geneid | 415 |
---|---|
ensemblid | ENSG00000157399.17 |
hgncid | 719 |
symbol | ARSL |
name | arylsulfatase L |
refseq_nuc | NM_000047.3 |
refseq_prot | NP_000038.2 |
ensembl_nuc | ENST00000381134.9 |
ensembl_prot | ENSP00000370526.3 |
mane_status | MANE Select |
chr | chrX |
start | 2934521 |
end | 2964341 |
strand | - |
ver | v1.2 |
region | chrX:2934521-2964341 |
region5000 | chrX:2929521-2969341 |
regionname0 | ARSL_chrX_2934521_2964341 |
regionname5000 | ARSL_chrX_2929521_2969341 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 589 | 188 | 6 | 32 | 113 | 11 | 25 | 91 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002 | 1/0 | 589 | 102 | 51 | 24 | 19 | 2 | 5 | 15 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003 | 0/0 | 589 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0004 | 0/0 | 589 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0005 | 0/0 | 589 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0006 | 0/0 | 589 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0007 | 0/0 | 589 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0008 | 0/0 | 504 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0009 | 0/0 | 583 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0010 | 0/0 | 514 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0011 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0012 | 0/0 | 374 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0013 | 0/0 | 176 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0014 | 0/0 | 589 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
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 | 0/1 | 1770 | 168 | 4 | 21 | 112 | 8 | 22 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0002 | 1/0 | 1770 | 74 | 30 | 19 | 18 | 1 | 5 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0003 | 0/0 | 1770 | 14 | 12 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0004 | 0/0 | 1770 | 10 | 9 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0005 | 0/0 | 1770 | 10 | 8 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0006 | 0/0 | 1770 | 9 | 9 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0007 | 0/0 | 1770 | 9 | 0 | 7 | 0 | 0 | 2 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0008 | 0/0 | 1770 | 6 | 0 | 0 | 6 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0009 | 0/0 | 1770 | 5 | 0 | 2 | 0 | 2 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0010 | 0/0 | 1770 | 3 | 1 | 1 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0011 | 0/0 | 1770 | 3 | 0 | 0 | 3 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0012 | 0/0 | 1770 | 2 | 0 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0013 | 0/0 | 1770 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0014 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0015 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0016 | 0/0 | 1770 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0017 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0018 | 0/0 | 1771 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0019 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0020 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0021 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0022 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0023 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0024 | 0/0 | 1769 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0025 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
c0026 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
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 | 450 | 249 | 27 | 47 | 132 | 12 | 29 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0002 | 0/0 | 450 | 38 | 33 | 5 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0003 | 0/0 | 450 | 23 | 7 | 5 | 11 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0004 | 0/0 | 450 | 5 | 4 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0005 | 0/0 | 450 | 4 | 4 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0006 | 0/0 | 450 | 2 | 0 | 0 | 0 | 1 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0007 | 0/0 | 446 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0008 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0009 | 0/0 | 451 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0010 | 0/0 | 450 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0011 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0012 | 0/0 | 450 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
t0013 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
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 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1770 | 168 | 4 | 21 | 112 | 8 | 22 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0007 | 0/0 | 1770 | 9 | 0 | 7 | 0 | 0 | 2 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0009 | 0/0 | 1770 | 5 | 0 | 2 | 0 | 2 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0010 | 0/0 | 1770 | 3 | 1 | 1 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0014 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0016 | 0/0 | 1770 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0023 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0002 | 1/0 | 1770 | 74 | 30 | 19 | 18 | 1 | 5 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0003 | 0/0 | 1770 | 14 | 12 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0004 | 0/0 | 1770 | 10 | 9 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0012 | 0/0 | 1770 | 2 | 0 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0019 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0021 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0005 | 0/0 | 1770 | 10 | 8 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0013 | 0/0 | 1770 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0004c0006 | 0/0 | 1770 | 9 | 9 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0005c0008 | 0/0 | 1770 | 6 | 0 | 0 | 6 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0006c0011 | 0/0 | 1770 | 3 | 0 | 0 | 3 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0007c0022 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0008c0024 | 0/0 | 1769 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0009c0018 | 0/0 | 1771 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0010c0015 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0011c0017 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0012c0020 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0013c0025 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0014c0026 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2219 | 165 | 3 | 21 | 111 | 7 | 22 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0001t0002 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0001t0006 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0001t0012 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0007t0001 | 0/0 | 2219 | 8 | 0 | 7 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0007t0006 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0009t0001 | 0/0 | 2219 | 5 | 0 | 2 | 0 | 2 | 1 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0010t0001 | 0/0 | 2219 | 3 | 1 | 1 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0014t0001 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0016t0001 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0001c0023t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0002t0001 | 1/0 | 2219 | 39 | 10 | 14 | 8 | 1 | 5 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0002t0002 | 0/0 | 2219 | 13 | 12 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0002t0003 | 0/0 | 2219 | 18 | 5 | 3 | 10 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0002t0004 | 0/0 | 2219 | 3 | 2 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0002t0010 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0003t0001 | 0/0 | 2219 | 5 | 4 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0003t0002 | 0/0 | 2219 | 7 | 7 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0003t0007 | 0/0 | 2215 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0003t0009 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0004t0001 | 0/0 | 2219 | 3 | 3 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0004t0002 | 0/0 | 2219 | 3 | 2 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0004t0005 | 0/0 | 2219 | 3 | 3 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0004t0008 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0012t0002 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0012t0003 | 0/0 | 2219 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0019t0001 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0002c0021t0001 | 0/0 | 2219 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0005t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0005t0002 | 0/0 | 2219 | 5 | 3 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0005t0003 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0005t0004 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0013t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0003c0013t0002 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0004c0006t0001 | 0/0 | 2219 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0004c0006t0002 | 0/0 | 2219 | 7 | 7 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0005c0008t0001 | 0/0 | 2219 | 5 | 0 | 0 | 5 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0005c0008t0003 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0006c0011t0001 | 0/0 | 2219 | 3 | 0 | 0 | 3 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0007c0022t0001 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0008c0024t0005 | 0/0 | 2218 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0009c0018t0003 | 0/0 | 2220 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0010c0015t0013 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0011c0017t0011 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0012c0020t0001 | 0/0 | 2220 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0013c0025t0001 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
a0014c0026t0001 | 0/0 | 2219 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | copy fasta | chrX | 2929521 | 2969341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0007t0006g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0009t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0009t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0009t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0009t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0009t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0010t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0010t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0010t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0014t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0016t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0001c0023t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0002t0010g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0003t0009g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0004t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0012t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0012t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0019t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0002c0021t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0005t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0013t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0003c0013t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0004c0006t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0005c0008t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0005c0008t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0005c0008t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0005c0008t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0005c0008t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0005c0008t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0006c0011t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0006c0011t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0006c0011t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0007c0022t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0008c0024t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0009c0018t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0010c0015t0013g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0011c0017t0011g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0012c0020t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0013c0025t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
a0014c0026t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0021 | t0001 | g0171 | EUR | GBR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00099 | hp2 | a0001 | c0010 | t0001 | g0135 | EUR | GBR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00140 | hp1 | a0001 | c0009 | t0001 | g0207 | EUR | GBR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0201 | EUR | FIN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0117 | EUR | FIN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0236 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00423 | hp2 | a0002 | c0019 | t0001 | g0145 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00597 | hp2 | a0002 | c0002 | t0003 | g0249 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00642 | hp1 | a0001 | c0016 | t0001 | g0163 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00733 | hp1 | a0002 | c0004 | t0002 | g0025 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG00741 | hp2 | a0002 | c0003 | t0001 | g0210 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01070 | hp1 | a0003 | c0005 | t0002 | g0023 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01071 | hp2 | a0003 | c0005 | t0002 | g0022 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01099 | hp1 | a0001 | c0007 | t0001 | g0292 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01109 | hp1 | a0002 | c0003 | t0009 | g0040 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0277 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01168 | hp2 | a0001 | c0009 | t0001 | g0106 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01169 | hp1 | a0001 | c0009 | t0001 | g0199 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01175 | hp1 | a0002 | c0012 | t0002 | g0033 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01256 | hp1 | a0001 | c0007 | t0001 | g0309 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01261 | hp1 | a0002 | c0002 | t0004 | g0016 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0271 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0266 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0295 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01496 | hp1 | a0009 | c0018 | t0003 | g0315 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01516 | hp1 | a0001 | c0009 | t0001 | g0107 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01884 | hp1 | a0004 | c0006 | t0001 | g0245 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01891 | hp1 | a0002 | c0003 | t0002 | g0041 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0214 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0272 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01943 | hp1 | a0001 | c0007 | t0001 | g0307 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01952 | hp1 | a0001 | c0007 | t0001 | g0308 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01981 | hp1 | a0002 | c0012 | t0003 | g0312 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01981 | hp2 | a0002 | c0002 | t0003 | g0229 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01993 | hp2 | a0001 | c0007 | t0001 | g0311 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02004 | hp1 | a0001 | c0007 | t0001 | g0294 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0263 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02055 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02129 | hp1 | a0006 | c0011 | t0001 | g0221 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02145 | hp1 | a0002 | c0003 | t0001 | g0212 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02165 | hp2 | a0001 | c0014 | t0001 | g0204 | EAS | CDX | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02257 | hp1 | a0003 | c0005 | t0003 | g0216 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02257 | hp2 | a0001 | c0010 | t0001 | g0258 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02273 | hp2 | a0001 | c0007 | t0001 | g0313 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02280 | hp1 | a0003 | c0005 | t0001 | g0082 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02280 | hp2 | a0004 | c0006 | t0002 | g0003 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0317 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02293 | hp2 | a0002 | c0002 | t0003 | g0264 | AMR | PEL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02451 | hp1 | a0002 | c0003 | t0007 | g0011 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02451 | hp2 | a0004 | c0006 | t0002 | g0024 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02572 | hp1 | a0002 | c0002 | t0003 | g0238 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02615 | hp1 | a0002 | c0002 | t0003 | g0148 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02615 | hp2 | a0003 | c0013 | t0002 | g0035 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02622 | hp1 | a0002 | c0004 | t0005 | g0119 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0052 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02630 | hp2 | a0002 | c0002 | t0003 | g0235 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02647 | hp1 | a0003 | c0005 | t0002 | g0050 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02723 | hp1 | a0004 | c0006 | t0002 | g0042 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02723 | hp2 | a0002 | c0002 | t0002 | g0031 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02809 | hp1 | a0004 | c0006 | t0002 | g0003 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0217 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02895 | hp1 | a0002 | c0002 | t0004 | g0038 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0047 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02896 | hp2 | a0008 | c0024 | t0005 | g0113 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02897 | hp1 | a0002 | c0003 | t0002 | g0049 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02897 | hp2 | a0002 | c0002 | t0004 | g0028 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02922 | hp1 | a0002 | c0002 | t0003 | g0178 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02922 | hp2 | a0002 | c0002 | t0002 | g0036 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02965 | hp1 | a0003 | c0005 | t0002 | g0027 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02976 | hp2 | a0002 | c0004 | t0001 | g0115 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03041 | hp1 | a0002 | c0004 | t0002 | g0039 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03041 | hp2 | a0003 | c0005 | t0002 | g0032 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03098 | hp1 | a0002 | c0003 | t0001 | g0242 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03130 | hp1 | a0004 | c0006 | t0002 | g0030 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03139 | hp1 | a0003 | c0005 | t0004 | g0051 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03195 | hp1 | a0002 | c0003 | t0002 | g0048 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03209 | hp1 | a0002 | c0004 | t0008 | g0012 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03225 | hp1 | a0014 | c0026 | t0001 | g0098 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03453 | hp1 | a0003 | c0013 | t0001 | g0297 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03453 | hp2 | a0001 | c0023 | t0001 | g0132 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03486 | hp1 | a0002 | c0004 | t0001 | g0244 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03486 | hp2 | a0002 | c0003 | t0002 | g0037 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03516 | hp1 | a0004 | c0006 | t0002 | g0043 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03540 | hp2 | a0004 | c0006 | t0001 | g0282 | AFR | GWD | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03579 | hp1 | a0002 | c0002 | t0010 | g0014 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0280 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03704 | hp1 | a0001 | c0007 | t0006 | g0259 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0302 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03942 | hp1 | a0001 | c0007 | t0001 | g0071 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG04184 | hp2 | a0001 | c0009 | t0001 | g0278 | SAS | BEB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | STU | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18906 | hp1 | a0002 | c0004 | t0001 | g0286 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18906 | hp2 | a0002 | c0003 | t0002 | g0020 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18949 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18951 | hp1 | a0002 | c0002 | t0003 | g0250 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0248 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18962 | hp1 | a0005 | c0008 | t0001 | g0060 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18963 | hp1 | a0005 | c0008 | t0001 | g0128 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18964 | hp1 | a0005 | c0008 | t0001 | g0059 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18972 | hp1 | a0011 | c0017 | t0011 | g0268 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18973 | hp2 | a0002 | c0002 | t0003 | g0094 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18979 | hp2 | a0002 | c0002 | t0003 | g0254 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18991 | hp2 | a0005 | c0008 | t0001 | g0223 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18999 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19000 | hp1 | a0006 | c0011 | t0001 | g0070 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19004 | hp1 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19006 | hp1 | a0012 | c0020 | t0001 | g0251 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19030 | hp2 | a0003 | c0005 | t0004 | g0019 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19043 | hp1 | a0002 | c0004 | t0002 | g0029 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19055 | hp1 | a0007 | c0022 | t0001 | g0247 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19060 | hp1 | a0013 | c0025 | t0001 | g0181 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19063 | hp1 | a0006 | c0011 | t0001 | g0299 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19064 | hp1 | a0005 | c0008 | t0001 | g0129 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19066 | hp1 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19067 | hp1 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19076 | hp1 | a0010 | c0015 | t0013 | g0288 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19078 | hp2 | a0005 | c0008 | t0003 | g0127 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19090 | hp2 | a0002 | c0002 | t0003 | g0112 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | YRI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA20129 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | ASW | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA20129 | hp2 | a0002 | c0003 | t0002 | g0021 | AFR | ASW | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0283 | EUR | TSI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0159 | SAS | GIH | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01123 | hp1 | a0001 | c0010 | t0001 | g0310 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0314 | AMR | CLM | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0081 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02559 | hp1 | a0002 | c0004 | t0005 | g0130 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG02559 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG03471 | hp1 | a0004 | c0006 | t0002 | g0045 | AFR | MSL | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
HG06807 | hp2 | a0002 | c0004 | t0005 | g0180 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA20300 | hp1 | a0003 | c0005 | t0003 | g0215 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0209 | AFR | USA | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0046 | AFR | LWK | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0285 | REF | REF | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0116 | REF | REF | ARSL_chrX_2929521_2969341 | ARSL | chrX | 2929521 | 2969341 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2934866
|
A | AG | 1 | a0009 | 1 | HG01496.hp1 | frameshift_variant | HIGH | c.1735dupC | p.Leu579fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1873/2219 | 1735/1770 | 579/589 | chrX | 2934866 | ||
chrX:2934885
|
A | AG | 1 | a0011 | 1 | NA18972.hp1 | frameshift_variant | HIGH | c.1716dupC | p.Cys573fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1854/2219 | 1716/1770 | 572/589 | chrX | 2934885 | ||
chrX:2935094
|
TC | T | 1 | a0008 | 1 | HG02896.hp2 | frameshift_variant | HIGH | c.1507delG | p.Glu503fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1645/2219 | 1507/1770 | 503/589 | chrX | 2935094 | ||
chrX:2935112
|
A | AC | 1 | a0010 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.1489dupG | p.Val497fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1627/2219 | 1489/1770 | 497/589 | chrX | 2935112 | ||
chrX:2935169
|
TG | T | 1 | a0008 | 1 | HG02896.hp2 | frameshift_variant | HIGH | c.1432delC | p.His478fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1570/2219 | 1432/1770 | 478/589 | chrX | 2935169 | ||
chrX:2935184
|
G | GT | 1 | a0008 | 1 | HG02896.hp2 | frameshift_variant | HIGH | c.1417dupA | p.Thr473fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1555/2219 | 1417/1770 | 473/589 | chrX | 2935184 | ||
chrX:2938114
|
C | T | 6 | a0001a0006a0010others(3): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
missense_variant | MODERATE | c.1270G>A | p.Gly424Ser | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/11 | 1408/2219 | 1270/1770 | 424/589 | chrX | 2938114 | ||
chrX:2943085
|
C | CA | 1 | a0012 | 1 | NA19006.hp1 | frameshift_variant | HIGH | c.1105_1106insT | p.Gly369fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/11 | 1243/2219 | 1105/1770 | 369/589 | chrX | 2943085 | ||
chrX:2949311
|
GA | G | 1 | a0013 | 1 | NA19060.hp1 | frameshift_variant | HIGH | c.846delT | p.Leu283fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 984/2219 | 846/1770 | 282/589 | chrX | 2949311 | ||
chrX:2949344
|
T | TC | 1 | a0013 | 1 | NA19060.hp1 | frameshift_variant | HIGH | c.813dupG | p.Thr272fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 951/2219 | 813/1770 | 271/589 | chrX | 2949344 | ||
chrX:2949383
|
G | C | 2 | a0006a0007 | 4 | HG02129.hp1 NA19000.hp1 NA19055.hp1 others(1): Show |
missense_variant | MODERATE | c.775C>G | p.His259Asp | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 913/2219 | 775/1770 | 259/589 | chrX | 2949383 | ||
chrX:2949492
|
G | GT | 1 | a0013 | 1 | NA19060.hp1 | frameshift_variant | HIGH | c.665_666insA | p.Ser223fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 803/2219 | 665/1770 | 222/589 | chrX | 2949492 | ||
chrX:2949610
|
C | T | 1 | a0004 | 9 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.548G>A | p.Arg183His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 686/2219 | 548/1770 | 183/589 | chrX | 2949610 | ||
chrX:2949722
|
AT | A | 1 | a0013 | 1 | NA19060.hp1 | frameshift_variant | HIGH | c.435delA | p.Lys145fs | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 573/2219 | 435/1770 | 145/589 | chrX | 2949722 | ||
chrX:2955503
|
C | T | 1 | a0005 | 6 | NA18962.hp1 NA18963.hp1 NA18964.hp1 others(3): Show |
missense_variant | MODERATE | c.220G>A | p.Val74Met | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/11 | 358/2219 | 220/1770 | 74/589 | chrX | 2955503 | ||
chrX:2958302
|
T | C | 1 | a0003 | 12 | HG01070.hp1 HG01071.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.157A>G | p.Ile53Val | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/11 | 295/2219 | 157/1770 | 53/589 | chrX | 2958302 | ||
chrX:2958374
|
C | A | 1 | a0014 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.85G>T | p.Ala29Ser | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/11 | 223/2219 | 85/1770 | 29/589 | chrX | 2958374 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2934874
|
C | T | 1 | a0001c0009 | 5 | HG00140.hp1 HG01168.hp2 HG01169.hp1 others(2): Show |
synonymous_variant | LOW | c.1728G>A | p.Pro576Pro | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1866/2219 | 1728/1770 | 576/589 | chrX | 2934874 | ||
chrX:2934910
|
G | A | 12 | a0001c0001a0001c0007a0001c0009others(9): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
synonymous_variant | LOW | c.1692C>T | p.Asn564Asn | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 1830/2219 | 1692/1770 | 564/589 | chrX | 2934910 | ||
chrX:2936767
|
G | A | 1 | a0002c0019 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.1386C>T | p.His462His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/11 | 1524/2219 | 1386/1770 | 462/589 | chrX | 2936767 | ||
chrX:2943135
|
C | T | 1 | a0001c0014 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.1056G>A | p.Ser352Ser | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/11 | 1194/2219 | 1056/1770 | 352/589 | chrX | 2943135 | ||
chrX:2946092
|
G | A | 1 | a0002c0021 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.897C>T | p.His299His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/11 | 1035/2219 | 897/1770 | 299/589 | chrX | 2946092 | ||
chrX:2949372
|
C | T | 2 | a0001c0007a0002c0012 | 11 | HG01099.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
synonymous_variant | LOW | c.786G>A | p.Thr262Thr | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 924/2219 | 786/1770 | 262/589 | chrX | 2949372 | ||
chrX:2949609
|
G | A | 4 | a0001c0023a0002c0004a0003c0013others(1): Show | 14 | HG00733.hp1 HG02559.hp1 HG02615.hp2 others(11): Show |
synonymous_variant | LOW | c.549C>T | p.Arg183Arg | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 687/2219 | 549/1770 | 183/589 | chrX | 2949609 | ||
chrX:2949663
|
A | G | 1 | a0001c0010 | 3 | HG00099.hp2 HG01123.hp1 HG02257.hp2 |
synonymous_variant | LOW | c.495T>C | p.His165His | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/11 | 633/2219 | 495/1770 | 165/589 | chrX | 2949663 | ||
chrX:2958381
|
T | C | 3 | a0002c0003a0003c0005a0014c0026 | 25 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
synonymous_variant | LOW | c.78A>G | p.Ala26Ala | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/11 | 216/2219 | 78/1770 | 26/589 | chrX | 2958381 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2934558
|
C | G | 7 | a0002c0002t0003a0002c0002t0004a0002c0012t0003others(4): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*274G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 274 | chrX | 2934558 | |||||
chrX:2934561
|
C | T | 7 | a0002c0002t0003a0002c0002t0004a0002c0012t0003others(4): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*271G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 271 | chrX | 2934561 | |||||
chrX:2934567
|
C | T | 1 | a0002c0002t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*265G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 265 | chrX | 2934567 | |||||
chrX:2934641
|
A | AT | 1 | a0002c0003t0009 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 190 | chrX | 2934641 | |||||
chrX:2934651
|
T | A | 1 | a0001c0001t0012 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*181A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 181 | chrX | 2934651 | |||||
chrX:2934665
|
A | G | 3 | a0002c0004t0005a0002c0004t0008a0008c0024t0005 | 5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*167T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 167 | chrX | 2934665 | |||||
chrX:2934697
|
GT | G | 1 | a0010c0015t0013 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 134 | chrX | 2934697 | |||||
chrX:2934743
|
TG | T | 1 | a0011c0017t0011 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*88delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 88 | chrX | 2934743 | |||||
chrX:2934746
|
G | A | 2 | a0001c0001t0006a0001c0007t0006 | 2 | HG00323.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 11/11 | 86 | chrX | 2934746 | |||||
chrX:2960404
|
GTCTC | G | 1 | a0002c0003t0007 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8_-5delGAGA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/11 | 5 | chrX | 2960404 | |||||
chrX:2964339
|
A | G | 14 | a0001c0001t0002a0002c0002t0002a0002c0002t0004others(11): Show | 47 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(44): Show |
5_prime_UTR_variant | MODIFIER | c.-136T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/11 | 3939 | chrX | 2964339 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:2935242
|
G | A | 4 | a0002c0002t0001g0159a0002c0002t0001g0266a0002c0002t0001g0283others(1): Show | 4 | HG00099.hp1 HG01358.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1412-52C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935242 | ||||||
chrX:2935552
|
C | T | 6 | a0002c0004t0001g0115a0003c0005t0002g0022a0003c0005t0002g0023others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-362G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935552 | ||||||
chrX:2935667
|
TTTTTC | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(174): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1412-482_1412-478d others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935667 | ||||||
chrX:2935683
|
TTTTC | T | 13 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0104others(10): Show | 13 | HG00673.hp1 HG02027.hp1 HG03710.hp1 others(10): Show |
intron_variant | MODIFIER | c.1412-497_1412-494d others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935683 | ||||||
chrX:2935686
|
TCTTTTC | T | 6 | a0001c0001t0001g0064a0001c0001t0001g0097a0001c0001t0001g0123others(3): Show | 6 | HG02015.hp1 NA18959.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.1412-502_1412-497d others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935686 | ||||||
chrX:2935691
|
TC | T | 2 | a0002c0002t0004g0028a0005c0008t0003g0127 | 2 | HG02897.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1412-502delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935691 | ||||||
chrX:2935692
|
C | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(212): Show | 224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1412-502G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935692 | ||||||
chrX:2935692
|
CT | C | 8 | a0002c0002t0001g0213a0002c0002t0001g0277a0002c0002t0002g0015others(5): Show | 8 | HG01168.hp1 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1412-503delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935692 | ||||||
chrX:2935693
|
T | TTTTC | 3 | a0002c0002t0001g0131a0002c0004t0001g0286a0002c0004t0002g0029 | 3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1412-504_1412-503i others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935693 | ||||||
chrX:2935696
|
T | C | 1 | a0002c0019t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1412-506A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935696 | ||||||
chrX:2935707
|
T | A | 44 | a0001c0001t0001g0201a0002c0002t0001g0214a0002c0002t0002g0017others(41): Show | 46 | HG00280.hp1 HG00597.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1412-517A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935707 | ||||||
chrX:2935732
|
C | T | 2 | a0003c0013t0001g0297a0003c0013t0002g0035 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1412-542G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935732 | ||||||
chrX:2935824
|
T | C | 1 | a0002c0003t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1412-634A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935824 | ||||||
chrX:2935826
|
C | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0183a0001c0001t0001g0239others(2): Show | 5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1412-636G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2935826 | ||||||
chrX:2936128
|
G | T | 1 | a0002c0002t0002g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1411+614C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936128 | ||||||
chrX:2936175
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1411+567T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936175 | ||||||
chrX:2936303
|
C | G | 1 | a0002c0004t0002g0039 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1411+439G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936303 | ||||||
chrX:2936501
|
A | AC | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1411+240dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936501 | ||||||
chrX:2936621
|
C | T | 1 | a0002c0002t0002g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1411+121G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 10/10 | chrX | 2936621 | ||||||
chrX:2936908
|
C | T | 2 | a0002c0003t0001g0217a0002c0004t0002g0025 | 2 | HG00733.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1290-45G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2936908 | ||||||
chrX:2936994
|
G | T | 1 | a0001c0001t0001g0156 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1290-131C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2936994 | ||||||
chrX:2937130
|
G | A | 4 | a0003c0005t0003g0215a0003c0005t0003g0216a0003c0005t0004g0019others(1): Show | 4 | HG02257.hp1 HG03139.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1290-267C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937130 | ||||||
chrX:2937134
|
G | C | 34 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(31): Show | 35 | HG00597.hp2 HG00733.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.1290-271C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937134 | ||||||
chrX:2937158
|
T | C | 32 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(29): Show | 33 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.1290-295A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937158 | ||||||
chrX:2937164
|
C | A | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0182 | 3 | NA18983.hp1 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1290-301G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937164 | ||||||
chrX:2937326
|
G | A | 1 | a0002c0003t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1290-463C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937326 | ||||||
chrX:2937348
|
C | T | 1 | a0002c0003t0001g0212 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1290-485G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937348 | ||||||
chrX:2937393
|
C | CA | 4 | a0001c0001t0001g0274a0002c0002t0001g0131a0002c0004t0001g0286others(1): Show | 4 | NA18522.hp1 NA18906.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290-531dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937393 | ||||||
chrX:2937393
|
CA | C | 2 | a0001c0001t0001g0075a0001c0001t0001g0142 | 2 | HG00621.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1290-531delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937393 | ||||||
chrX:2937410
|
G | GA | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1290-548dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937410 | ||||||
chrX:2937410
|
GA | G | 1 | a0008c0024t0005g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1290-548delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937410 | ||||||
chrX:2937485
|
T | C | 5 | a0002c0004t0005g0119a0002c0004t0005g0130a0002c0004t0005g0180others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289+610A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937485 | ||||||
chrX:2937640
|
T | C | 3 | a0002c0002t0002g0046a0003c0013t0001g0297a0003c0013t0002g0035 | 3 | HG02615.hp2 HG03453.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1289+455A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937640 | ||||||
chrX:2937797
|
T | G | 9 | a0002c0003t0001g0209a0002c0003t0002g0020a0002c0003t0002g0021others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289+298A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937797 | ||||||
chrX:2937825
|
T | C | 3 | a0002c0002t0001g0213a0002c0002t0002g0044a0002c0003t0001g0242 | 3 | HG02486.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1289+270A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937825 | ||||||
chrX:2937877
|
G | C | 1 | a0001c0001t0001g0141 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1289+218C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 9/10 | chrX | 2937877 | ||||||
chrX:2938380
|
T | TTC | 201 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(198): Show | 208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1127-125_1127-124d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938380 | ||||||
chrX:2938380
|
TTC | T | 1 | a0002c0003t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1127-125_1127-124d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938380 | ||||||
chrX:2938382
|
C | T | 2 | a0002c0002t0001g0213a0002c0002t0002g0044 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1127-125G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938382 | ||||||
chrX:2938574
|
C | T | 3 | a0001c0001t0001g0093a0001c0001t0001g0218a0002c0002t0003g0238 | 3 | HG02572.hp1 NA18949.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1127-317G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938574 | ||||||
chrX:2938735
|
T | TC | 1 | a0010c0015t0013g0288 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1127-479dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938735 | ||||||
chrX:2938815
|
TG | T | 1 | a0010c0015t0013g0288 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1127-559delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938815 | ||||||
chrX:2938938
|
C | T | 1 | a0002c0003t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1127-681G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938938 | ||||||
chrX:2938966
|
TG | T | 1 | a0010c0015t0013g0288 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1127-710delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938966 | ||||||
chrX:2938987
|
TC | T | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1127-731delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2938987 | ||||||
chrX:2939003
|
G | GA | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1127-747dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939003 | ||||||
chrX:2939025
|
A | G | 1 | a0002c0003t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1127-768T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939025 | ||||||
chrX:2939041
|
T | TC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-785dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939041 | ||||||
chrX:2939088
|
G | C | 3 | a0002c0002t0001g0131a0002c0004t0001g0286a0002c0004t0002g0029 | 3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1127-831C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939088 | ||||||
chrX:2939100
|
TA | T | 1 | a0001c0001t0001g0123 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1127-844delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939100 | ||||||
chrX:2939146
|
C | CG | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-890dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939146 | ||||||
chrX:2939259
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1127-1002G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939259 | ||||||
chrX:2939269
|
A | AG | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1013dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939269 | ||||||
chrX:2939316
|
C | G | 2 | a0002c0003t0001g0210a0004c0006t0002g0003 | 3 | HG00741.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1127-1059G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939316 | ||||||
chrX:2939317
|
C | T | 6 | a0002c0002t0001g0214a0002c0002t0002g0052a0002c0002t0002g0053others(3): Show | 6 | HG00733.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1127-1060G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939317 | ||||||
chrX:2939324
|
G | A | 15 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(12): Show | 16 | HG00597.hp2 HG01123.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1127-1067C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939324 | ||||||
chrX:2939388
|
C | CG | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1132_1127-113 others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939388 | ||||||
chrX:2939416
|
C | T | 3 | a0002c0004t0002g0025a0003c0013t0001g0297a0003c0013t0002g0035 | 3 | HG00733.hp1 HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1127-1159G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939416 | ||||||
chrX:2939549
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1127-1292C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939549 | ||||||
chrX:2939583
|
C | T | 27 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(24): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1127-1326G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939583 | ||||||
chrX:2939636
|
A | G | 8 | a0002c0003t0001g0210a0002c0003t0001g0242a0002c0004t0005g0119others(5): Show | 9 | HG00741.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1127-1379T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939636 | ||||||
chrX:2939664
|
T | TA | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1408dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939664 | ||||||
chrX:2939716
|
A | AC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1127-1460dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939716 | ||||||
chrX:2939754
|
C | CG | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1498dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939754 | ||||||
chrX:2939772
|
C | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(235): Show | 247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1127-1515G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939772 | ||||||
chrX:2939813
|
T | A | 3 | a0002c0002t0001g0131a0002c0004t0001g0286a0002c0004t0002g0029 | 3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1127-1556A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939813 | ||||||
chrX:2939864
|
C | CT | 11 | a0001c0001t0001g0126a0001c0001t0001g0175a0002c0002t0001g0125others(8): Show | 11 | HG00423.hp2 HG01106.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1127-1608dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | ||||||
chrX:2939864
|
CT | C | 48 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0124others(45): Show | 50 | HG00140.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1127-1608delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | ||||||
chrX:2939864
|
CTT | C | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(157): Show | 167 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1127-1609_1127-160 others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | ||||||
chrX:2939864
|
CTTT | C | 15 | a0001c0001t0001g0064a0001c0001t0001g0103a0001c0001t0001g0122others(12): Show | 15 | HG01081.hp1 HG01169.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1127-1610_1127-160 others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939864 | ||||||
chrX:2939913
|
C | A | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1656G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939913 | ||||||
chrX:2939914
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1657T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939914 | ||||||
chrX:2939928
|
T | TG | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1672dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2939928 | ||||||
chrX:2940025
|
G | A | 1 | a0002c0004t0002g0025 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1127-1768C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940025 | ||||||
chrX:2940042
|
A | T | 1 | a0001c0001t0001g0192 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1127-1785T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940042 | ||||||
chrX:2940092
|
T | G | 27 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(24): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1127-1835A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940092 | ||||||
chrX:2940100
|
T | G | 1 | a0002c0019t0001g0145 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1127-1843A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940100 | ||||||
chrX:2940135
|
T | C | 1 | a0004c0006t0002g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1127-1878A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940135 | ||||||
chrX:2940157
|
T | A | 1 | a0002c0003t0001g0242 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1127-1900A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940157 | ||||||
chrX:2940159
|
C | T | 1 | a0002c0003t0001g0242 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1127-1902G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940159 | ||||||
chrX:2940165
|
G | GC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1127-1909dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940165 | ||||||
chrX:2940219
|
A | AC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1963dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940219 | ||||||
chrX:2940245
|
A | AG | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-1989dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940245 | ||||||
chrX:2940310
|
A | AC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-2054dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940310 | ||||||
chrX:2940379
|
A | AT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1127-2123dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940379 | ||||||
chrX:2940431
|
G | GC | 2 | a0001c0001t0001g0220a0012c0020t0001g0251 | 2 | NA18981.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1127-2175dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940431 | ||||||
chrX:2940549
|
G | GT | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1127-2293dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940549 | ||||||
chrX:2940562
|
G | T | 2 | a0001c0001t0006g0117a0001c0007t0006g0259 | 2 | HG00323.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1127-2305C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940562 | ||||||
chrX:2940582
|
A | AG | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1127-2326dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940582 | ||||||
chrX:2940607
|
A | AAT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1127-2351_1127-235 others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940607 | ||||||
chrX:2940655
|
A | G | 8 | a0002c0003t0001g0210a0002c0003t0001g0242a0002c0004t0005g0119others(5): Show | 9 | HG00741.hp2 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1127-2398T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940655 | ||||||
chrX:2940672
|
CCTG | C | 27 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(24): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+2390_1126+239 others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940672 | ||||||
chrX:2940723
|
G | GT | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+2341dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940723 | ||||||
chrX:2940756
|
C | CA | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+2308dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940756 | ||||||
chrX:2940777
|
A | AT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+2287dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940777 | ||||||
chrX:2940792
|
AG | A | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+2272delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940792 | ||||||
chrX:2940816
|
TC | T | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+2248delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940816 | ||||||
chrX:2940857
|
GC | G | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+2207delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940857 | ||||||
chrX:2940890
|
C | T | 6 | a0002c0004t0001g0115a0003c0005t0002g0022a0003c0005t0002g0023others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1126+2175G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940890 | ||||||
chrX:2940894
|
C | CT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+2170_1126+217 others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940894 | ||||||
chrX:2940947
|
A | C | 3 | a0002c0002t0001g0131a0002c0004t0001g0286a0002c0004t0002g0029 | 3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1126+2118T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940947 | ||||||
chrX:2940958
|
C | CA | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+2106dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940958 | ||||||
chrX:2940988
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1126+2077C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2940988 | ||||||
chrX:2941196
|
GC | G | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1868delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941196 | ||||||
chrX:2941247
|
C | CT | 3 | a0002c0002t0001g0095a0002c0002t0001g0151a0004c0006t0002g0003 | 4 | HG00423.hp1 HG01106.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1126+1817dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | ||||||
chrX:2941247
|
CT | C | 38 | a0001c0001t0001g0175a0002c0002t0001g0131a0002c0002t0001g0213others(35): Show | 39 | HG00597.hp2 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1126+1817delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | ||||||
chrX:2941247
|
CTT | C | 1 | a0002c0002t0003g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1126+1816_1126+181 others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | ||||||
chrX:2941247
|
CTTTTTTT others(3): Show |
C | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(184): Show | 194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1126+1808_1126+181 others(14): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | ||||||
chrX:2941247
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0001g0061a0001c0001t0001g0257a0001c0001t0001g0274others(2): Show | 5 | HG00408.hp1 HG01169.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1126+1807_1126+181 others(15): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941247 | ||||||
chrX:2941253
|
T | C | 1 | a0002c0003t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1126+1812A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941253 | ||||||
chrX:2941298
|
A | AG | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1766dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941298 | ||||||
chrX:2941401
|
C | T | 27 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(24): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+1664G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941401 | ||||||
chrX:2941411
|
C | CCA | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1653_1126+165 others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941411 | ||||||
chrX:2941411
|
C | T | 1 | a0002c0002t0001g0151 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1126+1654G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941411 | ||||||
chrX:2941412
|
A | C | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1653T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941412 | ||||||
chrX:2941420
|
A | T | 2 | a0002c0002t0001g0213a0002c0002t0002g0044 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1126+1645T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941420 | ||||||
chrX:2941459
|
TG | T | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1605delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941459 | ||||||
chrX:2941460
|
G | T | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1605C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941460 | ||||||
chrX:2941461
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1126+1604C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941461 | ||||||
chrX:2941472
|
C | CT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1592dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941472 | ||||||
chrX:2941488
|
CA | C | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1576delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941488 | ||||||
chrX:2941498
|
A | AC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1566dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941498 | ||||||
chrX:2941551
|
G | A | 28 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(25): Show | 29 | HG00597.hp2 HG00733.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.1126+1514C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941551 | ||||||
chrX:2941584
|
TC | T | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1480delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941584 | ||||||
chrX:2941619
|
C | A | 1 | a0002c0004t0001g0244 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1126+1446G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941619 | ||||||
chrX:2941664
|
GC | G | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1400delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941664 | ||||||
chrX:2941722
|
T | TC | 1 | a0001c0001t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+1342_1126+134 others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941722 | ||||||
chrX:2941761
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+1304T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941761 | ||||||
chrX:2941763
|
C | A | 1 | a0001c0001t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+1302G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941763 | ||||||
chrX:2941796
|
C | CT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1268dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941796 | ||||||
chrX:2941798
|
C | T | 5 | a0002c0002t0001g0214a0002c0002t0002g0052a0002c0002t0002g0053others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+1267G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941798 | ||||||
chrX:2941805
|
TC | T | 1 | a0001c0001t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+1259delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941805 | ||||||
chrX:2941838
|
C | T | 5 | a0002c0002t0001g0214a0002c0002t0002g0052a0002c0002t0002g0053others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1126+1227G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941838 | ||||||
chrX:2941928
|
A | AC | 1 | a0001c0001t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+1136dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941928 | ||||||
chrX:2941950
|
A | C | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1115T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941950 | ||||||
chrX:2941951
|
C | A | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1114G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941951 | ||||||
chrX:2941951
|
C | CA | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1113dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941951 | ||||||
chrX:2941951
|
CA | C | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1126+1113delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941951 | ||||||
chrX:2941952
|
A | C | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+1113T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2941952 | ||||||
chrX:2942000
|
G | GT | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1064dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942000 | ||||||
chrX:2942018
|
G | GA | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1046_1126+104 others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942018 | ||||||
chrX:2942056
|
T | TG | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+1008dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942056 | ||||||
chrX:2942066
|
G | T | 1 | a0002c0002t0002g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1126+999C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942066 | ||||||
chrX:2942084
|
G | GC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+980dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942084 | ||||||
chrX:2942104
|
AG | A | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+960delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942104 | ||||||
chrX:2942145
|
A | G | 1 | a0002c0002t0002g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1126+920T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942145 | ||||||
chrX:2942160
|
C | G | 1 | a0002c0003t0001g0242 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1126+905G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942160 | ||||||
chrX:2942248
|
G | GC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+816dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942248 | ||||||
chrX:2942266
|
A | C | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+799T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942266 | ||||||
chrX:2942269
|
T | TA | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+795dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942269 | ||||||
chrX:2942298
|
AT | A | 1 | a0001c0001t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1126+766delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942298 | ||||||
chrX:2942319
|
ACT | A | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+744_1126+745d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942319 | ||||||
chrX:2942352
|
C | T | 2 | a0003c0013t0001g0297a0003c0013t0002g0035 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1126+713G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942352 | ||||||
chrX:2942395
|
G | T | 3 | a0002c0002t0001g0131a0002c0004t0001g0286a0002c0004t0002g0029 | 3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1126+670C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942395 | ||||||
chrX:2942401
|
T | C | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(238): Show | 250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1126+664A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942401 | ||||||
chrX:2942416
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(243): Show | 255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1126+649A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942416 | ||||||
chrX:2942441
|
GC | G | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+623delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942441 | ||||||
chrX:2942449
|
G | GC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+615dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942449 | ||||||
chrX:2942480
|
C | T | 27 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(24): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.1126+585G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942480 | ||||||
chrX:2942507
|
G | GC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+557dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942507 | ||||||
chrX:2942548
|
T | TC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+516dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942548 | ||||||
chrX:2942560
|
G | GT | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+504_1126+505i others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942560 | ||||||
chrX:2942746
|
TG | T | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+318delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942746 | ||||||
chrX:2942793
|
T | TC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+271dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942793 | ||||||
chrX:2942814
|
A | AT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+250dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942814 | ||||||
chrX:2942849
|
A | AT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+215dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942849 | ||||||
chrX:2942867
|
T | TA | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+197dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942867 | ||||||
chrX:2942878
|
A | AC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+186dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942878 | ||||||
chrX:2942946
|
AG | A | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+118delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942946 | ||||||
chrX:2942997
|
G | GC | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1126+67dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2942997 | ||||||
chrX:2943004
|
TG | T | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1126+60delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2943004 | ||||||
chrX:2943063
|
AC | A | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | splice_donor_variant&intron_variant | HIGH | c.1126+1delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 8/10 | chrX | 2943063 | ||||||
chrX:2943280
|
C | CG | 1 | a0001c0001t0001g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.992-82dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943280 | ||||||
chrX:2943317
|
G | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0183a0001c0001t0001g0239others(2): Show | 5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-118C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943317 | ||||||
chrX:2943319
|
A | C | 5 | a0001c0001t0001g0054a0001c0001t0001g0183a0001c0001t0001g0239others(2): Show | 5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-120T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943319 | ||||||
chrX:2943418
|
G | C | 316 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(313): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.992-219C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943418 | ||||||
chrX:2943420
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.992-221T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943420 | ||||||
chrX:2943423
|
A | C | 27 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(24): Show | 28 | HG00597.hp2 HG01123.hp2 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.992-224T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943423 | ||||||
chrX:2943453
|
G | A | 1 | a0001c0014t0001g0204 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.992-254C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943453 | ||||||
chrX:2943488
|
TC | T | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-290delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943488 | ||||||
chrX:2943515
|
G | A | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-316C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943515 | ||||||
chrX:2943516
|
A | G | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-317T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943516 | ||||||
chrX:2943603
|
G | A | 1 | a0001c0001t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.992-404C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943603 | ||||||
chrX:2943666
|
C | T | 2 | a0002c0002t0002g0017a0002c0004t0002g0025 | 2 | HG00733.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.992-467G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943666 | ||||||
chrX:2943698
|
C | T | 2 | a0002c0002t0002g0017a0002c0004t0002g0025 | 2 | HG00733.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.992-499G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943698 | ||||||
chrX:2943706
|
C | T | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.992-507G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943706 | ||||||
chrX:2943741
|
C | CA | 10 | a0001c0001t0001g0087a0001c0001t0001g0194a0001c0007t0001g0071others(7): Show | 10 | HG01516.hp2 HG01981.hp1 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-543dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | ||||||
chrX:2943741
|
C | CAA | 4 | a0001c0001t0001g0065a0001c0001t0001g0184a0001c0001t0001g0274others(1): Show | 4 | HG01361.hp2 NA19082.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-544_992-543dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | ||||||
chrX:2943741
|
CA | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0054others(140): Show | 147 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.992-543delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | ||||||
chrX:2943741
|
CAA | C | 35 | a0001c0001t0001g0058a0001c0001t0001g0064a0001c0001t0001g0067others(32): Show | 35 | HG00323.hp1 HG00673.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.992-544_992-543del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | ||||||
chrX:2943741
|
CAAA | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0104others(2): Show | 5 | HG02027.hp1 HG04184.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-545_992-543del others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | ||||||
chrX:2943741
|
CAAAA | C | 3 | a0002c0002t0002g0017a0002c0004t0002g0025a0006c0011t0001g0299 | 3 | HG00733.hp1 NA19063.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.992-546_992-543del others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943741 | ||||||
chrX:2943793
|
G | GAGA | 3 | a0002c0002t0001g0131a0002c0004t0001g0286a0002c0004t0002g0029 | 3 | NA18522.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.992-597_992-595dup others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943793 | ||||||
chrX:2943815
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.992-616T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2943815 | ||||||
chrX:2944035
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.992-836G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944035 | ||||||
chrX:2944048
|
G | GC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-850dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944048 | ||||||
chrX:2944178
|
A | G | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0182 | 3 | NA18983.hp1 NA18985.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.992-979T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944178 | ||||||
chrX:2944186
|
T | G | 24 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0073others(21): Show | 25 | HG00597.hp2 HG01261.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.992-987A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944186 | ||||||
chrX:2944193
|
T | C | 11 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0100others(8): Show | 11 | HG01175.hp2 HG01496.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.992-994A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944193 | ||||||
chrX:2944194
|
C | G | 11 | a0001c0001t0001g0076a0001c0001t0001g0083a0001c0001t0001g0100others(8): Show | 11 | HG01175.hp2 HG01496.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.992-995G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944194 | ||||||
chrX:2944200
|
A | C | 6 | a0002c0004t0001g0115a0002c0004t0005g0119a0002c0004t0005g0130others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.992-1001T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944200 | ||||||
chrX:2944223
|
A | T | 1 | a0004c0006t0001g0282 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.992-1024T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944223 | ||||||
chrX:2944226
|
C | T | 20 | a0001c0001t0001g0175a0002c0002t0001g0125a0002c0002t0001g0131others(17): Show | 20 | HG00733.hp1 HG01884.hp1 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.992-1027G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944226 | ||||||
chrX:2944230
|
C | CG | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-1032dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944230 | ||||||
chrX:2944230
|
C | T | 2 | a0002c0002t0001g0213a0002c0002t0002g0044 | 2 | HG02486.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.992-1031G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944230 | ||||||
chrX:2944238
|
A | G | 5 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1039T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944238 | ||||||
chrX:2944239
|
A | AG | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-1041dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944239 | ||||||
chrX:2944252
|
G | A | 1 | a0002c0002t0003g0249 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.992-1053C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944252 | ||||||
chrX:2944262
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.992-1063A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944262 | ||||||
chrX:2944266
|
C | T | 2 | a0002c0002t0001g0172a0002c0002t0001g0187 | 2 | NA18972.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.992-1067G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944266 | ||||||
chrX:2944267
|
A | C | 5 | a0001c0001t0001g0054a0001c0001t0001g0183a0001c0001t0001g0239others(2): Show | 5 | HG02165.hp1 NA18950.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1068T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944267 | ||||||
chrX:2944272
|
G | GGTGAAA | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-1079_992-1074d others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944272 | ||||||
chrX:2944274
|
T | A | 5 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1075A>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944274 | ||||||
chrX:2944296
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0252a0001c0001t0001g0253others(1): Show | 4 | NA18946.hp2 NA18954.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-1097C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944296 | ||||||
chrX:2944314
|
C | T | 2 | a0002c0002t0001g0056a0002c0002t0001g0057 | 2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.992-1115G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944314 | ||||||
chrX:2944315
|
A | G | 4 | a0001c0001t0001g0111a0002c0002t0001g0056a0002c0002t0001g0057others(1): Show | 4 | HG00639.hp2 HG01074.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-1116T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944315 | ||||||
chrX:2944323
|
G | A | 8 | a0001c0001t0001g0175a0002c0004t0002g0039a0004c0006t0001g0245others(5): Show | 8 | HG01884.hp1 HG02015.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.992-1124C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944323 | ||||||
chrX:2944326
|
T | C | 6 | a0004c0006t0001g0245a0004c0006t0002g0024a0004c0006t0002g0030others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-1127A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944326 | ||||||
chrX:2944335
|
A | T | 10 | a0002c0002t0002g0046a0002c0003t0001g0242a0003c0013t0001g0297others(7): Show | 10 | HG01884.hp1 HG02451.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.992-1136T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944335 | ||||||
chrX:2944346
|
C | A | 1 | a0004c0006t0001g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.992-1147G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944346 | ||||||
chrX:2944347
|
C | G | 1 | a0004c0006t0001g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.992-1148G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944347 | ||||||
chrX:2944432
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0198 | 3 | HG02040.hp1 HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.992-1233G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944432 | ||||||
chrX:2944433
|
A | G | 6 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0198others(3): Show | 6 | HG02040.hp1 HG02083.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-1234T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944433 | ||||||
chrX:2944453
|
C | CA | 8 | a0001c0001t0001g0093a0001c0001t0001g0103a0001c0001t0001g0121others(5): Show | 8 | HG02486.hp1 HG02622.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.992-1255dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944453 | ||||||
chrX:2944453
|
CA | C | 2 | a0001c0001t0001g0275a0001c0001t0001g0276 | 2 | NA18995.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.992-1255delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944453 | ||||||
chrX:2944461
|
AAAC | A | 5 | a0002c0004t0005g0119a0002c0004t0005g0130a0002c0004t0005g0180others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1265_992-1263d others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944461 | ||||||
chrX:2944462
|
AAC | A | 1 | a0002c0004t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.992-1265_992-1264d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944462 | ||||||
chrX:2944463
|
AC | A | 14 | a0001c0001t0001g0175a0002c0002t0001g0131a0002c0002t0002g0017others(11): Show | 14 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.992-1265delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944463 | ||||||
chrX:2944466
|
A | C | 5 | a0002c0004t0005g0119a0002c0004t0005g0130a0002c0004t0005g0180others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1267T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944466 | ||||||
chrX:2944472
|
AC | A | 1 | a0011c0017t0011g0268 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.992-1274delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944472 | ||||||
chrX:2944473
|
C | CA | 3 | a0001c0001t0001g0110a0002c0002t0001g0159a0002c0003t0007g0011 | 3 | HG02451.hp1 NA19081.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.992-1275dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944473 | ||||||
chrX:2944473
|
CA | C | 14 | a0001c0001t0001g0123a0001c0001t0001g0134a0001c0001t0001g0226others(11): Show | 14 | HG00738.hp1 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.992-1275delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944473 | ||||||
chrX:2944473
|
CAA | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(164): Show | 174 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.992-1276_992-1275d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944473 | ||||||
chrX:2944475
|
A | C | 1 | a0011c0017t0011g0268 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.992-1276T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944475 | ||||||
chrX:2944477
|
A | C | 5 | a0002c0002t0001g0131a0002c0004t0001g0115a0002c0004t0001g0286others(2): Show | 5 | HG00733.hp1 HG02976.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-1278T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944477 | ||||||
chrX:2944482
|
A | C | 49 | a0001c0001t0001g0175a0002c0002t0001g0131a0002c0002t0001g0214others(46): Show | 51 | HG00597.hp2 HG00733.hp1 HG00741.hp2 others(48): Show |
intron_variant | MODIFIER | c.992-1283T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944482 | ||||||
chrX:2944508
|
G | GTC | 5 | a0002c0004t0005g0119a0002c0004t0005g0130a0002c0004t0005g0180others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1310_992-1309i others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944508 | ||||||
chrX:2944509
|
C | A | 5 | a0002c0004t0005g0119a0002c0004t0005g0130a0002c0004t0005g0180others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.992-1310G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944509 | ||||||
chrX:2944509
|
C | CCA | 3 | a0002c0002t0001g0149a0002c0002t0001g0186a0002c0002t0002g0018 | 3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.992-1312_992-1311d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944509 | ||||||
chrX:2944562
|
G | GA | 1 | a0011c0017t0011g0268 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.992-1364dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944562 | ||||||
chrX:2944568
|
A | AT | 7 | a0002c0004t0005g0119a0002c0004t0005g0130a0002c0004t0005g0180others(4): Show | 7 | HG02559.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.992-1370dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944568 | ||||||
chrX:2944568
|
AT | A | 1 | a0002c0002t0003g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.992-1370delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944568 | ||||||
chrX:2944594
|
A | AC | 6 | a0001c0001t0001g0121a0001c0001t0001g0200a0001c0001t0001g0274others(3): Show | 6 | HG01243.hp1 HG01361.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-1396dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944594 | ||||||
chrX:2944597
|
C | CA | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.992-1399dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944597 | ||||||
chrX:2944629
|
TG | T | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.991+1368delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944629 | ||||||
chrX:2944680
|
T | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(174): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.991+1318A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944680 | ||||||
chrX:2944808
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.991+1190C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944808 | ||||||
chrX:2944809
|
G | GC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.991+1188dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944809 | ||||||
chrX:2944873
|
G | A | 5 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+1125C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944873 | ||||||
chrX:2944873
|
GA | G | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.991+1124delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944873 | ||||||
chrX:2944916
|
A | G | 2 | a0002c0002t0003g0314a0009c0018t0003g0315 | 2 | HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.991+1082T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944916 | ||||||
chrX:2944961
|
GGAA | G | 6 | a0004c0006t0001g0245a0004c0006t0002g0024a0004c0006t0002g0030others(3): Show | 6 | HG01884.hp1 HG02451.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.991+1034_991+1036d others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2944961 | ||||||
chrX:2945005
|
T | TAAGAAG | 3 | a0002c0002t0001g0213a0002c0002t0002g0044a0002c0003t0001g0242 | 3 | HG02486.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.991+987_991+992dup others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945005 | ||||||
chrX:2945005
|
TAAG | T | 2 | a0002c0004t0001g0115a0002c0004t0002g0039 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.991+990_991+992del others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945005 | ||||||
chrX:2945005
|
TAAGAAG | T | 1 | a0001c0001t0001g0166 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.991+987_991+992del others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945005 | ||||||
chrX:2945011
|
G | C | 1 | a0002c0002t0001g0291 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.991+987C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945011 | ||||||
chrX:2945036
|
A | AG | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.991+961dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945036 | ||||||
chrX:2945058
|
A | AG | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.991+939dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945058 | ||||||
chrX:2945097
|
TG | T | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.991+900delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945097 | ||||||
chrX:2945101
|
GGA | G | 1 | a0001c0001t0001g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.991+895_991+896del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945101 | ||||||
chrX:2945107
|
G | C | 1 | a0002c0002t0001g0291 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.991+891C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945107 | ||||||
chrX:2945211
|
C | G | 5 | a0002c0004t0005g0119a0002c0004t0005g0130a0002c0004t0005g0180others(2): Show | 5 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.991+787G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945211 | ||||||
chrX:2945248
|
G | A | 2 | a0003c0013t0001g0297a0003c0013t0002g0035 | 2 | HG02615.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.991+750C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945248 | ||||||
chrX:2945433
|
T | C | 7 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.991+565A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945433 | ||||||
chrX:2945443
|
CCACATGG | C | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.991+548_991+554del others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945443 | ||||||
chrX:2945502
|
T | C | 2 | a0002c0002t0001g0125a0002c0003t0007g0011 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.991+496A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945502 | ||||||
chrX:2945537
|
C | T | 3 | a0002c0002t0001g0149a0002c0002t0001g0186a0002c0002t0002g0018 | 3 | HG01243.hp1 HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.991+461G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945537 | ||||||
chrX:2945554
|
A | AG | 1 | a0001c0001t0001g0274 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.991+443dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945554 | ||||||
chrX:2945608
|
T | C | 5 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+390A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945608 | ||||||
chrX:2945667
|
TG | T | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.991+330delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945667 | ||||||
chrX:2945686
|
A | G | 1 | a0002c0003t0001g0210 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.991+312T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945686 | ||||||
chrX:2945805
|
G | A | 5 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.991+193C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945805 | ||||||
chrX:2945938
|
TC | T | 2 | a0003c0005t0002g0032a0003c0005t0002g0050 | 2 | HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.991+59delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 7/10 | chrX | 2945938 | ||||||
chrX:2946292
|
GA | G | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.855-159delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946292 | ||||||
chrX:2946322
|
C | CT | 16 | a0001c0001t0001g0093a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01175.hp2 HG02145.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.855-189dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
C | CTT | 3 | a0002c0002t0002g0026a0002c0002t0004g0028a0002c0002t0004g0038 | 3 | HG02895.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.855-190_855-189dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CT | C | 23 | a0001c0001t0001g0075a0001c0001t0001g0168a0001c0001t0001g0188others(20): Show | 23 | HG00733.hp1 HG01069.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.855-189delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CTT | C | 1 | a0002c0004t0002g0039 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.855-190_855-189del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CTTTTTT | C | 5 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.855-194_855-189del others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CTTTTTTT | C | 6 | a0002c0002t0001g0125a0002c0002t0001g0272a0002c0003t0007g0011others(3): Show | 7 | HG01884.hp1 HG01928.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.855-195_855-189del others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CTTTTTTT others(1): Show |
C | 11 | a0001c0001t0001g0274a0001c0014t0001g0204a0001c0016t0001g0163others(8): Show | 11 | HG00642.hp1 HG01433.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.855-196_855-189del others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CTTTTTTT others(2): Show |
C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(70): Show | 78 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.855-197_855-189del others(9): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0303a0010c0015t0013g0288 | 2 | HG01169.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.855-198_855-189del others(10): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946322
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0006g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.855-200_855-189del others(12): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946322 | ||||||
chrX:2946496
|
GC | G | 2 | a0002c0002t0002g0002a0002c0002t0002g0013 | 3 | HG02055.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.855-363delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946496 | ||||||
chrX:2946505
|
A | AT | 53 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0069others(50): Show | 54 | HG00408.hp1 HG00741.hp2 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.855-372dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | ||||||
chrX:2946505
|
A | ATT | 6 | a0001c0001t0001g0173a0001c0001t0001g0188a0002c0003t0007g0011others(3): Show | 6 | HG02451.hp1 HG02451.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.855-373_855-372dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | ||||||
chrX:2946505
|
A | ATTT | 1 | a0002c0002t0001g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.855-374_855-372dup others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | ||||||
chrX:2946505
|
AT | A | 90 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(87): Show | 94 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.855-372delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | ||||||
chrX:2946505
|
ATT | A | 2 | a0001c0001t0001g0182a0002c0004t0002g0039 | 2 | HG03041.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.855-373_855-372del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | ||||||
chrX:2946505
|
ATTTTTTT | A | 1 | a0001c0023t0001g0132 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.855-378_855-372del others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | ||||||
chrX:2946505
|
ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0296 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.855-386_855-372del others(15): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946505 | ||||||
chrX:2946580
|
C | T | 1 | a0001c0009t0001g0278 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.855-446G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946580 | ||||||
chrX:2946599
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.855-465G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946599 | ||||||
chrX:2946750
|
A | G | 5 | a0002c0002t0001g0246a0002c0002t0002g0002a0002c0002t0002g0013others(2): Show | 6 | HG01884.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.855-616T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946750 | ||||||
chrX:2946827
|
A | C | 2 | a0001c0001t0001g0084a0001c0001t0001g0222 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.855-693T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946827 | ||||||
chrX:2946969
|
A | G | 4 | a0003c0005t0003g0215a0003c0005t0003g0216a0003c0005t0004g0019others(1): Show | 4 | HG02257.hp1 HG03139.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.855-835T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2946969 | ||||||
chrX:2947039
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.855-905G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947039 | ||||||
chrX:2947040
|
G | A | 3 | a0002c0002t0002g0046a0002c0003t0001g0217a0002c0003t0001g0242 | 3 | HG02809.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.855-906C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947040 | ||||||
chrX:2947089
|
TG | T | 1 | a0001c0001t0001g0136 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.855-956delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947089 | ||||||
chrX:2947124
|
C | T | 3 | a0002c0002t0002g0026a0002c0002t0004g0028a0002c0002t0004g0038 | 3 | HG02895.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.855-990G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947124 | ||||||
chrX:2947141
|
G | A | 2 | a0001c0001t0001g0158a0002c0002t0001g0280 | 2 | HG03669.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.855-1007C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947141 | ||||||
chrX:2947235
|
TC | T | 1 | a0001c0001t0001g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.855-1102delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947235 | ||||||
chrX:2947243
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.855-1109C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947243 | ||||||
chrX:2947255
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(124): Show | 134 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.855-1121C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947255 | ||||||
chrX:2947529
|
T | TC | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.855-1396dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947529 | ||||||
chrX:2947815
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.854+1489C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947815 | ||||||
chrX:2947889
|
A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 129 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.854+1415T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2947889 | ||||||
chrX:2948120
|
C | CA | 5 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027others(2): Show | 5 | HG01070.hp1 HG01071.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+1183dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948120 | ||||||
chrX:2948191
|
G | T | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.854+1113C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948191 | ||||||
chrX:2948341
|
G | C | 3 | a0002c0002t0002g0026a0002c0002t0004g0028a0002c0002t0004g0038 | 3 | HG02895.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.854+963C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948341 | ||||||
chrX:2948371
|
C | CT | 7 | a0002c0002t0001g0125a0002c0002t0003g0081a0002c0002t0003g0148others(4): Show | 7 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.854+932dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948371 | ||||||
chrX:2948615
|
C | T | 3 | a0002c0002t0002g0046a0002c0003t0001g0217a0002c0003t0001g0242 | 3 | HG02809.hp2 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.854+689G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948615 | ||||||
chrX:2948739
|
C | T | 2 | a0002c0004t0001g0286a0002c0004t0002g0029 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.854+565G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948739 | ||||||
chrX:2948853
|
T | C | 1 | a0002c0003t0007g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.854+451A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948853 | ||||||
chrX:2948898
|
C | T | 2 | a0002c0002t0002g0002a0002c0002t0002g0013 | 3 | HG02055.hp1 HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.854+406G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948898 | ||||||
chrX:2948901
|
T | TA | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+402_854+403ins others(1): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948901 | ||||||
chrX:2948910
|
C | CA | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+393_854+394ins others(1): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948910 | ||||||
chrX:2948929
|
C | CT | 1 | a0003c0005t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.854+374dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948929 | ||||||
chrX:2948929
|
C | CTT | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+373_854+374dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948929 | ||||||
chrX:2948982
|
A | AT | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+321dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948982 | ||||||
chrX:2948989
|
C | T | 2 | a0002c0004t0001g0115a0002c0004t0002g0039 | 2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.854+315G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2948989 | ||||||
chrX:2949001
|
C | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(92): Show | 101 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.854+303G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949001 | ||||||
chrX:2949119
|
CG | C | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+184delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949119 | ||||||
chrX:2949138
|
C | T | 6 | a0001c0023t0001g0132a0002c0004t0005g0119a0002c0004t0005g0130others(3): Show | 6 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.854+166G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949138 | ||||||
chrX:2949198
|
TG | T | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+105delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949198 | ||||||
chrX:2949224
|
C | A | 8 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0094others(5): Show | 9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.854+80G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949224 | ||||||
chrX:2949231
|
GA | G | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+72delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949231 | ||||||
chrX:2949283
|
A | AG | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.854+20dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 6/10 | chrX | 2949283 | ||||||
chrX:2949733
|
AG | A | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | splice_region_variant&intron_variant | LOW | c.431-7delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2949733 | ||||||
chrX:2949931
|
TA | T | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-205delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2949931 | ||||||
chrX:2949960
|
T | TG | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-234dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2949960 | ||||||
chrX:2950133
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0304a0001c0001t0001g0305 | 3 | NA18964.hp2 NA19064.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.431-406C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950133 | ||||||
chrX:2950167
|
T | C | 1 | a0002c0003t0007g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.431-440A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950167 | ||||||
chrX:2950187
|
CTG | C | 1 | a0002c0002t0003g0178 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-462_431-461del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950187 | ||||||
chrX:2950191
|
G | GT | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-465dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950191 | ||||||
chrX:2950352
|
A | AC | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-626dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950352 | ||||||
chrX:2950365
|
A | AC | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-639dupG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950365 | ||||||
chrX:2950398
|
T | C | 7 | a0001c0023t0001g0132a0002c0004t0001g0244a0002c0004t0005g0119others(4): Show | 7 | HG02559.hp1 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.431-671A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950398 | ||||||
chrX:2950443
|
C | T | 2 | a0002c0002t0001g0172a0002c0002t0001g0187 | 2 | NA18972.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.431-716G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950443 | ||||||
chrX:2950513
|
A | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(109): Show | 117 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.431-786T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950513 | ||||||
chrX:2950595
|
TG | T | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-869delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950595 | ||||||
chrX:2950716
|
AC | A | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-990delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950716 | ||||||
chrX:2950832
|
GACACAGA others(6): Show |
G | 1 | a0001c0001t0001g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.431-1118_431-1106d others(15): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950832 | ||||||
chrX:2950880
|
TC | T | 8 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0094others(5): Show | 9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1154delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2950880 | ||||||
chrX:2951089
|
C | CT | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.431-1363dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951089 | ||||||
chrX:2951104
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.431-1377G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951104 | ||||||
chrX:2951321
|
C | T | 8 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0094others(5): Show | 9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-1594G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951321 | ||||||
chrX:2951598
|
G | T | 3 | a0002c0003t0001g0212a0002c0003t0001g0217a0002c0003t0001g0242 | 3 | HG02145.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.430+1545C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951598 | ||||||
chrX:2951614
|
C | CA | 16 | a0001c0001t0001g0080a0001c0001t0001g0093a0001c0001t0001g0123others(13): Show | 16 | HG01106.hp1 HG01175.hp2 HG03834.hp1 others(13): Show |
intron_variant | MODIFIER | c.430+1528dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951614 | ||||||
chrX:2951614
|
CA | C | 7 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0001g0305others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1528delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951614 | ||||||
chrX:2951614
|
CAA | C | 41 | a0001c0023t0001g0132a0002c0002t0002g0026a0002c0002t0004g0028others(38): Show | 42 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.430+1527_430+1528d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951614 | ||||||
chrX:2951624
|
A | G | 1 | a0002c0002t0001g0272 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.430+1519T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951624 | ||||||
chrX:2951800
|
T | TA | 2 | a0002c0002t0001g0213a0002c0003t0007g0011 | 2 | HG02451.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.430+1342dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951800 | ||||||
chrX:2951800
|
TA | T | 72 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(69): Show | 77 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.430+1342delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951800 | ||||||
chrX:2951800
|
TAA | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0255a0001c0001t0001g0304others(1): Show | 4 | HG01169.hp1 NA18957.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1341_430+1342d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951800 | ||||||
chrX:2951850
|
G | A | 25 | a0001c0001t0001g0055a0001c0001t0001g0063a0001c0001t0001g0067others(22): Show | 26 | HG01081.hp2 HG01192.hp1 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.430+1293C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951850 | ||||||
chrX:2951874
|
G | GT | 15 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0103others(12): Show | 15 | HG00735.hp2 HG01175.hp2 HG02027.hp1 others(12): Show |
intron_variant | MODIFIER | c.430+1268dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | ||||||
chrX:2951874
|
G | GTT | 7 | a0002c0003t0001g0210a0002c0003t0002g0020a0002c0003t0002g0021others(4): Show | 7 | HG00741.hp2 HG01891.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1267_430+1268d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | ||||||
chrX:2951874
|
G | GTTT | 3 | a0002c0003t0001g0217a0002c0003t0001g0242a0002c0003t0002g0037 | 3 | HG02809.hp2 HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.430+1266_430+1268d others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | ||||||
chrX:2951874
|
G | GTTTT | 2 | a0002c0003t0001g0212a0002c0003t0009g0040 | 2 | HG01109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.430+1265_430+1268d others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | ||||||
chrX:2951874
|
GT | G | 20 | a0001c0001t0001g0253a0001c0023t0001g0132a0002c0004t0001g0115others(17): Show | 21 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.430+1268delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | ||||||
chrX:2951874
|
GTTTTTTT | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(76): Show | 85 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.430+1262_430+1268d others(9): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951874 | ||||||
chrX:2951893
|
T | TA | 1 | a0001c0001t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.430+1249dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951893 | ||||||
chrX:2951905
|
C | G | 88 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0061others(85): Show | 90 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.430+1238G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951905 | ||||||
chrX:2951961
|
TC | T | 1 | a0002c0002t0001g0066 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.430+1181delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951961 | ||||||
chrX:2951990
|
T | TA | 16 | a0001c0023t0001g0132a0002c0002t0002g0026a0002c0002t0004g0028others(13): Show | 16 | HG02280.hp1 HG02559.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.430+1152dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2951990 | ||||||
chrX:2952117
|
G | C | 1 | a0001c0001t0001g0156 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.430+1026C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952117 | ||||||
chrX:2952272
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 132 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.430+871G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952272 | ||||||
chrX:2952347
|
C | G | 21 | a0001c0023t0001g0132a0002c0002t0002g0026a0002c0002t0004g0028others(18): Show | 21 | HG01070.hp1 HG01071.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.430+796G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952347 | ||||||
chrX:2952412
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0177a0001c0001t0001g0195others(4): Show | 8 | HG00323.hp2 HG00639.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+731G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952412 | ||||||
chrX:2952502
|
G | A | 11 | a0001c0001t0001g0067a0001c0001t0001g0093a0001c0001t0001g0104others(8): Show | 12 | HG01081.hp2 HG01192.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+641C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952502 | ||||||
chrX:2952517
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.430+626G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952517 | ||||||
chrX:2952669
|
G | A | 1 | a0004c0006t0001g0245 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.430+474C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952669 | ||||||
chrX:2952676
|
G | T | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.430+467C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952676 | ||||||
chrX:2952970
|
G | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(88): Show | 97 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.430+173C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2952970 | ||||||
chrX:2953005
|
A | G | 3 | a0002c0002t0002g0026a0002c0002t0004g0028a0002c0002t0004g0038 | 3 | HG02895.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.430+138T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2953005 | ||||||
chrX:2953135
|
G | A | 8 | a0002c0002t0003g0005a0002c0002t0003g0068a0002c0002t0003g0094others(5): Show | 9 | HG00597.hp2 NA18949.hp2 NA18951.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.430+8C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 5/10 | chrX | 2953135 | ||||||
chrX:2953411
|
C | T | 3 | a0002c0003t0001g0212a0002c0003t0001g0217a0002c0003t0001g0242 | 3 | HG02145.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.308-146G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953411 | ||||||
chrX:2953433
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(66): Show | 74 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.308-168C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953433 | ||||||
chrX:2953490
|
T | C | 20 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0001g0212others(17): Show | 21 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.308-225A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953490 | ||||||
chrX:2953716
|
C | T | 7 | a0004c0006t0001g0245a0004c0006t0002g0003a0004c0006t0002g0024others(4): Show | 8 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.308-451G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953716 | ||||||
chrX:2953899
|
T | G | 1 | a0001c0009t0001g0107 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.308-634A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2953899 | ||||||
chrX:2954125
|
C | A | 1 | a0014c0026t0001g0098 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.308-860G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954125 | ||||||
chrX:2954289
|
G | GT | 1 | a0012c0020t0001g0251 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.308-1025dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954289 | ||||||
chrX:2954293
|
TTTTG | T | 1 | a0002c0004t0001g0115 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.308-1032_308-1029d others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954293 | ||||||
chrX:2954556
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.307+860T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954556 | ||||||
chrX:2954586
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.307+830C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954586 | ||||||
chrX:2954628
|
G | GTATTAT | 10 | a0002c0003t0001g0212a0002c0003t0001g0217a0002c0003t0001g0242others(7): Show | 11 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.307+782_307+787dup others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954628 | ||||||
chrX:2954628
|
G | GTATTATT others(2): Show |
10 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0002g0020others(7): Show | 10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.307+779_307+787dup others(9): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954628 | ||||||
chrX:2954726
|
G | C | 15 | a0001c0001t0001g0065a0001c0001t0001g0105a0001c0001t0001g0161others(12): Show | 15 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.307+690C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954726 | ||||||
chrX:2954738
|
C | T | 1 | a0013c0025t0001g0181 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.307+678G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954738 | ||||||
chrX:2954932
|
G | A | 1 | a0001c0023t0001g0132 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.307+484C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954932 | ||||||
chrX:2954981
|
TG | T | 1 | a0001c0009t0001g0199 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.307+434delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2954981 | ||||||
chrX:2955207
|
G | A | 7 | a0001c0001t0001g0164a0001c0001t0001g0200a0003c0005t0002g0022others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.307+209C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2955207 | ||||||
chrX:2955272
|
A | C | 35 | a0001c0023t0001g0132a0002c0002t0001g0131a0002c0002t0002g0026others(32): Show | 36 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.307+144T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2955272 | ||||||
chrX:2955315
|
T | G | 3 | a0002c0003t0001g0212a0002c0003t0001g0217a0002c0003t0001g0242 | 3 | HG02145.hp1 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.307+101A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2955315 | ||||||
chrX:2955334
|
T | TA | 1 | a0005c0008t0001g0060 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.307+81dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 4/10 | chrX | 2955334 | ||||||
chrX:2955597
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.186-60A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955597 | ||||||
chrX:2955804
|
C | A | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(61): Show | 69 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.186-267G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955804 | ||||||
chrX:2955857
|
T | C | 4 | a0001c0009t0001g0106a0001c0009t0001g0107a0001c0009t0001g0199others(1): Show | 4 | HG00140.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-320A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955857 | ||||||
chrX:2955939
|
G | C | 22 | a0002c0002t0002g0044a0002c0003t0001g0209a0002c0003t0001g0210others(19): Show | 23 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.186-402C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2955939 | ||||||
chrX:2956045
|
T | C | 10 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0002g0020others(7): Show | 10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-508A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956045 | ||||||
chrX:2956106
|
G | A | 22 | a0002c0002t0002g0044a0002c0003t0001g0212a0002c0003t0001g0217others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.186-569C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956106 | ||||||
chrX:2956355
|
C | T | 9 | a0002c0003t0001g0209a0002c0003t0002g0020a0002c0003t0002g0021others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.186-818G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956355 | ||||||
chrX:2956390
|
TG | T | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.186-854delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956390 | ||||||
chrX:2956413
|
T | C | 14 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0001g0212others(11): Show | 14 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-876A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956413 | ||||||
chrX:2956720
|
TC | T | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.186-1184delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956720 | ||||||
chrX:2956788
|
C | T | 14 | a0002c0003t0001g0209a0002c0003t0001g0212a0002c0003t0001g0217others(11): Show | 14 | HG01109.hp1 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.186-1251G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956788 | ||||||
chrX:2956804
|
G | T | 15 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0001g0212others(12): Show | 15 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.186-1267C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956804 | ||||||
chrX:2956913
|
A | AT | 2 | a0001c0001t0001g0084a0001c0001t0001g0222 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.185+1360dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956913 | ||||||
chrX:2956937
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.185+1337T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956937 | ||||||
chrX:2956971
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.185+1303G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956971 | ||||||
chrX:2956987
|
T | C | 13 | a0002c0002t0002g0044a0003c0005t0002g0022a0003c0005t0002g0023others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1287A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956987 | ||||||
chrX:2956988
|
G | A | 13 | a0002c0002t0002g0044a0003c0005t0002g0022a0003c0005t0002g0023others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1286C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956988 | ||||||
chrX:2956997
|
A | T | 13 | a0002c0002t0002g0044a0003c0005t0002g0022a0003c0005t0002g0023others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1277T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2956997 | ||||||
chrX:2957003
|
C | CTTG | 13 | a0002c0002t0002g0044a0003c0005t0002g0022a0003c0005t0002g0023others(10): Show | 14 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.185+1270_185+1271i others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957003 | ||||||
chrX:2957010
|
A | AG | 1 | a0001c0001t0001g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.185+1263dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957010 | ||||||
chrX:2957028
|
T | C | 10 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0002g0020others(7): Show | 10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+1246A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957028 | ||||||
chrX:2957048
|
C | T | 3 | a0006c0011t0001g0070a0006c0011t0001g0221a0006c0011t0001g0299 | 3 | HG02129.hp1 NA19000.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.185+1226G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957048 | ||||||
chrX:2957076
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.185+1198G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957076 | ||||||
chrX:2957093
|
C | T | 1 | a0002c0003t0007g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.185+1181G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957093 | ||||||
chrX:2957145
|
C | CG | 1 | a0001c0001t0001g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.185+1128dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957145 | ||||||
chrX:2957145
|
C | T | 1 | a0002c0002t0002g0046 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.185+1129G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957145 | ||||||
chrX:2957215
|
C | T | 15 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0001g0212others(12): Show | 15 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.185+1059G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957215 | ||||||
chrX:2957220
|
C | CAAA | 7 | a0002c0002t0002g0044a0003c0005t0002g0027a0004c0006t0001g0245others(4): Show | 8 | HG01884.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+1051_185+1053d others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | ||||||
chrX:2957220
|
C | CAAAA | 7 | a0002c0003t0002g0020a0003c0005t0002g0022a0003c0005t0002g0023others(4): Show | 7 | HG01070.hp1 HG01071.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+1050_185+1053d others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | ||||||
chrX:2957220
|
C | CAAAAA | 10 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0001g0212others(7): Show | 10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+1049_185+1053d others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | ||||||
chrX:2957220
|
C | CAAAAAA | 4 | a0002c0003t0001g0217a0002c0003t0001g0242a0002c0003t0007g0011others(1): Show | 4 | HG02451.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+1048_185+1053d others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | ||||||
chrX:2957220
|
C | CAAAAAAA others(1): Show |
4 | a0003c0005t0003g0215a0003c0005t0003g0216a0003c0005t0004g0019others(1): Show | 4 | HG02257.hp1 HG03139.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+1046_185+1053d others(10): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | ||||||
chrX:2957220
|
C | CAAAAAAA others(2): Show |
1 | a0003c0005t0001g0082 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.185+1045_185+1053d others(11): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | ||||||
chrX:2957220
|
CA | C | 3 | a0002c0002t0001g0214a0002c0002t0002g0052a0002c0002t0002g0053 | 3 | HG01891.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.185+1053delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957220 | ||||||
chrX:2957232
|
AT | A | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185+1041delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957232 | ||||||
chrX:2957443
|
TC | T | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185+830delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957443 | ||||||
chrX:2957462
|
A | T | 1 | a0001c0001t0001g0167 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.185+812T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957462 | ||||||
chrX:2957466
|
TG | T | 1 | a0001c0001t0001g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.185+807delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957466 | ||||||
chrX:2957479
|
C | CG | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185+794dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957479 | ||||||
chrX:2957513
|
A | AG | 1 | a0001c0001t0001g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.185+760dupC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957513 | ||||||
chrX:2957632
|
C | T | 1 | a0002c0002t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.185+642G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957632 | ||||||
chrX:2957688
|
A | G | 2 | a0002c0002t0002g0017a0002c0004t0002g0025 | 2 | HG00733.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.185+586T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957688 | ||||||
chrX:2957708
|
C | CA | 24 | a0001c0001t0001g0167a0001c0001t0001g0255a0001c0001t0001g0265others(21): Show | 26 | HG00597.hp2 HG01361.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.185+565dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957708 | ||||||
chrX:2957708
|
C | CAA | 7 | a0002c0002t0002g0017a0002c0004t0002g0025a0003c0005t0002g0022others(4): Show | 7 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+564_185+565dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957708 | ||||||
chrX:2957708
|
C | CAAA | 11 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0002g0020others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+563_185+565dup others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957708 | ||||||
chrX:2957708
|
CA | C | 5 | a0001c0001t0001g0064a0001c0001t0001g0099a0001c0001t0001g0177others(2): Show | 5 | HG00323.hp2 HG02735.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.185+565delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957708 | ||||||
chrX:2957724
|
AAG | A | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185+548_185+549del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957724 | ||||||
chrX:2957727
|
A | G | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185+547T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957727 | ||||||
chrX:2957851
|
C | CT | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.185+422dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957851 | ||||||
chrX:2957901
|
TC | T | 1 | a0001c0001t0001g0255 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.185+372delG | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957901 | ||||||
chrX:2957944
|
C | T | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185+330G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2957944 | ||||||
chrX:2958149
|
C | A | 10 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0002g0020others(7): Show | 10 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+125G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2958149 | ||||||
chrX:2958173
|
T | C | 2 | a0001c0001t0001g0191a0001c0001t0001g0200 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.185+101A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2958173 | ||||||
chrX:2958238
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.185+36A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 3/10 | chrX | 2958238 | ||||||
chrX:2958461
|
G | A | 16 | a0002c0002t0002g0044a0002c0002t0003g0005a0002c0002t0003g0068others(13): Show | 18 | HG00597.hp2 HG01884.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.24-26C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958461 | ||||||
chrX:2958641
|
G | T | 4 | a0002c0003t0001g0212a0002c0003t0001g0217a0002c0003t0001g0242others(1): Show | 4 | HG02145.hp1 HG02809.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.24-206C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958641 | ||||||
chrX:2958642
|
G | GT | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.24-208dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958642 | ||||||
chrX:2958642
|
G | T | 25 | a0002c0003t0001g0209a0002c0003t0001g0210a0002c0003t0001g0212others(22): Show | 25 | HG00741.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.24-207C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958642 | ||||||
chrX:2958647
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0287a0002c0003t0002g0041 | 3 | HG01891.hp1 HG04184.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.24-212A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958647 | ||||||
chrX:2958848
|
G | A | 1 | a0002c0002t0002g0015 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.24-413C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958848 | ||||||
chrX:2958924
|
C | CT | 1 | a0001c0001t0001g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.24-490dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2958924 | ||||||
chrX:2959031
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.24-596T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959031 | ||||||
chrX:2959409
|
G | A | 1 | a0002c0003t0007g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.23+969C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959409 | ||||||
chrX:2959447
|
C | A | 5 | a0003c0005t0001g0082a0003c0005t0003g0215a0003c0005t0003g0216others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.23+931G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959447 | ||||||
chrX:2959560
|
TG | T | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.23+817delC | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959560 | ||||||
chrX:2959691
|
C | T | 11 | a0002c0002t0001g0213a0002c0002t0002g0044a0002c0002t0004g0028others(8): Show | 12 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.23+687G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959691 | ||||||
chrX:2959758
|
C | G | 8 | a0001c0001t0001g0054a0001c0001t0001g0067a0001c0001t0001g0093others(5): Show | 8 | HG02155.hp2 HG02165.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+620G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959758 | ||||||
chrX:2959794
|
G | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(56): Show | 63 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.23+584C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959794 | ||||||
chrX:2959835
|
T | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(111): Show | 121 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.23+543A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959835 | ||||||
chrX:2959902
|
GA | G | 1 | a0001c0001t0001g0239 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.23+475delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959902 | ||||||
chrX:2959941
|
G | GAGAA | 17 | a0001c0001t0001g0079a0002c0002t0002g0044a0002c0002t0003g0005others(14): Show | 19 | HG00597.hp2 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.23+433_23+436dupTT others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | ||||||
chrX:2959941
|
G | GAGAAAGA others(1): Show |
2 | a0002c0002t0003g0248a0002c0002t0003g0250 | 2 | NA18951.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.23+429_23+436dupTT others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | ||||||
chrX:2959941
|
GAGAA | G | 22 | a0001c0007t0001g0309a0002c0002t0002g0002a0002c0002t0002g0013others(19): Show | 23 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.23+433_23+436delTT others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | ||||||
chrX:2959941
|
GAGAAAGA others(1): Show |
G | 1 | a0002c0003t0007g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.23+429_23+436delTT others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | ||||||
chrX:2959941
|
GAGAAAGA others(9): Show |
G | 1 | a0001c0001t0001g0191 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.23+421_23+436delTT others(14): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959941 | ||||||
chrX:2959967
|
GAGAA | G | 1 | a0001c0001t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.23+407_23+410delTT others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2959967 | ||||||
chrX:2960014
|
A | C | 1 | a0001c0001t0001g0104 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.23+364T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960014 | ||||||
chrX:2960025
|
T | G | 4 | a0003c0005t0003g0215a0003c0005t0003g0216a0003c0005t0004g0019others(1): Show | 4 | HG02257.hp1 HG03139.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.23+353A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960025 | ||||||
chrX:2960030
|
G | T | 3 | a0003c0005t0002g0022a0003c0005t0002g0023a0003c0005t0002g0027 | 3 | HG01070.hp1 HG01071.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.23+348C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960030 | ||||||
chrX:2960035
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.23+343G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960035 | ||||||
chrX:2960040
|
C | T | 6 | a0001c0001t0001g0076a0001c0001t0001g0173a0001c0001t0001g0174others(3): Show | 6 | HG01175.hp2 HG01496.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.23+338G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960040 | ||||||
chrX:2960085
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.23+293G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960085 | ||||||
chrX:2960118
|
A | C | 1 | a0002c0003t0002g0020 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.23+260T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960118 | ||||||
chrX:2960121
|
T | G | 7 | a0002c0002t0002g0002a0002c0002t0002g0013a0003c0005t0002g0022others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+257A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960121 | ||||||
chrX:2960130
|
G | A | 7 | a0002c0002t0002g0002a0002c0002t0002g0013a0003c0005t0002g0022others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+248C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960130 | ||||||
chrX:2960131
|
T | C | 7 | a0002c0002t0002g0002a0002c0002t0002g0013a0003c0005t0002g0022others(4): Show | 8 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.23+247A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960131 | ||||||
chrX:2960135
|
G | A | 97 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0058others(94): Show | 101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.23+243C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960135 | ||||||
chrX:2960137
|
C | T | 2 | a0002c0002t0002g0026a0002c0004t0001g0286 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.23+241G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960137 | ||||||
chrX:2960138
|
A | G | 115 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0058others(112): Show | 120 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.23+240T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960138 | ||||||
chrX:2960138
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.23+240T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960138 | ||||||
chrX:2960139
|
G | T | 2 | a0002c0002t0001g0266a0002c0021t0001g0171 | 2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.23+239C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960139 | ||||||
chrX:2960141
|
C | T | 2 | a0002c0002t0001g0266a0002c0021t0001g0171 | 2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.23+237G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960141 | ||||||
chrX:2960144
|
C | T | 1 | a0001c0007t0001g0308 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.23+234G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960144 | ||||||
chrX:2960149
|
G | A | 2 | a0002c0002t0001g0266a0002c0021t0001g0171 | 2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.23+229C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960149 | ||||||
chrX:2960159
|
C | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0189a0001c0001t0001g0233others(4): Show | 7 | NA18957.hp1 NA18969.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.23+219G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960159 | ||||||
chrX:2960184
|
G | C | 2 | a0002c0002t0001g0172a0002c0002t0001g0187 | 2 | NA18972.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.23+194C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960184 | ||||||
chrX:2960185
|
T | C | 11 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0100others(8): Show | 11 | HG01175.hp2 HG01258.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.23+193A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960185 | ||||||
chrX:2960193
|
C | T | 92 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(89): Show | 98 | HG00140.hp1 HG00323.hp2 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.23+185G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960193 | ||||||
chrX:2960215
|
G | A | 65 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(62): Show | 69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.23+163C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960215 | ||||||
chrX:2960221
|
A | G | 1 | a0001c0001t0001g0219 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.23+157T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960221 | ||||||
chrX:2960240
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.23+138C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960240 | ||||||
chrX:2960247
|
C | T | 1 | a0001c0001t0006g0117 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.23+131G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960247 | ||||||
chrX:2960255
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(308): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.23+123A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960255 | ||||||
chrX:2960263
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0008others(97): Show | 106 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.23+115G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960263 | ||||||
chrX:2960268
|
C | CA | 39 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0077others(36): Show | 41 | HG00323.hp2 HG01070.hp1 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.23+109dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
C | CAA | 49 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0078others(46): Show | 50 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.23+108_23+109dupTT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
C | CAAA | 17 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0080others(14): Show | 20 | HG00140.hp1 HG00408.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.23+107_23+109dupTT others(1): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
C | CAAAA | 1 | a0001c0001t0001g0208 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.23+106_23+109dupTT others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
C | CAAAAAA | 1 | a0001c0001t0002g0034 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.23+104_23+109dupTT others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
CA | C | 18 | a0001c0001t0001g0069a0001c0001t0001g0100a0001c0001t0001g0101others(15): Show | 18 | HG01943.hp1 HG01993.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.23+109delT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
CAAAAAA | C | 9 | a0002c0003t0001g0209a0002c0003t0002g0020a0002c0003t0002g0021others(6): Show | 9 | HG01109.hp1 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.23+104_23+109delTT others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
CAAAAAAA | C | 18 | a0001c0001t0001g0111a0002c0002t0001g0213a0002c0002t0002g0044others(15): Show | 20 | HG00597.hp2 HG00639.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.23+103_23+109delTT others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
CAAAAAAA others(1): Show |
C | 2 | a0001c0001t0001g0110a0002c0002t0003g0248 | 2 | NA18954.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.23+102_23+109delTT others(6): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960268
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0083a0001c0001t0001g0104a0001c0001t0001g0109 | 3 | NA18948.hp1 NA19002.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.23+99_23+109delTTT others(8): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960268 | ||||||
chrX:2960320
|
G | GAGAA | 11 | a0001c0001t0001g0211a0002c0003t0001g0209a0002c0003t0001g0210others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.23+54_23+57dupTTCT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960320 | ||||||
chrX:2960320
|
G | GAGAAAGA others(1): Show |
5 | a0002c0003t0001g0212a0002c0003t0001g0217a0002c0003t0001g0242others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.23+50_23+57dupTTCT others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 2/10 | chrX | 2960320 | ||||||
chrX:2960516
|
C | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0067a0001c0001t0001g0093others(1): Show | 4 | HG02165.hp1 NA18949.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-96G>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960516 | ||||||
chrX:2960519
|
G | A | 1 | a0002c0004t0001g0244 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-20-99C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960519 | ||||||
chrX:2960520
|
T | G | 1 | a0003c0013t0001g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-20-100A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960520 | ||||||
chrX:2960704
|
T | C | 10 | a0002c0002t0001g0213a0002c0002t0001g0214a0002c0002t0003g0081others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-20-284A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960704 | ||||||
chrX:2960830
|
CAG | C | 1 | a0002c0002t0001g0317 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-20-412_-20-411del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960830 | ||||||
chrX:2960882
|
G | C | 1 | a0003c0005t0004g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-20-462C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960882 | ||||||
chrX:2960883
|
A | G | 1 | a0007c0022t0001g0247 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-20-463T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960883 | ||||||
chrX:2960905
|
T | C | 7 | a0001c0001t0001g0058a0002c0002t0002g0044a0003c0005t0004g0019others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-20-485A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960905 | ||||||
chrX:2960996
|
AT | A | 13 | a0002c0002t0002g0036a0002c0002t0002g0044a0002c0003t0002g0037others(10): Show | 13 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.-20-577delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2960996 | ||||||
chrX:2961192
|
G | GA | 1 | a0001c0001t0012g0062 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-20-773dupT | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961192 | ||||||
chrX:2961253
|
G | C | 4 | a0002c0002t0001g0243a0002c0002t0001g0246a0002c0004t0001g0244others(1): Show | 4 | HG01884.hp2 HG02280.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-833C>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961253 | ||||||
chrX:2961256
|
C | A | 1 | a0001c0001t0001g0281 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-20-836G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961256 | ||||||
chrX:2961270
|
CAGGAA | C | 1 | a0002c0002t0001g0066 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-20-855_-20-851del others(5): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961270 | ||||||
chrX:2961394
|
T | C | 29 | a0001c0001t0001g0061a0001c0001t0001g0083a0001c0001t0001g0084others(26): Show | 29 | HG00408.hp1 HG00597.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-20-974A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961394 | ||||||
chrX:2961533
|
C | A | 8 | a0002c0002t0002g0017a0002c0002t0002g0018a0002c0002t0003g0235others(5): Show | 8 | HG01243.hp1 HG02630.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-1113G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961533 | ||||||
chrX:2961695
|
A | G | 8 | a0002c0002t0001g0237a0002c0002t0002g0031a0002c0002t0003g0238others(5): Show | 8 | HG02572.hp1 HG02723.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-20-1275T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961695 | ||||||
chrX:2961708
|
T | C | 1 | a0002c0002t0001g0236 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-20-1288A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961708 | ||||||
chrX:2961827
|
A | T | 1 | a0002c0002t0001g0108 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-20-1407T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961827 | ||||||
chrX:2961858
|
G | GT | 18 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0093others(15): Show | 19 | HG00733.hp1 HG00735.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-20-1439dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961858 | ||||||
chrX:2961858
|
GT | G | 12 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0001g0241others(9): Show | 12 | HG01070.hp2 HG02572.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-20-1439delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961858 | ||||||
chrX:2961865
|
T | G | 5 | a0001c0001t0002g0034a0002c0002t0002g0036a0002c0003t0002g0037others(2): Show | 5 | HG02615.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1445A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961865 | ||||||
chrX:2961871
|
T | C | 3 | a0001c0001t0001g0092a0001c0001t0012g0062a0002c0002t0003g0005 | 4 | NA18988.hp1 NA18999.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1451A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961871 | ||||||
chrX:2961891
|
A | AT | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG00438.hp2 NA18955.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-20-1472dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2961891 | ||||||
chrX:2962154
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-20-1734T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962154 | ||||||
chrX:2962181
|
C | A | 5 | a0001c0001t0002g0034a0002c0002t0002g0036a0002c0003t0002g0037others(2): Show | 5 | HG02615.hp2 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-20-1761G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962181 | ||||||
chrX:2962417
|
G | A | 1 | a0003c0005t0002g0032 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-21+1807C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962417 | ||||||
chrX:2962454
|
G | A | 15 | a0002c0002t0001g0243a0002c0002t0001g0246a0002c0002t0002g0018others(12): Show | 15 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-21+1770C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962454 | ||||||
chrX:2962476
|
C | T | 1 | a0002c0003t0007g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-21+1748G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962476 | ||||||
chrX:2962481
|
T | C | 8 | a0002c0002t0002g0044a0002c0003t0002g0041a0002c0003t0009g0040others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+1743A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962481 | ||||||
chrX:2962525
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-21+1699A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962525 | ||||||
chrX:2962629
|
A | T | 8 | a0002c0002t0002g0044a0002c0003t0002g0041a0002c0003t0009g0040others(5): Show | 8 | HG01109.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-21+1595T>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962629 | ||||||
chrX:2962721
|
A | G | 11 | a0001c0001t0002g0034a0002c0002t0002g0031a0002c0002t0002g0036others(8): Show | 11 | HG02615.hp2 HG02630.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.-21+1503T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962721 | ||||||
chrX:2962735
|
C | T | 15 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0015others(12): Show | 16 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-21+1489G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962735 | ||||||
chrX:2962736
|
A | G | 40 | a0001c0001t0002g0034a0002c0002t0002g0002a0002c0002t0002g0013others(37): Show | 42 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.-21+1488T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962736 | ||||||
chrX:2962751
|
A | C | 2 | a0002c0003t0002g0020a0002c0003t0002g0021 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21+1473T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962751 | ||||||
chrX:2962835
|
GAT | G | 14 | a0002c0002t0001g0246a0002c0002t0002g0018a0002c0002t0002g0031others(11): Show | 14 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-21+1387_-21+1388d others(4): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962835 | ||||||
chrX:2962853
|
T | C | 53 | a0001c0001t0001g0009a0001c0001t0001g0063a0001c0001t0001g0096others(50): Show | 55 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-21+1371A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962853 | ||||||
chrX:2962987
|
C | T | 2 | a0002c0003t0002g0020a0002c0003t0002g0021 | 2 | NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-21+1237G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2962987 | ||||||
chrX:2963063
|
C | T | 6 | a0002c0002t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+1161G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963063 | ||||||
chrX:2963119
|
G | A | 5 | a0001c0001t0001g0284a0001c0001t0001g0285a0002c0002t0001g0010others(2): Show | 6 | HG01081.hp1 HG01081.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+1105C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963119 | ||||||
chrX:2963135
|
G | A | 1 | a0002c0004t0001g0286 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-21+1089C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963135 | ||||||
chrX:2963159
|
T | G | 8 | a0002c0002t0002g0018a0002c0002t0002g0052a0002c0002t0002g0053others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-21+1065A>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963159 | ||||||
chrX:2963166
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-21+1058C>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963166 | ||||||
chrX:2963201
|
T | C | 13 | a0002c0002t0002g0044a0002c0002t0002g0046a0002c0003t0002g0041others(10): Show | 13 | HG01109.hp1 HG01891.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-21+1023A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963201 | ||||||
chrX:2963287
|
A | G | 1 | a0003c0005t0002g0032 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-21+937T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963287 | ||||||
chrX:2963424
|
C | T | 1 | a0005c0008t0001g0059 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-21+800G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963424 | ||||||
chrX:2963430
|
C | A | 44 | a0001c0001t0002g0034a0002c0002t0002g0002a0002c0002t0002g0013others(41): Show | 46 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.-21+794G>T | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963430 | ||||||
chrX:2963476
|
T | C | 6 | a0002c0002t0002g0018a0002c0003t0002g0020a0002c0003t0002g0021others(3): Show | 6 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.-21+748A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963476 | ||||||
chrX:2963533
|
C | CT | 40 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0065others(37): Show | 42 | HG00423.hp1 HG00597.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.-21+690dupA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | ||||||
chrX:2963533
|
C | CTT | 3 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0012g0062 | 3 | HG00408.hp1 HG02056.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-21+689_-21+690dup others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | ||||||
chrX:2963533
|
CT | C | 27 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0293others(24): Show | 28 | HG00733.hp1 HG01069.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.-21+690delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | ||||||
chrX:2963533
|
CTT | C | 20 | a0001c0001t0002g0034a0002c0002t0002g0036a0002c0002t0002g0044others(17): Show | 20 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-21+689_-21+690del others(2): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | ||||||
chrX:2963533
|
CTTT | C | 8 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0015others(5): Show | 9 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+688_-21+690del others(3): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | ||||||
chrX:2963533
|
CTTTTTTT | C | 1 | a0001c0001t0001g0306 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-21+684_-21+690del others(7): Show |
ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963533 | ||||||
chrX:2963603
|
C | T | 8 | a0002c0002t0002g0002a0002c0002t0002g0013a0002c0002t0002g0015others(5): Show | 9 | HG01261.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-21+621G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963603 | ||||||
chrX:2963608
|
A | G | 2 | a0005c0008t0001g0059a0005c0008t0001g0060 | 2 | NA18962.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-21+616T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963608 | ||||||
chrX:2963709
|
G | T | 1 | a0001c0001t0001g0058 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-21+515C>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963709 | ||||||
chrX:2963710
|
AT | A | 2 | a0002c0002t0002g0052a0002c0002t0002g0053 | 2 | HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-21+513delA | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963710 | ||||||
chrX:2963978
|
T | C | 11 | a0001c0001t0001g0316a0001c0007t0001g0307a0001c0007t0001g0308others(8): Show | 11 | HG01123.hp1 HG01123.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.-21+246A>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2963978 | ||||||
chrX:2964041
|
C | T | 2 | a0002c0002t0001g0056a0002c0002t0001g0057 | 2 | NA18986.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.-21+183G>A | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2964041 | ||||||
chrX:2964105
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-21+119T>C | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2964105 | ||||||
chrX:2964203
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-21+21T>G | ARSL | ENSG00000157399.17 | transcript | ENST00000381134.9 | protein_coding | 1/10 | chrX | 2964203 |