geneid | 5048 |
---|---|
ensemblid | ENSG00000007168.14 |
hgncid | 8574 |
symbol | PAFAH1B1 |
name | platelet activating factor acetylhydrolase 1b regulatory subunit 1 |
refseq_nuc | NM_000430.4 |
refseq_prot | NP_000421.1 |
ensembl_nuc | ENST00000397195.10 |
ensembl_prot | ENSP00000380378.4 |
mane_status | MANE Select |
chr | chr17 |
start | 2593654 |
end | 2685615 |
strand | + |
ver | v1.2 |
region | chr17:2593654-2685615 |
region5000 | chr17:2588654-2690615 |
regionname0 | PAFAH1B1_chr17_2593654_2685615 |
regionname5000 | PAFAH1B1_chr17_2588654_2690615 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 410 | 280 | 82 | 62 | 88 | 12 | 34 | 64 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1233 | 266 | 69 | 62 | 88 | 11 | 34 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
c0002 | 0/0 | 1233 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
c0003 | 0/0 | 1233 | 5 | 5 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
c0004 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
c0005 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4357 | 78 | 20 | 25 | 17 | 5 | 10 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0002 | 0/0 | 4355 | 48 | 1 | 7 | 29 | 4 | 7 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0003 | 1/0 | 4357 | 32 | 3 | 7 | 19 | 1 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0004 | 0/0 | 4357 | 26 | 9 | 9 | 1 | 1 | 6 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0005 | 0/0 | 4357 | 19 | 0 | 6 | 11 | 0 | 2 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0006 | 0/0 | 4355 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0007 | 0/0 | 4357 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0008 | 0/0 | 4364 | 7 | 6 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0009 | 0/0 | 4357 | 6 | 0 | 0 | 5 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0010 | 0/0 | 4357 | 6 | 6 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0011 | 0/0 | 4355 | 6 | 1 | 3 | 1 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0012 | 0/0 | 4364 | 5 | 4 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0013 | 0/0 | 4357 | 2 | 2 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0014 | 0/0 | 4357 | 2 | 0 | 0 | 0 | 0 | 2 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0015 | 0/0 | 4364 | 2 | 0 | 1 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0016 | 0/0 | 4357 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0017 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0018 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0019 | 0/0 | 4355 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0020 | 0/0 | 4355 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0021 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0022 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0023 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0024 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0025 | 0/0 | 4357 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0026 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0027 | 0/0 | 4355 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0028 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0029 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0030 | 0/0 | 4355 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0031 | 0/0 | 4355 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0032 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0033 | 0/0 | 4357 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0034 | 0/0 | 4372 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0035 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0036 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0037 | 0/0 | 4357 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0038 | 0/0 | 4357 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0039 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0040 | 0/0 | 4363 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0041 | 0/0 | 4364 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
t0042 | 0/0 | 4364 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1233 | 266 | 69 | 62 | 88 | 11 | 34 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0002 | 0/0 | 1233 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0003 | 0/0 | 1233 | 5 | 5 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0004 | 0/0 | 1233 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0005 | 0/0 | 1233 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5589 | 77 | 20 | 25 | 17 | 4 | 10 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0002 | 0/0 | 5587 | 48 | 1 | 7 | 29 | 4 | 7 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0003 | 1/0 | 5589 | 32 | 3 | 7 | 19 | 1 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0004 | 0/0 | 5589 | 26 | 9 | 9 | 1 | 1 | 6 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0005 | 0/0 | 5589 | 19 | 0 | 6 | 11 | 0 | 2 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0007 | 0/0 | 5589 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0008 | 0/0 | 5596 | 7 | 6 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0009 | 0/0 | 5589 | 6 | 0 | 0 | 5 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0010 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0011 | 0/0 | 5587 | 6 | 1 | 3 | 1 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0012 | 0/0 | 5596 | 5 | 4 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0013 | 0/0 | 5589 | 2 | 2 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0014 | 0/0 | 5589 | 2 | 0 | 0 | 0 | 0 | 2 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0015 | 0/0 | 5596 | 2 | 0 | 1 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0016 | 0/0 | 5589 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0017 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0018 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0019 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0020 | 0/0 | 5587 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0021 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0022 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0023 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0024 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0025 | 0/0 | 5589 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0026 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0027 | 0/0 | 5587 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0028 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0029 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0030 | 0/0 | 5587 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0031 | 0/0 | 5587 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0032 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0033 | 0/0 | 5589 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0034 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0035 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0037 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0038 | 0/0 | 5589 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0039 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0040 | 0/0 | 5595 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0041 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0001t0042 | 0/0 | 5596 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0002t0006 | 0/0 | 5587 | 7 | 7 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0003t0010 | 0/0 | 5589 | 5 | 5 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0004t0036 | 0/0 | 5589 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
a0001c0005t0001 | 0/0 | 5589 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | copy fasta | chr17 | 2588654 | 2690615 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0031 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0008g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0009g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0009g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0009g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0009g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0010g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0011g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0011g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0011g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0011g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0011g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0012g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0012g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0012g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0013g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0014g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0014g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0015g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0015g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0019g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0020g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0021g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0023g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0024g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0025g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0026g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0027g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0029g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0030g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0031g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0032g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0033g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0034g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0035g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0037g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0038g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0039g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0040g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0041g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0001t0042g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0002t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0002t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0003t0010g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0003t0010g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0003t0010g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0003t0010g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0003t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0004t0036g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
a0001c0005t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | GBR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00323 | hp1 | a0001 | c0001 | t0009 | g0088 | EUR | FIN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0087 | EUR | FIN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00438 | hp2 | a0001 | c0001 | t0011 | g0270 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0084 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0203 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01109 | hp1 | a0001 | c0001 | t0015 | g0017 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0143 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01167 | hp2 | a0001 | c0001 | t0040 | g0074 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0250 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01243 | hp1 | a0001 | c0001 | t0039 | g0146 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01243 | hp2 | a0001 | c0001 | t0025 | g0032 | AMR | PUR | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0235 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0276 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0229 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0063 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0011 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0138 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0100 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0230 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0265 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0168 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0101 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01993 | hp2 | a0001 | c0001 | t0011 | g0242 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02004 | hp2 | a0001 | c0001 | t0011 | g0239 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02055 | hp1 | a0001 | c0002 | t0006 | g0190 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0196 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02165 | hp1 | a0001 | c0001 | t0034 | g0251 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02165 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | CDX | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0144 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02258 | hp1 | a0001 | c0001 | t0022 | g0183 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0099 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02273 | hp2 | a0001 | c0001 | t0011 | g0241 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0191 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0098 | AMR | PEL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0137 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02572 | hp2 | a0001 | c0001 | t0030 | g0106 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02602 | hp2 | a0001 | c0001 | t0038 | g0238 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0014 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0181 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02647 | hp1 | a0001 | c0002 | t0006 | g0189 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02647 | hp2 | a0001 | c0003 | t0010 | g0179 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0211 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02698 | hp1 | a0001 | c0001 | t0011 | g0233 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02723 | hp1 | a0001 | c0001 | t0035 | g0204 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0192 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02738 | hp2 | a0001 | c0001 | t0027 | g0159 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02809 | hp1 | a0001 | c0002 | t0006 | g0188 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0022 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02886 | hp2 | a0001 | c0003 | t0010 | g0178 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02896 | hp1 | a0001 | c0003 | t0010 | g0177 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0012 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0199 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02976 | hp1 | a0001 | c0003 | t0010 | g0175 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03017 | hp2 | a0001 | c0001 | t0014 | g0049 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03041 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03041 | hp2 | a0001 | c0002 | t0006 | g0186 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03130 | hp2 | a0001 | c0002 | t0006 | g0185 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03139 | hp1 | a0001 | c0001 | t0032 | g0197 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03195 | hp1 | a0001 | c0003 | t0010 | g0176 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03209 | hp1 | a0001 | c0001 | t0026 | g0093 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03209 | hp2 | a0001 | c0001 | t0029 | g0182 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03225 | hp2 | a0001 | c0001 | t0042 | g0015 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0243 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03453 | hp1 | a0001 | c0001 | t0013 | g0218 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03453 | hp2 | a0001 | c0001 | t0037 | g0272 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0247 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0244 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0016 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0274 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03579 | hp2 | a0001 | c0001 | t0023 | g0135 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03704 | hp2 | a0001 | c0001 | t0031 | g0091 | SAS | PJL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0092 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0248 | SAS | BEB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04199 | hp2 | a0001 | c0001 | t0015 | g0280 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04204 | hp1 | a0001 | c0001 | t0012 | g0279 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0044 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG04228 | hp2 | a0001 | c0001 | t0014 | g0048 | SAS | STU | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | YRI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18522 | hp2 | a0001 | c0001 | t0012 | g0013 | AFR | YRI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | CHB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0085 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18946 | hp2 | a0001 | c0001 | t0033 | g0026 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18948 | hp2 | a0001 | c0001 | t0009 | g0062 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18954 | hp2 | a0001 | c0001 | t0009 | g0058 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0090 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18968 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18979 | hp2 | a0001 | c0001 | t0020 | g0226 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18983 | hp1 | a0001 | c0001 | t0019 | g0268 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18983 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0167 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19030 | hp1 | a0001 | c0004 | t0036 | g0205 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19043 | hp2 | a0001 | c0001 | t0024 | g0193 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19060 | hp2 | a0001 | c0001 | t0009 | g0107 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19063 | hp1 | a0001 | c0001 | t0009 | g0083 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0140 | AFR | ASW | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | ASW | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0237 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0208 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20805 | hp2 | a0001 | c0005 | t0001 | g0094 | EUR | TSI | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0082 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | CLM | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02109 | hp2 | a0001 | c0002 | t0006 | g0187 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03471 | hp1 | a0001 | c0001 | t0013 | g0253 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG03471 | hp2 | a0001 | c0001 | t0021 | g0180 | AFR | MSL | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG06807 | hp1 | a0001 | c0001 | t0028 | g0018 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0142 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20300 | hp1 | a0001 | c0001 | t0041 | g0139 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA20300 | hp2 | a0001 | c0001 | t0011 | g0240 | AFR | USA | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
NA21309 | hp2 | a0001 | c0001 | t0017 | g0010 | AFR | LWK | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0160 | REF | REF | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0031 | REF | REF | PAFAH1B1_chr17_2588654_2690615 | PAFAH1B1 | chr17 | 2588654 | 2690615 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:2670237
|
C | T | 1 | a0001c0003 | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
synonymous_variant | LOW | c.474C>T | p.Phe158Phe | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/11 | 1017/5589 | 474/1233 | 158/410 | chr17 | 2670237 | ||
chr17:2674081
|
A | T | 1 | a0001c0002 | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
synonymous_variant | LOW | c.693A>T | p.Thr231Thr | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/11 | 1236/5589 | 693/1233 | 231/410 | chr17 | 2674081 | ||
chr17:2674168
|
A | G | 1 | a0001c0005 | 1 | NA20805.hp2 | synonymous_variant | LOW | c.780A>G | p.Val260Val | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/11 | 1323/5589 | 780/1233 | 260/410 | chr17 | 2674168 | ||
chr17:2680220
|
T | C | 1 | a0001c0004 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1059T>C | p.Ile353Ile | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/11 | 1602/5589 | 1059/1233 | 353/410 | chr17 | 2680220 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:2593657
|
C | CGGAGCT | 7 | a0001c0001t0008a0001c0001t0012a0001c0001t0015others(4): Show | 18 | HG01109.hp1 HG01167.hp1 HG01167.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-534_-529dupTGGAGC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44620 | INFO_REALIGN_3_PRIME | chr17 | 2593657 | ||||
chr17:2593717
|
G | T | 1 | a0001c0001t0038 | 1 | HG02602.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-480G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | chr17 | 2593717 | ||||||
chr17:2593891
|
C | A | 1 | a0001c0001t0013 | 2 | HG03453.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-306C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44398 | chr17 | 2593891 | |||||
chr17:2593898
|
C | T | 3 | a0001c0001t0007a0001c0001t0037a0001c0004t0036 | 9 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-299C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44391 | chr17 | 2593898 | |||||
chr17:2593902
|
C | CCCTCCCT others(8): Show |
1 | a0001c0001t0034 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-284_-270dupTCCTTC others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44361 | INFO_REALIGN_3_PRIME | chr17 | 2593902 | ||||
chr17:2593927
|
C | T | 1 | a0001c0001t0035 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-270C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/11 | 44362 | chr17 | 2593927 | |||||
chr17:2638186
|
T | C | 1 | a0001c0001t0014 | 2 | HG03017.hp2 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-103T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/11 | 103 | chr17 | 2638186 | |||||
chr17:2638205
|
A | T | 1 | a0001c0001t0038 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/11 | 84 | chr17 | 2638205 | |||||
chr17:2638240
|
A | C | 1 | a0001c0001t0033 | 1 | NA18946.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/11 | 49 | chr17 | 2638240 | |||||
chr17:2681819
|
C | T | 6 | a0001c0001t0004a0001c0001t0011a0001c0001t0032others(3): Show | 36 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*17C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 17 | chr17 | 2681819 | |||||
chr17:2681866
|
A | AC | 5 | a0001c0001t0008a0001c0001t0012a0001c0001t0015others(2): Show | 16 | HG01109.hp1 HG01167.hp1 HG01884.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*68dupC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 69 | INFO_REALIGN_3_PRIME | chr17 | 2681866 | ||||
chr17:2682488
|
T | A | 2 | a0001c0001t0009a0001c0001t0016 | 7 | HG00323.hp1 NA18944.hp1 NA18948.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*686T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 686 | chr17 | 2682488 | |||||
chr17:2682503
|
C | T | 1 | a0001c0002t0006 | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*701C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 701 | chr17 | 2682503 | |||||
chr17:2682855
|
G | A | 3 | a0001c0001t0017a0001c0001t0018a0001c0004t0036 | 3 | HG02809.hp2 NA19030.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1053G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1053 | chr17 | 2682855 | |||||
chr17:2682935
|
A | G | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(23): Show | 215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*1133A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1133 | chr17 | 2682935 | |||||
chr17:2682955
|
C | T | 1 | a0001c0001t0023 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1153 | chr17 | 2682955 | |||||
chr17:2683180
|
G | A | 2 | a0001c0001t0024a0001c0002t0006 | 8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1378G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1378 | chr17 | 2683180 | |||||
chr17:2683264
|
C | G | 1 | a0001c0001t0022 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1462 | chr17 | 2683264 | |||||
chr17:2683716
|
A | T | 3 | a0001c0001t0005a0001c0001t0031a0001c0001t0033 | 21 | HG00597.hp2 HG00609.hp1 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1914A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1914 | chr17 | 2683716 | |||||
chr17:2683733
|
GAA | G | 1 | a0001c0002t0006 | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1934_*1935delAA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 2683733 | ||||
chr17:2683793
|
T | C | 5 | a0001c0001t0008a0001c0001t0025a0001c0001t0026others(2): Show | 11 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1991T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 1991 | chr17 | 2683793 | |||||
chr17:2683942
|
A | G | 5 | a0001c0001t0012a0001c0001t0018a0001c0001t0022others(2): Show | 9 | HG02258.hp1 HG02572.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2140A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 2140 | chr17 | 2683942 | |||||
chr17:2683988
|
C | T | 1 | a0001c0001t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2186C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 2186 | chr17 | 2683988 | |||||
chr17:2684594
|
T | C | 1 | a0001c0001t0027 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2792T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 2792 | chr17 | 2684594 | |||||
chr17:2684865
|
G | A | 1 | a0001c0001t0019 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3063G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3063 | chr17 | 2684865 | |||||
chr17:2684989
|
C | T | 11 | a0001c0001t0010a0001c0001t0017a0001c0001t0021others(8): Show | 15 | HG02630.hp2 HG02647.hp2 HG02886.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3187C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3187 | chr17 | 2684989 | |||||
chr17:2685165
|
A | G | 1 | a0001c0001t0028 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3363A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3363 | chr17 | 2685165 | |||||
chr17:2685428
|
TAA | T | 7 | a0001c0001t0002a0001c0001t0011a0001c0001t0019others(4): Show | 59 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3627_*3628delAA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3627 | chr17 | 2685428 | |||||
chr17:2685473
|
A | G | 1 | a0001c0001t0016 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3671A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 11/11 | 3671 | chr17 | 2685473 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:2594030
|
C | T | 2 | a0001c0001t0012g0279a0001c0001t0015g0280 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-191+24C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594030 | ||||||
chr17:2594149
|
T | G | 1 | a0001c0001t0016g0001 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-191+143T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594149 | ||||||
chr17:2594424
|
G | A | 1 | a0001c0001t0003g0002 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-191+418G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594424 | ||||||
chr17:2594755
|
A | G | 84 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(81): Show | 84 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-191+749A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594755 | ||||||
chr17:2594816
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-191+810G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594816 | ||||||
chr17:2594912
|
G | A | 1 | a0001c0001t0007g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-191+906G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2594912 | ||||||
chr17:2595054
|
G | A | 1 | a0001c0001t0005g0004 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-191+1048G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595054 | ||||||
chr17:2595162
|
TCTTTC | T | 8 | a0001c0001t0004g0198a0001c0001t0004g0199a0001c0001t0004g0200others(5): Show | 8 | HG01070.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+1160_-191+116 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595162 | |||||
chr17:2595260
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-191+1254C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595260 | ||||||
chr17:2595340
|
G | T | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-191+1334G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595340 | ||||||
chr17:2595421
|
C | CTTTTT | 62 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0217others(59): Show | 62 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.-191+1427_-191+143 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595421 | |||||
chr17:2595421
|
C | CTTTTTT | 11 | a0001c0001t0003g0277a0001c0001t0003g0278a0001c0001t0004g0275others(8): Show | 11 | HG00438.hp2 HG01257.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.-191+1426_-191+143 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595421 | |||||
chr17:2595421
|
CT | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(13): Show | 16 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-191+1431delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595421 | |||||
chr17:2595435
|
T | TTTTTC | 17 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(14): Show | 17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-191+1431_-191+143 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595435 | |||||
chr17:2595477
|
CAT | C | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+1473_-191+147 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2595477 | |||||
chr17:2595566
|
A | G | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+1560A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595566 | ||||||
chr17:2595599
|
G | T | 20 | a0001c0001t0003g0002a0001c0001t0003g0216a0001c0001t0003g0254others(17): Show | 20 | HG01346.hp1 HG01496.hp2 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.-191+1593G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2595599 | ||||||
chr17:2596184
|
G | A | 1 | a0001c0001t0012g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-191+2178G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596184 | ||||||
chr17:2596196
|
A | G | 9 | a0001c0001t0003g0011a0001c0001t0012g0012a0001c0001t0012g0013others(6): Show | 9 | HG01109.hp1 HG01515.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-191+2190A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596196 | ||||||
chr17:2596253
|
C | T | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+2247C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596253 | ||||||
chr17:2596293
|
G | T | 1 | a0001c0001t0013g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-191+2287G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596293 | ||||||
chr17:2596608
|
C | T | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191+2602C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596608 | ||||||
chr17:2596652
|
A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+2646A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596652 | ||||||
chr17:2596780
|
C | G | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191+2774C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596780 | ||||||
chr17:2596986
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0028g0018 | 3 | HG02559.hp2 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-191+2980G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2596986 | ||||||
chr17:2597011
|
A | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+3005A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597011 | ||||||
chr17:2597024
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-191+3018G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597024 | ||||||
chr17:2597149
|
G | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+3143G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597149 | ||||||
chr17:2597399
|
G | T | 74 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(71): Show | 74 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.-191+3393G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597399 | ||||||
chr17:2597403
|
C | CT | 52 | a0001c0001t0001g0154a0001c0001t0001g0160a0001c0001t0001g0161others(49): Show | 52 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-191+3422dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | |||||
chr17:2597403
|
C | CTT | 15 | a0001c0001t0001g0021a0001c0001t0001g0174a0001c0001t0003g0216others(12): Show | 15 | HG02055.hp2 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.-191+3421_-191+342 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | |||||
chr17:2597403
|
C | CTTT | 35 | a0001c0001t0002g0234a0001c0001t0004g0198a0001c0001t0004g0199others(32): Show | 35 | HG00733.hp1 HG01070.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.-191+3420_-191+342 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | |||||
chr17:2597403
|
CT | C | 30 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(27): Show | 30 | HG01070.hp2 HG01099.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.-191+3422delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | |||||
chr17:2597403
|
CTT | C | 6 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-191+3421_-191+342 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597403 | |||||
chr17:2597433
|
G | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.-191+3427G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597433 | ||||||
chr17:2597652
|
G | C | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+3646G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597652 | ||||||
chr17:2597679
|
A | G | 78 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(75): Show | 78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+3673A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2597679 | ||||||
chr17:2597742
|
TTCTC | T | 77 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(74): Show | 77 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.-191+3741_-191+374 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597742 | |||||
chr17:2597781
|
A | AGT | 79 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(76): Show | 79 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(76): Show |
intron_variant | MODIFIER | c.-191+3792_-191+379 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2597781 | |||||
chr17:2598105
|
C | T | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+4099C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598105 | ||||||
chr17:2598152
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG01243.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-191+4146G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598152 | ||||||
chr17:2598256
|
T | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0153 | 2 | HG00642.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-191+4250T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598256 | ||||||
chr17:2598474
|
C | T | 5 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(2): Show | 5 | HG00558.hp1 NA18612.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+4468C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2598474 | ||||||
chr17:2599092
|
T | C | 78 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(75): Show | 78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+5086T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599092 | ||||||
chr17:2599347
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-191+5341C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599347 | ||||||
chr17:2599402
|
T | G | 2 | a0001c0001t0004g0228a0001c0001t0004g0252 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-191+5396T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599402 | ||||||
chr17:2599656
|
A | G | 1 | a0001c0001t0015g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-191+5650A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599656 | ||||||
chr17:2599712
|
A | G | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+5706A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599712 | ||||||
chr17:2599767
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-191+5761C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599767 | ||||||
chr17:2599876
|
A | C | 1 | a0001c0001t0001g0147 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-191+5870A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2599876 | ||||||
chr17:2599971
|
C | CT | 49 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(46): Show | 49 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.-191+5990dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | |||||
chr17:2599971
|
C | CTT | 5 | a0001c0001t0001g0145a0001c0001t0012g0016a0001c0001t0022g0183others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+5989_-191+599 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | |||||
chr17:2599971
|
CT | C | 76 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 76 | HG00733.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.-191+5990delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | |||||
chr17:2599971
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+5978_-191+599 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2599971 | |||||
chr17:2600103
|
C | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-191+6097C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600103 | ||||||
chr17:2600104
|
C | T | 18 | a0001c0001t0002g0122a0001c0001t0008g0137a0001c0001t0008g0138others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-191+6098C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600104 | ||||||
chr17:2600154
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-191+6148A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600154 | ||||||
chr17:2600250
|
C | A | 19 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(16): Show | 19 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.-191+6244C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600250 | ||||||
chr17:2600283
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-191+6277T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600283 | ||||||
chr17:2600568
|
C | CA | 98 | a0001c0001t0001g0040a0001c0001t0001g0123a0001c0001t0001g0154others(95): Show | 98 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.-191+6580dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2600568 | |||||
chr17:2600568
|
C | CAA | 7 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0254others(4): Show | 7 | HG01261.hp2 HG01952.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+6579_-191+658 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2600568 | |||||
chr17:2600587
|
C | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+6581C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600587 | ||||||
chr17:2600769
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+6763G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600769 | ||||||
chr17:2600819
|
T | C | 77 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(74): Show | 77 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.-191+6813T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600819 | ||||||
chr17:2600864
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+6858C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600864 | ||||||
chr17:2600932
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-191+6926A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600932 | ||||||
chr17:2600952
|
G | A | 1 | a0001c0001t0025g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-191+6946G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600952 | ||||||
chr17:2600974
|
T | C | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0016 | 3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-191+6968T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2600974 | ||||||
chr17:2601254
|
C | T | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-191+7248C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601254 | ||||||
chr17:2601409
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-191+7403A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601409 | ||||||
chr17:2601508
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+7502C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601508 | ||||||
chr17:2601511
|
G | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+7505G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601511 | ||||||
chr17:2601566
|
C | T | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+7560C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601566 | ||||||
chr17:2601584
|
G | GGT | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+7580_-191+758 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2601584 | |||||
chr17:2601593
|
C | T | 1 | a0001c0001t0005g0004 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-191+7587C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601593 | ||||||
chr17:2601693
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-191+7687C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601693 | ||||||
chr17:2601993
|
A | G | 76 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(73): Show | 76 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-191+7987A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2601993 | ||||||
chr17:2602089
|
TACCATGA others(7): Show |
T | 3 | a0001c0001t0001g0040a0001c0001t0002g0118a0001c0001t0002g0119 | 3 | HG00544.hp1 HG03492.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-191+8084_-191+809 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602089 | ||||||
chr17:2602251
|
G | GA | 33 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0042others(30): Show | 33 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.-191+8255dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2602251 | |||||
chr17:2602264
|
A | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+8258A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602264 | ||||||
chr17:2602539
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-191+8533C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602539 | ||||||
chr17:2602807
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-191+8801G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602807 | ||||||
chr17:2602908
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-191+8902G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2602908 | ||||||
chr17:2603335
|
T | C | 3 | a0001c0001t0002g0038a0001c0001t0002g0057a0001c0001t0002g0156 | 3 | NA18944.hp2 NA18952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-191+9329T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603335 | ||||||
chr17:2603538
|
T | C | 73 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(70): Show | 73 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.-191+9532T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603538 | ||||||
chr17:2603741
|
C | CT | 29 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0229others(26): Show | 29 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.-191+9749dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2603741 | |||||
chr17:2603741
|
CT | C | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+9749delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2603741 | |||||
chr17:2603836
|
G | A | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+9830G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603836 | ||||||
chr17:2603894
|
C | T | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-191+9888C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603894 | ||||||
chr17:2603971
|
C | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-191+9965C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2603971 | ||||||
chr17:2604015
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0002g0115 | 3 | HG00544.hp2 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-191+10009C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604015 | ||||||
chr17:2604067
|
G | C | 1 | a0001c0001t0005g0059 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-191+10061G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604067 | ||||||
chr17:2604127
|
T | C | 12 | a0001c0001t0003g0216a0001c0001t0003g0254a0001c0001t0003g0255others(9): Show | 12 | NA18947.hp1 NA18952.hp2 NA18965.hp1 others(9): Show |
intron_variant | MODIFIER | c.-191+10121T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604127 | ||||||
chr17:2604198
|
C | T | 2 | a0001c0001t0004g0228a0001c0001t0004g0252 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-191+10192C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604198 | ||||||
chr17:2604203
|
A | G | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-191+10197A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604203 | ||||||
chr17:2604291
|
G | C | 7 | a0001c0001t0003g0002a0001c0001t0003g0264a0001c0001t0003g0265others(4): Show | 7 | HG01346.hp1 HG01496.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+10285G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604291 | ||||||
chr17:2604318
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191+10312G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604318 | ||||||
chr17:2604493
|
T | C | 2 | a0001c0001t0004g0228a0001c0001t0004g0252 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-191+10487T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604493 | ||||||
chr17:2604689
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-191+10683T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604689 | ||||||
chr17:2604809
|
C | CA | 9 | a0001c0001t0004g0198a0001c0002t0006g0185a0001c0002t0006g0186others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-191+10813dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2604809 | |||||
chr17:2604955
|
G | A | 96 | a0001c0001t0001g0184a0001c0001t0001g0220a0001c0001t0002g0234others(93): Show | 96 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.-191+10949G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2604955 | ||||||
chr17:2605002
|
G | C | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-191+10996G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605002 | ||||||
chr17:2605056
|
T | C | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+11050T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605056 | ||||||
chr17:2605085
|
C | T | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-191+11079C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605085 | ||||||
chr17:2605258
|
T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+11252T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605258 | ||||||
chr17:2605617
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-191+11611G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605617 | ||||||
chr17:2605619
|
G | A | 1 | a0001c0001t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-191+11613G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605619 | ||||||
chr17:2605689
|
C | G | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+11683C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605689 | ||||||
chr17:2605762
|
G | T | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-191+11756G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605762 | ||||||
chr17:2605785
|
G | T | 9 | a0001c0001t0001g0109a0001c0001t0002g0039a0001c0001t0002g0108others(6): Show | 9 | HG00438.hp1 HG00558.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.-191+11779G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605785 | ||||||
chr17:2605855
|
A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+11849A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605855 | ||||||
chr17:2605866
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-191+11860G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605866 | ||||||
chr17:2605871
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-191+11865T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605871 | ||||||
chr17:2605903
|
G | T | 3 | a0001c0001t0003g0217a0001c0001t0013g0218a0001c0001t0013g0253 | 3 | HG03453.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-191+11897G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2605903 | ||||||
chr17:2606002
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-191+11996A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606002 | ||||||
chr17:2606067
|
C | T | 74 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(71): Show | 74 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.-191+12061C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606067 | ||||||
chr17:2606426
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-191+12420C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606426 | ||||||
chr17:2606525
|
G | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-191+12519G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606525 | ||||||
chr17:2606732
|
G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+12726G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606732 | ||||||
chr17:2606803
|
C | T | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-191+12797C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606803 | ||||||
chr17:2606810
|
C | CT | 21 | a0001c0001t0001g0132a0001c0001t0001g0145a0001c0001t0001g0174others(18): Show | 21 | HG00438.hp1 HG00438.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.-191+12831dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | |||||
chr17:2606810
|
CT | C | 29 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0027others(26): Show | 29 | HG00733.hp2 HG01243.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.-191+12831delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | |||||
chr17:2606810
|
CTT | C | 9 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(6): Show | 9 | HG01891.hp1 HG02647.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-191+12830_-191+12 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | |||||
chr17:2606810
|
CTTTT | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+12828_-191+12 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2606810 | |||||
chr17:2606859
|
G | A | 78 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(75): Show | 78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+12853G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606859 | ||||||
chr17:2606885
|
C | T | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-191+12879C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2606885 | ||||||
chr17:2607018
|
G | A | 77 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(74): Show | 77 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.-191+13012G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607018 | ||||||
chr17:2607085
|
C | T | 78 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(75): Show | 78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+13079C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607085 | ||||||
chr17:2607244
|
G | A | 3 | a0001c0001t0004g0275a0001c0001t0013g0218a0001c0001t0013g0253 | 3 | HG02486.hp2 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-191+13238G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607244 | ||||||
chr17:2607497
|
T | C | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0016 | 3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-191+13491T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607497 | ||||||
chr17:2607518
|
T | C | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-191+13512T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607518 | ||||||
chr17:2607558
|
C | G | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-191+13552C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607558 | ||||||
chr17:2607567
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-191+13561C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2607567 | ||||||
chr17:2608099
|
T | G | 1 | a0001c0001t0020g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-191+14093T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608099 | ||||||
chr17:2608281
|
G | T | 3 | a0001c0001t0003g0217a0001c0001t0013g0218a0001c0001t0013g0253 | 3 | HG03453.hp1 HG03471.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-191+14275G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608281 | ||||||
chr17:2608316
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-191+14310C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608316 | ||||||
chr17:2608402
|
T | C | 18 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-191+14396T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608402 | ||||||
chr17:2608545
|
G | A | 1 | a0001c0001t0022g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-191+14539G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608545 | ||||||
chr17:2608624
|
A | T | 1 | a0001c0001t0030g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-191+14618A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608624 | ||||||
chr17:2608782
|
G | C | 1 | a0001c0001t0002g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-191+14776G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608782 | ||||||
chr17:2608826
|
A | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+14820A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2608826 | ||||||
chr17:2609191
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-191+15185C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609191 | ||||||
chr17:2609530
|
T | G | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-191+15524T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609530 | ||||||
chr17:2609581
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-191+15575C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609581 | ||||||
chr17:2609621
|
C | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-191+15615C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609621 | ||||||
chr17:2609656
|
C | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+15650C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609656 | ||||||
chr17:2609689
|
T | G | 1 | a0001c0001t0003g0278 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-191+15683T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609689 | ||||||
chr17:2609756
|
C | T | 18 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-191+15750C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2609756 | ||||||
chr17:2610394
|
A | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-191+16388A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2610394 | ||||||
chr17:2610691
|
T | C | 1 | a0001c0001t0042g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-191+16685T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2610691 | ||||||
chr17:2610857
|
C | T | 4 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0122others(1): Show | 4 | HG02015.hp1 NA18612.hp1 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191+16851C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2610857 | ||||||
chr17:2611265
|
C | T | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-191+17259C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611265 | ||||||
chr17:2611479
|
A | AT | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-191+17473_-191+17 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611479 | ||||||
chr17:2611479
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-191+17473A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611479 | ||||||
chr17:2611693
|
C | T | 1 | a0001c0001t0004g0248 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-191+17687C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611693 | ||||||
chr17:2611694
|
G | A | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-191+17688G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611694 | ||||||
chr17:2611707
|
C | G | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-191+17701C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2611707 | ||||||
chr17:2612210
|
C | CT | 13 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0105others(10): Show | 13 | HG01261.hp1 HG01433.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.-191+18220dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2612210 | |||||
chr17:2612303
|
G | A | 269 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(266): Show | 269 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.-191+18297G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612303 | ||||||
chr17:2612344
|
C | G | 1 | a0001c0001t0002g0169 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-191+18338C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612344 | ||||||
chr17:2612351
|
G | A | 3 | a0001c0001t0001g0128a0001c0001t0002g0133a0001c0001t0002g0136 | 3 | HG02735.hp1 HG04199.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-191+18345G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612351 | ||||||
chr17:2612522
|
A | G | 8 | a0001c0001t0003g0102a0001c0001t0005g0098a0001c0001t0005g0099others(5): Show | 8 | HG00558.hp2 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.-191+18516A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612522 | ||||||
chr17:2612588
|
C | T | 2 | a0001c0001t0012g0279a0001c0001t0015g0280 | 2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-191+18582C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612588 | ||||||
chr17:2612732
|
C | A | 1 | a0001c0001t0003g0224 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-191+18726C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612732 | ||||||
chr17:2612775
|
T | C | 2 | a0001c0001t0010g0181a0001c0001t0021g0180 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-191+18769T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612775 | ||||||
chr17:2612908
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-191+18902C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612908 | ||||||
chr17:2612975
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-191+18969C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2612975 | ||||||
chr17:2613004
|
A | G | 1 | a0001c0001t0003g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-191+18998A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613004 | ||||||
chr17:2613042
|
T | TA | 6 | a0001c0001t0001g0042a0001c0001t0001g0145a0001c0001t0001g0154others(3): Show | 6 | HG01433.hp2 HG02572.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.-191+19054dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | |||||
chr17:2613042
|
TA | T | 33 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(30): Show | 33 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.-191+19054delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | |||||
chr17:2613042
|
TAA | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-191+19053_-191+19 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | |||||
chr17:2613042
|
TAAA | T | 72 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(69): Show | 72 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.-191+19052_-191+19 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613042 | |||||
chr17:2613115
|
TTTTC | T | 72 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(69): Show | 72 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.-191+19117_-191+19 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2613115 | |||||
chr17:2613435
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-191+19429T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613435 | ||||||
chr17:2613474
|
C | A | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-191+19468C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613474 | ||||||
chr17:2613518
|
G | T | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-191+19512G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613518 | ||||||
chr17:2613640
|
T | C | 97 | a0001c0001t0001g0184a0001c0001t0001g0220a0001c0001t0002g0234others(94): Show | 97 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.-191+19634T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613640 | ||||||
chr17:2613667
|
C | T | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-191+19661C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613667 | ||||||
chr17:2613697
|
A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+19691A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613697 | ||||||
chr17:2613737
|
C | T | 3 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208 | 3 | HG00099.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-191+19731C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613737 | ||||||
chr17:2613828
|
G | T | 78 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(75): Show | 78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+19822G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613828 | ||||||
chr17:2613839
|
C | T | 2 | a0001c0001t0008g0143a0001c0001t0008g0144 | 2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-191+19833C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613839 | ||||||
chr17:2613855
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-191+19849G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613855 | ||||||
chr17:2613928
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-191+19922G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2613928 | ||||||
chr17:2614021
|
G | GT | 94 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(91): Show | 94 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.-191+20036dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | |||||
chr17:2614021
|
G | GTT | 27 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0037others(24): Show | 27 | HG00733.hp2 HG00741.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.-191+20035_-191+20 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | |||||
chr17:2614021
|
G | GTTT | 21 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0003g0011others(18): Show | 21 | HG01167.hp1 HG01243.hp1 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.-191+20034_-191+20 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | |||||
chr17:2614021
|
G | GTTTT | 15 | a0001c0001t0001g0008a0001c0001t0003g0224a0001c0001t0008g0141others(12): Show | 15 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-191+20033_-191+20 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | |||||
chr17:2614021
|
G | GTTTTT | 52 | a0001c0001t0001g0184a0001c0001t0001g0220a0001c0001t0002g0234others(49): Show | 52 | HG00733.hp1 HG00738.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.-191+20032_-191+20 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | |||||
chr17:2614021
|
G | GTTTTTT | 20 | a0001c0001t0003g0216a0001c0001t0003g0223a0001c0001t0003g0254others(17): Show | 20 | HG00438.hp2 HG01496.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.-191+20031_-191+20 others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2614021 | |||||
chr17:2614207
|
G | A | 3 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008 | 3 | HG02258.hp2 HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-191+20201G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614207 | ||||||
chr17:2614263
|
A | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-191+20257A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614263 | ||||||
chr17:2614414
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-191+20408A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614414 | ||||||
chr17:2614483
|
A | T | 1 | a0001c0001t0004g0246 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-191+20477A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614483 | ||||||
chr17:2614786
|
C | G | 24 | a0001c0001t0001g0024a0001c0001t0001g0042a0001c0001t0001g0045others(21): Show | 24 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.-191+20780C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614786 | ||||||
chr17:2614804
|
T | C | 13 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(10): Show | 13 | HG00735.hp2 HG01099.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.-191+20798T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614804 | ||||||
chr17:2614811
|
C | T | 1 | a0001c0001t0008g0144 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-191+20805C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2614811 | ||||||
chr17:2615011
|
T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-191+21005T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615011 | ||||||
chr17:2615038
|
C | CTCCA | 78 | a0001c0001t0001g0220a0001c0001t0002g0234a0001c0001t0003g0002others(75): Show | 78 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.-191+21033_-191+21 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2615038 | |||||
chr17:2615086
|
A | G | 1 | a0001c0001t0002g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-191+21080A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615086 | ||||||
chr17:2615271
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-191+21265C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615271 | ||||||
chr17:2615365
|
A | G | 71 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0216others(68): Show | 71 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.-191+21359A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615365 | ||||||
chr17:2615432
|
A | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 109 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.-191+21426A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615432 | ||||||
chr17:2615480
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-191+21474G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615480 | ||||||
chr17:2615555
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-191+21549C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615555 | ||||||
chr17:2615578
|
C | T | 92 | a0001c0001t0001g0184a0001c0001t0002g0234a0001c0001t0003g0002others(89): Show | 92 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.-191+21572C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615578 | ||||||
chr17:2615852
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-191+21846G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2615852 | ||||||
chr17:2616011
|
G | T | 1 | a0001c0001t0008g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-191+22005G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616011 | ||||||
chr17:2616027
|
C | G | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-191+22021C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616027 | ||||||
chr17:2616060
|
A | G | 1 | a0001c0001t0008g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-190-22039A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616060 | ||||||
chr17:2616313
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-190-21786C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616313 | ||||||
chr17:2616335
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-190-21764G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616335 | ||||||
chr17:2616337
|
G | A | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-21762G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616337 | ||||||
chr17:2616440
|
C | T | 27 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0229others(24): Show | 27 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-190-21659C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616440 | ||||||
chr17:2616504
|
A | G | 1 | a0001c0001t0009g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-190-21595A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616504 | ||||||
chr17:2616672
|
C | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-21427C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616672 | ||||||
chr17:2616834
|
C | T | 13 | a0001c0001t0023g0135a0001c0002t0006g0185a0001c0002t0006g0186others(10): Show | 13 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190-21265C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2616834 | ||||||
chr17:2617063
|
A | C | 2 | a0001c0001t0004g0228a0001c0001t0004g0252 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-190-21036A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617063 | ||||||
chr17:2617321
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-20778C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617321 | ||||||
chr17:2617342
|
C | A | 4 | a0001c0001t0003g0217a0001c0001t0013g0218a0001c0001t0013g0253others(1): Show | 4 | HG03453.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-20757C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617342 | ||||||
chr17:2617412
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-20687T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617412 | ||||||
chr17:2617645
|
TGGTGGCT others(324): Show |
T | 1 | a0001c0003t0010g0175 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-190-20416_-190-20 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2617645 | |||||
chr17:2617977
|
G | A | 4 | a0001c0001t0003g0217a0001c0001t0013g0218a0001c0001t0013g0253others(1): Show | 4 | HG03453.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-20122G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2617977 | ||||||
chr17:2618063
|
A | T | 1 | a0001c0005t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-190-20036A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618063 | ||||||
chr17:2618228
|
G | A | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-19871G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618228 | ||||||
chr17:2618489
|
A | G | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0016 | 3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-190-19610A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618489 | ||||||
chr17:2618631
|
T | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-19468T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618631 | ||||||
chr17:2618837
|
G | A | 113 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(110): Show | 113 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(110): Show |
intron_variant | MODIFIER | c.-190-19262G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618837 | ||||||
chr17:2618954
|
C | CA | 45 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0040others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-190-19122dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | |||||
chr17:2618954
|
C | CAA | 13 | a0001c0001t0001g0165a0001c0001t0002g0038a0001c0001t0002g0057others(10): Show | 13 | HG00558.hp1 HG00597.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-190-19123_-190-19 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | |||||
chr17:2618954
|
CA | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(88): Show | 91 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.-190-19122delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | |||||
chr17:2618954
|
CAA | C | 7 | a0001c0001t0003g0217a0001c0001t0004g0198a0001c0001t0004g0202others(4): Show | 7 | HG01070.hp1 HG02922.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-19123_-190-19 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | |||||
chr17:2618954
|
CAAA | C | 11 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-190-19124_-190-19 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2618954 | |||||
chr17:2618995
|
A | G | 1 | a0001c0001t0003g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-190-19104A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2618995 | ||||||
chr17:2619199
|
T | C | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-18900T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619199 | ||||||
chr17:2619273
|
C | T | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-190-18826C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619273 | ||||||
chr17:2619364
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-190-18735G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619364 | ||||||
chr17:2619382
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-18717C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619382 | ||||||
chr17:2619405
|
A | T | 6 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(3): Show | 6 | HG01071.hp1 HG01074.hp2 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190-18694A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619405 | ||||||
chr17:2619406
|
T | A | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-18693T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2619406 | ||||||
chr17:2619534
|
C | CTGTTTTT others(3): Show |
93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.-190-18563_-190-18 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619534 | |||||
chr17:2619534
|
C | CTGTTTTT others(4): Show |
17 | a0001c0001t0001g0184a0001c0001t0003g0225a0001c0001t0003g0227others(14): Show | 17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190-18554_-190-18 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619534 | |||||
chr17:2619534
|
CTGTTTTT others(4): Show |
C | 25 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0042others(22): Show | 25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-190-18554_-190-18 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619534 | |||||
chr17:2619536
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0015g0017a0001c0001t0032g0197 | 2 | HG01109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-190-18554_-190-18 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619536 | |||||
chr17:2619536
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-18562_-190-18 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2619536 | |||||
chr17:2620052
|
G | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-18047G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620052 | ||||||
chr17:2620584
|
C | T | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-17515C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620584 | ||||||
chr17:2620595
|
T | A | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-190-17504T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620595 | ||||||
chr17:2620626
|
G | T | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-17473G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620626 | ||||||
chr17:2620697
|
A | G | 1 | a0001c0001t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-190-17402A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620697 | ||||||
chr17:2620908
|
A | G | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-190-17191A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2620908 | ||||||
chr17:2620972
|
TC | T | 19 | a0001c0001t0001g0184a0001c0001t0003g0217a0001c0001t0013g0218others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-190-17125delC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2620972 | |||||
chr17:2621038
|
G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-17061G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621038 | ||||||
chr17:2621049
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-17050T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621049 | ||||||
chr17:2621082
|
TTC | T | 4 | a0001c0001t0003g0002a0001c0001t0003g0264a0001c0001t0003g0265others(1): Show | 4 | HG01346.hp1 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-17015_-190-17 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621082 | |||||
chr17:2621227
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 119 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-16872T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621227 | ||||||
chr17:2621572
|
T | TA | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-16525dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621572 | |||||
chr17:2621605
|
GTCTTTT | G | 7 | a0001c0001t0001g0184a0001c0001t0007g0196a0001c0001t0007g0213others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT | G | 12 | a0001c0001t0003g0219a0001c0001t0003g0223a0001c0001t0003g0261others(9): Show | 12 | HG00735.hp1 HG01978.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(13): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(1): Show |
G | 32 | a0001c0001t0003g0002a0001c0001t0003g0216a0001c0001t0003g0221others(29): Show | 32 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(2): Show |
G | 21 | a0001c0001t0002g0234a0001c0001t0003g0217a0001c0001t0004g0202others(18): Show | 21 | HG01168.hp2 HG01255.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(15): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(3): Show |
G | 2 | a0001c0001t0004g0198a0001c0001t0004g0276 | 2 | HG01257.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(4): Show |
G | 7 | a0001c0001t0018g0022a0001c0001t0023g0135a0001c0003t0010g0175others(4): Show | 7 | HG02647.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(5): Show |
G | 2 | a0001c0001t0012g0014a0001c0001t0015g0017 | 2 | HG01109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(6): Show |
G | 15 | a0001c0001t0008g0138a0001c0001t0008g0140a0001c0001t0008g0141others(12): Show | 15 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(19): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(7): Show |
G | 6 | a0001c0001t0003g0011a0001c0001t0003g0225a0001c0001t0003g0227others(3): Show | 6 | HG01515.hp2 HG02451.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(20): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(11): Show |
G | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-190-16492_-190-16 others(24): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621605
|
GTCTTTTT others(12): Show |
G | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-190-16492_-190-16 others(25): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621605 | |||||
chr17:2621607
|
C | T | 1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-190-16492C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621607 | ||||||
chr17:2621607
|
CT | C | 23 | a0001c0001t0001g0021a0001c0001t0001g0061a0001c0001t0001g0066others(20): Show | 23 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-16456delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTT | C | 25 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(22): Show | 25 | HG00609.hp1 HG00609.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-190-16457_-190-16 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTTT | C | 21 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(18): Show | 21 | HG00597.hp2 HG01099.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.-190-16458_-190-16 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0005g0004a0001c0001t0005g0089a0001c0001t0005g0090 | 3 | HG02074.hp1 HG02165.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-190-16467_-190-16 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0002g0081a0001c0001t0005g0082 | 2 | HG01123.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.-190-16469_-190-16 others(20): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTTTTTTT others(8): Show |
C | 40 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0078others(37): Show | 40 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.-190-16470_-190-16 others(21): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTTTTTTT others(9): Show |
C | 4 | a0001c0001t0001g0019a0001c0001t0001g0174a0001c0001t0002g0170others(1): Show | 4 | HG02896.hp2 NA18947.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-16471_-190-16 others(22): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-190-16473_-190-16 others(24): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621607
|
CTTTTTTT others(12): Show |
C | 26 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0042others(23): Show | 26 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-16474_-190-16 others(25): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621607 | |||||
chr17:2621619
|
T | G | 1 | a0001c0001t0002g0234 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-190-16480T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621619 | ||||||
chr17:2621627
|
T | G | 1 | a0001c0001t0002g0122 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-190-16472T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621627 | ||||||
chr17:2621633
|
T | C | 1 | a0001c0001t0003g0278 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-190-16466T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621633 | ||||||
chr17:2621665
|
G | A | 5 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0002g0122others(2): Show | 5 | HG02015.hp1 NA18612.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-16434G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621665 | ||||||
chr17:2621719
|
A | G | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 122 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.-190-16380A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621719 | ||||||
chr17:2621721
|
G | GC | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.-190-16378_-190-16 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621721 | ||||||
chr17:2621745
|
C | G | 4 | a0001c0001t0003g0217a0001c0001t0013g0218a0001c0001t0013g0253others(1): Show | 4 | HG03453.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-16354C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621745 | ||||||
chr17:2621787
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.-190-16312G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621787 | ||||||
chr17:2621881
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 60 | HG00438.hp2 HG00733.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.-190-16218T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2621881 | ||||||
chr17:2621949
|
TATTAC | T | 8 | a0001c0001t0023g0135a0001c0002t0006g0185a0001c0002t0006g0186others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-190-16146_-190-16 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2621949 | |||||
chr17:2622163
|
A | G | 5 | a0001c0001t0002g0234a0001c0001t0011g0239a0001c0001t0011g0240others(2): Show | 5 | HG01993.hp2 HG02004.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-15936A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622163 | ||||||
chr17:2622234
|
G | A | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-15865G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622234 | ||||||
chr17:2622801
|
G | C | 3 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208 | 3 | HG00099.hp2 HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-190-15298G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622801 | ||||||
chr17:2622927
|
C | T | 3 | a0001c0001t0002g0038a0001c0001t0002g0057a0001c0001t0002g0156 | 3 | NA18944.hp2 NA18952.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-190-15172C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622927 | ||||||
chr17:2622987
|
C | G | 1 | a0001c0001t0035g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-190-15112C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2622987 | ||||||
chr17:2623010
|
A | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(107): Show | 110 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(107): Show |
intron_variant | MODIFIER | c.-190-15089A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623010 | ||||||
chr17:2623040
|
A | G | 1 | a0001c0001t0029g0182 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-190-15059A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623040 | ||||||
chr17:2623079
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-190-15020A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623079 | ||||||
chr17:2623181
|
A | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-14918A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623181 | ||||||
chr17:2623261
|
CT | C | 154 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(151): Show | 154 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.-190-14816delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623261 | |||||
chr17:2623261
|
CTT | C | 75 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0216others(72): Show | 75 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-190-14817_-190-14 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623261 | |||||
chr17:2623266
|
T | C | 6 | a0001c0002t0006g0186a0001c0002t0006g0187a0001c0002t0006g0188others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-190-14833T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623266 | ||||||
chr17:2623267
|
T | C | 1 | a0001c0002t0006g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-190-14832T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623267 | ||||||
chr17:2623267
|
T | G | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-190-14832T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623267 | ||||||
chr17:2623283
|
T | C | 1 | a0001c0001t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-190-14816T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623283 | ||||||
chr17:2623308
|
C | T | 1 | a0001c0001t0001g0003 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-190-14791C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623308 | ||||||
chr17:2623460
|
A | G | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 119 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-14639A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623460 | ||||||
chr17:2623473
|
TGGTC | T | 6 | a0001c0001t0023g0135a0001c0003t0010g0175a0001c0003t0010g0176others(3): Show | 6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-190-14625_-190-14 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623473 | ||||||
chr17:2623630
|
G | GT | 16 | a0001c0001t0002g0080a0001c0001t0008g0138a0001c0001t0008g0140others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-190-14455dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623630 | |||||
chr17:2623752
|
A | AGGTAGCT others(14): Show |
51 | a0001c0001t0002g0234a0001c0001t0003g0217a0001c0001t0003g0225others(48): Show | 51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.-190-14346_-190-14 others(27): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623752 | |||||
chr17:2623752
|
A | AGGTAGCT others(35): Show |
1 | a0001c0001t0009g0058 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-190-14326_-190-14 others(48): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2623752 | |||||
chr17:2623770
|
C | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0161 | 2 | NA18960.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-190-14329C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623770 | ||||||
chr17:2623774
|
A | G | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0216others(69): Show | 72 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-14325A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2623774 | ||||||
chr17:2624027
|
A | T | 1 | a0001c0001t0001g0068 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-190-14072A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624027 | ||||||
chr17:2624144
|
G | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-13955G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624144 | ||||||
chr17:2624373
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0002g0153 | 2 | HG00642.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-190-13726C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624373 | ||||||
chr17:2624646
|
G | C | 118 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(115): Show | 118 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(115): Show |
intron_variant | MODIFIER | c.-190-13453G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624646 | ||||||
chr17:2624660
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-190-13439G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624660 | ||||||
chr17:2624734
|
G | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0002g0115 | 3 | HG00544.hp2 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-190-13365G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624734 | ||||||
chr17:2624901
|
A | G | 1 | a0001c0001t0002g0064 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-190-13198A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2624901 | ||||||
chr17:2625023
|
A | AT | 53 | a0001c0001t0001g0020a0001c0001t0001g0040a0001c0001t0001g0128others(50): Show | 53 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.-190-13063dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2625023 | |||||
chr17:2625062
|
G | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-13037G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625062 | ||||||
chr17:2625111
|
T | C | 1 | a0001c0001t0030g0106 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-190-12988T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625111 | ||||||
chr17:2625537
|
A | G | 6 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0027others(3): Show | 6 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-190-12562A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625537 | ||||||
chr17:2625541
|
C | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-12558C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625541 | ||||||
chr17:2625673
|
C | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-12426C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625673 | ||||||
chr17:2625706
|
G | T | 76 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0216others(73): Show | 76 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-190-12393G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625706 | ||||||
chr17:2625966
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG01109.hp1 HG01515.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190-12133A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2625966 | ||||||
chr17:2626015
|
C | A | 1 | a0001c0001t0002g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-190-12084C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626015 | ||||||
chr17:2626104
|
T | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(106): Show | 109 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.-190-11995T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626104 | ||||||
chr17:2626143
|
A | G | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-11956A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626143 | ||||||
chr17:2626259
|
A | G | 75 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0216others(72): Show | 75 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.-190-11840A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626259 | ||||||
chr17:2626294
|
G | A | 76 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0216others(73): Show | 76 | HG00438.hp2 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.-190-11805G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626294 | ||||||
chr17:2626385
|
G | C | 1 | a0001c0001t0002g0153 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-190-11714G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626385 | ||||||
chr17:2626493
|
T | C | 1 | a0001c0001t0009g0083 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-190-11606T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626493 | ||||||
chr17:2626553
|
T | TC | 25 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0025others(22): Show | 25 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-190-11528dupC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
T | TCC | 28 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0033others(25): Show | 28 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.-190-11529_-190-11 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
T | TCCC | 17 | a0001c0001t0001g0061a0001c0001t0001g0070a0001c0001t0001g0114others(14): Show | 17 | HG00558.hp2 HG00597.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-190-11530_-190-11 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
T | TCCCC | 17 | a0001c0001t0001g0021a0001c0001t0002g0111a0001c0001t0004g0250others(14): Show | 17 | HG00438.hp1 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-190-11531_-190-11 others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
T | TCCCCCCC others(4): Show |
2 | a0001c0001t0001g0041a0001c0001t0030g0106 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-190-11538_-190-11 others(17): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
T | TCCCCCCC others(5): Show |
1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-11539_-190-11 others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
TC | T | 23 | a0001c0001t0001g0040a0001c0001t0001g0076a0001c0001t0001g0112others(20): Show | 23 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-190-11528delC | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
TCC | T | 19 | a0001c0001t0001g0123a0001c0001t0001g0128a0001c0001t0002g0038others(16): Show | 19 | HG00558.hp1 HG00733.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-190-11529_-190-11 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626553
|
TCCC | T | 21 | a0001c0001t0001g0184a0001c0001t0002g0207a0001c0001t0013g0218others(18): Show | 21 | HG00099.hp2 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-190-11530_-190-11 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626553 | |||||
chr17:2626558
|
C | CCCG | 13 | a0001c0001t0003g0261a0001c0001t0003g0265a0001c0001t0003g0269others(10): Show | 13 | HG01978.hp1 HG02055.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.-190-11539_-190-11 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626558 | |||||
chr17:2626559
|
C | CCG | 17 | a0001c0001t0003g0002a0001c0001t0003g0221a0001c0001t0003g0222others(14): Show | 17 | HG01070.hp1 HG01255.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.-190-11539_-190-11 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2626559 | |||||
chr17:2626560
|
C | A | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-190-11539C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626560 | ||||||
chr17:2626560
|
C | CG | 18 | a0001c0001t0003g0254a0001c0001t0003g0255a0001c0001t0003g0259others(15): Show | 18 | HG00733.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-190-11539_-190-11 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626560 | ||||||
chr17:2626561
|
C | G | 11 | a0001c0001t0001g0123a0001c0001t0002g0234a0001c0001t0004g0198others(8): Show | 11 | HG01074.hp1 HG02155.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-190-11538C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626561 | ||||||
chr17:2626563
|
C | A | 1 | a0001c0001t0002g0155 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-190-11536C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626563 | ||||||
chr17:2626564
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-11535C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626564 | ||||||
chr17:2626566
|
C | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG01168.hp1 HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-190-11533C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626566 | ||||||
chr17:2626571
|
C | T | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-11528C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626571 | ||||||
chr17:2626572
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-190-11527G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626572 | ||||||
chr17:2626624
|
G | A | 1 | a0001c0001t0015g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-190-11475G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626624 | ||||||
chr17:2626640
|
T | C | 124 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(121): Show | 124 | HG00438.hp2 HG00642.hp2 HG00733.hp1 others(121): Show |
intron_variant | MODIFIER | c.-190-11459T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626640 | ||||||
chr17:2626643
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-11456C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626643 | ||||||
chr17:2626756
|
T | C | 1 | a0001c0001t0011g0233 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-190-11343T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626756 | ||||||
chr17:2626781
|
C | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-11318C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626781 | ||||||
chr17:2626799
|
C | T | 1 | a0001c0002t0006g0189 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-190-11300C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2626799 | ||||||
chr17:2627061
|
T | A | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-190-11038T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627061 | ||||||
chr17:2627314
|
G | T | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-10785G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627314 | ||||||
chr17:2627516
|
G | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-10583G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627516 | ||||||
chr17:2627555
|
C | G | 1 | a0001c0001t0005g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-190-10544C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627555 | ||||||
chr17:2627584
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-190-10515G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627584 | ||||||
chr17:2627834
|
G | C | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-10265G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627834 | ||||||
chr17:2627977
|
G | C | 1 | a0001c0001t0001g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-190-10122G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2627977 | ||||||
chr17:2628081
|
T | A | 26 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0042others(23): Show | 26 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-10018T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628081 | ||||||
chr17:2628123
|
G | A | 1 | a0001c0001t0011g0270 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-190-9976G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628123 | ||||||
chr17:2628157
|
G | A | 1 | a0001c0001t0035g0204 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-190-9942G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628157 | ||||||
chr17:2628195
|
T | C | 2 | a0001c0001t0002g0073a0001c0001t0002g0157 | 2 | NA18979.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-190-9904T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628195 | ||||||
chr17:2628219
|
A | G | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-190-9880A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628219 | ||||||
chr17:2628296
|
T | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-190-9803T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628296 | ||||||
chr17:2628505
|
T | C | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-9594T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628505 | ||||||
chr17:2628657
|
G | T | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-190-9442G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628657 | ||||||
chr17:2628758
|
G | A | 73 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(70): Show | 73 | HG00558.hp2 HG00735.hp1 HG01109.hp1 others(70): Show |
intron_variant | MODIFIER | c.-190-9341G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628758 | ||||||
chr17:2628852
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 119 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-9247T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628852 | ||||||
chr17:2628978
|
T | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 26 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-9121T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2628978 | ||||||
chr17:2629049
|
ATTTATCT | A | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-9046_-190-904 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2629049 | |||||
chr17:2629473
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-190-8626C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629473 | ||||||
chr17:2629571
|
G | A | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-8528G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629571 | ||||||
chr17:2629583
|
A | G | 27 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0229others(24): Show | 27 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.-190-8516A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629583 | ||||||
chr17:2629624
|
C | T | 1 | a0001c0002t0006g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-190-8475C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2629624 | ||||||
chr17:2630206
|
A | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-7893A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630206 | ||||||
chr17:2630276
|
G | A | 76 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(73): Show | 76 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.-190-7823G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630276 | ||||||
chr17:2630281
|
GCAGTTCT others(649): Show |
G | 1 | a0001c0001t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-190-7813_-190-715 others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2630281 | |||||
chr17:2630329
|
G | C | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-7770G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630329 | ||||||
chr17:2630394
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-190-7705C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630394 | ||||||
chr17:2630426
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-7673G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630426 | ||||||
chr17:2630553
|
G | A | 1 | a0001c0005t0001g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-190-7546G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630553 | ||||||
chr17:2630780
|
C | T | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-7319C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2630780 | ||||||
chr17:2631059
|
G | C | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-190-7040G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631059 | ||||||
chr17:2631361
|
G | A | 1 | a0001c0001t0034g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-190-6738G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631361 | ||||||
chr17:2631416
|
A | G | 11 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0126others(8): Show | 11 | HG00642.hp2 HG02015.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-190-6683A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631416 | ||||||
chr17:2631527
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-190-6572C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631527 | ||||||
chr17:2631624
|
G | T | 5 | a0001c0001t0004g0230a0001c0001t0004g0231a0001c0001t0004g0235others(2): Show | 5 | HG01255.hp2 HG01257.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-6475G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631624 | ||||||
chr17:2631643
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-190-6456A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631643 | ||||||
chr17:2631666
|
C | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-190-6433C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631666 | ||||||
chr17:2631669
|
C | T | 3 | a0001c0001t0005g0059a0001c0001t0005g0084a0001c0001t0005g0092 | 3 | HG00597.hp2 HG03927.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-190-6430C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631669 | ||||||
chr17:2631676
|
G | A | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-190-6423G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631676 | ||||||
chr17:2631683
|
A | G | 1 | a0001c0003t0010g0178 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-190-6416A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631683 | ||||||
chr17:2631983
|
A | G | 2 | a0001c0001t0007g0213a0001c0001t0007g0274 | 2 | HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-190-6116A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2631983 | ||||||
chr17:2632026
|
T | C | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(119): Show | 122 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(119): Show |
intron_variant | MODIFIER | c.-190-6073T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632026 | ||||||
chr17:2632160
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-190-5939C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632160 | ||||||
chr17:2632353
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-190-5746G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632353 | ||||||
chr17:2632432
|
C | G | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-5667C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632432 | ||||||
chr17:2632573
|
G | T | 77 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(74): Show | 77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-190-5526G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632573 | ||||||
chr17:2632584
|
C | T | 7 | a0001c0001t0008g0137a0001c0001t0008g0140a0001c0001t0008g0141others(4): Show | 7 | HG01167.hp1 HG02257.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-5515C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2632584 | ||||||
chr17:2633148
|
TTTTTTCT others(5): Show |
T | 1 | a0001c0001t0037g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-190-4941_-190-493 others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633148 | |||||
chr17:2633175
|
CT | C | 9 | a0001c0001t0008g0137a0001c0001t0008g0138a0001c0001t0008g0140others(6): Show | 9 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-190-4912delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633175 | |||||
chr17:2633225
|
T | A | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-4874T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633225 | ||||||
chr17:2633337
|
T | G | 2 | a0001c0001t0017g0010a0001c0004t0036g0205 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-190-4762T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633337 | ||||||
chr17:2633475
|
C | CT | 28 | a0001c0001t0002g0063a0001c0001t0002g0079a0001c0001t0002g0081others(25): Show | 28 | HG00558.hp2 HG00741.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.-190-4611dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633475 | |||||
chr17:2633658
|
C | A | 1 | a0001c0001t0012g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-190-4441C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633658 | ||||||
chr17:2633788
|
T | C | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(116): Show | 119 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(116): Show |
intron_variant | MODIFIER | c.-190-4311T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633788 | ||||||
chr17:2633889
|
G | A | 1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-190-4210G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633889 | ||||||
chr17:2633920
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-4179C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633920 | ||||||
chr17:2633961
|
C | CT | 22 | a0001c0001t0001g0095a0001c0001t0002g0038a0001c0001t0002g0081others(19): Show | 22 | HG00597.hp2 HG01123.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-190-4116dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | |||||
chr17:2633961
|
C | CTT | 10 | a0001c0001t0001g0078a0001c0001t0001g0105a0001c0001t0001g0160others(7): Show | 10 | HG00323.hp1 HG00323.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-190-4117_-190-411 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | |||||
chr17:2633961
|
CT | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(35): Show | 38 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.-190-4116delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | |||||
chr17:2633961
|
CTT | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0184a0001c0001t0012g0279others(9): Show | 12 | HG01891.hp1 HG02647.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.-190-4117_-190-411 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | |||||
chr17:2633961
|
CTTTT | C | 71 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(68): Show | 71 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-190-4119_-190-411 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | |||||
chr17:2633961
|
CTTTTT | C | 7 | a0001c0001t0003g0277a0001c0001t0004g0228a0001c0001t0004g0229others(4): Show | 7 | HG01257.hp2 HG01261.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-4120_-190-411 others(9): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2633961 | |||||
chr17:2633997
|
G | A | 77 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(74): Show | 77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-190-4102G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2633997 | ||||||
chr17:2634159
|
G | A | 7 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0072others(4): Show | 7 | NA18943.hp2 NA18951.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-3940G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634159 | ||||||
chr17:2634207
|
C | A | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-190-3892C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634207 | ||||||
chr17:2634257
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 26 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.-190-3842C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634257 | ||||||
chr17:2634323
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-190-3776G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634323 | ||||||
chr17:2634425
|
C | T | 1 | a0001c0001t0012g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-190-3674C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634425 | ||||||
chr17:2634608
|
C | A | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-190-3491C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634608 | ||||||
chr17:2634673
|
T | C | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-3426T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634673 | ||||||
chr17:2634754
|
T | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-3345T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634754 | ||||||
chr17:2634854
|
T | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-3245T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634854 | ||||||
chr17:2634902
|
G | C | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-3197G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634902 | ||||||
chr17:2634979
|
A | G | 1 | a0001c0001t0002g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-190-3120A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634979 | ||||||
chr17:2634991
|
C | G | 1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-190-3108C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2634991 | ||||||
chr17:2635121
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-190-2978C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635121 | ||||||
chr17:2635124
|
G | C | 77 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(74): Show | 77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.-190-2975G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635124 | ||||||
chr17:2635126
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-190-2973G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635126 | ||||||
chr17:2635184
|
A | C | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-2915A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635184 | ||||||
chr17:2635219
|
G | C | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-2880G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635219 | ||||||
chr17:2635515
|
G | A | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0016 | 3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-190-2584G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635515 | ||||||
chr17:2635646
|
A | C | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-2453A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635646 | ||||||
chr17:2635667
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-190-2432T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635667 | ||||||
chr17:2635760
|
G | T | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-190-2339G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635760 | ||||||
chr17:2635820
|
G | A | 1 | a0001c0001t0027g0159 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-190-2279G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635820 | ||||||
chr17:2635934
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-190-2165C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635934 | ||||||
chr17:2635953
|
C | CA | 14 | a0001c0001t0001g0053a0001c0001t0003g0217a0001c0001t0003g0265others(11): Show | 14 | HG01261.hp1 HG01884.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.-190-2126dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | |||||
chr17:2635953
|
CA | C | 24 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(21): Show | 24 | HG00099.hp1 HG01099.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-190-2126delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | |||||
chr17:2635953
|
CAA | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(12): Show | 15 | HG00099.hp2 HG01123.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.-190-2127_-190-212 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | |||||
chr17:2635953
|
CAAA | C | 36 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0128others(33): Show | 36 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.-190-2128_-190-212 others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2635953 | |||||
chr17:2635984
|
T | A | 1 | a0001c0001t0005g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-190-2115T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2635984 | ||||||
chr17:2636124
|
T | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-190-1975T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636124 | ||||||
chr17:2636235
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-190-1864A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636235 | ||||||
chr17:2636327
|
G | A | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-190-1772G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636327 | ||||||
chr17:2636405
|
T | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-1694T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636405 | ||||||
chr17:2636664
|
G | A | 1 | a0001c0001t0042g0015 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-190-1435G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636664 | ||||||
chr17:2636690
|
C | T | 3 | a0001c0001t0010g0181a0001c0001t0021g0180a0001c0001t0022g0183 | 3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-190-1409C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636690 | ||||||
chr17:2636691
|
G | A | 1 | a0001c0001t0004g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-190-1408G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636691 | ||||||
chr17:2636817
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-190-1282G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636817 | ||||||
chr17:2636921
|
G | A | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.-190-1178G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2636921 | ||||||
chr17:2637240
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-190-859A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637240 | ||||||
chr17:2637263
|
G | A | 3 | a0001c0001t0012g0279a0001c0001t0015g0280a0001c0001t0042g0015 | 3 | HG03225.hp2 HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-190-836G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637263 | ||||||
chr17:2637416
|
CA | C | 227 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 227 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.-190-673delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2637416 | |||||
chr17:2637474
|
C | T | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-190-625C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637474 | ||||||
chr17:2637666
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-190-433T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637666 | ||||||
chr17:2637848
|
A | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-190-251A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637848 | ||||||
chr17:2637916
|
T | C | 1 | a0001c0001t0031g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-190-183T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | chr17 | 2637916 | ||||||
chr17:2637973
|
AATC | A | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-190-119_-190-117d others(5): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 2637973 | |||||
chr17:2638386
|
A | T | 1 | a0001c0001t0002g0080 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32+66A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638386 | ||||||
chr17:2638667
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+347C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638667 | ||||||
chr17:2638798
|
T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+478T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638798 | ||||||
chr17:2638844
|
A | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+524A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638844 | ||||||
chr17:2638897
|
C | CTTATTT | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+592_32+597dupAT others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2638897 | |||||
chr17:2638928
|
C | T | 2 | a0001c0001t0008g0137a0001c0001t0008g0142 | 2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.32+608C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638928 | ||||||
chr17:2638930
|
C | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+610C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638930 | ||||||
chr17:2638960
|
C | T | 18 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.32+640C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2638960 | ||||||
chr17:2639018
|
A | G | 1 | a0001c0001t0007g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.32+698A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639018 | ||||||
chr17:2639603
|
C | CT | 18 | a0001c0001t0003g0011a0001c0001t0003g0102a0001c0001t0008g0137others(15): Show | 18 | HG00558.hp2 HG01109.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.32+1294dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2639603 | |||||
chr17:2639656
|
G | T | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+1336G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639656 | ||||||
chr17:2639676
|
A | G | 1 | a0001c0001t0011g0242 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.32+1356A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639676 | ||||||
chr17:2639844
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.32+1524C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639844 | ||||||
chr17:2639887
|
C | A | 3 | a0001c0001t0002g0063a0001c0001t0002g0079a0001c0001t0002g0120 | 3 | HG00741.hp2 HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.32+1567C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2639887 | ||||||
chr17:2640139
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.32+1819T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640139 | ||||||
chr17:2640167
|
C | A | 93 | a0001c0001t0001g0184a0001c0001t0002g0234a0001c0001t0003g0002others(90): Show | 93 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.32+1847C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640167 | ||||||
chr17:2640375
|
C | CT | 19 | a0001c0001t0001g0006a0001c0001t0001g0184a0001c0001t0002g0206others(16): Show | 19 | HG00733.hp2 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.32+2071dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640375 | |||||
chr17:2640375
|
C | CTT | 6 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+2070_32+2071dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640375 | |||||
chr17:2640375
|
CT | C | 78 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0068others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+2071delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640375 | |||||
chr17:2640412
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+2092A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640412 | ||||||
chr17:2640451
|
C | CT | 19 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0002g0111others(16): Show | 19 | HG00438.hp1 HG00544.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.32+2149dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640451 | |||||
chr17:2640451
|
C | CTT | 10 | a0001c0001t0001g0184a0001c0001t0021g0180a0001c0001t0022g0183others(7): Show | 10 | HG01891.hp1 HG02258.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.32+2148_32+2149dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2640451 | |||||
chr17:2640602
|
C | G | 5 | a0001c0001t0002g0234a0001c0001t0011g0239a0001c0001t0011g0240others(2): Show | 5 | HG01993.hp2 HG02004.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+2282C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640602 | ||||||
chr17:2640602
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+2282C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640602 | ||||||
chr17:2640926
|
G | T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+2606G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2640926 | ||||||
chr17:2641083
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+2763T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641083 | ||||||
chr17:2641091
|
C | T | 2 | a0001c0001t0002g0073a0001c0001t0002g0157 | 2 | NA18979.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.32+2771C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641091 | ||||||
chr17:2641186
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.32+2866A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641186 | ||||||
chr17:2641261
|
C | T | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+2941C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641261 | ||||||
chr17:2641430
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.32+3110A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641430 | ||||||
chr17:2641443
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.32+3123G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641443 | ||||||
chr17:2641452
|
C | T | 1 | a0001c0001t0004g0236 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.32+3132C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641452 | ||||||
chr17:2641669
|
T | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+3349T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641669 | ||||||
chr17:2641755
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+3435C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641755 | ||||||
chr17:2641868
|
C | G | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+3548C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2641868 | ||||||
chr17:2642079
|
T | C | 4 | a0001c0001t0002g0073a0001c0001t0002g0104a0001c0001t0002g0157others(1): Show | 4 | HG04184.hp1 NA18979.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+3759T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642079 | ||||||
chr17:2642179
|
A | G | 35 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(32): Show | 35 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.32+3859A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642179 | ||||||
chr17:2642377
|
T | G | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+4057T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642377 | ||||||
chr17:2642417
|
T | A | 1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.32+4097T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642417 | ||||||
chr17:2642510
|
A | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.32+4190A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642510 | ||||||
chr17:2642696
|
G | A | 1 | a0001c0001t0026g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.32+4376G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642696 | ||||||
chr17:2642907
|
A | G | 4 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(1): Show | 4 | HG01243.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+4587A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642907 | ||||||
chr17:2642968
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0071 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.32+4648C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2642968 | ||||||
chr17:2643031
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.32+4711A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643031 | ||||||
chr17:2643039
|
A | G | 3 | a0001c0001t0004g0202a0001c0001t0004g0203a0001c0001t0032g0197 | 3 | HG01070.hp1 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.32+4719A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643039 | ||||||
chr17:2643046
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(42): Show | 45 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.32+4726C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643046 | ||||||
chr17:2643047
|
CTCTT | C | 4 | a0001c0001t0004g0244a0001c0001t0004g0247a0001c0001t0004g0250others(1): Show | 4 | HG01168.hp2 HG02486.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+4732_32+4735del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2643047 | |||||
chr17:2643112
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.32+4792G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643112 | ||||||
chr17:2643155
|
T | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+4835T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643155 | ||||||
chr17:2643171
|
C | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.32+4851C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643171 | ||||||
chr17:2643307
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.32+4987C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643307 | ||||||
chr17:2643319
|
A | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+4999A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643319 | ||||||
chr17:2643489
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.32+5169C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643489 | ||||||
chr17:2643554
|
CT | C | 93 | a0001c0001t0001g0078a0001c0001t0001g0095a0001c0001t0001g0174others(90): Show | 93 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.32+5246delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2643554 | |||||
chr17:2643613
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.32+5293G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643613 | ||||||
chr17:2643797
|
C | G | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+5477C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643797 | ||||||
chr17:2643862
|
C | A | 1 | a0001c0001t0005g0098 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.32+5542C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2643862 | ||||||
chr17:2644118
|
C | T | 77 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(74): Show | 77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.32+5798C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644118 | ||||||
chr17:2644171
|
T | C | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+5851T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644171 | ||||||
chr17:2644377
|
A | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0147others(2): Show | 5 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.32+6057A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644377 | ||||||
chr17:2644474
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+6154C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644474 | ||||||
chr17:2644529
|
G | A | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.32+6209G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644529 | ||||||
chr17:2644902
|
A | G | 1 | a0001c0001t0003g0255 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.32+6582A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2644902 | ||||||
chr17:2645075
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.32+6755C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645075 | ||||||
chr17:2645146
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.32+6826C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645146 | ||||||
chr17:2645319
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+6999C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645319 | ||||||
chr17:2645550
|
A | G | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+7230A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645550 | ||||||
chr17:2645607
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.32+7287T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645607 | ||||||
chr17:2645609
|
A | T | 1 | a0001c0001t0005g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.32+7289A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645609 | ||||||
chr17:2645623
|
A | T | 21 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(18): Show | 21 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.32+7303A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645623 | ||||||
chr17:2645992
|
T | A | 1 | a0001c0001t0003g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.32+7672T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2645992 | ||||||
chr17:2646198
|
T | C | 2 | a0001c0001t0012g0013a0001c0001t0012g0016 | 2 | HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.32+7878T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2646198 | ||||||
chr17:2646436
|
TGAGGTCA others(3): Show |
T | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.32+8118_32+8127del others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2646436 | |||||
chr17:2646652
|
TAATAA | T | 4 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0224others(1): Show | 4 | NA18946.hp1 NA18979.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.32+8339_32+8343del others(5): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2646652 | |||||
chr17:2646933
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.32+8613G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2646933 | ||||||
chr17:2646951
|
G | T | 1 | a0001c0001t0013g0253 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.32+8631G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2646951 | ||||||
chr17:2646982
|
A | G | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+8662A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2646982 | ||||||
chr17:2647121
|
A | G | 27 | a0001c0001t0001g0128a0001c0001t0001g0154a0001c0001t0002g0038others(24): Show | 27 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.32+8801A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647121 | ||||||
chr17:2647213
|
C | T | 1 | a0001c0001t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.32+8893C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647213 | ||||||
chr17:2647282
|
C | T | 1 | a0001c0001t0004g0245 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.32+8962C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647282 | ||||||
chr17:2647302
|
G | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+8982G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647302 | ||||||
chr17:2647305
|
G | T | 1 | a0001c0001t0001g0134 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.32+8985G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647305 | ||||||
chr17:2647659
|
A | G | 1 | a0001c0001t0041g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.32+9339A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647659 | ||||||
chr17:2647964
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+9644G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2647964 | ||||||
chr17:2648146
|
A | G | 2 | a0001c0001t0003g0256a0001c0001t0003g0263 | 2 | NA18968.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.32+9826A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648146 | ||||||
chr17:2648147
|
T | A | 1 | a0001c0001t0001g0126 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.32+9827T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648147 | ||||||
chr17:2648246
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.32+9926G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648246 | ||||||
chr17:2648419
|
G | A | 1 | a0001c0001t0031g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.32+10099G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648419 | ||||||
chr17:2648468
|
A | G | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+10148A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648468 | ||||||
chr17:2648532
|
G | T | 1 | a0001c0001t0038g0238 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.32+10212G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648532 | ||||||
chr17:2648533
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0002g0118 | 2 | HG00544.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.32+10213C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648533 | ||||||
chr17:2648653
|
G | T | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+10333G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648653 | ||||||
chr17:2648677
|
C | CA | 51 | a0001c0001t0001g0068a0001c0001t0002g0234a0001c0001t0003g0217others(48): Show | 51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.32+10373dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648677 | |||||
chr17:2648677
|
CA | C | 7 | a0001c0001t0001g0114a0001c0001t0003g0221a0001c0001t0003g0222others(4): Show | 7 | HG02074.hp2 HG02965.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.32+10373delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648677 | |||||
chr17:2648759
|
G | GT | 87 | a0001c0001t0001g0145a0001c0001t0002g0036a0001c0001t0002g0054others(84): Show | 87 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.32+10441dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648759 | |||||
chr17:2648762
|
A | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.32+10442A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648762 | ||||||
chr17:2648805
|
C | T | 4 | a0001c0001t0002g0038a0001c0001t0002g0057a0001c0001t0002g0064others(1): Show | 4 | HG00597.hp1 NA18944.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+10485C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648805 | ||||||
chr17:2648925
|
ATATT | A | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+10607_32+10610d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2648925 | |||||
chr17:2648960
|
G | A | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.32+10640G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2648960 | ||||||
chr17:2649088
|
G | A | 76 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(73): Show | 76 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.32+10768G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649088 | ||||||
chr17:2649140
|
CTG | C | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+10821_32+10822d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649140 | ||||||
chr17:2649182
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.32+10862A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649182 | ||||||
chr17:2649214
|
C | CA | 21 | a0001c0001t0001g0053a0001c0001t0001g0184a0001c0001t0002g0111others(18): Show | 21 | HG00438.hp1 HG01261.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.32+10912dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2649214 | |||||
chr17:2649214
|
CA | C | 7 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 7 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.32+10912delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2649214 | |||||
chr17:2649598
|
C | G | 4 | a0001c0001t0002g0063a0001c0001t0002g0079a0001c0001t0002g0120others(1): Show | 4 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.32+11278C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649598 | ||||||
chr17:2649858
|
A | G | 253 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.32+11538A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2649858 | ||||||
chr17:2650271
|
GGAGGCCG others(17): Show |
G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.32+11956_32+11979d others(26): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650271 | |||||
chr17:2650278
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.32+11958G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650278 | ||||||
chr17:2650282
|
C | T | 42 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0078others(39): Show | 42 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.32+11962C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650282 | ||||||
chr17:2650334
|
A | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.32+12014A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650334 | ||||||
chr17:2650436
|
C | T | 1 | a0001c0001t0003g0254 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.32+12116C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650436 | ||||||
chr17:2650507
|
A | G | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.32+12187A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650507 | ||||||
chr17:2650510
|
T | TA | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(90): Show | 93 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.32+12206dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650510 | |||||
chr17:2650542
|
G | A | 29 | a0001c0001t0001g0105a0001c0001t0001g0160a0001c0001t0002g0081others(26): Show | 29 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.32+12222G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650542 | ||||||
chr17:2650639
|
CA | C | 174 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 174 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.32+12340delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650639 | |||||
chr17:2650639
|
CAAAAAAA others(1): Show |
C | 77 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(74): Show | 77 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.32+12333_32+12340d others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2650639 | |||||
chr17:2650770
|
G | A | 72 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(69): Show | 72 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.32+12450G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650770 | ||||||
chr17:2650907
|
A | G | 16 | a0001c0001t0004g0192a0001c0001t0004g0229a0001c0001t0004g0230others(13): Show | 16 | HG00733.hp1 HG01168.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.32+12587A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650907 | ||||||
chr17:2650908
|
T | C | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.32+12588T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650908 | ||||||
chr17:2650994
|
G | A | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+12674G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2650994 | ||||||
chr17:2651036
|
A | G | 78 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(75): Show | 78 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(75): Show |
intron_variant | MODIFIER | c.32+12716A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651036 | ||||||
chr17:2651291
|
T | G | 1 | a0001c0001t0004g0237 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.32+12971T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651291 | ||||||
chr17:2651359
|
C | T | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.32+13039C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651359 | ||||||
chr17:2651395
|
G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.32+13075G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651395 | ||||||
chr17:2651413
|
C | CA | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(22): Show | 25 | HG00323.hp1 HG00597.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.32+13114dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2651413 | |||||
chr17:2651413
|
CA | C | 36 | a0001c0001t0002g0153a0001c0001t0003g0002a0001c0001t0003g0102others(33): Show | 36 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(33): Show |
intron_variant | MODIFIER | c.32+13114delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2651413 | |||||
chr17:2651425
|
A | G | 1 | a0001c0001t0009g0062 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.32+13105A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651425 | ||||||
chr17:2651574
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.32+13254G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651574 | ||||||
chr17:2651645
|
G | A | 1 | a0001c0001t0002g0166 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.32+13325G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651645 | ||||||
chr17:2651668
|
CTTAAA | C | 79 | a0001c0001t0002g0234a0001c0001t0003g0002a0001c0001t0003g0102others(76): Show | 79 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.32+13352_32+13356d others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2651668 | |||||
chr17:2651712
|
T | C | 2 | a0001c0001t0014g0048a0001c0001t0014g0049 | 2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.32+13392T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651712 | ||||||
chr17:2651760
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.32+13440C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651760 | ||||||
chr17:2651937
|
A | G | 27 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0229others(24): Show | 27 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.33-13435A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651937 | ||||||
chr17:2651941
|
G | A | 37 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(34): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-13431G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651941 | ||||||
chr17:2651979
|
C | T | 163 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.33-13393C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2651979 | ||||||
chr17:2652058
|
A | G | 182 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 182 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.33-13314A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652058 | ||||||
chr17:2652064
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.33-13308A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652064 | ||||||
chr17:2652107
|
A | G | 99 | a0001c0001t0001g0184a0001c0001t0002g0234a0001c0001t0003g0002others(96): Show | 99 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.33-13265A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652107 | ||||||
chr17:2652134
|
A | G | 1 | a0001c0001t0031g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-13238A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652134 | ||||||
chr17:2652150
|
G | A | 6 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(3): Show | 6 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13222G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652150 | ||||||
chr17:2652161
|
C | CA | 219 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.33-13210dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652161 | |||||
chr17:2652162
|
A | AG | 13 | a0001c0001t0001g0003a0001c0001t0001g0025a0001c0001t0001g0027others(10): Show | 13 | HG01099.hp2 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-13210_33-13209i others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652162 | ||||||
chr17:2652177
|
A | G | 51 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0052others(48): Show | 51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.33-13195A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652177 | ||||||
chr17:2652187
|
A | G | 10 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(7): Show | 10 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.33-13185A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652187 | ||||||
chr17:2652193
|
G | T | 58 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(55): Show | 58 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.33-13179G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652193 | ||||||
chr17:2652204
|
A | T | 1 | a0001c0001t0001g0034 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.33-13168A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652204 | ||||||
chr17:2652206
|
C | G | 160 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.33-13166C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652206 | ||||||
chr17:2652207
|
G | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 75 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.33-13165G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652207 | ||||||
chr17:2652213
|
A | G | 37 | a0001c0001t0001g0113a0001c0001t0001g0184a0001c0001t0002g0158others(34): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-13159A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652213 | ||||||
chr17:2652215
|
C | T | 1 | a0001c0001t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.33-13157C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652215 | ||||||
chr17:2652216
|
C | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.33-13156C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652216 | ||||||
chr17:2652217
|
T | C | 187 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(184): Show | 187 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.33-13155T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652217 | ||||||
chr17:2652224
|
C | A | 2 | a0001c0001t0010g0181a0001c0001t0021g0180 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-13148C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652224 | ||||||
chr17:2652226
|
C | T | 33 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(30): Show | 33 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.33-13146C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652226 | ||||||
chr17:2652268
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-13104G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652268 | ||||||
chr17:2652275
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-13097C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652275 | ||||||
chr17:2652276
|
G | A | 51 | a0001c0001t0001g0172a0001c0001t0001g0184a0001c0001t0002g0234others(48): Show | 51 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.33-13096G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652276 | ||||||
chr17:2652282
|
G | A | 6 | a0001c0001t0023g0135a0001c0003t0010g0175a0001c0003t0010g0176others(3): Show | 6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-13090G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652282 | ||||||
chr17:2652283
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-13089C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652283 | ||||||
chr17:2652283
|
CG | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-13086delG | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652283 | |||||
chr17:2652287
|
T | C | 234 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.33-13085T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652287 | ||||||
chr17:2652294
|
A | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-13078A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652294 | ||||||
chr17:2652298
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0025others(46): Show | 49 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.33-13074C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652298 | ||||||
chr17:2652337
|
C | A | 6 | a0001c0001t0002g0081a0001c0001t0005g0098a0001c0001t0005g0099others(3): Show | 6 | HG01123.hp2 HG01934.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-13035C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652337 | ||||||
chr17:2652356
|
A | C | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-13016A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652356 | ||||||
chr17:2652364
|
A | G | 5 | a0001c0001t0003g0225a0001c0001t0003g0227a0001c0001t0013g0218others(2): Show | 5 | HG02809.hp2 HG02976.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-13008A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652364 | ||||||
chr17:2652374
|
C | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-12998C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652374 | ||||||
chr17:2652377
|
T | C | 2 | a0001c0001t0004g0243a0001c0001t0004g0248 | 2 | HG03239.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.33-12995T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652377 | ||||||
chr17:2652382
|
T | C | 1 | a0001c0001t0001g0160 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.33-12990T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652382 | ||||||
chr17:2652395
|
G | A | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-12977G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652395 | ||||||
chr17:2652402
|
G | A | 6 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(3): Show | 6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-12970G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652402 | ||||||
chr17:2652414
|
C | CAAACA | 3 | a0001c0001t0010g0181a0001c0001t0021g0180a0001c0001t0022g0183 | 3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-12944_33-12940d others(7): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652414 | |||||
chr17:2652421
|
A | AC | 4 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0224others(1): Show | 4 | NA18946.hp1 NA18979.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-12951_33-12950i others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652421 | ||||||
chr17:2652423
|
C | A | 4 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0224others(1): Show | 4 | NA18946.hp1 NA18979.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-12949C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652423 | ||||||
chr17:2652429
|
A | C | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-12943A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652429 | ||||||
chr17:2652576
|
A | AT | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(98): Show | 101 | HG00438.hp2 HG00558.hp2 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.33-12795dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2652576 | |||||
chr17:2652832
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.33-12540A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652832 | ||||||
chr17:2652842
|
T | C | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-12530T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652842 | ||||||
chr17:2652986
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-12386C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2652986 | ||||||
chr17:2653019
|
C | T | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-12353C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653019 | ||||||
chr17:2653180
|
A | G | 1 | a0001c0001t0003g0219 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.33-12192A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653180 | ||||||
chr17:2653332
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.33-12040A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653332 | ||||||
chr17:2653418
|
T | TA | 37 | a0001c0001t0001g0069a0001c0001t0001g0071a0001c0001t0002g0234others(34): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-11942dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2653418 | |||||
chr17:2653418
|
TA | T | 35 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(32): Show | 35 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-11942delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2653418 | |||||
chr17:2653668
|
G | A | 1 | a0001c0001t0002g0077 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.33-11704G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653668 | ||||||
chr17:2653673
|
C | T | 44 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0078others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.33-11699C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653673 | ||||||
chr17:2653677
|
T | C | 37 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(34): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-11695T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653677 | ||||||
chr17:2653806
|
T | A | 18 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.33-11566T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653806 | ||||||
chr17:2653953
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.33-11419C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2653953 | ||||||
chr17:2654045
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0161 | 2 | NA18960.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.33-11327G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654045 | ||||||
chr17:2654112
|
C | T | 41 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(38): Show | 41 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.33-11260C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654112 | ||||||
chr17:2654154
|
C | A | 18 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.33-11218C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654154 | ||||||
chr17:2654190
|
CT | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.33-11165delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2654190 | |||||
chr17:2654369
|
T | C | 4 | a0001c0001t0002g0063a0001c0001t0002g0079a0001c0001t0002g0120others(1): Show | 4 | HG00741.hp2 HG01123.hp1 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.33-11003T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654369 | ||||||
chr17:2654421
|
C | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0075a0001c0001t0001g0086 | 3 | NA18943.hp2 NA19009.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.33-10951C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654421 | ||||||
chr17:2654471
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.33-10901G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654471 | ||||||
chr17:2654672
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 48 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-10700G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654672 | ||||||
chr17:2654683
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-10689C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654683 | ||||||
chr17:2654762
|
C | G | 38 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(35): Show | 38 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.33-10610C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654762 | ||||||
chr17:2654785
|
G | A | 25 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0042others(22): Show | 25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-10587G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654785 | ||||||
chr17:2654948
|
T | C | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.33-10424T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654948 | ||||||
chr17:2654954
|
C | CT | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG02055.hp2 HG02258.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.33-10404dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2654954 | |||||
chr17:2654954
|
CT | C | 7 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0002g0080others(4): Show | 7 | HG00099.hp2 HG01070.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-10404delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2654954 | |||||
chr17:2654969
|
A | T | 17 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(14): Show | 17 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.33-10403A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2654969 | ||||||
chr17:2655047
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.33-10325G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655047 | ||||||
chr17:2655048
|
C | T | 1 | a0001c0001t0004g0232 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.33-10324C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655048 | ||||||
chr17:2655099
|
T | C | 232 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 232 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.33-10273T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655099 | ||||||
chr17:2655181
|
A | ATGTG | 6 | a0001c0001t0002g0151a0001c0003t0010g0175a0001c0003t0010g0176others(3): Show | 6 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-10190_33-10189i others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655181 | |||||
chr17:2655181
|
A | ATGTGTGT others(3): Show |
6 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0188others(3): Show | 6 | HG02055.hp1 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-10190_33-10189i others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655181 | |||||
chr17:2655181
|
A | ATGTGTGT others(5): Show |
1 | a0001c0002t0006g0187 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.33-10190_33-10189i others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655181 | |||||
chr17:2655183
|
A | ATG | 9 | a0001c0001t0001g0041a0001c0001t0001g0078a0001c0001t0002g0136others(6): Show | 9 | HG00735.hp1 HG01516.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.33-10157_33-10156d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | ATGTG | 8 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(5): Show | 8 | HG00438.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-10159_33-10156d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | ATGTGTG | 5 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0003g0225others(2): Show | 5 | HG02717.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-10161_33-10156d others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | ATGTGTGT others(1): Show |
28 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(25): Show | 28 | HG00558.hp2 HG01346.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.33-10163_33-10156d others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0003g0266a0001c0001t0007g0213a0001c0001t0007g0215others(1): Show | 4 | HG02486.hp1 HG02630.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-10165_33-10156d others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | ATGTGTGT others(5): Show |
3 | a0001c0001t0003g0222a0001c0001t0003g0259a0001c0001t0022g0183 | 3 | HG02258.hp1 NA18946.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.33-10167_33-10156d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | ATGTGTGT others(7): Show |
1 | a0001c0001t0021g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.33-10169_33-10156d others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0010g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.33-10171_33-10156d others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
A | G | 17 | a0001c0001t0001g0184a0001c0001t0002g0150a0001c0001t0002g0151others(14): Show | 17 | HG00558.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.33-10189A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655183 | ||||||
chr17:2655183
|
ATG | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.33-10157_33-10156d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
ATGTGTGT others(3): Show |
A | 2 | a0001c0001t0002g0234a0001c0004t0036g0205 | 2 | HG02155.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.33-10165_33-10156d others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655183
|
ATGTGTGT others(5): Show |
A | 5 | a0001c0001t0002g0108a0001c0001t0002g0171a0001c0001t0002g0194others(2): Show | 5 | HG03453.hp1 HG03471.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-10167_33-10156d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655183 | |||||
chr17:2655236
|
G | A | 2 | a0001c0001t0004g0229a0001c0001t0004g0237 | 2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.33-10136G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655236 | ||||||
chr17:2655255
|
A | G | 1 | a0001c0001t0009g0107 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.33-10117A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655255 | ||||||
chr17:2655490
|
A | G | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-9882A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655490 | ||||||
chr17:2655569
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-9803G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655569 | ||||||
chr17:2655645
|
G | A | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-9727G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655645 | ||||||
chr17:2655679
|
A | AT | 3 | a0001c0001t0002g0055a0001c0001t0002g0122a0001c0001t0002g0155 | 3 | HG02015.hp1 NA18943.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.33-9691dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655679 | |||||
chr17:2655724
|
T | C | 1 | a0001c0001t0001g0160 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.33-9648T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655724 | ||||||
chr17:2655762
|
C | T | 25 | a0001c0001t0001g0024a0001c0001t0001g0037a0001c0001t0001g0042others(22): Show | 25 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.33-9610C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655762 | ||||||
chr17:2655784
|
G | GA | 7 | a0001c0001t0002g0038a0001c0001t0002g0057a0001c0001t0002g0064others(4): Show | 7 | HG00597.hp1 HG01934.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-9575dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2655784 | |||||
chr17:2655923
|
G | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0145 | 2 | HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.33-9449G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655923 | ||||||
chr17:2655955
|
C | T | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-9417C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655955 | ||||||
chr17:2655986
|
C | T | 14 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 14 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-9386C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655986 | ||||||
chr17:2655988
|
A | G | 1 | a0001c0001t0031g0091 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.33-9384A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2655988 | ||||||
chr17:2656025
|
T | C | 2 | a0001c0001t0002g0150a0001c0001t0002g0151 | 2 | HG00558.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.33-9347T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656025 | ||||||
chr17:2656068
|
A | G | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.33-9304A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656068 | ||||||
chr17:2656101
|
T | G | 169 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.33-9271T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656101 | ||||||
chr17:2656145
|
C | T | 5 | a0001c0001t0002g0206a0001c0001t0002g0207a0001c0001t0002g0208others(2): Show | 5 | HG00099.hp2 HG00733.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-9227C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656145 | ||||||
chr17:2656255
|
C | T | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.33-9117C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656255 | ||||||
chr17:2656333
|
C | T | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-9039C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656333 | ||||||
chr17:2656368
|
T | C | 1 | a0001c0001t0026g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-9004T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656368 | ||||||
chr17:2656416
|
C | A | 8 | a0001c0001t0002g0081a0001c0001t0005g0098a0001c0001t0005g0099others(5): Show | 8 | HG01123.hp2 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-8956C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656416 | ||||||
chr17:2656481
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.33-8891C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656481 | ||||||
chr17:2656503
|
A | C | 1 | a0001c0001t0004g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.33-8869A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656503 | ||||||
chr17:2656589
|
A | G | 166 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(163): Show | 166 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.33-8783A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656589 | ||||||
chr17:2656627
|
C | T | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.33-8745C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2656627 | ||||||
chr17:2656871
|
GTCTGTT | G | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.33-8491_33-8486del others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2656871 | |||||
chr17:2657022
|
C | T | 1 | a0001c0001t0037g0272 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.33-8350C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657022 | ||||||
chr17:2657137
|
A | T | 38 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(35): Show | 38 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.33-8235A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657137 | ||||||
chr17:2657304
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.33-8068C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657304 | ||||||
chr17:2657312
|
T | C | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.33-8060T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657312 | ||||||
chr17:2657405
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-7967C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657405 | ||||||
chr17:2657413
|
A | T | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(63): Show | 66 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(63): Show |
intron_variant | MODIFIER | c.33-7959A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657413 | ||||||
chr17:2657524
|
G | A | 1 | a0001c0001t0026g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.33-7848G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657524 | ||||||
chr17:2657601
|
C | T | 1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-7771C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657601 | ||||||
chr17:2657708
|
C | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.33-7664C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657708 | ||||||
chr17:2657875
|
T | C | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 46 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-7497T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2657875 | ||||||
chr17:2658003
|
T | C | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 48 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-7369T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658003 | ||||||
chr17:2658204
|
A | G | 1 | a0001c0001t0007g0274 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.33-7168A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658204 | ||||||
chr17:2658530
|
A | C | 69 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(66): Show | 69 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.33-6842A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658530 | ||||||
chr17:2658574
|
C | T | 35 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(32): Show | 35 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.33-6798C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658574 | ||||||
chr17:2658599
|
A | G | 1 | a0001c0001t0004g0250 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.33-6773A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658599 | ||||||
chr17:2658658
|
C | T | 7 | a0001c0001t0001g0184a0001c0001t0029g0182a0001c0003t0010g0175others(4): Show | 7 | HG01891.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-6714C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658658 | ||||||
chr17:2658801
|
T | G | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 46 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-6571T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658801 | ||||||
chr17:2658859
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(45): Show | 48 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(45): Show |
intron_variant | MODIFIER | c.33-6513G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658859 | ||||||
chr17:2658946
|
T | C | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.33-6426T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2658946 | ||||||
chr17:2659184
|
G | A | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-6188G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659184 | ||||||
chr17:2659245
|
CA | C | 41 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(38): Show | 41 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(38): Show |
intron_variant | MODIFIER | c.33-6116delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2659245 | |||||
chr17:2659276
|
C | T | 1 | a0001c0001t0004g0248 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.33-6096C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659276 | ||||||
chr17:2659295
|
T | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132 | 3 | HG02257.hp1 HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.33-6077T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659295 | ||||||
chr17:2659382
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.33-5990C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659382 | ||||||
chr17:2659430
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0002g0087 | 2 | HG00323.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.33-5942G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659430 | ||||||
chr17:2659472
|
G | T | 8 | a0001c0001t0007g0196a0001c0001t0007g0213a0001c0001t0007g0214others(5): Show | 8 | HG02055.hp2 HG02486.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.33-5900G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659472 | ||||||
chr17:2659520
|
C | CA | 34 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0069others(31): Show | 34 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.33-5831dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2659520 | |||||
chr17:2659520
|
C | CAA | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-5832_33-5831dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2659520 | |||||
chr17:2659656
|
C | A | 1 | a0001c0001t0002g0194 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.33-5716C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659656 | ||||||
chr17:2659722
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.33-5650A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659722 | ||||||
chr17:2659916
|
A | G | 168 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.33-5456A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659916 | ||||||
chr17:2659967
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(166): Show | 169 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.33-5405T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2659967 | ||||||
chr17:2660127
|
C | T | 1 | a0001c0001t0004g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.33-5245C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660127 | ||||||
chr17:2660176
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0116a0001c0001t0002g0115 | 3 | HG00544.hp2 NA18948.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.33-5196T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660176 | ||||||
chr17:2660206
|
C | CTTA | 48 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(45): Show | 48 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.33-5165_33-5163dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2660206 | |||||
chr17:2660225
|
C | CT | 5 | a0001c0001t0002g0104a0001c0001t0002g0166a0001c0001t0003g0255others(2): Show | 5 | HG00323.hp1 HG01255.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-5134dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2660225 | |||||
chr17:2660225
|
CT | C | 5 | a0001c0001t0001g0061a0001c0001t0002g0194a0001c0001t0005g0152others(2): Show | 5 | HG02622.hp2 HG02698.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-5134delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2660225 | |||||
chr17:2660238
|
T | A | 1 | a0001c0001t0005g0059 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.33-5134T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660238 | ||||||
chr17:2660349
|
G | A | 62 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(59): Show | 62 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(59): Show |
intron_variant | MODIFIER | c.33-5023G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660349 | ||||||
chr17:2660453
|
T | G | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.33-4919T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660453 | ||||||
chr17:2660915
|
C | T | 37 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(34): Show | 37 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-4457C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660915 | ||||||
chr17:2660973
|
G | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(45): Show | 48 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.33-4399G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660973 | ||||||
chr17:2660992
|
C | G | 1 | a0001c0004t0036g0205 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.33-4380C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2660992 | ||||||
chr17:2661043
|
A | G | 1 | a0001c0001t0004g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.33-4329A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661043 | ||||||
chr17:2661094
|
G | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-4278G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661094 | ||||||
chr17:2661191
|
T | C | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-4181T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661191 | ||||||
chr17:2661238
|
T | C | 1 | a0001c0001t0022g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.33-4134T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661238 | ||||||
chr17:2661614
|
T | C | 278 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(275): Show | 278 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.33-3758T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661614 | ||||||
chr17:2661715
|
T | C | 37 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(34): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-3657T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661715 | ||||||
chr17:2661983
|
G | A | 1 | a0001c0001t0007g0196 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.33-3389G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2661983 | ||||||
chr17:2662005
|
T | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.33-3367T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662005 | ||||||
chr17:2662042
|
C | CA | 50 | a0001c0001t0001g0003a0001c0001t0001g0037a0001c0001t0001g0047others(47): Show | 50 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.33-3307dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662042 | |||||
chr17:2662042
|
C | CAA | 9 | a0001c0001t0001g0021a0001c0001t0001g0076a0001c0001t0001g0112others(6): Show | 9 | HG00438.hp2 HG00738.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.33-3308_33-3307dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662042 | |||||
chr17:2662042
|
CA | C | 40 | a0001c0001t0001g0147a0001c0001t0002g0149a0001c0001t0003g0002others(37): Show | 40 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(37): Show |
intron_variant | MODIFIER | c.33-3307delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662042 | |||||
chr17:2662180
|
G | T | 3 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201 | 3 | HG01884.hp1 HG02559.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.33-3192G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662180 | ||||||
chr17:2662184
|
G | C | 66 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(63): Show | 66 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(63): Show |
intron_variant | MODIFIER | c.33-3188G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662184 | ||||||
chr17:2662246
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.33-3126G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662246 | ||||||
chr17:2662276
|
C | T | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-3096C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662276 | ||||||
chr17:2662343
|
T | C | 15 | a0001c0001t0001g0184a0001c0001t0023g0135a0001c0001t0029g0182others(12): Show | 15 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.33-3029T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662343 | ||||||
chr17:2662378
|
T | G | 3 | a0001c0001t0001g0076a0001c0001t0001g0112a0001c0001t0002g0055 | 3 | HG01169.hp1 HG01169.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.33-2994T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662378 | ||||||
chr17:2662378
|
T | TGTG | 4 | a0001c0001t0001g0042a0001c0001t0001g0061a0001c0001t0002g0158others(1): Show | 4 | HG01243.hp2 HG01433.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2994_33-2993ins others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662378 | ||||||
chr17:2662378
|
T | TTG | 50 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0025others(47): Show | 50 | HG00609.hp2 HG00733.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.33-2949_33-2948dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
T | TTGTG | 43 | a0001c0001t0001g0020a0001c0001t0001g0037a0001c0001t0001g0047others(40): Show | 43 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.33-2951_33-2948dup others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
T | TTGTGTG | 22 | a0001c0001t0001g0040a0001c0001t0001g0103a0001c0001t0001g0105others(19): Show | 22 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.33-2953_33-2948dup others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
T | TTGTGTGT others(1): Show |
13 | a0001c0001t0001g0109a0001c0001t0001g0154a0001c0001t0001g0162others(10): Show | 13 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.33-2955_33-2948dup others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0002g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.33-2957_33-2948dup others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0002g0120 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.33-2961_33-2948dup others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
TTG | T | 17 | a0001c0001t0001g0023a0001c0001t0001g0053a0001c0001t0001g0070others(14): Show | 17 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.33-2949_33-2948del others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
TTGTG | T | 37 | a0001c0001t0003g0002a0001c0001t0003g0011a0001c0001t0003g0102others(34): Show | 37 | HG00558.hp2 HG00735.hp1 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.33-2951_33-2948del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
TTGTGTGT others(3): Show |
T | 21 | a0001c0001t0001g0184a0001c0001t0004g0230a0001c0001t0004g0231others(18): Show | 21 | HG01255.hp2 HG01257.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.33-2957_33-2948del others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
TTGTGTGT others(5): Show |
T | 24 | a0001c0001t0001g0006a0001c0001t0002g0234a0001c0001t0003g0217others(21): Show | 24 | HG00438.hp2 HG00733.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.33-2959_33-2948del others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
TTGTGTGT others(7): Show |
T | 6 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-2961_33-2948del others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
TTGTGTGT others(9): Show |
T | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.33-2963_33-2948del others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662378
|
TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0165 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.33-2967_33-2948del others(20): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2662378 | |||||
chr17:2662419
|
T | C | 1 | a0001c0003t0010g0176 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.33-2953T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662419 | ||||||
chr17:2662423
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-2949T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662423 | ||||||
chr17:2662674
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.33-2698G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662674 | ||||||
chr17:2662822
|
C | T | 1 | a0001c0001t0005g0090 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.33-2550C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662822 | ||||||
chr17:2662866
|
T | G | 8 | a0001c0001t0010g0181a0001c0001t0021g0180a0001c0001t0022g0183others(5): Show | 8 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.33-2506T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662866 | ||||||
chr17:2662868
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.33-2504T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662868 | ||||||
chr17:2662957
|
T | C | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-2415T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2662957 | ||||||
chr17:2663081
|
C | A | 60 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(57): Show | 60 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.33-2291C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663081 | ||||||
chr17:2663113
|
CTAAA | C | 4 | a0001c0001t0004g0202a0001c0001t0004g0203a0001c0001t0032g0197others(1): Show | 4 | HG01070.hp1 HG02723.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2254_33-2251del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663113 | |||||
chr17:2663118
|
TAAAG | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | HG01261.hp1 HG01516.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-2244_33-2241del others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663118 | |||||
chr17:2663472
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0220 | 2 | HG00738.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.33-1900C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663472 | ||||||
chr17:2663556
|
G | GTTC | 3 | a0001c0001t0002g0063a0001c0001t0002g0079a0001c0001t0002g0120 | 3 | HG00741.hp2 HG01255.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.33-1812_33-1810dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663556 | |||||
chr17:2663573
|
TA | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.33-1797delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663573 | |||||
chr17:2663579
|
A | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.33-1793A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663579 | ||||||
chr17:2663594
|
G | A | 1 | a0001c0001t0025g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.33-1778G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663594 | ||||||
chr17:2663701
|
A | AT | 217 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.33-1657dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663701 | |||||
chr17:2663701
|
A | ATT | 14 | a0001c0001t0001g0165a0001c0001t0002g0157a0001c0001t0004g0248others(11): Show | 14 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.33-1658_33-1657dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663701 | |||||
chr17:2663701
|
A | ATTT | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-1659_33-1657dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663701 | |||||
chr17:2663720
|
CAG | C | 32 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(29): Show | 32 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.33-1649_33-1648del others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2663720 | |||||
chr17:2663808
|
C | T | 1 | a0001c0001t0005g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.33-1564C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663808 | ||||||
chr17:2663914
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.33-1458C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663914 | ||||||
chr17:2663928
|
C | T | 1 | a0001c0001t0005g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.33-1444C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663928 | ||||||
chr17:2663975
|
G | A | 1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.33-1397G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2663975 | ||||||
chr17:2664027
|
G | A | 37 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(34): Show | 37 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.33-1345G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664027 | ||||||
chr17:2664032
|
G | C | 2 | a0001c0001t0012g0012a0001c0001t0015g0017 | 2 | HG01109.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.33-1340G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664032 | ||||||
chr17:2664193
|
A | G | 1 | a0001c0001t0004g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.33-1179A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664193 | ||||||
chr17:2664407
|
C | CT | 14 | a0001c0001t0001g0132a0001c0001t0004g0192a0001c0001t0004g0248others(11): Show | 14 | HG00597.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-949dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664407 | |||||
chr17:2664407
|
C | CTT | 7 | a0001c0002t0006g0185a0001c0002t0006g0186a0001c0002t0006g0187others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.33-950_33-949dupTT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664407 | |||||
chr17:2664407
|
CT | C | 46 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(43): Show | 46 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(43): Show |
intron_variant | MODIFIER | c.33-949delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664407 | |||||
chr17:2664466
|
T | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.33-906T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664466 | ||||||
chr17:2664554
|
T | G | 2 | a0001c0001t0004g0228a0001c0001t0004g0252 | 2 | HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.33-818T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664554 | ||||||
chr17:2664633
|
G | C | 5 | a0001c0003t0010g0175a0001c0003t0010g0176a0001c0003t0010g0177others(2): Show | 5 | HG02647.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.33-739G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664633 | ||||||
chr17:2664665
|
G | GCGCGCTC others(3): Show |
3 | a0001c0001t0003g0256a0001c0001t0003g0263a0001c0001t0003g0265 | 3 | HG01978.hp1 NA18968.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.33-706_33-705insGC others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(5): Show |
6 | a0001c0001t0003g0002a0001c0001t0007g0196a0001c0001t0007g0213others(3): Show | 6 | HG01943.hp2 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-706_33-705insGC others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(7): Show |
14 | a0001c0001t0003g0102a0001c0001t0003g0216a0001c0001t0003g0255others(11): Show | 14 | HG00558.hp2 HG02486.hp1 HG03130.hp1 others(11): Show |
intron_variant | MODIFIER | c.33-706_33-705insGC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(9): Show |
5 | a0001c0001t0003g0254a0001c0001t0003g0261a0001c0001t0003g0262others(2): Show | 5 | HG01346.hp1 NA18947.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.33-706_33-705insGC others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(11): Show |
1 | a0001c0001t0003g0267 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(21): Show |
1 | a0001c0001t0003g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(26): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(29): Show |
1 | a0001c0001t0020g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(34): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(33): Show |
1 | a0001c0001t0003g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(38): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCGCTC others(35): Show |
2 | a0001c0001t0003g0222a0001c0001t0003g0224 | 2 | NA18946.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.33-706_33-705insGC others(40): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCTCTC others(5): Show |
1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.33-706_33-705insGC others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCGCTCTC others(31): Show |
1 | a0001c0001t0003g0219 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.33-706_33-705insGC others(36): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCT | 7 | a0001c0001t0001g0125a0001c0001t0001g0174a0001c0001t0002g0080others(4): Show | 7 | HG02293.hp2 HG02683.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-680_33-679dupCT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(3): Show |
2 | a0001c0001t0001g0184a0001c0001t0022g0183 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(7): Show |
2 | a0001c0001t0010g0181a0001c0001t0021g0180 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(11): Show |
1 | a0001c0001t0023g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.33-704_33-703insGC others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(3): Show |
1 | a0001c0002t0006g0186 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.33-704_33-703insGC others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(5): Show |
2 | a0001c0003t0010g0177a0001c0003t0010g0178 | 2 | HG02886.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(7): Show |
6 | a0001c0002t0006g0185a0001c0002t0006g0187a0001c0002t0006g0188others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-704_33-703insGC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(9): Show |
1 | a0001c0002t0006g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.33-704_33-703insGC others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCGCTC others(11): Show |
2 | a0001c0002t0006g0189a0001c0003t0010g0176 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.33-704_33-703insGC others(16): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCT | 3 | a0001c0001t0001g0041a0001c0001t0002g0158a0001c0001t0017g0010 | 3 | HG03225.hp1 HG03654.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.33-682_33-679dupCT others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664665
|
G | GCTCTCTC others(1): Show |
4 | a0001c0001t0001g0154a0001c0001t0002g0118a0001c0001t0003g0011others(1): Show | 4 | HG00544.hp1 HG01515.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.33-686_33-679dupCT others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664665 | |||||
chr17:2664680
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0011g0239 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.33-683_33-670delTC others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664680 | |||||
chr17:2664684
|
CTCTCTCT others(3): Show |
C | 20 | a0001c0001t0002g0234a0001c0001t0004g0198a0001c0001t0004g0199others(17): Show | 20 | HG00438.hp2 HG01070.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.33-679_33-670delTT others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664684 | |||||
chr17:2664686
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0028g0018 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.33-686C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664686 | ||||||
chr17:2664686
|
CTCTCTCT others(1): Show |
C | 17 | a0001c0001t0004g0192a0001c0001t0004g0229a0001c0001t0004g0230others(14): Show | 17 | HG00733.hp1 HG01168.hp2 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.33-678_33-671delTT others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664686 | |||||
chr17:2664688
|
CTCTCTT | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(39): Show | 42 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.33-678_33-673delTT others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664688 | |||||
chr17:2664690
|
CTCTT | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(10): Show | 13 | HG00099.hp1 HG01071.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.33-678_33-675delTT others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664690 | |||||
chr17:2664694
|
T | C | 183 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0024others(180): Show | 183 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.33-678T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664694 | ||||||
chr17:2664734
|
G | A | 6 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0016others(3): Show | 6 | HG02622.hp2 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.33-638G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664734 | ||||||
chr17:2664838
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(4): Show | 7 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.33-534T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664838 | ||||||
chr17:2664891
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.33-481A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2664891 | ||||||
chr17:2664981
|
G | GTATA | 213 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.33-390_33-387dupTA others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | 2664981 | |||||
chr17:2665012
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.33-360A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665012 | ||||||
chr17:2665107
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.33-265T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665107 | ||||||
chr17:2665190
|
CAG | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(3): Show | 6 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.33-181_33-180delAG | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665190 | ||||||
chr17:2665298
|
T | C | 1 | a0001c0001t0015g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.33-74T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 2/10 | chr17 | 2665298 | ||||||
chr17:2665683
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212 | 3 | HG01071.hp1 HG01074.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.117+227C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 3/10 | chr17 | 2665683 | ||||||
chr17:2666002
|
T | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.118-14T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 3/10 | chr17 | 2666002 | ||||||
chr17:2666133
|
T | C | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+43T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666133 | ||||||
chr17:2666139
|
C | T | 2 | a0001c0001t0017g0010a0001c0004t0036g0205 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.192+49C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666139 | ||||||
chr17:2666201
|
T | C | 1 | a0001c0001t0011g0239 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.192+111T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666201 | ||||||
chr17:2666264
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+174T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666264 | ||||||
chr17:2666764
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.193-228G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666764 | ||||||
chr17:2666902
|
C | T | 1 | a0001c0001t0022g0183 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193-90C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 4/10 | chr17 | 2666902 | ||||||
chr17:2667301
|
TCCAGCCT others(1033): Show |
T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+107_399+1146de others(1): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 2667301 | |||||
chr17:2667757
|
G | A | 273 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.399+559G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2667757 | ||||||
chr17:2667965
|
G | C | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.399+767G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2667965 | ||||||
chr17:2667985
|
G | C | 4 | a0001c0001t0002g0038a0001c0001t0002g0057a0001c0001t0002g0064others(1): Show | 4 | HG00597.hp1 NA18944.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+787G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2667985 | ||||||
chr17:2668114
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.399+916C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668114 | ||||||
chr17:2668195
|
G | A | 37 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(34): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.399+997G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668195 | ||||||
chr17:2668374
|
A | G | 38 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(35): Show | 38 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(35): Show |
intron_variant | MODIFIER | c.399+1176A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668374 | ||||||
chr17:2668597
|
T | C | 165 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.399+1399T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668597 | ||||||
chr17:2668780
|
C | T | 37 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(34): Show | 37 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.400-1383C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2668780 | ||||||
chr17:2669064
|
T | A | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.400-1099T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669064 | ||||||
chr17:2669265
|
A | AT | 38 | a0001c0001t0002g0234a0001c0001t0003g0224a0001c0001t0004g0192others(35): Show | 38 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.400-882dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 2669265 | |||||
chr17:2669265
|
A | ATT | 19 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(16): Show | 19 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.400-883_400-882dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 2669265 | |||||
chr17:2669452
|
C | T | 1 | a0001c0001t0005g0152 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.400-711C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669452 | ||||||
chr17:2669478
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.400-685A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669478 | ||||||
chr17:2669484
|
G | T | 18 | a0001c0001t0003g0011a0001c0001t0008g0137a0001c0001t0008g0138others(15): Show | 18 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.400-679G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669484 | ||||||
chr17:2669506
|
G | A | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.400-657G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669506 | ||||||
chr17:2669879
|
A | G | 218 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.400-284A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2669879 | ||||||
chr17:2670042
|
T | G | 1 | a0001c0001t0005g0059 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.400-121T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 5/10 | chr17 | 2670042 | ||||||
chr17:2670358
|
C | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.568+27C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670358 | ||||||
chr17:2670564
|
C | T | 236 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.568+233C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670564 | ||||||
chr17:2670612
|
T | G | 18 | a0001c0001t0001g0184a0001c0001t0010g0181a0001c0001t0021g0180others(15): Show | 18 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.568+281T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670612 | ||||||
chr17:2670818
|
C | G | 1 | a0001c0003t0010g0177 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.568+487C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670818 | ||||||
chr17:2670892
|
C | T | 17 | a0001c0001t0008g0137a0001c0001t0008g0138a0001c0001t0008g0140others(14): Show | 17 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.568+561C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2670892 | ||||||
chr17:2671247
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.568+916C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671247 | ||||||
chr17:2671365
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.568+1034C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671365 | ||||||
chr17:2671369
|
C | T | 1 | a0001c0001t0004g0200 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.568+1038C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671369 | ||||||
chr17:2671497
|
G | A | 1 | a0001c0001t0011g0240 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.569-1158G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671497 | ||||||
chr17:2671527
|
G | A | 117 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(114): Show | 117 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.569-1128G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671527 | ||||||
chr17:2671559
|
T | C | 1 | a0001c0001t0005g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.569-1096T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671559 | ||||||
chr17:2671568
|
C | CT | 47 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(44): Show | 47 | HG00438.hp2 HG00733.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.569-1087_569-1086i others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671568 | ||||||
chr17:2671569
|
A | AT | 5 | a0001c0001t0004g0199a0001c0001t0004g0200a0001c0001t0004g0201others(2): Show | 5 | HG01884.hp1 HG02559.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-1074dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2671569 | |||||
chr17:2671569
|
A | T | 255 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.569-1086A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671569 | ||||||
chr17:2671596
|
C | CT | 23 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0128others(20): Show | 23 | HG01070.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.569-1038dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2671596 | |||||
chr17:2671596
|
CT | C | 21 | a0001c0001t0002g0063a0001c0001t0002g0164a0001c0001t0003g0225others(18): Show | 21 | HG01109.hp1 HG01167.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.569-1038delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2671596 | |||||
chr17:2671651
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-1004G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671651 | ||||||
chr17:2671675
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.569-980T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671675 | ||||||
chr17:2671881
|
G | T | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.569-774G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671881 | ||||||
chr17:2671980
|
C | G | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-675C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2671980 | ||||||
chr17:2672049
|
G | A | 157 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.569-606G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672049 | ||||||
chr17:2672132
|
T | G | 1 | a0001c0001t0009g0058 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.569-523T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672132 | ||||||
chr17:2672197
|
G | A | 1 | a0001c0001t0004g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.569-458G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672197 | ||||||
chr17:2672285
|
C | CA | 118 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(115): Show | 118 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.569-343dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | |||||
chr17:2672285
|
C | CAA | 81 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0035others(78): Show | 81 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.569-344_569-343dup others(2): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | |||||
chr17:2672285
|
C | CAAA | 21 | a0001c0001t0001g0066a0001c0001t0001g0124a0001c0001t0001g0134others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.569-345_569-343dup others(3): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | |||||
chr17:2672285
|
CA | C | 9 | a0001c0001t0003g0011a0001c0001t0008g0143a0001c0001t0021g0180others(6): Show | 9 | HG01167.hp1 HG01515.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.569-343delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | |||||
chr17:2672285
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.569-353_569-343del others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 2672285 | |||||
chr17:2672325
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0046a0001c0001t0001g0121others(2): Show | 5 | HG00738.hp1 HG01099.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.569-330G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 6/10 | chr17 | 2672325 | ||||||
chr17:2673064
|
G | A | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671+307G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673064 | ||||||
chr17:2673068
|
C | CA | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.671+320dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 2673068 | |||||
chr17:2673141
|
C | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.671+384C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673141 | ||||||
chr17:2673405
|
A | C | 1 | a0001c0001t0003g0011 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.671+648A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673405 | ||||||
chr17:2673426
|
T | A | 1 | a0001c0001t0001g0127 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.672-634T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673426 | ||||||
chr17:2673442
|
G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.672-618G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673442 | ||||||
chr17:2673491
|
T | G | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672-569T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673491 | ||||||
chr17:2673502
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0071 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.672-558G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673502 | ||||||
chr17:2673797
|
C | T | 218 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.672-263C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673797 | ||||||
chr17:2673883
|
A | T | 14 | a0001c0001t0001g0042a0001c0001t0001g0045a0001c0001t0001g0046others(11): Show | 14 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.672-177A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673883 | ||||||
chr17:2673936
|
T | A | 1 | a0001c0001t0019g0268 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.672-124T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2673936 | ||||||
chr17:2674050
|
A | C | 11 | a0001c0001t0010g0181a0001c0001t0017g0010a0001c0001t0021g0180others(8): Show | 11 | HG02258.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.672-10A>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 7/10 | chr17 | 2674050 | ||||||
chr17:2674556
|
T | C | 2 | a0001c0001t0004g0249a0001c0001t0004g0276 | 2 | HG01257.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.900+268T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674556 | ||||||
chr17:2674686
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.900+398T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674686 | ||||||
chr17:2674723
|
T | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.900+435T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674723 | ||||||
chr17:2674741
|
C | T | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.900+453C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674741 | ||||||
chr17:2674781
|
C | G | 3 | a0001c0001t0010g0181a0001c0001t0021g0180a0001c0001t0022g0183 | 3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.900+493C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2674781 | ||||||
chr17:2675071
|
G | A | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.900+783G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675071 | ||||||
chr17:2675080
|
C | A | 38 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(35): Show | 38 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.900+792C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675080 | ||||||
chr17:2675256
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.900+968G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675256 | ||||||
chr17:2675354
|
G | T | 195 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.900+1066G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675354 | ||||||
chr17:2675393
|
C | G | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.900+1105C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675393 | ||||||
chr17:2675634
|
C | CT | 120 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0023others(117): Show | 120 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.901-856dupT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 2675634 | |||||
chr17:2675634
|
CT | C | 7 | a0001c0001t0001g0006a0001c0001t0002g0149a0001c0001t0003g0011others(4): Show | 7 | HG01515.hp2 HG02258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.901-856delT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 2675634 | |||||
chr17:2675662
|
A | G | 1 | a0001c0001t0007g0215 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.901-843A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675662 | ||||||
chr17:2675675
|
A | G | 1 | a0001c0001t0005g0168 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.901-830A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675675 | ||||||
chr17:2675775
|
A | G | 10 | a0001c0001t0001g0184a0001c0001t0024g0193a0001c0001t0029g0182others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.901-730A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675775 | ||||||
chr17:2675782
|
A | G | 1 | a0001c0001t0003g0221 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.901-723A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2675782 | ||||||
chr17:2676106
|
G | T | 1 | a0001c0001t0002g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.901-399G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676106 | ||||||
chr17:2676116
|
G | A | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.901-389G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676116 | ||||||
chr17:2676138
|
C | G | 1 | a0001c0001t0002g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.901-367C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676138 | ||||||
chr17:2676149
|
C | T | 38 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(35): Show | 38 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.901-356C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676149 | ||||||
chr17:2676159
|
T | C | 277 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(274): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.901-346T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676159 | ||||||
chr17:2676249
|
G | A | 6 | a0001c0001t0001g0195a0001c0003t0010g0175a0001c0003t0010g0176others(3): Show | 6 | HG01099.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.901-256G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676249 | ||||||
chr17:2676296
|
T | G | 10 | a0001c0001t0003g0011a0001c0001t0012g0012a0001c0001t0012g0013others(7): Show | 10 | HG01109.hp1 HG01515.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.901-209T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676296 | ||||||
chr17:2676303
|
G | A | 3 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0016 | 3 | HG02622.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.901-202G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676303 | ||||||
chr17:2676417
|
A | AAT | 3 | a0001c0001t0010g0181a0001c0001t0021g0180a0001c0001t0022g0183 | 3 | HG02258.hp1 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.901-81_901-80dupAT | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 2676417 | |||||
chr17:2676426
|
C | G | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.901-79C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 8/10 | chr17 | 2676426 | ||||||
chr17:2676706
|
G | A | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1002+100G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2676706 | ||||||
chr17:2676889
|
G | A | 1 | a0001c0001t0012g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1002+283G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2676889 | ||||||
chr17:2676971
|
G | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.1002+365G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2676971 | ||||||
chr17:2677077
|
C | T | 8 | a0001c0001t0024g0193a0001c0002t0006g0185a0001c0002t0006g0186others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1002+471C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677077 | ||||||
chr17:2677358
|
A | G | 1 | a0001c0001t0011g0241 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1002+752A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677358 | ||||||
chr17:2677415
|
G | T | 2 | a0001c0001t0013g0218a0001c0001t0013g0253 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1002+809G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677415 | ||||||
chr17:2677502
|
T | A | 1 | a0001c0001t0004g0250 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1002+896T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677502 | ||||||
chr17:2677523
|
C | T | 1 | a0001c0001t0019g0268 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1002+917C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677523 | ||||||
chr17:2677527
|
CAT | C | 35 | a0001c0001t0003g0002a0001c0001t0003g0102a0001c0001t0003g0216others(32): Show | 35 | HG00558.hp2 HG00735.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.1002+924_1002+925d others(4): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2677527 | |||||
chr17:2677778
|
C | T | 1 | a0001c0001t0012g0279 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1002+1172C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677778 | ||||||
chr17:2677785
|
C | T | 1 | a0001c0001t0018g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1002+1179C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677785 | ||||||
chr17:2677801
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1002+1195C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677801 | ||||||
chr17:2677827
|
C | T | 1 | a0001c0001t0004g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1002+1221C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677827 | ||||||
chr17:2677856
|
A | AAAAT | 164 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.1002+1270_1002+127 others(8): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2677856 | |||||
chr17:2677856
|
A | AAAATAAA others(1): Show |
3 | a0001c0001t0008g0137a0001c0001t0008g0140a0001c0001t0008g0142 | 3 | HG02451.hp1 HG06807.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1002+1266_1002+127 others(12): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2677856 | |||||
chr17:2677899
|
C | G | 1 | a0001c0001t0002g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1002+1293C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677899 | ||||||
chr17:2677966
|
A | G | 12 | a0001c0001t0001g0078a0001c0001t0001g0162a0001c0001t0002g0039others(9): Show | 12 | HG00323.hp2 HG00438.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.1002+1360A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2677966 | ||||||
chr17:2678114
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+1508G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678114 | ||||||
chr17:2678237
|
G | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1002+1631G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678237 | ||||||
chr17:2678334
|
G | A | 1 | a0001c0001t0001g0160 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1002+1728G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678334 | ||||||
chr17:2678383
|
CAA | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+1778_1002+177 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678383 | ||||||
chr17:2678400
|
C | CA | 63 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(60): Show | 63 | HG00438.hp2 HG00544.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.1003-1745dupA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | |||||
chr17:2678400
|
C | CAA | 15 | a0001c0001t0002g0115a0001c0001t0004g0192a0001c0001t0004g0201others(12): Show | 15 | HG00544.hp2 HG01952.hp1 HG01993.hp2 others(12): Show |
intron_variant | MODIFIER | c.1003-1746_1003-174 others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | |||||
chr17:2678400
|
CA | C | 10 | a0001c0001t0001g0184a0001c0001t0002g0055a0001c0001t0024g0193others(7): Show | 10 | HG01891.hp1 HG02015.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1003-1745delA | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | |||||
chr17:2678400
|
CAAAAAAA | C | 27 | a0001c0001t0001g0105a0001c0001t0001g0160a0001c0001t0005g0004others(24): Show | 27 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1003-1751_1003-174 others(11): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2678400 | |||||
chr17:2678434
|
C | T | 2 | a0001c0001t0001g0184a0001c0001t0029g0182 | 2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1003-1730C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678434 | ||||||
chr17:2678514
|
C | T | 1 | a0001c0001t0041g0139 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1003-1650C>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678514 | ||||||
chr17:2678579
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003-1585G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2678579 | ||||||
chr17:2679015
|
T | G | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1003-1149T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679015 | ||||||
chr17:2679045
|
CGTACATG others(4): Show |
C | 1 | a0001c0001t0002g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1003-1115_1003-110 others(15): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679045 | |||||
chr17:2679152
|
G | A | 5 | a0001c0001t0004g0230a0001c0001t0004g0231a0001c0001t0004g0235others(2): Show | 5 | HG01255.hp2 HG01257.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-1012G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679152 | ||||||
chr17:2679198
|
C | A | 6 | a0001c0001t0012g0013a0001c0001t0012g0014a0001c0001t0012g0016others(3): Show | 6 | HG02622.hp2 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-966C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679198 | ||||||
chr17:2679361
|
GATGATTA others(9): Show |
G | 209 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.1003-796_1003-781d others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679361 | |||||
chr17:2679458
|
TTGGATGG others(17): Show |
T | 262 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1003-639_1003-616d others(26): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679458 | |||||
chr17:2679478
|
TTGGATGG others(25): Show |
T | 1 | a0001c0001t0002g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1003-671_1003-640d others(34): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679478 | |||||
chr17:2679502
|
TTGGATGG others(25): Show |
T | 2 | a0001c0001t0017g0010a0001c0004t0036g0205 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1003-643_1003-612d others(34): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679502 | |||||
chr17:2679506
|
ATGGATGG others(13): Show |
A | 10 | a0001c0001t0003g0011a0001c0001t0003g0225a0001c0001t0003g0227others(7): Show | 10 | HG01515.hp2 HG02622.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1003-639_1003-620d others(22): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679506 | |||||
chr17:2679514
|
ATGGATGG others(5): Show |
A | 2 | a0001c0001t0001g0019a0001c0001t0028g0018 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-639_1003-628d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679514 | |||||
chr17:2679540
|
G | C | 1 | a0001c0001t0015g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1003-624G>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679540 | ||||||
chr17:2679541
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0028g0018 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-623G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679541 | ||||||
chr17:2679542
|
A | T | 2 | a0001c0001t0001g0019a0001c0001t0028g0018 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-622A>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679542 | ||||||
chr17:2679544
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0028g0018 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-620G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679544 | ||||||
chr17:2679584
|
GGATA | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0028g0018 | 3 | HG02559.hp2 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-572_1003-569d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679584 | |||||
chr17:2679610
|
A | G | 36 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(33): Show | 36 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1003-554A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679610 | ||||||
chr17:2679614
|
ATGGATGA others(1): Show |
A | 24 | a0001c0001t0001g0037a0001c0001t0001g0046a0001c0001t0001g0065others(21): Show | 24 | HG01071.hp1 HG01074.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1003-535_1003-528d others(10): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679614 | |||||
chr17:2679618
|
ATGAT | A | 36 | a0001c0001t0002g0234a0001c0001t0004g0192a0001c0001t0004g0198others(33): Show | 36 | HG00438.hp2 HG00733.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1003-543_1003-540d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679618 | |||||
chr17:2679622
|
TTGGATGA others(5): Show |
T | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0224others(3): Show | 6 | NA18946.hp1 NA18979.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-535_1003-524d others(14): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679622 | |||||
chr17:2679622
|
TTGGATGA others(9): Show |
T | 1 | a0001c0001t0008g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1003-535_1003-520d others(18): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679622 | |||||
chr17:2679626
|
ATGAT | A | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.1003-535_1003-532d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679626 | |||||
chr17:2679627
|
T | TG | 6 | a0001c0001t0002g0044a0001c0001t0002g0080a0001c0001t0012g0012others(3): Show | 6 | HG02738.hp2 HG02965.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-536dupG | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679627 | |||||
chr17:2679629
|
A | G | 53 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0067others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1003-535A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679629 | ||||||
chr17:2679630
|
T | A | 53 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0067others(50): Show | 53 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1003-534T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679630 | ||||||
chr17:2679630
|
T | TGGA | 6 | a0001c0001t0002g0044a0001c0001t0002g0080a0001c0001t0012g0012others(3): Show | 6 | HG02738.hp2 HG02965.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1003-534_1003-533i others(5): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679630 | ||||||
chr17:2679630
|
TTGGA | T | 2 | a0001c0001t0004g0249a0001c0001t0004g0276 | 2 | HG01257.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1003-496_1003-493d others(6): Show |
PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 2679630 | |||||
chr17:2679814
|
C | A | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1003-350C>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679814 | ||||||
chr17:2679896
|
T | G | 1 | a0001c0001t0024g0193 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1003-268T>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679896 | ||||||
chr17:2679930
|
T | C | 2 | a0001c0001t0003g0225a0001c0001t0003g0227 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1003-234T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679930 | ||||||
chr17:2679980
|
G | A | 1 | a0001c0001t0002g0073 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1003-184G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679980 | ||||||
chr17:2679984
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0028g0018 | 2 | HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1003-180G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 9/10 | chr17 | 2679984 | ||||||
chr17:2680682
|
G | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.1159+362G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2680682 | ||||||
chr17:2680684
|
T | C | 1 | a0001c0001t0017g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1159+364T>C | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2680684 | ||||||
chr17:2680817
|
C | G | 239 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.1159+497C>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2680817 | ||||||
chr17:2681370
|
T | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0078others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1160-359T>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681370 | ||||||
chr17:2681452
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1160-277G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681452 | ||||||
chr17:2681540
|
G | T | 4 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0132others(1): Show | 4 | HG01891.hp2 HG02257.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160-189G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681540 | ||||||
chr17:2681596
|
G | T | 8 | a0001c0001t0012g0012a0001c0001t0012g0013a0001c0001t0012g0014others(5): Show | 8 | HG01109.hp1 HG02622.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-133G>T | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681596 | ||||||
chr17:2681601
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1160-128A>G | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681601 | ||||||
chr17:2681652
|
G | A | 44 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0078others(41): Show | 44 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.1160-77G>A | PAFAH1B1 | ENSG00000007168.14 | transcript | ENST00000397195.10 | protein_coding | 10/10 | chr17 | 2681652 |