16 | HG00438.hp2 HG00597.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.3749-529C>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350575 | ||||||
chr14:21350614
|
C | G | 1 | a0010c0014t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3749-490C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350614 | ||||||
chr14:21350616
|
C | G | 1 | a0010c0014t0001g0276 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3749-488C>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350616 | ||||||
chr14:21350668
|
T | G | 14 | a0008c0009t0001g0110a0008c0009t0001g0114a0008c0009t0001g0253others(11): Show | 14 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.3749-436T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350668 | ||||||
chr14:21350747
|
A | C | 1 | a0001c0001t0001g0195 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3749-357A>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350747 | ||||||
chr14:21350884
|
T | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3749-220T>G | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350884 | ||||||
chr14:21350885
|
T | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3749-219T>A | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350885 | ||||||
chr14:21350886
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3749-218C>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350886 | ||||||
chr14:21350888
|
G | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0123others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3749-216G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350888 | ||||||
chr14:21350902
|
G | T | 293 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.3749-202G>T | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21350902 | ||||||
chr14:21350983
|
A | AT | 9 | a0001c0001t0001g0150a0001c0001t0001g0151a0003c0003t0001g0046others(6): Show | 9 | HG01261.hp2 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3749-119dupT | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr14 | 21350983 | |||||
chr14:21351081
|
T | C | 1 | a0012c0017t0001g0323 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3749-23T>C | RPGRIP1 | ENSG00000092200.13 | transcript | ENST00000400017.7 | protein_coding | 24/24 | chr14 | 21351081 |