geneid | 5064 |
---|---|
ensemblid | ENSG00000099864.18 |
hgncid | 8594 |
symbol | PALM |
name | paralemmin |
refseq_nuc | NM_002579.3 |
refseq_prot | NP_002570.2 |
ensembl_nuc | ENST00000338448.10 |
ensembl_prot | ENSP00000341911.4 |
mane_status | MANE Select |
chr | chr19 |
start | 708935 |
end | 748329 |
strand | + |
ver | v1.2 |
region | chr19:708935-748329 |
region5000 | chr19:703935-753329 |
regionname0 | PALM_chr19_708935_748329 |
regionname5000 | PALM_chr19_703935_753329 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 387 | 219 | 67 | 32 | 89 | 4 | 27 | 67 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002 | 1/1 | 387 | 181 | 23 | 48 | 77 | 12 | 19 | 52 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0003 | 0/0 | 387 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0004 | 0/0 | 387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0005 | 0/0 | 387 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0006 | 0/0 | 387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
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 | 1164 | 134 | 19 | 43 | 45 | 10 | 15 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0002 | 0/0 | 1164 | 122 | 42 | 14 | 44 | 3 | 19 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0003 | 0/0 | 1164 | 55 | 24 | 15 | 10 | 1 | 5 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0004 | 0/0 | 1164 | 38 | 0 | 2 | 33 | 0 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0005 | 0/0 | 1164 | 27 | 0 | 1 | 26 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0006 | 0/0 | 1164 | 7 | 4 | 2 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0007 | 0/0 | 1164 | 6 | 0 | 0 | 6 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0008 | 0/0 | 1164 | 4 | 0 | 0 | 0 | 1 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0009 | 0/0 | 1164 | 3 | 0 | 2 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0010 | 0/0 | 1164 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0011 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0012 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0013 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0014 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0015 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
c0016 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1728 | 124 | 26 | 34 | 39 | 5 | 18 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0002 | 0/0 | 1728 | 111 | 36 | 30 | 23 | 8 | 14 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0003 | 0/0 | 1728 | 60 | 0 | 2 | 55 | 0 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0004 | 0/0 | 1728 | 38 | 2 | 2 | 27 | 0 | 7 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0005 | 0/0 | 1728 | 16 | 0 | 0 | 13 | 0 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0006 | 0/0 | 1728 | 12 | 10 | 1 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0007 | 0/0 | 1728 | 6 | 6 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0008 | 0/0 | 1728 | 4 | 3 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0009 | 0/0 | 1728 | 4 | 1 | 2 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0010 | 0/0 | 1728 | 3 | 2 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0011 | 0/0 | 1728 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0012 | 0/0 | 1728 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0013 | 0/0 | 1728 | 2 | 0 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0014 | 0/0 | 1728 | 2 | 1 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0015 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0016 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0017 | 0/0 | 1729 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0018 | 0/0 | 1729 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0019 | 0/0 | 1729 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0020 | 0/0 | 1729 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0021 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0022 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0023 | 0/0 | 1728 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0024 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0025 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0026 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0027 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0028 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0029 | 0/0 | 1728 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0030 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0031 | 0/0 | 1728 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
t0032 | 0/0 | 1728 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 1164 | 122 | 42 | 14 | 44 | 3 | 19 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003 | 0/0 | 1164 | 55 | 24 | 15 | 10 | 1 | 5 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0004 | 0/0 | 1164 | 38 | 0 | 2 | 33 | 0 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0010 | 0/0 | 1164 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0014 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0016 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001 | 1/1 | 1164 | 134 | 19 | 43 | 45 | 10 | 15 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0005 | 0/0 | 1164 | 27 | 0 | 1 | 26 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0006 | 0/0 | 1164 | 7 | 4 | 2 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0007 | 0/0 | 1164 | 6 | 0 | 0 | 6 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0008 | 0/0 | 1164 | 4 | 0 | 0 | 0 | 1 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0009 | 0/0 | 1164 | 3 | 0 | 2 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0003c0015 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0004c0012 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0005c0011 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0006c0013 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 2891 | 27 | 7 | 4 | 7 | 1 | 8 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0002 | 0/0 | 2891 | 43 | 28 | 5 | 6 | 1 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0004 | 0/0 | 2891 | 25 | 0 | 2 | 18 | 0 | 5 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0005 | 0/0 | 2891 | 14 | 0 | 0 | 11 | 0 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0006 | 0/0 | 2891 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0007 | 0/0 | 2891 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0008 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0010 | 0/0 | 2891 | 3 | 2 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0012 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0013 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0015 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0026 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0027 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0002t0031 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0001 | 0/0 | 2891 | 37 | 11 | 10 | 10 | 1 | 5 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0002 | 0/0 | 2891 | 3 | 2 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0006 | 0/0 | 2891 | 8 | 7 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0007 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0014 | 0/0 | 2891 | 2 | 1 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0016 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0017 | 0/0 | 2892 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0022 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0003t0032 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0004t0003 | 0/0 | 2891 | 34 | 0 | 2 | 29 | 0 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0004t0018 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0004t0024 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0004t0025 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0004t0028 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0010t0003 | 0/0 | 2891 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0014t0001 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0001c0016t0001 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0001 | 1/1 | 2891 | 49 | 4 | 15 | 20 | 3 | 5 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0002 | 0/0 | 2891 | 61 | 6 | 24 | 17 | 6 | 8 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0004 | 0/0 | 2891 | 6 | 2 | 0 | 2 | 0 | 2 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0005 | 0/0 | 2891 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0006 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0007 | 0/0 | 2891 | 3 | 3 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0008 | 0/0 | 2891 | 2 | 1 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0009 | 0/0 | 2891 | 4 | 1 | 2 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0011 | 0/0 | 2891 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0012 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0013 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0020 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0001t0030 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0005t0003 | 0/0 | 2891 | 24 | 0 | 0 | 24 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0005t0004 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0005t0019 | 0/0 | 2892 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0005t0029 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0006t0001 | 0/0 | 2891 | 3 | 1 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0006t0006 | 0/0 | 2891 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0006t0008 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0006t0021 | 0/0 | 2891 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0007t0004 | 0/0 | 2891 | 6 | 0 | 0 | 6 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0008t0002 | 0/0 | 2891 | 4 | 0 | 0 | 0 | 1 | 3 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0009t0001 | 0/0 | 2891 | 2 | 0 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0002c0009t0023 | 0/0 | 2891 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0003c0015t0001 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0004c0012t0001 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0005c0011t0001 | 0/0 | 2891 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
a0006c0013t0001 | 0/0 | 2891 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | copy fasta | chr19 | 703935 | 753329 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0004g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0005g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0006g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0008g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0010g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0010g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0012g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0013g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0026g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0027g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0002t0031g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0002g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0006g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0014g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0014g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0016g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0017g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0022g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0003t0032g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0018g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0024g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0025g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0004t0028g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0010t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0010t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0014t0001g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0001c0016t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0216 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0002g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0004g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0007g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0008g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0009g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0009g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0009g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0011g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0012g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0013g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0020g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0001t0030g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0019g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0005t0029g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0006t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0006t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0006t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0006t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0006t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0006t0021g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0007t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0007t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0007t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0007t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0007t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0007t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0008t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0008t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0008t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0008t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0009t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0009t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0002c0009t0023g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0003c0015t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0004c0012t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0005c0011t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
a0006c0013t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0378 | EUR | GBR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00099 | hp2 | a0002 | c0001 | t0002 | g0084 | EUR | GBR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00140 | hp1 | a0002 | c0001 | t0002 | g0212 | EUR | GBR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00140 | hp2 | a0002 | c0001 | t0002 | g0081 | EUR | GBR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0357 | EUR | FIN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00280 | hp2 | a0002 | c0001 | t0009 | g0313 | EUR | FIN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00323 | hp1 | a0002 | c0008 | t0002 | g0172 | EUR | FIN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00323 | hp2 | a0002 | c0009 | t0023 | g0083 | EUR | FIN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00408 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00408 | hp2 | a0001 | c0004 | t0003 | g0051 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00423 | hp1 | a0005 | c0011 | t0001 | g0308 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00423 | hp2 | a0002 | c0001 | t0011 | g0191 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00438 | hp2 | a0002 | c0005 | t0003 | g0181 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00544 | hp1 | a0001 | c0002 | t0004 | g0251 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00544 | hp2 | a0002 | c0007 | t0004 | g0073 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00597 | hp1 | a0001 | c0004 | t0003 | g0088 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00597 | hp2 | a0001 | c0002 | t0005 | g0326 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00609 | hp1 | a0002 | c0005 | t0003 | g0244 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00609 | hp2 | a0001 | c0004 | t0003 | g0069 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00621 | hp2 | a0002 | c0005 | t0003 | g0194 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0214 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00639 | hp2 | a0002 | c0001 | t0002 | g0160 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00642 | hp1 | a0002 | c0001 | t0002 | g0227 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00673 | hp1 | a0002 | c0005 | t0003 | g0077 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00673 | hp2 | a0002 | c0005 | t0003 | g0235 | EAS | CHS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0351 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0331 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00735 | hp2 | a0001 | c0002 | t0004 | g0254 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00738 | hp1 | a0002 | c0001 | t0009 | g0167 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00738 | hp2 | a0001 | c0003 | t0022 | g0037 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0122 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01069 | hp1 | a0001 | c0003 | t0002 | g0385 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01069 | hp2 | a0002 | c0001 | t0002 | g0008 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01070 | hp1 | a0002 | c0001 | t0002 | g0057 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0215 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01071 | hp1 | a0002 | c0001 | t0002 | g0008 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01071 | hp2 | a0001 | c0003 | t0001 | g0217 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0211 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01074 | hp2 | a0001 | c0002 | t0010 | g0030 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01081 | hp1 | a0002 | c0001 | t0002 | g0148 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0383 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01099 | hp1 | a0002 | c0001 | t0002 | g0230 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01099 | hp2 | a0001 | c0003 | t0017 | g0350 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01106 | hp1 | a0002 | c0001 | t0002 | g0041 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01106 | hp2 | a0001 | c0002 | t0013 | g0379 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01109 | hp1 | a0002 | c0001 | t0008 | g0023 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01109 | hp2 | a0002 | c0006 | t0001 | g0206 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01167 | hp1 | a0002 | c0001 | t0009 | g0213 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01167 | hp2 | a0002 | c0001 | t0001 | g0355 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0218 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01168 | hp2 | a0002 | c0001 | t0001 | g0292 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01169 | hp1 | a0002 | c0001 | t0001 | g0291 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01169 | hp2 | a0002 | c0001 | t0001 | g0354 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0358 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0239 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01192 | hp1 | a0002 | c0001 | t0001 | g0352 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01192 | hp2 | a0001 | c0002 | t0027 | g0047 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01243 | hp1 | a0001 | c0003 | t0006 | g0376 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01243 | hp2 | a0001 | c0002 | t0002 | g0353 | AMR | PUR | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01255 | hp1 | a0002 | c0001 | t0013 | g0330 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01255 | hp2 | a0002 | c0001 | t0002 | g0380 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01256 | hp1 | a0002 | c0001 | t0001 | g0297 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01256 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01257 | hp1 | a0002 | c0009 | t0001 | g0290 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0153 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01258 | hp1 | a0002 | c0001 | t0001 | g0003 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01258 | hp2 | a0002 | c0001 | t0001 | g0151 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0112 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01261 | hp2 | a0002 | c0001 | t0002 | g0282 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01358 | hp1 | a0001 | c0004 | t0003 | g0016 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01358 | hp2 | a0002 | c0001 | t0002 | g0002 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01361 | hp1 | a0002 | c0001 | t0002 | g0226 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01433 | hp1 | a0002 | c0001 | t0001 | g0062 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01433 | hp2 | a0002 | c0001 | t0002 | g0082 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01496 | hp1 | a0002 | c0001 | t0001 | g0157 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01496 | hp2 | a0002 | c0009 | t0001 | g0281 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01516 | hp1 | a0002 | c0001 | t0002 | g0209 | EUR | IBS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0097 | EUR | IBS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01517 | hp1 | a0002 | c0001 | t0001 | g0356 | EUR | IBS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01517 | hp2 | a0002 | c0001 | t0002 | g0210 | EUR | IBS | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01884 | hp1 | a0002 | c0001 | t0030 | g0096 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01884 | hp2 | a0001 | c0002 | t0008 | g0371 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01891 | hp1 | a0001 | c0003 | t0006 | g0034 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0370 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01934 | hp1 | a0002 | c0001 | t0002 | g0170 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01934 | hp2 | a0002 | c0001 | t0002 | g0002 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01943 | hp1 | a0002 | c0001 | t0001 | g0204 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01943 | hp2 | a0002 | c0001 | t0002 | g0038 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01975 | hp1 | a0002 | c0001 | t0002 | g0208 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01975 | hp2 | a0002 | c0005 | t0029 | g0315 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01978 | hp1 | a0001 | c0003 | t0014 | g0278 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01978 | hp2 | a0001 | c0004 | t0003 | g0016 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01981 | hp1 | a0002 | c0006 | t0001 | g0173 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01981 | hp2 | a0001 | c0014 | t0001 | g0382 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01993 | hp1 | a0002 | c0001 | t0002 | g0042 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0103 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02004 | hp1 | a0002 | c0001 | t0002 | g0036 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02004 | hp2 | a0002 | c0001 | t0002 | g0162 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02015 | hp1 | a0002 | c0005 | t0003 | g0147 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02015 | hp2 | a0002 | c0001 | t0002 | g0342 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02027 | hp1 | a0002 | c0001 | t0002 | g0061 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02040 | hp1 | a0002 | c0001 | t0011 | g0186 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02040 | hp2 | a0001 | c0004 | t0003 | g0322 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02056 | hp1 | a0002 | c0001 | t0004 | g0284 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02056 | hp2 | a0002 | c0001 | t0001 | g0283 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02071 | hp1 | a0002 | c0001 | t0002 | g0070 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02071 | hp2 | a0001 | c0002 | t0004 | g0018 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02074 | hp2 | a0002 | c0001 | t0002 | g0066 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02080 | hp1 | a0002 | c0001 | t0001 | g0055 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02080 | hp2 | a0001 | c0004 | t0003 | g0001 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02083 | hp1 | a0001 | c0002 | t0004 | g0197 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02083 | hp2 | a0001 | c0002 | t0005 | g0104 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02129 | hp1 | a0002 | c0001 | t0002 | g0184 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0245 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02132 | hp1 | a0001 | c0002 | t0012 | g0074 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02132 | hp2 | a0001 | c0002 | t0004 | g0130 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02135 | hp1 | a0001 | c0002 | t0005 | g0087 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02135 | hp2 | a0002 | c0001 | t0002 | g0324 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02145 | hp2 | a0002 | c0001 | t0001 | g0046 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02148 | hp1 | a0002 | c0001 | t0002 | g0161 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02148 | hp2 | a0001 | c0002 | t0004 | g0259 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02155 | hp1 | a0001 | c0002 | t0005 | g0246 | EAS | CDX | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02155 | hp2 | a0002 | c0001 | t0001 | g0294 | EAS | CDX | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02165 | hp1 | a0002 | c0001 | t0002 | g0323 | EAS | CDX | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02165 | hp2 | a0001 | c0004 | t0003 | g0132 | EAS | CDX | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0033 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02257 | hp2 | a0001 | c0003 | t0006 | g0373 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02258 | hp1 | a0002 | c0001 | t0007 | g0277 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02258 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02273 | hp1 | a0002 | c0001 | t0002 | g0175 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0039 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02280 | hp1 | a0002 | c0006 | t0001 | g0049 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02280 | hp2 | a0002 | c0006 | t0008 | g0024 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02300 | hp1 | a0002 | c0001 | t0001 | g0319 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0314 | AMR | PEL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0265 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02451 | hp2 | a0001 | c0003 | t0016 | g0271 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02523 | hp1 | a0001 | c0002 | t0031 | g0258 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02523 | hp2 | a0002 | c0001 | t0002 | g0064 | EAS | KHV | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02602 | hp1 | a0001 | c0002 | t0005 | g0334 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02602 | hp2 | a0002 | c0001 | t0002 | g0343 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02622 | hp1 | a0001 | c0003 | t0007 | g0272 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0043 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02630 | hp1 | a0001 | c0003 | t0014 | g0275 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02647 | hp1 | a0001 | c0002 | t0007 | g0274 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0031 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02698 | hp2 | a0002 | c0001 | t0001 | g0056 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02717 | hp1 | a0001 | c0003 | t0006 | g0374 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02717 | hp2 | a0001 | c0003 | t0006 | g0118 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0367 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02735 | hp1 | a0002 | c0001 | t0002 | g0150 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02735 | hp2 | a0001 | c0003 | t0001 | g0123 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0109 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0360 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02818 | hp1 | a0001 | c0002 | t0026 | g0263 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0361 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0347 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0268 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0368 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02922 | hp1 | a0001 | c0003 | t0006 | g0346 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02922 | hp2 | a0002 | c0001 | t0001 | g0169 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02965 | hp1 | a0006 | c0013 | t0001 | g0080 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02970 | hp1 | a0002 | c0001 | t0001 | g0119 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02970 | hp2 | a0001 | c0002 | t0002 | g0262 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02976 | hp1 | a0001 | c0003 | t0006 | g0241 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0202 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03041 | hp1 | a0002 | c0001 | t0002 | g0179 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0369 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03098 | hp2 | a0001 | c0003 | t0006 | g0375 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03130 | hp1 | a0002 | c0001 | t0007 | g0276 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0362 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03139 | hp2 | a0002 | c0001 | t0009 | g0065 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03209 | hp2 | a0002 | c0001 | t0004 | g0339 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0372 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03225 | hp2 | a0002 | c0001 | t0007 | g0273 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03239 | hp2 | a0002 | c0001 | t0004 | g0312 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03486 | hp1 | a0002 | c0001 | t0002 | g0022 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03486 | hp2 | a0002 | c0001 | t0002 | g0240 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03490 | hp1 | a0002 | c0001 | t0002 | g0341 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03490 | hp2 | a0001 | c0002 | t0004 | g0013 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03491 | hp1 | a0002 | c0001 | t0002 | g0048 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03491 | hp2 | a0001 | c0003 | t0001 | g0079 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03492 | hp1 | a0001 | c0002 | t0004 | g0013 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03492 | hp2 | a0001 | c0003 | t0001 | g0075 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03516 | hp2 | a0001 | c0002 | t0015 | g0242 | AFR | ESN | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03540 | hp2 | a0001 | c0002 | t0007 | g0020 | AFR | GWD | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03579 | hp1 | a0002 | c0001 | t0004 | g0338 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0201 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03669 | hp1 | a0001 | c0004 | t0003 | g0138 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03669 | hp2 | a0002 | c0001 | t0004 | g0377 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03688 | hp1 | a0002 | c0008 | t0002 | g0307 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03688 | hp2 | a0001 | c0002 | t0005 | g0237 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03710 | hp1 | a0002 | c0001 | t0002 | g0174 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0180 | SAS | PJL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0270 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03831 | hp2 | a0002 | c0001 | t0002 | g0269 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0060 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0318 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03927 | hp1 | a0002 | c0006 | t0021 | g0359 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03927 | hp2 | a0001 | c0004 | t0003 | g0221 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0236 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03942 | hp2 | a0001 | c0002 | t0004 | g0286 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04115 | hp1 | a0002 | c0001 | t0001 | g0068 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04115 | hp2 | a0001 | c0002 | t0005 | g0335 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0050 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04184 | hp2 | a0001 | c0004 | t0003 | g0139 | SAS | BEB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0337 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04199 | hp2 | a0002 | c0008 | t0002 | g0040 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04204 | hp1 | a0001 | c0002 | t0004 | g0340 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04204 | hp2 | a0002 | c0008 | t0002 | g0067 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04228 | hp1 | a0001 | c0002 | t0004 | g0164 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG04228 | hp2 | a0002 | c0001 | t0001 | g0348 | SAS | STU | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18522 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | YRI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | YRI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18612 | hp1 | a0002 | c0001 | t0001 | g0188 | EAS | CHB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18612 | hp2 | a0002 | c0001 | t0002 | g0192 | EAS | CHB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18747 | hp1 | a0002 | c0001 | t0001 | g0165 | EAS | CHB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18747 | hp2 | a0001 | c0004 | t0003 | g0125 | EAS | CHB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | YRI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0108 | AFR | YRI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18939 | hp1 | a0001 | c0004 | t0003 | g0001 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18939 | hp2 | a0002 | c0005 | t0004 | g0158 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18941 | hp1 | a0001 | c0002 | t0004 | g0144 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18941 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18942 | hp1 | a0002 | c0005 | t0003 | g0345 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18942 | hp2 | a0001 | c0004 | t0003 | g0128 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18943 | hp1 | a0001 | c0002 | t0005 | g0223 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18943 | hp2 | a0002 | c0005 | t0003 | g0078 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18944 | hp1 | a0001 | c0002 | t0005 | g0106 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18944 | hp2 | a0002 | c0001 | t0004 | g0124 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18945 | hp1 | a0002 | c0001 | t0012 | g0249 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18945 | hp2 | a0002 | c0005 | t0003 | g0120 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18947 | hp2 | a0002 | c0001 | t0005 | g0089 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18948 | hp1 | a0001 | c0002 | t0004 | g0298 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18948 | hp2 | a0001 | c0010 | t0003 | g0295 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0127 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18950 | hp1 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18950 | hp2 | a0002 | c0001 | t0002 | g0327 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18951 | hp1 | a0002 | c0001 | t0005 | g0189 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18951 | hp2 | a0001 | c0002 | t0005 | g0247 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18952 | hp1 | a0001 | c0004 | t0003 | g0222 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18953 | hp1 | a0002 | c0005 | t0003 | g0094 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18953 | hp2 | a0001 | c0004 | t0003 | g0305 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18954 | hp1 | a0002 | c0005 | t0003 | g0121 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18954 | hp2 | a0002 | c0001 | t0002 | g0178 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18956 | hp1 | a0001 | c0002 | t0004 | g0111 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18956 | hp2 | a0001 | c0002 | t0004 | g0017 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18959 | hp1 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18959 | hp2 | a0001 | c0004 | t0003 | g0320 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18960 | hp1 | a0001 | c0002 | t0005 | g0141 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0325 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18963 | hp1 | a0001 | c0002 | t0005 | g0193 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18963 | hp2 | a0001 | c0002 | t0004 | g0253 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18964 | hp1 | a0001 | c0004 | t0003 | g0098 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18964 | hp2 | a0001 | c0003 | t0001 | g0145 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18965 | hp1 | a0002 | c0005 | t0003 | g0288 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18965 | hp2 | a0001 | c0003 | t0001 | g0287 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18966 | hp1 | a0001 | c0002 | t0004 | g0293 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18966 | hp2 | a0002 | c0005 | t0003 | g0310 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18967 | hp1 | a0002 | c0007 | t0004 | g0163 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18967 | hp2 | a0002 | c0005 | t0019 | g0176 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18968 | hp1 | a0001 | c0002 | t0004 | g0199 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18968 | hp2 | a0001 | c0004 | t0024 | g0126 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18970 | hp1 | a0001 | c0004 | t0003 | g0001 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0238 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18971 | hp1 | a0002 | c0001 | t0002 | g0168 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18971 | hp2 | a0001 | c0004 | t0003 | g0007 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18973 | hp1 | a0001 | c0004 | t0003 | g0086 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18973 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18980 | hp1 | a0001 | c0004 | t0003 | g0300 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18980 | hp2 | a0002 | c0005 | t0003 | g0344 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18983 | hp1 | a0002 | c0005 | t0003 | g0071 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18983 | hp2 | a0002 | c0005 | t0003 | g0304 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18984 | hp1 | a0001 | c0010 | t0003 | g0296 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18984 | hp2 | a0001 | c0002 | t0004 | g0136 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18986 | hp1 | a0002 | c0001 | t0001 | g0185 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18986 | hp2 | a0001 | c0004 | t0003 | g0007 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18990 | hp1 | a0001 | c0004 | t0003 | g0131 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18991 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18991 | hp2 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18994 | hp2 | a0001 | c0002 | t0004 | g0243 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18995 | hp1 | a0001 | c0004 | t0003 | g0328 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18997 | hp1 | a0002 | c0001 | t0002 | g0285 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18997 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18998 | hp1 | a0001 | c0002 | t0004 | g0053 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18998 | hp2 | a0001 | c0004 | t0003 | g0336 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18999 | hp1 | a0001 | c0004 | t0028 | g0135 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA18999 | hp2 | a0002 | c0001 | t0001 | g0090 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19000 | hp1 | a0001 | c0004 | t0003 | g0092 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19000 | hp2 | a0002 | c0005 | t0003 | g0232 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19003 | hp1 | a0001 | c0004 | t0018 | g0133 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19003 | hp2 | a0002 | c0007 | t0004 | g0159 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19005 | hp1 | a0001 | c0004 | t0003 | g0321 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19005 | hp2 | a0002 | c0001 | t0002 | g0063 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19007 | hp1 | a0001 | c0004 | t0003 | g0306 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19009 | hp1 | a0002 | c0005 | t0003 | g0072 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0317 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19010 | hp1 | a0001 | c0004 | t0003 | g0102 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19010 | hp2 | a0002 | c0001 | t0001 | g0187 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19011 | hp1 | a0001 | c0004 | t0003 | g0085 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19011 | hp2 | a0001 | c0003 | t0001 | g0116 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19012 | hp1 | a0001 | c0002 | t0005 | g0220 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19012 | hp2 | a0002 | c0007 | t0004 | g0228 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0149 | AFR | LWK | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19030 | hp2 | a0002 | c0006 | t0006 | g0280 | AFR | LWK | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19043 | hp1 | a0001 | c0016 | t0001 | g0349 | AFR | LWK | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0363 | AFR | LWK | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19054 | hp1 | a0002 | c0001 | t0002 | g0156 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19054 | hp2 | a0001 | c0004 | t0003 | g0101 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19055 | hp1 | a0002 | c0005 | t0003 | g0301 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19055 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19056 | hp1 | a0002 | c0001 | t0001 | g0303 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19063 | hp1 | a0002 | c0001 | t0020 | g0332 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19064 | hp1 | a0001 | c0004 | t0025 | g0154 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19064 | hp2 | a0003 | c0015 | t0001 | g0134 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19065 | hp1 | a0002 | c0005 | t0003 | g0316 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19065 | hp2 | a0001 | c0002 | t0004 | g0255 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19068 | hp1 | a0002 | c0007 | t0004 | g0146 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0299 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19070 | hp1 | a0002 | c0005 | t0003 | g0311 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19070 | hp2 | a0002 | c0005 | t0003 | g0195 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0054 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19074 | hp2 | a0002 | c0005 | t0003 | g0182 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19085 | hp1 | a0002 | c0001 | t0001 | g0333 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19085 | hp2 | a0002 | c0001 | t0002 | g0190 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19087 | hp1 | a0001 | c0002 | t0005 | g0143 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19087 | hp2 | a0002 | c0007 | t0004 | g0196 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19088 | hp1 | a0002 | c0001 | t0001 | g0099 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19088 | hp2 | a0001 | c0004 | t0003 | g0114 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19090 | hp1 | a0002 | c0001 | t0001 | g0044 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19090 | hp2 | a0002 | c0005 | t0003 | g0166 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19091 | hp1 | a0002 | c0001 | t0001 | g0309 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19091 | hp2 | a0001 | c0004 | t0003 | g0129 | EAS | JPT | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0381 | AFR | YRI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA19240 | hp2 | a0001 | c0002 | t0002 | g0365 | AFR | YRI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | ASW | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0289 | AFR | ASW | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20752 | hp1 | a0002 | c0001 | t0001 | g0329 | EUR | TSI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20752 | hp2 | a0001 | c0002 | t0006 | g0029 | EUR | TSI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20805 | hp1 | a0002 | c0001 | t0002 | g0171 | EUR | TSI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0155 | EUR | TSI | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20905 | hp1 | a0002 | c0001 | t0002 | g0231 | SAS | GIH | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20905 | hp2 | a0002 | c0001 | t0002 | g0229 | SAS | GIH | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01123 | hp1 | a0002 | c0001 | t0002 | g0207 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG01123 | hp2 | a0002 | c0001 | t0002 | g0177 | AMR | CLM | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02109 | hp1 | a0002 | c0001 | t0001 | g0003 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02109 | hp2 | a0002 | c0006 | t0006 | g0279 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02486 | hp1 | a0002 | c0001 | t0002 | g0117 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02559 | hp1 | a0002 | c0001 | t0002 | g0366 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG02559 | hp2 | a0001 | c0003 | t0032 | g0021 | AFR | ACB | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03471 | hp1 | a0002 | c0001 | t0006 | g0095 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG03471 | hp2 | a0001 | c0002 | t0010 | g0203 | AFR | MSL | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG06807 | hp1 | a0001 | c0002 | t0010 | g0261 | AFR | USA | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | USA | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20300 | hp1 | a0002 | c0001 | t0002 | g0384 | AFR | USA | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | USA | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA21309 | hp1 | a0002 | c0001 | t0008 | g0058 | AFR | LWK | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
NA21309 | hp2 | a0004 | c0012 | t0001 | g0364 | AFR | LWK | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0152 | REF | REF | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0001 | g0216 | REF | REF | PALM_chr19_703935_753329 | PALM | chr19 | 703935 | 753329 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:731144
|
A | G | 2 | a0001a0003 | 220 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(217): Show |
missense_variant | MODERATE | c.319A>G | p.Thr107Ala | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/9 | 531/2891 | 319/1164 | 107/387 | chr19 | 731144 | ||
chr19:736022
|
A | T | 1 | a0006 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.446A>T | p.Lys149Met | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/9 | 658/2891 | 446/1164 | 149/387 | chr19 | 736022 | ||
chr19:746311
|
G | A | 1 | a0005 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.661G>A | p.Glu221Lys | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 873/2891 | 661/1164 | 221/387 | chr19 | 746311 | ||
chr19:746458
|
C | T | 1 | a0004 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.808C>T | p.Arg270Trp | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1020/2891 | 808/1164 | 270/387 | chr19 | 746458 | ||
chr19:746540
|
C | T | 1 | a0003 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.890C>T | p.Pro297Leu | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1102/2891 | 890/1164 | 297/387 | chr19 | 746540 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:731176
|
A | G | 1 | a0002c0009 | 3 | HG00323.hp2 HG01257.hp1 HG01496.hp2 |
synonymous_variant | LOW | c.351A>G | p.Pro117Pro | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/9 | 563/2891 | 351/1164 | 117/387 | chr19 | 731176 | ||
chr19:746307
|
C | T | 1 | a0001c0016 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.657C>T | p.Thr219Thr | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 869/2891 | 657/1164 | 219/387 | chr19 | 746307 | ||
chr19:746310
|
C | A | 1 | a0002c0007 | 6 | HG00544.hp2 NA18967.hp1 NA19003.hp2 others(3): Show |
synonymous_variant | LOW | c.660C>A | p.Ala220Ala | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 872/2891 | 660/1164 | 220/387 | chr19 | 746310 | ||
chr19:746409
|
G | A | 4 | a0001c0004a0001c0010a0001c0014others(1): Show | 68 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(65): Show |
synonymous_variant | LOW | c.759G>A | p.Ala253Ala | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 971/2891 | 759/1164 | 253/387 | chr19 | 746409 | ||
chr19:746526
|
C | T | 1 | a0001c0010 | 2 | NA18948.hp2 NA18984.hp1 |
synonymous_variant | LOW | c.876C>T | p.Pro292Pro | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1088/2891 | 876/1164 | 292/387 | chr19 | 746526 | ||
chr19:746541
|
G | A | 1 | a0002c0008 | 4 | HG00323.hp1 HG03688.hp1 HG04199.hp2 others(1): Show |
synonymous_variant | LOW | c.891G>A | p.Pro297Pro | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1103/2891 | 891/1164 | 297/387 | chr19 | 746541 | ||
chr19:746712
|
C | T | 6 | a0001c0003a0001c0014a0001c0016others(3): Show | 66 | HG00099.hp1 HG00639.hp1 HG00738.hp2 others(63): Show |
synonymous_variant | LOW | c.1062C>T | p.Ala354Ala | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1274/2891 | 1062/1164 | 354/387 | chr19 | 746712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:709001
|
G | A | 1 | a0001c0002t0015 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-146G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/9 | 146 | chr19 | 709001 | |||||
chr19:709032
|
C | A | 1 | a0001c0003t0016 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-115C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/9 | 115 | chr19 | 709032 | |||||
chr19:709042
|
C | G | 1 | a0001c0002t0031 | 1 | HG02523.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/9 | 105 | chr19 | 709042 | |||||
chr19:709042
|
C | T | 6 | a0001c0002t0007a0001c0003t0007a0001c0003t0014others(3): Show | 10 | HG01978.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-105C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/9 | 105 | chr19 | 709042 | |||||
chr19:709070
|
T | G | 6 | a0001c0002t0007a0001c0003t0007a0001c0003t0014others(3): Show | 10 | HG01978.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-77T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/9 | 77 | chr19 | 709070 | |||||
chr19:709093
|
A | C | 1 | a0002c0001t0030 | 1 | HG01884.hp1 | 5_prime_UTR_variant | MODIFIER | c.-54A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/9 | 54 | chr19 | 709093 | |||||
chr19:746828
|
A | AC | 4 | a0001c0003t0017a0001c0004t0018a0002c0001t0020others(1): Show | 4 | HG01099.hp2 NA18967.hp2 NA19003.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*18dupC | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 19 | INFO_REALIGN_3_PRIME | chr19 | 746828 | ||||
chr19:746881
|
G | T | 1 | a0002c0005t0029 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 67 | chr19 | 746881 | |||||
chr19:746979
|
C | A | 1 | a0002c0006t0021 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*165C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 165 | chr19 | 746979 | |||||
chr19:747023
|
C | T | 2 | a0001c0002t0013a0002c0001t0013 | 2 | HG01106.hp2 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*209C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 209 | chr19 | 747023 | |||||
chr19:747150
|
A | G | 39 | a0001c0002t0002a0001c0002t0004a0001c0002t0005others(36): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
3_prime_UTR_variant | MODIFIER | c.*336A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 336 | chr19 | 747150 | |||||
chr19:747224
|
G | C | 1 | a0001c0004t0018 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 410 | chr19 | 747224 | |||||
chr19:747225
|
C | G | 1 | a0001c0004t0018 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 411 | chr19 | 747225 | |||||
chr19:747245
|
C | T | 2 | a0001c0002t0010a0001c0004t0028 | 4 | HG01074.hp2 HG03471.hp2 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*431C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 431 | chr19 | 747245 | |||||
chr19:747299
|
C | T | 1 | a0002c0001t0009 | 4 | HG00280.hp2 HG00738.hp1 HG01167.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*485C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 485 | chr19 | 747299 | |||||
chr19:747311
|
C | T | 1 | a0001c0002t0027 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*497C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 497 | chr19 | 747311 | |||||
chr19:747362
|
G | C | 9 | a0001c0004t0003a0001c0004t0018a0001c0004t0024others(6): Show | 66 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*548G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 548 | chr19 | 747362 | |||||
chr19:747405
|
T | C | 4 | a0001c0002t0008a0002c0001t0008a0002c0001t0030others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*591T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 591 | chr19 | 747405 | |||||
chr19:747461
|
G | A | 1 | a0001c0003t0022 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*647G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 647 | chr19 | 747461 | |||||
chr19:747473
|
C | T | 5 | a0001c0002t0004a0002c0001t0004a0002c0001t0020others(2): Show | 39 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*659C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 659 | chr19 | 747473 | |||||
chr19:747658
|
T | A | 1 | a0001c0004t0018 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*844T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 844 | chr19 | 747658 | |||||
chr19:747664
|
T | A | 4 | a0001c0002t0008a0002c0001t0008a0002c0001t0030others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*850T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 850 | chr19 | 747664 | |||||
chr19:747847
|
C | A | 2 | a0001c0002t0005a0002c0001t0005 | 16 | HG00597.hp2 HG02083.hp2 HG02135.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1033C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1033 | chr19 | 747847 | |||||
chr19:747848
|
C | A | 1 | a0001c0004t0024 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1034C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1034 | chr19 | 747848 | |||||
chr19:747849
|
A | G | 1 | a0001c0004t0024 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1035A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1035 | chr19 | 747849 | |||||
chr19:747893
|
C | T | 1 | a0001c0002t0027 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1079C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1079 | chr19 | 747893 | |||||
chr19:748083
|
C | T | 8 | a0001c0002t0006a0001c0002t0012a0001c0002t0026others(5): Show | 16 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1269C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1269 | chr19 | 748083 | |||||
chr19:748139
|
G | A | 1 | a0001c0004t0025 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1325G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1325 | chr19 | 748139 | |||||
chr19:748161
|
C | A | 1 | a0002c0001t0011 | 2 | HG00423.hp2 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1347C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1347 | chr19 | 748161 | |||||
chr19:748162
|
G | A | 1 | a0001c0002t0026 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1348 | chr19 | 748162 | |||||
chr19:748179
|
C | T | 1 | a0002c0009t0023 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1365C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 9/9 | 1365 | chr19 | 748179 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:709237
|
T | C | 3 | a0001c0002t0004g0017a0001c0002t0004g0018a0001c0002t0004g0019 | 3 | HG00408.hp1 HG02071.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.5+86T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709237 | ||||||
chr19:709335
|
G | C | 2 | a0001c0002t0007g0020a0001c0003t0032g0021 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.5+184G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709335 | ||||||
chr19:709391
|
G | A | 9 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0005others(6): Show | 11 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.5+240G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709391 | ||||||
chr19:709411
|
A | C | 5 | a0001c0003t0001g0383a0001c0003t0002g0385a0001c0004t0003g0016others(2): Show | 6 | HG01069.hp1 HG01081.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+260A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709411 | ||||||
chr19:709425
|
G | A | 7 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0006g0029others(4): Show | 7 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.5+274G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709425 | ||||||
chr19:709592
|
C | T | 1 | a0001c0003t0001g0381 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5+441C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709592 | ||||||
chr19:709601
|
G | A | 7 | a0001c0003t0001g0039a0001c0003t0022g0037a0002c0001t0002g0036others(4): Show | 7 | HG00738.hp2 HG01106.hp1 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+450G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709601 | ||||||
chr19:709613
|
C | A | 1 | a0001c0003t0002g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5+462C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709613 | ||||||
chr19:709675
|
C | T | 3 | a0001c0002t0013g0379a0001c0003t0001g0378a0002c0001t0002g0380 | 3 | HG00099.hp1 HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.5+524C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709675 | ||||||
chr19:709803
|
C | T | 1 | a0002c0001t0004g0377 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5+652C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709803 | ||||||
chr19:709902
|
C | CTG | 41 | a0001c0002t0001g0028a0001c0002t0001g0248a0001c0002t0001g0256others(38): Show | 45 | HG00544.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.5+760_5+761dupTG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 709902 | |||||
chr19:709911
|
T | TG | 58 | a0001c0002t0001g0045a0001c0002t0001g0060a0001c0002t0002g0006others(55): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.5+770dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 709911 | |||||
chr19:709912
|
G | GT | 46 | a0001c0002t0001g0357a0001c0002t0002g0014a0001c0002t0002g0015others(43): Show | 50 | HG00280.hp1 HG01167.hp2 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.5+761_5+762insT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709912 | ||||||
chr19:709913
|
G | T | 81 | a0001c0002t0001g0028a0001c0002t0001g0299a0001c0002t0001g0302others(78): Show | 85 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.5+762G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709913 | ||||||
chr19:709914
|
G | T | 31 | a0001c0002t0001g0357a0001c0002t0002g0014a0001c0002t0002g0015others(28): Show | 35 | HG00280.hp1 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.5+763G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709914 | ||||||
chr19:709935
|
C | G | 1 | a0002c0006t0008g0024 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5+784C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709935 | ||||||
chr19:709970
|
G | T | 1 | a0002c0005t0003g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5+819G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709970 | ||||||
chr19:709971
|
T | C | 1 | a0002c0005t0003g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5+820T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709971 | ||||||
chr19:709982
|
C | T | 1 | a0002c0001t0001g0348 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.5+831C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 709982 | ||||||
chr19:710050
|
T | G | 165 | a0001c0002t0001g0028a0001c0002t0001g0110a0001c0002t0001g0248others(162): Show | 174 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.5+899T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710050 | ||||||
chr19:710073
|
C | G | 3 | a0001c0003t0006g0374a0001c0003t0006g0375a0001c0003t0006g0376 | 3 | HG01243.hp1 HG02717.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.5+922C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710073 | ||||||
chr19:710105
|
T | G | 17 | a0001c0002t0002g0268a0001c0002t0007g0020a0001c0002t0007g0274others(14): Show | 17 | HG01109.hp1 HG01884.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.5+954T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710105 | ||||||
chr19:710135
|
A | T | 3 | a0002c0001t0002g0022a0002c0001t0008g0023a0002c0006t0008g0024 | 3 | HG01109.hp1 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5+984A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710135 | ||||||
chr19:710144
|
C | T | 39 | a0001c0002t0001g0110a0001c0002t0001g0248a0001c0002t0001g0256others(36): Show | 41 | HG00544.hp1 HG00609.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.5+993C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710144 | ||||||
chr19:710201
|
C | T | 3 | a0002c0001t0002g0022a0002c0001t0008g0023a0002c0006t0008g0024 | 3 | HG01109.hp1 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5+1050C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710201 | ||||||
chr19:710261
|
C | A | 13 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0005others(10): Show | 15 | HG01109.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+1110C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710261 | ||||||
chr19:710348
|
A | AC | 7 | a0001c0002t0001g0045a0001c0002t0002g0112a0001c0002t0004g0111others(4): Show | 7 | HG01192.hp1 HG01261.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+1201dupC | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 710348 | |||||
chr19:710411
|
A | C | 1 | a0001c0002t0002g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.5+1260A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710411 | ||||||
chr19:710417
|
A | C | 1 | a0001c0002t0001g0110 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.5+1266A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710417 | ||||||
chr19:710450
|
A | G | 16 | a0001c0002t0001g0260a0001c0002t0001g0265a0001c0002t0002g0100others(13): Show | 17 | HG00733.hp1 HG00733.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.5+1299A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710450 | ||||||
chr19:710537
|
G | A | 2 | a0002c0001t0004g0338a0002c0001t0004g0339 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5+1386G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710537 | ||||||
chr19:710647
|
T | C | 19 | a0001c0002t0001g0260a0001c0002t0001g0265a0001c0002t0002g0262others(16): Show | 20 | HG00733.hp1 HG00733.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.5+1496T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710647 | ||||||
chr19:710651
|
G | GC | 56 | a0001c0002t0001g0028a0001c0002t0001g0110a0001c0002t0001g0233others(53): Show | 56 | HG00597.hp1 HG00621.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.5+1510dupC | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 710651 | |||||
chr19:710651
|
GC | G | 23 | a0001c0002t0001g0115a0001c0002t0001g0357a0001c0002t0002g0014others(20): Show | 26 | HG00280.hp1 HG01167.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.5+1510delC | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 710651 | |||||
chr19:710653
|
C | G | 16 | a0001c0002t0001g0260a0001c0002t0001g0265a0001c0002t0002g0262others(13): Show | 17 | HG00733.hp1 HG00733.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.5+1502C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710653 | ||||||
chr19:710653
|
C | T | 3 | a0002c0001t0002g0022a0002c0001t0008g0023a0002c0006t0008g0024 | 3 | HG01109.hp1 HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5+1502C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710653 | ||||||
chr19:710654
|
C | G | 4 | a0001c0003t0006g0241a0002c0001t0002g0240a0002c0001t0006g0095others(1): Show | 4 | HG01884.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+1503C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710654 | ||||||
chr19:710656
|
C | A | 1 | a0001c0002t0002g0353 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.5+1505C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710656 | ||||||
chr19:710661
|
C | A | 4 | a0002c0001t0001g0352a0002c0001t0002g0022a0002c0001t0008g0023others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+1510C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710661 | ||||||
chr19:710662
|
A | C | 2 | a0001c0002t0004g0286a0002c0001t0001g0352 | 2 | HG01192.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.5+1511A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710662 | ||||||
chr19:710663
|
C | A | 1 | a0002c0001t0002g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5+1512C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710663 | ||||||
chr19:710692
|
CG | C | 338 | a0001c0002t0001g0009a0001c0002t0001g0028a0001c0002t0001g0060others(335): Show | 355 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.5+1547delG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 710692 | |||||
chr19:710693
|
G | C | 1 | a0002c0005t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.5+1542G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710693 | ||||||
chr19:710768
|
T | C | 15 | a0001c0002t0001g0357a0001c0002t0002g0014a0001c0002t0002g0360others(12): Show | 18 | HG00280.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.5+1617T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710768 | ||||||
chr19:710831
|
G | C | 29 | a0001c0002t0001g0357a0001c0002t0002g0014a0001c0002t0002g0360others(26): Show | 32 | HG00280.hp1 HG01167.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.5+1680G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710831 | ||||||
chr19:710847
|
G | T | 15 | a0001c0002t0001g0357a0001c0002t0002g0014a0001c0002t0002g0360others(12): Show | 18 | HG00280.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.5+1696G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710847 | ||||||
chr19:710850
|
C | T | 5 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0003t0001g0031others(2): Show | 5 | HG01891.hp1 HG02257.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.5+1699C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710850 | ||||||
chr19:710852
|
A | C | 293 | a0001c0002t0001g0009a0001c0002t0001g0060a0001c0002t0001g0110others(290): Show | 308 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.5+1701A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710852 | ||||||
chr19:710886
|
G | A | 17 | a0001c0002t0001g0260a0001c0002t0001g0265a0001c0002t0002g0262others(14): Show | 18 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.5+1735G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710886 | ||||||
chr19:710906
|
C | G | 2 | a0001c0003t0007g0272a0001c0003t0016g0271 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.5+1755C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710906 | ||||||
chr19:710968
|
C | G | 2 | a0002c0001t0004g0338a0002c0001t0004g0339 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5+1817C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710968 | ||||||
chr19:710969
|
C | G | 5 | a0001c0003t0002g0043a0002c0001t0002g0022a0002c0001t0008g0023others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+1818C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710969 | ||||||
chr19:710988
|
G | T | 2 | a0002c0001t0004g0338a0002c0001t0004g0339 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5+1837G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 710988 | ||||||
chr19:711029
|
A | T | 1 | a0002c0001t0004g0338 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.5+1878A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711029 | ||||||
chr19:711236
|
C | T | 5 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0005others(2): Show | 7 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+2085C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711236 | ||||||
chr19:711242
|
C | T | 3 | a0001c0002t0010g0203a0002c0001t0004g0338a0002c0001t0004g0339 | 3 | HG03209.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5+2091C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711242 | ||||||
chr19:711334
|
G | A | 1 | a0001c0004t0003g0101 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.5+2183G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711334 | ||||||
chr19:711422
|
A | G | 1 | a0002c0001t0001g0238 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.5+2271A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711422 | ||||||
chr19:711541
|
T | C | 1 | a0002c0001t0002g0048 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.5+2390T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711541 | ||||||
chr19:711549
|
A | G | 1 | a0002c0001t0002g0082 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.5+2398A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711549 | ||||||
chr19:711637
|
C | A | 31 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0205others(28): Show | 33 | HG00642.hp2 HG00733.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.5+2486C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711637 | ||||||
chr19:711647
|
G | T | 2 | a0002c0001t0001g0044a0002c0001t0001g0099 | 2 | NA19088.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.5+2496G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711647 | ||||||
chr19:711750
|
A | G | 1 | a0001c0003t0006g0375 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5+2599A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711750 | ||||||
chr19:711753
|
G | A | 1 | a0002c0006t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5+2602G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711753 | ||||||
chr19:711817
|
T | C | 1 | a0001c0002t0004g0243 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.5+2666T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711817 | ||||||
chr19:711857
|
C | T | 1 | a0002c0001t0008g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.5+2706C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711857 | ||||||
chr19:711870
|
T | A | 1 | a0002c0009t0023g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5+2719T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711870 | ||||||
chr19:711871
|
C | A | 1 | a0002c0009t0023g0083 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.5+2720C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711871 | ||||||
chr19:711886
|
C | A | 3 | a0002c0001t0001g0003a0002c0001t0001g0354a0002c0001t0001g0355 | 5 | HG01167.hp2 HG01169.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+2735C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711886 | ||||||
chr19:711917
|
T | C | 3 | a0001c0002t0002g0268a0001c0003t0006g0241a0002c0001t0006g0095 | 3 | HG02895.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5+2766T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 711917 | ||||||
chr19:712045
|
C | CA | 13 | a0001c0002t0001g0357a0001c0003t0001g0358a0002c0001t0001g0003others(10): Show | 15 | HG00280.hp1 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+2895dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 712045 | |||||
chr19:712079
|
G | C | 41 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0205others(38): Show | 45 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.5+2928G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712079 | ||||||
chr19:712089
|
C | A | 1 | a0001c0002t0005g0334 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5+2938C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712089 | ||||||
chr19:712118
|
G | T | 65 | a0001c0002t0001g0028a0001c0002t0001g0299a0001c0002t0001g0302others(62): Show | 70 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.5+2967G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712118 | ||||||
chr19:712197
|
AT | A | 3 | a0001c0002t0002g0268a0001c0003t0006g0241a0002c0001t0006g0095 | 3 | HG02895.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5+3051delT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 712197 | |||||
chr19:712265
|
C | T | 3 | a0001c0002t0002g0268a0001c0003t0006g0241a0002c0001t0006g0095 | 3 | HG02895.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5+3114C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712265 | ||||||
chr19:712266
|
G | A | 1 | a0002c0001t0004g0124 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.5+3115G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712266 | ||||||
chr19:712275
|
G | C | 4 | a0001c0002t0001g0270a0001c0002t0004g0340a0002c0006t0006g0279others(1): Show | 4 | HG02109.hp2 HG03831.hp1 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+3124G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712275 | ||||||
chr19:712340
|
T | C | 162 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(159): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.5+3189T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712340 | ||||||
chr19:712351
|
C | T | 137 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0299others(134): Show | 146 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.5+3200C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712351 | ||||||
chr19:712476
|
T | C | 13 | a0001c0002t0001g0357a0001c0003t0001g0358a0002c0001t0001g0003others(10): Show | 15 | HG00280.hp1 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+3325T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712476 | ||||||
chr19:712504
|
C | A | 1 | a0002c0007t0004g0146 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.5+3353C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712504 | ||||||
chr19:712625
|
C | T | 6 | a0001c0002t0027g0047a0001c0003t0006g0118a0002c0001t0001g0046others(3): Show | 6 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+3474C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712625 | ||||||
chr19:712629
|
T | C | 158 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(155): Show | 169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.5+3478T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712629 | ||||||
chr19:712680
|
G | GT | 40 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0205others(37): Show | 45 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.5+3538dupT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 712680 | |||||
chr19:712707
|
T | G | 1 | a0002c0001t0001g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5+3556T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712707 | ||||||
chr19:712721
|
A | G | 1 | a0002c0001t0001g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.5+3570A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712721 | ||||||
chr19:712837
|
A | G | 1 | a0001c0002t0002g0201 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5+3686A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712837 | ||||||
chr19:712872
|
C | T | 149 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(146): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.5+3721C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712872 | ||||||
chr19:712960
|
G | T | 3 | a0001c0002t0002g0268a0001c0003t0006g0241a0002c0001t0006g0095 | 3 | HG02895.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5+3809G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 712960 | ||||||
chr19:713132
|
G | T | 75 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0011others(72): Show | 79 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.5+3981G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713132 | ||||||
chr19:713148
|
C | T | 167 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(164): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.5+3997C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713148 | ||||||
chr19:713175
|
G | GGC | 168 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(165): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.5+4026_5+4027dupCG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 713175 | |||||
chr19:713346
|
T | G | 6 | a0001c0002t0027g0047a0001c0003t0006g0118a0002c0001t0001g0046others(3): Show | 6 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+4195T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713346 | ||||||
chr19:713424
|
T | C | 6 | a0001c0002t0027g0047a0001c0003t0006g0118a0002c0001t0001g0046others(3): Show | 6 | HG01192.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5+4273T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713424 | ||||||
chr19:713441
|
A | G | 164 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(161): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.5+4290A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713441 | ||||||
chr19:713504
|
G | T | 1 | a0001c0002t0001g0270 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5+4353G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713504 | ||||||
chr19:713518
|
G | A | 355 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(352): Show | 374 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.5+4367G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713518 | ||||||
chr19:713524
|
T | C | 1 | a0001c0002t0012g0074 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5+4373T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713524 | ||||||
chr19:713530
|
G | A | 1 | a0001c0004t0003g0125 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.5+4379G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713530 | ||||||
chr19:713611
|
C | T | 1 | a0001c0002t0002g0011 | 2 | NA18990.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.5+4460C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713611 | ||||||
chr19:713680
|
G | C | 1 | a0001c0003t0001g0214 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5+4529G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713680 | ||||||
chr19:713682
|
G | A | 3 | a0001c0004t0003g0300a0002c0001t0001g0012a0002c0005t0003g0301 | 4 | NA18941.hp2 NA18973.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+4531G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713682 | ||||||
chr19:713770
|
C | T | 1 | a0001c0003t0014g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.5+4619C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713770 | ||||||
chr19:713772
|
G | A | 1 | a0002c0001t0002g0148 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.5+4621G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713772 | ||||||
chr19:713814
|
T | A | 1 | a0001c0003t0006g0346 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5+4663T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713814 | ||||||
chr19:713908
|
C | CT | 9 | a0001c0002t0001g0219a0001c0002t0002g0112a0001c0002t0004g0286others(6): Show | 9 | HG01261.hp1 HG01361.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5+4771dupT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 713908 | |||||
chr19:713908
|
CT | C | 126 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(123): Show | 136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.5+4771delT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 713908 | |||||
chr19:713912
|
T | C | 52 | a0001c0002t0002g0011a0001c0002t0004g0053a0001c0002t0004g0130others(49): Show | 56 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.5+4761T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713912 | ||||||
chr19:713916
|
T | C | 52 | a0001c0002t0002g0011a0001c0002t0004g0053a0001c0002t0004g0130others(49): Show | 56 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.5+4765T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713916 | ||||||
chr19:713978
|
C | T | 1 | a0001c0003t0001g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5+4827C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 713978 | ||||||
chr19:714121
|
G | A | 1 | a0002c0001t0002g0150 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5+4970G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714121 | ||||||
chr19:714171
|
C | G | 2 | a0001c0002t0002g0035a0001c0003t0006g0034 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5+5020C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714171 | ||||||
chr19:714234
|
T | G | 181 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(178): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.5+5083T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714234 | ||||||
chr19:714282
|
C | T | 180 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(177): Show | 193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.5+5131C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714282 | ||||||
chr19:714330
|
G | A | 3 | a0001c0002t0002g0268a0001c0003t0006g0241a0002c0001t0006g0095 | 3 | HG02895.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.5+5179G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714330 | ||||||
chr19:714358
|
C | CT | 54 | a0001c0002t0002g0011a0001c0002t0002g0331a0001c0002t0004g0053others(51): Show | 58 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.5+5225dupT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 714358 | |||||
chr19:714358
|
CT | C | 14 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0205others(11): Show | 15 | HG00642.hp2 HG01070.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+5225delT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 714358 | |||||
chr19:714412
|
G | A | 3 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0003t0006g0034 | 3 | HG01891.hp1 HG02572.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.5+5261G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714412 | ||||||
chr19:714419
|
C | G | 2 | a0002c0006t0006g0279a0002c0006t0006g0280 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.5+5268C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714419 | ||||||
chr19:714503
|
C | T | 41 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0183others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.5+5352C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714503 | ||||||
chr19:714507
|
C | T | 1 | a0002c0001t0002g0150 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.5+5356C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714507 | ||||||
chr19:714537
|
T | C | 1 | a0001c0002t0001g0302 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5+5386T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714537 | ||||||
chr19:714545
|
A | G | 4 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0025others(1): Show | 5 | HG02055.hp2 HG02258.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.5+5394A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714545 | ||||||
chr19:714716
|
C | T | 181 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(178): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.5+5565C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714716 | ||||||
chr19:714739
|
C | T | 181 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(178): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.5+5588C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714739 | ||||||
chr19:714751
|
G | A | 1 | a0002c0001t0001g0202 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.5+5600G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714751 | ||||||
chr19:714920
|
G | A | 53 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0032others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.5+5769G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714920 | ||||||
chr19:714936
|
T | C | 4 | a0001c0002t0007g0274a0001c0003t0014g0275a0002c0001t0007g0273others(1): Show | 4 | HG02630.hp1 HG02647.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+5785T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714936 | ||||||
chr19:714980
|
T | C | 10 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0006g0029others(7): Show | 10 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.5+5829T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 714980 | ||||||
chr19:715405
|
C | T | 2 | a0002c0001t0001g0333a0002c0001t0004g0284 | 2 | HG02056.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.5+6254C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715405 | ||||||
chr19:715607
|
G | C | 20 | a0001c0002t0001g0357a0001c0003t0001g0358a0002c0001t0001g0003others(17): Show | 22 | HG00280.hp1 HG01167.hp2 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.5+6456G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715607 | ||||||
chr19:715646
|
G | A | 3 | a0001c0003t0001g0180a0002c0001t0001g0068a0002c0001t0002g0150 | 3 | HG02735.hp1 HG03710.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.5+6495G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715646 | ||||||
chr19:715649
|
A | G | 1 | a0002c0001t0002g0179 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.5+6498A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715649 | ||||||
chr19:715656
|
G | A | 1 | a0002c0001t0020g0332 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.5+6505G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715656 | ||||||
chr19:715765
|
T | C | 237 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(234): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.5+6614T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715765 | ||||||
chr19:715780
|
C | G | 349 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(346): Show | 368 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.5+6629C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715780 | ||||||
chr19:715914
|
G | A | 1 | a0001c0002t0004g0144 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.5+6763G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715914 | ||||||
chr19:715924
|
G | C | 1 | a0001c0004t0003g0328 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.5+6773G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715924 | ||||||
chr19:715962
|
C | T | 2 | a0001c0002t0001g0009a0006c0013t0001g0080 | 3 | HG02965.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.5+6811C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 715962 | ||||||
chr19:716139
|
T | C | 181 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(178): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.5+6988T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716139 | ||||||
chr19:716149
|
C | T | 2 | a0001c0003t0001g0123a0001c0004t0003g0222 | 2 | HG02735.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.5+6998C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716149 | ||||||
chr19:716188
|
G | C | 181 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(178): Show | 194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.5+7037G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716188 | ||||||
chr19:716363
|
T | C | 14 | a0001c0002t0002g0015a0001c0002t0002g0353a0001c0002t0002g0365others(11): Show | 15 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.5+7212T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716363 | ||||||
chr19:716395
|
G | A | 1 | a0002c0001t0007g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5+7244G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716395 | ||||||
chr19:716411
|
C | CA | 90 | a0001c0002t0001g0234a0001c0002t0001g0256a0001c0002t0001g0299others(87): Show | 93 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.5+7275dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 716411 | |||||
chr19:716411
|
CA | C | 15 | a0001c0002t0005g0247a0001c0003t0001g0079a0001c0003t0001g0287others(12): Show | 15 | HG01070.hp1 HG01099.hp2 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+7275delA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 716411 | |||||
chr19:716627
|
C | G | 2 | a0002c0001t0001g0046a0002c0001t0001g0119 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.5+7476C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716627 | ||||||
chr19:716872
|
C | T | 2 | a0001c0002t0001g0200a0001c0003t0001g0236 | 2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5+7721C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716872 | ||||||
chr19:716880
|
A | G | 15 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0140others(12): Show | 15 | HG00609.hp1 HG02129.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+7729A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716880 | ||||||
chr19:716908
|
G | T | 1 | a0002c0001t0001g0093 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.5+7757G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 716908 | ||||||
chr19:717024
|
G | A | 18 | a0001c0002t0001g0357a0001c0003t0001g0358a0002c0001t0001g0003others(15): Show | 20 | HG00280.hp1 HG01167.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.5+7873G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717024 | ||||||
chr19:717077
|
G | A | 1 | a0001c0003t0001g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5+7926G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717077 | ||||||
chr19:717087
|
G | A | 7 | a0001c0002t0002g0014a0001c0002t0002g0059a0001c0002t0002g0225others(4): Show | 8 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+7936G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717087 | ||||||
chr19:717150
|
A | G | 238 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(235): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.5+7999A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717150 | ||||||
chr19:717185
|
C | T | 1 | a0002c0001t0002g0212 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5+8034C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717185 | ||||||
chr19:717289
|
C | T | 126 | a0001c0002t0001g0142a0001c0002t0001g0233a0001c0002t0001g0234others(123): Show | 130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.5+8138C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717289 | ||||||
chr19:717292
|
C | T | 1 | a0001c0004t0003g0098 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5+8141C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717292 | ||||||
chr19:717293
|
A | G | 15 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0140others(12): Show | 15 | HG00609.hp1 HG02129.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.5+8142A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717293 | ||||||
chr19:717398
|
C | T | 1 | a0001c0003t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.5+8247C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717398 | ||||||
chr19:717463
|
C | A | 15 | a0001c0002t0002g0015a0001c0002t0002g0353a0001c0002t0002g0365others(12): Show | 16 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.5+8312C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717463 | ||||||
chr19:717463
|
C | T | 2 | a0001c0002t0005g0326a0002c0005t0003g0345 | 2 | HG00597.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.5+8312C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717463 | ||||||
chr19:717486
|
T | C | 220 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(217): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.5+8335T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717486 | ||||||
chr19:717487
|
C | T | 1 | a0001c0003t0022g0037 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5+8336C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717487 | ||||||
chr19:717606
|
T | A | 1 | a0002c0005t0003g0181 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.5+8455T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717606 | ||||||
chr19:717664
|
G | A | 51 | a0001c0002t0002g0011a0001c0002t0004g0053a0001c0002t0004g0130others(48): Show | 55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.6-8474G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717664 | ||||||
chr19:717713
|
G | C | 1 | a0001c0003t0016g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6-8425G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717713 | ||||||
chr19:717725
|
A | G | 85 | a0001c0002t0001g0110a0001c0002t0001g0115a0001c0002t0001g0233others(82): Show | 89 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.6-8413A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717725 | ||||||
chr19:717743
|
A | G | 3 | a0001c0002t0004g0017a0001c0002t0004g0019a0001c0002t0004g0144 | 3 | HG00408.hp1 NA18941.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.6-8395A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717743 | ||||||
chr19:717803
|
C | G | 1 | a0001c0004t0003g0222 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.6-8335C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717803 | ||||||
chr19:717857
|
T | C | 2 | a0002c0001t0002g0285a0002c0005t0003g0288 | 2 | NA18965.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.6-8281T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 717857 | ||||||
chr19:718038
|
C | T | 1 | a0002c0001t0001g0056 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6-8100C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718038 | ||||||
chr19:718203
|
A | T | 53 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0032others(50): Show | 53 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.6-7935A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718203 | ||||||
chr19:718318
|
C | G | 1 | a0002c0001t0002g0041 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.6-7820C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718318 | ||||||
chr19:718338
|
T | C | 4 | a0001c0002t0001g0009a0001c0002t0002g0025a0001c0002t0010g0203others(1): Show | 5 | HG02965.hp1 HG03098.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-7800T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718338 | ||||||
chr19:718362
|
C | T | 1 | a0001c0002t0004g0255 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.6-7776C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718362 | ||||||
chr19:718514
|
C | G | 3 | a0002c0001t0001g0314a0002c0001t0009g0313a0002c0005t0029g0315 | 3 | HG00280.hp2 HG01975.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.6-7624C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718514 | ||||||
chr19:718515
|
G | A | 1 | a0001c0003t0006g0034 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.6-7623G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718515 | ||||||
chr19:718586
|
A | G | 74 | a0001c0002t0001g0142a0001c0002t0001g0233a0001c0002t0001g0318others(71): Show | 78 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.6-7552A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718586 | ||||||
chr19:718617
|
C | T | 87 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(84): Show | 94 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.6-7521C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718617 | ||||||
chr19:718645
|
G | A | 3 | a0001c0002t0007g0274a0002c0001t0007g0273a0002c0001t0007g0276 | 3 | HG02647.hp1 HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.6-7493G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718645 | ||||||
chr19:718757
|
A | AG | 75 | a0001c0002t0001g0142a0001c0002t0001g0233a0001c0002t0002g0011others(72): Show | 79 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.6-7379dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 718757 | |||||
chr19:718794
|
G | C | 74 | a0001c0002t0001g0142a0001c0002t0001g0233a0001c0002t0001g0318others(71): Show | 78 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.6-7344G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718794 | ||||||
chr19:718839
|
TGGGGCTT others(7): Show |
T | 1 | a0002c0001t0002g0177 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6-7288_6-7275delCT others(12): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 718839 | |||||
chr19:718958
|
A | T | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-7180A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 718958 | ||||||
chr19:719031
|
C | A | 3 | a0001c0002t0001g0260a0001c0003t0001g0123a0001c0003t0022g0037 | 3 | HG00733.hp2 HG00738.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.6-7107C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719031 | ||||||
chr19:719092
|
A | G | 1 | a0002c0005t0003g0194 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.6-7046A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719092 | ||||||
chr19:719130
|
G | A | 18 | a0001c0002t0001g0110a0001c0002t0001g0248a0001c0002t0001g0256others(15): Show | 18 | HG00544.hp1 HG00621.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.6-7008G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719130 | ||||||
chr19:719179
|
G | C | 7 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0003t0001g0033others(4): Show | 7 | HG01891.hp1 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-6959G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719179 | ||||||
chr19:719214
|
G | T | 8 | a0002c0001t0001g0297a0002c0001t0002g0008a0002c0001t0002g0057others(5): Show | 9 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-6924G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719214 | ||||||
chr19:719295
|
C | G | 41 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0183others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.6-6843C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719295 | ||||||
chr19:719322
|
C | T | 238 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(235): Show | 251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.6-6816C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719322 | ||||||
chr19:719529
|
A | G | 2 | a0001c0003t0006g0241a0002c0001t0006g0095 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.6-6609A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719529 | ||||||
chr19:719615
|
T | C | 208 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(205): Show | 219 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.6-6523T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719615 | ||||||
chr19:719684
|
G | A | 19 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0097others(16): Show | 19 | HG00609.hp1 HG00735.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.6-6454G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719684 | ||||||
chr19:719722
|
A | G | 6 | a0001c0002t0002g0025a0002c0001t0002g0022a0002c0001t0008g0023others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-6416A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719722 | ||||||
chr19:719764
|
C | A | 6 | a0001c0002t0002g0025a0002c0001t0002g0022a0002c0001t0008g0023others(3): Show | 6 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.6-6374C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719764 | ||||||
chr19:719785
|
TGAACGCC others(4): Show |
T | 1 | a0002c0001t0004g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.6-6349_6-6339delCG others(9): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 719785 | |||||
chr19:719802
|
C | T | 51 | a0001c0002t0001g0233a0001c0002t0002g0011a0001c0002t0004g0053others(48): Show | 55 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.6-6336C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719802 | ||||||
chr19:719809
|
G | T | 1 | a0002c0006t0021g0359 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.6-6329G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719809 | ||||||
chr19:719859
|
A | C | 41 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0183others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.6-6279A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719859 | ||||||
chr19:719870
|
G | T | 41 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0183others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.6-6268G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719870 | ||||||
chr19:719952
|
G | A | 1 | a0002c0001t0001g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6-6186G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719952 | ||||||
chr19:719992
|
G | C | 18 | a0001c0002t0001g0357a0001c0003t0001g0358a0002c0001t0001g0003others(15): Show | 20 | HG00280.hp1 HG01167.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.6-6146G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 719992 | ||||||
chr19:720041
|
GC | G | 18 | a0001c0002t0002g0005a0001c0002t0002g0015a0001c0002t0002g0027others(15): Show | 20 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.6-6091delC | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720041 | |||||
chr19:720062
|
G | T | 72 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(69): Show | 76 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.6-6076G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720062 | ||||||
chr19:720223
|
C | G | 1 | a0001c0003t0001g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6-5915C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720223 | ||||||
chr19:720301
|
C | T | 2 | a0002c0001t0001g0329a0002c0001t0013g0330 | 2 | HG01255.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.6-5837C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720301 | ||||||
chr19:720325
|
G | GAGGGGGG others(112): Show |
15 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0097others(12): Show | 15 | HG00609.hp1 HG00735.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.6-5771_6-5770insAT others(117): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720325 | |||||
chr19:720325
|
G | GAGGGGGG others(113): Show |
2 | a0001c0002t0005g0143a0002c0001t0002g0282 | 2 | HG01261.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.6-5806_6-5805insGC others(118): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720325 | |||||
chr19:720325
|
G | GAGGGGGG others(114): Show |
1 | a0001c0002t0005g0335 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.6-5806_6-5805insGC others(119): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720325 | |||||
chr19:720326
|
A | AG | 15 | a0001c0002t0001g0028a0001c0002t0004g0286a0001c0003t0001g0127others(12): Show | 15 | HG00438.hp2 HG01168.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.6-5806dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720326 | |||||
chr19:720326
|
A | AGGGGGGC others(113): Show |
1 | a0001c0002t0005g0106 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.6-5771_6-5770insAT others(118): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720326 | |||||
chr19:720356
|
AGGCGAGG others(21): Show |
A | 1 | a0002c0001t0001g0003 | 3 | HG01256.hp2 HG01258.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.6-5771_6-5744delCG others(26): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720356 | |||||
chr19:720372
|
A | AGGCCCGG others(112): Show |
46 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(43): Show | 50 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.6-5697_6-5696insAC others(117): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720372 | |||||
chr19:720372
|
A | G | 19 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0097others(16): Show | 19 | HG00609.hp1 HG00735.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.6-5766A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720372 | ||||||
chr19:720390
|
G | GGGGGGCG others(168): Show |
17 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0265others(14): Show | 19 | HG00733.hp1 HG01099.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.6-5694_6-5520dupAA others(173): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720390 | |||||
chr19:720405
|
T | TGGGGAGG others(84): Show |
1 | a0001c0004t0003g0322 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.6-5697_6-5696insAC others(89): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720405 | |||||
chr19:720417
|
A | AGGGGGGC others(114): Show |
1 | a0001c0004t0003g0139 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.6-5697_6-5696insAC others(119): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720417 | |||||
chr19:720442
|
G | A | 2 | a0001c0004t0003g0138a0001c0004t0003g0221 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.6-5696G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720442 | ||||||
chr19:720445
|
A | AG | 17 | a0001c0002t0001g0200a0001c0002t0004g0199a0001c0002t0004g0254others(14): Show | 17 | HG00735.hp2 HG01168.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.6-5687dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720445 | |||||
chr19:720445
|
A | AGGGGGGC others(170): Show |
1 | a0001c0003t0001g0031 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.6-5540_6-5539insGC others(175): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720445 | |||||
chr19:720445
|
A | AGGGGGGC others(113): Show |
2 | a0001c0004t0003g0138a0001c0004t0003g0221 | 2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.6-5651_6-5650insTC others(118): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720445 | |||||
chr19:720445
|
A | AGGGGGGG others(169): Show |
1 | a0001c0002t0001g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6-5687_6-5686insGC others(174): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720445 | |||||
chr19:720455
|
A | C | 44 | a0001c0002t0001g0009a0001c0002t0001g0234a0001c0002t0001g0299others(41): Show | 45 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.6-5683A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720455 | ||||||
chr19:720508
|
A | AGGGGGGC others(169): Show |
1 | a0001c0002t0001g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.6-5520_6-5519insAA others(174): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720508 | |||||
chr19:720520
|
G | T | 1 | a0001c0002t0004g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.6-5618G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720520 | ||||||
chr19:720527
|
G | A | 18 | a0001c0002t0002g0005a0001c0002t0002g0015a0001c0002t0002g0027others(15): Show | 20 | HG01243.hp1 HG01243.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.6-5611G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720527 | ||||||
chr19:720565
|
AGGGGGCG others(21): Show |
A | 1 | a0002c0005t0003g0182 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.6-5535_6-5508delGG others(26): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720565 | |||||
chr19:720592
|
A | AG | 12 | a0001c0002t0002g0112a0001c0002t0002g0257a0001c0002t0004g0019others(9): Show | 12 | HG00408.hp1 HG00673.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.6-5540dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720592 | |||||
chr19:720592
|
A | AGGGGGGC others(169): Show |
1 | a0001c0003t0001g0122 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6-5520_6-5519insAA others(174): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720592 | |||||
chr19:720620
|
A | AG | 10 | a0001c0002t0001g0028a0001c0002t0001g0256a0001c0002t0001g0337others(7): Show | 10 | HG00323.hp1 HG00621.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.6-5512dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720620 | |||||
chr19:720627
|
C | G | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-5511C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720627 | ||||||
chr19:720628
|
G | C | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-5510G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720628 | ||||||
chr19:720629
|
C | G | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-5509C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720629 | ||||||
chr19:720639
|
C | G | 190 | a0001c0002t0001g0009a0001c0002t0001g0028a0001c0002t0001g0142others(187): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.6-5499C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720639 | ||||||
chr19:720647
|
A | AG | 11 | a0001c0002t0001g0028a0001c0002t0004g0199a0001c0002t0012g0074others(8): Show | 11 | HG00741.hp1 HG01192.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.6-5485dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720647 | |||||
chr19:720692
|
CCG | C | 2 | a0001c0002t0002g0006a0001c0002t0002g0224 | 3 | HG02055.hp1 HG03139.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.6-5441_6-5440delCG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720692 | |||||
chr19:720709
|
G | T | 2 | a0001c0002t0001g0009a0006c0013t0001g0080 | 3 | HG02965.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.6-5429G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720709 | ||||||
chr19:720715
|
CT | C | 2 | a0001c0002t0002g0005a0001c0002t0002g0027 | 3 | HG02145.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.6-5422delT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720715 | ||||||
chr19:720761
|
A | G | 1 | a0001c0002t0001g0302 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6-5377A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720761 | ||||||
chr19:720768
|
A | AC | 4 | a0001c0002t0001g0219a0001c0003t0001g0218a0001c0004t0003g0086others(1): Show | 4 | HG01168.hp1 HG01361.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-5368dupC | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 720768 | |||||
chr19:720815
|
C | T | 1 | a0002c0001t0002g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.6-5323C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720815 | ||||||
chr19:720834
|
G | A | 12 | a0001c0002t0001g0009a0001c0002t0002g0032a0001c0002t0002g0035others(9): Show | 13 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-5304G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720834 | ||||||
chr19:720867
|
T | A | 1 | a0001c0002t0004g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.6-5271T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720867 | ||||||
chr19:720881
|
G | C | 2 | a0001c0002t0007g0020a0001c0003t0032g0021 | 2 | HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.6-5257G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720881 | ||||||
chr19:720933
|
G | T | 4 | a0001c0002t0001g0260a0001c0002t0010g0261a0001c0003t0001g0123others(1): Show | 4 | HG00733.hp2 HG00738.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-5205G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 720933 | ||||||
chr19:721080
|
G | A | 2 | a0001c0002t0002g0360a0001c0002t0002g0361 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.6-5058G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721080 | ||||||
chr19:721086
|
G | A | 1 | a0002c0006t0006g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6-5052G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721086 | ||||||
chr19:721168
|
G | C | 1 | a0002c0001t0001g0204 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.6-4970G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721168 | ||||||
chr19:721179
|
G | A | 1 | a0001c0002t0004g0018 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.6-4959G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721179 | ||||||
chr19:721194
|
G | T | 31 | a0001c0002t0001g0009a0001c0002t0001g0357a0001c0002t0002g0032others(28): Show | 34 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(31): Show |
intron_variant | MODIFIER | c.6-4944G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721194 | ||||||
chr19:721270
|
A | G | 2 | a0002c0005t0003g0311a0002c0005t0003g0316 | 2 | NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.6-4868A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721270 | ||||||
chr19:721304
|
C | T | 1 | a0002c0001t0001g0012 | 2 | NA18941.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.6-4834C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721304 | ||||||
chr19:721357
|
C | T | 135 | a0001c0002t0001g0060a0001c0002t0001g0110a0001c0002t0001g0115others(132): Show | 140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.6-4781C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721357 | ||||||
chr19:721857
|
C | CA | 39 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0183others(36): Show | 39 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.6-4278dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 721857 | |||||
chr19:721890
|
A | G | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-4248A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721890 | ||||||
chr19:721909
|
A | T | 17 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0097others(14): Show | 17 | HG00735.hp1 HG01261.hp2 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.6-4229A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721909 | ||||||
chr19:721948
|
T | C | 5 | a0002c0001t0002g0022a0002c0001t0006g0095a0002c0001t0008g0023others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-4190T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 721948 | ||||||
chr19:722009
|
T | C | 5 | a0001c0002t0002g0005a0001c0002t0002g0027a0002c0006t0001g0049others(2): Show | 6 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-4129T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722009 | ||||||
chr19:722044
|
G | A | 1 | a0001c0002t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6-4094G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722044 | ||||||
chr19:722064
|
A | G | 67 | a0001c0002t0001g0009a0001c0002t0001g0234a0001c0002t0001g0299others(64): Show | 70 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.6-4074A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722064 | ||||||
chr19:722074
|
A | G | 83 | a0001c0002t0001g0234a0001c0002t0001g0270a0001c0002t0001g0299others(80): Show | 88 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.6-4064A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722074 | ||||||
chr19:722104
|
G | T | 1 | a0002c0001t0002g0048 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6-4034G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722104 | ||||||
chr19:722110
|
G | A | 356 | a0001c0002t0001g0009a0001c0002t0001g0028a0001c0002t0001g0060others(353): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.6-4028G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722110 | ||||||
chr19:722119
|
C | T | 1 | a0002c0005t0003g0345 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.6-4019C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722119 | ||||||
chr19:722129
|
A | G | 5 | a0002c0001t0002g0022a0002c0001t0006g0095a0002c0001t0008g0023others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-4009A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722129 | ||||||
chr19:722131
|
G | C | 296 | a0001c0002t0001g0028a0001c0002t0001g0060a0001c0002t0001g0110others(293): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.6-4007G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722131 | ||||||
chr19:722160
|
C | T | 1 | a0002c0001t0001g0091 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.6-3978C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722160 | ||||||
chr19:722161
|
G | A | 105 | a0001c0002t0001g0060a0001c0002t0001g0110a0001c0002t0001g0115others(102): Show | 109 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.6-3977G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722161 | ||||||
chr19:722161
|
G | C | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-3977G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722161 | ||||||
chr19:722162
|
C | T | 1 | a0002c0001t0002g0324 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.6-3976C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722162 | ||||||
chr19:722164
|
C | T | 1 | a0001c0002t0004g0019 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6-3974C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722164 | ||||||
chr19:722165
|
G | A | 243 | a0001c0002t0001g0009a0001c0002t0001g0028a0001c0002t0001g0142others(240): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.6-3973G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722165 | ||||||
chr19:722169
|
C | T | 239 | a0001c0002t0001g0009a0001c0002t0001g0028a0001c0002t0001g0142others(236): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.6-3969C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722169 | ||||||
chr19:722170
|
G | A | 106 | a0001c0002t0001g0060a0001c0002t0001g0110a0001c0002t0001g0115others(103): Show | 110 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.6-3968G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722170 | ||||||
chr19:722177
|
C | G | 2 | a0001c0002t0001g0142a0001c0002t0005g0141 | 2 | NA18960.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.6-3961C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722177 | ||||||
chr19:722206
|
G | C | 4 | a0001c0002t0004g0017a0001c0002t0004g0018a0001c0002t0004g0019others(1): Show | 4 | HG00408.hp1 HG02071.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-3932G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722206 | ||||||
chr19:722210
|
A | G | 4 | a0001c0002t0004g0017a0001c0002t0004g0018a0001c0002t0004g0019others(1): Show | 4 | HG00408.hp1 HG02071.hp2 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.6-3928A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722210 | ||||||
chr19:722528
|
C | T | 77 | a0001c0002t0001g0110a0001c0002t0001g0115a0001c0002t0001g0256others(74): Show | 81 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.6-3610C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722528 | ||||||
chr19:722578
|
A | T | 2 | a0001c0004t0003g0320a0001c0004t0003g0321 | 2 | NA18959.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.6-3560A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722578 | ||||||
chr19:722651
|
G | T | 1 | a0001c0002t0015g0242 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6-3487G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722651 | ||||||
chr19:722685
|
A | G | 1 | a0001c0002t0004g0298 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.6-3453A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722685 | ||||||
chr19:722741
|
G | C | 2 | a0002c0006t0006g0279a0002c0006t0006g0280 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.6-3397G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722741 | ||||||
chr19:722939
|
G | A | 1 | a0002c0001t0009g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.6-3199G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 722939 | ||||||
chr19:723004
|
A | C | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-3134A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723004 | ||||||
chr19:723026
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.6-3112C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723026 | ||||||
chr19:723051
|
T | G | 1 | a0002c0005t0003g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.6-3087T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723051 | ||||||
chr19:723064
|
C | T | 171 | a0001c0002t0001g0060a0001c0002t0001g0110a0001c0002t0001g0115others(168): Show | 178 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.6-3074C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723064 | ||||||
chr19:723076
|
C | T | 7 | a0001c0002t0001g0142a0001c0002t0004g0243a0001c0002t0005g0141others(4): Show | 7 | HG02155.hp1 NA18943.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-3062C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723076 | ||||||
chr19:723100
|
C | G | 58 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0005others(55): Show | 60 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.6-3038C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723100 | ||||||
chr19:723205
|
G | A | 46 | a0001c0002t0001g0028a0001c0002t0001g0337a0001c0002t0002g0004others(43): Show | 49 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(46): Show |
intron_variant | MODIFIER | c.6-2933G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723205 | ||||||
chr19:723477
|
G | A | 4 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0003t0016g0271others(1): Show | 5 | HG02055.hp2 HG02451.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-2661G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723477 | ||||||
chr19:723518
|
G | T | 1 | a0001c0003t0014g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.6-2620G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723518 | ||||||
chr19:723600
|
T | G | 1 | a0001c0004t0003g0129 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.6-2538T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723600 | ||||||
chr19:723649
|
C | CG | 305 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(302): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.6-2488dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 723649 | |||||
chr19:723780
|
C | T | 2 | a0001c0002t0008g0371a0001c0002t0010g0203 | 2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.6-2358C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723780 | ||||||
chr19:723791
|
C | T | 5 | a0002c0001t0002g0022a0002c0001t0006g0095a0002c0001t0008g0023others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.6-2347C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723791 | ||||||
chr19:723838
|
C | T | 1 | a0002c0001t0002g0171 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.6-2300C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723838 | ||||||
chr19:723842
|
C | T | 1 | a0002c0005t0003g0345 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.6-2296C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723842 | ||||||
chr19:723847
|
C | T | 1 | a0002c0001t0002g0192 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.6-2291C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 723847 | ||||||
chr19:724025
|
TGGGGTG | T | 55 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0001g0302others(52): Show | 59 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.6-2106_6-2101delGG others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 724025 | |||||
chr19:724108
|
T | TG | 12 | a0001c0002t0001g0009a0001c0002t0002g0014a0001c0002t0002g0059others(9): Show | 14 | HG01884.hp2 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.6-2029dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr19 | 724108 | |||||
chr19:724155
|
C | T | 1 | a0002c0001t0002g0048 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6-1983C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 724155 | ||||||
chr19:724299
|
A | G | 232 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(229): Show | 243 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.6-1839A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 724299 | ||||||
chr19:724617
|
G | A | 19 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0005others(16): Show | 20 | HG00735.hp1 HG01516.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.6-1521G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 724617 | ||||||
chr19:724622
|
T | A | 166 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(163): Show | 173 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.6-1516T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 724622 | ||||||
chr19:724720
|
A | T | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6-1418A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 724720 | ||||||
chr19:724873
|
C | T | 1 | a0001c0002t0001g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.6-1265C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 724873 | ||||||
chr19:724903
|
C | A | 11 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0006g0029others(8): Show | 11 | HG01074.hp2 HG01891.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.6-1235C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 724903 | ||||||
chr19:725066
|
G | A | 13 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0140others(10): Show | 13 | HG02129.hp2 HG02155.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-1072G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725066 | ||||||
chr19:725168
|
C | T | 62 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(59): Show | 66 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.6-970C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725168 | ||||||
chr19:725296
|
C | T | 10 | a0001c0002t0005g0247a0002c0001t0002g0022a0002c0001t0002g0082others(7): Show | 10 | HG01109.hp1 HG01433.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.6-842C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725296 | ||||||
chr19:725367
|
T | C | 2 | a0001c0002t0001g0028a0001c0002t0002g0004 | 3 | HG02055.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.6-771T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725367 | ||||||
chr19:725434
|
A | G | 1 | a0001c0002t0005g0106 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.6-704A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725434 | ||||||
chr19:725458
|
A | G | 282 | a0001c0002t0001g0028a0001c0002t0001g0115a0001c0002t0001g0142others(279): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.6-680A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725458 | ||||||
chr19:725459
|
G | C | 13 | a0001c0002t0001g0142a0001c0002t0001g0318a0001c0002t0002g0140others(10): Show | 13 | HG02129.hp2 HG02155.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.6-679G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725459 | ||||||
chr19:725492
|
C | T | 1 | a0002c0001t0001g0319 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.6-646C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725492 | ||||||
chr19:725558
|
G | C | 278 | a0001c0002t0001g0115a0001c0002t0001g0142a0001c0002t0001g0233others(275): Show | 290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.6-580G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725558 | ||||||
chr19:725772
|
G | A | 8 | a0001c0002t0001g0110a0001c0002t0001g0256a0001c0002t0002g0107others(5): Show | 8 | HG00544.hp1 HG00621.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-366G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725772 | ||||||
chr19:725867
|
C | T | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6-271C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725867 | ||||||
chr19:725876
|
C | G | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6-262C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725876 | ||||||
chr19:725937
|
C | T | 1 | a0002c0001t0001g0169 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6-201C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725937 | ||||||
chr19:725939
|
C | T | 202 | a0001c0002t0001g0115a0001c0002t0001g0234a0001c0002t0001g0299others(199): Show | 209 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.6-199C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 725939 | ||||||
chr19:726043
|
A | T | 1 | a0004c0012t0001g0364 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.6-95A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 726043 | ||||||
chr19:726069
|
G | T | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.6-69G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 726069 | ||||||
chr19:726078
|
C | T | 1 | a0001c0002t0004g0243 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.6-60C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 726078 | ||||||
chr19:726088
|
G | A | 1 | a0001c0002t0010g0030 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.6-50G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 726088 | ||||||
chr19:726098
|
G | T | 62 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0005others(59): Show | 64 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.6-40G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 1/8 | chr19 | 726098 | ||||||
chr19:726200
|
G | A | 16 | a0001c0002t0002g0006a0001c0002t0002g0032a0001c0002t0002g0035others(13): Show | 17 | HG01074.hp2 HG01891.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.57+11G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726200 | ||||||
chr19:726236
|
G | A | 1 | a0002c0005t0003g0244 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.57+47G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726236 | ||||||
chr19:726346
|
A | G | 4 | a0002c0005t0003g0304a0002c0005t0003g0310a0002c0005t0003g0311others(1): Show | 4 | NA18966.hp2 NA18983.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+157A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726346 | ||||||
chr19:726482
|
G | A | 73 | a0001c0002t0001g0234a0001c0002t0001g0299a0001c0002t0002g0005others(70): Show | 75 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.57+293G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726482 | ||||||
chr19:726748
|
C | T | 8 | a0001c0002t0001g0265a0001c0002t0002g0262a0001c0002t0002g0264others(5): Show | 8 | HG02451.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-260C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726748 | ||||||
chr19:726754
|
T | C | 1 | a0002c0005t0003g0310 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.58-254T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726754 | ||||||
chr19:726778
|
C | G | 1 | a0001c0003t0001g0381 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.58-230C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726778 | ||||||
chr19:726832
|
G | A | 73 | a0001c0002t0002g0025a0001c0002t0004g0164a0001c0002t0004g0340others(70): Show | 76 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.58-176G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726832 | ||||||
chr19:726862
|
C | T | 1 | a0001c0004t0028g0135 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.58-146C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726862 | ||||||
chr19:726884
|
C | T | 11 | a0002c0001t0001g0204a0002c0001t0001g0291a0002c0001t0001g0292others(8): Show | 11 | HG00323.hp2 HG01168.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-124C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726884 | ||||||
chr19:726910
|
G | A | 80 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0004g0164others(77): Show | 84 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.58-98G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726910 | ||||||
chr19:726963
|
G | A | 2 | a0002c0001t0002g0061a0002c0001t0002g0066 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.58-45G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726963 | ||||||
chr19:726974
|
G | A | 1 | a0001c0003t0002g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.58-34G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 2/8 | chr19 | 726974 | ||||||
chr19:727097
|
G | A | 3 | a0001c0004t0003g0007a0001c0004t0003g0320a0001c0004t0003g0321 | 4 | NA18959.hp2 NA18971.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+9G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727097 | ||||||
chr19:727105
|
G | A | 53 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(50): Show | 56 | HG00544.hp1 HG00621.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.138+17G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727105 | ||||||
chr19:727128
|
C | T | 1 | a0001c0002t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.138+40C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727128 | ||||||
chr19:727139
|
C | T | 1 | a0001c0002t0002g0103 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.138+51C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727139 | ||||||
chr19:727149
|
G | A | 1 | a0002c0009t0001g0290 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.138+61G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727149 | ||||||
chr19:727167
|
G | T | 1 | a0001c0004t0003g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.138+79G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727167 | ||||||
chr19:727181
|
T | TCCCAACC others(105): Show |
2 | a0001c0002t0004g0130a0001c0004t0003g0336 | 2 | HG02132.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.138+137_138+138ins others(112): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 727181 | |||||
chr19:727225
|
C | CAACCCT | 220 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(217): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.138+137_138+138ins others(6): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727225 | ||||||
chr19:727226
|
G | A | 11 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0006others(8): Show | 13 | HG01074.hp2 HG01109.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+138G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727226 | ||||||
chr19:727237
|
C | CGACCCCG others(5): Show |
4 | a0001c0002t0001g0219a0001c0002t0002g0006a0001c0002t0002g0224others(1): Show | 5 | HG01361.hp2 HG01978.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+160_138+161ins others(12): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 727237 | |||||
chr19:727237
|
C | CGACCCT | 220 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(217): Show | 228 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.138+154_138+155ins others(6): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 727237 | |||||
chr19:727237
|
C | T | 8 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0010g0030others(5): Show | 9 | HG01074.hp2 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.138+149C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727237 | ||||||
chr19:727238
|
G | A | 50 | a0001c0002t0001g0142a0001c0002t0001g0233a0001c0002t0001g0248others(47): Show | 53 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.138+150G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727238 | ||||||
chr19:727243
|
C | CGACCCTG others(10): Show |
1 | a0001c0002t0002g0004 | 2 | HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.138+160_138+161ins others(17): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 727243 | |||||
chr19:727243
|
C | CGACCCTG others(5): Show |
2 | a0001c0002t0001g0028a0001c0002t0010g0030 | 2 | HG01074.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.138+160_138+161ins others(12): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr19 | 727243 | |||||
chr19:727249
|
C | T | 2 | a0002c0001t0001g0291a0002c0001t0001g0292 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.138+161C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727249 | ||||||
chr19:727262
|
A | G | 24 | a0001c0002t0002g0011a0001c0003t0001g0054a0001c0003t0001g0105others(21): Show | 26 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.138+174A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727262 | ||||||
chr19:727310
|
C | A | 279 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(276): Show | 292 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.138+222C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727310 | ||||||
chr19:727401
|
C | G | 37 | a0001c0002t0001g0337a0001c0003t0001g0287a0002c0001t0001g0012others(34): Show | 38 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(35): Show |
intron_variant | MODIFIER | c.139-163C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727401 | ||||||
chr19:727418
|
C | T | 1 | a0001c0002t0002g0112 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139-146C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727418 | ||||||
chr19:727448
|
C | A | 57 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(54): Show | 62 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.139-116C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727448 | ||||||
chr19:727475
|
G | A | 5 | a0002c0001t0002g0022a0002c0001t0006g0095a0002c0001t0008g0023others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-89G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727475 | ||||||
chr19:727544
|
C | G | 139 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(136): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.139-20C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727544 | ||||||
chr19:727550
|
T | C | 134 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(131): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.139-14T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727550 | ||||||
chr19:727552
|
C | T | 134 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(131): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.139-12C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 3/8 | chr19 | 727552 | ||||||
chr19:727754
|
C | T | 28 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0149others(25): Show | 31 | HG00642.hp2 HG00733.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.269+60C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 727754 | ||||||
chr19:727803
|
C | T | 1 | a0002c0001t0001g0348 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.269+109C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 727803 | ||||||
chr19:727919
|
G | A | 1 | a0002c0001t0002g0022 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.269+225G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 727919 | ||||||
chr19:727986
|
GCGTCGAG others(37): Show |
G | 126 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(123): Show | 135 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.269+303_269+346del others(44): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 727986 | |||||
chr19:727997
|
C | G | 1 | a0001c0002t0031g0258 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.269+303C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 727997 | ||||||
chr19:727997
|
CTGGGTCC others(37): Show |
C | 2 | a0001c0002t0001g0009a0001c0003t0001g0381 | 3 | HG03209.hp1 HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.269+321_269+364del others(44): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 727997 | |||||
chr19:728035
|
G | A | 1 | a0001c0002t0002g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.269+341G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728035 | ||||||
chr19:728043
|
G | A | 1 | a0001c0002t0027g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.269+349G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728043 | ||||||
chr19:728095
|
C | T | 51 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(48): Show | 56 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.269+401C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728095 | ||||||
chr19:728132
|
G | A | 1 | a0005c0011t0001g0308 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.269+438G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728132 | ||||||
chr19:728173
|
G | A | 1 | a0001c0014t0001g0382 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.269+479G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728173 | ||||||
chr19:728177
|
G | A | 1 | a0001c0002t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.269+483G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728177 | ||||||
chr19:728220
|
G | A | 14 | a0001c0002t0004g0017a0001c0002t0004g0018a0001c0002t0004g0019others(11): Show | 14 | HG00408.hp1 HG00597.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.269+526G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728220 | ||||||
chr19:728236
|
G | A | 5 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0007g0020others(2): Show | 6 | HG01884.hp2 HG02055.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.269+542G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728236 | ||||||
chr19:728310
|
G | A | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.269+616G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728310 | ||||||
chr19:728398
|
C | G | 16 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0270others(13): Show | 16 | HG00741.hp2 HG02083.hp2 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.269+704C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728398 | ||||||
chr19:728416
|
C | T | 135 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(132): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.269+722C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728416 | ||||||
chr19:728450
|
T | A | 1 | a0001c0004t0024g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.269+756T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728450 | ||||||
chr19:728469
|
G | A | 168 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(165): Show | 179 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.269+775G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728469 | ||||||
chr19:728470
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.269+776T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728470 | ||||||
chr19:728476
|
G | T | 164 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(161): Show | 175 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.269+782G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728476 | ||||||
chr19:728536
|
G | A | 1 | a0002c0005t0003g0235 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.269+842G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728536 | ||||||
chr19:728626
|
C | T | 117 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(114): Show | 124 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.269+932C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728626 | ||||||
chr19:728628
|
T | C | 171 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(168): Show | 183 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.269+934T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728628 | ||||||
chr19:728726
|
A | G | 12 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(9): Show | 13 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.269+1032A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728726 | ||||||
chr19:728731
|
C | T | 3 | a0001c0004t0003g0007a0001c0004t0003g0320a0001c0004t0003g0321 | 4 | NA18959.hp2 NA18971.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+1037C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728731 | ||||||
chr19:728746
|
G | A | 7 | a0001c0002t0001g0149a0001c0002t0002g0351a0001c0002t0004g0013others(4): Show | 8 | HG00733.hp1 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.269+1052G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728746 | ||||||
chr19:728799
|
C | T | 111 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(108): Show | 117 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.269+1105C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728799 | ||||||
chr19:728810
|
T | C | 6 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(3): Show | 7 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.269+1116T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728810 | ||||||
chr19:728872
|
C | T | 2 | a0001c0002t0005g0220a0001c0002t0005g0334 | 2 | HG02602.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.269+1178C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728872 | ||||||
chr19:728879
|
C | T | 42 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0015g0242others(39): Show | 43 | HG00423.hp1 HG01891.hp1 HG01975.hp2 others(40): Show |
intron_variant | MODIFIER | c.269+1185C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728879 | ||||||
chr19:728963
|
C | T | 4 | a0001c0003t0001g0026a0001c0003t0001g0369a0001c0003t0001g0370others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+1269C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728963 | ||||||
chr19:728983
|
A | G | 232 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(229): Show | 245 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.269+1289A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 728983 | ||||||
chr19:729027
|
A | G | 2 | a0002c0001t0001g0291a0002c0001t0001g0292 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.269+1333A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729027 | ||||||
chr19:729037
|
G | A | 2 | a0002c0006t0006g0279a0002c0006t0006g0280 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.269+1343G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729037 | ||||||
chr19:729049
|
C | T | 230 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(227): Show | 243 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.269+1355C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729049 | ||||||
chr19:729089
|
G | A | 54 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(51): Show | 59 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.269+1395G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729089 | ||||||
chr19:729180
|
AG | A | 190 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(187): Show | 202 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.269+1488delG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729180 | |||||
chr19:729292
|
C | A | 1 | a0002c0001t0002g0041 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.269+1598C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729292 | ||||||
chr19:729385
|
C | T | 1 | a0001c0003t0002g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.269+1691C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729385 | ||||||
chr19:729455
|
C | T | 125 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(122): Show | 132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.270-1640C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729455 | ||||||
chr19:729458
|
C | CT | 51 | a0001c0002t0001g0149a0001c0002t0001g0256a0001c0002t0001g0302others(48): Show | 53 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.270-1612dupT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729458 | |||||
chr19:729458
|
C | CTT | 21 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0270others(18): Show | 21 | HG02055.hp2 HG02083.hp2 HG02129.hp2 others(18): Show |
intron_variant | MODIFIER | c.270-1613_270-1612d others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729458 | |||||
chr19:729458
|
CT | C | 72 | a0001c0002t0001g0265a0001c0002t0004g0144a0001c0003t0001g0218others(69): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.270-1612delT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729458 | |||||
chr19:729458
|
CTTTTTTT others(3): Show |
C | 11 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0007g0020others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.270-1621_270-1612d others(12): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729458 | |||||
chr19:729458
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.270-1622_270-1612d others(13): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729458 | |||||
chr19:729481
|
T | TTG | 45 | a0001c0002t0001g0233a0001c0002t0002g0011a0001c0002t0004g0111others(42): Show | 50 | HG00408.hp2 HG00597.hp1 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.270-1613_270-1612i others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729481 | |||||
chr19:729481
|
T | TTTG | 7 | a0001c0002t0001g0248a0001c0002t0005g0193a0001c0004t0003g0086others(4): Show | 7 | HG01981.hp2 HG02027.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.270-1613_270-1611d others(5): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr19 | 729481 | |||||
chr19:729517
|
G | C | 3 | a0002c0001t0001g0314a0002c0001t0001g0352a0002c0001t0009g0313 | 3 | HG00280.hp2 HG01192.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.270-1578G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729517 | ||||||
chr19:729567
|
G | A | 194 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(191): Show | 206 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.270-1528G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729567 | ||||||
chr19:729586
|
C | T | 1 | a0002c0001t0002g0175 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.270-1509C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729586 | ||||||
chr19:729684
|
A | G | 1 | a0002c0001t0001g0012 | 2 | NA18941.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.270-1411A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729684 | ||||||
chr19:729728
|
C | T | 17 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0270others(14): Show | 17 | HG00741.hp2 HG02083.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.270-1367C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729728 | ||||||
chr19:729756
|
C | T | 2 | a0001c0002t0001g0219a0001c0003t0001g0214 | 2 | HG00639.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.270-1339C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729756 | ||||||
chr19:729850
|
G | T | 17 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0270others(14): Show | 17 | HG00741.hp2 HG02083.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.270-1245G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729850 | ||||||
chr19:729953
|
G | A | 1 | a0001c0004t0003g0322 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.270-1142G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 729953 | ||||||
chr19:730030
|
T | C | 195 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(192): Show | 207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.270-1065T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730030 | ||||||
chr19:730052
|
G | A | 36 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(33): Show | 37 | HG00423.hp1 HG01975.hp2 HG02056.hp1 others(34): Show |
intron_variant | MODIFIER | c.270-1043G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730052 | ||||||
chr19:730160
|
C | G | 1 | a0002c0001t0002g0162 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.270-935C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730160 | ||||||
chr19:730206
|
G | A | 1 | a0001c0004t0024g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.270-889G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730206 | ||||||
chr19:730206
|
G | GA | 194 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(191): Show | 206 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.270-889_270-888ins others(1): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730206 | ||||||
chr19:730235
|
A | G | 195 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(192): Show | 207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.270-860A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730235 | ||||||
chr19:730273
|
C | G | 125 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(122): Show | 132 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.270-822C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730273 | ||||||
chr19:730297
|
G | A | 195 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(192): Show | 207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.270-798G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730297 | ||||||
chr19:730343
|
C | T | 1 | a0001c0002t0002g0059 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.270-752C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730343 | ||||||
chr19:730369
|
C | T | 1 | a0001c0002t0013g0379 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.270-726C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730369 | ||||||
chr19:730603
|
C | T | 1 | a0006c0013t0001g0080 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.270-492C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 730603 | ||||||
chr19:731055
|
G | C | 195 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(192): Show | 207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.270-40G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 731055 | ||||||
chr19:731077
|
G | C | 195 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(192): Show | 207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.270-18G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 731077 | ||||||
chr19:731078
|
G | T | 195 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(192): Show | 207 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.270-17G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 4/8 | chr19 | 731078 | ||||||
chr19:731337
|
A | C | 3 | a0001c0003t0001g0052a0001c0003t0001g0325a0003c0015t0001g0134 | 3 | NA18960.hp2 NA19056.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.420+92A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731337 | ||||||
chr19:731382
|
C | G | 12 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(9): Show | 13 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.420+137C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731382 | ||||||
chr19:731384
|
G | A | 189 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(186): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.420+139G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731384 | ||||||
chr19:731386
|
A | G | 83 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(80): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.420+141A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731386 | ||||||
chr19:731484
|
G | A | 189 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(186): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.420+239G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731484 | ||||||
chr19:731542
|
G | A | 189 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(186): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.420+297G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731542 | ||||||
chr19:731563
|
A | G | 136 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0006others(133): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.420+318A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731563 | ||||||
chr19:731573
|
A | ATCAGAAG others(33): Show |
1 | a0001c0003t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.420+346_420+385dup others(40): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 731573 | |||||
chr19:731573
|
A | G | 124 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(121): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.420+328A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731573 | ||||||
chr19:731582
|
G | A | 1 | a0001c0002t0002g0025 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.420+337G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731582 | ||||||
chr19:731582
|
G | T | 12 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(9): Show | 13 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.420+337G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731582 | ||||||
chr19:731590
|
A | AAGCAGGA others(75): Show |
1 | a0001c0002t0002g0025 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.420+357_420+358ins others(82): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 731590 | |||||
chr19:731590
|
A | AAGCAGGA others(117): Show |
1 | a0001c0002t0001g0357 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.420+357_420+358ins others(124): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 731590 | |||||
chr19:731590
|
A | AAGCAGGA others(35): Show |
130 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(127): Show | 136 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.420+357_420+358ins others(42): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 731590 | |||||
chr19:731590
|
A | AAGCAGGA others(77): Show |
2 | a0001c0002t0004g0254a0001c0002t0004g0259 | 2 | HG00735.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.420+357_420+358ins others(84): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 731590 | |||||
chr19:731590
|
A | AAGCAGGA others(35): Show |
1 | a0002c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.420+359_420+400dup others(42): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 731590 | |||||
chr19:731590
|
A | AGC | 13 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(10): Show | 14 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.420+345_420+346ins others(2): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731590 | ||||||
chr19:731590
|
A | AGCAGCAG others(37): Show |
124 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(121): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.420+345_420+346ins others(44): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731590 | ||||||
chr19:731603
|
G | A | 53 | a0001c0002t0001g0233a0001c0002t0001g0248a0001c0002t0002g0011others(50): Show | 58 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.420+358G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731603 | ||||||
chr19:731613
|
G | A | 1 | a0001c0003t0001g0033 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.420+368G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731613 | ||||||
chr19:731699
|
C | A | 69 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0248others(66): Show | 74 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.420+454C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 731699 | ||||||
chr19:732008
|
T | A | 2 | a0002c0005t0003g0344a0002c0005t0019g0176 | 2 | NA18967.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.420+763T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732008 | ||||||
chr19:732029
|
T | C | 2 | a0002c0001t0002g0061a0002c0001t0002g0066 | 2 | HG02027.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.420+784T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732029 | ||||||
chr19:732042
|
T | C | 2 | a0001c0002t0002g0025a0001c0016t0001g0349 | 2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.420+797T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732042 | ||||||
chr19:732080
|
G | A | 1 | a0002c0001t0030g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.420+835G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732080 | ||||||
chr19:732123
|
C | T | 17 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0270others(14): Show | 17 | HG00741.hp2 HG02083.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.420+878C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732123 | ||||||
chr19:732228
|
T | C | 1 | a0001c0002t0007g0274 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.420+983T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732228 | ||||||
chr19:732442
|
C | T | 1 | a0002c0001t0001g0152 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.420+1197C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732442 | ||||||
chr19:732475
|
A | T | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.420+1230A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732475 | ||||||
chr19:732621
|
G | C | 1 | a0002c0001t0002g0184 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.420+1376G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732621 | ||||||
chr19:732675
|
C | T | 1 | a0002c0001t0030g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.420+1430C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732675 | ||||||
chr19:732764
|
T | A | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.421-1409T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732764 | ||||||
chr19:732797
|
G | A | 1 | a0002c0005t0003g0147 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.421-1376G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732797 | ||||||
chr19:732800
|
G | C | 1 | a0002c0001t0002g0150 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.421-1373G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732800 | ||||||
chr19:732880
|
T | C | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.421-1293T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 732880 | ||||||
chr19:732939
|
G | GT | 16 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(13): Show | 17 | HG01099.hp1 HG01192.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-1223dupT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 732939 | |||||
chr19:732939
|
GT | G | 51 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(48): Show | 56 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.421-1223delT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr19 | 732939 | |||||
chr19:733076
|
G | A | 1 | a0001c0003t0001g0266 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.421-1097G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733076 | ||||||
chr19:733090
|
C | A | 2 | a0001c0002t0004g0254a0001c0002t0004g0259 | 2 | HG00735.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.421-1083C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733090 | ||||||
chr19:733173
|
G | A | 17 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0270others(14): Show | 17 | HG00741.hp2 HG02083.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.421-1000G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733173 | ||||||
chr19:733245
|
G | A | 2 | a0002c0006t0006g0279a0002c0006t0006g0280 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.421-928G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733245 | ||||||
chr19:733426
|
T | C | 34 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(31): Show | 35 | HG00423.hp1 HG01975.hp2 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.421-747T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733426 | ||||||
chr19:733496
|
G | T | 1 | a0002c0001t0002g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.421-677G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733496 | ||||||
chr19:733634
|
G | A | 11 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(8): Show | 12 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-539G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733634 | ||||||
chr19:733656
|
G | A | 1 | a0005c0011t0001g0308 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.421-517G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733656 | ||||||
chr19:733671
|
G | T | 1 | a0002c0001t0008g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.421-502G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733671 | ||||||
chr19:733674
|
G | A | 152 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(149): Show | 159 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.421-499G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733674 | ||||||
chr19:733708
|
G | C | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.421-465G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733708 | ||||||
chr19:733713
|
C | T | 1 | a0002c0001t0008g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.421-460C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733713 | ||||||
chr19:733732
|
A | T | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.421-441A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733732 | ||||||
chr19:733736
|
C | T | 24 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0234others(21): Show | 25 | HG00741.hp2 HG02055.hp2 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.421-437C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733736 | ||||||
chr19:733761
|
T | C | 240 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(237): Show | 254 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.421-412T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733761 | ||||||
chr19:733784
|
C | T | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.421-389C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733784 | ||||||
chr19:733854
|
C | T | 5 | a0002c0001t0002g0022a0002c0001t0006g0095a0002c0001t0008g0023others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-319C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733854 | ||||||
chr19:733855
|
G | A | 3 | a0001c0002t0004g0017a0001c0002t0004g0019a0001c0002t0004g0144 | 3 | HG00408.hp1 NA18941.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.421-318G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733855 | ||||||
chr19:733951
|
A | T | 3 | a0001c0003t0001g0031a0001c0003t0001g0109a0001c0003t0002g0108 | 3 | HG02647.hp2 HG02809.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.421-222A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733951 | ||||||
chr19:733962
|
G | T | 1 | a0001c0002t0002g0368 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.421-211G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 733962 | ||||||
chr19:734055
|
C | T | 1 | a0002c0001t0002g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.421-118C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 734055 | ||||||
chr19:734061
|
C | T | 2 | a0001c0002t0002g0025a0001c0016t0001g0349 | 2 | HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.421-112C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 734061 | ||||||
chr19:734077
|
C | G | 37 | a0001c0002t0005g0193a0001c0004t0003g0092a0001c0004t0003g0300others(34): Show | 38 | HG00423.hp1 HG01975.hp2 HG02056.hp1 others(35): Show |
intron_variant | MODIFIER | c.421-96C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 734077 | ||||||
chr19:734087
|
C | T | 1 | a0002c0001t0002g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.421-86C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 734087 | ||||||
chr19:734091
|
C | G | 1 | a0002c0005t0003g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.421-82C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 734091 | ||||||
chr19:734129
|
C | T | 1 | a0002c0001t0002g0343 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.421-44C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 5/8 | chr19 | 734129 | ||||||
chr19:734326
|
G | A | 24 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0234others(21): Show | 25 | HG00741.hp2 HG02055.hp2 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.442+132G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734326 | ||||||
chr19:734326
|
G | C | 1 | a0001c0002t0002g0362 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.442+132G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734326 | ||||||
chr19:734369
|
G | C | 1 | a0002c0001t0030g0096 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.442+175G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734369 | ||||||
chr19:734371
|
C | T | 85 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(82): Show | 91 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.442+177C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734371 | ||||||
chr19:734381
|
G | C | 3 | a0002c0001t0002g0240a0002c0001t0007g0273a0002c0001t0007g0276 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.442+187G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734381 | ||||||
chr19:734419
|
G | A | 1 | a0001c0002t0002g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.442+225G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734419 | ||||||
chr19:734421
|
C | T | 22 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0234others(19): Show | 23 | HG00741.hp2 HG02055.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.442+227C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734421 | ||||||
chr19:734483
|
C | T | 1 | a0001c0003t0014g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.442+289C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734483 | ||||||
chr19:734491
|
C | T | 1 | a0001c0014t0001g0382 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.442+297C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734491 | ||||||
chr19:734520
|
A | C | 7 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0015g0242others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.442+326A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734520 | ||||||
chr19:734542
|
A | G | 3 | a0001c0002t0001g0260a0001c0002t0004g0164a0001c0002t0004g0340 | 3 | HG00733.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.442+348A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734542 | ||||||
chr19:734714
|
A | G | 324 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(321): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.442+520A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734714 | ||||||
chr19:734736
|
G | A | 5 | a0001c0002t0002g0351a0001c0003t0001g0122a0001c0003t0001g0123others(2): Show | 5 | HG00733.hp1 HG00741.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+542G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734736 | ||||||
chr19:734778
|
G | C | 1 | a0002c0001t0004g0377 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.442+584G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734778 | ||||||
chr19:734851
|
C | T | 73 | a0002c0001t0001g0137a0002c0001t0001g0151a0002c0001t0001g0153others(70): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.442+657C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734851 | ||||||
chr19:734990
|
T | C | 37 | a0001c0002t0001g0233a0002c0001t0001g0046a0002c0001t0001g0055others(34): Show | 37 | HG00423.hp2 HG00738.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.442+796T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 734990 | ||||||
chr19:735017
|
T | C | 35 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(32): Show | 36 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.442+823T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735017 | ||||||
chr19:735034
|
A | G | 13 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(10): Show | 14 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.442+840A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735034 | ||||||
chr19:735060
|
G | T | 7 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(4): Show | 8 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+866G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735060 | ||||||
chr19:735097
|
C | T | 5 | a0002c0001t0002g0081a0002c0001t0002g0207a0002c0001t0002g0209others(2): Show | 5 | HG00140.hp1 HG00140.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+903C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735097 | ||||||
chr19:735105
|
G | T | 1 | a0001c0002t0001g0198 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.442+911G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735105 | ||||||
chr19:735111
|
G | A | 73 | a0002c0001t0001g0137a0002c0001t0001g0151a0002c0001t0001g0153others(70): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.443-908G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735111 | ||||||
chr19:735132
|
CTGTGTCT others(42): Show |
C | 98 | a0001c0002t0002g0006a0001c0002t0002g0032a0001c0002t0002g0035others(95): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.443-810_443-762del others(49): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735132 | |||||
chr19:735205
|
GTGTCCTG others(41): Show |
G | 1 | a0002c0001t0002g0380 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.443-813_443-766del others(48): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735205 | ||||||
chr19:735209
|
C | T | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-810C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735209 | ||||||
chr19:735210
|
C | T | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-809C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735210 | ||||||
chr19:735211
|
T | G | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-808T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735211 | ||||||
chr19:735219
|
G | C | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-800G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735219 | ||||||
chr19:735231
|
T | TGTGTCTG others(254): Show |
1 | a0001c0004t0003g0300 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.443-778_443-777ins others(261): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735231 | |||||
chr19:735231
|
T | TGTGTCTG others(177): Show |
9 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0025others(6): Show | 10 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.443-768_443-767ins others(184): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735231 | |||||
chr19:735231
|
T | TGTGTCTG others(254): Show |
51 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(48): Show | 56 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.443-768_443-767ins others(261): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735231 | |||||
chr19:735231
|
T | TGTGTCTG others(254): Show |
18 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0270others(15): Show | 18 | HG00741.hp2 HG02083.hp2 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.443-768_443-767ins others(261): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735231 | |||||
chr19:735232
|
G | GTGTCTGG others(177): Show |
2 | a0002c0001t0001g0056a0002c0001t0004g0312 | 2 | HG02698.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.443-768_443-767ins others(184): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735232 | |||||
chr19:735232
|
G | GTGTCTGG others(177): Show |
1 | a0001c0004t0024g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.443-768_443-767ins others(184): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735232 | |||||
chr19:735244
|
C | CCAGGTGC others(23): Show |
143 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(140): Show | 150 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.443-768_443-767ins others(30): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735244 | |||||
chr19:735258
|
T | C | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-761T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735258 | ||||||
chr19:735259
|
T | C | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-760T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735259 | ||||||
chr19:735260
|
G | A | 1 | a0001c0004t0024g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.443-759G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735260 | ||||||
chr19:735268
|
C | G | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-751C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735268 | ||||||
chr19:735268
|
C | T | 1 | a0001c0003t0006g0118 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.443-751C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735268 | ||||||
chr19:735275
|
G | A | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-744G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735275 | ||||||
chr19:735278
|
T | C | 53 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(50): Show | 58 | HG00099.hp1 HG00408.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.443-741T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735278 | ||||||
chr19:735288
|
G | A | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-731G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735288 | ||||||
chr19:735301
|
T | C | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-718T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735301 | ||||||
chr19:735309
|
A | G | 30 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0234others(27): Show | 31 | HG00099.hp1 HG00741.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.443-710A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735309 | ||||||
chr19:735311
|
G | A | 32 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(29): Show | 33 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.443-708G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735311 | ||||||
chr19:735321
|
CCA | C | 117 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0234others(114): Show | 124 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.443-695_443-694del others(2): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735321 | |||||
chr19:735323
|
A | AGGTTCCT others(453): Show |
2 | a0002c0006t0006g0279a0002c0006t0006g0280 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.443-696_443-695ins others(460): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735323 | ||||||
chr19:735323
|
A | AGGTTCCT others(68): Show |
106 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(103): Show | 112 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.443-696_443-695ins others(75): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735323 | ||||||
chr19:735329
|
G | T | 34 | a0001c0002t0002g0363a0001c0004t0003g0306a0002c0001t0001g0012others(31): Show | 35 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-690G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735329 | ||||||
chr19:735338
|
C | T | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.443-681C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735338 | ||||||
chr19:735338
|
CGGGTGTC others(224): Show |
C | 13 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(10): Show | 14 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-662_443-432del | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735338 | |||||
chr19:735349
|
G | A | 34 | a0001c0002t0002g0363a0001c0004t0003g0306a0002c0001t0001g0012others(31): Show | 35 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(32): Show |
intron_variant | MODIFIER | c.443-670G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735349 | ||||||
chr19:735357
|
T | C | 39 | a0001c0002t0002g0363a0001c0004t0003g0306a0001c0004t0024g0126others(36): Show | 40 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(37): Show |
intron_variant | MODIFIER | c.443-662T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735357 | ||||||
chr19:735388
|
A | G | 188 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(185): Show | 200 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.443-631A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735388 | ||||||
chr19:735390
|
G | A | 1 | a0002c0008t0002g0307 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.443-629G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735390 | ||||||
chr19:735406
|
T | G | 222 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(219): Show | 235 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.443-613T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735406 | ||||||
chr19:735415
|
C | T | 6 | a0001c0002t0001g0009a0001c0002t0001g0265a0001c0003t0014g0278others(3): Show | 7 | HG01978.hp1 HG02109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-604C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735415 | ||||||
chr19:735416
|
G | A | 1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.443-603G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735416 | ||||||
chr19:735426
|
A | G | 225 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(222): Show | 238 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.443-593A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735426 | ||||||
chr19:735426
|
ATGGGATC others(301): Show |
A | 72 | a0002c0001t0001g0137a0002c0001t0001g0151a0002c0001t0001g0153others(69): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.443-554_443-247del | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735426 | |||||
chr19:735427
|
TGGGATCC others(302): Show |
T | 1 | a0002c0001t0002g0380 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.443-589_443-281del | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735427 | |||||
chr19:735434
|
C | T | 162 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(159): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.443-585C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735434 | ||||||
chr19:735444
|
A | G | 17 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0270others(14): Show | 17 | HG00741.hp2 HG02083.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.443-575A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735444 | ||||||
chr19:735465
|
A | G | 106 | a0001c0002t0001g0028a0001c0002t0001g0248a0001c0002t0002g0004others(103): Show | 113 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.443-554A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735465 | ||||||
chr19:735465
|
ATGTCTGG others(301): Show |
A | 7 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0015g0242others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-444_443-137del | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735465 | |||||
chr19:735469
|
C | G | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.443-550C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735469 | ||||||
chr19:735483
|
G | T | 52 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(49): Show | 57 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.443-536G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735483 | ||||||
chr19:735492
|
C | T | 53 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(50): Show | 58 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.443-527C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735492 | ||||||
chr19:735511
|
T | C | 117 | a0001c0002t0001g0142a0001c0002t0001g0234a0001c0002t0001g0248others(114): Show | 124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.443-508T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735511 | ||||||
chr19:735512
|
G | C | 1 | a0001c0004t0003g0051 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.443-507G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735512 | ||||||
chr19:735513
|
T | TGTGTCTG others(98): Show |
7 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(4): Show | 8 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-499_443-498ins others(105): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735513 | |||||
chr19:735521
|
A | G | 7 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(4): Show | 8 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-498A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735521 | ||||||
chr19:735542
|
G | A | 109 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(106): Show | 115 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.443-477G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735542 | ||||||
chr19:735542
|
G | GTGTCTGG others(147): Show |
2 | a0002c0001t0001g0291a0002c0001t0001g0292 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.443-460_443-459ins others(154): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735542 | |||||
chr19:735546
|
C | G | 53 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(50): Show | 58 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.443-473C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735546 | ||||||
chr19:735560
|
T | G | 46 | a0001c0002t0002g0025a0001c0002t0002g0363a0001c0002t0004g0076others(43): Show | 47 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.443-459T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735560 | ||||||
chr19:735569
|
T | C | 207 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(204): Show | 219 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.443-450T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735569 | ||||||
chr19:735580
|
G | A | 17 | a0001c0002t0002g0006a0001c0002t0002g0025a0001c0002t0002g0224others(14): Show | 18 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.443-439G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735580 | ||||||
chr19:735588
|
C | T | 8 | a0001c0002t0004g0076a0001c0002t0004g0197a0001c0002t0004g0199others(5): Show | 8 | HG00609.hp1 HG01978.hp1 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-431C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735588 | ||||||
chr19:735619
|
G | A | 42 | a0001c0002t0001g0028a0001c0002t0001g0142a0001c0002t0001g0234others(39): Show | 44 | HG00609.hp1 HG00741.hp2 HG01192.hp2 others(41): Show |
intron_variant | MODIFIER | c.443-400G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735619 | ||||||
chr19:735637
|
G | GCCTGTGT others(70): Show |
1 | a0001c0004t0024g0126 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.443-373_443-297dup others(77): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735637 | |||||
chr19:735648
|
G | T | 13 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(10): Show | 14 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-371G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735648 | ||||||
chr19:735665
|
C | T | 132 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(129): Show | 139 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.443-354C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735665 | ||||||
chr19:735696
|
G | A | 5 | a0001c0002t0004g0076a0001c0002t0004g0197a0001c0002t0004g0199others(2): Show | 5 | HG00609.hp1 HG02083.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-323G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735696 | ||||||
chr19:735700
|
C | G | 1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.443-319C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735700 | ||||||
chr19:735714
|
T | G | 13 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(10): Show | 14 | HG01192.hp2 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-305T>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735714 | ||||||
chr19:735723
|
T | C | 21 | a0001c0002t0002g0006a0001c0002t0002g0224a0001c0002t0002g0268others(18): Show | 22 | HG00609.hp1 HG01192.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.443-296T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735723 | ||||||
chr19:735723
|
T | TGGGTGTC others(147): Show |
1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.443-243_443-242ins others(154): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr19 | 735723 | |||||
chr19:735736
|
G | A | 2 | a0001c0002t0006g0029a0001c0003t0002g0043 | 2 | HG02622.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.443-283G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735736 | ||||||
chr19:735791
|
G | T | 1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.443-228G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735791 | ||||||
chr19:735800
|
C | T | 1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.443-219C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735800 | ||||||
chr19:735819
|
T | C | 1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.443-200T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 6/8 | chr19 | 735819 | ||||||
chr19:736153
|
TGGGGCG | T | 7 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0015g0242others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.502+82_502+87delGG others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 736153 | |||||
chr19:736158
|
C | CG | 8 | a0001c0002t0001g0028a0001c0002t0004g0254a0001c0002t0004g0259others(5): Show | 8 | HG00438.hp2 HG00735.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+85dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 736158 | |||||
chr19:736175
|
T | C | 1 | a0001c0002t0002g0097 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.502+97T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736175 | ||||||
chr19:736195
|
G | A | 35 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(32): Show | 36 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+117G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736195 | ||||||
chr19:736236
|
G | C | 7 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(4): Show | 8 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+158G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736236 | ||||||
chr19:736295
|
C | T | 1 | a0002c0001t0007g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.502+217C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736295 | ||||||
chr19:736296
|
G | A | 35 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(32): Show | 36 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+218G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736296 | ||||||
chr19:736382
|
C | T | 7 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0262others(4): Show | 8 | HG02055.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.502+304C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736382 | ||||||
chr19:736393
|
C | T | 120 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(117): Show | 126 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.502+315C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736393 | ||||||
chr19:736395
|
C | A | 2 | a0002c0006t0006g0279a0002c0006t0006g0280 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.502+317C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736395 | ||||||
chr19:736447
|
A | G | 330 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(327): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.502+369A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736447 | ||||||
chr19:736476
|
G | A | 1 | a0001c0004t0003g0138 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.502+398G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736476 | ||||||
chr19:736491
|
C | T | 54 | a0001c0002t0001g0248a0001c0002t0002g0011a0001c0002t0004g0111others(51): Show | 59 | HG00408.hp2 HG00597.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.502+413C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736491 | ||||||
chr19:736494
|
C | T | 1 | a0001c0003t0001g0109 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.502+416C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736494 | ||||||
chr19:736581
|
C | T | 35 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(32): Show | 36 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+503C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736581 | ||||||
chr19:736673
|
C | T | 2 | a0002c0006t0006g0279a0002c0006t0006g0280 | 2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.502+595C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736673 | ||||||
chr19:736822
|
G | A | 35 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(32): Show | 36 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.502+744G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736822 | ||||||
chr19:736834
|
G | A | 7 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0015g0242others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.502+756G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736834 | ||||||
chr19:736875
|
G | A | 1 | a0002c0001t0001g0099 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.502+797G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736875 | ||||||
chr19:736888
|
T | C | 2 | a0002c0001t0012g0249a0002c0005t0003g0345 | 2 | NA18942.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.502+810T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736888 | ||||||
chr19:736946
|
G | A | 1 | a0001c0002t0007g0020 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.502+868G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 736946 | ||||||
chr19:737008
|
G | A | 1 | a0001c0004t0003g0114 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.502+930G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737008 | ||||||
chr19:737032
|
G | A | 49 | a0001c0003t0006g0373a0002c0001t0001g0137a0002c0001t0001g0297others(46): Show | 52 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.502+954G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737032 | ||||||
chr19:737049
|
G | A | 1 | a0001c0003t0006g0373 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.502+971G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737049 | ||||||
chr19:737123
|
A | T | 130 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(127): Show | 136 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.502+1045A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737123 | ||||||
chr19:737161
|
C | T | 1 | a0002c0006t0006g0279 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.502+1083C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737161 | ||||||
chr19:737171
|
T | C | 1 | a0002c0001t0007g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.502+1093T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737171 | ||||||
chr19:737280
|
C | G | 1 | a0001c0002t0010g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.502+1202C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737280 | ||||||
chr19:737497
|
G | A | 1 | a0001c0002t0001g0248 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.502+1419G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737497 | ||||||
chr19:737557
|
C | G | 2 | a0002c0001t0001g0291a0002c0001t0001g0292 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.502+1479C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737557 | ||||||
chr19:737557
|
CAG | C | 33 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(30): Show | 34 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.502+1480_502+1481d others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737557 | ||||||
chr19:737590
|
G | A | 1 | a0005c0011t0001g0308 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.502+1512G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737590 | ||||||
chr19:737608
|
A | G | 33 | a0002c0001t0001g0012a0002c0001t0001g0044a0002c0001t0001g0050others(30): Show | 34 | HG00280.hp2 HG00423.hp1 HG01975.hp2 others(31): Show |
intron_variant | MODIFIER | c.502+1530A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737608 | ||||||
chr19:737621
|
G | GCAAGGCA others(24): Show |
2 | a0001c0002t0004g0251a0001c0003t0001g0252 | 2 | HG00544.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.502+1564_502+1594d others(33): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr19 | 737621 | |||||
chr19:737697
|
A | G | 30 | a0001c0002t0001g0233a0002c0001t0001g0055a0002c0001t0001g0090others(27): Show | 30 | HG00423.hp2 HG00738.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.502+1619A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737697 | ||||||
chr19:737698
|
C | T | 37 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0205others(34): Show | 39 | HG00280.hp2 HG00423.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.502+1620C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737698 | ||||||
chr19:737778
|
C | T | 1 | a0002c0001t0002g0285 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.502+1700C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737778 | ||||||
chr19:737803
|
A | G | 37 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0205others(34): Show | 39 | HG00280.hp2 HG00423.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.502+1725A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737803 | ||||||
chr19:737889
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.502+1811G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737889 | ||||||
chr19:737924
|
G | A | 15 | a0001c0002t0001g0142a0001c0002t0001g0299a0001c0002t0002g0140others(12): Show | 15 | HG02083.hp2 HG02129.hp2 HG02155.hp1 others(12): Show |
intron_variant | MODIFIER | c.502+1846G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737924 | ||||||
chr19:737949
|
T | C | 26 | a0001c0002t0001g0149a0001c0002t0002g0268a0002c0001t0001g0151others(23): Show | 26 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.502+1871T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737949 | ||||||
chr19:737951
|
C | G | 2 | a0002c0005t0003g0147a0002c0005t0004g0158 | 2 | HG02015.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.502+1873C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 737951 | ||||||
chr19:738113
|
A | G | 332 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(329): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.502+2035A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738113 | ||||||
chr19:738200
|
G | A | 90 | a0001c0002t0001g0115a0001c0002t0001g0200a0001c0002t0001g0260others(87): Show | 94 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.502+2122G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738200 | ||||||
chr19:738342
|
C | G | 4 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0015g0242others(1): Show | 4 | HG02572.hp1 HG03486.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-2010C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738342 | ||||||
chr19:738394
|
C | T | 34 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0110others(31): Show | 36 | HG00423.hp1 HG00642.hp2 HG01975.hp2 others(33): Show |
intron_variant | MODIFIER | c.503-1958C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738394 | ||||||
chr19:738424
|
CCTTAGGC others(5): Show |
C | 1 | a0002c0001t0001g0185 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.503-1927_503-1916d others(14): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738424 | ||||||
chr19:738637
|
G | A | 2 | a0001c0002t0002g0140a0002c0001t0002g0341 | 2 | HG03490.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.503-1715G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738637 | ||||||
chr19:738727
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.503-1625G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738727 | ||||||
chr19:738750
|
G | A | 2 | a0001c0002t0001g0149a0001c0002t0002g0268 | 2 | HG02895.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.503-1602G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738750 | ||||||
chr19:738793
|
G | A | 65 | a0001c0002t0001g0115a0001c0002t0001g0302a0001c0002t0001g0337others(62): Show | 68 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.503-1559G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738793 | ||||||
chr19:738811
|
G | A | 1 | a0001c0003t0001g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.503-1541G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738811 | ||||||
chr19:738832
|
G | A | 1 | a0002c0001t0002g0178 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.503-1520G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738832 | ||||||
chr19:738907
|
T | C | 2 | a0001c0003t0001g0122a0001c0003t0017g0350 | 2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.503-1445T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738907 | ||||||
chr19:738952
|
G | A | 1 | a0001c0002t0001g0149 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503-1400G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 738952 | ||||||
chr19:739004
|
C | T | 2 | a0002c0006t0001g0049a0006c0013t0001g0080 | 2 | HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.503-1348C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739004 | ||||||
chr19:739140
|
A | T | 3 | a0002c0001t0002g0240a0002c0001t0007g0273a0002c0001t0007g0276 | 3 | HG03130.hp1 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.503-1212A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739140 | ||||||
chr19:739407
|
C | T | 1 | a0001c0002t0006g0029 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.503-945C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739407 | ||||||
chr19:739550
|
G | A | 1 | a0002c0008t0002g0067 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.503-802G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739550 | ||||||
chr19:739750
|
T | C | 67 | a0001c0002t0001g0248a0001c0003t0001g0052a0001c0003t0001g0325others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.503-602T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739750 | ||||||
chr19:739809
|
C | G | 4 | a0001c0002t0008g0371a0002c0001t0006g0095a0002c0001t0030g0096others(1): Show | 4 | HG01884.hp1 HG01884.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-543C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739809 | ||||||
chr19:739866
|
C | T | 6 | a0001c0002t0002g0004a0001c0002t0002g0262a0001c0002t0002g0264others(3): Show | 7 | HG02818.hp2 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-486C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739866 | ||||||
chr19:739918
|
A | G | 3 | a0001c0002t0001g0299a0002c0001t0001g0303a0002c0001t0001g0309 | 3 | NA19056.hp1 NA19068.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.503-434A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739918 | ||||||
chr19:739928
|
G | C | 1 | a0002c0006t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.503-424G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739928 | ||||||
chr19:739955
|
G | A | 65 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(62): Show | 69 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.503-397G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739955 | ||||||
chr19:739998
|
G | T | 30 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(27): Show | 32 | HG00423.hp1 HG00642.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.503-354G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 739998 | ||||||
chr19:740149
|
G | A | 6 | a0001c0002t0002g0004a0001c0002t0002g0262a0001c0002t0002g0264others(3): Show | 7 | HG02818.hp2 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-203G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 740149 | ||||||
chr19:740198
|
G | A | 30 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(27): Show | 32 | HG00423.hp1 HG00642.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.503-154G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 740198 | ||||||
chr19:740272
|
C | T | 72 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0014others(69): Show | 79 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.503-80C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 740272 | ||||||
chr19:740275
|
C | A | 1 | a0002c0001t0001g0356 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.503-77C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 740275 | ||||||
chr19:740300
|
G | C | 1 | a0001c0004t0003g0092 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.503-52G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 740300 | ||||||
chr19:740312
|
G | A | 14 | a0002c0005t0003g0071a0002c0005t0003g0072a0002c0005t0003g0120others(11): Show | 14 | HG00438.hp2 HG00621.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.503-40G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 740312 | ||||||
chr19:740314
|
G | A | 4 | a0001c0003t0001g0054a0001c0003t0001g0116a0001c0003t0001g0252others(1): Show | 4 | NA18959.hp1 NA19009.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-38G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 7/8 | chr19 | 740314 | ||||||
chr19:740560
|
T | C | 372 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(369): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.634+77T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 740560 | ||||||
chr19:740581
|
GA | G | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+99delA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 740581 | ||||||
chr19:740661
|
C | G | 1 | a0002c0006t0001g0206 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.634+178C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 740661 | ||||||
chr19:740758
|
A | G | 81 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0014others(78): Show | 88 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.634+275A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 740758 | ||||||
chr19:740763
|
C | T | 3 | a0001c0002t0001g0299a0002c0001t0001g0303a0002c0001t0001g0309 | 3 | NA19056.hp1 NA19068.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.634+280C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 740763 | ||||||
chr19:740892
|
A | T | 92 | a0001c0002t0001g0009a0001c0002t0001g0265a0001c0002t0005g0087others(89): Show | 97 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.634+409A>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 740892 | ||||||
chr19:740911
|
G | A | 37 | a0001c0002t0001g0028a0001c0002t0002g0004a0001c0002t0002g0006others(34): Show | 39 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.634+428G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 740911 | ||||||
chr19:740968
|
C | CA | 29 | a0001c0002t0001g0233a0001c0002t0001g0234a0001c0002t0002g0032others(26): Show | 29 | HG00423.hp2 HG00438.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.634+506dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 740968 | |||||
chr19:740968
|
CA | C | 87 | a0001c0002t0002g0103a0001c0002t0002g0368a0001c0002t0004g0144others(84): Show | 91 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.634+506delA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 740968 | |||||
chr19:740968
|
CAAAAAAA | C | 6 | a0001c0002t0002g0004a0001c0002t0002g0262a0001c0002t0002g0264others(3): Show | 7 | HG02818.hp2 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+500_634+506del others(7): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 740968 | |||||
chr19:741211
|
G | C | 23 | a0001c0002t0002g0097a0001c0002t0002g0201a0001c0002t0002g0250others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(20): Show |
intron_variant | MODIFIER | c.634+728G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741211 | ||||||
chr19:741234
|
A | G | 1 | a0001c0003t0001g0267 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.634+751A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741234 | ||||||
chr19:741242
|
G | A | 15 | a0001c0002t0005g0087a0001c0002t0005g0104a0001c0002t0005g0106others(12): Show | 15 | HG00597.hp2 HG02083.hp2 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.634+759G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741242 | ||||||
chr19:741376
|
G | A | 1 | a0001c0002t0002g0363 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.634+893G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741376 | ||||||
chr19:741381
|
TGGGCTGC others(16): Show |
T | 19 | a0001c0002t0004g0019a0001c0002t0004g0076a0001c0002t0004g0197others(16): Show | 19 | HG00408.hp1 HG00597.hp2 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.634+909_634+931del others(23): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741381 | |||||
chr19:741392
|
A | AGTGAGGG others(16): Show |
11 | a0001c0002t0002g0004a0001c0002t0002g0262a0001c0002t0002g0264others(8): Show | 12 | HG02004.hp1 HG02647.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.634+989_634+1011du others(24): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741392 | |||||
chr19:741392
|
A | G | 224 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0045others(221): Show | 232 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.634+909A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741392 | ||||||
chr19:741404
|
C | CGGGCTGC others(16): Show |
9 | a0001c0002t0001g0028a0001c0002t0008g0371a0001c0003t0014g0278others(6): Show | 9 | HG01884.hp1 HG01884.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+943_634+944ins others(23): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741404 | |||||
chr19:741404
|
C | T | 145 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(142): Show | 148 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.634+921C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741404 | ||||||
chr19:741427
|
C | T | 72 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0014others(69): Show | 79 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.634+944C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741427 | ||||||
chr19:741431
|
C | G | 1 | a0002c0001t0008g0058 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.634+948C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741431 | ||||||
chr19:741450
|
C | CG | 4 | a0001c0002t0027g0047a0002c0001t0002g0070a0002c0001t0002g0184others(1): Show | 4 | HG01192.hp2 HG02071.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+970dupG | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741450 | |||||
chr19:741451
|
G | GGGCTGCA others(16): Show |
1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.634+990_634+991ins others(23): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741451 | |||||
chr19:741458
|
AGGGGTGA others(54): Show |
A | 3 | a0001c0002t0002g0006a0001c0002t0002g0224a0002c0001t0008g0023 | 4 | HG01109.hp1 HG02055.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1012_634+1072d others(63): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741458 | |||||
chr19:741472
|
A | C | 3 | a0002c0005t0003g0311a0002c0005t0003g0316a0002c0005t0019g0176 | 3 | NA18967.hp2 NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.634+989A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741472 | ||||||
chr19:741473
|
C | T | 3 | a0002c0005t0003g0311a0002c0005t0003g0316a0002c0005t0019g0176 | 3 | NA18967.hp2 NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.634+990C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741473 | ||||||
chr19:741473
|
CGGGCTGC others(16): Show |
C | 4 | a0001c0002t0001g0009a0001c0002t0001g0265a0002c0001t0001g0046others(1): Show | 5 | HG02145.hp2 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+1012_634+1034d others(25): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741473 | |||||
chr19:741481
|
AGGGGTGA others(31): Show |
A | 3 | a0002c0005t0003g0311a0002c0005t0003g0316a0002c0005t0019g0176 | 3 | NA18967.hp2 NA19065.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.634+1012_634+1049d others(40): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741481 | |||||
chr19:741486
|
T | C | 6 | a0001c0003t0006g0034a0001c0003t0006g0346a0001c0003t0006g0373others(3): Show | 6 | HG01891.hp1 HG02109.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+1003T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741486 | ||||||
chr19:741494
|
G | A | 1 | a0001c0003t0002g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.634+1011G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741494 | ||||||
chr19:741495
|
C | A | 151 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(148): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.634+1012C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741495 | ||||||
chr19:741496
|
T | C | 151 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(148): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.634+1013T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741496 | ||||||
chr19:741504
|
AGGGGTGA others(8): Show |
A | 207 | a0001c0002t0001g0009a0001c0002t0001g0142a0001c0002t0001g0149others(204): Show | 213 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.634+1040_634+1054d others(17): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741504 | |||||
chr19:741516
|
A | AGCTGGGC others(1): Show |
145 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(142): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.634+1034_634+1035i others(10): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741516 | |||||
chr19:741518
|
A | C | 145 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(142): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.634+1035A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741518 | ||||||
chr19:741519
|
C | A | 145 | a0001c0002t0001g0010a0001c0002t0001g0028a0001c0002t0001g0045others(142): Show | 154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.634+1036C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741519 | ||||||
chr19:741519
|
C | CGGGCTGC others(1): Show |
4 | a0001c0002t0002g0112a0002c0001t0001g0314a0002c0001t0002g0117others(1): Show | 4 | HG01261.hp1 HG02300.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1039_634+1040i others(10): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741519 | |||||
chr19:741519
|
C | CGGGCTGC others(24): Show |
1 | a0001c0002t0008g0371 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.634+1039_634+1040i others(33): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 741519 | |||||
chr19:741535
|
G | T | 1 | a0002c0001t0002g0036 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.634+1052G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741535 | ||||||
chr19:741557
|
C | T | 1 | a0002c0001t0002g0048 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.634+1074C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741557 | ||||||
chr19:741709
|
C | A | 13 | a0001c0003t0006g0034a0001c0003t0006g0118a0001c0003t0006g0241others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.634+1226C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741709 | ||||||
chr19:741751
|
G | T | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.634+1268G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741751 | ||||||
chr19:741758
|
G | A | 30 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(27): Show | 32 | HG00423.hp1 HG00642.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.634+1275G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741758 | ||||||
chr19:741816
|
G | T | 1 | a0002c0001t0002g0324 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.634+1333G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741816 | ||||||
chr19:741825
|
C | G | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+1342C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741825 | ||||||
chr19:741949
|
C | T | 1 | a0002c0006t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.634+1466C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741949 | ||||||
chr19:741959
|
G | T | 1 | a0002c0001t0002g0229 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.634+1476G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741959 | ||||||
chr19:741973
|
A | C | 8 | a0001c0002t0008g0371a0002c0001t0002g0117a0002c0001t0006g0095others(5): Show | 8 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.634+1490A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741973 | ||||||
chr19:741985
|
C | T | 2 | a0001c0002t0006g0029a0001c0003t0002g0043 | 2 | HG02622.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.634+1502C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741985 | ||||||
chr19:741998
|
C | G | 1 | a0001c0002t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.634+1515C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 741998 | ||||||
chr19:742037
|
C | T | 1 | a0002c0001t0002g0174 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.634+1554C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742037 | ||||||
chr19:742082
|
G | A | 1 | a0002c0001t0002g0081 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.634+1599G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742082 | ||||||
chr19:742326
|
C | T | 2 | a0002c0001t0001g0151a0002c0001t0001g0153 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.634+1843C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742326 | ||||||
chr19:742559
|
C | T | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+2076C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742559 | ||||||
chr19:742616
|
A | AAAAAG | 35 | a0001c0002t0004g0013a0001c0002t0004g0017a0001c0002t0004g0018others(32): Show | 36 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.634+2136_634+2137i others(7): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 742616 | |||||
chr19:742616
|
A | AAAAG | 184 | a0001c0002t0001g0009a0001c0002t0001g0010a0001c0002t0001g0028others(181): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.634+2141_634+2144d others(6): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 742616 | |||||
chr19:742616
|
A | AAAG | 67 | a0001c0002t0001g0265a0001c0003t0001g0052a0001c0003t0001g0325others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+2135_634+2136i others(5): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 742616 | |||||
chr19:742616
|
A | G | 6 | a0001c0002t0002g0004a0001c0002t0002g0262a0001c0002t0002g0264others(3): Show | 7 | HG02818.hp2 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+2133A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742616 | ||||||
chr19:742681
|
C | T | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+2198C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742681 | ||||||
chr19:742884
|
C | T | 3 | a0001c0002t0002g0006a0001c0002t0002g0224a0002c0001t0008g0023 | 4 | HG01109.hp1 HG02055.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+2401C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742884 | ||||||
chr19:742915
|
C | T | 12 | a0001c0003t0006g0034a0001c0003t0006g0118a0001c0003t0006g0241others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.634+2432C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742915 | ||||||
chr19:742958
|
C | A | 3 | a0002c0001t0001g0169a0002c0001t0004g0338a0002c0001t0004g0339 | 3 | HG02922.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.634+2475C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742958 | ||||||
chr19:742999
|
G | A | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+2516G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 742999 | ||||||
chr19:743024
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.634+2541C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743024 | ||||||
chr19:743049
|
G | A | 1 | a0002c0006t0001g0206 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.634+2566G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743049 | ||||||
chr19:743207
|
G | C | 3 | a0001c0004t0003g0051a0002c0005t0003g0147a0002c0005t0004g0158 | 3 | HG00408.hp2 HG02015.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.634+2724G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743207 | ||||||
chr19:743221
|
T | C | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.634+2738T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743221 | ||||||
chr19:743351
|
CT | C | 10 | a0001c0002t0002g0004a0001c0002t0002g0262a0001c0002t0002g0264others(7): Show | 11 | HG02647.hp1 HG02818.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.634+2869delT | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743351 | ||||||
chr19:743362
|
G | A | 3 | a0001c0002t0001g0060a0002c0001t0001g0050a0002c0001t0001g0319 | 3 | HG02300.hp1 HG03834.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.634+2879G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743362 | ||||||
chr19:743539
|
C | T | 1 | a0001c0003t0014g0278 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.635-2746C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743539 | ||||||
chr19:743563
|
G | GAA | 3 | a0001c0004t0003g0092a0001c0004t0003g0300a0002c0005t0003g0301 | 3 | NA18980.hp1 NA19000.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.635-2720_635-2719d others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 743563 | |||||
chr19:743589
|
T | C | 21 | a0001c0002t0002g0097a0001c0002t0002g0201a0001c0002t0002g0250others(18): Show | 21 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(18): Show |
intron_variant | MODIFIER | c.635-2696T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743589 | ||||||
chr19:743633
|
C | T | 6 | a0001c0002t0001g0009a0001c0002t0001g0265a0001c0002t0010g0030others(3): Show | 7 | HG01074.hp2 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-2652C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743633 | ||||||
chr19:743654
|
G | T | 1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.635-2631G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743654 | ||||||
chr19:743655
|
C | T | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.635-2630C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743655 | ||||||
chr19:743714
|
G | T | 1 | a0001c0004t0003g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.635-2571G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743714 | ||||||
chr19:743786
|
C | T | 5 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0085others(2): Show | 5 | NA18960.hp2 NA18990.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.635-2499C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743786 | ||||||
chr19:743789
|
C | T | 2 | a0001c0002t0002g0331a0002c0001t0002g0148 | 2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.635-2496C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743789 | ||||||
chr19:743849
|
A | G | 2 | a0001c0002t0001g0110a0001c0002t0001g0256 | 2 | NA18949.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.635-2436A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743849 | ||||||
chr19:743932
|
A | G | 2 | a0002c0001t0002g0064a0002c0001t0002g0168 | 2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.635-2353A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 743932 | ||||||
chr19:744004
|
T | C | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.635-2281T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744004 | ||||||
chr19:744122
|
C | T | 28 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(25): Show | 30 | HG00423.hp1 HG00642.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.635-2163C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744122 | ||||||
chr19:744128
|
T | C | 216 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(213): Show | 223 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.635-2157T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744128 | ||||||
chr19:744134
|
C | T | 75 | a0001c0002t0001g0142a0001c0002t0001g0198a0001c0002t0001g0200others(72): Show | 75 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.635-2151C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744134 | ||||||
chr19:744166
|
T | C | 216 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(213): Show | 223 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.635-2119T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744166 | ||||||
chr19:744188
|
C | A | 89 | a0001c0002t0002g0004a0001c0002t0002g0005a0001c0002t0002g0011others(86): Show | 97 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.635-2097C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744188 | ||||||
chr19:744206
|
C | T | 2 | a0002c0001t0001g0062a0002c0001t0001g0157 | 2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.635-2079C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744206 | ||||||
chr19:744230
|
C | A | 3 | a0002c0001t0006g0095a0002c0001t0030g0096a0002c0006t0008g0024 | 3 | HG01884.hp1 HG02280.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.635-2055C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744230 | ||||||
chr19:744257
|
A | G | 188 | a0001c0002t0001g0142a0001c0002t0001g0149a0001c0002t0001g0198others(185): Show | 193 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.635-2028A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744257 | ||||||
chr19:744273
|
G | A | 1 | a0001c0002t0027g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.635-2012G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744273 | ||||||
chr19:744357
|
A | G | 229 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(226): Show | 236 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.635-1928A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744357 | ||||||
chr19:744399
|
C | CA | 96 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(93): Show | 102 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.635-1871dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 744399 | |||||
chr19:744399
|
C | CAA | 110 | a0001c0002t0001g0142a0001c0002t0001g0149a0001c0002t0001g0198others(107): Show | 111 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.635-1872_635-1871d others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 744399 | |||||
chr19:744399
|
C | CAAA | 7 | a0001c0003t0001g0239a0001c0003t0001g0358a0002c0007t0004g0073others(4): Show | 7 | HG00544.hp2 HG01175.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-1873_635-1871d others(5): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 744399 | |||||
chr19:744399
|
CA | C | 13 | a0001c0002t0002g0004a0001c0002t0002g0262a0001c0002t0002g0264others(10): Show | 14 | HG01255.hp1 HG02602.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.635-1871delA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 744399 | |||||
chr19:744501
|
G | C | 117 | a0001c0002t0001g0142a0001c0002t0001g0149a0001c0002t0001g0198others(114): Show | 118 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.635-1784G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744501 | ||||||
chr19:744626
|
G | T | 1 | a0002c0006t0008g0024 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.635-1659G>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744626 | ||||||
chr19:744762
|
C | T | 11 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0262others(8): Show | 12 | HG02647.hp1 HG02818.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.635-1523C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744762 | ||||||
chr19:744765
|
G | C | 1 | a0002c0008t0002g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.635-1520G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744765 | ||||||
chr19:744809
|
G | A | 1 | a0002c0001t0001g0068 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.635-1476G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744809 | ||||||
chr19:744850
|
C | T | 1 | a0001c0004t0003g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.635-1435C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744850 | ||||||
chr19:744851
|
G | A | 1 | a0002c0006t0001g0206 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.635-1434G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744851 | ||||||
chr19:744880
|
G | C | 119 | a0001c0002t0001g0142a0001c0002t0001g0149a0001c0002t0001g0198others(116): Show | 120 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.635-1405G>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744880 | ||||||
chr19:744885
|
C | A | 1 | a0002c0001t0008g0023 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.635-1400C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744885 | ||||||
chr19:744885
|
C | CA | 7 | a0001c0002t0008g0371a0002c0001t0002g0117a0002c0001t0006g0095others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.635-1389dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 744885 | |||||
chr19:744896
|
AGC | A | 119 | a0001c0002t0001g0142a0001c0002t0001g0149a0001c0002t0001g0198others(116): Show | 120 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.635-1388_635-1387d others(4): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744896 | ||||||
chr19:744901
|
C | T | 37 | a0001c0002t0004g0013a0001c0002t0004g0017a0001c0002t0004g0018others(34): Show | 38 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.635-1384C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744901 | ||||||
chr19:744917
|
C | T | 1 | a0002c0001t0002g0160 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.635-1368C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744917 | ||||||
chr19:744944
|
C | G | 4 | a0001c0002t0002g0262a0001c0002t0002g0264a0001c0002t0002g0365others(1): Show | 4 | HG02970.hp2 HG03540.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-1341C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744944 | ||||||
chr19:744999
|
G | A | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.635-1286G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 744999 | ||||||
chr19:745041
|
G | A | 1 | a0002c0001t0002g0207 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.635-1244G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745041 | ||||||
chr19:745073
|
T | TA | 67 | a0001c0003t0001g0052a0001c0003t0001g0325a0001c0004t0003g0001others(64): Show | 71 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.635-1211dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 745073 | |||||
chr19:745122
|
G | A | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.635-1163G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745122 | ||||||
chr19:745344
|
C | T | 36 | a0001c0002t0002g0004a0001c0002t0002g0025a0001c0002t0002g0097others(33): Show | 37 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(34): Show |
intron_variant | MODIFIER | c.635-941C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745344 | ||||||
chr19:745345
|
G | A | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.635-940G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745345 | ||||||
chr19:745374
|
C | G | 8 | a0001c0002t0008g0371a0002c0001t0002g0117a0002c0001t0006g0095others(5): Show | 8 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.635-911C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745374 | ||||||
chr19:745422
|
G | A | 13 | a0001c0003t0002g0043a0001c0003t0006g0034a0001c0003t0006g0118others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.635-863G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745422 | ||||||
chr19:745432
|
G | A | 6 | a0001c0002t0002g0014a0001c0002t0002g0059a0001c0002t0002g0225others(3): Show | 7 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.635-853G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745432 | ||||||
chr19:745497
|
C | G | 18 | a0001c0002t0001g0009a0001c0002t0001g0265a0001c0002t0006g0029others(15): Show | 19 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.635-788C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745497 | ||||||
chr19:745626
|
C | A | 13 | a0001c0003t0002g0043a0001c0003t0006g0034a0001c0003t0006g0118others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.635-659C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745626 | ||||||
chr19:745627
|
G | A | 77 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0014others(74): Show | 84 | HG00280.hp2 HG00323.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.635-658G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745627 | ||||||
chr19:745675
|
G | A | 330 | a0001c0002t0001g0010a0001c0002t0001g0045a0001c0002t0001g0060others(327): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.635-610G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745675 | ||||||
chr19:745686
|
G | GA | 252 | a0001c0002t0001g0142a0001c0002t0001g0149a0001c0002t0001g0198others(249): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.635-583dupA | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 745686 | |||||
chr19:745686
|
G | GAA | 6 | a0001c0002t0002g0032a0001c0002t0002g0361a0001c0002t0004g0254others(3): Show | 6 | HG00735.hp2 HG01175.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-584_635-583dup others(2): Show |
PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr19 | 745686 | |||||
chr19:745737
|
C | G | 2 | a0002c0001t0004g0338a0002c0001t0004g0339 | 2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.635-548C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745737 | ||||||
chr19:745807
|
C | A | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.635-478C>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745807 | ||||||
chr19:745857
|
G | A | 5 | a0001c0002t0001g0009a0001c0002t0001g0265a0001c0002t0006g0029others(2): Show | 6 | HG02145.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-428G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745857 | ||||||
chr19:745919
|
G | A | 37 | a0001c0002t0004g0013a0001c0002t0004g0017a0001c0002t0004g0018others(34): Show | 38 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.635-366G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745919 | ||||||
chr19:745937
|
A | G | 1 | a0001c0002t0002g0268 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.635-348A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 745937 | ||||||
chr19:746036
|
C | T | 96 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0014others(93): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.635-249C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746036 | ||||||
chr19:746049
|
C | G | 1 | a0002c0001t0001g0319 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.635-236C>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746049 | ||||||
chr19:746066
|
T | A | 1 | a0001c0003t0014g0275 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.635-219T>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746066 | ||||||
chr19:746083
|
A | G | 1 | a0001c0002t0004g0199 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.635-202A>G | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746083 | ||||||
chr19:746084
|
C | T | 1 | a0001c0003t0001g0026 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.635-201C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746084 | ||||||
chr19:746085
|
G | A | 13 | a0001c0002t0002g0004a0001c0002t0002g0006a0001c0002t0002g0025others(10): Show | 15 | HG02055.hp1 HG02647.hp1 HG02818.hp2 others(12): Show |
intron_variant | MODIFIER | c.635-200G>A | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746085 | ||||||
chr19:746148
|
A | C | 1 | a0001c0002t0002g0367 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.635-137A>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746148 | ||||||
chr19:746206
|
C | T | 96 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0014others(93): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.635-79C>T | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746206 | ||||||
chr19:746209
|
T | C | 1 | a0001c0002t0008g0371 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.635-76T>C | PALM | ENSG00000099864.18 | transcript | ENST00000338448.10 | protein_coding | 8/8 | chr19 | 746209 |