geneid | 29929 |
---|---|
ensemblid | ENSG00000088035.18 |
hgncid | 23157 |
symbol | ALG6 |
name | ALG6 alpha-1,3-glucosyltransferase |
refseq_nuc | NM_013339.4 |
refseq_prot | NP_037471.2 |
ensembl_nuc | ENST00000263440.6 |
ensembl_prot | ENSP00000263440.5 |
mane_status | MANE Select |
chr | chr1 |
start | 63367627 |
end | 63438553 |
strand | + |
ver | v1.2 |
region | chr1:63367627-63438553 |
region5000 | chr1:63362627-63443553 |
regionname0 | ALG6_chr1_63367627_63438553 |
regionname5000 | ALG6_chr1_63362627_63443553 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 507 | 307 | 75 | 44 | 145 | 7 | 36 | 113 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0002 | 1/1 | 507 | 74 | 9 | 16 | 37 | 3 | 7 | 33 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0003 | 0/0 | 507 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0004 | 0/0 | 507 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0005 | 0/0 | 507 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0006 | 0/0 | 507 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
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 | 0/0 | 1524 | 291 | 61 | 43 | 144 | 7 | 36 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0002 | 1/1 | 1524 | 74 | 9 | 16 | 37 | 3 | 7 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0003 | 0/0 | 1524 | 8 | 7 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0004 | 0/0 | 1524 | 7 | 7 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0005 | 0/0 | 1524 | 4 | 0 | 4 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0006 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0007 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0008 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
c0009 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
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 | 1802 | 125 | 9 | 21 | 76 | 5 | 12 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0002 | 0/0 | 1802 | 120 | 17 | 23 | 58 | 4 | 18 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0003 | 0/0 | 1798 | 79 | 13 | 16 | 40 | 1 | 9 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0004 | 0/0 | 1798 | 20 | 17 | 2 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0005 | 0/0 | 1802 | 7 | 0 | 0 | 3 | 0 | 4 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0006 | 0/0 | 1802 | 6 | 6 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0007 | 0/0 | 1798 | 6 | 5 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0008 | 0/0 | 1798 | 5 | 5 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0009 | 0/0 | 1802 | 4 | 3 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0010 | 0/0 | 1802 | 3 | 3 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0011 | 0/0 | 1802 | 3 | 3 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0012 | 0/0 | 1802 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0013 | 0/0 | 1798 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0014 | 0/0 | 1802 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0015 | 0/0 | 1802 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0016 | 0/0 | 1802 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0017 | 0/0 | 1802 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0018 | 0/0 | 1802 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0019 | 0/0 | 1802 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
t0020 | 0/0 | 1803 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
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 | 2 | 1 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
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 | 0/0 | 1524 | 291 | 61 | 43 | 144 | 7 | 36 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0003 | 0/0 | 1524 | 8 | 7 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0004 | 0/0 | 1524 | 7 | 7 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0007 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0002c0002 | 1/1 | 1524 | 74 | 9 | 16 | 37 | 3 | 7 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0003c0005 | 0/0 | 1524 | 4 | 0 | 4 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0004c0008 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0005c0006 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0006c0009 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3325 | 52 | 0 | 5 | 39 | 2 | 6 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0002 | 0/0 | 3325 | 119 | 17 | 23 | 58 | 4 | 17 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0003 | 0/0 | 3321 | 74 | 12 | 12 | 40 | 1 | 9 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0004 | 0/0 | 3321 | 19 | 16 | 2 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0005 | 0/0 | 3325 | 6 | 0 | 0 | 3 | 0 | 3 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0007 | 0/0 | 3321 | 6 | 5 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0008 | 0/0 | 3321 | 5 | 5 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0010 | 0/0 | 3325 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0011 | 0/0 | 3325 | 3 | 3 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0013 | 0/0 | 3321 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0015 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0017 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0018 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0001t0019 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0003t0009 | 0/0 | 3325 | 4 | 3 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0003t0010 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0003t0012 | 0/0 | 3325 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0003t0014 | 0/0 | 3325 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0004t0004 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0004t0006 | 0/0 | 3325 | 6 | 6 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0001c0007t0001 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0002c0002t0001 | 1/1 | 3325 | 72 | 9 | 16 | 36 | 3 | 6 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0002c0002t0005 | 0/0 | 3325 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0002c0002t0016 | 0/0 | 3325 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0003c0005t0003 | 0/0 | 3321 | 4 | 0 | 4 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0004c0008t0003 | 0/0 | 3321 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0005c0006t0002 | 0/0 | 3325 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
a0006c0009t0020 | 0/0 | 3326 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | copy fasta | chr1 | 63362627 | 63443553 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0007g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0008g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0008g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0008g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0008g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0010g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0010g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0013g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0015g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0017g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0018g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0001t0019g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0009g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0010g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0012g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0003t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0004t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0004t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0004t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0004t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0004t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0004t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0004t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0001c0007t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0009 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0005g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0002c0002t0016g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0003c0005t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0003c0005t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0003c0005t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0003c0005t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0004c0008t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0005c0006t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
a0006c0009t0020g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0364 | EUR | GBR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0366 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00733 | hp1 | a0003 | c0005 | t0003 | g0141 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0314 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG00741 | hp2 | a0003 | c0005 | t0003 | g0104 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01069 | hp2 | a0003 | c0005 | t0003 | g0120 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0312 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01071 | hp1 | a0003 | c0005 | t0003 | g0005 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0377 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0181 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01192 | hp1 | a0001 | c0003 | t0009 | g0192 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0165 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | CLM | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0076 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0315 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0311 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | IBS | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01891 | hp2 | a0001 | c0004 | t0006 | g0198 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01934 | hp2 | a0001 | c0001 | t0007 | g0145 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0372 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0376 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02129 | hp2 | a0002 | c0002 | t0016 | g0188 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0317 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | CDX | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0059 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0330 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02280 | hp2 | a0001 | c0004 | t0006 | g0325 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0146 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0334 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0235 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02615 | hp1 | a0001 | c0004 | t0006 | g0199 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02622 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02622 | hp2 | a0001 | c0003 | t0009 | g0194 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02647 | hp1 | a0001 | c0003 | t0009 | g0193 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0362 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0269 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0258 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0186 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02809 | hp2 | a0001 | c0004 | t0004 | g0200 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02818 | hp1 | a0001 | c0004 | t0006 | g0201 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0333 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02886 | hp2 | a0001 | c0001 | t0008 | g0234 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0326 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0327 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02922 | hp2 | a0001 | c0001 | t0015 | g0380 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02965 | hp1 | a0001 | c0004 | t0006 | g0231 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0103 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0182 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0332 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0108 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0237 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0057 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03195 | hp2 | a0001 | c0003 | t0012 | g0238 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0190 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0236 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03453 | hp2 | a0001 | c0001 | t0011 | g0191 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0369 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0011 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03516 | hp1 | a0006 | c0009 | t0020 | g0322 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0233 | AFR | ESN | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0060 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03579 | hp2 | a0001 | c0004 | t0006 | g0156 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0336 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0056 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0338 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0337 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03710 | hp1 | a0005 | c0006 | t0002 | g0284 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0316 | SAS | PJL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03831 | hp1 | a0002 | c0002 | t0005 | g0100 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0276 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0124 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0329 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0152 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0209 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0373 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0139 | SAS | STU | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0319 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18522 | hp2 | a0001 | c0003 | t0012 | g0239 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | CHB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0232 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0349 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18956 | hp1 | a0001 | c0001 | t0018 | g0004 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0357 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18966 | hp1 | a0001 | c0007 | t0001 | g0094 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18971 | hp2 | a0001 | c0001 | t0019 | g0147 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0344 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18980 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0354 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0355 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0343 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0356 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18997 | hp1 | a0001 | c0001 | t0013 | g0155 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0378 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0328 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0352 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19011 | hp2 | a0001 | c0001 | t0017 | g0035 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | LWK | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19043 | hp2 | a0001 | c0003 | t0014 | g0240 | AFR | LWK | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0342 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0341 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19059 | hp1 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0348 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0359 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19072 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0358 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0361 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | ASW | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ASW | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0313 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0122 | EUR | TSI | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0374 | SAS | GIH | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | GIH | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0379 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02559 | hp1 | a0004 | c0008 | t0003 | g0203 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG06807 | hp1 | a0001 | c0003 | t0010 | g0324 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
NA20300 | hp2 | a0001 | c0003 | t0009 | g0195 | AFR | USA | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0009 | REF | REF | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0163 | REF | REF | ALG6_chr1_63362627_63443553 | ALG6 | chr1 | 63362627 | 63443553 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:63406361
|
T | C | 1 | a0003 | 4 | HG00733.hp1 HG00741.hp2 HG01069.hp2 others(1): Show |
missense_variant | MODERATE | c.391T>C | p.Tyr131His | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/15 | 659/3325 | 391/1524 | 131/507 | chr1 | 63406361 | ||
chr1:63411329
|
G | T | 1 | a0006 | 1 | HG03516.hp1 | missense_variant&splice_region_variant | MODERATE | c.678G>T | p.Lys226Asn | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/15 | 946/3325 | 678/1524 | 226/507 | chr1 | 63411329 | ||
chr1:63411996
|
A | G | 1 | a0004 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.751A>G | p.Thr251Ala | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/15 | 1019/3325 | 751/1524 | 251/507 | chr1 | 63411996 | ||
chr1:63415881
|
C | T | 5 | a0001a0003a0004others(2): Show | 314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
missense_variant | MODERATE | c.911C>T | p.Ser304Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/15 | 1179/3325 | 911/1524 | 304/507 | chr1 | 63415881 | ||
chr1:63419415
|
G | C | 1 | a0005 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1033G>C | p.Glu345Gln | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/15 | 1301/3325 | 1033/1524 | 345/507 | chr1 | 63419415 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:63411971
|
C | T | 1 | a0001c0004 | 7 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.726C>T | p.Phe242Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/15 | 994/3325 | 726/1524 | 242/507 | chr1 | 63411971 | ||
chr1:63415951
|
T | C | 2 | a0001c0003a0001c0004 | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
synonymous_variant | LOW | c.981T>C | p.Phe327Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/15 | 1249/3325 | 981/1524 | 327/507 | chr1 | 63415951 | ||
chr1:63436948
|
C | T | 1 | a0001c0007 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.1452C>T | p.Phe484Phe | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1720/3325 | 1452/1524 | 484/507 | chr1 | 63436948 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:63367683
|
G | C | 1 | a0001c0001t0013 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/15 | 3295 | chr1 | 63367683 | |||||
chr1:63367684
|
C | G | 1 | a0001c0001t0013 | 1 | NA18997.hp1 | 5_prime_UTR_variant | MODIFIER | c.-211C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/15 | 3294 | chr1 | 63367684 | |||||
chr1:63370842
|
C | G | 11 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(8): Show | 102 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(99): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-136C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/15 | chr1 | 63370842 | ||||||
chr1:63370857
|
T | G | 2 | a0001c0003t0012a0001c0003t0014 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-121T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/15 | 121 | chr1 | 63370857 | |||||
chr1:63437195
|
G | T | 1 | a0001c0001t0018 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 175 | chr1 | 63437195 | |||||
chr1:63437207
|
A | G | 1 | a0001c0001t0017 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*187A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 187 | chr1 | 63437207 | |||||
chr1:63437530
|
T | C | 1 | a0001c0001t0015 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*510T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 510 | chr1 | 63437530 | |||||
chr1:63437781
|
T | C | 19 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(16): Show | 251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*761T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 761 | chr1 | 63437781 | |||||
chr1:63437807
|
CATTAT | C | 8 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(5): Show | 111 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*795_*799delTATAT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 795 | INFO_REALIGN_3_PRIME | chr1 | 63437807 | ||||
chr1:63437821
|
T | C | 1 | a0002c0002t0016 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 801 | chr1 | 63437821 | |||||
chr1:63437864
|
T | C | 2 | a0001c0001t0007a0001c0001t0008 | 11 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*844T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 844 | chr1 | 63437864 | |||||
chr1:63437981
|
C | T | 1 | a0001c0001t0011 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*961C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 961 | chr1 | 63437981 | |||||
chr1:63438156
|
C | T | 1 | a0001c0001t0011 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1136C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1136 | chr1 | 63438156 | |||||
chr1:63438175
|
A | AT | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(6): Show | 112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1156dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1157 | INFO_REALIGN_3_PRIME | chr1 | 63438175 | ||||
chr1:63438342
|
A | G | 3 | a0001c0003t0009a0001c0003t0014a0001c0004t0006 | 11 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1322A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1322 | chr1 | 63438342 | |||||
chr1:63438435
|
T | G | 3 | a0001c0001t0010a0001c0001t0011a0001c0003t0010 | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1415T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1415 | chr1 | 63438435 | |||||
chr1:63438454
|
T | C | 3 | a0001c0001t0010a0001c0001t0011a0001c0003t0010 | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1434T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 15/15 | 1434 | chr1 | 63438454 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:63367765
|
C | G | 57 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0001g0360others(54): Show | 57 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(54): Show |
intron_variant | MODIFIER | c.-208+78C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367765 | ||||||
chr1:63367779
|
G | T | 46 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0001g0360others(43): Show | 46 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.-208+92G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367779 | ||||||
chr1:63367802
|
C | G | 3 | a0001c0001t0004g0332a0001c0001t0010g0333a0001c0001t0010g0334 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-208+115C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367802 | ||||||
chr1:63367903
|
G | T | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-208+216G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367903 | ||||||
chr1:63367953
|
A | C | 3 | a0001c0001t0004g0332a0001c0001t0010g0333a0001c0001t0010g0334 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-208+266A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63367953 | ||||||
chr1:63368022
|
C | T | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-208+335C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368022 | ||||||
chr1:63368024
|
C | T | 12 | a0001c0001t0001g0320a0002c0002t0001g0008a0002c0002t0001g0311others(9): Show | 13 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.-208+337C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368024 | ||||||
chr1:63368409
|
A | G | 71 | a0001c0001t0001g0247a0001c0001t0001g0285a0001c0001t0001g0286others(68): Show | 72 | HG00408.hp2 HG00423.hp2 HG01261.hp1 others(69): Show |
intron_variant | MODIFIER | c.-208+722A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368409 | ||||||
chr1:63368540
|
G | A | 1 | a0002c0002t0001g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-208+853G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368540 | ||||||
chr1:63368599
|
C | T | 3 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-208+912C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368599 | ||||||
chr1:63368742
|
C | T | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-208+1055C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368742 | ||||||
chr1:63368764
|
G | A | 2 | a0001c0001t0005g0010a0001c0001t0005g0011 | 2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-208+1077G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368764 | ||||||
chr1:63368783
|
G | A | 1 | a0001c0001t0003g0012 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-208+1096G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368783 | ||||||
chr1:63368806
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-208+1119T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368806 | ||||||
chr1:63368850
|
G | A | 161 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(158): Show | 165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-208+1163G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368850 | ||||||
chr1:63368853
|
A | G | 161 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(158): Show | 165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.-208+1166A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368853 | ||||||
chr1:63368924
|
G | C | 12 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-208+1237G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63368924 | ||||||
chr1:63369022
|
C | T | 6 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(3): Show | 6 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-208+1335C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369022 | ||||||
chr1:63369063
|
C | CATATG | 4 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0003t0010g0324others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-208+1382_-208+138 others(9): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63369063 | |||||
chr1:63369143
|
C | T | 27 | a0001c0001t0001g0004a0001c0001t0001g0078a0001c0001t0001g0079others(24): Show | 27 | HG00408.hp1 HG00423.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.-208+1456C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369143 | ||||||
chr1:63369351
|
G | A | 13 | a0001c0001t0001g0320a0001c0001t0004g0098a0002c0002t0001g0008others(10): Show | 14 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-207-1420G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369351 | ||||||
chr1:63369366
|
C | T | 1 | a0001c0004t0006g0231 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-207-1405C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369366 | ||||||
chr1:63369402
|
G | T | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207-1369G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369402 | ||||||
chr1:63369438
|
G | C | 3 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015 | 3 | NA18986.hp1 NA19005.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-207-1333G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369438 | ||||||
chr1:63369457
|
C | T | 21 | a0001c0001t0003g0012a0001c0001t0003g0211a0001c0001t0003g0212others(18): Show | 21 | HG00544.hp1 HG00558.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.-207-1314C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369457 | ||||||
chr1:63369569
|
C | T | 4 | a0001c0001t0002g0069a0001c0001t0002g0070a0001c0001t0002g0071others(1): Show | 4 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-207-1202C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369569 | ||||||
chr1:63369629
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-207-1142C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369629 | ||||||
chr1:63369639
|
G | GA | 20 | a0001c0001t0001g0320a0001c0001t0001g0338a0001c0001t0002g0241others(17): Show | 21 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.-207-1123dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63369639 | |||||
chr1:63369822
|
A | AT | 6 | a0001c0001t0002g0007a0001c0001t0002g0306a0001c0001t0002g0307others(3): Show | 7 | HG01496.hp2 HG01952.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207-940dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63369822 | |||||
chr1:63369950
|
C | T | 1 | a0001c0001t0002g0305 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-207-821C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369950 | ||||||
chr1:63369968
|
G | A | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207-803G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63369968 | ||||||
chr1:63370055
|
T | C | 84 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(81): Show | 85 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.-207-716T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370055 | ||||||
chr1:63370158
|
C | G | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-207-613C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370158 | ||||||
chr1:63370161
|
T | TA | 82 | a0001c0001t0002g0244a0001c0001t0003g0005a0001c0001t0003g0012others(79): Show | 83 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.-207-595dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63370161 | |||||
chr1:63370161
|
TA | T | 7 | a0001c0001t0001g0097a0001c0001t0002g0304a0001c0001t0003g0210others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-207-595delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 63370161 | |||||
chr1:63370221
|
C | T | 1 | a0002c0002t0001g0209 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-207-550C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370221 | ||||||
chr1:63370230
|
A | G | 347 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(344): Show | 353 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.-207-541A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370230 | ||||||
chr1:63370231
|
T | G | 5 | a0002c0002t0001g0340a0002c0002t0001g0341a0002c0002t0001g0342others(2): Show | 5 | NA18973.hp2 NA18991.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.-207-540T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370231 | ||||||
chr1:63370300
|
A | G | 3 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-207-471A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370300 | ||||||
chr1:63370389
|
C | T | 1 | a0001c0003t0014g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-207-382C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370389 | ||||||
chr1:63370390
|
G | A | 3 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159 | 3 | HG01167.hp1 HG01169.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-207-381G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370390 | ||||||
chr1:63370424
|
G | A | 1 | a0002c0002t0001g0328 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-207-347G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370424 | ||||||
chr1:63370466
|
A | G | 1 | a0001c0001t0003g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-207-305A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370466 | ||||||
chr1:63370674
|
T | C | 7 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191others(4): Show | 7 | HG01192.hp1 HG02622.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-207-97T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 1/14 | chr1 | 63370674 | ||||||
chr1:63371079
|
T | TA | 7 | a0001c0001t0001g0247a0001c0001t0002g0013a0001c0001t0002g0016others(4): Show | 7 | HG01891.hp1 NA18953.hp1 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+30dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63371079 | |||||
chr1:63371135
|
A | G | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+76A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371135 | ||||||
chr1:63371148
|
T | G | 6 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(3): Show | 6 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+89T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371148 | ||||||
chr1:63371383
|
G | A | 1 | a0002c0002t0001g0345 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.82+324G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371383 | ||||||
chr1:63371411
|
G | A | 1 | a0002c0002t0001g0311 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.82+352G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371411 | ||||||
chr1:63371416
|
G | A | 1 | a0002c0002t0001g0311 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.82+357G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371416 | ||||||
chr1:63371532
|
C | T | 1 | a0002c0002t0001g0321 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.82+473C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371532 | ||||||
chr1:63371589
|
C | T | 6 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(3): Show | 6 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+530C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371589 | ||||||
chr1:63371625
|
T | G | 1 | a0001c0001t0003g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.82+566T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371625 | ||||||
chr1:63371627
|
C | G | 1 | a0001c0001t0002g0303 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.82+568C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371627 | ||||||
chr1:63371753
|
C | T | 160 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(157): Show | 164 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.82+694C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371753 | ||||||
chr1:63371762
|
G | A | 1 | a0001c0001t0002g0249 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.82+703G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371762 | ||||||
chr1:63371892
|
C | T | 1 | a0002c0002t0001g0379 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82+833C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63371892 | ||||||
chr1:63372025
|
C | T | 7 | a0001c0004t0004g0200a0001c0004t0006g0156a0001c0004t0006g0198others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+966C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372025 | ||||||
chr1:63372217
|
A | G | 12 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.82+1158A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372217 | ||||||
chr1:63372344
|
A | G | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+1285A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372344 | ||||||
chr1:63372604
|
A | C | 1 | a0001c0001t0013g0155 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.82+1545A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372604 | ||||||
chr1:63372706
|
C | T | 161 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(158): Show | 165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.82+1647C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372706 | ||||||
chr1:63372763
|
T | G | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+1704T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372763 | ||||||
chr1:63372825
|
A | G | 1 | a0002c0002t0016g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.82+1766A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63372825 | ||||||
chr1:63373094
|
G | A | 1 | a0001c0001t0004g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+2035G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373094 | ||||||
chr1:63373125
|
G | C | 12 | a0001c0001t0001g0320a0002c0002t0001g0008a0002c0002t0001g0311others(9): Show | 13 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.82+2066G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373125 | ||||||
chr1:63373136
|
A | G | 1 | a0001c0001t0015g0380 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.82+2077A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373136 | ||||||
chr1:63373437
|
T | C | 5 | a0002c0002t0001g0345a0002c0002t0001g0346a0002c0002t0001g0347others(2): Show | 5 | NA18946.hp2 NA18962.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2378T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373437 | ||||||
chr1:63373464
|
G | A | 3 | a0001c0001t0004g0332a0001c0001t0010g0333a0001c0001t0010g0334 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82+2405G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373464 | ||||||
chr1:63373531
|
G | A | 4 | a0002c0002t0001g0350a0002c0002t0001g0351a0002c0002t0001g0352others(1): Show | 4 | NA18939.hp1 NA18953.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+2472G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373531 | ||||||
chr1:63373594
|
C | CA | 6 | a0001c0001t0002g0017a0001c0001t0002g0160a0001c0001t0003g0101others(3): Show | 6 | HG01070.hp1 HG02738.hp2 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+2544dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373594 | |||||
chr1:63373657
|
C | CT | 6 | a0001c0001t0002g0066a0001c0001t0002g0067a0001c0001t0002g0241others(3): Show | 6 | HG01952.hp2 HG02109.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.82+2598_82+2599ins others(1): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373657 | ||||||
chr1:63373657
|
CA | C | 5 | a0001c0001t0002g0250a0001c0003t0012g0238a0001c0003t0012g0239others(2): Show | 5 | HG01070.hp2 HG03195.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2599delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373657 | ||||||
chr1:63373658
|
A | AT | 8 | a0001c0001t0004g0187a0001c0001t0008g0234a0001c0001t0008g0235others(5): Show | 8 | HG02145.hp2 HG02572.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2619dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | |||||
chr1:63373658
|
A | ATT | 10 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(7): Show | 10 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+2618_82+2619dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | |||||
chr1:63373658
|
A | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(169): Show | 177 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.82+2599A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373658 | ||||||
chr1:63373658
|
AT | A | 89 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(86): Show | 90 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.82+2619delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | |||||
chr1:63373658
|
ATT | A | 47 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0001g0360others(44): Show | 47 | HG00140.hp2 HG00438.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.82+2618_82+2619del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63373658 | |||||
chr1:63373714
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.82+2655G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373714 | ||||||
chr1:63373913
|
C | T | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82+2854C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373913 | ||||||
chr1:63373914
|
G | A | 3 | a0001c0001t0004g0332a0001c0001t0010g0333a0001c0001t0010g0334 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82+2855G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373914 | ||||||
chr1:63373944
|
A | G | 1 | a0001c0001t0005g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.82+2885A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63373944 | ||||||
chr1:63374043
|
C | T | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+2984C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374043 | ||||||
chr1:63374083
|
A | T | 1 | a0001c0001t0013g0155 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.82+3024A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374083 | ||||||
chr1:63374189
|
G | A | 3 | a0001c0004t0006g0156a0001c0004t0006g0198a0001c0004t0006g0199 | 3 | HG01891.hp2 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.82+3130G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374189 | ||||||
chr1:63374246
|
A | T | 101 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(98): Show | 102 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.82+3187A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374246 | ||||||
chr1:63374278
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.82+3219G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374278 | ||||||
chr1:63374394
|
G | A | 9 | a0001c0001t0002g0331a0001c0001t0004g0326a0001c0001t0004g0327others(6): Show | 9 | HG02280.hp1 HG02280.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+3335G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374394 | ||||||
chr1:63374401
|
G | A | 3 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.82+3342G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374401 | ||||||
chr1:63374456
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.82+3397C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374456 | ||||||
chr1:63374496
|
C | T | 3 | a0001c0001t0004g0332a0001c0001t0010g0333a0001c0001t0010g0334 | 3 | HG02572.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82+3437C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374496 | ||||||
chr1:63374522
|
G | A | 4 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0003t0010g0324others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+3463G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374522 | ||||||
chr1:63374585
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82+3526G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374585 | ||||||
chr1:63374628
|
CA | C | 334 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(331): Show | 339 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(336): Show |
intron_variant | MODIFIER | c.82+3581delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63374628 | |||||
chr1:63374734
|
A | G | 3 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240 | 3 | HG03195.hp2 NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.82+3675A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374734 | ||||||
chr1:63374832
|
T | C | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+3773T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63374832 | ||||||
chr1:63375026
|
A | T | 1 | a0001c0001t0002g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.82+3967A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375026 | ||||||
chr1:63375071
|
C | T | 2 | a0001c0001t0004g0326a0001c0001t0004g0327 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.82+4012C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375071 | ||||||
chr1:63375093
|
C | A | 5 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0001t0011g0189others(2): Show | 5 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+4034C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375093 | ||||||
chr1:63375199
|
TAA | T | 138 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0001g0363others(135): Show | 139 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(136): Show |
intron_variant | MODIFIER | c.82+4149_82+4150del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375199 | |||||
chr1:63375309
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82+4250A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375309 | ||||||
chr1:63375333
|
T | C | 3 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0003t0010g0324 | 3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+4274T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375333 | ||||||
chr1:63375410
|
A | AT | 81 | a0001c0001t0001g0064a0001c0001t0001g0092a0001c0001t0001g0093others(78): Show | 81 | HG00140.hp2 HG00438.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.82+4378dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | |||||
chr1:63375410
|
A | ATT | 10 | a0001c0001t0001g0377a0001c0001t0001g0378a0001c0001t0002g0241others(7): Show | 11 | HG01106.hp1 HG01175.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+4377_82+4378dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | |||||
chr1:63375410
|
AT | A | 10 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0021others(7): Show | 10 | HG01358.hp1 HG01993.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.82+4378delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | |||||
chr1:63375410
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0003g0102 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.82+4368_82+4378del others(11): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | |||||
chr1:63375410
|
ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.82+4367_82+4378del others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63375410 | |||||
chr1:63375424
|
TTTTTTTT others(7): Show |
T | 4 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240others(1): Show | 4 | HG02965.hp1 HG03195.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+4366_82+4379del others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375424 | ||||||
chr1:63375438
|
C | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+4379C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375438 | ||||||
chr1:63375740
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.82+4681A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63375740 | ||||||
chr1:63376033
|
C | CAGTCATG others(282): Show |
3 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0003t0010g0324 | 3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+4985_82+4986ins others(289): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63376033 | |||||
chr1:63376133
|
G | C | 3 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0003t0010g0324 | 3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+5074G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376133 | ||||||
chr1:63376172
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.82+5113C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376172 | ||||||
chr1:63376339
|
C | T | 1 | a0001c0004t0006g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.82+5280C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376339 | ||||||
chr1:63376581
|
A | G | 1 | a0001c0001t0002g0298 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.82+5522A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376581 | ||||||
chr1:63376607
|
A | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+5548A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376607 | ||||||
chr1:63376745
|
T | G | 1 | a0001c0001t0003g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.82+5686T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376745 | ||||||
chr1:63376904
|
T | C | 1 | a0002c0002t0001g0323 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+5845T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376904 | ||||||
chr1:63376905
|
C | T | 1 | a0002c0002t0001g0323 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+5846C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376905 | ||||||
chr1:63376906
|
T | C | 1 | a0002c0002t0001g0323 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+5847T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63376906 | ||||||
chr1:63377251
|
T | G | 1 | a0001c0001t0003g0213 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.82+6192T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377251 | ||||||
chr1:63377301
|
G | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(155): Show | 162 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.82+6242G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377301 | ||||||
chr1:63377467
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0002g0249 | 2 | NA18962.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.82+6408A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377467 | ||||||
chr1:63377523
|
C | T | 92 | a0001c0001t0001g0320a0001c0001t0003g0005a0001c0001t0003g0012others(89): Show | 92 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.82+6464C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377523 | ||||||
chr1:63377641
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.82+6582T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377641 | ||||||
chr1:63377764
|
C | G | 1 | a0001c0001t0004g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+6705C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377764 | ||||||
chr1:63377816
|
C | G | 4 | a0001c0001t0003g0212a0001c0001t0003g0224a0001c0001t0003g0225others(1): Show | 4 | HG01358.hp2 HG01978.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+6757C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63377816 | ||||||
chr1:63378085
|
A | G | 1 | a0001c0004t0006g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.82+7026A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378085 | ||||||
chr1:63378461
|
A | G | 1 | a0001c0001t0002g0310 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.82+7402A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378461 | ||||||
chr1:63378503
|
T | A | 3 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0003t0010g0324 | 3 | HG02895.hp1 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.82+7444T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378503 | ||||||
chr1:63378762
|
A | T | 5 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0001t0010g0333others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+7703A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378762 | ||||||
chr1:63378782
|
C | G | 105 | a0001c0001t0001g0320a0001c0001t0002g0178a0001c0001t0002g0179others(102): Show | 105 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(102): Show |
intron_variant | MODIFIER | c.82+7723C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378782 | ||||||
chr1:63378839
|
G | C | 110 | a0001c0001t0001g0320a0001c0001t0002g0178a0001c0001t0002g0179others(107): Show | 110 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(107): Show |
intron_variant | MODIFIER | c.82+7780G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378839 | ||||||
chr1:63378864
|
G | GT | 102 | a0001c0001t0001g0320a0001c0001t0002g0178a0001c0001t0002g0179others(99): Show | 102 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(99): Show |
intron_variant | MODIFIER | c.82+7817dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63378864 | |||||
chr1:63378864
|
G | T | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+7805G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378864 | ||||||
chr1:63378867
|
T | TG | 4 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0003g0111others(1): Show | 4 | NA18939.hp2 NA18957.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+7808_82+7809ins others(1): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63378867 | ||||||
chr1:63378943
|
C | CT | 110 | a0001c0001t0001g0320a0001c0001t0002g0178a0001c0001t0002g0179others(107): Show | 110 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(107): Show |
intron_variant | MODIFIER | c.82+7889dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63378943 | |||||
chr1:63379064
|
G | A | 11 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(8): Show | 11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.82+8005G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379064 | ||||||
chr1:63379065
|
T | C | 76 | a0001c0001t0001g0320a0001c0001t0003g0005a0001c0001t0003g0012others(73): Show | 76 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.82+8006T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379065 | ||||||
chr1:63379299
|
C | T | 156 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(153): Show | 160 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.82+8240C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379299 | ||||||
chr1:63379370
|
TAGG | T | 5 | a0001c0001t0004g0326a0001c0001t0004g0327a0001c0001t0010g0333others(2): Show | 5 | HG02572.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+8314_82+8316del others(3): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63379370 | |||||
chr1:63379396
|
G | A | 1 | a0001c0001t0004g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.82+8337G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379396 | ||||||
chr1:63379459
|
G | GAGATAGT others(6): Show |
1 | a0001c0001t0002g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.82+8400_82+8401ins others(13): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379459 | ||||||
chr1:63379460
|
C | A | 1 | a0001c0001t0002g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.82+8401C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379460 | ||||||
chr1:63379520
|
C | T | 2 | a0001c0001t0002g0242a0001c0001t0002g0243 | 2 | NA19003.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.82+8461C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379520 | ||||||
chr1:63379547
|
C | T | 296 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(293): Show | 301 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.82+8488C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379547 | ||||||
chr1:63379582
|
G | A | 1 | a0001c0001t0001g0363 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82+8523G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379582 | ||||||
chr1:63379659
|
A | C | 1 | a0001c0001t0001g0376 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.82+8600A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379659 | ||||||
chr1:63379721
|
A | G | 4 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240others(1): Show | 4 | HG03195.hp2 HG03516.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+8662A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379721 | ||||||
chr1:63379722
|
C | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+8663C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63379722 | ||||||
chr1:63380075
|
G | A | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82+9016G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380075 | ||||||
chr1:63380312
|
C | T | 1 | a0001c0001t0002g0021 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.82+9253C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380312 | ||||||
chr1:63380338
|
G | A | 1 | a0001c0001t0004g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82+9279G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380338 | ||||||
chr1:63380435
|
GTAACTTA others(12): Show |
G | 6 | a0001c0004t0004g0200a0001c0004t0006g0156a0001c0004t0006g0198others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+9379_82+9397del others(19): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63380435 | |||||
chr1:63380577
|
T | C | 7 | a0002c0002t0001g0202a0002c0002t0001g0323a0002c0002t0001g0328others(4): Show | 7 | HG02280.hp1 HG03471.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+9518T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380577 | ||||||
chr1:63380583
|
T | C | 1 | a0001c0001t0003g0102 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.82+9524T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380583 | ||||||
chr1:63380589
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+9530G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380589 | ||||||
chr1:63380648
|
A | G | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+9589A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380648 | ||||||
chr1:63380821
|
A | G | 1 | a0001c0001t0002g0304 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.82+9762A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63380821 | ||||||
chr1:63381099
|
T | C | 244 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(241): Show | 248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.82+10040T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381099 | ||||||
chr1:63381122
|
C | T | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+10063C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381122 | ||||||
chr1:63381176
|
C | T | 73 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(70): Show | 73 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.82+10117C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381176 | ||||||
chr1:63381181
|
G | A | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+10122G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381181 | ||||||
chr1:63381182
|
C | T | 1 | a0001c0004t0006g0201 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82+10123C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381182 | ||||||
chr1:63381322
|
C | T | 4 | a0002c0002t0001g0350a0002c0002t0001g0351a0002c0002t0001g0352others(1): Show | 4 | NA18939.hp1 NA18953.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+10263C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381322 | ||||||
chr1:63381326
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.82+10267C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381326 | ||||||
chr1:63381334
|
G | T | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+10275G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381334 | ||||||
chr1:63381385
|
C | T | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.82+10326C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381385 | ||||||
chr1:63381424
|
A | G | 6 | a0001c0004t0004g0200a0001c0004t0006g0156a0001c0004t0006g0198others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+10365A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381424 | ||||||
chr1:63381560
|
C | T | 5 | a0002c0002t0001g0166a0002c0002t0001g0167a0002c0002t0001g0168others(2): Show | 5 | NA18941.hp1 NA18950.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+10501C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381560 | ||||||
chr1:63381643
|
T | G | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.82+10584T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381643 | ||||||
chr1:63381664
|
AGGGAG | A | 142 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(139): Show | 146 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.82+10626_82+10630d others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63381664 | |||||
chr1:63381693
|
A | G | 1 | a0002c0002t0005g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.82+10634A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381693 | ||||||
chr1:63381747
|
C | T | 24 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(21): Show | 24 | HG01167.hp2 HG02145.hp2 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.82+10688C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381747 | ||||||
chr1:63381825
|
C | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+10766C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381825 | ||||||
chr1:63381852
|
G | T | 1 | a0002c0002t0001g0165 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.82+10793G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381852 | ||||||
chr1:63381897
|
T | C | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+10838T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63381897 | ||||||
chr1:63382164
|
T | A | 9 | a0001c0001t0003g0210a0001c0001t0004g0098a0002c0002t0001g0345others(6): Show | 9 | HG01243.hp1 HG02559.hp1 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+11105T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382164 | ||||||
chr1:63382165
|
A | T | 4 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0004t0006g0325others(1): Show | 4 | HG01516.hp1 HG01517.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+11106A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382165 | ||||||
chr1:63382221
|
A | G | 5 | a0001c0001t0003g0101a0001c0001t0003g0137a0001c0001t0003g0138others(2): Show | 5 | HG02071.hp2 NA18964.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+11162A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382221 | ||||||
chr1:63382286
|
C | T | 1 | a0002c0002t0001g0323 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.82+11227C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382286 | ||||||
chr1:63382505
|
C | T | 18 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0204others(15): Show | 18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.82+11446C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382505 | ||||||
chr1:63382506
|
G | A | 5 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108others(2): Show | 6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+11447G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382506 | ||||||
chr1:63382538
|
G | A | 2 | a0001c0003t0012g0238a0001c0003t0012g0239 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.82+11479G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382538 | ||||||
chr1:63382583
|
C | T | 1 | a0001c0001t0001g0375 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82+11524C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382583 | ||||||
chr1:63382640
|
AGTTTTTT others(17): Show |
A | 19 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(16): Show | 19 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.82+11592_82+11615d others(26): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382640 | |||||
chr1:63382642
|
TTTTTTTT others(6): Show |
T | 120 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(117): Show | 124 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.82+11592_82+11604d others(15): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382642 | |||||
chr1:63382642
|
TTTTTTTT others(16): Show |
T | 1 | a0001c0001t0004g0185 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.82+11592_82+11614d others(25): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382642 | |||||
chr1:63382645
|
TTTTTTGT others(3): Show |
T | 1 | a0001c0001t0003g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.82+11592_82+11601d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382645 | |||||
chr1:63382650
|
T | G | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+11591T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382650 | ||||||
chr1:63382650
|
TGTTTGTT others(8): Show |
T | 7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.82+11592_82+11606d others(17): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382650 | ||||||
chr1:63382651
|
G | T | 143 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.82+11592G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382651 | ||||||
chr1:63382655
|
G | T | 1 | a0001c0004t0004g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.82+11596G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382655 | ||||||
chr1:63382655
|
GTTTTTTT others(7): Show |
G | 157 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(154): Show | 158 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.82+11620_82+11633d others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382655 | |||||
chr1:63382656
|
TTTTTTTT others(16): Show |
T | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82+11606_82+11628d others(25): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382656 | |||||
chr1:63382659
|
T | G | 3 | a0001c0001t0002g0241a0001c0001t0002g0252a0001c0001t0002g0291 | 3 | NA19000.hp2 NA19087.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.82+11600T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382659 | ||||||
chr1:63382666
|
TTTTTTTT others(6): Show |
T | 10 | a0001c0001t0001g0055a0001c0001t0001g0090a0001c0001t0001g0091others(7): Show | 10 | HG01168.hp2 HG01433.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.82+11620_82+11632d others(15): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382666 | |||||
chr1:63382667
|
TTTTTTTT others(5): Show |
T | 1 | a0001c0001t0002g0241 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.82+11620_82+11631d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63382667 | |||||
chr1:63382669
|
T | G | 128 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(125): Show | 132 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.82+11610T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382669 | ||||||
chr1:63382673
|
T | G | 125 | a0001c0001t0001g0078a0001c0001t0002g0002a0001c0001t0002g0003others(122): Show | 129 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.82+11614T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382673 | ||||||
chr1:63382674
|
T | G | 6 | a0001c0001t0003g0115a0001c0001t0007g0108a0001c0001t0008g0234others(3): Show | 6 | HG02572.hp2 HG02886.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+11615T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382674 | ||||||
chr1:63382680
|
T | G | 1 | a0001c0001t0003g0136 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.82+11621T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382680 | ||||||
chr1:63382684
|
T | G | 2 | a0001c0001t0004g0332a0001c0001t0013g0155 | 2 | HG03098.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.82+11625T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382684 | ||||||
chr1:63382685
|
T | G | 21 | a0001c0001t0002g0331a0001c0001t0003g0101a0001c0001t0003g0153others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.82+11626T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382685 | ||||||
chr1:63382737
|
G | A | 18 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0001g0363others(15): Show | 18 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.82+11678G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382737 | ||||||
chr1:63382745
|
G | A | 38 | a0001c0001t0002g0051a0001c0001t0002g0242a0001c0001t0002g0243others(35): Show | 38 | HG00408.hp2 HG00423.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.82+11686G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382745 | ||||||
chr1:63382769
|
G | A | 75 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(72): Show | 75 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.82+11710G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382769 | ||||||
chr1:63382822
|
C | T | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.82+11763C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382822 | ||||||
chr1:63382833
|
A | G | 26 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(23): Show | 26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.82+11774A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382833 | ||||||
chr1:63382867
|
A | G | 26 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(23): Show | 26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.82+11808A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382867 | ||||||
chr1:63382879
|
T | C | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.82+11820T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382879 | ||||||
chr1:63382898
|
G | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.82+11839G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382898 | ||||||
chr1:63382922
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.82+11863C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382922 | ||||||
chr1:63382927
|
C | T | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+11868C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382927 | ||||||
chr1:63382965
|
C | T | 1 | a0001c0001t0002g0249 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.82+11906C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63382965 | ||||||
chr1:63383073
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82+12014A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383073 | ||||||
chr1:63383093
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82+12034G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383093 | ||||||
chr1:63383093
|
G | T | 7 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0016others(4): Show | 9 | HG01192.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.82+12034G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383093 | ||||||
chr1:63383145
|
C | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.82+12086C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383145 | ||||||
chr1:63383355
|
C | T | 1 | a0002c0002t0001g0318 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.82+12296C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383355 | ||||||
chr1:63383357
|
A | G | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.82+12298A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383357 | ||||||
chr1:63383860
|
C | T | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.83-12653C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383860 | ||||||
chr1:63383964
|
C | T | 1 | a0001c0003t0012g0239 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.83-12549C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63383964 | ||||||
chr1:63384193
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-12320G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384193 | ||||||
chr1:63384343
|
A | G | 26 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(23): Show | 26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.83-12170A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384343 | ||||||
chr1:63384373
|
C | T | 1 | a0001c0001t0002g0299 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.83-12140C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384373 | ||||||
chr1:63384387
|
G | A | 1 | a0002c0002t0001g0355 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.83-12126G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384387 | ||||||
chr1:63384509
|
C | T | 1 | a0002c0002t0001g0343 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.83-12004C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384509 | ||||||
chr1:63384621
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.83-11892G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384621 | ||||||
chr1:63384712
|
C | T | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.83-11801C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384712 | ||||||
chr1:63384717
|
T | A | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-11796T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63384717 | ||||||
chr1:63385001
|
A | G | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83-11512A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385001 | ||||||
chr1:63385184
|
C | CT | 14 | a0002c0002t0001g0073a0002c0002t0001g0074a0002c0002t0001g0075others(11): Show | 14 | HG02280.hp1 NA18906.hp1 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.83-11296dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CT | C | 39 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0096others(36): Show | 40 | HG00438.hp2 HG00639.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.83-11296delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CTT | C | 57 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(54): Show | 58 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.83-11297_83-11296d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CTTTT | C | 10 | a0001c0001t0003g0197a0001c0001t0004g0187a0001c0001t0008g0235others(7): Show | 10 | HG01192.hp1 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-11299_83-11296d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CTTTTT | C | 48 | a0001c0001t0003g0005a0001c0001t0003g0102a0001c0001t0003g0109others(45): Show | 48 | HG00733.hp1 HG00741.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.83-11300_83-11296d others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CTTTTTT | C | 57 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0012others(54): Show | 57 | HG00544.hp1 HG00558.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.83-11301_83-11296d others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0002g0020a0001c0001t0002g0296a0005c0006t0002g0284 | 3 | HG02027.hp1 HG02818.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.83-11307_83-11296d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CTTTTTTT others(6): Show |
C | 117 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(114): Show | 121 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.83-11308_83-11296d others(15): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385184
|
CTTTTTTT others(7): Show |
C | 7 | a0001c0001t0001g0365a0001c0001t0001g0366a0001c0001t0001g0367others(4): Show | 7 | HG00438.hp1 HG02165.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-11309_83-11296d others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385184 | |||||
chr1:63385205
|
T | C | 14 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0016others(11): Show | 16 | HG01106.hp2 HG01192.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-11308T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385205 | ||||||
chr1:63385372
|
G | A | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-11141G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385372 | ||||||
chr1:63385693
|
T | C | 21 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-10820T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385693 | ||||||
chr1:63385700
|
G | C | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-10813G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385700 | ||||||
chr1:63385749
|
T | C | 21 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-10764T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63385749 | ||||||
chr1:63385880
|
A | ATTC | 309 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(306): Show | 314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.83-10630_83-10628d others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63385880 | |||||
chr1:63386194
|
T | C | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83-10319T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386194 | ||||||
chr1:63386230
|
G | A | 1 | a0001c0001t0003g0154 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.83-10283G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386230 | ||||||
chr1:63386250
|
A | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.83-10263A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386250 | ||||||
chr1:63386270
|
G | GT | 23 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(20): Show | 23 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.83-10234dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63386270 | |||||
chr1:63386562
|
A | G | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.83-9951A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386562 | ||||||
chr1:63386570
|
G | A | 90 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.83-9943G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386570 | ||||||
chr1:63386574
|
C | A | 1 | a0004c0008t0003g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.83-9939C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386574 | ||||||
chr1:63386710
|
C | T | 2 | a0001c0001t0003g0153a0001c0001t0013g0155 | 2 | NA18997.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.83-9803C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386710 | ||||||
chr1:63386751
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.83-9762G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386751 | ||||||
chr1:63386806
|
C | A | 20 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(17): Show | 20 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.83-9707C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386806 | ||||||
chr1:63386888
|
T | C | 6 | a0001c0001t0003g0102a0001c0001t0003g0122a0001c0001t0003g0123others(3): Show | 6 | HG01884.hp1 HG02293.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-9625T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386888 | ||||||
chr1:63386933
|
C | T | 23 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(20): Show | 23 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.83-9580C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63386933 | ||||||
chr1:63387208
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.83-9305G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387208 | ||||||
chr1:63387532
|
C | CT | 15 | a0001c0001t0001g0055a0001c0001t0001g0090a0001c0001t0001g0097others(12): Show | 15 | HG00438.hp2 HG01361.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.83-8954dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387532
|
C | CTTT | 59 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0245others(56): Show | 59 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.83-8956_83-8954dup others(3): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387532
|
C | CTTTT | 32 | a0001c0001t0002g0014a0001c0001t0002g0046a0001c0001t0002g0047others(29): Show | 32 | HG01168.hp2 HG01175.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.83-8957_83-8954dup others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387532
|
C | CTTTTT | 63 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(60): Show | 67 | HG00408.hp2 HG00558.hp2 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.83-8958_83-8954dup others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387532
|
C | CTTTTTT | 44 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0002g0020others(41): Show | 44 | HG00423.hp2 HG00639.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.83-8959_83-8954dup others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387532
|
C | CTTTTTTT | 9 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0063others(6): Show | 9 | HG00544.hp2 HG01358.hp1 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.83-8960_83-8954dup others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387532
|
CT | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0247a0001c0001t0001g0285others(5): Show | 8 | HG00738.hp2 HG01070.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-8954delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387532
|
CTTTTTTT | C | 19 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(16): Show | 19 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.83-8960_83-8954del others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63387532 | |||||
chr1:63387635
|
A | C | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-8878A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387635 | ||||||
chr1:63387652
|
C | T | 1 | a0001c0001t0007g0006 | 2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.83-8861C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387652 | ||||||
chr1:63387742
|
G | C | 31 | a0002c0002t0001g0054a0002c0002t0001g0073a0002c0002t0001g0074others(28): Show | 31 | HG00738.hp2 HG01517.hp1 HG02109.hp2 others(28): Show |
intron_variant | MODIFIER | c.83-8771G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63387742 | ||||||
chr1:63388019
|
C | T | 5 | a0001c0001t0001g0004a0001c0001t0001g0079a0001c0001t0001g0089others(2): Show | 5 | NA18946.hp1 NA18956.hp1 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-8494C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388019 | ||||||
chr1:63388076
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.83-8437C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388076 | ||||||
chr1:63388210
|
C | T | 2 | a0001c0001t0004g0326a0001c0001t0004g0327 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.83-8303C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388210 | ||||||
chr1:63388427
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-8086A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388427 | ||||||
chr1:63388493
|
C | T | 2 | a0002c0002t0001g0355a0002c0002t0001g0356 | 2 | NA18988.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.83-8020C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388493 | ||||||
chr1:63388609
|
T | G | 10 | a0002c0002t0001g0202a0002c0002t0001g0319a0002c0002t0001g0321others(7): Show | 10 | HG02132.hp2 HG02280.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.83-7904T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388609 | ||||||
chr1:63388651
|
C | T | 1 | a0002c0002t0001g0318 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.83-7862C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63388651 | ||||||
chr1:63389075
|
G | T | 3 | a0001c0001t0002g0295a0001c0001t0002g0296a0001c0001t0002g0303 | 3 | HG02027.hp1 NA18959.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.83-7438G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389075 | ||||||
chr1:63389078
|
C | G | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-7435C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389078 | ||||||
chr1:63389165
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83-7348C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389165 | ||||||
chr1:63389359
|
C | T | 1 | a0001c0001t0002g0045 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.83-7154C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389359 | ||||||
chr1:63389410
|
A | G | 1 | a0002c0002t0001g0186 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.83-7103A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389410 | ||||||
chr1:63389746
|
G | A | 1 | a0002c0002t0001g0352 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.83-6767G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389746 | ||||||
chr1:63389830
|
A | G | 21 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-6683A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389830 | ||||||
chr1:63389849
|
G | A | 21 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-6664G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389849 | ||||||
chr1:63389945
|
C | G | 7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-6568C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389945 | ||||||
chr1:63389954
|
G | C | 2 | a0001c0001t0003g0196a0001c0001t0004g0057 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.83-6559G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63389954 | ||||||
chr1:63390029
|
C | A | 2 | a0001c0001t0003g0196a0001c0001t0004g0057 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.83-6484C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390029 | ||||||
chr1:63390128
|
G | A | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-6385G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390128 | ||||||
chr1:63390154
|
C | T | 2 | a0001c0001t0002g0268a0001c0001t0002g0269 | 2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.83-6359C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390154 | ||||||
chr1:63390351
|
G | A | 3 | a0002c0002t0001g0319a0002c0002t0001g0321a0002c0002t0005g0100 | 3 | HG02132.hp2 HG03831.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.83-6162G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390351 | ||||||
chr1:63390359
|
T | C | 2 | a0001c0001t0002g0036a0001c0001t0017g0035 | 2 | NA18968.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.83-6154T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390359 | ||||||
chr1:63390389
|
G | C | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-6124G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390389 | ||||||
chr1:63390436
|
A | G | 1 | a0002c0002t0001g0359 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.83-6077A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390436 | ||||||
chr1:63390451
|
C | G | 1 | a0001c0001t0003g0149 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.83-6062C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390451 | ||||||
chr1:63390458
|
C | T | 2 | a0001c0001t0002g0254a0001c0001t0002g0275 | 2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.83-6055C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390458 | ||||||
chr1:63390609
|
A | T | 1 | a0001c0001t0007g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-5904A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390609 | ||||||
chr1:63390724
|
C | T | 42 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(39): Show | 42 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.83-5789C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390724 | ||||||
chr1:63390980
|
A | G | 312 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(309): Show | 317 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(314): Show |
intron_variant | MODIFIER | c.83-5533A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63390980 | ||||||
chr1:63391011
|
G | T | 2 | a0001c0001t0004g0326a0001c0001t0004g0327 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.83-5502G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391011 | ||||||
chr1:63391038
|
G | A | 7 | a0001c0004t0004g0200a0001c0004t0006g0156a0001c0004t0006g0198others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-5475G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391038 | ||||||
chr1:63391047
|
G | T | 1 | a0001c0001t0002g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.83-5466G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391047 | ||||||
chr1:63391184
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.83-5329C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391184 | ||||||
chr1:63391221
|
C | T | 92 | a0001c0001t0002g0331a0001c0001t0003g0005a0001c0001t0003g0012others(89): Show | 92 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.83-5292C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391221 | ||||||
chr1:63391318
|
T | C | 1 | a0001c0001t0003g0211 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.83-5195T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391318 | ||||||
chr1:63391447
|
C | T | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-5066C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391447 | ||||||
chr1:63391483
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.83-5030C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391483 | ||||||
chr1:63391632
|
T | C | 2 | a0002c0002t0001g0180a0002c0002t0001g0232 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.83-4881T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391632 | ||||||
chr1:63391764
|
T | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.83-4749T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391764 | ||||||
chr1:63391998
|
A | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.83-4515A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63391998 | ||||||
chr1:63392172
|
A | AT | 40 | a0001c0001t0002g0331a0001c0001t0003g0101a0001c0001t0003g0102others(37): Show | 40 | HG01167.hp2 HG01884.hp1 HG02015.hp2 others(37): Show |
intron_variant | MODIFIER | c.83-4327dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63392172 | |||||
chr1:63392226
|
A | G | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-4287A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392226 | ||||||
chr1:63392239
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-4274C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392239 | ||||||
chr1:63392451
|
A | G | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.83-4062A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392451 | ||||||
chr1:63392612
|
C | T | 124 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(121): Show | 128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.83-3901C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392612 | ||||||
chr1:63392627
|
T | C | 1 | a0001c0001t0002g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.83-3886T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392627 | ||||||
chr1:63392631
|
C | T | 1 | a0002c0002t0001g0379 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.83-3882C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392631 | ||||||
chr1:63392667
|
G | A | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3846G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63392667 | ||||||
chr1:63393224
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-3289C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393224 | ||||||
chr1:63393239
|
G | A | 1 | a0002c0002t0001g0009 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.83-3274G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393239 | ||||||
chr1:63393375
|
C | T | 310 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(307): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.83-3138C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393375 | ||||||
chr1:63393469
|
G | A | 2 | a0001c0001t0002g0254a0001c0001t0002g0275 | 2 | HG01261.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.83-3044G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393469 | ||||||
chr1:63393500
|
A | T | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.83-3013A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393500 | ||||||
chr1:63393817
|
G | T | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.83-2696G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393817 | ||||||
chr1:63393819
|
C | T | 1 | a0001c0001t0005g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.83-2694C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63393819 | ||||||
chr1:63393927
|
TAGAG | T | 5 | a0001c0001t0004g0098a0001c0001t0008g0234a0001c0001t0008g0235others(2): Show | 5 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-2582_83-2579del others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr1 | 63393927 | |||||
chr1:63394065
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.83-2448T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394065 | ||||||
chr1:63394187
|
T | C | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2326T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394187 | ||||||
chr1:63394246
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0135 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.83-2267A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394246 | ||||||
chr1:63394376
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.83-2137T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394376 | ||||||
chr1:63394440
|
C | T | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2073C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394440 | ||||||
chr1:63394652
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.83-1861G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394652 | ||||||
chr1:63394734
|
A | G | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-1779A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394734 | ||||||
chr1:63394856
|
T | C | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-1657T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63394856 | ||||||
chr1:63395115
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.83-1398C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395115 | ||||||
chr1:63395144
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.83-1369G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395144 | ||||||
chr1:63395156
|
G | A | 2 | a0001c0001t0002g0255a0001c0001t0002g0256 | 2 | HG00408.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.83-1357G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395156 | ||||||
chr1:63395281
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.83-1232G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395281 | ||||||
chr1:63395342
|
T | G | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.83-1171T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395342 | ||||||
chr1:63395366
|
C | T | 90 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.83-1147C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395366 | ||||||
chr1:63395461
|
C | T | 124 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(121): Show | 128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.83-1052C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395461 | ||||||
chr1:63395540
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0050 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.83-973C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395540 | ||||||
chr1:63395550
|
G | A | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-963G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395550 | ||||||
chr1:63395602
|
T | C | 1 | a0002c0002t0001g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.83-911T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395602 | ||||||
chr1:63395655
|
A | G | 1 | a0001c0001t0002g0291 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.83-858A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395655 | ||||||
chr1:63395658
|
G | T | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.83-855G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395658 | ||||||
chr1:63395790
|
C | A | 23 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(20): Show | 23 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.83-723C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63395790 | ||||||
chr1:63396032
|
A | G | 1 | a0002c0002t0001g0359 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.83-481A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396032 | ||||||
chr1:63396096
|
A | G | 1 | a0002c0002t0001g0328 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.83-417A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396096 | ||||||
chr1:63396179
|
C | T | 1 | a0001c0001t0015g0380 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.83-334C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396179 | ||||||
chr1:63396239
|
T | G | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.83-274T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 2/14 | chr1 | 63396239 | ||||||
chr1:63396621
|
T | C | 1 | a0001c0001t0007g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.167+24T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63396621 | ||||||
chr1:63396745
|
T | C | 2 | a0001c0001t0004g0098a0004c0008t0003g0203 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.167+148T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63396745 | ||||||
chr1:63396940
|
G | A | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.167+343G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63396940 | ||||||
chr1:63397023
|
G | A | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.167+426G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397023 | ||||||
chr1:63397069
|
G | A | 379 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(376): Show | 385 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(382): Show |
intron_variant | MODIFIER | c.167+472G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397069 | ||||||
chr1:63397077
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+480G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397077 | ||||||
chr1:63397147
|
A | G | 1 | a0001c0001t0003g0012 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.167+550A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397147 | ||||||
chr1:63397251
|
T | G | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.167+654T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397251 | ||||||
chr1:63397516
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.167+919A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397516 | ||||||
chr1:63397565
|
T | TG | 310 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(307): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.167+969dupG | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63397565 | |||||
chr1:63397592
|
C | T | 1 | a0001c0001t0007g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.167+995C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397592 | ||||||
chr1:63397593
|
G | A | 1 | a0001c0003t0009g0192 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.167+996G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397593 | ||||||
chr1:63397847
|
T | C | 1 | a0001c0001t0001g0372 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.167+1250T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397847 | ||||||
chr1:63397850
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.167+1253A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397850 | ||||||
chr1:63397897
|
T | C | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.167+1300T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397897 | ||||||
chr1:63397911
|
C | T | 90 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.167+1314C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397911 | ||||||
chr1:63397928
|
C | T | 21 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.167+1331C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63397928 | ||||||
chr1:63398253
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+1656G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398253 | ||||||
chr1:63398262
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+1665T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398262 | ||||||
chr1:63398507
|
C | T | 1 | a0001c0001t0004g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.167+1910C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398507 | ||||||
chr1:63398589
|
T | C | 1 | a0001c0001t0003g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.167+1992T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398589 | ||||||
chr1:63398597
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.167+2000C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398597 | ||||||
chr1:63398666
|
A | G | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.167+2069A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398666 | ||||||
chr1:63398715
|
T | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.167+2118T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398715 | ||||||
chr1:63398717
|
C | T | 68 | a0001c0001t0002g0017a0001c0001t0002g0027a0001c0001t0002g0028others(65): Show | 69 | HG00408.hp2 HG00423.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.167+2120C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398717 | ||||||
chr1:63398770
|
T | C | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.167+2173T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398770 | ||||||
chr1:63398871
|
A | C | 11 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(8): Show | 11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.167+2274A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398871 | ||||||
chr1:63398888
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.167+2291A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63398888 | ||||||
chr1:63399055
|
A | G | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.167+2458A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399055 | ||||||
chr1:63399332
|
A | G | 2 | a0001c0001t0002g0014a0001c0001t0002g0015 | 2 | NA18986.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.167+2735A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399332 | ||||||
chr1:63399384
|
G | A | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.167+2787G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399384 | ||||||
chr1:63399650
|
G | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.168-2604G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399650 | ||||||
chr1:63399689
|
TA | T | 20 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(17): Show | 20 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.168-2562delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63399689 | |||||
chr1:63399694
|
A | C | 20 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(17): Show | 20 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.168-2560A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399694 | ||||||
chr1:63399714
|
T | A | 7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2540T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399714 | ||||||
chr1:63399786
|
G | A | 1 | a0001c0001t0002g0362 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-2468G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399786 | ||||||
chr1:63399834
|
A | G | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168-2420A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399834 | ||||||
chr1:63399911
|
G | A | 7 | a0001c0001t0002g0027a0001c0001t0004g0001a0001c0001t0004g0026others(4): Show | 8 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.168-2343G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399911 | ||||||
chr1:63399923
|
G | A | 7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2331G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399923 | ||||||
chr1:63399934
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.168-2320C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399934 | ||||||
chr1:63399939
|
G | A | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.168-2315G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63399939 | ||||||
chr1:63400086
|
C | T | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-2168C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400086 | ||||||
chr1:63400092
|
G | A | 1 | a0001c0001t0002g0257 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.168-2162G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400092 | ||||||
chr1:63400194
|
C | CA | 28 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0055others(25): Show | 29 | HG00140.hp1 HG01192.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.168-2047dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400194 | |||||
chr1:63400205
|
A | T | 1 | a0002c0002t0005g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.168-2049A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400205 | ||||||
chr1:63400206
|
A | AT | 6 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0095others(3): Show | 6 | HG00408.hp1 HG00438.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2048_168-2047i others(3): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400206 | ||||||
chr1:63400206
|
A | T | 4 | a0001c0001t0011g0190a0001c0001t0011g0191a0002c0002t0001g0167others(1): Show | 4 | HG03209.hp1 HG03453.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-2048A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400206 | ||||||
chr1:63400207
|
AT | A | 113 | a0001c0001t0001g0366a0001c0001t0002g0003a0001c0001t0002g0007others(110): Show | 116 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.168-2046delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | ||||||
chr1:63400207
|
ATAT | A | 5 | a0001c0001t0002g0362a0001c0001t0003g0099a0001c0001t0003g0137others(2): Show | 5 | HG01934.hp2 HG02451.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2046_168-2044d others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | ||||||
chr1:63400207
|
ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0363a0001c0001t0001g0371 | 2 | NA18952.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.168-2046_168-2028d others(21): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | ||||||
chr1:63400207
|
ATATATAT others(106): Show |
A | 17 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0079others(14): Show | 17 | HG00423.hp1 HG02027.hp2 HG04184.hp1 others(14): Show |
intron_variant | MODIFIER | c.168-2046_168-1934d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400207 | ||||||
chr1:63400208
|
T | A | 130 | a0001c0001t0001g0297a0001c0001t0001g0335a0001c0001t0001g0338others(127): Show | 132 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.168-2046T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400208 | ||||||
chr1:63400209
|
ATATATAT others(105): Show |
A | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.168-2032_168-1921d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400209 | |||||
chr1:63400210
|
T | A | 201 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0013others(198): Show | 204 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(201): Show |
intron_variant | MODIFIER | c.168-2044T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400210 | ||||||
chr1:63400212
|
T | A | 124 | a0001c0001t0002g0007a0001c0001t0002g0013a0001c0001t0002g0029others(121): Show | 126 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.168-2042T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400212 | ||||||
chr1:63400213
|
ATATATAT others(25): Show |
A | 1 | a0001c0001t0004g0326 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.168-2032_168-2001d others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400213 | |||||
chr1:63400214
|
T | A | 99 | a0001c0001t0002g0051a0001c0001t0002g0178a0001c0001t0002g0179others(96): Show | 100 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(97): Show |
intron_variant | MODIFIER | c.168-2040T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400214 | ||||||
chr1:63400215
|
ATATATAC others(23): Show |
A | 6 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(3): Show | 6 | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-2032_168-2003d others(32): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400215 | |||||
chr1:63400215
|
ATATATAC others(61): Show |
A | 2 | a0001c0001t0001g0320a0001c0001t0005g0139 | 2 | HG04184.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.168-2032_168-1965d others(70): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400215 | |||||
chr1:63400216
|
T | A | 90 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.168-2038T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400216 | ||||||
chr1:63400218
|
T | A | 88 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.168-2036T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400218 | ||||||
chr1:63400219
|
ATACG | A | 6 | a0001c0001t0001g0335a0001c0001t0001g0372a0001c0001t0001g0377others(3): Show | 7 | HG01106.hp1 HG01952.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2032_168-2029d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400219 | |||||
chr1:63400220
|
T | A | 88 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.168-2034T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400220 | ||||||
chr1:63400221
|
ACG | A | 95 | a0001c0001t0001g0297a0001c0001t0001g0338a0001c0001t0001g0364others(92): Show | 97 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.168-2032_168-2031d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | ||||||
chr1:63400221
|
ACGT | A | 46 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0109others(43): Show | 46 | HG00544.hp1 HG00733.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.168-2032_168-2030d others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | ||||||
chr1:63400221
|
ACGTATAT others(27): Show |
A | 1 | a0001c0001t0004g0327 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.168-2032_168-1999d others(36): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | ||||||
chr1:63400221
|
ACGTATAT others(55): Show |
A | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-2032_168-1971d others(64): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | ||||||
chr1:63400221
|
ACGTATAT others(79): Show |
A | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-2032_168-1947d others(88): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400221 | ||||||
chr1:63400222
|
C | A | 40 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0099others(37): Show | 40 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.168-2032C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | ||||||
chr1:63400222
|
C | T | 58 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0020others(55): Show | 60 | HG00408.hp2 HG01070.hp1 HG01081.hp1 others(57): Show |
intron_variant | MODIFIER | c.168-2032C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | ||||||
chr1:63400222
|
CGTATATA others(109): Show |
C | 2 | a0001c0001t0001g0086a0001c0007t0001g0094 | 2 | HG00408.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.168-2031_168-1916d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | ||||||
chr1:63400222
|
CGTATATA others(133): Show |
C | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.168-2031_168-1892d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400222 | ||||||
chr1:63400223
|
G | A | 122 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0055others(119): Show | 124 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.168-2031G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400223 | ||||||
chr1:63400223
|
G | GTA | 6 | a0002c0002t0001g0075a0002c0002t0001g0166a0002c0002t0001g0173others(3): Show | 6 | HG01243.hp2 HG02132.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.168-2012_168-2011d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400223 | |||||
chr1:63400224
|
T | A | 15 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0102others(12): Show | 15 | HG00738.hp1 HG00741.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.168-2030T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400224 | ||||||
chr1:63400226
|
T | A | 46 | a0001c0001t0003g0005a0001c0001t0003g0109a0001c0001t0003g0110others(43): Show | 46 | HG00544.hp1 HG00733.hp1 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.168-2028T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400226 | ||||||
chr1:63400226
|
T | C | 12 | a0001c0001t0001g0297a0001c0001t0001g0338a0001c0001t0001g0364others(9): Show | 12 | HG00140.hp2 HG02056.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.168-2028T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400226 | ||||||
chr1:63400228
|
T | A | 8 | a0001c0001t0003g0112a0001c0001t0003g0118a0001c0001t0003g0210others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2026T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400228 | ||||||
chr1:63400228
|
T | C | 7 | a0001c0001t0001g0335a0001c0001t0001g0366a0001c0001t0001g0372others(4): Show | 8 | HG00438.hp1 HG01106.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2026T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400228 | ||||||
chr1:63400230
|
T | A | 3 | a0001c0001t0003g0210a0001c0003t0009g0192a0001c0003t0009g0195 | 3 | HG01192.hp1 HG01243.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.168-2024T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400230 | ||||||
chr1:63400230
|
T | C | 5 | a0001c0001t0007g0145a0001c0001t0007g0146a0001c0001t0011g0189others(2): Show | 5 | HG01934.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-2024T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400230 | ||||||
chr1:63400231
|
ATATATAT others(45): Show |
A | 1 | a0002c0002t0001g0323 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.168-1972_168-1921d others(54): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400231 | |||||
chr1:63400232
|
T | A | 2 | a0001c0003t0009g0192a0001c0003t0009g0195 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.168-2022T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400232 | ||||||
chr1:63400233
|
ATATATAT others(29): Show |
A | 1 | a0001c0001t0001g0367 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.168-2010_168-1975d others(38): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400233 | |||||
chr1:63400233
|
ATATATAT others(43): Show |
A | 1 | a0002c0002t0001g0319 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.168-2010_168-1961d others(52): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400233 | |||||
chr1:63400234
|
T | C | 2 | a0001c0001t0004g0098a0004c0008t0003g0203 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-2020T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400234 | ||||||
chr1:63400235
|
ATATATAT others(41): Show |
A | 1 | a0002c0002t0005g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.168-2010_168-1963d others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400235 | |||||
chr1:63400235
|
ATATATAT others(107): Show |
A | 1 | a0001c0001t0001g0095 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.168-2010_168-1897d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400235 | |||||
chr1:63400236
|
T | C | 2 | a0001c0001t0004g0098a0004c0008t0003g0203 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-2018T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400236 | ||||||
chr1:63400237
|
ATATATAC others(25): Show |
A | 1 | a0001c0001t0001g0365 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.168-2010_168-1979d others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400237 | |||||
chr1:63400237
|
ATATATAC others(105): Show |
A | 3 | a0001c0001t0001g0080a0001c0001t0001g0090a0001c0001t0001g0097 | 3 | NA18957.hp1 NA18978.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.168-2010_168-1899d others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400237 | |||||
chr1:63400238
|
T | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0362a0001c0001t0004g0098others(1): Show | 5 | HG01192.hp2 HG02559.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2016T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400238 | ||||||
chr1:63400239
|
ATATACGT others(23): Show |
A | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168-2010_168-1981d others(32): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400239 | |||||
chr1:63400239
|
ATATACGT others(37): Show |
A | 27 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0247others(24): Show | 27 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.168-2010_168-1967d others(46): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400239 | |||||
chr1:63400240
|
T | C | 12 | a0001c0001t0002g0002a0001c0001t0002g0362a0001c0001t0003g0196others(9): Show | 13 | HG01167.hp2 HG01192.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.168-2014T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400240 | ||||||
chr1:63400241
|
A | G | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-2013A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400241 | ||||||
chr1:63400241
|
ATACGTAT others(21): Show |
A | 2 | a0001c0001t0001g0338a0001c0001t0001g0369 | 2 | HG03490.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.168-2010_168-1983d others(30): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400241 | |||||
chr1:63400241
|
ATACGTAT others(35): Show |
A | 42 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(39): Show | 42 | HG00423.hp2 HG00544.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.168-2010_168-1969d others(44): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400241 | |||||
chr1:63400241
|
ATACGTAT others(49): Show |
A | 5 | a0001c0001t0002g0306a0001c0001t0002g0307a0001c0001t0002g0308others(2): Show | 5 | HG01496.hp2 HG01952.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2010_168-1955d others(58): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400241 | |||||
chr1:63400242
|
T | C | 10 | a0001c0001t0002g0002a0001c0001t0002g0362a0001c0001t0003g0196others(7): Show | 11 | HG01167.hp2 HG01192.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-2012T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400242 | ||||||
chr1:63400243
|
ACG | A | 27 | a0001c0001t0001g0335a0001c0001t0001g0364a0001c0001t0001g0366others(24): Show | 28 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.168-2010_168-2009d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | ||||||
chr1:63400243
|
ACGTATAT others(5): Show |
A | 1 | a0001c0003t0009g0194 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.168-2010_168-1999d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | ||||||
chr1:63400243
|
ACGTATAT others(19): Show |
A | 2 | a0001c0001t0001g0374a0001c0001t0001g0375 | 2 | HG02165.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.168-2010_168-1985d others(28): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | ||||||
chr1:63400243
|
ACGTATAT others(33): Show |
A | 82 | a0001c0001t0001g0055a0001c0001t0001g0297a0001c0001t0002g0003others(79): Show | 83 | HG00544.hp1 HG00558.hp2 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.168-2010_168-1971d others(42): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | ||||||
chr1:63400243
|
ACGTATAT others(47): Show |
A | 5 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(2): Show | 6 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2010_168-1957d others(56): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400243 | ||||||
chr1:63400244
|
C | T | 5 | a0001c0001t0002g0031a0001c0001t0011g0189a0001c0001t0011g0190others(2): Show | 5 | HG00639.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-2010C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | ||||||
chr1:63400244
|
CGTATATA others(15): Show |
C | 2 | a0001c0001t0002g0331a0001c0001t0004g0332 | 2 | HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.168-2009_168-1988d others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | ||||||
chr1:63400244
|
CGTATATA others(19): Show |
C | 7 | a0001c0001t0003g0196a0001c0001t0004g0181a0001c0001t0004g0182others(4): Show | 7 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-2009_168-1984d others(28): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | ||||||
chr1:63400244
|
CGTATATA others(39): Show |
C | 50 | a0001c0001t0002g0017a0001c0001t0002g0020a0001c0001t0002g0023others(47): Show | 51 | HG00408.hp2 HG01070.hp1 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.168-2009_168-1964d others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400244 | ||||||
chr1:63400245
|
G | A | 14 | a0001c0001t0001g0363a0001c0001t0001g0371a0001c0001t0002g0002others(11): Show | 15 | HG00639.hp2 HG00738.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-2009G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400245 | ||||||
chr1:63400246
|
T | C | 5 | a0001c0001t0002g0027a0001c0001t0002g0037a0001c0001t0002g0178others(2): Show | 5 | HG00738.hp1 HG02155.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-2008T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400246 | ||||||
chr1:63400247
|
A | ATATATAC others(1): Show |
3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-2001_168-2000i others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400247 | |||||
chr1:63400248
|
T | C | 6 | a0001c0001t0002g0027a0001c0001t0002g0037a0001c0001t0002g0178others(3): Show | 6 | HG00738.hp1 HG02155.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-2006T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400248 | ||||||
chr1:63400250
|
T | C | 7 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0037others(4): Show | 7 | HG00639.hp2 HG00738.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2004T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400250 | ||||||
chr1:63400252
|
T | C | 8 | a0001c0001t0002g0027a0001c0001t0002g0031a0001c0001t0002g0037others(5): Show | 8 | HG00639.hp2 HG00738.hp1 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-2002T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400252 | ||||||
chr1:63400254
|
T | C | 7 | a0001c0001t0002g0031a0001c0001t0003g0152a0001c0001t0004g0098others(4): Show | 7 | HG00639.hp2 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-2000T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400254 | ||||||
chr1:63400255
|
G | A | 37 | a0001c0001t0001g0335a0001c0001t0001g0363a0001c0001t0001g0364others(34): Show | 37 | HG00140.hp2 HG00438.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.168-1999G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400255 | ||||||
chr1:63400255
|
G | GTA | 2 | a0001c0001t0002g0002a0001c0001t0002g0362 | 3 | HG01192.hp2 HG02683.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.168-1988_168-1987d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400255 | |||||
chr1:63400256
|
T | C | 3 | a0001c0001t0002g0031a0001c0001t0003g0152a0001c0004t0006g0325 | 3 | HG00639.hp2 HG02280.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.168-1998T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400256 | ||||||
chr1:63400258
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168-1996T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400258 | ||||||
chr1:63400262
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1992T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400262 | ||||||
chr1:63400263
|
A | G | 5 | a0001c0001t0002g0027a0001c0001t0002g0037a0001c0001t0002g0178others(2): Show | 5 | HG00738.hp1 HG02155.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.168-1991A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400263 | ||||||
chr1:63400264
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1990T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400264 | ||||||
chr1:63400265
|
ATACG | A | 7 | a0001c0001t0001g0363a0001c0001t0001g0371a0001c0001t0002g0027others(4): Show | 7 | HG00738.hp1 HG02155.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.168-1986_168-1983d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400265 | |||||
chr1:63400266
|
T | C | 10 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(7): Show | 10 | HG01243.hp1 HG02647.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-1988T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400266 | ||||||
chr1:63400267
|
A | G | 2 | a0001c0001t0002g0031a0001c0004t0006g0325 | 2 | HG00639.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.168-1987A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400267 | ||||||
chr1:63400267
|
ACG | A | 4 | a0001c0003t0009g0192a0001c0003t0009g0194a0001c0003t0009g0195others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1986_168-1985d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400267 | ||||||
chr1:63400268
|
C | T | 3 | a0001c0001t0002g0031a0001c0001t0003g0152a0001c0004t0006g0325 | 3 | HG00639.hp2 HG02280.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.168-1986C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400268 | ||||||
chr1:63400268
|
CGTATATA others(15): Show |
C | 2 | a0001c0003t0012g0239a0001c0003t0014g0240 | 2 | NA18522.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.168-1985_168-1964d others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400268 | ||||||
chr1:63400268
|
CGTATATA others(17): Show |
C | 1 | a0001c0003t0009g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.168-1985_168-1962d others(26): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400268 | ||||||
chr1:63400269
|
G | A | 12 | a0001c0001t0002g0031a0001c0001t0002g0331a0001c0001t0003g0204others(9): Show | 12 | HG00639.hp2 HG01243.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.168-1985G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400269 | ||||||
chr1:63400269
|
G | GTA | 7 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159others(4): Show | 7 | HG01167.hp1 HG01169.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1974_168-1973d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400269 | |||||
chr1:63400269
|
G | GTATA | 44 | a0002c0002t0001g0008a0002c0002t0001g0009a0002c0002t0001g0053others(41): Show | 45 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.168-1976_168-1973d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400269 | |||||
chr1:63400270
|
T | C | 9 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 9 | HG02895.hp1 HG02896.hp1 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1984T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400270 | ||||||
chr1:63400271
|
ATATATAT others(43): Show |
A | 7 | a0002c0002t0001g0180a0002c0002t0001g0232a0002c0002t0001g0233others(4): Show | 7 | HG02280.hp1 HG03516.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1972_168-1923d others(52): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400271 | |||||
chr1:63400273
|
A | ATATATAT others(21): Show |
3 | a0002c0002t0001g0073a0002c0002t0001g0074a0002c0002t0001g0075 | 3 | NA18944.hp1 NA18945.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.168-1973_168-1972i others(30): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400273 | |||||
chr1:63400273
|
ATATATAT others(41): Show |
A | 2 | a0002c0002t0001g0321a0002c0002t0001g0329 | 2 | HG02132.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.168-1972_168-1925d others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400273 | |||||
chr1:63400273
|
ATATATAT others(57): Show |
A | 3 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108 | 4 | HG02559.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1972_168-1909d others(66): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400273 | |||||
chr1:63400278
|
TATAC | T | 13 | a0001c0001t0001g0335a0001c0001t0001g0364a0001c0001t0001g0366others(10): Show | 13 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.168-1975_168-1972d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400278 | ||||||
chr1:63400279
|
A | G | 3 | a0001c0001t0003g0210a0001c0001t0004g0098a0004c0008t0003g0203 | 3 | HG01243.hp1 HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-1975A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400279 | ||||||
chr1:63400280
|
T | C | 8 | a0001c0001t0002g0002a0001c0001t0002g0362a0001c0001t0011g0189others(5): Show | 9 | HG01192.hp1 HG01192.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1974T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400280 | ||||||
chr1:63400281
|
A | G | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1973A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400281 | ||||||
chr1:63400281
|
ACG | A | 7 | a0001c0001t0001g0363a0001c0001t0001g0365a0001c0001t0001g0367others(4): Show | 7 | HG01243.hp1 HG02165.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1972_168-1971d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400281 | ||||||
chr1:63400281
|
ACGTATAT others(83): Show |
A | 2 | a0001c0001t0004g0098a0004c0008t0003g0203 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.168-1972_168-1883d others(92): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400281 | ||||||
chr1:63400282
|
C | T | 9 | a0001c0001t0002g0331a0001c0001t0004g0332a0001c0001t0011g0189others(6): Show | 9 | HG02622.hp1 HG02976.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.168-1972C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400282 | ||||||
chr1:63400282
|
CGTAT | C | 3 | a0001c0001t0001g0338a0001c0001t0001g0369a0001c0001t0001g0374 | 3 | HG03490.hp2 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.168-1971_168-1968d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400282 | ||||||
chr1:63400282
|
CGTATATA others(51): Show |
C | 2 | a0001c0001t0002g0002a0001c0001t0002g0362 | 3 | HG01192.hp2 HG02683.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.168-1971_168-1914d others(60): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400282 | ||||||
chr1:63400283
|
G | A | 10 | a0001c0001t0002g0331a0001c0001t0011g0189a0001c0001t0011g0190others(7): Show | 10 | HG01192.hp1 HG02622.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.168-1971G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400283 | ||||||
chr1:63400284
|
T | C | 3 | a0001c0003t0009g0192a0001c0003t0009g0195a0001c0003t0012g0238 | 3 | HG01192.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.168-1970T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400284 | ||||||
chr1:63400285
|
A | ACG | 3 | a0002c0002t0001g0354a0002c0002t0001g0355a0002c0002t0001g0356 | 3 | NA18985.hp2 NA18988.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.168-1969_168-1968i others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400285 | ||||||
chr1:63400286
|
T | C | 3 | a0001c0003t0009g0192a0001c0003t0009g0195a0001c0003t0012g0238 | 3 | HG01192.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.168-1968T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400286 | ||||||
chr1:63400288
|
T | C | 7 | a0001c0001t0003g0144a0001c0004t0004g0200a0001c0004t0006g0156others(4): Show | 7 | HG01891.hp2 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.168-1966T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400288 | ||||||
chr1:63400289
|
A | G | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1965A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400289 | ||||||
chr1:63400290
|
T | C | 134 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(131): Show | 135 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.168-1964T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400290 | ||||||
chr1:63400292
|
T | C | 190 | a0001c0001t0001g0050a0001c0001t0002g0003a0001c0001t0002g0013others(187): Show | 192 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.168-1962T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400292 | ||||||
chr1:63400294
|
T | C | 216 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0055others(213): Show | 218 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.168-1960T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400294 | ||||||
chr1:63400296
|
C | T | 6 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191others(3): Show | 6 | HG01192.hp1 HG02622.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-1958C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400296 | ||||||
chr1:63400296
|
CGTATATA others(37): Show |
C | 6 | a0001c0001t0002g0027a0001c0001t0002g0037a0001c0001t0002g0178others(3): Show | 6 | HG00738.hp1 HG02155.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-1957_168-1914d others(46): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400296 | ||||||
chr1:63400297
|
G | A | 194 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(191): Show | 196 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.168-1957G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400297 | ||||||
chr1:63400298
|
T | C | 2 | a0001c0001t0003g0124a0001c0003t0010g0324 | 2 | HG03834.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.168-1956T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400298 | ||||||
chr1:63400299
|
ATATATAT others(1): Show |
A | 3 | a0001c0003t0009g0192a0001c0003t0009g0195a0001c0003t0012g0238 | 3 | HG01192.hp1 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.168-1947_168-1940d others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400299 | |||||
chr1:63400301
|
ATATATGT others(29): Show |
A | 13 | a0001c0001t0001g0335a0001c0001t0001g0364a0001c0001t0001g0366others(10): Show | 13 | HG00140.hp2 HG00438.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.168-1947_168-1912d others(38): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400301 | |||||
chr1:63400304
|
T | C | 10 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(7): Show | 11 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.168-1950T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400304 | ||||||
chr1:63400305
|
ATGTATAT others(25): Show |
A | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1947_168-1916d others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400305 | |||||
chr1:63400306
|
T | C | 30 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(27): Show | 31 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(28): Show |
intron_variant | MODIFIER | c.168-1948T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400306 | ||||||
chr1:63400306
|
T | TATAC | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1948_168-1947i others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400306 | ||||||
chr1:63400307
|
G | A | 14 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(11): Show | 15 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1947G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400307 | ||||||
chr1:63400308
|
T | C | 14 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(11): Show | 15 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1946T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400308 | ||||||
chr1:63400310
|
T | C | 14 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(11): Show | 15 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.168-1944T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400310 | ||||||
chr1:63400316
|
T | C | 1 | a0002c0002t0001g0162 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.168-1938T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400316 | ||||||
chr1:63400317
|
A | G | 4 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191others(1): Show | 4 | HG01261.hp2 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1937A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400317 | ||||||
chr1:63400319
|
ACG | A | 117 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(114): Show | 119 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.168-1934_168-1933d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400319 | ||||||
chr1:63400320
|
C | T | 17 | a0001c0001t0002g0007a0001c0001t0002g0036a0001c0001t0002g0042others(14): Show | 18 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.168-1934C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400320 | ||||||
chr1:63400321
|
G | A | 24 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0079others(21): Show | 24 | HG00423.hp1 HG02027.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.168-1933G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400321 | ||||||
chr1:63400321
|
G | GTA | 41 | a0002c0002t0001g0009a0002c0002t0001g0053a0002c0002t0001g0054others(38): Show | 41 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.168-1920_168-1919d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400321 | |||||
chr1:63400322
|
T | C | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-1932T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400322 | ||||||
chr1:63400324
|
T | C | 120 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(117): Show | 122 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.168-1930T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400324 | ||||||
chr1:63400325
|
A | G | 119 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(116): Show | 121 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.168-1929A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400325 | ||||||
chr1:63400325
|
ATATATAT others(5): Show |
A | 8 | a0001c0001t0001g0338a0001c0001t0001g0363a0001c0001t0001g0365others(5): Show | 8 | HG03490.hp2 HG03491.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.168-1918_168-1907d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400325 | |||||
chr1:63400327
|
ATATATAT others(3): Show |
A | 10 | a0001c0001t0001g0247a0001c0001t0001g0285a0001c0001t0001g0286others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG04115.hp1 others(7): Show |
intron_variant | MODIFIER | c.168-1918_168-1909d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400327 | |||||
chr1:63400329
|
ATATATAC others(1): Show |
A | 4 | a0001c0001t0001g0018a0001c0001t0001g0050a0001c0001t0001g0055others(1): Show | 4 | HG00140.hp1 HG01433.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1918_168-1911d others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400329 | |||||
chr1:63400330
|
T | C | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1924T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400330 | ||||||
chr1:63400331
|
A | G | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1923A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400331 | ||||||
chr1:63400331
|
ATATACG | A | 96 | a0001c0001t0001g0375a0001c0001t0002g0031a0001c0001t0002g0331others(93): Show | 96 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.168-1918_168-1913d others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400331 | |||||
chr1:63400336
|
C | T | 4 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191others(1): Show | 4 | HG02622.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.168-1918C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400336 | ||||||
chr1:63400336
|
CGT | C | 120 | a0001c0001t0001g0078a0001c0001t0002g0003a0001c0001t0002g0013others(117): Show | 122 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.168-1917_168-1916d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400336 | ||||||
chr1:63400337
|
G | A | 22 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0079others(19): Show | 22 | HG00423.hp1 HG02027.hp2 HG02523.hp2 others(19): Show |
intron_variant | MODIFIER | c.168-1917G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400337 | ||||||
chr1:63400338
|
T | C | 75 | a0001c0001t0002g0031a0001c0001t0003g0005a0001c0001t0003g0012others(72): Show | 75 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.168-1916T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400338 | ||||||
chr1:63400339
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-1915A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400339 | ||||||
chr1:63400340
|
T | C | 210 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0014others(207): Show | 212 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(209): Show |
intron_variant | MODIFIER | c.168-1914T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400340 | ||||||
chr1:63400342
|
T | C | 4 | a0001c0001t0003g0210a0001c0001t0011g0189a0001c0001t0011g0190others(1): Show | 4 | HG01243.hp1 HG02622.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.168-1912T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400342 | ||||||
chr1:63400347
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.168-1907A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400347 | ||||||
chr1:63400348
|
T | C | 15 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(12): Show | 16 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.168-1906T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400348 | ||||||
chr1:63400349
|
G | A | 40 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0078others(37): Show | 41 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.168-1905G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400349 | ||||||
chr1:63400350
|
T | C | 17 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(14): Show | 18 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.168-1904T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400350 | ||||||
chr1:63400351
|
A | G | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.168-1903A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400351 | ||||||
chr1:63400359
|
A | G | 13 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(10): Show | 14 | HG00738.hp1 HG01074.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.168-1895A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400359 | ||||||
chr1:63400361
|
G | A | 11 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(8): Show | 12 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.168-1893G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400361 | ||||||
chr1:63400361
|
G | GTA | 22 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0204others(19): Show | 22 | HG01167.hp2 HG02145.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.168-1885_168-1884d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63400361 | |||||
chr1:63400370
|
T | C | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.168-1884T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400370 | ||||||
chr1:63400370
|
T | TAC | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.168-1884_168-1883i others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400370 | ||||||
chr1:63400427
|
A | C | 1 | a0002c0002t0001g0315 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.168-1827A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400427 | ||||||
chr1:63400587
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1667G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400587 | ||||||
chr1:63400788
|
T | C | 2 | a0001c0001t0003g0122a0001c0001t0003g0148 | 2 | HG01884.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.168-1466T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400788 | ||||||
chr1:63400930
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1324G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400930 | ||||||
chr1:63400931
|
C | G | 1 | a0001c0001t0002g0178 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168-1323C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400931 | ||||||
chr1:63400994
|
G | A | 1 | a0001c0001t0001g0365 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.168-1260G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63400994 | ||||||
chr1:63401015
|
CA | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.168-1235delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63401015 | |||||
chr1:63401020
|
G | T | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168-1234G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401020 | ||||||
chr1:63401041
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.168-1213A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401041 | ||||||
chr1:63401157
|
T | A | 1 | a0001c0001t0002g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.168-1097T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401157 | ||||||
chr1:63401179
|
G | C | 1 | a0001c0001t0002g0362 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.168-1075G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401179 | ||||||
chr1:63401264
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.168-990G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401264 | ||||||
chr1:63401414
|
G | A | 1 | a0002c0002t0001g0330 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168-840G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401414 | ||||||
chr1:63401503
|
T | G | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168-751T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401503 | ||||||
chr1:63401580
|
C | T | 2 | a0001c0001t0007g0145a0001c0001t0007g0146 | 2 | HG01934.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.168-674C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401580 | ||||||
chr1:63401584
|
T | TA | 17 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(14): Show | 18 | HG00544.hp1 HG01074.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.168-656dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 63401584 | |||||
chr1:63401599
|
C | G | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.168-655C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401599 | ||||||
chr1:63401610
|
G | A | 90 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.168-644G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401610 | ||||||
chr1:63401614
|
T | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.168-640T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401614 | ||||||
chr1:63401642
|
A | G | 5 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108others(2): Show | 6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.168-612A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401642 | ||||||
chr1:63401671
|
C | T | 2 | a0001c0001t0003g0122a0001c0001t0003g0148 | 2 | HG01884.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.168-583C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401671 | ||||||
chr1:63401740
|
T | C | 1 | a0001c0001t0002g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.168-514T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401740 | ||||||
chr1:63401822
|
T | G | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.168-432T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401822 | ||||||
chr1:63401946
|
A | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.168-308A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401946 | ||||||
chr1:63401947
|
C | T | 243 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(240): Show | 247 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(244): Show |
intron_variant | MODIFIER | c.168-307C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 3/14 | chr1 | 63401947 | ||||||
chr1:63402385
|
C | T | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.257+42C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402385 | ||||||
chr1:63402460
|
A | AT | 153 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(150): Show | 155 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.257+141dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402460 | |||||
chr1:63402460
|
A | ATT | 13 | a0001c0001t0001g0085a0001c0001t0001g0088a0001c0001t0001g0360others(10): Show | 13 | HG01168.hp2 HG01169.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+140_257+141dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402460 | |||||
chr1:63402460
|
AT | A | 31 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0065others(28): Show | 31 | HG01069.hp1 HG01070.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.257+141delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402460 | |||||
chr1:63402515
|
G | GGA | 4 | a0001c0001t0003g0099a0001c0001t0003g0125a0001c0001t0003g0131others(1): Show | 4 | NA18947.hp1 NA18981.hp2 NA19059.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+174_257+175dup others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63402515 | |||||
chr1:63402518
|
G | A | 1 | a0001c0001t0008g0059 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.257+175G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402518 | ||||||
chr1:63402586
|
C | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.257+243C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402586 | ||||||
chr1:63402655
|
C | T | 1 | a0001c0001t0003g0012 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.257+312C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402655 | ||||||
chr1:63402677
|
A | G | 309 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(306): Show | 314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.257+334A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402677 | ||||||
chr1:63402849
|
C | G | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.257+506C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402849 | ||||||
chr1:63402924
|
A | G | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+581A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402924 | ||||||
chr1:63402938
|
T | C | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.257+595T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63402938 | ||||||
chr1:63403027
|
G | A | 7 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0016others(4): Show | 9 | HG01192.hp2 HG01891.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+684G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403027 | ||||||
chr1:63403052
|
G | A | 1 | a0001c0001t0003g0226 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.257+709G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403052 | ||||||
chr1:63403087
|
T | G | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.257+744T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403087 | ||||||
chr1:63403094
|
C | CA | 15 | a0001c0001t0001g0081a0001c0001t0001g0088a0001c0001t0001g0297others(12): Show | 15 | HG00438.hp1 HG00741.hp1 HG02080.hp2 others(12): Show |
intron_variant | MODIFIER | c.257+777dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63403094 | |||||
chr1:63403094
|
CA | C | 107 | a0001c0001t0001g0365a0001c0001t0002g0024a0001c0001t0002g0032others(104): Show | 107 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.257+777delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63403094 | |||||
chr1:63403094
|
CAA | C | 119 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(116): Show | 123 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.257+776_257+777del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr1 | 63403094 | |||||
chr1:63403179
|
T | C | 244 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(241): Show | 248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.257+836T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403179 | ||||||
chr1:63403315
|
G | A | 26 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(23): Show | 26 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(23): Show |
intron_variant | MODIFIER | c.257+972G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403315 | ||||||
chr1:63403502
|
A | G | 244 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(241): Show | 248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.258-951A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403502 | ||||||
chr1:63403534
|
A | G | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-919A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403534 | ||||||
chr1:63403674
|
G | C | 21 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.258-779G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403674 | ||||||
chr1:63403695
|
C | CT | 310 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(307): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.258-758_258-757ins others(1): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403695 | ||||||
chr1:63403751
|
T | C | 1 | a0001c0001t0002g0273 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.258-702T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403751 | ||||||
chr1:63403767
|
T | C | 3 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0302 | 3 | HG02683.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.258-686T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403767 | ||||||
chr1:63403816
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.258-637C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403816 | ||||||
chr1:63403817
|
G | A | 90 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0003g0005others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.258-636G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403817 | ||||||
chr1:63403893
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.258-560G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63403893 | ||||||
chr1:63404168
|
A | G | 7 | a0001c0001t0002g0279a0001c0001t0002g0282a0001c0001t0002g0291others(4): Show | 7 | HG02027.hp1 HG02056.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-285A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63404168 | ||||||
chr1:63404428
|
T | C | 6 | a0002c0002t0001g0054a0002c0002t0001g0340a0002c0002t0001g0341others(3): Show | 6 | NA18973.hp2 NA18991.hp2 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-25T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63404428 | ||||||
chr1:63404431
|
G | A | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.258-22G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 4/14 | chr1 | 63404431 | ||||||
chr1:63404624
|
TACTG | T | 21 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0197others(18): Show | 21 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.346+87_346+90delGA others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr1 | 63404624 | |||||
chr1:63404780
|
C | G | 1 | a0001c0001t0002g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.346+239C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63404780 | ||||||
chr1:63404893
|
G | A | 1 | a0001c0004t0006g0156 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.346+352G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63404893 | ||||||
chr1:63405086
|
A | T | 1 | a0001c0001t0002g0296 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.346+545A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405086 | ||||||
chr1:63405223
|
C | T | 1 | a0004c0008t0003g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.346+682C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405223 | ||||||
chr1:63405242
|
C | T | 118 | a0001c0001t0002g0331a0001c0001t0003g0005a0001c0001t0003g0012others(115): Show | 118 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(115): Show |
intron_variant | MODIFIER | c.346+701C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405242 | ||||||
chr1:63405285
|
C | G | 1 | a0001c0001t0005g0106 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.346+744C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405285 | ||||||
chr1:63405459
|
T | A | 1 | a0001c0001t0002g0249 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.347-858T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405459 | ||||||
chr1:63405478
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.347-839C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405478 | ||||||
chr1:63405794
|
A | G | 6 | a0001c0001t0002g0331a0001c0001t0010g0333a0001c0001t0010g0334others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-523A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405794 | ||||||
chr1:63405879
|
T | A | 1 | a0001c0001t0001g0375 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.347-438T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405879 | ||||||
chr1:63405948
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.347-369T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405948 | ||||||
chr1:63405951
|
C | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.347-366C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405951 | ||||||
chr1:63405969
|
T | C | 124 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(121): Show | 128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.347-348T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63405969 | ||||||
chr1:63406087
|
T | C | 88 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.347-230T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406087 | ||||||
chr1:63406109
|
G | A | 6 | a0001c0001t0002g0331a0001c0001t0010g0333a0001c0001t0010g0334others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-208G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406109 | ||||||
chr1:63406153
|
A | G | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.347-164A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406153 | ||||||
chr1:63406210
|
A | G | 124 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(121): Show | 128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.347-107A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 5/14 | chr1 | 63406210 | ||||||
chr1:63406427
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.429+28G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406427 | ||||||
chr1:63406445
|
T | C | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.429+46T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406445 | ||||||
chr1:63406617
|
C | A | 3 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0001t0001g0375 | 3 | HG00438.hp1 HG02165.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.429+218C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406617 | ||||||
chr1:63406655
|
T | C | 3 | a0001c0001t0003g0102a0001c0001t0003g0124a0001c0001t0003g0152 | 3 | HG02738.hp2 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.429+256T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406655 | ||||||
chr1:63406688
|
T | C | 18 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0204others(15): Show | 18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.429+289T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406688 | ||||||
chr1:63406929
|
T | C | 88 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.430-133T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406929 | ||||||
chr1:63406944
|
G | T | 1 | a0001c0001t0002g0179 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.430-118G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63406944 | ||||||
chr1:63407059
|
C | T | 1 | a0001c0001t0002g0023 | 1 | HG02698.hp2 | splice_region_variant&intron_variant | LOW | c.430-3C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 6/14 | chr1 | 63407059 | ||||||
chr1:63407194
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.494+68G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407194 | ||||||
chr1:63407195
|
C | T | 1 | a0002c0002t0001g0355 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.494+69C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407195 | ||||||
chr1:63407200
|
A | G | 244 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(241): Show | 248 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(245): Show |
intron_variant | MODIFIER | c.494+74A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407200 | ||||||
chr1:63407343
|
T | C | 1 | a0003c0005t0003g0104 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.494+217T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407343 | ||||||
chr1:63407779
|
T | C | 148 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(145): Show | 152 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.494+653T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407779 | ||||||
chr1:63407795
|
GT | G | 73 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(70): Show | 73 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.494+673delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 63407795 | |||||
chr1:63407835
|
G | A | 4 | a0001c0001t0001g0320a0001c0001t0005g0010a0001c0001t0005g0011others(1): Show | 4 | HG03491.hp2 HG04115.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+709G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63407835 | ||||||
chr1:63408040
|
G | A | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.494+914G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408040 | ||||||
chr1:63408405
|
A | T | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.494+1279A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408405 | ||||||
chr1:63408511
|
A | G | 148 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(145): Show | 152 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.494+1385A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408511 | ||||||
chr1:63408530
|
A | G | 6 | a0001c0001t0002g0331a0001c0001t0010g0333a0001c0001t0010g0334others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.494+1404A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63408530 | ||||||
chr1:63409071
|
T | C | 96 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0331others(93): Show | 96 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(93): Show |
intron_variant | MODIFIER | c.494+1945T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409071 | ||||||
chr1:63409245
|
T | C | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.495-1901T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409245 | ||||||
chr1:63409344
|
C | T | 381 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(378): Show | 387 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(384): Show |
intron_variant | MODIFIER | c.495-1802C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409344 | ||||||
chr1:63409352
|
G | A | 2 | a0002c0002t0001g0357a0002c0002t0001g0361 | 2 | NA18961.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.495-1794G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409352 | ||||||
chr1:63409357
|
A | G | 3 | a0002c0002t0001g0009a0002c0002t0001g0161a0002c0002t0001g0175 | 3 | HG00741.hp1 HG01168.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.495-1789A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409357 | ||||||
chr1:63409403
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.495-1743T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409403 | ||||||
chr1:63409565
|
A | C | 1 | a0002c0002t0001g0359 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.495-1581A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409565 | ||||||
chr1:63409604
|
A | G | 1 | a0001c0004t0004g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.495-1542A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409604 | ||||||
chr1:63409643
|
A | T | 1 | a0001c0001t0002g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.495-1503A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409643 | ||||||
chr1:63409669
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.495-1477C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409669 | ||||||
chr1:63409695
|
T | C | 6 | a0001c0001t0002g0331a0001c0001t0010g0333a0001c0001t0010g0334others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.495-1451T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409695 | ||||||
chr1:63409746
|
A | G | 1 | a0001c0001t0001g0289 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.495-1400A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409746 | ||||||
chr1:63409880
|
C | A | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-1266C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409880 | ||||||
chr1:63409965
|
A | G | 3 | a0002c0002t0001g0341a0002c0002t0001g0342a0002c0002t0001g0344 | 3 | NA18973.hp2 NA19054.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.495-1181A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63409965 | ||||||
chr1:63410031
|
C | T | 4 | a0002c0002t0001g0157a0002c0002t0001g0158a0002c0002t0001g0159others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-1115C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410031 | ||||||
chr1:63410050
|
G | A | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.495-1096G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410050 | ||||||
chr1:63410164
|
T | C | 23 | a0001c0001t0002g0013a0001c0001t0002g0014a0001c0001t0002g0015others(20): Show | 23 | HG00544.hp2 HG00558.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.495-982T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410164 | ||||||
chr1:63410312
|
T | A | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.495-834T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410312 | ||||||
chr1:63410394
|
C | G | 1 | a0001c0001t0002g0292 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.495-752C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410394 | ||||||
chr1:63410444
|
T | C | 87 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(84): Show | 87 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.495-702T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410444 | ||||||
chr1:63410500
|
C | T | 4 | a0001c0001t0002g0246a0001c0001t0002g0250a0001c0001t0002g0257others(1): Show | 4 | HG02071.hp1 NA18948.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-646C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410500 | ||||||
chr1:63410617
|
G | T | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.495-529G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410617 | ||||||
chr1:63410678
|
T | C | 88 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.495-468T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410678 | ||||||
chr1:63410696
|
T | G | 310 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(307): Show | 315 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.495-450T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410696 | ||||||
chr1:63410729
|
A | G | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495-417A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410729 | ||||||
chr1:63410753
|
G | T | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.495-393G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410753 | ||||||
chr1:63410803
|
C | T | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.495-343C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410803 | ||||||
chr1:63410823
|
T | C | 1 | a0001c0001t0001g0373 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.495-323T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410823 | ||||||
chr1:63410913
|
G | A | 1 | a0002c0002t0016g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.495-233G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63410913 | ||||||
chr1:63411008
|
G | A | 7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.495-138G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63411008 | ||||||
chr1:63411015
|
T | C | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.495-131T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 7/14 | chr1 | 63411015 | ||||||
chr1:63411400
|
A | C | 1 | a0001c0001t0002g0002 | 2 | HG01192.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.680+69A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411400 | ||||||
chr1:63411459
|
G | T | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.680+128G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411459 | ||||||
chr1:63411483
|
T | G | 1 | a0001c0001t0001g0364 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.680+152T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411483 | ||||||
chr1:63411716
|
T | A | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.681-210T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411716 | ||||||
chr1:63411718
|
A | G | 1 | a0002c0002t0001g0348 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.681-208A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411718 | ||||||
chr1:63411743
|
C | T | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.681-183C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411743 | ||||||
chr1:63411829
|
A | G | 1 | a0001c0001t0003g0101 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.681-97A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 8/14 | chr1 | 63411829 | ||||||
chr1:63412128
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.816+67G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412128 | ||||||
chr1:63412262
|
C | T | 19 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0204others(16): Show | 19 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.816+201C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412262 | ||||||
chr1:63412360
|
A | C | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.816+299A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412360 | ||||||
chr1:63412380
|
C | T | 1 | a0001c0001t0002g0039 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.816+319C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412380 | ||||||
chr1:63412431
|
G | C | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.816+370G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412431 | ||||||
chr1:63412896
|
A | G | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.816+835A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412896 | ||||||
chr1:63412960
|
C | T | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.816+899C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63412960 | ||||||
chr1:63413056
|
T | A | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.816+995T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413056 | ||||||
chr1:63413096
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.817-965T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413096 | ||||||
chr1:63413106
|
T | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.817-955T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413106 | ||||||
chr1:63413194
|
A | T | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.817-867A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413194 | ||||||
chr1:63413393
|
T | G | 6 | a0001c0001t0002g0331a0001c0001t0010g0333a0001c0001t0010g0334others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.817-668T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413393 | ||||||
chr1:63413435
|
C | T | 88 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(85): Show | 88 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(85): Show |
intron_variant | MODIFIER | c.817-626C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413435 | ||||||
chr1:63413436
|
A | G | 1 | a0001c0004t0006g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.817-625A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413436 | ||||||
chr1:63413451
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.817-610G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413451 | ||||||
chr1:63413562
|
A | G | 1 | a0001c0001t0008g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.817-499A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413562 | ||||||
chr1:63413732
|
A | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.817-329A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413732 | ||||||
chr1:63413769
|
A | G | 148 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(145): Show | 152 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.817-292A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413769 | ||||||
chr1:63413783
|
G | T | 1 | a0001c0001t0003g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.817-278G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413783 | ||||||
chr1:63413788
|
G | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(2): Show | 5 | HG00639.hp2 HG01255.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.817-273G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413788 | ||||||
chr1:63413795
|
G | A | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.817-266G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413795 | ||||||
chr1:63413902
|
G | A | 1 | a0001c0001t0015g0380 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.817-159G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63413902 | ||||||
chr1:63414021
|
C | T | 1 | a0001c0001t0007g0145 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.817-40C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 9/14 | chr1 | 63414021 | ||||||
chr1:63414213
|
T | C | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.902+67T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414213 | ||||||
chr1:63414331
|
A | G | 6 | a0001c0001t0002g0331a0001c0001t0010g0333a0001c0001t0010g0334others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.902+185A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414331 | ||||||
chr1:63414400
|
C | T | 2 | a0001c0001t0002g0279a0001c0001t0002g0294 | 2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.902+254C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414400 | ||||||
chr1:63414485
|
G | A | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.902+339G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414485 | ||||||
chr1:63414739
|
A | G | 1 | a0001c0001t0003g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.902+593A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414739 | ||||||
chr1:63414754
|
A | C | 221 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(218): Show | 225 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(222): Show |
intron_variant | MODIFIER | c.902+608A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414754 | ||||||
chr1:63414851
|
A | G | 5 | a0001c0001t0002g0246a0001c0001t0002g0250a0001c0001t0002g0257others(2): Show | 5 | HG02071.hp1 NA18948.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.902+705A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414851 | ||||||
chr1:63414881
|
G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0050 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.902+735G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414881 | ||||||
chr1:63414932
|
G | A | 2 | a0001c0001t0002g0252a0001c0001t0002g0265 | 2 | NA18983.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.902+786G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414932 | ||||||
chr1:63414977
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.902+831A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63414977 | ||||||
chr1:63415027
|
G | A | 72 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(69): Show | 72 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.903-846G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415027 | ||||||
chr1:63415100
|
A | G | 2 | a0001c0001t0003g0132a0001c0001t0003g0135 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.903-773A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415100 | ||||||
chr1:63415145
|
C | A | 13 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.903-728C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415145 | ||||||
chr1:63415224
|
T | C | 22 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(19): Show | 22 | HG00738.hp1 HG01192.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.903-649T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415224 | ||||||
chr1:63415226
|
G | A | 5 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0031others(2): Show | 5 | HG00639.hp2 HG01255.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.903-647G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415226 | ||||||
chr1:63415662
|
G | A | 1 | a0002c0002t0001g0329 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.903-211G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415662 | ||||||
chr1:63415678
|
G | C | 1 | a0002c0002t0001g0165 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.903-195G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415678 | ||||||
chr1:63415678
|
GTA | G | 121 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(118): Show | 125 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.903-183_903-182del others(2): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 63415678 | |||||
chr1:63415837
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0048 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.903-36A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415837 | ||||||
chr1:63415843
|
A | T | 13 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.903-30A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415843 | ||||||
chr1:63415850
|
T | A | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.903-23T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 10/14 | chr1 | 63415850 | ||||||
chr1:63415993
|
C | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.987+36C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63415993 | ||||||
chr1:63416193
|
A | G | 2 | a0001c0001t0003g0134a0001c0001t0004g0056 | 2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.987+236A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416193 | ||||||
chr1:63416244
|
A | G | 3 | a0001c0001t0002g0019a0001c0001t0002g0021a0001c0001t0002g0302 | 3 | HG02683.hp1 HG04204.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.987+287A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416244 | ||||||
chr1:63416263
|
G | A | 42 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(39): Show | 42 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.987+306G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416263 | ||||||
chr1:63416313
|
T | G | 1 | a0002c0002t0001g0343 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.987+356T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416313 | ||||||
chr1:63416319
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0002g0032 | 2 | HG01884.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.987+362C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416319 | ||||||
chr1:63416332
|
T | C | 5 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108others(2): Show | 6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+375T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416332 | ||||||
chr1:63416559
|
G | A | 1 | a0002c0002t0001g0311 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.987+602G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416559 | ||||||
chr1:63416614
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.987+657G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416614 | ||||||
chr1:63416665
|
G | A | 5 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108others(2): Show | 6 | HG01934.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.987+708G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416665 | ||||||
chr1:63416841
|
TA | T | 120 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0331others(117): Show | 120 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.987+886delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 63416841 | |||||
chr1:63416984
|
A | G | 1 | a0001c0001t0004g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.987+1027A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63416984 | ||||||
chr1:63417007
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.987+1050T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417007 | ||||||
chr1:63417085
|
G | A | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(4): Show | 7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1128G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417085 | ||||||
chr1:63417201
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.987+1244T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417201 | ||||||
chr1:63417402
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.987+1445G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417402 | ||||||
chr1:63417459
|
T | C | 11 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(8): Show | 11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.987+1502T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417459 | ||||||
chr1:63417651
|
A | G | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.987+1694A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417651 | ||||||
chr1:63417744
|
C | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.988-1626C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63417744 | ||||||
chr1:63418048
|
C | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.988-1322C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418048 | ||||||
chr1:63418048
|
C | T | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.988-1322C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418048 | ||||||
chr1:63418091
|
G | A | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.988-1279G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418091 | ||||||
chr1:63418099
|
A | G | 1 | a0001c0001t0002g0274 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.988-1271A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418099 | ||||||
chr1:63418244
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.988-1126G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418244 | ||||||
chr1:63418255
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.988-1115G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418255 | ||||||
chr1:63418267
|
T | C | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.988-1103T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418267 | ||||||
chr1:63418341
|
A | G | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.988-1029A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418341 | ||||||
chr1:63418393
|
A | G | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.988-977A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418393 | ||||||
chr1:63418422
|
T | C | 10 | a0002c0002t0001g0202a0002c0002t0001g0319a0002c0002t0001g0321others(7): Show | 10 | HG02132.hp2 HG02280.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.988-948T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418422 | ||||||
chr1:63418614
|
A | G | 2 | a0002c0002t0001g0232a0002c0002t0001g0233 | 2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.988-756A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418614 | ||||||
chr1:63418616
|
G | T | 1 | a0001c0001t0002g0041 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.988-754G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418616 | ||||||
chr1:63418750
|
G | T | 11 | a0001c0001t0002g0007a0001c0001t0002g0069a0001c0001t0002g0070others(8): Show | 12 | HG01074.hp2 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.988-620G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418750 | ||||||
chr1:63418785
|
T | C | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(4): Show | 7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-585T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418785 | ||||||
chr1:63418914
|
T | A | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-456T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418914 | ||||||
chr1:63418988
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.988-382A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63418988 | ||||||
chr1:63419038
|
G | T | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(4): Show | 7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-332G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419038 | ||||||
chr1:63419097
|
G | A | 1 | a0001c0001t0002g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.988-273G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419097 | ||||||
chr1:63419129
|
G | A | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(4): Show | 7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.988-241G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419129 | ||||||
chr1:63419205
|
T | C | 2 | a0001c0003t0010g0324a0001c0004t0006g0325 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.988-165T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419205 | ||||||
chr1:63419228
|
G | A | 1 | a0002c0002t0001g0330 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.988-142G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 11/14 | chr1 | 63419228 | ||||||
chr1:63419551
|
T | G | 81 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(78): Show | 81 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.1058+111T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419551 | ||||||
chr1:63419594
|
G | T | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+154G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419594 | ||||||
chr1:63419828
|
T | G | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+388T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419828 | ||||||
chr1:63419841
|
C | T | 1 | a0002c0002t0001g0176 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1058+401C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419841 | ||||||
chr1:63419847
|
CT | C | 120 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0331others(117): Show | 120 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(117): Show |
intron_variant | MODIFIER | c.1058+414delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63419847 | |||||
chr1:63419920
|
A | C | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(4): Show | 7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+480A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63419920 | ||||||
chr1:63420132
|
T | A | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(4): Show | 7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+692T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420132 | ||||||
chr1:63420200
|
G | C | 97 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(94): Show | 97 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1058+760G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420200 | ||||||
chr1:63420363
|
G | A | 1 | a0001c0004t0004g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1058+923G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420363 | ||||||
chr1:63420418
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+978G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420418 | ||||||
chr1:63420444
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+1004G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420444 | ||||||
chr1:63420536
|
T | C | 7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+1096T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420536 | ||||||
chr1:63420545
|
A | G | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1058+1105A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420545 | ||||||
chr1:63420625
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1058+1185C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420625 | ||||||
chr1:63420662
|
C | T | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1058+1222C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420662 | ||||||
chr1:63420775
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1058+1335T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420775 | ||||||
chr1:63420778
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1058+1338T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420778 | ||||||
chr1:63420779
|
T | C | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+1339T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420779 | ||||||
chr1:63420786
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1058+1346A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420786 | ||||||
chr1:63420840
|
G | A | 1 | a0002c0002t0001g0346 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1058+1400G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420840 | ||||||
chr1:63420860
|
C | CA | 66 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0064others(63): Show | 67 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1058+1436dupA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63420860 | |||||
chr1:63420860
|
CA | C | 90 | a0001c0001t0002g0179a0001c0001t0002g0331a0001c0001t0003g0005others(87): Show | 90 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(87): Show |
intron_variant | MODIFIER | c.1058+1436delA | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63420860 | |||||
chr1:63420860
|
CAA | C | 29 | a0001c0001t0002g0178a0001c0001t0003g0112a0001c0001t0003g0113others(26): Show | 29 | HG01069.hp2 HG01167.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1058+1435_1058+143 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63420860 | |||||
chr1:63420892
|
T | A | 3 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0001t0001g0375 | 3 | HG00438.hp1 HG02165.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1058+1452T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420892 | ||||||
chr1:63420896
|
G | A | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+1456G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420896 | ||||||
chr1:63420975
|
C | T | 4 | a0001c0001t0002g0241a0001c0001t0002g0283a0001c0001t0002g0293others(1): Show | 4 | NA18942.hp1 NA18990.hp1 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+1535C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63420975 | ||||||
chr1:63421029
|
T | C | 2 | a0002c0002t0001g0157a0002c0002t0001g0159 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1058+1589T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421029 | ||||||
chr1:63421161
|
C | T | 5 | a0001c0001t0001g0055a0001c0001t0001g0320a0001c0001t0005g0010others(2): Show | 5 | HG01433.hp2 HG03491.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+1721C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421161 | ||||||
chr1:63421330
|
T | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1058+1890T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421330 | ||||||
chr1:63421396
|
T | C | 124 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(121): Show | 128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1058+1956T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421396 | ||||||
chr1:63421584
|
T | A | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1058+2144T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421584 | ||||||
chr1:63421728
|
A | G | 1 | a0001c0001t0002g0261 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1058+2288A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421728 | ||||||
chr1:63421843
|
A | G | 353 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(350): Show | 358 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(355): Show |
intron_variant | MODIFIER | c.1058+2403A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421843 | ||||||
chr1:63421911
|
G | A | 1 | a0002c0002t0001g0359 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1058+2471G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63421911 | ||||||
chr1:63422082
|
AATAAATA others(1): Show |
A | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+2660_1058+266 others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422082 | |||||
chr1:63422088
|
TATATAAA others(7): Show |
T | 7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2662_1058+267 others(18): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422088 | |||||
chr1:63422098
|
TATAAATA others(3): Show |
T | 1 | a0001c0001t0001g0080 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1058+2662_1058+267 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422098 | |||||
chr1:63422108
|
AAT | A | 65 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(62): Show | 66 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.1058+2676_1058+267 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422108 | |||||
chr1:63422110
|
T | A | 1 | a0001c0001t0001g0080 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1058+2670T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422110 | ||||||
chr1:63422114
|
TATAAATA others(5): Show |
T | 74 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(71): Show | 74 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1058+2690_1058+270 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422114 | |||||
chr1:63422120
|
T | TATATATA others(55): Show |
1 | a0001c0001t0002g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2685_1058+268 others(66): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422120 | |||||
chr1:63422124
|
T | TATAA | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2685_1058+268 others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422124 | |||||
chr1:63422126
|
A | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2686A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422126 | ||||||
chr1:63422130
|
A | T | 1 | a0001c0001t0002g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2690A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422130 | ||||||
chr1:63422135
|
A | T | 1 | a0001c0001t0002g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2695A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422135 | ||||||
chr1:63422137
|
A | ATAACTAT others(1): Show |
6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2697_1058+269 others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422137 | ||||||
chr1:63422138
|
A | T | 1 | a0001c0001t0002g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2698A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422138 | ||||||
chr1:63422141
|
A | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2701A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422141 | ||||||
chr1:63422142
|
T | G | 1 | a0001c0001t0002g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2702T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422142 | ||||||
chr1:63422147
|
A | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2707A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422147 | ||||||
chr1:63422148
|
A | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2708A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422148 | ||||||
chr1:63422154
|
A | T | 1 | a0001c0001t0002g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2714A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422154 | ||||||
chr1:63422154
|
AAT | A | 280 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(277): Show | 285 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1058+2724_1058+272 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422154 | |||||
chr1:63422154
|
AATATAT | A | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+2720_1058+272 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422154 | |||||
chr1:63422157
|
A | C | 1 | a0001c0001t0002g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1058+2717A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422157 | ||||||
chr1:63422160
|
T | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1058+2720T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422160 | ||||||
chr1:63422160
|
T | TATCTATA others(3): Show |
6 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(3): Show | 6 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2722_1058+272 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422160 | |||||
chr1:63422167
|
C | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2727C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422167 | ||||||
chr1:63422167
|
CTA | C | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+2729_1058+273 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422167 | |||||
chr1:63422168
|
T | G | 1 | a0001c0001t0002g0032 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1058+2728T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422168 | ||||||
chr1:63422171
|
G | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2731G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422171 | ||||||
chr1:63422172
|
A | T | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2732A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422172 | ||||||
chr1:63422181
|
T | A | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2741T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422181 | ||||||
chr1:63422182
|
T | G | 7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2742T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422182 | ||||||
chr1:63422197
|
CTA | C | 3 | a0001c0001t0001g0338a0001c0001t0001g0369a0001c0001t0001g0374 | 3 | HG03490.hp2 HG03688.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1058+2761_1058+276 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422197 | |||||
chr1:63422202
|
T | G | 2 | a0001c0001t0004g0326a0001c0001t0004g0327 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1058+2762T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422202 | ||||||
chr1:63422204
|
AATATAAA others(103): Show |
A | 2 | a0001c0001t0004g0326a0001c0001t0004g0327 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1058+2770_1058+287 others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422204 | |||||
chr1:63422210
|
A | AATATATA others(61): Show |
1 | a0005c0006t0002g0284 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1058+2785_1058+278 others(72): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422210 | |||||
chr1:63422210
|
A | G | 1 | a0001c0001t0004g0184 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1058+2770A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422210 | ||||||
chr1:63422210
|
AATATATA others(39): Show |
A | 1 | a0002c0002t0005g0100 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1058+2776_1058+282 others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422210 | |||||
chr1:63422219
|
T | C | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2779T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422219 | ||||||
chr1:63422220
|
TATATAAA others(5): Show |
T | 95 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(92): Show | 95 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1058+2786_1058+279 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422220 | |||||
chr1:63422226
|
A | AATATAAA others(29): Show |
1 | a0002c0002t0001g0171 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1058+2837_1058+287 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422226 | |||||
chr1:63422226
|
A | G | 124 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(121): Show | 128 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.1058+2786A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422226 | ||||||
chr1:63422232
|
A | AATATATA others(57): Show |
1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2800_1058+280 others(68): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422232 | |||||
chr1:63422237
|
A | C | 95 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(92): Show | 95 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1058+2797A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422237 | ||||||
chr1:63422238
|
T | G | 79 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(76): Show | 79 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.1058+2798T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422238 | ||||||
chr1:63422238
|
T | TATATTTA others(5): Show |
7 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(4): Show | 7 | HG01106.hp2 HG01358.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+2802_1058+280 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | |||||
chr1:63422238
|
T | TATCTATA others(3): Show |
14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | |||||
chr1:63422238
|
T | TATCTATA others(49): Show |
1 | a0001c0001t0002g0160 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1058+2800_1058+280 others(60): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | |||||
chr1:63422238
|
T | TATCTATA others(49): Show |
104 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(101): Show | 108 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(60): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | |||||
chr1:63422238
|
T | TATCTATA others(73): Show |
3 | a0001c0001t0002g0021a0001c0001t0002g0268a0001c0001t0002g0304 | 3 | HG03704.hp1 NA18964.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(84): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | |||||
chr1:63422238
|
T | TATCTATA others(93): Show |
2 | a0001c0001t0002g0020a0001c0001t0002g0067 | 2 | HG02109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(104): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | |||||
chr1:63422238
|
T | TATCTATA others(71): Show |
1 | a0001c0001t0002g0248 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1058+2800_1058+280 others(82): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422238 | |||||
chr1:63422240
|
T | TCTATATG others(1): Show |
5 | a0001c0001t0002g0036a0001c0001t0002g0042a0001c0001t0002g0282others(2): Show | 5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2800_1058+280 others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422240 | ||||||
chr1:63422244
|
A | T | 5 | a0001c0001t0002g0036a0001c0001t0002g0042a0001c0001t0002g0282others(2): Show | 5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2804A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422244 | ||||||
chr1:63422246
|
T | A | 5 | a0001c0001t0002g0036a0001c0001t0002g0042a0001c0001t0002g0282others(2): Show | 5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2806T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422246 | ||||||
chr1:63422261
|
A | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0096 | 2 | NA18962.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1058+2821A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422261 | ||||||
chr1:63422262
|
G | A | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2822G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422262 | ||||||
chr1:63422262
|
G | T | 1 | a0001c0001t0001g0367 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1058+2822G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422262 | ||||||
chr1:63422270
|
T | C | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058+2830T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422270 | ||||||
chr1:63422273
|
A | C | 1 | a0001c0001t0002g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1058+2833A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422273 | ||||||
chr1:63422274
|
T | G | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2834T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422274 | ||||||
chr1:63422274
|
T | TATATAAA others(17): Show |
1 | a0001c0001t0001g0287 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1058+2849_1058+287 others(28): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422274 | |||||
chr1:63422274
|
T | TATATTTA others(5): Show |
1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2838_1058+283 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422274 | |||||
chr1:63422274
|
T | TATATTTA others(65): Show |
5 | a0001c0001t0002g0036a0001c0001t0002g0042a0001c0001t0002g0282others(2): Show | 5 | HG02165.hp2 HG02257.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+2838_1058+283 others(76): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422274 | |||||
chr1:63422277
|
A | C | 101 | a0001c0001t0002g0331a0001c0001t0003g0005a0001c0001t0003g0012others(98): Show | 101 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.1058+2837A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422277 | ||||||
chr1:63422283
|
ATATATAT others(23): Show |
A | 101 | a0001c0001t0002g0331a0001c0001t0003g0005a0001c0001t0003g0012others(98): Show | 101 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(98): Show |
intron_variant | MODIFIER | c.1058+2851_1058+288 others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422283 | |||||
chr1:63422297
|
A | C | 1 | a0001c0001t0002g0293 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1058+2857A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422297 | ||||||
chr1:63422313
|
C | A | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2873C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422313 | ||||||
chr1:63422315
|
A | T | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2875A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422315 | ||||||
chr1:63422320
|
T | TA | 11 | a0001c0003t0010g0324a0001c0003t0012g0238a0001c0003t0012g0239others(8): Show | 11 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1058+2880_1058+288 others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422320 | ||||||
chr1:63422320
|
T | TC | 4 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+2880_1058+288 others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422320 | ||||||
chr1:63422322
|
A | ATATAAAT | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2882_1058+288 others(11): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422322 | ||||||
chr1:63422331
|
C | T | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2891C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422331 | ||||||
chr1:63422336
|
G | T | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2896G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422336 | ||||||
chr1:63422337
|
G | A | 14 | a0001c0003t0009g0192a0001c0003t0009g0194a0001c0003t0009g0195others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2897G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422337 | ||||||
chr1:63422337
|
G | C | 1 | a0001c0003t0009g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1058+2897G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422337 | ||||||
chr1:63422338
|
A | G | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1058+2898A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422338 | ||||||
chr1:63422344
|
A | AAT | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2911_1058+291 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422344 | |||||
chr1:63422353
|
C | T | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2913C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422353 | ||||||
chr1:63422354
|
TATATAA | T | 95 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(92): Show | 95 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.1058+2926_1058+293 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422354 | |||||
chr1:63422360
|
A | G | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2920A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422360 | ||||||
chr1:63422360
|
A | T | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2920A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422360 | ||||||
chr1:63422364
|
TAAATATA others(37): Show |
T | 2 | a0001c0001t0003g0216a0001c0001t0003g0217 | 2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2926_1058+296 others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422364 | |||||
chr1:63422365
|
A | G | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2925A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422365 | ||||||
chr1:63422375
|
A | ATTTATAT others(12): Show |
4 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+2935_1058+293 others(23): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422375 | ||||||
chr1:63422375
|
A | G | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2935A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422375 | ||||||
chr1:63422376
|
A | T | 10 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240others(7): Show | 10 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058+2936A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422376 | ||||||
chr1:63422377
|
G | A | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2937G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422377 | ||||||
chr1:63422377
|
G | GA | 4 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(1): Show | 4 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+2937_1058+293 others(5): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422377 | ||||||
chr1:63422377
|
G | T | 10 | a0001c0003t0012g0238a0001c0003t0012g0239a0001c0003t0014g0240others(7): Show | 10 | HG01891.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1058+2937G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422377 | ||||||
chr1:63422379
|
A | ATATAGAT others(61): Show |
2 | a0001c0003t0012g0238a0001c0004t0006g0231 | 2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1058+2941_1058+294 others(72): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422379 | |||||
chr1:63422379
|
A | ATATAGAT others(37): Show |
6 | a0001c0003t0012g0239a0001c0004t0004g0200a0001c0004t0006g0156others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+2941_1058+294 others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422379 | |||||
chr1:63422379
|
A | ATATAGAT others(13): Show |
2 | a0001c0003t0014g0240a0001c0004t0006g0325 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1058+2941_1058+294 others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422379 | |||||
chr1:63422388
|
TATAAATA others(37): Show |
T | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+2952_1058+299 others(48): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422388 | |||||
chr1:63422391
|
A | ATG | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2951_1058+295 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422391 | ||||||
chr1:63422396
|
TATATCTA others(29): Show |
T | 11 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(8): Show | 11 | HG01167.hp2 HG02145.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1058+2961_1058+299 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422396 | |||||
chr1:63422397
|
A | C | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1058+2957A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422397 | ||||||
chr1:63422398
|
T | A | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2958T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422398 | ||||||
chr1:63422398
|
TATCTATA others(27): Show |
T | 80 | a0001c0001t0002g0331a0001c0001t0003g0005a0001c0001t0003g0012others(77): Show | 80 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.1058+2961_1058+299 others(38): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422398 | |||||
chr1:63422398
|
TATCTATA others(39): Show |
T | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058+2961_1058+300 others(50): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422398 | |||||
chr1:63422401
|
C | A | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2961C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422401 | ||||||
chr1:63422402
|
TATATAA | T | 64 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(61): Show | 65 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1058+2974_1058+297 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422402 | |||||
chr1:63422406
|
T | G | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2966T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422406 | ||||||
chr1:63422407
|
A | G | 14 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(11): Show | 14 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1058+2967A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422407 | ||||||
chr1:63422408
|
A | AATATATA others(13): Show |
1 | a0001c0001t0001g0320 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1058+2973_1058+297 others(24): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422408 | |||||
chr1:63422408
|
AATATAAA others(23): Show |
A | 129 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(126): Show | 133 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1058+3016_1058+304 others(34): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422408 | |||||
chr1:63422408
|
AATATAAA others(35): Show |
A | 1 | a0001c0001t0010g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1058+2980_1058+302 others(46): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422408 | |||||
chr1:63422409
|
A | G | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2969A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422409 | ||||||
chr1:63422414
|
AATATATA others(29): Show |
A | 1 | a0001c0001t0010g0334 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1058+2980_1058+301 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422414 | |||||
chr1:63422415
|
A | G | 2 | a0001c0001t0003g0216a0001c0001t0003g0217 | 2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2975A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422415 | ||||||
chr1:63422420
|
T | A | 2 | a0001c0001t0003g0216a0001c0001t0003g0217 | 2 | NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2980T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422420 | ||||||
chr1:63422426
|
A | T | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2986A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422426 | ||||||
chr1:63422426
|
AATATAAA others(5): Show |
A | 2 | a0002c0002t0001g0172a0002c0002t0001g0177 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1058+3010_1058+302 others(16): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422426 | |||||
chr1:63422431
|
A | C | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1058+2991A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422431 | ||||||
chr1:63422432
|
A | T | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0003t0010g0324 | 3 | HG06807.hp1 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1058+2992A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422432 | ||||||
chr1:63422434
|
T | TATATATA others(7): Show |
1 | a0001c0004t0006g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1058+3001_1058+300 others(18): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422434 | |||||
chr1:63422438
|
T | A | 98 | a0001c0001t0002g0331a0001c0001t0003g0005a0001c0001t0003g0012others(95): Show | 98 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.1058+2998T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422438 | ||||||
chr1:63422438
|
T | TATAAGTA others(29): Show |
6 | a0001c0004t0004g0200a0001c0004t0006g0156a0001c0004t0006g0198others(3): Show | 6 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+3001_1058+300 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422438 | |||||
chr1:63422438
|
T | TATAAGTA others(29): Show |
7 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(4): Show | 7 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+3001_1058+300 others(40): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422438 | |||||
chr1:63422450
|
T | A | 4 | a0001c0001t0003g0197a0001c0001t0011g0189a0001c0001t0011g0190others(1): Show | 4 | HG02622.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+3010T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422450 | ||||||
chr1:63422450
|
T | TATCTATA others(3): Show |
1 | a0001c0004t0006g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1058+3012_1058+301 others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63422450 | |||||
chr1:63422462
|
A | T | 1 | a0001c0004t0006g0325 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1058+3022A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422462 | ||||||
chr1:63422493
|
A | G | 1 | a0004c0008t0003g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1058+3053A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422493 | ||||||
chr1:63422638
|
C | T | 1 | a0001c0003t0009g0194 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1058+3198C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422638 | ||||||
chr1:63422895
|
C | T | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1058+3455C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422895 | ||||||
chr1:63422936
|
C | T | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+3496C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422936 | ||||||
chr1:63422937
|
G | A | 1 | a0001c0001t0003g0197 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1058+3497G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63422937 | ||||||
chr1:63423020
|
T | C | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+3580T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423020 | ||||||
chr1:63423024
|
A | AT | 180 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(177): Show | 181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1058+3601dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63423024 | |||||
chr1:63423024
|
A | ATT | 9 | a0001c0001t0001g0064a0001c0001t0001g0297a0001c0001t0002g0178others(6): Show | 9 | HG00738.hp1 HG01243.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1058+3600_1058+360 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63423024 | |||||
chr1:63423024
|
AT | A | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1058+3601delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63423024 | |||||
chr1:63423169
|
G | A | 3 | a0001c0001t0002g0017a0001c0001t0002g0028a0001c0001t0002g0032 | 3 | HG01070.hp1 HG01884.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1058+3729G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423169 | ||||||
chr1:63423181
|
G | A | 1 | a0001c0001t0002g0007 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1058+3741G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423181 | ||||||
chr1:63423346
|
A | G | 24 | a0001c0001t0001g0004a0001c0001t0001g0064a0001c0001t0001g0078others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.1058+3906A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423346 | ||||||
chr1:63423473
|
G | A | 123 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(120): Show | 127 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.1058+4033G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423473 | ||||||
chr1:63423808
|
C | T | 1 | a0002c0002t0001g0074 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1058+4368C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423808 | ||||||
chr1:63423963
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1058+4523C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423963 | ||||||
chr1:63423989
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1058+4549C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63423989 | ||||||
chr1:63424265
|
C | T | 1 | a0001c0001t0002g0269 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1059-4468C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424265 | ||||||
chr1:63424274
|
G | A | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-4459G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424274 | ||||||
chr1:63424286
|
G | A | 15 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(12): Show | 15 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059-4447G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424286 | ||||||
chr1:63424375
|
G | A | 72 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(69): Show | 72 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.1059-4358G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424375 | ||||||
chr1:63424419
|
G | A | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-4314G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424419 | ||||||
chr1:63424439
|
G | A | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1059-4294G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424439 | ||||||
chr1:63424496
|
A | C | 1 | a0001c0003t0014g0240 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1059-4237A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424496 | ||||||
chr1:63424704
|
C | T | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1059-4029C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424704 | ||||||
chr1:63424774
|
A | AT | 28 | a0001c0001t0002g0179a0001c0001t0002g0331a0001c0001t0003g0102others(25): Show | 28 | HG00738.hp1 HG01192.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1059-3937dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | |||||
chr1:63424774
|
A | ATT | 7 | a0001c0001t0003g0115a0001c0001t0008g0234a0001c0001t0008g0235others(4): Show | 7 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-3938_1059-393 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | |||||
chr1:63424774
|
A | ATTT | 7 | a0001c0003t0010g0324a0001c0004t0004g0200a0001c0004t0006g0156others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-3939_1059-393 others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | |||||
chr1:63424774
|
AT | A | 16 | a0001c0001t0001g0360a0001c0001t0002g0052a0001c0001t0002g0310others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.1059-3937delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | |||||
chr1:63424774
|
ATT | A | 129 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(126): Show | 133 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1059-3938_1059-393 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | |||||
chr1:63424774
|
ATTT | A | 9 | a0001c0001t0002g0041a0001c0001t0002g0047a0001c0001t0002g0076others(6): Show | 9 | HG01167.hp2 HG01516.hp1 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059-3939_1059-393 others(7): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63424774 | |||||
chr1:63424820
|
C | T | 1 | a0005c0006t0002g0284 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1059-3913C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424820 | ||||||
chr1:63424821
|
G | A | 97 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(94): Show | 97 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1059-3912G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63424821 | ||||||
chr1:63425092
|
A | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059-3641A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425092 | ||||||
chr1:63425164
|
C | T | 22 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(19): Show | 22 | HG00738.hp1 HG01192.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059-3569C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425164 | ||||||
chr1:63425409
|
A | G | 97 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(94): Show | 97 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(94): Show |
intron_variant | MODIFIER | c.1059-3324A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425409 | ||||||
chr1:63425491
|
G | A | 2 | a0001c0001t0004g0098a0004c0008t0003g0203 | 2 | HG02559.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1059-3242G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425491 | ||||||
chr1:63425524
|
G | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-3209G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425524 | ||||||
chr1:63425706
|
A | G | 243 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(240): Show | 247 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(244): Show |
intron_variant | MODIFIER | c.1059-3027A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425706 | ||||||
chr1:63425721
|
A | G | 116 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0331others(113): Show | 116 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(113): Show |
intron_variant | MODIFIER | c.1059-3012A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425721 | ||||||
chr1:63425813
|
C | A | 71 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(68): Show | 71 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.1059-2920C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425813 | ||||||
chr1:63425827
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1059-2906G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425827 | ||||||
chr1:63425838
|
G | C | 1 | a0001c0001t0001g0290 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1059-2895G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425838 | ||||||
chr1:63425876
|
G | A | 19 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0204others(16): Show | 19 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1059-2857G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425876 | ||||||
chr1:63425903
|
C | T | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059-2830C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425903 | ||||||
chr1:63425923
|
C | T | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059-2810C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425923 | ||||||
chr1:63425963
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1059-2770G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63425963 | ||||||
chr1:63426129
|
A | G | 1 | a0001c0001t0003g0149 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1059-2604A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426129 | ||||||
chr1:63426151
|
G | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-2582G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426151 | ||||||
chr1:63426184
|
G | T | 74 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(71): Show | 74 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.1059-2549G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426184 | ||||||
chr1:63426301
|
T | C | 243 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(240): Show | 247 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(244): Show |
intron_variant | MODIFIER | c.1059-2432T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426301 | ||||||
chr1:63426498
|
G | A | 4 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0116others(1): Show | 4 | HG02698.hp1 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-2235G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426498 | ||||||
chr1:63426569
|
G | A | 3 | a0001c0001t0001g0366a0001c0001t0001g0367a0001c0001t0001g0375 | 3 | HG00438.hp1 HG02165.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1059-2164G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426569 | ||||||
chr1:63426643
|
A | C | 1 | a0001c0003t0010g0324 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1059-2090A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426643 | ||||||
chr1:63426681
|
C | A | 66 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1059-2052C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63426681 | ||||||
chr1:63427040
|
C | T | 18 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0204others(15): Show | 18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1059-1693C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427040 | ||||||
chr1:63427069
|
C | T | 1 | a0001c0007t0001g0094 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1059-1664C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427069 | ||||||
chr1:63427086
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1059-1647C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427086 | ||||||
chr1:63427167
|
A | AT | 38 | a0001c0001t0001g0064a0001c0001t0001g0081a0001c0001t0001g0084others(35): Show | 39 | HG00438.hp1 HG00738.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059-1547dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427167 | |||||
chr1:63427167
|
AT | A | 22 | a0001c0001t0001g0247a0001c0001t0003g0123a0001c0001t0003g0128others(19): Show | 22 | HG01069.hp1 HG01192.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1059-1547delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427167 | |||||
chr1:63427167
|
ATT | A | 73 | a0001c0001t0002g0331a0001c0001t0003g0005a0001c0001t0003g0012others(70): Show | 73 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.1059-1548_1059-154 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427167 | |||||
chr1:63427204
|
G | A | 7 | a0001c0001t0002g0331a0001c0004t0004g0200a0001c0004t0006g0156others(4): Show | 7 | HG01891.hp2 HG02615.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-1529G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427204 | ||||||
chr1:63427282
|
C | A | 1 | a0002c0002t0001g0379 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1059-1451C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427282 | ||||||
chr1:63427329
|
T | C | 117 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(114): Show | 120 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1059-1404T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427329 | ||||||
chr1:63427537
|
C | A | 1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1059-1196C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427537 | ||||||
chr1:63427647
|
G | A | 1 | a0001c0001t0007g0103 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1059-1086G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427647 | ||||||
chr1:63427649
|
C | A | 4 | a0001c0001t0008g0234a0001c0001t0008g0235a0001c0001t0008g0236others(1): Show | 4 | HG02572.hp2 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-1084C>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427649 | ||||||
chr1:63427723
|
A | G | 304 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(301): Show | 309 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.1059-1010A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427723 | ||||||
chr1:63427757
|
T | C | 248 | a0001c0001t0001g0080a0001c0001t0002g0002a0001c0001t0002g0003others(245): Show | 253 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(250): Show |
intron_variant | MODIFIER | c.1059-976T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427757 | ||||||
chr1:63427787
|
C | CT | 39 | a0001c0001t0001g0064a0001c0001t0001g0092a0001c0001t0001g0297others(36): Show | 39 | HG00741.hp1 HG01175.hp1 HG01175.hp2 others(36): Show |
intron_variant | MODIFIER | c.1059-923dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427787 | |||||
chr1:63427787
|
C | CTT | 7 | a0001c0001t0002g0241a0001c0004t0004g0200a0001c0004t0006g0156others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-924_1059-923d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427787 | |||||
chr1:63427787
|
CT | C | 30 | a0001c0001t0002g0014a0001c0001t0002g0029a0001c0001t0002g0178others(27): Show | 31 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059-923delT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr1 | 63427787 | |||||
chr1:63427944
|
T | G | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059-789T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63427944 | ||||||
chr1:63428016
|
G | A | 1 | a0002c0002t0001g0317 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1059-717G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428016 | ||||||
chr1:63428253
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059-480T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428253 | ||||||
chr1:63428488
|
T | G | 117 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(114): Show | 120 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1059-245T>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428488 | ||||||
chr1:63428502
|
G | T | 1 | a0001c0001t0002g0291 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1059-231G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 12/14 | chr1 | 63428502 | ||||||
chr1:63428822
|
T | A | 1 | a0001c0001t0002g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1127+21T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 13/14 | chr1 | 63428822 | ||||||
chr1:63428887
|
T | C | 13 | a0001c0001t0002g0331a0001c0003t0009g0192a0001c0003t0009g0193others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1128-41T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 13/14 | chr1 | 63428887 | ||||||
chr1:63429334
|
A | G | 1 | a0001c0001t0007g0103 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1326+208A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429334 | ||||||
chr1:63429534
|
C | G | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326+408C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429534 | ||||||
chr1:63429550
|
G | T | 1 | a0001c0001t0002g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1326+424G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429550 | ||||||
chr1:63429800
|
A | G | 110 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(107): Show | 112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.1326+674A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429800 | ||||||
chr1:63429850
|
A | AGT | 83 | a0001c0001t0001g0004a0001c0001t0001g0050a0001c0001t0001g0055others(80): Show | 84 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1326+757_1326+758d others(4): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
A | AGTGT | 130 | a0001c0001t0001g0018a0001c0001t0001g0083a0001c0001t0001g0335others(127): Show | 133 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.1326+755_1326+758d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
A | AGTGTGT | 21 | a0001c0001t0002g0020a0001c0001t0002g0033a0001c0001t0002g0040others(18): Show | 21 | HG00558.hp2 HG00738.hp1 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.1326+753_1326+758d others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
A | AGTGTGTG others(1): Show |
40 | a0001c0001t0001g0364a0001c0001t0002g0019a0001c0001t0002g0022others(37): Show | 40 | HG00140.hp2 HG00544.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.1326+751_1326+758d others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
A | AGTGTGTG others(3): Show |
5 | a0001c0001t0002g0063a0001c0001t0002g0178a0001c0001t0003g0127others(2): Show | 5 | HG00544.hp2 HG00558.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326+749_1326+758d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
A | AGTGTGTG others(5): Show |
1 | a0001c0001t0004g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1326+747_1326+758d others(14): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
AGTGT | A | 7 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108others(4): Show | 8 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326+755_1326+758d others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
AGTGTGTG others(3): Show |
A | 1 | a0001c0001t0001g0079 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1326+749_1326+758d others(12): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429850
|
AGTGTGTG others(11): Show |
A | 1 | a0001c0001t0002g0298 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1326+741_1326+758d others(20): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63429850 | |||||
chr1:63429975
|
T | C | 2 | a0001c0001t0003g0132a0001c0001t0003g0135 | 2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1326+849T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63429975 | ||||||
chr1:63430031
|
C | T | 2 | a0001c0001t0003g0196a0001c0001t0004g0057 | 2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1326+905C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430031 | ||||||
chr1:63430037
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1326+911C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430037 | ||||||
chr1:63430171
|
G | A | 75 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(72): Show | 75 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1326+1045G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430171 | ||||||
chr1:63430179
|
T | C | 246 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(243): Show | 251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
intron_variant | MODIFIER | c.1326+1053T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430179 | ||||||
chr1:63430235
|
T | C | 13 | a0001c0001t0002g0331a0001c0003t0009g0192a0001c0003t0009g0193others(10): Show | 13 | HG01192.hp1 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1326+1109T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430235 | ||||||
chr1:63430258
|
A | G | 1 | a0001c0001t0002g0302 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1326+1132A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430258 | ||||||
chr1:63430530
|
G | T | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1326+1404G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430530 | ||||||
chr1:63430735
|
T | C | 1 | a0006c0009t0020g0322 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326+1609T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430735 | ||||||
chr1:63430772
|
T | C | 1 | a0001c0001t0002g0263 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1326+1646T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430772 | ||||||
chr1:63430830
|
CTG | C | 5 | a0001c0004t0006g0156a0001c0004t0006g0198a0001c0004t0006g0199others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326+1710_1326+171 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63430830 | |||||
chr1:63430903
|
A | G | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1326+1777A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63430903 | ||||||
chr1:63431452
|
T | C | 6 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108others(3): Show | 7 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326+2326T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431452 | ||||||
chr1:63431458
|
C | T | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326+2332C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431458 | ||||||
chr1:63431620
|
G | A | 1 | a0002c0002t0001g0359 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1326+2494G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431620 | ||||||
chr1:63431654
|
G | T | 1 | a0001c0001t0001g0368 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1326+2528G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431654 | ||||||
chr1:63431655
|
G | A | 1 | a0001c0001t0001g0368 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1326+2529G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431655 | ||||||
chr1:63431656
|
A | G | 1 | a0001c0001t0001g0368 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1326+2530A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431656 | ||||||
chr1:63431761
|
G | A | 110 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(107): Show | 112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.1326+2635G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431761 | ||||||
chr1:63431848
|
A | T | 1 | a0002c0002t0001g0354 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1326+2722A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431848 | ||||||
chr1:63431885
|
C | T | 7 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0010g0333others(4): Show | 7 | HG00738.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1326+2759C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431885 | ||||||
chr1:63431938
|
A | T | 18 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0204others(15): Show | 18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1326+2812A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63431938 | ||||||
chr1:63432245
|
T | A | 2 | a0001c0003t0010g0324a0001c0004t0006g0325 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1326+3119T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432245 | ||||||
chr1:63432258
|
G | GT | 219 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(216): Show | 223 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.1326+3133dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63432258 | |||||
chr1:63432258
|
G | GTT | 6 | a0001c0001t0002g0246a0001c0001t0003g0122a0001c0001t0003g0133others(3): Show | 6 | HG01884.hp1 HG02015.hp2 NA19043.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326+3133_1326+313 others(6): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63432258 | |||||
chr1:63432258
|
G | GTTTTTT | 6 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0034others(3): Show | 7 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1326+3133_1326+313 others(10): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63432258 | |||||
chr1:63432260
|
G | T | 351 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(348): Show | 356 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(353): Show |
intron_variant | MODIFIER | c.1326+3134G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432260 | ||||||
chr1:63432283
|
T | C | 1 | a0001c0001t0003g0140 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1326+3157T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432283 | ||||||
chr1:63432739
|
C | T | 130 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0331others(127): Show | 132 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1326+3613C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432739 | ||||||
chr1:63432920
|
T | C | 1 | a0002c0002t0001g0073 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1326+3794T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63432920 | ||||||
chr1:63433053
|
C | G | 2 | a0002c0002t0001g0172a0002c0002t0001g0177 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1327-3770C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433053 | ||||||
chr1:63433158
|
G | A | 2 | a0001c0001t0010g0333a0001c0001t0010g0334 | 2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1327-3665G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433158 | ||||||
chr1:63433221
|
G | A | 130 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0331others(127): Show | 132 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1327-3602G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433221 | ||||||
chr1:63433230
|
C | T | 1 | a0002c0002t0001g0165 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1327-3593C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433230 | ||||||
chr1:63433238
|
G | T | 110 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(107): Show | 112 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(109): Show |
intron_variant | MODIFIER | c.1327-3585G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433238 | ||||||
chr1:63433260
|
A | G | 18 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0204others(15): Show | 18 | HG01167.hp2 HG02145.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1327-3563A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433260 | ||||||
chr1:63433270
|
G | A | 6 | a0001c0001t0007g0006a0001c0001t0007g0103a0001c0001t0007g0108others(3): Show | 7 | HG01934.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-3553G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433270 | ||||||
chr1:63433475
|
G | T | 1 | a0001c0001t0002g0241 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1327-3348G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433475 | ||||||
chr1:63433663
|
C | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0179 | 2 | HG00738.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1327-3160C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433663 | ||||||
chr1:63433714
|
T | C | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1327-3109T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433714 | ||||||
chr1:63433752
|
G | A | 6 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0034others(3): Show | 7 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-3071G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433752 | ||||||
chr1:63433973
|
T | C | 10 | a0001c0001t0002g0015a0001c0001t0002g0245a0001c0001t0002g0252others(7): Show | 10 | HG00423.hp2 NA18963.hp1 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1327-2850T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433973 | ||||||
chr1:63433981
|
G | C | 1 | a0002c0002t0001g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1327-2842G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63433981 | ||||||
chr1:63434111
|
T | A | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-2712T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434111 | ||||||
chr1:63434149
|
A | G | 2 | a0001c0003t0010g0324a0001c0004t0006g0325 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1327-2674A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434149 | ||||||
chr1:63434337
|
A | G | 2 | a0001c0001t0003g0113a0001c0001t0003g0121 | 2 | HG01256.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1327-2486A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434337 | ||||||
chr1:63434399
|
G | A | 92 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(89): Show | 94 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1327-2424G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434399 | ||||||
chr1:63434462
|
A | G | 246 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(243): Show | 251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
intron_variant | MODIFIER | c.1327-2361A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434462 | ||||||
chr1:63434479
|
G | A | 1 | a0001c0001t0002g0041 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1327-2344G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434479 | ||||||
chr1:63434588
|
T | C | 5 | a0001c0001t0010g0333a0001c0001t0010g0334a0001c0001t0011g0189others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-2235T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434588 | ||||||
chr1:63434603
|
G | GT | 116 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(113): Show | 119 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1327-2213dupT | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63434603 | |||||
chr1:63434639
|
C | T | 3 | a0001c0001t0011g0189a0001c0001t0011g0190a0001c0001t0011g0191 | 3 | HG02622.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1327-2184C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434639 | ||||||
chr1:63434640
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1327-2183G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434640 | ||||||
chr1:63434666
|
G | A | 1 | a0002c0002t0001g0319 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1327-2157G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434666 | ||||||
chr1:63434727
|
G | A | 1 | a0001c0001t0002g0331 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1327-2096G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434727 | ||||||
chr1:63434823
|
G | T | 30 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0204others(27): Show | 30 | HG01167.hp2 HG01192.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1327-2000G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434823 | ||||||
chr1:63434824
|
T | C | 30 | a0001c0001t0002g0331a0001c0001t0003g0196a0001c0001t0003g0204others(27): Show | 30 | HG01167.hp2 HG01192.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1327-1999T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434824 | ||||||
chr1:63434850
|
G | A | 5 | a0001c0001t0001g0363a0001c0001t0001g0368a0001c0001t0001g0370others(2): Show | 5 | NA18940.hp2 NA18944.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-1973G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434850 | ||||||
chr1:63434875
|
G | T | 1 | a0001c0001t0003g0210 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1327-1948G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434875 | ||||||
chr1:63434963
|
G | T | 1 | a0001c0001t0010g0334 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1327-1860G>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434963 | ||||||
chr1:63434973
|
A | C | 1 | a0001c0001t0001g0092 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1327-1850A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63434973 | ||||||
chr1:63435060
|
T | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(60): Show | 63 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1327-1763T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435060 | ||||||
chr1:63435068
|
G | A | 246 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(243): Show | 251 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(248): Show |
intron_variant | MODIFIER | c.1327-1755G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435068 | ||||||
chr1:63435087
|
A | T | 1 | a0002c0002t0001g0164 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1327-1736A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435087 | ||||||
chr1:63435111
|
T | C | 1 | a0001c0001t0002g0362 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1327-1712T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435111 | ||||||
chr1:63435116
|
A | T | 92 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(89): Show | 94 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1327-1707A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435116 | ||||||
chr1:63435164
|
G | A | 86 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(83): Show | 87 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1327-1659G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435164 | ||||||
chr1:63435230
|
G | A | 92 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(89): Show | 94 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1327-1593G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435230 | ||||||
chr1:63435680
|
A | G | 1 | a0001c0001t0004g0098 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1327-1143A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435680 | ||||||
chr1:63435723
|
T | A | 116 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(113): Show | 119 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.1327-1100T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435723 | ||||||
chr1:63435757
|
T | A | 309 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(306): Show | 314 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.1327-1066T>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435757 | ||||||
chr1:63435762
|
C | CTCAG | 5 | a0001c0003t0009g0192a0001c0003t0009g0193a0001c0003t0009g0194others(2): Show | 5 | HG01192.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1327-1057_1327-105 others(8): Show |
ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 63435762 | |||||
chr1:63435820
|
A | C | 1 | a0001c0001t0002g0037 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1327-1003A>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435820 | ||||||
chr1:63435951
|
G | C | 130 | a0001c0001t0002g0178a0001c0001t0002g0179a0001c0001t0002g0331others(127): Show | 132 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(129): Show |
intron_variant | MODIFIER | c.1327-872G>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63435951 | ||||||
chr1:63436085
|
C | T | 2 | a0001c0003t0012g0238a0001c0003t0012g0239 | 2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1327-738C>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436085 | ||||||
chr1:63436086
|
G | A | 2 | a0001c0001t0002g0251a0001c0001t0002g0260 | 2 | NA18945.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1327-737G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436086 | ||||||
chr1:63436250
|
A | T | 6 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0034others(3): Show | 7 | HG01081.hp1 HG02055.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1327-573A>T | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436250 | ||||||
chr1:63436274
|
T | C | 3 | a0001c0001t0005g0105a0001c0001t0005g0106a0001c0001t0005g0107 | 3 | HG00438.hp2 NA18747.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1327-549T>C | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436274 | ||||||
chr1:63436382
|
C | G | 1 | a0001c0003t0009g0193 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1327-441C>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436382 | ||||||
chr1:63436526
|
G | A | 75 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0099others(72): Show | 75 | HG00544.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.1327-297G>A | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436526 | ||||||
chr1:63436596
|
A | G | 2 | a0002c0002t0001g0336a0002c0002t0001g0337 | 2 | HG03669.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1327-227A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436596 | ||||||
chr1:63436760
|
A | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0050others(34): Show | 37 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.1327-63A>G | ALG6 | ENSG00000088035.18 | transcript | ENST00000263440.6 | protein_coding | 14/14 | chr1 | 63436760 |