geneid | 8899 |
---|---|
ensemblid | ENSG00000112739.17 |
hgncid | 17346 |
symbol | PRPF4B |
name | pre-mRNA processing factor 4B |
refseq_nuc | NM_003913.5 |
refseq_prot | NP_003904.3 |
ensembl_nuc | ENST00000337659.11 |
ensembl_prot | ENSP00000337194.6 |
mane_status | MANE Select |
chr | chr6 |
start | 4021300 |
end | 4064983 |
strand | + |
ver | v1.2 |
region | chr6:4021300-4064983 |
region5000 | chr6:4016300-4069983 |
regionname0 | PRPF4B_chr6_4021300_4064983 |
regionname5000 | PRPF4B_chr6_4016300_4069983 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1007 | 259 | 60 | 49 | 104 | 13 | 32 | 79 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002 | 1/0 | 1007 | 106 | 25 | 22 | 45 | 5 | 8 | 32 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0003 | 0/0 | 1007 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0004 | 0/0 | 1007 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0005 | 0/0 | 1007 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3024 | 239 | 46 | 48 | 104 | 13 | 27 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0002 | 1/0 | 3024 | 91 | 14 | 19 | 45 | 4 | 8 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0003 | 0/0 | 3024 | 13 | 10 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0004 | 0/0 | 3024 | 6 | 6 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0005 | 0/0 | 3024 | 5 | 5 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0006 | 0/0 | 3024 | 3 | 0 | 0 | 0 | 0 | 3 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0007 | 0/0 | 3024 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0008 | 0/0 | 3024 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0009 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0010 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0011 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0012 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0013 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0014 | 0/0 | 3024 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
c0015 | 0/0 | 3024 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4494 | 155 | 17 | 30 | 63 | 12 | 32 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0002 | 0/0 | 4494 | 84 | 14 | 16 | 43 | 4 | 7 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0003 | 0/0 | 4495 | 46 | 0 | 14 | 32 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0004 | 0/0 | 4495 | 23 | 20 | 3 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0005 | 0/0 | 4494 | 13 | 10 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0006 | 0/0 | 4494 | 11 | 10 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0007 | 0/0 | 4494 | 4 | 0 | 0 | 4 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0008 | 0/0 | 4494 | 3 | 0 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0009 | 0/0 | 4494 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0010 | 0/0 | 4494 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0011 | 0/0 | 4494 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0012 | 1/0 | 4494 | 2 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0013 | 0/0 | 4494 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0014 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0015 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0016 | 0/0 | 4495 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0017 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0018 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0019 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0020 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0021 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0022 | 0/0 | 4494 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0023 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0024 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0025 | 0/0 | 4482 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0026 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0027 | 0/0 | 4494 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0028 | 0/0 | 4494 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
t0029 | 0/0 | 4495 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0017 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3024 | 239 | 46 | 48 | 104 | 13 | 27 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0004 | 0/0 | 3024 | 6 | 6 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0005 | 0/0 | 3024 | 5 | 5 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0006 | 0/0 | 3024 | 3 | 0 | 0 | 0 | 0 | 3 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0007 | 0/0 | 3024 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0011 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0012 | 0/0 | 3024 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0015 | 0/0 | 3024 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002 | 1/0 | 3024 | 91 | 14 | 19 | 45 | 4 | 8 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0003 | 0/0 | 3024 | 13 | 10 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0008 | 0/0 | 3024 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0009 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0003c0014 | 0/0 | 3024 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0004c0013 | 0/0 | 3024 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0005c0010 | 0/0 | 3024 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7517 | 146 | 17 | 29 | 61 | 12 | 26 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0002 | 0/0 | 7517 | 2 | 1 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0003 | 0/0 | 7518 | 45 | 0 | 13 | 32 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0004 | 0/0 | 7518 | 23 | 20 | 3 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0006 | 0/0 | 7517 | 3 | 2 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0007 | 0/0 | 7517 | 4 | 0 | 0 | 4 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0008 | 0/0 | 7517 | 3 | 0 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0009 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0014 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0015 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0016 | 0/0 | 7518 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0017 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0020 | 0/0 | 7517 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0021 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0022 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0025 | 0/0 | 7505 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0026 | 0/0 | 7517 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0001t0029 | 0/0 | 7518 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0004t0010 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0004t0011 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0005t0006 | 0/0 | 7517 | 5 | 5 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0006t0001 | 0/0 | 7517 | 3 | 0 | 0 | 0 | 0 | 3 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0007t0006 | 0/0 | 7517 | 3 | 3 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0011t0001 | 0/0 | 7517 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0012t0001 | 0/0 | 7517 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0001c0015t0003 | 0/0 | 7518 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0001 | 0/0 | 7517 | 2 | 0 | 0 | 1 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0002 | 0/0 | 7517 | 81 | 13 | 15 | 42 | 4 | 7 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0012 | 1/0 | 7517 | 2 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0013 | 0/0 | 7517 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0023 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0024 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0027 | 0/0 | 7517 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0002t0028 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0003t0005 | 0/0 | 7517 | 13 | 10 | 2 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0008t0002 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0002c0009t0018 | 0/0 | 7517 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0003c0014t0001 | 0/0 | 7517 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0004c0013t0019 | 0/0 | 7517 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
a0005c0010t0001 | 0/0 | 7517 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | copy fasta | chr6 | 4016300 | 4069983 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0017 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0001 | 0/0 | 7 | 0 | 6 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0006g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0007g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0007g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0008g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0008g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0014g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0015g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0016g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0017g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0020g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0021g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0022g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0025g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0026g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0001t0029g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0004t0010g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0004t0010g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0004t0010g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0004t0011g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0004t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0004t0011g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0005t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0005t0006g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0005t0006g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0005t0006g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0005t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0006t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0006t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0006t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0007t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0007t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0007t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0011t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0012t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0001c0015t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0012g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0012g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0013g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0013g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0023g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0024g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0027g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0002t0028g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0003t0005g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0008t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0002c0009t0018g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0003c0014t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0004c0013t0019g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
a0005c0010t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0331 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | GBR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0156 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00323 | hp2 | a0001 | c0001 | t0008 | g0042 | EUR | FIN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00621 | hp1 | a0001 | c0001 | t0015 | g0018 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00639 | hp1 | a0002 | c0002 | t0024 | g0183 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00735 | hp1 | a0002 | c0003 | t0005 | g0201 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00738 | hp1 | a0002 | c0003 | t0005 | g0126 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0187 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG00741 | hp2 | a0003 | c0014 | t0001 | g0332 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01070 | hp1 | a0001 | c0015 | t0003 | g0005 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0176 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01099 | hp1 | a0002 | c0002 | t0023 | g0198 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01106 | hp2 | a0002 | c0002 | t0012 | g0205 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0095 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0182 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0188 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01257 | hp2 | a0001 | c0001 | t0008 | g0051 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0050 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0009 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0180 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01517 | hp2 | a0002 | c0002 | t0002 | g0181 | EUR | IBS | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01884 | hp1 | a0001 | c0004 | t0011 | g0235 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0199 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0166 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01975 | hp1 | a0002 | c0002 | t0028 | g0154 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0324 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0196 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02004 | hp2 | a0002 | c0008 | t0002 | g0167 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02055 | hp1 | a0001 | c0005 | t0006 | g0321 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02055 | hp2 | a0001 | c0001 | t0026 | g0300 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02080 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0128 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02145 | hp1 | a0002 | c0003 | t0005 | g0117 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02155 | hp2 | a0001 | c0001 | t0022 | g0215 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02257 | hp1 | a0001 | c0005 | t0006 | g0212 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0189 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0168 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02280 | hp2 | a0002 | c0002 | t0002 | g0142 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0186 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0206 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02572 | hp1 | a0002 | c0002 | t0027 | g0190 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02615 | hp1 | a0002 | c0003 | t0005 | g0116 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0178 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02630 | hp2 | a0002 | c0003 | t0005 | g0124 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02647 | hp2 | a0002 | c0002 | t0002 | g0179 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02717 | hp1 | a0002 | c0003 | t0005 | g0118 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0073 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0091 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0177 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02738 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02738 | hp2 | a0001 | c0006 | t0001 | g0297 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0221 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02922 | hp1 | a0002 | c0003 | t0005 | g0122 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02922 | hp2 | a0001 | c0007 | t0006 | g0306 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0341 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0191 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02976 | hp2 | a0002 | c0003 | t0005 | g0120 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0209 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03017 | hp2 | a0001 | c0011 | t0001 | g0036 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03041 | hp1 | a0001 | c0001 | t0016 | g0304 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03098 | hp2 | a0001 | c0004 | t0011 | g0234 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03139 | hp1 | a0001 | c0005 | t0006 | g0318 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03195 | hp1 | a0002 | c0003 | t0005 | g0121 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0194 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03209 | hp1 | a0002 | c0003 | t0005 | g0115 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03453 | hp2 | a0001 | c0005 | t0006 | g0319 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0130 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03516 | hp2 | a0001 | c0005 | t0006 | g0320 | AFR | ESN | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03540 | hp1 | a0001 | c0004 | t0010 | g0308 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0292 | AFR | GWD | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03579 | hp2 | a0002 | c0003 | t0005 | g0125 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0197 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0338 | SAS | PJL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03927 | hp1 | a0001 | c0006 | t0001 | g0223 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03942 | hp1 | a0001 | c0006 | t0001 | g0323 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0173 | SAS | BEB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04199 | hp1 | a0001 | c0012 | t0001 | g0336 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04204 | hp1 | a0001 | c0001 | t0020 | g0302 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0149 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18522 | hp1 | a0002 | c0009 | t0018 | g0322 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18906 | hp1 | a0001 | c0004 | t0010 | g0288 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0011 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18942 | hp2 | a0001 | c0001 | t0007 | g0262 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18951 | hp1 | a0001 | c0001 | t0007 | g0232 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18951 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18954 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18956 | hp1 | a0002 | c0002 | t0013 | g0175 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18969 | hp1 | a0001 | c0001 | t0017 | g0286 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18978 | hp1 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18983 | hp1 | a0001 | c0001 | t0014 | g0016 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0147 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0208 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18999 | hp1 | a0001 | c0001 | t0021 | g0265 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19006 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19010 | hp2 | a0001 | c0001 | t0025 | g0244 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19011 | hp1 | a0001 | c0001 | t0007 | g0245 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19030 | hp2 | a0001 | c0004 | t0010 | g0295 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19043 | hp2 | a0004 | c0013 | t0019 | g0291 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19060 | hp1 | a0002 | c0002 | t0013 | g0151 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19060 | hp2 | a0001 | c0001 | t0007 | g0246 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19066 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19067 | hp1 | a0005 | c0010 | t0001 | g0337 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19068 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0143 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0081 | AFR | YRI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20805 | hp1 | a0002 | c0003 | t0005 | g0123 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0274 | EUR | TSI | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | GIH | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | GIH | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0136 | AMR | CLM | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02486 | hp1 | a0001 | c0004 | t0011 | g0233 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | ACB | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03471 | hp1 | a0001 | c0007 | t0006 | g0307 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG03471 | hp2 | a0002 | c0002 | t0002 | g0192 | AFR | MSL | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG06807 | hp1 | a0001 | c0007 | t0006 | g0211 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0185 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20300 | hp1 | a0001 | c0001 | t0029 | g0060 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | USA | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA21309 | hp1 | a0002 | c0003 | t0005 | g0119 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0210 | AFR | LWK | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0017 | REF | REF | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0012 | g0204 | REF | REF | PRPF4B_chr6_4016300_4069983 | PRPF4B | chr6 | 4016300 | 4069983 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4031764
|
A | G | 4 | a0001a0003a0004others(1): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
missense_variant | MODERATE | c.247A>G | p.Ile83Val | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 373/7517 | 247/3024 | 83/1007 | chr6 | 4031764 | ||
chr6:4031926
|
T | G | 1 | a0005 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.409T>G | p.Leu137Val | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 535/7517 | 409/3024 | 137/1007 | chr6 | 4031926 | ||
chr6:4032439
|
C | G | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.922C>G | p.Arg308Gly | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 1048/7517 | 922/3024 | 308/1007 | chr6 | 4032439 | ||
chr6:4037422
|
A | G | 1 | a0004 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.1264A>G | p.Ser422Gly | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/15 | 1390/7517 | 1264/3024 | 422/1007 | chr6 | 4037422 | ||
chr6:4064981
|
T | C | 1 | a0001 | 3 | HG00323.hp2 HG01257.hp2 HG01258.hp1 |
splice_region_variant | LOW | c.*4365T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | chr6 | 4064981 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4031610
|
A | T | 1 | a0001c0015 | 1 | HG01070.hp1 | synonymous_variant | LOW | c.93A>T | p.Val31Val | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 219/7517 | 93/3024 | 31/1007 | chr6 | 4031610 | ||
chr6:4031721
|
A | G | 1 | a0001c0007 | 3 | HG02922.hp2 HG03471.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.204A>G | p.Lys68Lys | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 330/7517 | 204/3024 | 68/1007 | chr6 | 4031721 | ||
chr6:4032606
|
A | T | 1 | a0002c0009 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1089A>T | p.Ser363Ser | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/15 | 1215/7517 | 1089/3024 | 363/1007 | chr6 | 4032606 | ||
chr6:4037550
|
A | G | 1 | a0004c0013 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1392A>G | p.Arg464Arg | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/15 | 1518/7517 | 1392/3024 | 464/1007 | chr6 | 4037550 | ||
chr6:4040823
|
C | T | 1 | a0001c0012 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1464C>T | p.Arg488Arg | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/15 | 1590/7517 | 1464/3024 | 488/1007 | chr6 | 4040823 | ||
chr6:4043980
|
A | G | 1 | a0002c0003 | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
synonymous_variant | LOW | c.1818A>G | p.Ser606Ser | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/15 | 1944/7517 | 1818/3024 | 606/1007 | chr6 | 4043980 | ||
chr6:4049087
|
C | T | 1 | a0001c0005 | 5 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(2): Show |
synonymous_variant | LOW | c.2007C>T | p.Thr669Thr | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/15 | 2133/7517 | 2007/3024 | 669/1007 | chr6 | 4049087 | ||
chr6:4051996
|
A | G | 1 | a0001c0004 | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
synonymous_variant | LOW | c.2214A>G | p.Lys738Lys | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/15 | 2340/7517 | 2214/3024 | 738/1007 | chr6 | 4051996 | ||
chr6:4052014
|
T | C | 1 | a0002c0008 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.2232T>C | p.Pro744Pro | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/15 | 2358/7517 | 2232/3024 | 744/1007 | chr6 | 4052014 | ||
chr6:4052083
|
C | T | 1 | a0001c0006 | 3 | HG02738.hp2 HG03927.hp1 HG03942.hp1 |
synonymous_variant | LOW | c.2301C>T | p.Phe767Phe | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/15 | 2427/7517 | 2301/3024 | 767/1007 | chr6 | 4052083 | ||
chr6:4060529
|
G | A | 1 | a0001c0011 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.2937G>A | p.Leu979Leu | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3063/7517 | 2937/3024 | 979/1007 | chr6 | 4060529 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4021320
|
A | G | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | 366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
5_prime_UTR_variant | MODIFIER | c.-106A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 106 | chr6 | 4021320 | |||||
chr6:4021365
|
C | A | 1 | a0001c0001t0014 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-61C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 61 | chr6 | 4021365 | |||||
chr6:4021366
|
C | A | 1 | a0001c0001t0015 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-60C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 60 | chr6 | 4021366 | |||||
chr6:4021391
|
G | T | 1 | a0002c0002t0013 | 2 | NA18956.hp1 NA19060.hp1 |
5_prime_UTR_variant | MODIFIER | c.-35G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/15 | 35 | chr6 | 4021391 | |||||
chr6:4061239
|
C | T | 1 | a0001c0001t0029 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 623 | chr6 | 4061239 | |||||
chr6:4061296
|
G | A | 1 | a0001c0001t0016 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 680 | chr6 | 4061296 | |||||
chr6:4061465
|
C | T | 1 | a0002c0002t0028 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 849 | chr6 | 4061465 | |||||
chr6:4061537
|
C | A | 5 | a0001c0001t0003a0001c0001t0004a0001c0001t0016others(2): Show | 71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*921C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 921 | chr6 | 4061537 | |||||
chr6:4061613
|
C | G | 1 | a0002c0002t0027 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*997C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 997 | chr6 | 4061613 | |||||
chr6:4061672
|
T | A | 1 | a0001c0001t0017 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1056T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1056 | chr6 | 4061672 | |||||
chr6:4061699
|
C | T | 1 | a0001c0001t0026 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1083C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1083 | chr6 | 4061699 | |||||
chr6:4061864
|
T | G | 1 | a0002c0009t0018 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1248T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1248 | chr6 | 4061864 | |||||
chr6:4062142
|
A | T | 2 | a0001c0004t0010a0001c0004t0011 | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1526A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1526 | chr6 | 4062142 | |||||
chr6:4062431
|
A | G | 3 | a0001c0001t0003a0001c0001t0029a0001c0015t0003 | 47 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1815A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 1815 | chr6 | 4062431 | |||||
chr6:4062781
|
GAGTGAAG others(5): Show |
G | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2166_*2177delAGTG others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2166 | chr6 | 4062781 | |||||
chr6:4062795
|
A | C | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2179A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2179 | chr6 | 4062795 | |||||
chr6:4062799
|
A | C | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2183A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2183 | chr6 | 4062799 | |||||
chr6:4062803
|
C | T | 1 | a0001c0001t0025 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2187C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2187 | chr6 | 4062803 | |||||
chr6:4062947
|
G | GT | 5 | a0001c0001t0003a0001c0001t0004a0001c0001t0016others(2): Show | 71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2334dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2335 | INFO_REALIGN_3_PRIME | chr6 | 4062947 | ||||
chr6:4062986
|
C | T | 1 | a0002c0002t0024 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2370C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2370 | chr6 | 4062986 | |||||
chr6:4063306
|
C | T | 1 | a0002c0003t0005 | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2690C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2690 | chr6 | 4063306 | |||||
chr6:4063447
|
G | A | 29 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(26): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*2831G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 2831 | chr6 | 4063447 | |||||
chr6:4063862
|
G | A | 1 | a0002c0002t0023 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3246G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3246 | chr6 | 4063862 | |||||
chr6:4064094
|
G | A | 1 | a0004c0013t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3478G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3478 | chr6 | 4064094 | |||||
chr6:4064107
|
A | G | 1 | a0002c0003t0005 | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3491A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3491 | chr6 | 4064107 | |||||
chr6:4064304
|
T | C | 1 | a0001c0001t0020 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3688T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3688 | chr6 | 4064304 | |||||
chr6:4064431
|
A | G | 1 | a0001c0001t0022 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3815A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3815 | chr6 | 4064431 | |||||
chr6:4064469
|
G | A | 1 | a0001c0001t0021 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3853G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3853 | chr6 | 4064469 | |||||
chr6:4064477
|
G | A | 3 | a0001c0001t0006a0001c0005t0006a0001c0007t0006 | 11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3861G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3861 | chr6 | 4064477 | |||||
chr6:4064552
|
T | C | 1 | a0001c0001t0007 | 4 | NA18942.hp2 NA18951.hp1 NA19011.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3936T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 3936 | chr6 | 4064552 | |||||
chr6:4064712
|
A | G | 1 | a0001c0001t0009 | 3 | HG02895.hp1 HG02896.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4096A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 4096 | chr6 | 4064712 | |||||
chr6:4064769
|
A | G | 1 | a0001c0004t0011 | 3 | HG01884.hp1 HG02486.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4153A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 15/15 | 4153 | chr6 | 4064769 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:4021476
|
C | T | 2 | a0001c0001t0001g0342a0001c0001t0001g0343 | 2 | HG02027.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.41+10C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021476 | ||||||
chr6:4021653
|
T | C | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0023others(99): Show | 112 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.41+187T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021653 | ||||||
chr6:4021781
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41+315C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021781 | ||||||
chr6:4021865
|
C | T | 16 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0327others(13): Show | 16 | HG00140.hp1 HG00408.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.41+399C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021865 | ||||||
chr6:4021975
|
C | G | 1 | a0002c0002t0002g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.41+509C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021975 | ||||||
chr6:4021979
|
C | T | 1 | a0001c0006t0001g0323 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.41+513C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4021979 | ||||||
chr6:4022085
|
C | T | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.41+619C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022085 | ||||||
chr6:4022154
|
A | AT | 7 | a0001c0001t0001g0214a0001c0001t0001g0216a0001c0001t0001g0217others(4): Show | 7 | HG01515.hp2 HG01517.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+710dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | |||||
chr6:4022154
|
A | ATT | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(122): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.41+709_41+710dupTT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | |||||
chr6:4022154
|
A | ATTT | 79 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(76): Show | 90 | HG00609.hp1 HG00621.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.41+708_41+710dupTT others(1): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | |||||
chr6:4022154
|
A | ATTTT | 27 | a0001c0001t0001g0106a0001c0001t0001g0309a0001c0001t0001g0310others(24): Show | 27 | HG00544.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.41+707_41+710dupTT others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | |||||
chr6:4022154
|
AT | A | 92 | a0001c0001t0001g0200a0002c0002t0001g0131a0002c0002t0001g0195others(89): Show | 96 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.41+710delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022154 | |||||
chr6:4022226
|
G | C | 13 | a0002c0003t0005g0115a0002c0003t0005g0116a0002c0003t0005g0117others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+760G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022226 | ||||||
chr6:4022249
|
A | C | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41+783A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022249 | ||||||
chr6:4022304
|
G | GA | 17 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(14): Show | 17 | HG00673.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.41+851dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022304 | |||||
chr6:4022304
|
GA | G | 57 | a0001c0001t0001g0200a0001c0001t0001g0290a0001c0001t0001g0317others(54): Show | 58 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.41+851delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022304 | |||||
chr6:4022354
|
C | A | 1 | a0001c0001t0009g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41+888C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022354 | ||||||
chr6:4022360
|
G | A | 13 | a0002c0003t0005g0115a0002c0003t0005g0116a0002c0003t0005g0117others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+894G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022360 | ||||||
chr6:4022377
|
A | G | 258 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(255): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.41+911A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022377 | ||||||
chr6:4022381
|
C | G | 1 | a0001c0004t0010g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+915C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022381 | ||||||
chr6:4022453
|
GTTTT | G | 10 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0005t0006g0212others(7): Show | 11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+996_41+999delTT others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022453 | |||||
chr6:4022459
|
T | C | 1 | a0002c0002t0002g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+993T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022459 | ||||||
chr6:4022461
|
T | TG | 231 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(228): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.41+995_41+996insG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022461 | ||||||
chr6:4022476
|
T | G | 10 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0005t0006g0212others(7): Show | 11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+1010T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022476 | ||||||
chr6:4022477
|
TG | T | 10 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0005t0006g0212others(7): Show | 11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+1012delG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022477 | ||||||
chr6:4022478
|
G | GT | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(203): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.41+1021dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022478 | |||||
chr6:4022479
|
T | G | 12 | a0002c0002t0002g0020a0002c0002t0002g0180a0002c0002t0002g0181others(9): Show | 12 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+1013T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022479 | ||||||
chr6:4022639
|
A | G | 3 | a0001c0006t0001g0223a0001c0006t0001g0297a0001c0006t0001g0323 | 3 | HG02738.hp2 HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.41+1173A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022639 | ||||||
chr6:4022826
|
G | C | 1 | a0001c0001t0001g0224 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.41+1360G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022826 | ||||||
chr6:4022910
|
C | T | 63 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(60): Show | 71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.41+1444C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022910 | ||||||
chr6:4022913
|
ATTCAT | A | 7 | a0002c0002t0001g0195a0002c0002t0002g0176a0002c0002t0002g0177others(4): Show | 7 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+1451_41+1455del others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4022913 | |||||
chr6:4022975
|
C | G | 1 | a0001c0004t0010g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.41+1509C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4022975 | ||||||
chr6:4023134
|
A | G | 1 | a0001c0001t0001g0339 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.41+1668A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023134 | ||||||
chr6:4023175
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41+1709A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023175 | ||||||
chr6:4023193
|
G | A | 3 | a0001c0001t0009g0213a0001c0001t0009g0220a0001c0001t0009g0221 | 3 | HG02895.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.41+1727G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023193 | ||||||
chr6:4023380
|
AAC | A | 3 | a0001c0001t0009g0213a0001c0001t0009g0220a0001c0001t0009g0221 | 3 | HG02895.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.41+1918_41+1919del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4023380 | |||||
chr6:4023447
|
T | C | 1 | a0002c0002t0002g0127 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.41+1981T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023447 | ||||||
chr6:4023507
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.41+2041G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023507 | ||||||
chr6:4023618
|
C | G | 1 | a0002c0002t0013g0175 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.41+2152C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023618 | ||||||
chr6:4023716
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.41+2250G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023716 | ||||||
chr6:4023872
|
A | AT | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.41+2419dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4023872 | |||||
chr6:4023890
|
C | T | 7 | a0001c0001t0001g0219a0001c0001t0001g0284a0001c0001t0001g0285others(4): Show | 7 | NA18944.hp2 NA18969.hp1 NA19057.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+2424C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023890 | ||||||
chr6:4023891
|
G | A | 1 | a0001c0005t0006g0318 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.41+2425G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4023891 | ||||||
chr6:4024159
|
C | G | 2 | a0001c0001t0008g0050a0001c0001t0008g0051 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.41+2693C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024159 | ||||||
chr6:4024160
|
G | A | 2 | a0001c0001t0004g0073a0001c0001t0006g0012 | 3 | HG01081.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.41+2694G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024160 | ||||||
chr6:4024280
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.41+2814G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024280 | ||||||
chr6:4024306
|
C | G | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.41+2840C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024306 | ||||||
chr6:4024330
|
C | G | 13 | a0002c0003t0005g0115a0002c0003t0005g0116a0002c0003t0005g0117others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.41+2864C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024330 | ||||||
chr6:4024538
|
CACTAAG | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(136): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.41+3077_41+3082del others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4024538 | |||||
chr6:4024642
|
G | C | 1 | a0002c0002t0002g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.41+3176G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024642 | ||||||
chr6:4024743
|
C | G | 1 | a0001c0001t0001g0219 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.41+3277C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024743 | ||||||
chr6:4024763
|
G | A | 4 | a0002c0002t0002g0180a0002c0002t0002g0181a0002c0002t0002g0182others(1): Show | 4 | HG01109.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+3297G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024763 | ||||||
chr6:4024879
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0312 | 3 | NA18939.hp1 NA18994.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.41+3413C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024879 | ||||||
chr6:4024932
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.41+3466C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4024932 | ||||||
chr6:4025021
|
C | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(135): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.41+3555C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025021 | ||||||
chr6:4025038
|
C | G | 10 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0005t0006g0212others(7): Show | 11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.41+3572C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025038 | ||||||
chr6:4025281
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.41+3815A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025281 | ||||||
chr6:4025388
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0312 | 3 | NA18939.hp1 NA18994.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.41+3922A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025388 | ||||||
chr6:4025431
|
G | C | 1 | a0001c0001t0003g0059 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.41+3965G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025431 | ||||||
chr6:4025493
|
C | G | 80 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(77): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.41+4027C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025493 | ||||||
chr6:4025529
|
G | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.41+4063G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025529 | ||||||
chr6:4025602
|
A | C | 80 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(77): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.41+4136A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025602 | ||||||
chr6:4025641
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41+4175T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025641 | ||||||
chr6:4025674
|
C | G | 1 | a0001c0004t0010g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.41+4208C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025674 | ||||||
chr6:4025697
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.41+4231T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025697 | ||||||
chr6:4025795
|
G | C | 3 | a0001c0007t0006g0211a0001c0007t0006g0306a0001c0007t0006g0307 | 3 | HG02922.hp2 HG03471.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.41+4329G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4025795 | ||||||
chr6:4026057
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.41+4591A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026057 | ||||||
chr6:4026088
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.41+4622G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026088 | ||||||
chr6:4026144
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0227a0001c0001t0001g0228others(5): Show | 8 | HG00621.hp1 HG02080.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.41+4678G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026144 | ||||||
chr6:4026163
|
G | A | 2 | a0001c0001t0004g0074a0001c0001t0004g0075 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.41+4697G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026163 | ||||||
chr6:4026302
|
C | G | 1 | a0001c0001t0001g0283 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.41+4836C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026302 | ||||||
chr6:4026303
|
CT | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.41+4853delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4026303 | |||||
chr6:4026330
|
T | C | 1 | a0001c0001t0007g0232 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.41+4864T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026330 | ||||||
chr6:4026369
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(129): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.41+4903C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026369 | ||||||
chr6:4026462
|
C | G | 1 | a0001c0001t0006g0012 | 2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.41+4996C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026462 | ||||||
chr6:4026479
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.41+5013T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026479 | ||||||
chr6:4026482
|
T | C | 7 | a0002c0002t0001g0195a0002c0002t0002g0176a0002c0002t0002g0177others(4): Show | 7 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+5016T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026482 | ||||||
chr6:4026720
|
A | G | 1 | a0001c0001t0001g0279 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.42-4839A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026720 | ||||||
chr6:4026901
|
G | C | 1 | a0002c0002t0002g0128 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.42-4658G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026901 | ||||||
chr6:4026954
|
A | G | 1 | a0001c0001t0004g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.42-4605A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026954 | ||||||
chr6:4026964
|
C | T | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.42-4595C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4026964 | ||||||
chr6:4027275
|
A | G | 2 | a0001c0001t0008g0050a0001c0001t0008g0051 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.42-4284A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027275 | ||||||
chr6:4027335
|
C | A | 1 | a0002c0002t0002g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.42-4224C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027335 | ||||||
chr6:4027592
|
C | CG | 18 | a0001c0001t0001g0225a0001c0001t0001g0240a0001c0001t0001g0241others(15): Show | 18 | HG01952.hp1 HG02055.hp2 HG02273.hp2 others(15): Show |
intron_variant | MODIFIER | c.42-3965dupG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | |||||
chr6:4027592
|
C | CGG | 9 | a0001c0001t0001g0053a0001c0001t0001g0214a0001c0001t0001g0219others(6): Show | 9 | HG01975.hp2 HG02970.hp1 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.42-3966_42-3965dup others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | |||||
chr6:4027592
|
CGGA | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0031others(11): Show | 14 | HG00323.hp1 HG00609.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-3964_42-3962del others(3): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | |||||
chr6:4027592
|
CGGAG | C | 3 | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0001g0034 | 4 | HG01256.hp1 HG01258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-3964_42-3961del others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027592 | |||||
chr6:4027593
|
GGA | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0024others(44): Show | 50 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.42-3964_42-3963del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027593 | |||||
chr6:4027594
|
GA | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(81): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.42-3964delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027594 | ||||||
chr6:4027595
|
A | G | 95 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(92): Show | 99 | HG00438.hp2 HG00741.hp1 HG01069.hp2 others(96): Show |
intron_variant | MODIFIER | c.42-3964A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027595 | ||||||
chr6:4027600
|
T | C | 2 | a0001c0001t0001g0024a0001c0004t0010g0308 | 2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.42-3959T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027600 | ||||||
chr6:4027600
|
T | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(236): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.42-3959T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027600 | ||||||
chr6:4027600
|
T | TG | 13 | a0002c0002t0001g0131a0002c0002t0001g0195a0002c0002t0002g0129others(10): Show | 13 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-3952dupG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4027600 | |||||
chr6:4027603
|
G | T | 7 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(4): Show | 7 | HG01255.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-3956G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027603 | ||||||
chr6:4027608
|
T | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(13): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.42-3951T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027608 | ||||||
chr6:4027613
|
T | G | 2 | a0001c0001t0001g0227a0001c0001t0003g0083 | 2 | HG02040.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.42-3946T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027613 | ||||||
chr6:4027712
|
G | A | 1 | a0001c0004t0010g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.42-3847G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027712 | ||||||
chr6:4027948
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.42-3611C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4027948 | ||||||
chr6:4028018
|
A | G | 283 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(280): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.42-3541A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028018 | ||||||
chr6:4028097
|
C | G | 1 | a0001c0004t0010g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.42-3462C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028097 | ||||||
chr6:4028427
|
G | A | 1 | a0002c0002t0024g0183 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.42-3132G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028427 | ||||||
chr6:4028437
|
G | C | 1 | a0001c0001t0004g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.42-3122G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028437 | ||||||
chr6:4028587
|
A | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(78): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-2972A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028587 | ||||||
chr6:4028826
|
C | T | 1 | a0002c0002t0002g0177 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.42-2733C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028826 | ||||||
chr6:4028830
|
A | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(135): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.42-2729A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028830 | ||||||
chr6:4028845
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.42-2714C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028845 | ||||||
chr6:4028875
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.42-2684A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028875 | ||||||
chr6:4028894
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.42-2665C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028894 | ||||||
chr6:4028963
|
T | C | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.42-2596T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028963 | ||||||
chr6:4028968
|
C | T | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.42-2591C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028968 | ||||||
chr6:4028969
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.42-2590C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028969 | ||||||
chr6:4028976
|
TATC | T | 4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG00099.hp2 HG00280.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-2582_42-2580del others(3): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4028976 | ||||||
chr6:4029012
|
C | CT | 15 | a0002c0002t0001g0195a0002c0002t0002g0011a0002c0002t0002g0137others(12): Show | 16 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.42-2526dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
C | CTTTTTTT others(5): Show |
2 | a0002c0003t0005g0116a0002c0003t0005g0117 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.42-2537_42-2526dup others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
C | CTTTTTTT others(6): Show |
8 | a0002c0003t0005g0115a0002c0003t0005g0118a0002c0003t0005g0119others(5): Show | 8 | HG02630.hp2 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-2538_42-2526dup others(13): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
C | CTTTTTTT others(7): Show |
4 | a0002c0002t0002g0179a0002c0003t0005g0125a0002c0003t0005g0126others(1): Show | 4 | HG00735.hp1 HG00738.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-2539_42-2526dup others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
C | CTTTTTTT others(8): Show |
3 | a0002c0002t0002g0180a0002c0002t0002g0184a0002c0002t0002g0185 | 3 | HG01516.hp2 HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.42-2540_42-2526dup others(15): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
C | CTTTTTTT others(9): Show |
5 | a0002c0002t0002g0181a0002c0002t0002g0186a0002c0002t0002g0192others(2): Show | 5 | HG01517.hp2 HG02293.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-2541_42-2526dup others(16): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
C | CTTTTTTT others(10): Show |
6 | a0002c0002t0002g0020a0002c0002t0002g0182a0002c0002t0002g0187others(3): Show | 6 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.42-2542_42-2526dup others(17): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
C | CTTTTTTT others(11): Show |
2 | a0002c0002t0002g0193a0002c0002t0002g0194 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.42-2543_42-2526dup others(18): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029012
|
CTTTTTTT others(5): Show |
C | 242 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(239): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.42-2537_42-2526del others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029012 | |||||
chr6:4029036
|
TGA | T | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.42-2520_42-2519del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029036 | |||||
chr6:4029074
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0239a0001c0001t0001g0279others(2): Show | 5 | NA18955.hp1 NA18956.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-2485C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029074 | ||||||
chr6:4029115
|
G | A | 20 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(17): Show | 20 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-2444G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029115 | ||||||
chr6:4029226
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.42-2333G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029226 | ||||||
chr6:4029238
|
G | A | 1 | a0001c0001t0009g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.42-2321G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029238 | ||||||
chr6:4029339
|
AT | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(204): Show | 224 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.42-2199delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029339 | |||||
chr6:4029339
|
ATT | A | 12 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0038others(9): Show | 12 | HG00099.hp2 HG01168.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-2200_42-2199del others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029339 | |||||
chr6:4029343
|
T | A | 1 | a0002c0002t0002g0137 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.42-2216T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029343 | ||||||
chr6:4029380
|
G | A | 10 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0005t0006g0212others(7): Show | 11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.42-2179G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029380 | ||||||
chr6:4029403
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.42-2156G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029403 | ||||||
chr6:4029496
|
A | G | 4 | a0002c0002t0002g0136a0002c0002t0002g0166a0002c0002t0002g0168others(1): Show | 4 | HG01123.hp2 HG01943.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-2063A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029496 | ||||||
chr6:4029711
|
C | T | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.42-1848C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029711 | ||||||
chr6:4029768
|
G | A | 1 | a0001c0001t0004g0316 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.42-1791G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029768 | ||||||
chr6:4029888
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.42-1671A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029888 | ||||||
chr6:4029938
|
C | CT | 13 | a0001c0001t0001g0048a0001c0001t0001g0071a0001c0001t0001g0290others(10): Show | 13 | HG00735.hp2 HG01074.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-1605dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr6 | 4029938 | |||||
chr6:4029939
|
T | C | 9 | a0001c0001t0006g0012a0001c0005t0006g0212a0001c0005t0006g0318others(6): Show | 10 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.42-1620T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4029939 | ||||||
chr6:4030202
|
C | G | 5 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0011g0233others(2): Show | 5 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-1357C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030202 | ||||||
chr6:4030260
|
G | T | 80 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(77): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.42-1299G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030260 | ||||||
chr6:4030306
|
T | C | 20 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(17): Show | 20 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-1253T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030306 | ||||||
chr6:4030320
|
T | A | 4 | a0001c0001t0007g0232a0001c0001t0007g0245a0001c0001t0007g0246others(1): Show | 4 | NA18942.hp2 NA18951.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-1239T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030320 | ||||||
chr6:4030415
|
C | T | 1 | a0002c0003t0005g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.42-1144C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030415 | ||||||
chr6:4030474
|
T | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(78): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-1085T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030474 | ||||||
chr6:4030481
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.42-1078A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030481 | ||||||
chr6:4030599
|
T | G | 1 | a0001c0001t0001g0311 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.42-960T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030599 | ||||||
chr6:4030679
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.42-880A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030679 | ||||||
chr6:4030717
|
A | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(78): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-842A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030717 | ||||||
chr6:4030759
|
G | C | 5 | a0002c0002t0002g0129a0002c0002t0002g0139a0002c0002t0002g0140others(2): Show | 5 | NA18954.hp2 NA18971.hp2 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-800G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030759 | ||||||
chr6:4030775
|
A | T | 9 | a0002c0002t0002g0010a0002c0002t0002g0127a0002c0002t0002g0128others(6): Show | 10 | HG00408.hp1 HG00544.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-784A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030775 | ||||||
chr6:4030777
|
T | A | 9 | a0002c0002t0002g0010a0002c0002t0002g0127a0002c0002t0002g0128others(6): Show | 10 | HG00408.hp1 HG00544.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-782T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030777 | ||||||
chr6:4030891
|
T | G | 1 | a0001c0001t0004g0111 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42-668T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030891 | ||||||
chr6:4030914
|
C | T | 81 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(78): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-645C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4030914 | ||||||
chr6:4031050
|
C | A | 7 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0075others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-509C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031050 | ||||||
chr6:4031138
|
G | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(38): Show | 48 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.42-421G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031138 | ||||||
chr6:4031225
|
T | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.42-334T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031225 | ||||||
chr6:4031393
|
G | A | 1 | a0002c0003t0005g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.42-166G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031393 | ||||||
chr6:4031482
|
A | G | 1 | a0002c0002t0002g0020 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.42-77A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 1/14 | chr6 | 4031482 | ||||||
chr6:4032831
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1238+76A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4032831 | ||||||
chr6:4032968
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1238+213A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4032968 | ||||||
chr6:4033172
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1238+417T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033172 | ||||||
chr6:4033602
|
A | G | 1 | a0001c0001t0020g0302 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1238+847A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033602 | ||||||
chr6:4033664
|
A | G | 1 | a0001c0005t0006g0212 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1238+909A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033664 | ||||||
chr6:4033677
|
G | A | 1 | a0002c0002t0002g0189 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1238+922G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033677 | ||||||
chr6:4033807
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1238+1052T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033807 | ||||||
chr6:4033825
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1238+1070T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033825 | ||||||
chr6:4033847
|
G | A | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1238+1092G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033847 | ||||||
chr6:4033966
|
A | G | 1 | a0002c0002t0002g0136 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1238+1211A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033966 | ||||||
chr6:4033997
|
TA | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(6): Show | 10 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(7): Show |
intron_variant | MODIFIER | c.1238+1243delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4033997 | ||||||
chr6:4034020
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1238+1265A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034020 | ||||||
chr6:4034143
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0048 | 3 | HG01070.hp2 HG01071.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1238+1388A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034143 | ||||||
chr6:4034157
|
AT | A | 142 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(139): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1238+1413delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4034157 | |||||
chr6:4034315
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1238+1560A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034315 | ||||||
chr6:4034401
|
A | G | 1 | a0002c0002t0002g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1238+1646A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034401 | ||||||
chr6:4034662
|
G | T | 1 | a0001c0001t0001g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1238+1907G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034662 | ||||||
chr6:4034698
|
T | C | 13 | a0002c0003t0005g0115a0002c0003t0005g0116a0002c0003t0005g0117others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1238+1943T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034698 | ||||||
chr6:4034774
|
G | A | 2 | a0001c0001t0001g0325a0001c0001t0001g0326 | 2 | HG01123.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1238+2019G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034774 | ||||||
chr6:4034870
|
G | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(136): Show | 147 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1238+2115G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034870 | ||||||
chr6:4034888
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1238+2133T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034888 | ||||||
chr6:4034935
|
A | C | 1 | a0001c0001t0004g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1238+2180A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034935 | ||||||
chr6:4034947
|
G | A | 4 | a0002c0002t0002g0142a0002c0002t0002g0143a0002c0002t0002g0144others(1): Show | 4 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1238+2192G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4034947 | ||||||
chr6:4035173
|
G | C | 2 | a0001c0001t0003g0065a0001c0001t0003g0066 | 2 | NA18939.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1239-2224G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035173 | ||||||
chr6:4035221
|
A | G | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239-2176A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035221 | ||||||
chr6:4035284
|
A | ATT | 7 | a0002c0002t0002g0149a0002c0002t0002g0177a0002c0002t0002g0189others(4): Show | 7 | HG00735.hp1 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239-2081_1239-208 others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTT | 7 | a0001c0005t0006g0321a0001c0007t0006g0306a0001c0007t0006g0307others(4): Show | 7 | HG01928.hp1 HG02055.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239-2084_1239-208 others(9): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(3): Show |
1 | a0002c0002t0002g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1239-2089_1239-208 others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(4): Show |
6 | a0002c0002t0002g0010a0002c0002t0002g0127a0002c0002t0002g0128others(3): Show | 7 | HG00408.hp1 HG01943.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239-2090_1239-208 others(15): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(5): Show |
17 | a0002c0002t0001g0131a0002c0002t0002g0008a0002c0002t0002g0011others(14): Show | 19 | HG00280.hp2 HG00438.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.1239-2091_1239-208 others(16): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(6): Show |
9 | a0002c0002t0002g0133a0002c0002t0002g0158a0002c0002t0002g0159others(6): Show | 9 | HG01192.hp1 HG02027.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239-2092_1239-208 others(17): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(7): Show |
3 | a0002c0002t0002g0161a0002c0002t0002g0165a0002c0002t0002g0172 | 3 | NA18612.hp2 NA19067.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1239-2093_1239-208 others(18): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(8): Show |
2 | a0002c0002t0002g0168a0002c0002t0002g0173 | 2 | HG02273.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1239-2094_1239-208 others(19): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(9): Show |
3 | a0002c0002t0002g0009a0002c0002t0002g0206a0002c0002t0002g0324 | 4 | HG00642.hp2 HG01515.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-2095_1239-208 others(20): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(10): Show |
1 | a0002c0002t0002g0135 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1239-2096_1239-208 others(21): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(11): Show |
1 | a0002c0002t0002g0162 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1239-2097_1239-208 others(22): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(12): Show |
1 | a0002c0002t0002g0207 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1239-2098_1239-208 others(23): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
A | ATTTTTTT others(18): Show |
1 | a0002c0002t0002g0134 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1239-2104_1239-208 others(29): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
AT | A | 14 | a0001c0001t0001g0056a0001c0001t0001g0311a0002c0002t0002g0179others(11): Show | 14 | HG02145.hp2 HG02293.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1239-2080delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATT | A | 13 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG00642.hp1 HG00738.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1239-2081_1239-208 others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATTT | A | 31 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0040others(28): Show | 31 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1239-2082_1239-208 others(7): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATTTT | A | 100 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(97): Show | 108 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1239-2083_1239-208 others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATTTTT | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0043a0001c0001t0001g0214others(5): Show | 8 | HG00323.hp2 HG01169.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239-2084_1239-208 others(9): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATTTTTT | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0071others(9): Show | 12 | HG00735.hp2 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239-2085_1239-208 others(10): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATTTTTTT | A | 31 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0027others(28): Show | 33 | HG00099.hp2 HG00280.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.1239-2086_1239-208 others(11): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATTTTTTT others(1): Show |
A | 38 | a0001c0001t0001g0023a0001c0001t0003g0001a0001c0001t0003g0005others(35): Show | 45 | HG00323.hp1 HG00609.hp1 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1239-2087_1239-208 others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035284
|
ATTTTTTT others(21): Show |
A | 3 | a0002c0002t0002g0138a0002c0002t0002g0145a0002c0002t0002g0146 | 3 | NA18951.hp2 NA19006.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1239-2107_1239-208 others(32): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4035284 | |||||
chr6:4035319
|
A | G | 1 | a0002c0002t0002g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1239-2078A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035319 | ||||||
chr6:4035340
|
T | C | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239-2057T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035340 | ||||||
chr6:4035371
|
T | G | 1 | a0001c0001t0001g0264 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1239-2026T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035371 | ||||||
chr6:4035417
|
G | A | 2 | a0002c0003t0005g0116a0002c0003t0005g0117 | 2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1239-1980G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035417 | ||||||
chr6:4035600
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1239-1797G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035600 | ||||||
chr6:4035838
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1239-1559A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035838 | ||||||
chr6:4035927
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1239-1470T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4035927 | ||||||
chr6:4036022
|
GACAA | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1239-1372_1239-136 others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036022 | |||||
chr6:4036038
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1239-1359A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036038 | ||||||
chr6:4036105
|
T | C | 1 | a0001c0001t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1239-1292T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036105 | ||||||
chr6:4036170
|
C | A | 1 | a0002c0002t0002g0196 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1239-1227C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036170 | ||||||
chr6:4036200
|
T | C | 2 | a0001c0005t0006g0319a0001c0005t0006g0320 | 2 | HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1239-1197T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036200 | ||||||
chr6:4036236
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1239-1161A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036236 | ||||||
chr6:4036307
|
T | C | 5 | a0001c0001t0006g0292a0001c0004t0011g0233a0001c0004t0011g0234others(2): Show | 5 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1239-1090T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036307 | ||||||
chr6:4036344
|
C | T | 3 | a0001c0005t0006g0318a0001c0005t0006g0319a0001c0005t0006g0320 | 3 | HG03139.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1239-1053C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036344 | ||||||
chr6:4036410
|
T | G | 3 | a0001c0005t0006g0318a0001c0005t0006g0319a0001c0005t0006g0320 | 3 | HG03139.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1239-987T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036410 | ||||||
chr6:4036419
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1239-978G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036419 | ||||||
chr6:4036511
|
C | G | 14 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(11): Show | 15 | HG01081.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1239-886C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036511 | ||||||
chr6:4036549
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.1239-848C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036549 | ||||||
chr6:4036735
|
A | G | 2 | a0001c0001t0001g0328a0005c0010t0001g0337 | 2 | HG02165.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1239-662A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036735 | ||||||
chr6:4036811
|
A | AC | 22 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(19): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.1239-581dupC | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036811 | |||||
chr6:4036862
|
A | G | 10 | a0001c0001t0004g0078a0001c0001t0004g0080a0001c0001t0004g0081others(7): Show | 10 | HG01884.hp2 HG02486.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239-535A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4036862 | ||||||
chr6:4036985
|
C | CA | 10 | a0002c0002t0002g0137a0002c0002t0002g0139a0002c0002t0002g0148others(7): Show | 10 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239-390dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | |||||
chr6:4036985
|
CAAA | C | 13 | a0002c0002t0002g0184a0002c0003t0005g0115a0002c0003t0005g0116others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1239-392_1239-390d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | |||||
chr6:4036985
|
CAAAA | C | 21 | a0001c0001t0001g0032a0001c0004t0011g0233a0001c0004t0011g0235others(18): Show | 21 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.1239-393_1239-390d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | |||||
chr6:4036985
|
CAAAAA | C | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(233): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1239-394_1239-390d others(7): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr6 | 4036985 | |||||
chr6:4037158
|
A | G | 2 | a0002c0002t0002g0184a0002c0002t0024g0183 | 2 | HG00639.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1239-239A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037158 | ||||||
chr6:4037224
|
A | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(235): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1239-173A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037224 | ||||||
chr6:4037322
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1239-75G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037322 | ||||||
chr6:4037348
|
C | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1239-49C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037348 | ||||||
chr6:4037360
|
T | C | 6 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0010g0308others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239-37T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 2/14 | chr6 | 4037360 | ||||||
chr6:4037857
|
A | AT | 10 | a0001c0001t0001g0274a0001c0001t0001g0294a0001c0001t0003g0114others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1412+302dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4037857 | |||||
chr6:4037857
|
AT | A | 7 | a0001c0001t0001g0214a0001c0001t0021g0265a0001c0004t0010g0288others(4): Show | 7 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412+302delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4037857 | |||||
chr6:4037896
|
T | C | 2 | a0001c0001t0001g0327a0001c0001t0001g0340 | 2 | HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1412+326T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4037896 | ||||||
chr6:4037911
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1412+341C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4037911 | ||||||
chr6:4038034
|
A | C | 1 | a0001c0001t0001g0282 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1412+464A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038034 | ||||||
chr6:4038045
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1412+475A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038045 | ||||||
chr6:4038121
|
T | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1412+551T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038121 | ||||||
chr6:4038122
|
G | A | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1412+552G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038122 | ||||||
chr6:4038264
|
C | T | 4 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0049others(1): Show | 4 | HG03017.hp2 HG03491.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412+694C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038264 | ||||||
chr6:4038282
|
G | GTTTTA | 4 | a0001c0001t0001g0294a0001c0005t0006g0319a0001c0005t0006g0320others(1): Show | 4 | HG02717.hp1 HG03453.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1412+737_1412+741d others(7): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4038282 | |||||
chr6:4038336
|
C | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1412+766C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038336 | ||||||
chr6:4038367
|
A | C | 35 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(32): Show | 42 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1412+797A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038367 | ||||||
chr6:4038393
|
T | C | 6 | a0002c0002t0002g0176a0002c0002t0002g0177a0002c0002t0002g0196others(3): Show | 6 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412+823T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038393 | ||||||
chr6:4038410
|
A | C | 1 | a0002c0002t0002g0186 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1412+840A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038410 | ||||||
chr6:4038462
|
G | T | 2 | a0002c0003t0005g0123a0002c0003t0005g0126 | 2 | HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1412+892G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038462 | ||||||
chr6:4038540
|
G | A | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1412+970G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038540 | ||||||
chr6:4038587
|
G | A | 1 | a0001c0001t0006g0012 | 2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1412+1017G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038587 | ||||||
chr6:4038718
|
C | T | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1412+1148C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4038718 | ||||||
chr6:4038919
|
C | CTT | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1412+1358_1412+135 others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr6 | 4038919 | |||||
chr6:4039087
|
A | G | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1412+1517A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039087 | ||||||
chr6:4039241
|
G | A | 265 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(262): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1413-1531G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039241 | ||||||
chr6:4039393
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1413-1379A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039393 | ||||||
chr6:4039602
|
C | G | 1 | a0001c0001t0004g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1413-1170C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039602 | ||||||
chr6:4039659
|
G | A | 6 | a0002c0002t0002g0176a0002c0002t0002g0177a0002c0002t0002g0196others(3): Show | 6 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1413-1113G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039659 | ||||||
chr6:4039747
|
C | T | 1 | a0001c0004t0010g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1413-1025C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039747 | ||||||
chr6:4039883
|
C | G | 20 | a0001c0001t0001g0294a0002c0002t0002g0020a0002c0002t0002g0179others(17): Show | 20 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1413-889C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039883 | ||||||
chr6:4039915
|
T | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1413-857T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4039915 | ||||||
chr6:4040009
|
C | T | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1413-763C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040009 | ||||||
chr6:4040113
|
C | T | 1 | a0001c0001t0003g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1413-659C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040113 | ||||||
chr6:4040114
|
G | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(1): Show | 4 | HG00099.hp2 HG00280.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1413-658G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040114 | ||||||
chr6:4040121
|
C | T | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1413-651C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040121 | ||||||
chr6:4040171
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1413-601C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040171 | ||||||
chr6:4040187
|
T | G | 3 | a0001c0005t0006g0318a0001c0005t0006g0319a0001c0005t0006g0320 | 3 | HG03139.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1413-585T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040187 | ||||||
chr6:4040217
|
T | C | 2 | a0002c0002t0002g0180a0002c0002t0002g0181 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1413-555T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040217 | ||||||
chr6:4040328
|
A | G | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1413-444A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040328 | ||||||
chr6:4040394
|
C | T | 1 | a0001c0001t0002g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1413-378C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040394 | ||||||
chr6:4040399
|
G | C | 2 | a0001c0001t0004g0082a0001c0001t0004g0316 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1413-373G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040399 | ||||||
chr6:4040401
|
G | T | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1413-371G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040401 | ||||||
chr6:4040523
|
T | C | 6 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0010g0308others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413-249T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040523 | ||||||
chr6:4040612
|
G | A | 1 | a0001c0004t0010g0295 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1413-160G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040612 | ||||||
chr6:4040688
|
A | G | 18 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(15): Show | 19 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
intron_variant | MODIFIER | c.1413-84A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040688 | ||||||
chr6:4040690
|
A | G | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1413-82A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040690 | ||||||
chr6:4040699
|
G | C | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1413-73G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 3/14 | chr6 | 4040699 | ||||||
chr6:4040978
|
T | C | 2 | a0001c0001t0004g0082a0001c0001t0004g0316 | 2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1568+51T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4040978 | ||||||
chr6:4040988
|
G | A | 11 | a0001c0001t0001g0294a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1568+61G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4040988 | ||||||
chr6:4041187
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1568+260A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041187 | ||||||
chr6:4041353
|
T | G | 1 | a0001c0005t0006g0319 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1568+426T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041353 | ||||||
chr6:4041445
|
C | T | 1 | a0002c0002t0002g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1568+518C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041445 | ||||||
chr6:4041650
|
T | C | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1568+723T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041650 | ||||||
chr6:4041683
|
C | CTTG | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1568+758_1568+760d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr6 | 4041683 | |||||
chr6:4041744
|
A | C | 19 | a0001c0001t0001g0294a0001c0001t0002g0341a0001c0001t0006g0012others(16): Show | 20 | HG01074.hp2 HG01081.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1569-743A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041744 | ||||||
chr6:4041754
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1569-733A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041754 | ||||||
chr6:4041987
|
A | C | 1 | a0002c0002t0002g0155 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1569-500A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4041987 | ||||||
chr6:4042006
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0015g0018a0002c0009t0018g0322 | 3 | HG00621.hp1 NA18522.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1569-481C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042006 | ||||||
chr6:4042068
|
G | A | 1 | a0002c0002t0002g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1569-419G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042068 | ||||||
chr6:4042103
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1569-384G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042103 | ||||||
chr6:4042163
|
G | A | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0026g0300 | 3 | HG01168.hp2 HG01169.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1569-324G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 4/14 | chr6 | 4042163 | ||||||
chr6:4042712
|
A | G | 1 | a0002c0002t0027g0190 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1650+144A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4042712 | ||||||
chr6:4042775
|
T | G | 6 | a0002c0002t0001g0131a0002c0002t0002g0150a0002c0002t0002g0156others(3): Show | 6 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1650+207T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4042775 | ||||||
chr6:4043025
|
G | A | 1 | a0001c0001t0001g0313 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1650+457G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043025 | ||||||
chr6:4043086
|
A | G | 1 | a0002c0002t0002g0172 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1650+518A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043086 | ||||||
chr6:4043181
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1650+613A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043181 | ||||||
chr6:4043219
|
C | T | 1 | a0001c0001t0004g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1651-594C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043219 | ||||||
chr6:4043248
|
G | A | 1 | a0002c0002t0002g0149 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1651-565G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043248 | ||||||
chr6:4043577
|
G | T | 1 | a0001c0001t0001g0249 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1651-236G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043577 | ||||||
chr6:4043613
|
A | C | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1651-200A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043613 | ||||||
chr6:4043653
|
A | G | 1 | a0001c0001t0001g0285 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1651-160A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043653 | ||||||
chr6:4043662
|
T | A | 12 | a0001c0001t0001g0294a0001c0001t0002g0341a0001c0001t0006g0012others(9): Show | 13 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1651-151T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043662 | ||||||
chr6:4043664
|
C | T | 9 | a0001c0001t0006g0292a0001c0005t0006g0212a0001c0005t0006g0318others(6): Show | 9 | HG02055.hp1 HG02257.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1651-149C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043664 | ||||||
chr6:4043665
|
A | G | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1651-148A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043665 | ||||||
chr6:4043738
|
G | A | 3 | a0002c0002t0002g0008a0002c0002t0002g0132a0002c0002t0002g0148 | 4 | NA18966.hp2 NA18980.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.1651-75G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 5/14 | chr6 | 4043738 | ||||||
chr6:4044039
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1861+16C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044039 | ||||||
chr6:4044063
|
G | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1861+40G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044063 | ||||||
chr6:4044092
|
G | C | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+69G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044092 | ||||||
chr6:4044110
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(256): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1861+87A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044110 | ||||||
chr6:4044252
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1861+229G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044252 | ||||||
chr6:4044384
|
T | C | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1861+361T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044384 | ||||||
chr6:4044393
|
C | G | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+370C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044393 | ||||||
chr6:4044510
|
T | C | 1 | a0001c0004t0010g0288 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1861+487T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044510 | ||||||
chr6:4044682
|
T | C | 1 | a0001c0012t0001g0336 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1861+659T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044682 | ||||||
chr6:4044708
|
A | G | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(2): Show | 5 | HG01074.hp1 HG01106.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+685A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044708 | ||||||
chr6:4044800
|
A | G | 1 | a0002c0002t0002g0156 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1861+777A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044800 | ||||||
chr6:4044814
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1861+791G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044814 | ||||||
chr6:4044845
|
G | GTTA | 69 | a0001c0001t0001g0045a0001c0001t0001g0227a0001c0001t0001g0251others(66): Show | 77 | HG00544.hp2 HG00609.hp1 HG01069.hp1 others(74): Show |
intron_variant | MODIFIER | c.1861+840_1861+842d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044845 | |||||
chr6:4044860
|
A | ATTT | 13 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0044others(10): Show | 14 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1861+839_1861+840i others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044860 | |||||
chr6:4044860
|
A | T | 7 | a0002c0002t0002g0179a0002c0003t0005g0116a0002c0003t0005g0117others(4): Show | 7 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1861+837A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044860 | ||||||
chr6:4044862
|
TA | T | 5 | a0001c0005t0006g0318a0001c0005t0006g0319a0001c0005t0006g0320others(2): Show | 5 | HG02922.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1861+840delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044862 | ||||||
chr6:4044863
|
A | ATT | 17 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(14): Show | 18 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.1861+854_1861+855d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | |||||
chr6:4044863
|
A | ATTT | 111 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0014others(108): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.1861+853_1861+855d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | |||||
chr6:4044863
|
A | ATTTT | 9 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0001g0056others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1861+852_1861+855d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | |||||
chr6:4044863
|
A | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0037a0001c0001t0001g0043others(39): Show | 43 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1861+840A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044863 | ||||||
chr6:4044863
|
AT | A | 7 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(4): Show | 8 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1861+855delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044863 | |||||
chr6:4044864
|
T | TTA | 6 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0033others(3): Show | 6 | HG01169.hp2 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1861+842_1861+843i others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4044864 | |||||
chr6:4044866
|
T | A | 3 | a0001c0001t0022g0215a0002c0002t0002g0166a0002c0002t0002g0186 | 3 | HG01943.hp2 HG02155.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1861+843T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044866 | ||||||
chr6:4044904
|
C | T | 7 | a0002c0003t0005g0115a0002c0003t0005g0118a0002c0003t0005g0119others(4): Show | 7 | HG02717.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1861+881C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4044904 | ||||||
chr6:4045008
|
G | A | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1861+985G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045008 | ||||||
chr6:4045097
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0252 | 3 | HG01516.hp1 HG03654.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1861+1074G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045097 | ||||||
chr6:4045168
|
C | T | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+1145C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045168 | ||||||
chr6:4045280
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1861+1257A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045280 | ||||||
chr6:4045358
|
G | A | 13 | a0002c0003t0005g0115a0002c0003t0005g0116a0002c0003t0005g0117others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1861+1335G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045358 | ||||||
chr6:4045469
|
C | T | 1 | a0002c0003t0005g0120 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1861+1446C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045469 | ||||||
chr6:4045599
|
A | C | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1861+1576A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045599 | ||||||
chr6:4045684
|
T | C | 1 | a0002c0002t0002g0135 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1862-1491T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045684 | ||||||
chr6:4045724
|
C | G | 1 | a0001c0001t0002g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1862-1451C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045724 | ||||||
chr6:4045745
|
A | G | 1 | a0001c0004t0011g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1862-1430A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045745 | ||||||
chr6:4045746
|
G | A | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1862-1429G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4045746 | ||||||
chr6:4046010
|
A | T | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1862-1165A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046010 | ||||||
chr6:4046082
|
G | A | 1 | a0002c0002t0002g0156 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1862-1093G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046082 | ||||||
chr6:4046316
|
A | G | 1 | a0001c0001t0003g0066 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1862-859A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046316 | ||||||
chr6:4046322
|
T | C | 13 | a0002c0003t0005g0115a0002c0003t0005g0116a0002c0003t0005g0117others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1862-853T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046322 | ||||||
chr6:4046364
|
G | T | 1 | a0001c0007t0006g0306 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1862-811G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046364 | ||||||
chr6:4046568
|
G | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1862-607G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046568 | ||||||
chr6:4046594
|
C | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1862-581C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046594 | ||||||
chr6:4046660
|
C | CT | 16 | a0001c0001t0001g0294a0001c0001t0002g0341a0001c0001t0003g0092others(13): Show | 17 | HG01081.hp2 HG02055.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1862-499dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr6 | 4046660 | |||||
chr6:4046663
|
T | C | 1 | a0001c0001t0001g0330 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1862-512T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046663 | ||||||
chr6:4046686
|
T | C | 3 | a0001c0001t0001g0327a0001c0001t0001g0338a0001c0001t0001g0340 | 3 | HG03710.hp2 HG03834.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1862-489T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046686 | ||||||
chr6:4046697
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(210): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.1862-478C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046697 | ||||||
chr6:4046711
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1862-464G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046711 | ||||||
chr6:4046815
|
G | C | 1 | a0001c0001t0004g0095 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1862-360G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4046815 | ||||||
chr6:4047005
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1862-170C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4047005 | ||||||
chr6:4047075
|
G | A | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1862-100G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 6/14 | chr6 | 4047075 | ||||||
chr6:4047363
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1935+115G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047363 | ||||||
chr6:4047382
|
ACT | A | 7 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0075others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1935+137_1935+138d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047382 | |||||
chr6:4047414
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1935+166A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047414 | ||||||
chr6:4047462
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1935+214T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047462 | ||||||
chr6:4047584
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1935+336A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047584 | ||||||
chr6:4047639
|
C | T | 1 | a0001c0001t0022g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1935+391C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047639 | ||||||
chr6:4047791
|
A | G | 1 | a0002c0003t0005g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1935+543A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047791 | ||||||
chr6:4047901
|
T | TAC | 29 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0035others(26): Show | 30 | HG00735.hp2 HG01099.hp1 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1935+697_1935+698d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
T | TACAC | 8 | a0001c0004t0010g0295a0002c0002t0002g0142a0002c0002t0002g0157others(5): Show | 8 | HG00738.hp2 HG02040.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1935+695_1935+698d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TAC | T | 48 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0027others(45): Show | 50 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1935+697_1935+698d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TACAC | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(109): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1935+695_1935+698d others(6): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TACACAC | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0030others(13): Show | 17 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1935+693_1935+698d others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TACACACA others(1): Show |
T | 29 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0053others(26): Show | 31 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.1935+691_1935+698d others(10): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TACACACA others(3): Show |
T | 22 | a0001c0001t0001g0018a0001c0001t0001g0227a0001c0001t0001g0228others(19): Show | 22 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.1935+689_1935+698d others(12): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TACACACA others(7): Show |
T | 8 | a0001c0001t0002g0341a0001c0001t0006g0292a0001c0005t0006g0318others(5): Show | 8 | HG02922.hp2 HG02965.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1935+685_1935+698d others(16): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TACACACA others(9): Show |
T | 2 | a0001c0005t0006g0212a0001c0005t0006g0321 | 2 | HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1935+683_1935+698d others(18): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047901
|
TACACACA others(15): Show |
T | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1935+677_1935+698d others(24): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4047901 | |||||
chr6:4047976
|
A | G | 1 | a0001c0001t0004g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1935+728A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4047976 | ||||||
chr6:4048006
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1935+758A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048006 | ||||||
chr6:4048046
|
G | T | 2 | a0002c0002t0002g0134a0002c0002t0002g0207 | 2 | HG00609.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.1935+798G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048046 | ||||||
chr6:4048058
|
T | A | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0273others(1): Show | 4 | HG00140.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1935+810T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048058 | ||||||
chr6:4048150
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1936-866G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048150 | ||||||
chr6:4048194
|
C | T | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1936-822C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048194 | ||||||
chr6:4048222
|
C | CA | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1936-787dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048222 | |||||
chr6:4048236
|
G | A | 4 | a0002c0002t0001g0131a0002c0002t0002g0150a0002c0002t0002g0160others(1): Show | 4 | HG00438.hp1 HG02080.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1936-780G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048236 | ||||||
chr6:4048310
|
C | T | 7 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0075others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1936-706C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048310 | ||||||
chr6:4048357
|
C | T | 6 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0010g0308others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-659C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048357 | ||||||
chr6:4048378
|
C | CA | 25 | a0001c0001t0002g0341a0001c0001t0003g0052a0001c0001t0003g0085others(22): Show | 25 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1936-619dupA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048378 | |||||
chr6:4048378
|
CA | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.1936-619delA | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048378 | |||||
chr6:4048378
|
CAA | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0058others(2): Show | 6 | HG01069.hp2 HG01993.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-620_1936-619d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048378 | |||||
chr6:4048464
|
G | T | 1 | a0001c0004t0011g0234 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1936-552G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048464 | ||||||
chr6:4048483
|
G | T | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1936-533G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048483 | ||||||
chr6:4048496
|
GAATGGTA others(5): Show |
G | 6 | a0002c0002t0002g0176a0002c0002t0002g0177a0002c0002t0002g0196others(3): Show | 6 | HG01074.hp2 HG01099.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1936-507_1936-496d others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048496 | |||||
chr6:4048618
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1936-398C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048618 | ||||||
chr6:4048662
|
A | G | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1936-354A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048662 | ||||||
chr6:4048733
|
C | CT | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1936-274dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr6 | 4048733 | |||||
chr6:4048803
|
TG | T | 10 | a0001c0001t0002g0341a0001c0001t0006g0292a0001c0005t0006g0212others(7): Show | 10 | HG02055.hp1 HG02257.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1936-212delG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048803 | ||||||
chr6:4048804
|
G | T | 1 | a0002c0003t0005g0122 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1936-212G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048804 | ||||||
chr6:4048805
|
T | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(128): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1936-211T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048805 | ||||||
chr6:4048806
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1936-210T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 7/14 | chr6 | 4048806 | ||||||
chr6:4049188
|
TG | T | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2026+84delG | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr6 | 4049188 | |||||
chr6:4049196
|
T | G | 1 | a0001c0001t0001g0241 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2026+90T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049196 | ||||||
chr6:4049245
|
A | G | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2026+139A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049245 | ||||||
chr6:4049260
|
C | T | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2026+154C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049260 | ||||||
chr6:4049366
|
T | C | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2026+260T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049366 | ||||||
chr6:4049726
|
T | C | 1 | a0001c0007t0006g0307 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.2027-6T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 8/14 | chr6 | 4049726 | ||||||
chr6:4050007
|
TGGAAACA others(312): Show |
T | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2174+145_2174+463d others(2): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4050007 | |||||
chr6:4050018
|
G | GT | 14 | a0002c0002t0002g0127a0002c0002t0002g0133a0002c0002t0002g0146others(11): Show | 14 | HG00621.hp2 HG01106.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.2174+165dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4050018 | |||||
chr6:4050443
|
A | G | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2174+564A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050443 | ||||||
chr6:4050460
|
C | T | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2174+581C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050460 | ||||||
chr6:4050469
|
T | C | 12 | a0001c0001t0001g0294a0001c0001t0002g0341a0001c0001t0006g0012others(9): Show | 13 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2174+590T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050469 | ||||||
chr6:4050503
|
C | T | 6 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0010g0308others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2174+624C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050503 | ||||||
chr6:4050707
|
G | A | 1 | a0002c0002t0002g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2174+828G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050707 | ||||||
chr6:4050817
|
A | G | 63 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(60): Show | 71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2174+938A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4050817 | ||||||
chr6:4050896
|
G | GTTGT | 15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0219others(12): Show | 16 | HG02129.hp2 NA18944.hp2 NA18954.hp1 others(13): Show |
intron_variant | MODIFIER | c.2174+1036_2174+103 others(8): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4050896 | |||||
chr6:4051029
|
C | A | 1 | a0002c0002t0002g0152 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2175-928C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051029 | ||||||
chr6:4051066
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2175-891C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051066 | ||||||
chr6:4051151
|
C | G | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2175-806C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051151 | ||||||
chr6:4051161
|
C | T | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2175-796C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051161 | ||||||
chr6:4051365
|
G | T | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2175-592G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051365 | ||||||
chr6:4051369
|
G | A | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2175-588G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051369 | ||||||
chr6:4051438
|
T | C | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2175-519T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051438 | ||||||
chr6:4051468
|
C | T | 1 | a0001c0001t0004g0022 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2175-489C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051468 | ||||||
chr6:4051674
|
A | T | 1 | a0001c0001t0022g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2175-283A>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051674 | ||||||
chr6:4051773
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2175-184T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051773 | ||||||
chr6:4051827
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2175-130A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051827 | ||||||
chr6:4051933
|
C | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2175-24C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051933 | ||||||
chr6:4051937
|
A | G | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2175-20A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | chr6 | 4051937 | ||||||
chr6:4051938
|
A | AT | 15 | a0001c0001t0001g0254a0001c0001t0001g0271a0002c0003t0005g0115others(12): Show | 15 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.2175-8dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr6 | 4051938 | |||||
chr6:4052110
|
G | A | 2 | a0001c0001t0001g0328a0005c0010t0001g0337 | 2 | HG02165.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2312+16G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052110 | ||||||
chr6:4052149
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(223): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.2312+55G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052149 | ||||||
chr6:4052160
|
G | A | 1 | a0002c0002t0002g0161 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2312+66G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052160 | ||||||
chr6:4052224
|
G | GT | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2312+135dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052224 | |||||
chr6:4052252
|
T | TTTG | 18 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(15): Show | 18 | HG01074.hp2 HG01099.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2312+183_2312+185d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052252 | |||||
chr6:4052252
|
TTTG | T | 23 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0021others(20): Show | 29 | HG01069.hp1 HG01070.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.2312+183_2312+185d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052252 | |||||
chr6:4052252
|
TTTGTTGT others(2): Show |
T | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2312+177_2312+185d others(11): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr6 | 4052252 | |||||
chr6:4052318
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2312+224G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052318 | ||||||
chr6:4052340
|
C | T | 1 | a0002c0002t0002g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2312+246C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052340 | ||||||
chr6:4052476
|
T | G | 1 | a0001c0001t0001g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2313-244T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052476 | ||||||
chr6:4052573
|
T | C | 1 | a0002c0002t0002g0132 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2313-147T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052573 | ||||||
chr6:4052592
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2313-128G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052592 | ||||||
chr6:4052618
|
G | A | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2313-102G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 10/14 | chr6 | 4052618 | ||||||
chr6:4053082
|
A | G | 1 | a0001c0001t0022g0215 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2466+209A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053082 | ||||||
chr6:4053122
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(268): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2466+249G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053122 | ||||||
chr6:4053130
|
A | G | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2466+257A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053130 | ||||||
chr6:4053192
|
T | C | 1 | a0002c0002t0002g0162 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2466+319T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053192 | ||||||
chr6:4053225
|
CT | C | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0045others(2): Show | 5 | HG01074.hp1 HG01106.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.2466+354delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053225 | |||||
chr6:4053367
|
G | T | 1 | a0001c0005t0006g0318 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2466+494G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053367 | ||||||
chr6:4053537
|
G | A | 2 | a0002c0002t0002g0134a0002c0002t0002g0207 | 2 | HG00609.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2466+664G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053537 | ||||||
chr6:4053560
|
A | AT | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2466+687_2466+688i others(3): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053560 | ||||||
chr6:4053573
|
A | G | 1 | a0004c0013t0019g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2466+700A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053573 | ||||||
chr6:4053655
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2466+782T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053655 | ||||||
chr6:4053656
|
G | A | 1 | a0001c0004t0010g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2466+783G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053656 | ||||||
chr6:4053738
|
A | C | 1 | a0002c0002t0002g0178 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2466+865A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053738 | ||||||
chr6:4053899
|
G | GCTTTTTT others(2): Show |
6 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0010g0308others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2466+1026_2466+102 others(13): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053899 | ||||||
chr6:4053903
|
T | G | 6 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0010g0308others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2466+1030T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4053903 | ||||||
chr6:4053903
|
T | TTTTTG | 22 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(19): Show | 23 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.2466+1051_2466+105 others(9): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | |||||
chr6:4053903
|
T | TTTTTGTT others(3): Show |
193 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(190): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2466+1046_2466+105 others(14): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | |||||
chr6:4053903
|
T | TTTTTGTT others(8): Show |
19 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(16): Show | 20 | HG01081.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+1041_2466+105 others(19): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | |||||
chr6:4053903
|
T | TTTTTGTT others(13): Show |
4 | a0001c0001t0009g0213a0001c0001t0009g0220a0001c0001t0009g0221others(1): Show | 4 | HG02257.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+1036_2466+105 others(24): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4053903 | |||||
chr6:4054000
|
C | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2466+1127C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054000 | ||||||
chr6:4054085
|
A | C | 7 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0075others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2466+1212A>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054085 | ||||||
chr6:4054460
|
A | AT | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2466+1589dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4054460 | |||||
chr6:4054487
|
G | C | 2 | a0001c0001t0003g0063a0001c0001t0003g0068 | 2 | NA18998.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2466+1614G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054487 | ||||||
chr6:4054515
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(263): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.2466+1642G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054515 | ||||||
chr6:4054517
|
T | A | 2 | a0001c0007t0006g0306a0001c0007t0006g0307 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2466+1644T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054517 | ||||||
chr6:4054611
|
T | G | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2467-1710T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054611 | ||||||
chr6:4054665
|
C | A | 1 | a0001c0001t0003g0093 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2467-1656C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054665 | ||||||
chr6:4054694
|
C | T | 13 | a0002c0003t0005g0115a0002c0003t0005g0116a0002c0003t0005g0117others(10): Show | 13 | HG00735.hp1 HG00738.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2467-1627C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054694 | ||||||
chr6:4054721
|
G | A | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2467-1600G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054721 | ||||||
chr6:4054740
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2467-1581G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054740 | ||||||
chr6:4054894
|
G | C | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2467-1427G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054894 | ||||||
chr6:4054961
|
T | C | 1 | a0001c0001t0025g0244 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2467-1360T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054961 | ||||||
chr6:4054964
|
A | G | 3 | a0002c0002t0002g0193a0002c0002t0002g0194a0002c0002t0027g0190 | 3 | HG02572.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2467-1357A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4054964 | ||||||
chr6:4055004
|
C | G | 6 | a0001c0004t0010g0288a0001c0004t0010g0295a0001c0004t0010g0308others(3): Show | 6 | HG01884.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2467-1317C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055004 | ||||||
chr6:4055004
|
C | T | 1 | a0002c0003t0005g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2467-1317C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055004 | ||||||
chr6:4055041
|
G | A | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2467-1280G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055041 | ||||||
chr6:4055182
|
A | G | 2 | a0001c0001t0006g0292a0001c0007t0006g0211 | 2 | HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2467-1139A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055182 | ||||||
chr6:4055473
|
T | A | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2467-848T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055473 | ||||||
chr6:4055553
|
G | C | 1 | a0002c0002t0002g0172 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2467-768G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055553 | ||||||
chr6:4055737
|
A | G | 2 | a0001c0001t0002g0341a0001c0001t0006g0012 | 3 | HG01081.hp2 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2467-584A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055737 | ||||||
chr6:4055770
|
G | C | 1 | a0002c0009t0018g0322 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2467-551G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055770 | ||||||
chr6:4055901
|
T | A | 1 | a0002c0002t0002g0206 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2467-420T>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055901 | ||||||
chr6:4055902
|
C | T | 7 | a0001c0001t0004g0073a0001c0001t0004g0074a0001c0001t0004g0075others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2467-419C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4055902 | ||||||
chr6:4056091
|
T | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(229): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2467-230T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | chr6 | 4056091 | ||||||
chr6:4056147
|
T | TAACTTTT others(82): Show |
1 | a0001c0004t0010g0308 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2467-164_2467-76du others(90): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr6 | 4056147 | |||||
chr6:4056494
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2581+59A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056494 | ||||||
chr6:4056831
|
T | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2582-205T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056831 | ||||||
chr6:4056926
|
T | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2582-110T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056926 | ||||||
chr6:4056939
|
C | T | 63 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0006others(60): Show | 71 | HG00609.hp1 HG01069.hp1 HG01070.hp1 others(68): Show |
intron_variant | MODIFIER | c.2582-97C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056939 | ||||||
chr6:4056966
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2582-70A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056966 | ||||||
chr6:4056999
|
C | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(243): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2582-37C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 12/14 | chr6 | 4056999 | ||||||
chr6:4057195
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
splice_region_variant&intron_variant | LOW | c.2733+8A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057195 | ||||||
chr6:4057308
|
T | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(14): Show | 18 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.2733+121T>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057308 | ||||||
chr6:4057380
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0200a0001c0001t0001g0293 | 3 | HG02809.hp1 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2733+193G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057380 | ||||||
chr6:4057393
|
G | T | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2733+206G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057393 | ||||||
chr6:4057538
|
A | G | 7 | a0002c0003t0005g0115a0002c0003t0005g0118a0002c0003t0005g0119others(4): Show | 7 | HG02717.hp1 HG02922.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2733+351A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057538 | ||||||
chr6:4057751
|
C | CT | 6 | a0001c0001t0002g0341a0002c0002t0002g0011a0002c0002t0002g0127others(3): Show | 7 | HG02040.hp1 HG02132.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2733+585dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | |||||
chr6:4057751
|
CT | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(149): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2733+585delT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | |||||
chr6:4057751
|
CTT | C | 107 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0024others(104): Show | 116 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.2733+584_2733+585d others(4): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | |||||
chr6:4057751
|
CTTT | C | 10 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(7): Show | 10 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2733+583_2733+585d others(5): Show |
PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr6 | 4057751 | |||||
chr6:4057777
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(224): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.2733+590C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057777 | ||||||
chr6:4057804
|
C | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2733+617C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057804 | ||||||
chr6:4057841
|
G | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0250a0001c0001t0001g0269others(1): Show | 4 | HG01167.hp2 HG01255.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.2733+654G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057841 | ||||||
chr6:4057903
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2733+716C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057903 | ||||||
chr6:4057911
|
G | T | 1 | a0001c0001t0001g0328 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2733+724G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057911 | ||||||
chr6:4057923
|
C | T | 1 | a0002c0002t0002g0199 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2733+736C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4057923 | ||||||
chr6:4058096
|
G | A | 1 | a0002c0002t0002g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2734-632G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058096 | ||||||
chr6:4058305
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2734-423G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058305 | ||||||
chr6:4058548
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(131): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2734-180C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058548 | ||||||
chr6:4058600
|
G | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG01891.hp2 HG02145.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2734-128G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 13/14 | chr6 | 4058600 | ||||||
chr6:4058834
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2820+20C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4058834 | ||||||
chr6:4058879
|
G | A | 1 | a0001c0001t0003g0094 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2820+65G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4058879 | ||||||
chr6:4058909
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2820+95A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4058909 | ||||||
chr6:4059002
|
G | C | 1 | a0001c0001t0001g0241 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2820+188G>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059002 | ||||||
chr6:4059045
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG03654.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2820+231G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059045 | ||||||
chr6:4059145
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.2820+331A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059145 | ||||||
chr6:4059187
|
A | G | 10 | a0001c0001t0006g0012a0001c0001t0006g0292a0001c0005t0006g0212others(7): Show | 11 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.2820+373A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059187 | ||||||
chr6:4059295
|
G | T | 1 | a0002c0003t0005g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2820+481G>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059295 | ||||||
chr6:4059298
|
C | T | 19 | a0002c0002t0002g0020a0002c0002t0002g0179a0002c0002t0002g0180others(16): Show | 19 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.2820+484C>T | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059298 | ||||||
chr6:4059308
|
C | G | 11 | a0001c0001t0002g0341a0001c0001t0006g0012a0001c0001t0006g0292others(8): Show | 12 | HG01081.hp2 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2820+494C>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059308 | ||||||
chr6:4059382
|
A | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2820+568A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059382 | ||||||
chr6:4059567
|
A | G | 1 | a0001c0001t0002g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2820+753A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059567 | ||||||
chr6:4059590
|
A | G | 4 | a0001c0001t0006g0292a0001c0007t0006g0211a0001c0007t0006g0306others(1): Show | 4 | HG02922.hp2 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2820+776A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059590 | ||||||
chr6:4059640
|
C | CT | 278 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(275): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2821-764dupT | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr6 | 4059640 | |||||
chr6:4059802
|
C | A | 1 | a0001c0001t0001g0250 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2821-611C>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059802 | ||||||
chr6:4059907
|
A | G | 12 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(9): Show | 12 | HG01891.hp2 HG02145.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.2821-506A>G | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4059907 | ||||||
chr6:4060143
|
G | A | 4 | a0001c0001t0003g0098a0001c0001t0003g0100a0001c0001t0003g0101others(1): Show | 4 | NA18944.hp1 NA18948.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.2821-270G>A | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4060143 | ||||||
chr6:4060181
|
T | C | 1 | a0001c0011t0001g0036 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2821-232T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4060181 | ||||||
chr6:4060380
|
T | C | 1 | a0001c0001t0002g0341 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2821-33T>C | PRPF4B | ENSG00000112739.17 | transcript | ENST00000337659.11 | protein_coding | 14/14 | chr6 | 4060380 |