geneid | 22 |
---|---|
ensemblid | ENSG00000131269.19 |
hgncid | 48 |
symbol | ABCB7 |
name | ATP binding cassette subfamily B member 7 |
refseq_nuc | NM_001271696.3 |
refseq_prot | NP_001258625.1 |
ensembl_nuc | ENST00000373394.8 |
ensembl_prot | ENSP00000362492.3 |
mane_status | MANE Select |
chr | chrX |
start | 75051048 |
end | 75156283 |
strand | - |
ver | v1.2 |
region | chrX:75051048-75156283 |
region5000 | chrX:75046048-75161283 |
regionname0 | ABCB7_chrX_75051048_75156283 |
regionname5000 | ABCB7_chrX_75046048_75161283 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 752 | 212 | 53 | 42 | 78 | 7 | 30 | 55 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0002 | 0/0 | 752 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0003 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0004 | 0/0 | 138 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0005 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2259 | 201 | 44 | 40 | 78 | 7 | 30 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
c0002 | 0/0 | 2259 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
c0003 | 0/0 | 2259 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
c0004 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
c0005 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
c0006 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
c0007 | 0/0 | 2261 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
c0008 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2340 | 96 | 11 | 12 | 62 | 2 | 9 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0002 | 1/1 | 2334 | 49 | 4 | 21 | 5 | 5 | 12 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0003 | 0/0 | 2344 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0004 | 0/0 | 2335 | 15 | 8 | 1 | 0 | 0 | 6 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0005 | 0/0 | 2341 | 6 | 1 | 1 | 4 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0006 | 0/0 | 2341 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0007 | 0/0 | 2340 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0008 | 0/0 | 2335 | 5 | 3 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0009 | 0/0 | 2339 | 4 | 1 | 1 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0010 | 0/0 | 2339 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0011 | 0/0 | 2341 | 4 | 0 | 0 | 2 | 0 | 2 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0012 | 0/0 | 2342 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0013 | 0/0 | 2336 | 3 | 2 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0014 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0015 | 0/0 | 2341 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0016 | 0/0 | 2340 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0017 | 0/0 | 2329 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0018 | 0/0 | 2341 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0019 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0020 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0021 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0022 | 0/0 | 2335 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0023 | 0/0 | 2336 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0024 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
t0025 | 0/0 | 2336 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2259 | 201 | 44 | 40 | 78 | 7 | 30 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0003 | 0/0 | 2259 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0004 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0006 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0002c0002 | 0/0 | 2259 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0003c0005 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0004c0007 | 0/0 | 2261 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0005c0008 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4598 | 95 | 10 | 12 | 62 | 2 | 9 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0002 | 1/1 | 4592 | 48 | 4 | 20 | 5 | 5 | 12 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0004 | 0/0 | 4593 | 14 | 8 | 0 | 0 | 0 | 6 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0005 | 0/0 | 4599 | 5 | 1 | 1 | 3 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0007 | 0/0 | 4598 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0008 | 0/0 | 4593 | 5 | 3 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0009 | 0/0 | 4597 | 4 | 1 | 1 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0010 | 0/0 | 4597 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0011 | 0/0 | 4599 | 4 | 0 | 0 | 2 | 0 | 2 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0013 | 0/0 | 4594 | 3 | 2 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0014 | 0/0 | 4598 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0015 | 0/0 | 4599 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0016 | 0/0 | 4598 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0017 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0019 | 0/0 | 4598 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0020 | 0/0 | 4598 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0021 | 0/0 | 4598 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0022 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0023 | 0/0 | 4594 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0024 | 0/0 | 4595 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0001t0025 | 0/0 | 4594 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0003t0006 | 0/0 | 4599 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0003t0012 | 0/0 | 4600 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0003t0018 | 0/0 | 4599 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0004t0004 | 0/0 | 4593 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0001c0006t0002 | 0/0 | 4592 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0002c0002t0003 | 0/0 | 4602 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0003c0005t0001 | 0/0 | 4598 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0004c0007t0005 | 0/0 | 4601 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
a0005c0008t0017 | 0/0 | 4587 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta | chrX | 75046048 | 75161283 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0008g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0008g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0009g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0009g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0010g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0010g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0011g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0011g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0013g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0013g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0013g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0014g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0015g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0015g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0016g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0016g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0017g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0019g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0020g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0021g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0022g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0024g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0001t0025g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0012g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0012g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0012g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0003t0018g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0004t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0001c0006t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0002c0002t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0003c0005t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0004c0007t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
a0005c0008t0017g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | GBR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | FIN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00609 | hp1 | a0001 | c0001 | t0011 | g0148 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0177 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00673 | hp1 | a0001 | c0001 | t0015 | g0037 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00735 | hp2 | a0002 | c0002 | t0003 | g0008 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG00738 | hp1 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01070 | hp2 | a0001 | c0001 | t0009 | g0185 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0107 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01099 | hp1 | a0001 | c0001 | t0022 | g0058 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01109 | hp1 | a0001 | c0001 | t0016 | g0217 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01167 | hp1 | a0001 | c0001 | t0025 | g0103 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01169 | hp2 | a0001 | c0001 | t0008 | g0105 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01243 | hp1 | a0001 | c0004 | t0004 | g0002 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01884 | hp1 | a0002 | c0002 | t0003 | g0014 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01884 | hp2 | a0001 | c0003 | t0006 | g0220 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01978 | hp2 | a0001 | c0001 | t0021 | g0149 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02015 | hp1 | a0001 | c0001 | t0013 | g0112 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0231 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02145 | hp1 | a0001 | c0001 | t0017 | g0086 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CDX | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02257 | hp1 | a0001 | c0001 | t0010 | g0201 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02257 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02273 | hp1 | a0001 | c0006 | t0002 | g0046 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02572 | hp1 | a0001 | c0003 | t0006 | g0224 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0160 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0157 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02630 | hp1 | a0001 | c0003 | t0012 | g0227 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02647 | hp1 | a0001 | c0003 | t0006 | g0221 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02717 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02723 | hp1 | a0001 | c0001 | t0010 | g0154 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02723 | hp2 | a0001 | c0003 | t0006 | g0223 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02735 | hp1 | a0001 | c0001 | t0011 | g0197 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0161 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02886 | hp2 | a0001 | c0003 | t0018 | g0219 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02965 | hp1 | a0001 | c0001 | t0020 | g0155 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02970 | hp1 | a0001 | c0003 | t0006 | g0222 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02970 | hp2 | a0002 | c0002 | t0003 | g0005 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02976 | hp1 | a0002 | c0002 | t0003 | g0020 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03041 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03098 | hp1 | a0002 | c0002 | t0003 | g0004 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03130 | hp1 | a0002 | c0002 | t0003 | g0013 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03139 | hp1 | a0002 | c0002 | t0003 | g0018 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03195 | hp2 | a0005 | c0008 | t0017 | g0085 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03225 | hp1 | a0001 | c0003 | t0012 | g0226 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03453 | hp1 | a0002 | c0002 | t0003 | g0021 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03486 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0108 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0109 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03516 | hp2 | a0002 | c0002 | t0003 | g0007 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0078 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0113 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG04184 | hp1 | a0001 | c0001 | t0011 | g0228 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG04199 | hp1 | a0001 | c0001 | t0023 | g0114 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18522 | hp1 | a0002 | c0002 | t0003 | g0006 | AFR | YRI | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18747 | hp1 | a0001 | c0001 | t0009 | g0027 | EAS | CHB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | YRI | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18967 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18985 | hp1 | a0001 | c0001 | t0011 | g0023 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19012 | hp1 | a0001 | c0001 | t0015 | g0038 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19030 | hp1 | a0001 | c0001 | t0024 | g0116 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19030 | hp2 | a0002 | c0002 | t0003 | g0012 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19067 | hp1 | a0004 | c0007 | t0005 | g0174 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19072 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA19091 | hp1 | a0001 | c0001 | t0019 | g0178 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | ASW | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA20129 | hp2 | a0001 | c0001 | t0008 | g0106 | AFR | ASW | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | TSI | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0019 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0204 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG02559 | hp2 | a0001 | c0003 | t0012 | g0225 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
HG03471 | hp1 | a0002 | c0002 | t0003 | g0016 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0230 | AFR | USA | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA21309 | hp1 | a0001 | c0001 | t0016 | g0216 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
NA21309 | hp2 | a0003 | c0005 | t0001 | g0003 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0087 | REF | REF | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0015 | REF | REF | ABCB7_chrX_75046048_75161283 | ABCB7 | chrX | 75046048 | 75161283 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:75065162
|
G | A | 1 | a0002 | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
missense_variant | MODERATE | c.1739C>T | p.Ala580Val | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/16 | 1750/4592 | 1739/2259 | 580/752 | chrX | 75065162 | ||
chrX:75098951
|
AC | A | 1 | a0004 | 1 | NA19067.hp1 | frameshift_variant | HIGH | c.443delG | p.Gly148fs | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/16 | 454/4592 | 443/2259 | 148/752 | chrX | 75098951 | ||
chrX:75098970
|
A | AAT | 1 | a0004 | 1 | NA19067.hp1 | frameshift_variant | HIGH | c.424_425insAT | p.Ile142fs | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/16 | 435/4592 | 424/2259 | 142/752 | chrX | 75098970 | ||
chrX:75098971
|
T | G | 1 | a0004 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.424A>C | p.Ile142Leu | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/16 | 435/4592 | 424/2259 | 142/752 | chrX | 75098971 | ||
chrX:75099004
|
T | TG | 1 | a0004 | 1 | NA19067.hp1 | frameshift_variant | HIGH | c.390dupC | p.Lys131fs | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/16 | 401/4592 | 390/2259 | 130/752 | chrX | 75099004 | ||
chrX:75099034
|
T | C | 1 | a0005 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.361A>G | p.Ile121Val | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/16 | 372/4592 | 361/2259 | 121/752 | chrX | 75099034 | ||
chrX:75156152
|
A | G | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.121T>C | p.Trp41Arg | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/16 | 132/4592 | 121/2259 | 41/752 | chrX | 75156152 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:75065161
|
T | C | 2 | a0001c0003a0002c0002 | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
synonymous_variant | LOW | c.1740A>G | p.Ala580Ala | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/16 | 1751/4592 | 1740/2259 | 580/752 | chrX | 75065161 | ||
chrX:75070410
|
A | G | 1 | a0001c0006 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.1320T>C | p.Asp440Asp | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/16 | 1331/4592 | 1320/2259 | 440/752 | chrX | 75070410 | ||
chrX:75156171
|
A | G | 1 | a0001c0004 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.102T>C | p.Val34Val | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/16 | 113/4592 | 102/2259 | 34/752 | chrX | 75156171 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:75051141
|
G | GA | 4 | a0001c0001t0011a0001c0001t0022a0001c0001t0023others(1): Show | 23 | HG00609.hp1 HG00735.hp2 HG00738.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2228dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 2228 | chrX | 75051141 | |||||
chrX:75051141
|
GA | G | 1 | a0001c0001t0010 | 4 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2228delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 2228 | chrX | 75051141 | |||||
chrX:75051304
|
C | A | 1 | a0001c0003t0006 | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2066G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 2066 | chrX | 75051304 | |||||
chrX:75051305
|
C | T | 1 | a0001c0003t0006 | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2065G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 2065 | chrX | 75051305 | |||||
chrX:75051463
|
C | A | 1 | a0001c0001t0007 | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1907G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 1907 | chrX | 75051463 | |||||
chrX:75051746
|
C | A | 1 | a0001c0003t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 1624 | chrX | 75051746 | |||||
chrX:75051846
|
G | A | 1 | a0001c0001t0014 | 2 | HG02615.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1524C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 1524 | chrX | 75051846 | |||||
chrX:75051878
|
C | T | 1 | a0001c0001t0019 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1492G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 1492 | chrX | 75051878 | |||||
chrX:75051937
|
T | G | 1 | a0001c0001t0020 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1433A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 1433 | chrX | 75051937 | |||||
chrX:75052134
|
G | GT | 1 | a0002c0002t0003 | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1235dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 1235 | chrX | 75052134 | |||||
chrX:75052284
|
G | A | 1 | a0001c0001t0022 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1086C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 1086 | chrX | 75052284 | |||||
chrX:75052418
|
G | A | 1 | a0001c0001t0021 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*952C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 952 | chrX | 75052418 | |||||
chrX:75052466
|
C | CA | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(12): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*903dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 903 | chrX | 75052466 | |||||
chrX:75052466
|
C | CAA | 5 | a0001c0001t0005a0001c0001t0013a0001c0001t0015others(2): Show | 12 | HG00639.hp2 HG00673.hp1 HG01167.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*902_*903dupTT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 903 | chrX | 75052466 | |||||
chrX:75052466
|
C | CAAA | 3 | a0001c0001t0024a0001c0003t0006a0001c0003t0018 | 7 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*901_*903dupTTT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 903 | chrX | 75052466 | |||||
chrX:75052466
|
C | CAAAA | 1 | a0001c0003t0012 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*900_*903dupTTTT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 903 | chrX | 75052466 | |||||
chrX:75052610
|
C | A | 2 | a0001c0001t0008a0001c0001t0025 | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*760G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 760 | chrX | 75052610 | |||||
chrX:75052777
|
C | CA | 1 | a0002c0002t0003 | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*592dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 592 | chrX | 75052777 | |||||
chrX:75052777
|
CA | C | 3 | a0001c0003t0006a0001c0003t0012a0001c0003t0018 | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*592delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 592 | chrX | 75052777 | |||||
chrX:75052793
|
C | CA | 1 | a0002c0002t0003 | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*576dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 576 | chrX | 75052793 | |||||
chrX:75052817
|
A | AAAAAG | 18 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(15): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*548_*552dupCTTTT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 552 | chrX | 75052817 | |||||
chrX:75052837
|
C | A | 1 | a0001c0001t0015 | 2 | HG00673.hp1 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*533G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 533 | chrX | 75052837 | |||||
chrX:75052922
|
C | G | 3 | a0001c0003t0006a0001c0003t0012a0001c0003t0018 | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*448G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 448 | chrX | 75052922 | |||||
chrX:75052931
|
T | C | 1 | a0001c0001t0016 | 2 | HG01109.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*439A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 439 | chrX | 75052931 | |||||
chrX:75053250
|
AATCTT | A | 2 | a0001c0001t0017a0005c0008t0017 | 2 | HG02145.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*115_*119delAAGAT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 16/16 | 115 | chrX | 75053250 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:75053609
|
C | T | 6 | a0001c0001t0001g0158a0001c0001t0007g0204a0001c0001t0007g0212others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044-24G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75053609 | ||||||
chrX:75053619
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2044-34C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75053619 | ||||||
chrX:75053854
|
G | C | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2044-269C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75053854 | ||||||
chrX:75053954
|
TAC | T | 1 | a0001c0001t0016g0216 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2044-371_2044-370d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75053954 | ||||||
chrX:75054257
|
A | C | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2044-672T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75054257 | ||||||
chrX:75054577
|
G | GT | 4 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0145others(1): Show | 4 | HG00408.hp1 NA18967.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044-993dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75054577 | ||||||
chrX:75054879
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2044-1294A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75054879 | ||||||
chrX:75054901
|
T | G | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2044-1316A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75054901 | ||||||
chrX:75054907
|
G | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2044-1322C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75054907 | ||||||
chrX:75055058
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2044-1473C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055058 | ||||||
chrX:75055314
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2044-1729G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055314 | ||||||
chrX:75055325
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0003c0005t0001g0003 | 3 | HG02258.hp1 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2044-1740A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055325 | ||||||
chrX:75055533
|
A | AC | 1 | a0001c0001t0004g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2044-1949dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055533 | ||||||
chrX:75055540
|
C | G | 1 | a0001c0001t0011g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2044-1955G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055540 | ||||||
chrX:75055553
|
C | CA | 22 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0065others(19): Show | 22 | HG01167.hp1 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.2044-1969dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055553 | ||||||
chrX:75055553
|
CA | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(108): Show | 112 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.2044-1969delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055553 | ||||||
chrX:75055553
|
CAA | C | 1 | a0001c0001t0001g0207 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2044-1970_2044-196 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055553 | ||||||
chrX:75055553
|
CAAAAA | C | 2 | a0001c0001t0002g0083a0001c0001t0004g0082 | 2 | HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2044-1973_2044-196 others(9): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055553 | ||||||
chrX:75055553
|
CAAAAAAA others(1): Show |
C | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2044-1976_2044-196 others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055553 | ||||||
chrX:75055559
|
A | C | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2044-1974T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055559 | ||||||
chrX:75055560
|
A | C | 6 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2044-1975T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055560 | ||||||
chrX:75055565
|
A | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2044-1980T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055565 | ||||||
chrX:75055581
|
A | C | 1 | a0001c0001t0002g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2044-1996T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055581 | ||||||
chrX:75055597
|
C | A | 1 | a0001c0001t0004g0049 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2044-2012G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055597 | ||||||
chrX:75055854
|
C | A | 1 | a0001c0001t0011g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2044-2269G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055854 | ||||||
chrX:75055858
|
A | AT | 16 | a0001c0001t0002g0110a0001c0001t0004g0049a0001c0001t0004g0050others(13): Show | 16 | HG01243.hp1 HG02015.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2044-2274dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055858 | ||||||
chrX:75055858
|
A | ATT | 2 | a0001c0001t0013g0230a0001c0001t0013g0231 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2044-2275_2044-227 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055858 | ||||||
chrX:75055959
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2044-2374A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055959 | ||||||
chrX:75055979
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02040.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2044-2394C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75055979 | ||||||
chrX:75056094
|
T | C | 1 | a0001c0001t0002g0089 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2044-2509A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75056094 | ||||||
chrX:75056215
|
T | C | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2044-2630A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75056215 | ||||||
chrX:75056241
|
G | A | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2044-2656C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75056241 | ||||||
chrX:75056250
|
C | G | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2044-2665G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75056250 | ||||||
chrX:75056294
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(150): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.2044-2709C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75056294 | ||||||
chrX:75056324
|
T | A | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2044-2739A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75056324 | ||||||
chrX:75056676
|
CA | C | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2044-3092delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75056676 | ||||||
chrX:75057731
|
G | T | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2043+2492C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75057731 | ||||||
chrX:75057763
|
C | CT | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2043+2459dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75057763 | ||||||
chrX:75057778
|
TG | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.2043+2444delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75057778 | ||||||
chrX:75058327
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2043+1896G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75058327 | ||||||
chrX:75058574
|
C | G | 1 | a0001c0003t0012g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2043+1649G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75058574 | ||||||
chrX:75059075
|
A | G | 2 | a0001c0001t0007g0212a0001c0001t0007g0213 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2043+1148T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059075 | ||||||
chrX:75059138
|
G | C | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2043+1085C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059138 | ||||||
chrX:75059283
|
G | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043+940C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059283 | ||||||
chrX:75059426
|
G | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043+797C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059426 | ||||||
chrX:75059473
|
G | GA | 1 | a0001c0001t0002g0076 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2043+749dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059473 | ||||||
chrX:75059508
|
T | C | 1 | a0001c0001t0005g0196 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2043+715A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059508 | ||||||
chrX:75059700
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2043+523A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059700 | ||||||
chrX:75059769
|
A | G | 26 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.2043+454T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75059769 | ||||||
chrX:75060009
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043+214A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75060009 | ||||||
chrX:75060016
|
TATA | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043+204_2043+206d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75060016 | ||||||
chrX:75060206
|
A | T | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2043+17T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 15/15 | chrX | 75060206 | ||||||
chrX:75060390
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1936-60A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75060390 | ||||||
chrX:75060406
|
C | G | 3 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0024g0116 | 3 | HG02109.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1936-76G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75060406 | ||||||
chrX:75060439
|
G | GT | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1936-110dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75060439 | ||||||
chrX:75060550
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.1936-220G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75060550 | ||||||
chrX:75060718
|
G | A | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1936-388C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75060718 | ||||||
chrX:75061371
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1935+957A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75061371 | ||||||
chrX:75061481
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1935+847G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75061481 | ||||||
chrX:75061612
|
C | G | 30 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0016g0216others(27): Show | 30 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1935+716G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75061612 | ||||||
chrX:75061905
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1935+423T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75061905 | ||||||
chrX:75062083
|
T | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1935+245A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75062083 | ||||||
chrX:75062320
|
T | C | 1 | a0001c0001t0011g0197 | 1 | HG02735.hp1 | splice_region_variant&intron_variant | LOW | c.1935+8A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 14/15 | chrX | 75062320 | ||||||
chrX:75062585
|
A | C | 1 | a0001c0001t0020g0155 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1832-154T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75062585 | ||||||
chrX:75062596
|
C | A | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1832-165G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75062596 | ||||||
chrX:75062670
|
G | C | 1 | a0001c0001t0001g0163 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1832-239C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75062670 | ||||||
chrX:75062681
|
T | C | 6 | a0001c0001t0001g0158a0001c0001t0007g0204a0001c0001t0007g0212others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1832-250A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75062681 | ||||||
chrX:75062697
|
A | T | 6 | a0001c0001t0001g0158a0001c0001t0007g0204a0001c0001t0007g0212others(3): Show | 6 | HG02280.hp2 HG02559.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1832-266T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75062697 | ||||||
chrX:75063116
|
G | C | 1 | a0001c0001t0013g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1832-685C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063116 | ||||||
chrX:75063192
|
TC | T | 1 | a0002c0002t0003g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1832-762delG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063192 | ||||||
chrX:75063280
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1832-849A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063280 | ||||||
chrX:75063291
|
T | C | 10 | a0001c0001t0010g0157a0001c0003t0006g0220a0001c0003t0006g0221others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1832-860A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063291 | ||||||
chrX:75063527
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0208a0001c0001t0001g0209 | 3 | HG01975.hp1 HG02630.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1832-1096G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063527 | ||||||
chrX:75063590
|
C | A | 5 | a0001c0001t0007g0204a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1832-1159G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063590 | ||||||
chrX:75063777
|
A | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1831+1293T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063777 | ||||||
chrX:75063962
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG02258.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1831+1108G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063962 | ||||||
chrX:75063980
|
G | A | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1831+1090C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75063980 | ||||||
chrX:75064011
|
G | T | 3 | a0002c0002t0003g0010a0002c0002t0003g0016a0002c0002t0003g0021 | 3 | HG00738.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1831+1059C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75064011 | ||||||
chrX:75064065
|
A | C | 1 | a0001c0001t0021g0149 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1831+1005T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75064065 | ||||||
chrX:75064460
|
CA | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1831+609delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75064460 | ||||||
chrX:75064855
|
G | GCTAA | 1 | a0001c0001t0024g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1831+214_1831+215i others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75064855 | ||||||
chrX:75064861
|
G | GA | 170 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(167): Show | 171 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1831+208dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75064861 | ||||||
chrX:75064861
|
G | GAA | 7 | a0001c0003t0006g0222a0001c0003t0006g0224a0001c0003t0012g0225others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1831+207_1831+208d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75064861 | ||||||
chrX:75064927
|
T | C | 1 | a0001c0001t0001g0176 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1831+143A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75064927 | ||||||
chrX:75065017
|
T | TA | 1 | a0001c0001t0002g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1831+52dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75065017 | ||||||
chrX:75065037
|
CAAG | C | 1 | a0001c0001t0001g0166 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1831+30_1831+32del others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75065037 | ||||||
chrX:75065046
|
G | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1831+24C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 13/15 | chrX | 75065046 | ||||||
chrX:75065284
|
ATCTC | A | 13 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1660-47_1660-44del others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75065284 | ||||||
chrX:75065302
|
T | A | 1 | a0002c0002t0003g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1660-61A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75065302 | ||||||
chrX:75065554
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1660-313T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75065554 | ||||||
chrX:75065941
|
G | C | 1 | a0002c0002t0003g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1660-700C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75065941 | ||||||
chrX:75065999
|
C | T | 5 | a0001c0001t0001g0184a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1660-758G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75065999 | ||||||
chrX:75066266
|
T | C | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1660-1025A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75066266 | ||||||
chrX:75066276
|
C | T | 1 | a0001c0001t0013g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1660-1035G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75066276 | ||||||
chrX:75066468
|
T | C | 1 | a0001c0001t0010g0154 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1660-1227A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75066468 | ||||||
chrX:75066577
|
A | G | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1660-1336T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75066577 | ||||||
chrX:75066686
|
C | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1660-1445G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75066686 | ||||||
chrX:75066688
|
TTAAA | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1660-1451_1660-144 others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75066688 | ||||||
chrX:75067620
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1659+1387C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75067620 | ||||||
chrX:75067780
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1659+1227G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75067780 | ||||||
chrX:75067825
|
T | C | 1 | a0002c0002t0003g0013 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1659+1182A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75067825 | ||||||
chrX:75067874
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1659+1133T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75067874 | ||||||
chrX:75068014
|
GATGTT | G | 6 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0013g0230others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1659+988_1659+992d others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75068014 | ||||||
chrX:75068127
|
CAT | C | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1659+878_1659+879d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75068127 | ||||||
chrX:75068483
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1659+524C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75068483 | ||||||
chrX:75068679
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1659+328A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75068679 | ||||||
chrX:75068846
|
CT | C | 1 | a0001c0001t0002g0056 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1659+160delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 12/15 | chrX | 75068846 | ||||||
chrX:75069227
|
GAAAT | G | 1 | a0001c0001t0016g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1529+60_1529+63del others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 11/15 | chrX | 75069227 | ||||||
chrX:75069509
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(174): Show | 178 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1366-55G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75069509 | ||||||
chrX:75069568
|
A | G | 2 | a0001c0001t0013g0230a0001c0001t0013g0231 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1366-114T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75069568 | ||||||
chrX:75069591
|
A | C | 1 | a0001c0001t0004g0050 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1366-137T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75069591 | ||||||
chrX:75069647
|
C | G | 1 | a0001c0006t0002g0046 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1366-193G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75069647 | ||||||
chrX:75069860
|
T | TTTTA | 11 | a0001c0001t0002g0077a0001c0001t0009g0036a0001c0001t0010g0154others(8): Show | 11 | HG02257.hp1 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1366-410_1366-407d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75069860 | ||||||
chrX:75069897
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1366-443G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75069897 | ||||||
chrX:75069914
|
G | C | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1365+451C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75069914 | ||||||
chrX:75070120
|
C | T | 2 | a0001c0001t0001g0203a0001c0001t0023g0114 | 2 | HG04199.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1365+245G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75070120 | ||||||
chrX:75070149
|
C | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1365+216G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75070149 | ||||||
chrX:75070362
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA18961.hp1 | splice_region_variant&intron_variant | LOW | c.1365+3A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 10/15 | chrX | 75070362 | ||||||
chrX:75070586
|
T | C | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1208-64A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 9/15 | chrX | 75070586 | ||||||
chrX:75070946
|
A | AAAT | 117 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1208-425_1208-424i others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 9/15 | chrX | 75070946 | ||||||
chrX:75071182
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1207+327G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 9/15 | chrX | 75071182 | ||||||
chrX:75071195
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207+314G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 9/15 | chrX | 75071195 | ||||||
chrX:75071892
|
G | C | 1 | a0001c0001t0004g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1033-209C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75071892 | ||||||
chrX:75072304
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1033-621G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75072304 | ||||||
chrX:75072479
|
C | T | 1 | a0001c0001t0004g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1033-796G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75072479 | ||||||
chrX:75072561
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1033-878T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75072561 | ||||||
chrX:75072727
|
G | A | 1 | a0001c0001t0013g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1032+962C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75072727 | ||||||
chrX:75072926
|
AT | A | 9 | a0001c0001t0001g0153a0001c0001t0002g0051a0001c0001t0009g0036others(6): Show | 9 | HG01167.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1032+762delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75072926 | ||||||
chrX:75072951
|
C | T | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1032+738G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75072951 | ||||||
chrX:75073316
|
G | A | 1 | a0001c0001t0001g0138 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1032+373C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75073316 | ||||||
chrX:75073677
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1032+12A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 8/15 | chrX | 75073677 | ||||||
chrX:75074324
|
A | T | 1 | a0001c0001t0002g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.856-368T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 6/15 | chrX | 75074324 | ||||||
chrX:75074553
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(113): Show | 117 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.856-597G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 6/15 | chrX | 75074553 | ||||||
chrX:75074999
|
G | GA | 7 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.855+362dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 6/15 | chrX | 75074999 | ||||||
chrX:75075738
|
A | G | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.587-108T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 5/15 | chrX | 75075738 | ||||||
chrX:75075810
|
C | T | 26 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.587-180G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 5/15 | chrX | 75075810 | ||||||
chrX:75076264
|
G | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+258C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 5/15 | chrX | 75076264 | ||||||
chrX:75077140
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-486A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077140 | ||||||
chrX:75077431
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-777T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077431 | ||||||
chrX:75077667
|
C | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-1013G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077667 | ||||||
chrX:75077749
|
C | A | 3 | a0001c0001t0002g0045a0001c0001t0017g0086a0005c0008t0017g0085 | 3 | HG02145.hp1 HG02818.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.454-1095G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077749 | ||||||
chrX:75077916
|
C | CT | 1 | a0001c0001t0023g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.454-1263dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077916 | ||||||
chrX:75077916
|
C | CTT | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-1264_454-1263d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077916 | ||||||
chrX:75077916
|
CT | C | 5 | a0001c0001t0001g0184a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-1263delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077916 | ||||||
chrX:75077916
|
CTT | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-1264_454-1263d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75077916 | ||||||
chrX:75078009
|
G | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-1355C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078009 | ||||||
chrX:75078420
|
T | C | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.454-1766A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078420 | ||||||
chrX:75078454
|
T | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.454-1800A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078454 | ||||||
chrX:75078544
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.454-1890T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078544 | ||||||
chrX:75078586
|
T | A | 39 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(36): Show | 39 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.454-1932A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078586 | ||||||
chrX:75078589
|
G | A | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.454-1935C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078589 | ||||||
chrX:75078782
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.454-2128T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078782 | ||||||
chrX:75078816
|
A | AC | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2163dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078816 | ||||||
chrX:75078839
|
T | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(150): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.454-2185A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078839 | ||||||
chrX:75078893
|
A | AT | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2240dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75078893 | ||||||
chrX:75079128
|
G | GA | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2475dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079128 | ||||||
chrX:75079166
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0003c0005t0001g0003 | 3 | HG02258.hp1 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.454-2512G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079166 | ||||||
chrX:75079172
|
T | C | 18 | a0001c0001t0002g0110a0001c0001t0004g0049a0001c0001t0004g0050others(15): Show | 18 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.454-2518A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079172 | ||||||
chrX:75079193
|
AG | A | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2540delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079193 | ||||||
chrX:75079255
|
T | TG | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2602_454-2601i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079255 | ||||||
chrX:75079279
|
AG | A | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2626delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079279 | ||||||
chrX:75079302
|
T | G | 5 | a0001c0001t0001g0184a0001c0001t0001g0189a0001c0001t0001g0190others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-2648A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079302 | ||||||
chrX:75079476
|
C | CA | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2823dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079476 | ||||||
chrX:75079490
|
TA | T | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.454-2837delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079490 | ||||||
chrX:75079546
|
A | T | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.454-2892T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079546 | ||||||
chrX:75079566
|
C | T | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.454-2912G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079566 | ||||||
chrX:75079581
|
G | C | 1 | a0001c0001t0001g0028 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.454-2927C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079581 | ||||||
chrX:75079621
|
CA | C | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2968delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079621 | ||||||
chrX:75079629
|
G | GA | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-2976dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079629 | ||||||
chrX:75079669
|
G | C | 1 | a0001c0001t0001g0179 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.454-3015C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079669 | ||||||
chrX:75079682
|
G | GT | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-3029dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079682 | ||||||
chrX:75079705
|
A | G | 5 | a0001c0001t0007g0204a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-3051T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079705 | ||||||
chrX:75079729
|
C | CA | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-3076_454-3075i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079729 | ||||||
chrX:75079764
|
A | AC | 1 | a0001c0001t0001g0167 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.454-3111dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079764 | ||||||
chrX:75079915
|
T | A | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-3261A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75079915 | ||||||
chrX:75080453
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.454-3799G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75080453 | ||||||
chrX:75080458
|
C | A | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-3804G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75080458 | ||||||
chrX:75080477
|
C | G | 26 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.454-3823G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75080477 | ||||||
chrX:75080809
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-4155A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75080809 | ||||||
chrX:75080876
|
A | T | 26 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.454-4222T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75080876 | ||||||
chrX:75081015
|
G | C | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.454-4361C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081015 | ||||||
chrX:75081118
|
AT | A | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-4465delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081118 | ||||||
chrX:75081180
|
AATAAG | A | 1 | a0001c0001t0001g0022 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.454-4531_454-4527d others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081180 | ||||||
chrX:75081278
|
G | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-4624C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081278 | ||||||
chrX:75081327
|
G | C | 1 | a0001c0001t0001g0029 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.454-4673C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081327 | ||||||
chrX:75081604
|
GT | G | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-4951delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081604 | ||||||
chrX:75081697
|
G | T | 4 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0054others(1): Show | 4 | HG02280.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.454-5043C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081697 | ||||||
chrX:75081727
|
C | T | 26 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.454-5073G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081727 | ||||||
chrX:75081879
|
T | TG | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-5226dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081879 | ||||||
chrX:75081923
|
G | GA | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-5270dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081923 | ||||||
chrX:75081968
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-5314G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75081968 | ||||||
chrX:75082034
|
A | G | 1 | a0001c0001t0011g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.454-5380T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082034 | ||||||
chrX:75082159
|
A | C | 1 | a0001c0001t0002g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.454-5505T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082159 | ||||||
chrX:75082183
|
G | GA | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-5530dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082183 | ||||||
chrX:75082361
|
A | AG | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-5708dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082361 | ||||||
chrX:75082492
|
G | C | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.454-5838C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082492 | ||||||
chrX:75082515
|
T | TG | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-5862dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082515 | ||||||
chrX:75082536
|
T | A | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.454-5882A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082536 | ||||||
chrX:75082771
|
GAA | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(95): Show | 99 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.454-6119_454-6118d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082771 | ||||||
chrX:75082940
|
A | G | 1 | a0001c0004t0004g0002 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.454-6286T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75082940 | ||||||
chrX:75083000
|
T | C | 6 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0013g0230others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.454-6346A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083000 | ||||||
chrX:75083267
|
T | C | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.454-6613A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083267 | ||||||
chrX:75083273
|
A | AC | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-6620dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083273 | ||||||
chrX:75083283
|
G | GT | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-6630dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083283 | ||||||
chrX:75083314
|
G | GC | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-6661dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083314 | ||||||
chrX:75083509
|
G | T | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.454-6855C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083509 | ||||||
chrX:75083614
|
C | CA | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-6961dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083614 | ||||||
chrX:75083614
|
CA | C | 30 | a0001c0001t0014g0159a0001c0001t0014g0160a0001c0001t0016g0216others(27): Show | 30 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.454-6961delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083614 | ||||||
chrX:75083711
|
A | AAT | 43 | a0001c0001t0001g0139a0001c0001t0001g0195a0001c0001t0002g0110others(40): Show | 43 | HG00735.hp2 HG00738.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.454-7059_454-7058d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083711 | ||||||
chrX:75083727
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.454-7073A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083727 | ||||||
chrX:75083866
|
T | C | 6 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.454-7212A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75083866 | ||||||
chrX:75084060
|
T | C | 1 | a0001c0001t0016g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.454-7406A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75084060 | ||||||
chrX:75084178
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.454-7524C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75084178 | ||||||
chrX:75084288
|
T | G | 177 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(174): Show | 178 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.454-7634A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75084288 | ||||||
chrX:75084576
|
G | A | 2 | a0001c0001t0001g0172a0001c0001t0001g0192 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.454-7922C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75084576 | ||||||
chrX:75084613
|
G | GA | 1 | a0001c0001t0002g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.454-7960dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75084613 | ||||||
chrX:75085259
|
C | T | 1 | a0001c0003t0012g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.454-8605G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085259 | ||||||
chrX:75085347
|
G | T | 1 | a0001c0001t0001g0132 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.454-8693C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085347 | ||||||
chrX:75085493
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0019g0178 | 2 | NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.454-8839A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085493 | ||||||
chrX:75085568
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.454-8914A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085568 | ||||||
chrX:75085851
|
A | AT | 27 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(24): Show | 27 | HG00621.hp1 HG00673.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.454-9198dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085851 | ||||||
chrX:75085851
|
AT | A | 26 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.454-9198delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085851 | ||||||
chrX:75085886
|
G | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-9232C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085886 | ||||||
chrX:75085908
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-9254T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085908 | ||||||
chrX:75085972
|
G | A | 2 | a0001c0003t0006g0222a0001c0003t0006g0224 | 2 | HG02572.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.454-9318C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75085972 | ||||||
chrX:75086033
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0163 | 2 | NA18986.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.454-9379C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75086033 | ||||||
chrX:75086143
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(150): Show | 154 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.454-9489T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75086143 | ||||||
chrX:75086164
|
A | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-9510T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75086164 | ||||||
chrX:75086300
|
A | G | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.454-9646T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75086300 | ||||||
chrX:75086316
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.454-9662T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75086316 | ||||||
chrX:75086999
|
A | G | 26 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(23): Show | 26 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.454-10345T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75086999 | ||||||
chrX:75087148
|
T | C | 1 | a0001c0001t0005g0196 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.454-10494A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75087148 | ||||||
chrX:75087458
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-10804A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75087458 | ||||||
chrX:75087491
|
C | T | 17 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(14): Show | 17 | HG00735.hp2 HG00738.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.454-10837G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75087491 | ||||||
chrX:75087525
|
TA | T | 1 | a0001c0001t0004g0108 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.454-10872delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75087525 | ||||||
chrX:75088333
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.453+10609C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088333 | ||||||
chrX:75088818
|
C | G | 2 | a0001c0001t0002g0062a0001c0001t0002g0073 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.453+10124G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088818 | ||||||
chrX:75088846
|
C | CA | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+10095dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088846 | ||||||
chrX:75088846
|
CA | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.453+10095delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088846 | ||||||
chrX:75088875
|
C | CA | 1 | a0001c0001t0001g0143 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.453+10066dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088875 | ||||||
chrX:75088878
|
A | C | 36 | a0001c0001t0001g0147a0001c0001t0001g0164a0001c0001t0001g0179others(33): Show | 36 | HG00735.hp2 HG00738.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.453+10064T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088878 | ||||||
chrX:75088881
|
A | C | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.453+10061T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088881 | ||||||
chrX:75088948
|
C | T | 6 | a0001c0001t0001g0182a0001c0001t0001g0184a0001c0001t0001g0189others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+9994G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75088948 | ||||||
chrX:75089002
|
GA | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+9939delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75089002 | ||||||
chrX:75089330
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.453+9612A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75089330 | ||||||
chrX:75089353
|
A | C | 1 | a0001c0001t0001g0170 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.453+9589T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75089353 | ||||||
chrX:75089376
|
T | C | 2 | a0001c0001t0013g0230a0001c0001t0013g0231 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.453+9566A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75089376 | ||||||
chrX:75089553
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+9389G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75089553 | ||||||
chrX:75089558
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(115): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.453+9384A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75089558 | ||||||
chrX:75089614
|
G | A | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.453+9328C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75089614 | ||||||
chrX:75090275
|
AT | A | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+8666delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090275 | ||||||
chrX:75090580
|
G | A | 1 | a0001c0001t0023g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.453+8362C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090580 | ||||||
chrX:75090580
|
G | GA | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.453+8361dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090580 | ||||||
chrX:75090791
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.453+8151C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090791 | ||||||
chrX:75090853
|
T | C | 6 | a0001c0001t0008g0048a0001c0001t0008g0104a0001c0001t0008g0105others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+8089A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090853 | ||||||
chrX:75090922
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+8020A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090922 | ||||||
chrX:75090930
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.453+8012A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090930 | ||||||
chrX:75090959
|
T | A | 1 | a0002c0002t0003g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.453+7983A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75090959 | ||||||
chrX:75091105
|
T | A | 16 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(13): Show | 16 | HG00639.hp2 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.453+7837A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091105 | ||||||
chrX:75091259
|
A | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7683T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091259 | ||||||
chrX:75091261
|
G | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7681C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091261 | ||||||
chrX:75091263
|
G | A | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7679C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091263 | ||||||
chrX:75091266
|
A | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7676T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091266 | ||||||
chrX:75091267
|
T | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7675A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091267 | ||||||
chrX:75091268
|
T | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7674A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091268 | ||||||
chrX:75091269
|
T | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7673A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091269 | ||||||
chrX:75091270
|
A | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7672T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091270 | ||||||
chrX:75091272
|
T | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7670A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091272 | ||||||
chrX:75091273
|
C | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7669G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091273 | ||||||
chrX:75091366
|
GA | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+7575delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091366 | ||||||
chrX:75091397
|
TA | T | 1 | a0001c0001t0001g0022 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.453+7544delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091397 | ||||||
chrX:75091675
|
G | GA | 10 | a0001c0001t0001g0120a0001c0001t0001g0171a0001c0001t0002g0059others(7): Show | 10 | HG01109.hp1 HG02523.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+7266dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091675 | ||||||
chrX:75091675
|
G | GAA | 7 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(4): Show | 7 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.453+7265_453+7266d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091675 | ||||||
chrX:75091675
|
GA | G | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.453+7266delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091675 | ||||||
chrX:75091924
|
G | T | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+7018C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75091924 | ||||||
chrX:75092281
|
AGT | A | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6659_453+6660d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092281 | ||||||
chrX:75092286
|
A | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6656T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092286 | ||||||
chrX:75092287
|
C | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6655G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092287 | ||||||
chrX:75092288
|
T | A | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6654A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092288 | ||||||
chrX:75092292
|
C | CG | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6649_453+6650i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092292 | ||||||
chrX:75092293
|
T | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6649A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092293 | ||||||
chrX:75092294
|
T | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6648A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092294 | ||||||
chrX:75092296
|
C | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6646G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092296 | ||||||
chrX:75092297
|
A | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6645T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092297 | ||||||
chrX:75092298
|
C | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6644G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092298 | ||||||
chrX:75092376
|
G | GA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+6565dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092376 | ||||||
chrX:75092475
|
C | T | 12 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(9): Show | 12 | HG00673.hp1 HG02056.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.453+6467G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092475 | ||||||
chrX:75092533
|
C | CA | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+6408dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092533 | ||||||
chrX:75092650
|
T | C | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.453+6292A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092650 | ||||||
chrX:75092724
|
A | C | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.453+6218T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092724 | ||||||
chrX:75092730
|
CA | C | 1 | a0001c0001t0001g0171 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.453+6211delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092730 | ||||||
chrX:75092792
|
A | C | 1 | a0001c0001t0001g0035 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.453+6150T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75092792 | ||||||
chrX:75093165
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+5777T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093165 | ||||||
chrX:75093221
|
A | AT | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+5720dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093221 | ||||||
chrX:75093276
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+5666T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093276 | ||||||
chrX:75093343
|
A | C | 2 | a0001c0003t0012g0226a0001c0003t0012g0227 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.453+5599T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093343 | ||||||
chrX:75093714
|
A | G | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.453+5228T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093714 | ||||||
chrX:75093762
|
T | TTAA | 212 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(209): Show | 213 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.453+5177_453+5179d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093762 | ||||||
chrX:75093762
|
T | TTAATAA | 1 | a0001c0001t0004g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.453+5174_453+5179d others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093762 | ||||||
chrX:75093942
|
G | GC | 1 | a0001c0001t0001g0171 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.453+4999dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75093942 | ||||||
chrX:75094019
|
C | CAT | 31 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0035others(28): Show | 31 | HG00408.hp1 HG00735.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.453+4921_453+4922d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094019
|
C | CATAT | 42 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0025others(39): Show | 43 | HG00621.hp1 HG00673.hp1 HG01258.hp1 others(40): Show |
intron_variant | MODIFIER | c.453+4919_453+4922d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094019
|
C | CATATAT | 30 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0118others(27): Show | 30 | HG01261.hp1 HG01952.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.453+4917_453+4922d others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094019
|
C | CATATATA others(1): Show |
29 | a0001c0001t0001g0034a0001c0001t0001g0117a0001c0001t0001g0119others(26): Show | 29 | HG00609.hp1 HG00639.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.453+4915_453+4922d others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094019
|
C | CATATATA others(3): Show |
5 | a0001c0001t0001g0024a0001c0001t0001g0139a0001c0001t0001g0169others(2): Show | 5 | HG01981.hp2 HG02135.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+4913_453+4922d others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094019
|
C | CATATATA others(5): Show |
3 | a0001c0001t0001g0186a0001c0001t0004g0113a0001c0001t0024g0116 | 3 | HG03942.hp1 NA18952.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.453+4911_453+4922d others(14): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094019
|
C | CATATATA others(7): Show |
1 | a0001c0001t0001g0176 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.453+4909_453+4922d others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094019
|
C | CATATATA others(9): Show |
1 | a0002c0002t0003g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.453+4907_453+4922d others(18): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094019 | ||||||
chrX:75094025
|
T | TATATATA | 1 | a0001c0001t0001g0171 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.453+4910_453+4916d others(9): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094025 | ||||||
chrX:75094036
|
ATATATAT others(11): Show |
A | 1 | a0001c0004t0004g0002 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.453+4888_453+4905d others(20): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094036 | ||||||
chrX:75094038
|
ATATATAT others(9): Show |
A | 50 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(47): Show | 50 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.453+4888_453+4903d others(18): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094038 | ||||||
chrX:75094040
|
ATATATAT others(7): Show |
A | 3 | a0001c0001t0002g0061a0001c0001t0002g0097a0001c0001t0002g0100 | 3 | HG01070.hp1 HG01168.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.453+4888_453+4901d others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094040 | ||||||
chrX:75094044
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0004g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.453+4888_453+4897d others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094044 | ||||||
chrX:75094046
|
ATATATAT others(1): Show |
A | 1 | a0001c0001t0001g0188 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.453+4888_453+4895d others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094046 | ||||||
chrX:75094048
|
ATATATC | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0184a0001c0001t0009g0185 | 3 | HG01070.hp2 HG01071.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.453+4888_453+4893d others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094048 | ||||||
chrX:75094050
|
A | ATATATAT others(9): Show |
1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.453+4891_453+4892i others(18): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094050 | ||||||
chrX:75094050
|
A | C | 1 | a0002c0002t0003g0014 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.453+4892T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094050 | ||||||
chrX:75094050
|
ATATC | A | 10 | a0001c0001t0001g0156a0001c0001t0001g0162a0001c0001t0001g0175others(7): Show | 10 | HG00323.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.453+4888_453+4891d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094050 | ||||||
chrX:75094052
|
ATC | A | 1 | a0001c0001t0001g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.453+4888_453+4889d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094052 | ||||||
chrX:75094054
|
C | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(142): Show | 146 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.453+4888G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094054 | ||||||
chrX:75094056
|
A | ATATATAT others(1): Show |
1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+4885_453+4886i others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094056 | ||||||
chrX:75094116
|
CTTTA | C | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.453+4822_453+4825d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094116 | ||||||
chrX:75094440
|
TG | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+4501delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094440 | ||||||
chrX:75094681
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.453+4261G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094681 | ||||||
chrX:75094796
|
T | TA | 1 | a0001c0001t0004g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.453+4145dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094796 | ||||||
chrX:75094966
|
CT | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3975delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094966 | ||||||
chrX:75094970
|
G | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3972C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094970 | ||||||
chrX:75094971
|
T | A | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3971A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094971 | ||||||
chrX:75094974
|
A | AG | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3967_453+3968i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094974 | ||||||
chrX:75094975
|
C | A | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3967G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094975 | ||||||
chrX:75094978
|
T | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3964A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094978 | ||||||
chrX:75094979
|
G | C | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3963C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094979 | ||||||
chrX:75094981
|
G | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3961C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094981 | ||||||
chrX:75094982
|
C | G | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3960G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094982 | ||||||
chrX:75094984
|
C | T | 1 | a0001c0001t0005g0135 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.453+3958G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75094984 | ||||||
chrX:75095393
|
G | C | 6 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+3549C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095393 | ||||||
chrX:75095403
|
GA | G | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.453+3538delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095403 | ||||||
chrX:75095497
|
G | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+3445C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095497 | ||||||
chrX:75095519
|
CA | C | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+3422delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095519 | ||||||
chrX:75095804
|
GT | G | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+3137delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095804 | ||||||
chrX:75095828
|
TA | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+3113delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095828 | ||||||
chrX:75095865
|
GT | G | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+3076delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095865 | ||||||
chrX:75095914
|
G | GA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+3027dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095914 | ||||||
chrX:75095941
|
T | TC | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+3000dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095941 | ||||||
chrX:75095983
|
A | AT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2958_453+2959i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75095983 | ||||||
chrX:75096029
|
CT | C | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2912delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096029 | ||||||
chrX:75096036
|
T | TA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2905dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096036 | ||||||
chrX:75096051
|
GA | G | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2890delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096051 | ||||||
chrX:75096134
|
CT | C | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.453+2807delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096134 | ||||||
chrX:75096169
|
A | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+2773T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096169 | ||||||
chrX:75096192
|
G | A | 4 | a0002c0002t0003g0010a0002c0002t0003g0013a0002c0002t0003g0016others(1): Show | 4 | HG00738.hp1 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+2750C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096192 | ||||||
chrX:75096198
|
TA | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2743delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096198 | ||||||
chrX:75096254
|
C | CA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2687dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096254 | ||||||
chrX:75096267
|
TG | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2674delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096267 | ||||||
chrX:75096335
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+2607T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096335 | ||||||
chrX:75096349
|
C | G | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2593G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096349 | ||||||
chrX:75096350
|
G | A | 12 | a0001c0001t0001g0001a0001c0001t0001g0140a0001c0001t0001g0141others(9): Show | 13 | NA18945.hp1 NA18952.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.453+2592C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096350 | ||||||
chrX:75096351
|
G | GA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2590_453+2591i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096351 | ||||||
chrX:75096408
|
TG | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2533delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096408 | ||||||
chrX:75096432
|
T | TA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2509dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096432 | ||||||
chrX:75096481
|
G | GA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2460dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096481 | ||||||
chrX:75096521
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.453+2421A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096521 | ||||||
chrX:75096543
|
T | TC | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2398dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096543 | ||||||
chrX:75096667
|
G | GC | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2274dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096667 | ||||||
chrX:75096715
|
C | T | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.453+2227G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096715 | ||||||
chrX:75096732
|
A | AT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2209dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096732 | ||||||
chrX:75096784
|
C | CT | 2 | a0001c0001t0002g0087a0001c0001t0002g0102 | 2 | HG04204.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.453+2157dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096784 | ||||||
chrX:75096784
|
CT | C | 6 | a0001c0001t0002g0068a0001c0003t0006g0220a0001c0003t0006g0221others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.453+2157delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096784 | ||||||
chrX:75096857
|
T | A | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+2085A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096857 | ||||||
chrX:75096901
|
C | A | 3 | a0001c0001t0001g0168a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | NA18955.hp1 NA18990.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.453+2041G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75096901 | ||||||
chrX:75097048
|
A | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(115): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.453+1894T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097048 | ||||||
chrX:75097058
|
TA | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1883delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097058 | ||||||
chrX:75097092
|
CA | C | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1849delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097092 | ||||||
chrX:75097166
|
G | GA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1775dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097166 | ||||||
chrX:75097224
|
C | CT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1717dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097224 | ||||||
chrX:75097237
|
A | AG | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1704dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097237 | ||||||
chrX:75097420
|
C | CG | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1521_453+1522i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097420 | ||||||
chrX:75097456
|
C | CT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1485dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097456 | ||||||
chrX:75097475
|
A | AT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1466dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097475 | ||||||
chrX:75097510
|
GA | G | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1431delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097510 | ||||||
chrX:75097644
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.453+1298A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097644 | ||||||
chrX:75097661
|
G | GT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1280dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097661 | ||||||
chrX:75097691
|
T | TA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1250dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097691 | ||||||
chrX:75097874
|
C | CA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+1067dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097874 | ||||||
chrX:75097949
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.453+993A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097949 | ||||||
chrX:75097995
|
CT | C | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+946delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75097995 | ||||||
chrX:75098025
|
G | A | 2 | a0001c0001t0007g0212a0001c0001t0007g0213 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.453+917C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098025 | ||||||
chrX:75098279
|
A | AT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+662_453+663ins others(1): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098279 | ||||||
chrX:75098283
|
T | TG | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+658dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098283 | ||||||
chrX:75098308
|
C | CA | 3 | a0001c0001t0001g0191a0001c0001t0001g0194a0001c0001t0005g0196 | 3 | HG02027.hp1 HG02132.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.453+633dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098308 | ||||||
chrX:75098308
|
CA | C | 1 | a0001c0001t0005g0146 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.453+633delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098308 | ||||||
chrX:75098309
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.453+633T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098309 | ||||||
chrX:75098476
|
G | GT | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+465dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098476 | ||||||
chrX:75098494
|
T | A | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+448A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098494 | ||||||
chrX:75098575
|
TC | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+366delG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098575 | ||||||
chrX:75098578
|
T | A | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+364A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098578 | ||||||
chrX:75098621
|
T | C | 4 | a0001c0001t0010g0154a0001c0001t0010g0157a0001c0001t0010g0161others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.453+321A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098621 | ||||||
chrX:75098775
|
T | TA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.453+166_453+167ins others(1): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 4/15 | chrX | 75098775 | ||||||
chrX:75099101
|
A | AT | 2 | a0001c0001t0002g0069a0001c0001t0002g0075 | 2 | HG02602.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.334-41dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099101 | ||||||
chrX:75099109
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-48G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099109 | ||||||
chrX:75099197
|
T | TA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.334-137dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099197 | ||||||
chrX:75099248
|
TA | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.334-188delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099248 | ||||||
chrX:75099261
|
C | CA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.334-201dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099261 | ||||||
chrX:75099388
|
C | CAAAA | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.334-331_334-328dup others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099388 | ||||||
chrX:75099433
|
T | C | 3 | a0001c0001t0002g0060a0001c0001t0002g0083a0001c0001t0004g0082 | 3 | HG00140.hp1 HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.334-372A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099433 | ||||||
chrX:75099478
|
T | C | 1 | a0001c0001t0001g0189 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.334-417A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099478 | ||||||
chrX:75099624
|
A | G | 1 | a0001c0003t0012g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.334-563T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099624 | ||||||
chrX:75099892
|
A | C | 1 | a0001c0001t0004g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.334-831T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099892 | ||||||
chrX:75099901
|
T | TA | 2 | a0001c0001t0001g0172a0001c0001t0001g0192 | 2 | NA18970.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.334-841dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099901 | ||||||
chrX:75099901
|
TA | T | 1 | a0001c0001t0001g0209 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.334-841delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099901 | ||||||
chrX:75099997
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0218 | 2 | NA18944.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.334-936G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75099997 | ||||||
chrX:75100017
|
T | C | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.334-956A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75100017 | ||||||
chrX:75100081
|
T | TA | 2 | a0001c0001t0001g0147a0002c0002t0003g0008 | 2 | HG00735.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.334-1021dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75100081 | ||||||
chrX:75100090
|
A | C | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.334-1029T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75100090 | ||||||
chrX:75100329
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.334-1268C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75100329 | ||||||
chrX:75100352
|
T | C | 1 | a0002c0002t0003g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.334-1291A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75100352 | ||||||
chrX:75100514
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.334-1453A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75100514 | ||||||
chrX:75100943
|
A | G | 77 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.334-1882T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75100943 | ||||||
chrX:75101034
|
GA | G | 1 | a0001c0001t0009g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.334-1974delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75101034 | ||||||
chrX:75101084
|
C | CA | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.334-2024dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75101084 | ||||||
chrX:75101377
|
A | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-2316T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75101377 | ||||||
chrX:75101408
|
C | T | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.334-2347G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75101408 | ||||||
chrX:75101546
|
C | T | 1 | a0001c0001t0004g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.334-2485G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75101546 | ||||||
chrX:75101553
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.334-2492C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75101553 | ||||||
chrX:75101572
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-2511T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75101572 | ||||||
chrX:75102165
|
G | A | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.334-3104C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75102165 | ||||||
chrX:75102252
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.334-3191G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75102252 | ||||||
chrX:75102648
|
A | T | 39 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(36): Show | 39 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.334-3587T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75102648 | ||||||
chrX:75102694
|
T | C | 217 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(214): Show | 218 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.334-3633A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75102694 | ||||||
chrX:75102864
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.334-3803C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75102864 | ||||||
chrX:75102868
|
T | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0087 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.334-3807A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75102868 | ||||||
chrX:75102978
|
A | AT | 1 | a0001c0001t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.334-3918dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75102978 | ||||||
chrX:75103335
|
C | T | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.334-4274G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75103335 | ||||||
chrX:75103449
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.334-4388G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75103449 | ||||||
chrX:75103691
|
C | T | 6 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-4630G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75103691 | ||||||
chrX:75103854
|
G | A | 117 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.334-4793C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75103854 | ||||||
chrX:75103892
|
G | T | 4 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(1): Show | 4 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-4831C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75103892 | ||||||
chrX:75103985
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.334-4924A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75103985 | ||||||
chrX:75103998
|
T | C | 2 | a0001c0003t0012g0226a0001c0003t0012g0227 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.334-4937A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75103998 | ||||||
chrX:75104042
|
T | C | 1 | a0001c0001t0007g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.334-4981A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104042 | ||||||
chrX:75104046
|
A | AGTTTTTT others(1): Show |
4 | a0001c0001t0001g0164a0001c0001t0010g0154a0001c0001t0010g0157others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-4993_334-4986d others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104046 | ||||||
chrX:75104047
|
G | GT | 12 | a0001c0001t0001g0199a0001c0001t0002g0066a0001c0001t0002g0079others(9): Show | 12 | HG00639.hp1 HG00735.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.334-4987dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTT | 8 | a0001c0001t0001g0187a0001c0001t0002g0063a0001c0001t0004g0049others(5): Show | 8 | HG00642.hp1 HG01243.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-4988_334-4987d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTT | 5 | a0001c0001t0002g0045a0001c0001t0002g0062a0001c0001t0002g0073others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-4989_334-4987d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTT | 6 | a0001c0001t0001g0153a0001c0001t0002g0093a0001c0001t0004g0099others(3): Show | 6 | HG01975.hp2 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-4990_334-4987d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTT | 1 | a0001c0001t0004g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.334-4991_334-4987d others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTT | 2 | a0001c0001t0002g0061a0001c0001t0016g0217 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.334-4992_334-4987d others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT | 4 | a0001c0001t0001g0032a0001c0001t0001g0034a0001c0001t0001g0041others(1): Show | 4 | HG02165.hp2 NA18984.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-4993_334-4987d others(9): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(2): Show |
2 | a0001c0001t0001g0158a0001c0001t0010g0161 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.334-4987_334-4986i others(11): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(3): Show |
1 | a0003c0005t0001g0003 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.334-4987_334-4986i others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(7): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0162 | 2 | HG00323.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.334-4987_334-4986i others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(9): Show |
2 | a0001c0001t0001g0203a0001c0001t0005g0122 | 2 | HG03516.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.334-4987_334-4986i others(18): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(10): Show |
1 | a0001c0001t0001g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.334-4987_334-4986i others(19): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(11): Show |
1 | a0001c0001t0001g0121 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.334-4987_334-4986i others(20): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(1): Show |
14 | a0001c0001t0001g0120a0001c0001t0001g0126a0001c0001t0001g0133others(11): Show | 14 | HG00408.hp1 HG01081.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.334-4994_334-4987d others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(2): Show |
27 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0029others(24): Show | 28 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.334-4995_334-4987d others(11): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(3): Show |
8 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0118others(5): Show | 8 | HG02129.hp1 HG02559.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.334-4996_334-4987d others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(4): Show |
8 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0040others(5): Show | 8 | HG01168.hp2 HG01169.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-4997_334-4987d others(13): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(5): Show |
4 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0166others(1): Show | 4 | HG01261.hp1 HG01358.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-4998_334-4987d others(14): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(6): Show |
9 | a0001c0001t0001g0039a0001c0001t0001g0170a0001c0001t0001g0172others(6): Show | 9 | HG01167.hp1 HG01169.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.334-4999_334-4987d others(15): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(7): Show |
11 | a0001c0001t0001g0163a0001c0001t0001g0167a0001c0001t0001g0169others(8): Show | 11 | HG01070.hp2 HG01081.hp1 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-5000_334-4987d others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(8): Show |
4 | a0001c0001t0001g0175a0001c0001t0001g0184a0001c0001t0001g0188others(1): Show | 4 | HG01071.hp1 HG03239.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-5001_334-4987d others(17): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(9): Show |
2 | a0001c0001t0001g0139a0001c0001t0002g0090 | 2 | HG01256.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.334-5002_334-4987d others(18): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(10): Show |
3 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0095 | 3 | HG01943.hp1 HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.334-5003_334-4987d others(19): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(11): Show |
4 | a0001c0001t0001g0191a0001c0001t0002g0044a0001c0001t0002g0064others(1): Show | 4 | HG00323.hp2 HG00673.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-5004_334-4987d others(20): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(12): Show |
3 | a0001c0001t0001g0210a0001c0001t0002g0043a0001c0001t0002g0077 | 3 | HG02897.hp1 NA19085.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.334-5005_334-4987d others(21): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(13): Show |
7 | a0001c0001t0001g0186a0001c0001t0002g0060a0001c0001t0002g0074others(4): Show | 7 | HG00140.hp1 HG00408.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.334-5006_334-4987d others(22): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(14): Show |
3 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0004g0082 | 3 | HG02698.hp1 HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.334-5007_334-4987d others(23): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(15): Show |
2 | a0001c0001t0002g0075a0001c0001t0002g0096 | 2 | HG01934.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.334-5008_334-4987d others(24): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(16): Show |
4 | a0001c0001t0002g0065a0001c0001t0002g0069a0001c0001t0002g0094others(1): Show | 4 | HG01928.hp1 HG02145.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-5009_334-4987d others(25): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(17): Show |
2 | a0001c0001t0001g0211a0001c0001t0002g0087 | 2 | HG02040.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.334-5010_334-4987d others(26): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0002g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.334-5011_334-4987d others(27): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(23): Show |
1 | a0001c0001t0004g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.334-5016_334-4987d others(32): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(24): Show |
1 | a0001c0001t0002g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.334-5017_334-4987d others(33): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(26): Show |
1 | a0001c0001t0002g0059 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.334-5019_334-4987d others(35): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
G | GTTTTTTT others(27): Show |
1 | a0001c0001t0002g0100 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.334-5020_334-4987d others(36): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GT | G | 5 | a0001c0001t0001g0152a0001c0001t0004g0052a0001c0001t0004g0054others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-4987delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTT | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0125a0001c0001t0002g0071others(2): Show | 5 | HG01258.hp1 HG01993.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.334-4988_334-4987d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTT | G | 2 | a0001c0001t0001g0206a0001c0001t0002g0072 | 2 | HG02523.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.334-4989_334-4987d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTT | G | 3 | a0001c0001t0001g0209a0001c0001t0002g0088a0001c0001t0004g0078 | 3 | HG01433.hp1 HG03688.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.334-4990_334-4987d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTT | G | 8 | a0001c0001t0001g0031a0001c0001t0002g0051a0001c0001t0002g0056others(5): Show | 8 | HG01099.hp1 HG01192.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-4991_334-4987d others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTT | G | 2 | a0001c0001t0001g0193a0001c0001t0002g0084 | 2 | HG01106.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.334-4992_334-4987d others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT | G | 1 | a0001c0001t0002g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.334-4993_334-4987d others(9): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT others(1): Show |
G | 1 | a0001c0001t0002g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.334-4994_334-4987d others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0001g0117 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.334-5000_334-4987d others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT others(9): Show |
G | 2 | a0001c0001t0001g0022a0001c0001t0001g0026 | 2 | HG00621.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.334-5002_334-4987d others(18): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT others(11): Show |
G | 2 | a0001c0001t0001g0129a0001c0001t0014g0160 | 2 | HG02615.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.334-5004_334-4987d others(20): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT others(12): Show |
G | 1 | a0001c0001t0014g0159 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.334-5005_334-4987d others(21): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT others(13): Show |
G | 1 | a0001c0003t0006g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.334-5006_334-4987d others(22): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104047
|
GTTTTTTT others(14): Show |
G | 8 | a0001c0003t0006g0220a0001c0003t0006g0222a0001c0003t0006g0223others(5): Show | 8 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.334-5007_334-4987d others(23): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104047 | ||||||
chrX:75104048
|
T | TTTTTTTG | 3 | a0001c0001t0001g0156a0001c0001t0009g0151a0001c0001t0020g0155 | 3 | HG02451.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.334-4988_334-4987i others(9): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104048 | ||||||
chrX:75104109
|
C | G | 4 | a0001c0001t0002g0059a0001c0001t0002g0071a0001c0001t0002g0072others(1): Show | 4 | HG00408.hp2 HG02165.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-5048G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104109 | ||||||
chrX:75104477
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.334-5416G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104477 | ||||||
chrX:75104522
|
CAAT | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG02040.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.334-5464_334-5462d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104522 | ||||||
chrX:75104575
|
A | C | 12 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0150others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.334-5514T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104575 | ||||||
chrX:75104976
|
T | C | 1 | a0001c0001t0007g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.334-5915A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75104976 | ||||||
chrX:75105111
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.334-6050A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75105111 | ||||||
chrX:75105593
|
T | C | 1 | a0001c0001t0005g0196 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.334-6532A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75105593 | ||||||
chrX:75105796
|
T | C | 1 | a0001c0001t0007g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.334-6735A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75105796 | ||||||
chrX:75105952
|
C | A | 6 | a0001c0001t0008g0048a0001c0001t0008g0104a0001c0001t0008g0105others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.334-6891G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75105952 | ||||||
chrX:75105970
|
CT | C | 1 | a0001c0001t0001g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.334-6910delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75105970 | ||||||
chrX:75106128
|
A | C | 1 | a0001c0001t0011g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.333+6758T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75106128 | ||||||
chrX:75106149
|
ATAAT | A | 1 | a0001c0001t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.333+6733_333+6736d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75106149 | ||||||
chrX:75106160
|
A | T | 1 | a0001c0001t0002g0059 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.333+6726T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75106160 | ||||||
chrX:75106294
|
C | T | 14 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0150others(11): Show | 14 | HG00323.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.333+6592G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75106294 | ||||||
chrX:75106566
|
C | T | 123 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.333+6320G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75106566 | ||||||
chrX:75106810
|
C | T | 2 | a0001c0001t0013g0230a0001c0001t0013g0231 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.333+6076G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75106810 | ||||||
chrX:75107851
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0042others(1): Show | 4 | NA18612.hp1 NA18747.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+5035C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75107851 | ||||||
chrX:75107911
|
T | G | 2 | a0001c0001t0007g0212a0001c0001t0007g0213 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.333+4975A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75107911 | ||||||
chrX:75107912
|
AG | A | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.333+4973delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75107912 | ||||||
chrX:75108017
|
C | G | 1 | a0001c0001t0001g0182 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.333+4869G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108017 | ||||||
chrX:75108078
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.333+4808A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108078 | ||||||
chrX:75108082
|
G | A | 2 | a0001c0001t0007g0212a0001c0001t0007g0213 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.333+4804C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108082 | ||||||
chrX:75108108
|
C | T | 5 | a0001c0001t0002g0062a0001c0001t0002g0073a0001c0001t0002g0079others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.333+4778G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108108 | ||||||
chrX:75108114
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+4772A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108114 | ||||||
chrX:75108581
|
G | GA | 19 | a0001c0001t0001g0162a0001c0001t0001g0181a0001c0001t0001g0203others(16): Show | 19 | HG00323.hp1 HG01081.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.333+4304dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108581 | ||||||
chrX:75108581
|
G | GAA | 2 | a0001c0003t0012g0225a0001c0003t0012g0227 | 2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.333+4303_333+4304d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108581 | ||||||
chrX:75108581
|
G | GAAA | 1 | a0001c0003t0012g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.333+4302_333+4304d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108581 | ||||||
chrX:75108581
|
GA | G | 3 | a0001c0001t0001g0168a0001c0001t0002g0047a0001c0001t0023g0114 | 3 | HG03579.hp1 HG04199.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.333+4304delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108581 | ||||||
chrX:75108595
|
A | C | 1 | a0001c0001t0002g0100 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.333+4291T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108595 | ||||||
chrX:75108596
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.333+4290G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108596 | ||||||
chrX:75108748
|
A | AG | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.333+4137dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108748 | ||||||
chrX:75108839
|
T | C | 2 | a0002c0002t0003g0008a0002c0002t0003g0011 | 2 | HG00735.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.333+4047A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75108839 | ||||||
chrX:75109055
|
C | T | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.333+3831G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75109055 | ||||||
chrX:75109176
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+3710A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75109176 | ||||||
chrX:75109240
|
G | A | 4 | a0001c0001t0010g0154a0001c0001t0010g0157a0001c0001t0010g0161others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.333+3646C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75109240 | ||||||
chrX:75109429
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+3457G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75109429 | ||||||
chrX:75110260
|
CA | C | 1 | a0001c0001t0009g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.333+2625delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75110260 | ||||||
chrX:75110273
|
AT | A | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.333+2612delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75110273 | ||||||
chrX:75110461
|
T | C | 77 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.333+2425A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75110461 | ||||||
chrX:75110768
|
TG | T | 2 | a0001c0001t0001g0180a0001c0001t0009g0036 | 2 | NA19072.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.333+2117delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75110768 | ||||||
chrX:75111016
|
TG | T | 1 | a0001c0001t0009g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.333+1869delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111016 | ||||||
chrX:75111049
|
AG | A | 1 | a0001c0001t0009g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.333+1836delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111049 | ||||||
chrX:75111053
|
GT | G | 59 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.333+1832delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111053 | ||||||
chrX:75111107
|
CA | C | 1 | a0001c0001t0009g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.333+1778delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111107 | ||||||
chrX:75111161
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.333+1725C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111161 | ||||||
chrX:75111164
|
A | ACC | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.333+1721_333+1722i others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111164 | ||||||
chrX:75111165
|
C | A | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.333+1721G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111165 | ||||||
chrX:75111249
|
TC | T | 1 | a0001c0001t0009g0036 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.333+1636delG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111249 | ||||||
chrX:75111442
|
C | A | 1 | a0001c0001t0002g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.333+1444G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111442 | ||||||
chrX:75111443
|
C | G | 1 | a0001c0001t0002g0072 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.333+1443G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111443 | ||||||
chrX:75111601
|
C | CTATT | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.333+1281_333+1284d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111601 | ||||||
chrX:75111899
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.333+987C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111899 | ||||||
chrX:75111901
|
C | T | 1 | a0004c0007t0005g0174 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.333+985G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75111901 | ||||||
chrX:75112553
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | NA18965.hp1 NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.333+333G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75112553 | ||||||
chrX:75112712
|
C | T | 1 | a0001c0003t0012g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.333+174G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75112712 | ||||||
chrX:75112750
|
G | GT | 180 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(177): Show | 181 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.333+135dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 3/15 | chrX | 75112750 | ||||||
chrX:75113964
|
C | T | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+790G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 2/15 | chrX | 75113964 | ||||||
chrX:75114222
|
T | A | 2 | a0001c0003t0006g0221a0001c0003t0006g0223 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.246+532A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 2/15 | chrX | 75114222 | ||||||
chrX:75114249
|
T | C | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+505A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 2/15 | chrX | 75114249 | ||||||
chrX:75114309
|
T | C | 1 | a0002c0002t0003g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.246+445A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 2/15 | chrX | 75114309 | ||||||
chrX:75114581
|
A | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+173T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 2/15 | chrX | 75114581 | ||||||
chrX:75114852
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.169-21A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75114852 | ||||||
chrX:75114945
|
AGAT | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-117_169-115del others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75114945 | ||||||
chrX:75114994
|
G | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | NA18965.hp1 NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.169-163C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75114994 | ||||||
chrX:75115019
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0042others(2): Show | 5 | NA18612.hp1 NA18747.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-188A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115019 | ||||||
chrX:75115020
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0042others(2): Show | 5 | NA18612.hp1 NA18747.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-189C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115020 | ||||||
chrX:75115040
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | NA18965.hp1 NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.169-209G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115040 | ||||||
chrX:75115044
|
C | A | 1 | a0001c0001t0011g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.169-213G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115044 | ||||||
chrX:75115058
|
T | A | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.169-227A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115058 | ||||||
chrX:75115145
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.169-314C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115145 | ||||||
chrX:75115181
|
T | A | 1 | a0001c0001t0013g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.169-350A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115181 | ||||||
chrX:75115197
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.169-366C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115197 | ||||||
chrX:75115266
|
C | CA | 103 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(100): Show | 103 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.169-436dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
C | CAA | 19 | a0001c0001t0001g0032a0001c0001t0001g0118a0001c0001t0001g0129others(16): Show | 19 | HG01106.hp1 HG01934.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-437_169-436dup others(2): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
C | CAAA | 7 | a0001c0001t0001g0120a0001c0001t0001g0171a0001c0001t0002g0110others(4): Show | 7 | HG01243.hp1 HG02896.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-438_169-436dup others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
C | CAAAA | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.169-439_169-436dup others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
C | CAAAAA | 2 | a0001c0001t0004g0099a0001c0001t0004g0111 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.169-440_169-436dup others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
C | CAAAAAA | 3 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0024g0116 | 3 | HG02109.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.169-441_169-436dup others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
C | CAAAAAAA | 4 | a0001c0001t0013g0230a0001c0001t0013g0231a0001c0001t0014g0159others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-442_169-436dup others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
CA | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0034others(8): Show | 11 | HG01884.hp2 HG02523.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-436delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
CAA | C | 1 | a0001c0003t0012g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.169-437_169-436del others(2): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
CAAA | C | 2 | a0001c0003t0012g0225a0001c0003t0012g0226 | 2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.169-438_169-436del others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0057 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.169-445_169-436del others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0210 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.169-446_169-436del others(11): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0002g0070a0001c0001t0002g0080 | 2 | HG01192.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.169-447_169-436del others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115266
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0004g0108a0001c0001t0004g0109 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.169-451_169-436del others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115266 | ||||||
chrX:75115290
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.169-469_169-460del others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115290 | ||||||
chrX:75115299
|
A | AT | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.169-469dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115299 | ||||||
chrX:75115300
|
T | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0229 | 2 | HG03491.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.169-469A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115300 | ||||||
chrX:75115341
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-510A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115341 | ||||||
chrX:75115410
|
C | CT | 58 | a0001c0001t0001g0022a0001c0001t0001g0039a0001c0001t0001g0124others(55): Show | 58 | HG00621.hp1 HG00642.hp1 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.169-580dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115410 | ||||||
chrX:75115410
|
C | CTT | 13 | a0001c0001t0002g0068a0001c0001t0002g0084a0001c0001t0016g0217others(10): Show | 13 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.169-581_169-580dup others(2): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115410 | ||||||
chrX:75115410
|
C | CTTT | 5 | a0001c0001t0014g0160a0001c0003t0006g0221a0001c0003t0006g0224others(2): Show | 5 | HG02559.hp2 HG02572.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-582_169-580dup others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115410 | ||||||
chrX:75115410
|
C | CTTTT | 1 | a0001c0001t0002g0081 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.169-583_169-580dup others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115410 | ||||||
chrX:75115410
|
CT | C | 9 | a0001c0001t0001g0134a0001c0001t0002g0090a0001c0001t0004g0067others(6): Show | 9 | HG01168.hp2 HG01256.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-580delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115410 | ||||||
chrX:75115410
|
CTTTTTTT | C | 1 | a0001c0001t0002g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.169-586_169-580del others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115410 | ||||||
chrX:75115420
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.169-589A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115420 | ||||||
chrX:75115580
|
C | T | 6 | a0001c0001t0002g0110a0001c0001t0004g0108a0001c0001t0004g0109others(3): Show | 6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-749G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115580 | ||||||
chrX:75115786
|
T | TG | 10 | a0001c0001t0001g0138a0001c0001t0001g0192a0001c0001t0002g0056others(7): Show | 10 | HG01192.hp1 HG01515.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-956dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115786 | ||||||
chrX:75115786
|
TG | T | 13 | a0001c0001t0008g0048a0001c0001t0008g0104a0001c0001t0008g0105others(10): Show | 13 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.169-956delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115786 | ||||||
chrX:75115797
|
G | C | 7 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092others(4): Show | 7 | HG01256.hp1 HG01928.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-966C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115797 | ||||||
chrX:75115874
|
T | G | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169-1043A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115874 | ||||||
chrX:75115994
|
T | C | 1 | a0001c0001t0004g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-1163A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75115994 | ||||||
chrX:75116063
|
T | C | 1 | a0001c0001t0024g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.169-1232A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75116063 | ||||||
chrX:75116171
|
C | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(95): Show | 99 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.169-1340G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75116171 | ||||||
chrX:75116254
|
A | G | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.169-1423T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75116254 | ||||||
chrX:75116654
|
T | C | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-1823A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75116654 | ||||||
chrX:75116663
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 8 | NA18945.hp1 NA18953.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.169-1832C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75116663 | ||||||
chrX:75117090
|
C | A | 6 | a0001c0001t0002g0110a0001c0001t0004g0108a0001c0001t0004g0109others(3): Show | 6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-2259G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117090 | ||||||
chrX:75117129
|
G | T | 1 | a0001c0001t0008g0107 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.169-2298C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117129 | ||||||
chrX:75117311
|
C | T | 1 | a0002c0002t0003g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.169-2480G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117311 | ||||||
chrX:75117317
|
GACTAT | G | 2 | a0001c0001t0004g0049a0001c0001t0004g0050 | 2 | HG02109.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.169-2491_169-2487d others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117317 | ||||||
chrX:75117436
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-2605T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117436 | ||||||
chrX:75117437
|
G | A | 77 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.169-2606C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117437 | ||||||
chrX:75117503
|
A | G | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169-2672T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117503 | ||||||
chrX:75117617
|
T | A | 1 | a0001c0001t0002g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.169-2786A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75117617 | ||||||
chrX:75118168
|
T | C | 1 | a0002c0002t0003g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.169-3337A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75118168 | ||||||
chrX:75118398
|
C | CT | 6 | a0001c0001t0002g0098a0001c0001t0002g0115a0001c0001t0004g0049others(3): Show | 6 | HG01074.hp1 HG02015.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-3568dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75118398 | ||||||
chrX:75118398
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG01975.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.169-3567G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75118398 | ||||||
chrX:75118398
|
CT | C | 1 | a0001c0001t0009g0151 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.169-3568delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75118398 | ||||||
chrX:75118558
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.169-3727C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75118558 | ||||||
chrX:75118561
|
G | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-3730C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75118561 | ||||||
chrX:75118785
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | NA18971.hp1 NA19005.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.169-3954G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75118785 | ||||||
chrX:75119022
|
G | A | 1 | a0002c0002t0003g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.169-4191C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119022 | ||||||
chrX:75119064
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.169-4233C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119064 | ||||||
chrX:75119236
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169-4405T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119236 | ||||||
chrX:75119276
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169-4445C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119276 | ||||||
chrX:75119333
|
G | T | 6 | a0001c0001t0002g0110a0001c0001t0004g0108a0001c0001t0004g0109others(3): Show | 6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-4502C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119333 | ||||||
chrX:75119555
|
C | T | 1 | a0002c0002t0003g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.169-4724G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119555 | ||||||
chrX:75119643
|
T | C | 1 | a0002c0002t0003g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-4812A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119643 | ||||||
chrX:75119713
|
T | A | 1 | a0001c0001t0005g0122 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.169-4882A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119713 | ||||||
chrX:75119749
|
G | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.169-4918C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119749 | ||||||
chrX:75119760
|
C | T | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.169-4929G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75119760 | ||||||
chrX:75120058
|
T | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-5227A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120058 | ||||||
chrX:75120291
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169-5460A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120291 | ||||||
chrX:75120426
|
TG | T | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169-5596delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120426 | ||||||
chrX:75120466
|
G | A | 77 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.169-5635C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120466 | ||||||
chrX:75120549
|
C | G | 1 | a0001c0001t0001g0163 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.169-5718G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120549 | ||||||
chrX:75120603
|
A | AAAAT | 123 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.169-5776_169-5773d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120603 | ||||||
chrX:75120628
|
A | G | 59 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-5797T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120628 | ||||||
chrX:75120633
|
CTG | C | 1 | a0001c0001t0001g0125 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.169-5804_169-5803d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120633 | ||||||
chrX:75120786
|
C | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-5955G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120786 | ||||||
chrX:75120829
|
G | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-5998C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120829 | ||||||
chrX:75120830
|
C | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-5999G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120830 | ||||||
chrX:75120901
|
G | T | 3 | a0001c0001t0002g0063a0001c0001t0002g0066a0001c0001t0004g0067 | 3 | HG00639.hp1 HG00642.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.169-6070C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75120901 | ||||||
chrX:75121186
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.169-6355C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75121186 | ||||||
chrX:75121288
|
C | CA | 2 | a0001c0001t0001g0022a0001c0001t0001g0158 | 2 | HG00621.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.169-6458dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75121288 | ||||||
chrX:75121288
|
CA | C | 10 | a0001c0001t0011g0023a0001c0003t0006g0220a0001c0003t0006g0221others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-6458delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75121288 | ||||||
chrX:75121412
|
A | C | 1 | a0001c0001t0002g0102 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.169-6581T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75121412 | ||||||
chrX:75121524
|
C | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-6693G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75121524 | ||||||
chrX:75121774
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.169-6943C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75121774 | ||||||
chrX:75122327
|
G | A | 4 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(1): Show | 4 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-7496C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122327 | ||||||
chrX:75122401
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0011g0023 | 3 | NA18983.hp1 NA18985.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.169-7570A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122401 | ||||||
chrX:75122442
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.169-7611G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122442 | ||||||
chrX:75122582
|
T | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-7751A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122582 | ||||||
chrX:75122859
|
G | GGTGTGT | 2 | a0001c0001t0017g0086a0005c0008t0017g0085 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.169-8029_169-8028i others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122859 | ||||||
chrX:75122861
|
G | GGT | 8 | a0001c0001t0002g0081a0001c0001t0014g0159a0001c0001t0014g0160others(5): Show | 8 | HG02615.hp1 HG02886.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-8032_169-8031d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGT | 5 | a0001c0001t0002g0110a0001c0001t0004g0108a0001c0001t0004g0109others(2): Show | 5 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-8034_169-8031d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGT | 53 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0001t0002g0051others(50): Show | 53 | HG00408.hp2 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.169-8036_169-8031d others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(1): Show |
15 | a0001c0001t0001g0144a0001c0001t0001g0218a0001c0001t0002g0043others(12): Show | 15 | HG00323.hp2 HG00642.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.169-8038_169-8031d others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(3): Show |
15 | a0001c0001t0001g0001a0001c0001t0001g0118a0001c0001t0001g0120others(12): Show | 16 | HG01081.hp2 HG01109.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.169-8040_169-8031d others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(5): Show |
29 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0119others(26): Show | 29 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.169-8042_169-8031d others(14): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(7): Show |
21 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0117others(18): Show | 21 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.169-8044_169-8031d others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(9): Show |
17 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0123others(14): Show | 17 | HG00609.hp1 HG01261.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.169-8046_169-8031d others(18): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(11): Show |
19 | a0001c0001t0001g0025a0001c0001t0001g0029a0001c0001t0001g0030others(16): Show | 19 | HG00639.hp2 HG01258.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.169-8048_169-8031d others(20): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(13): Show |
12 | a0001c0001t0001g0028a0001c0001t0001g0041a0001c0001t0001g0121others(9): Show | 12 | HG02074.hp1 HG02135.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-8050_169-8031d others(22): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(15): Show |
2 | a0001c0001t0001g0042a0001c0001t0001g0168 | 2 | NA18955.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.169-8052_169-8031d others(24): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(17): Show |
2 | a0001c0001t0001g0040a0001c0001t0011g0023 | 2 | NA18983.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.169-8054_169-8031d others(26): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GGTGTGTG others(19): Show |
1 | a0001c0001t0009g0027 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.169-8056_169-8031d others(28): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GTGTGTGT others(6): Show |
3 | a0001c0001t0001g0032a0001c0001t0001g0164a0001c0001t0001g0208 | 3 | HG01975.hp1 HG03041.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.169-8031_169-8030i others(15): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169-8031_169-8030i others(17): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | GTGTGTGT others(10): Show |
1 | a0001c0001t0015g0037 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.169-8031_169-8030i others(19): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
G | T | 2 | a0001c0001t0017g0086a0005c0008t0017g0085 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.169-8030C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
GGT | G | 11 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(8): Show | 11 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-8032_169-8031d others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
GGTGT | G | 1 | a0002c0002t0003g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169-8034_169-8031d others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75122861
|
GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0002g0060a0001c0001t0002g0083a0001c0001t0004g0082 | 3 | HG00140.hp1 HG02698.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.169-8038_169-8031d others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75122861 | ||||||
chrX:75123168
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169-8337A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75123168 | ||||||
chrX:75123239
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-8408A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75123239 | ||||||
chrX:75123757
|
TC | T | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169-8927delG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75123757 | ||||||
chrX:75123785
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169-8954C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75123785 | ||||||
chrX:75123799
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.169-8968C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75123799 | ||||||
chrX:75123940
|
G | A | 1 | a0001c0003t0012g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-9109C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75123940 | ||||||
chrX:75124268
|
T | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-9437A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75124268 | ||||||
chrX:75124294
|
T | A | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-9463A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75124294 | ||||||
chrX:75124301
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.169-9470A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75124301 | ||||||
chrX:75124386
|
A | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-9555T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75124386 | ||||||
chrX:75124457
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.169-9626A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75124457 | ||||||
chrX:75124652
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.169-9821C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75124652 | ||||||
chrX:75124967
|
G | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-10136C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75124967 | ||||||
chrX:75125294
|
C | A | 1 | a0001c0001t0021g0149 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.169-10463G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125294 | ||||||
chrX:75125305
|
T | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0087 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.169-10474A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125305 | ||||||
chrX:75125311
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.169-10480A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125311 | ||||||
chrX:75125502
|
A | G | 3 | a0001c0001t0001g0167a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | NA18971.hp1 NA19005.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.169-10671T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125502 | ||||||
chrX:75125658
|
G | A | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-10827C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125658 | ||||||
chrX:75125758
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.169-10927A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125758 | ||||||
chrX:75125776
|
CAATTG | C | 6 | a0001c0001t0008g0048a0001c0001t0008g0104a0001c0001t0008g0105others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-10950_169-1094 others(9): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125776 | ||||||
chrX:75125846
|
TC | T | 1 | a0001c0001t0002g0062 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.169-11016delG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125846 | ||||||
chrX:75125870
|
C | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-11039G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125870 | ||||||
chrX:75125914
|
T | C | 1 | a0001c0001t0005g0146 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.169-11083A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125914 | ||||||
chrX:75125970
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.169-11139G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75125970 | ||||||
chrX:75126103
|
T | C | 59 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-11272A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126103 | ||||||
chrX:75126159
|
G | A | 217 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(214): Show | 218 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.169-11328C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126159 | ||||||
chrX:75126185
|
C | T | 5 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.169-11354G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126185 | ||||||
chrX:75126252
|
A | G | 1 | a0001c0001t0004g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-11421T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126252 | ||||||
chrX:75126422
|
T | A | 4 | a0001c0001t0004g0052a0001c0001t0004g0053a0001c0001t0004g0054others(1): Show | 4 | HG02280.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-11591A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126422 | ||||||
chrX:75126553
|
T | A | 1 | a0001c0001t0002g0057 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.169-11722A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126553 | ||||||
chrX:75126763
|
G | A | 1 | a0001c0003t0012g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-11932C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126763 | ||||||
chrX:75126990
|
C | A | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.169-12159G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75126990 | ||||||
chrX:75127506
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-12675A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75127506 | ||||||
chrX:75127568
|
G | A | 2 | a0001c0003t0012g0226a0001c0003t0012g0227 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.169-12737C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75127568 | ||||||
chrX:75127717
|
G | A | 18 | a0001c0001t0002g0110a0001c0001t0004g0049a0001c0001t0004g0050others(15): Show | 18 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.169-12886C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75127717 | ||||||
chrX:75127756
|
T | C | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.169-12925A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75127756 | ||||||
chrX:75128084
|
A | G | 1 | a0001c0001t0001g0024 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.169-13253T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75128084 | ||||||
chrX:75128133
|
A | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0153a0003c0005t0001g0003 | 3 | HG02258.hp1 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.169-13302T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75128133 | ||||||
chrX:75128162
|
A | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-13331T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75128162 | ||||||
chrX:75128764
|
C | T | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-13933G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75128764 | ||||||
chrX:75129130
|
T | C | 13 | a0001c0001t0002g0110a0001c0001t0004g0049a0001c0001t0004g0050others(10): Show | 13 | HG01243.hp1 HG02015.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.169-14299A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129130 | ||||||
chrX:75129266
|
A | G | 1 | a0001c0001t0025g0103 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.169-14435T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129266 | ||||||
chrX:75129377
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-14546A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129377 | ||||||
chrX:75129434
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.169-14603A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129434 | ||||||
chrX:75129528
|
T | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.169-14697A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129528 | ||||||
chrX:75129606
|
A | AAT | 1 | a0001c0003t0012g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.169-14777_169-1477 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129606 | ||||||
chrX:75129606
|
AAT | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.169-14777_169-1477 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129606 | ||||||
chrX:75129623
|
T | A | 1 | a0001c0001t0002g0061 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.169-14792A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129623 | ||||||
chrX:75129708
|
A | G | 1 | a0001c0001t0013g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.169-14877T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75129708 | ||||||
chrX:75130052
|
A | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-15221T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75130052 | ||||||
chrX:75130248
|
A | C | 1 | a0001c0001t0009g0151 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.169-15417T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75130248 | ||||||
chrX:75130491
|
G | A | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.169-15660C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75130491 | ||||||
chrX:75130532
|
G | T | 1 | a0002c0002t0003g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.169-15701C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75130532 | ||||||
chrX:75130974
|
A | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-16143T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75130974 | ||||||
chrX:75131086
|
C | CA | 1 | a0001c0001t0001g0194 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.169-16256dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75131086 | ||||||
chrX:75131354
|
G | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-16523C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75131354 | ||||||
chrX:75131530
|
G | A | 1 | a0002c0002t0003g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.169-16699C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75131530 | ||||||
chrX:75131760
|
C | A | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.169-16929G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75131760 | ||||||
chrX:75131981
|
C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.169-17150G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75131981 | ||||||
chrX:75132010
|
A | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.169-17179T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75132010 | ||||||
chrX:75132247
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.169-17416T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75132247 | ||||||
chrX:75132859
|
G | A | 1 | a0001c0003t0012g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-18028C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75132859 | ||||||
chrX:75132898
|
C | T | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.169-18067G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75132898 | ||||||
chrX:75133216
|
C | G | 1 | a0001c0001t0001g0026 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.169-18385G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75133216 | ||||||
chrX:75133355
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.169-18524A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75133355 | ||||||
chrX:75133535
|
AT | A | 1 | a0001c0001t0001g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.169-18705delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75133535 | ||||||
chrX:75133732
|
A | G | 1 | a0001c0001t0011g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.169-18901T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75133732 | ||||||
chrX:75133739
|
G | A | 2 | a0001c0001t0017g0086a0005c0008t0017g0085 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.169-18908C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75133739 | ||||||
chrX:75134266
|
A | G | 6 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0013g0230others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-19435T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75134266 | ||||||
chrX:75134331
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.169-19500A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75134331 | ||||||
chrX:75134847
|
A | T | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.169-20016T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75134847 | ||||||
chrX:75135150
|
A | AC | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.169-20320dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135150 | ||||||
chrX:75135312
|
C | CA | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.169-20482dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135312 | ||||||
chrX:75135369
|
A | AT | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.169-20539dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135369 | ||||||
chrX:75135432
|
C | CAA | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.169-20603_169-2060 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135432 | ||||||
chrX:75135481
|
G | A | 11 | a0001c0001t0016g0216a0001c0001t0016g0217a0001c0003t0006g0220others(8): Show | 11 | HG01109.hp1 HG01884.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.168+20624C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135481 | ||||||
chrX:75135496
|
C | CA | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20608dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135496 | ||||||
chrX:75135766
|
A | AC | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20338dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135766 | ||||||
chrX:75135782
|
C | CT | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20322dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135782 | ||||||
chrX:75135807
|
A | AC | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20297dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135807 | ||||||
chrX:75135829
|
C | CT | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20275dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135829 | ||||||
chrX:75135883
|
TG | T | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20221delC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135883 | ||||||
chrX:75135964
|
T | TG | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20140dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135964 | ||||||
chrX:75135995
|
GA | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+20109delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75135995 | ||||||
chrX:75136104
|
C | CT | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+20000_168+2000 others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136104 | ||||||
chrX:75136130
|
T | TA | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19974dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136130 | ||||||
chrX:75136200
|
T | C | 1 | a0001c0001t0011g0148 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.168+19905A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136200 | ||||||
chrX:75136360
|
G | GA | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19744dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136360 | ||||||
chrX:75136378
|
A | AT | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19726dupA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136378 | ||||||
chrX:75136529
|
C | A | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.168+19576G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136529 | ||||||
chrX:75136597
|
C | CTGGAGGC others(1): Show |
9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+19500_168+1950 others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136597 | ||||||
chrX:75136811
|
T | TG | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19293dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136811 | ||||||
chrX:75136814
|
T | TG | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19290dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136814 | ||||||
chrX:75136850
|
T | TG | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19254dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136850 | ||||||
chrX:75136866
|
A | AC | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19238dupG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136866 | ||||||
chrX:75136909
|
G | A | 1 | a0001c0001t0005g0196 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.168+19196C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136909 | ||||||
chrX:75136964
|
T | TG | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19140dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136964 | ||||||
chrX:75136986
|
G | A | 1 | a0001c0001t0021g0149 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.168+19119C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75136986 | ||||||
chrX:75137032
|
T | TG | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+19072dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137032 | ||||||
chrX:75137091
|
T | C | 1 | a0001c0001t0002g0087 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.168+19014A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137091 | ||||||
chrX:75137107
|
T | TG | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+18997dupC | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137107 | ||||||
chrX:75137478
|
T | C | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.168+18627A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137478 | ||||||
chrX:75137620
|
T | C | 6 | a0001c0001t0002g0110a0001c0001t0004g0108a0001c0001t0004g0109others(3): Show | 6 | HG02015.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+18485A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137620 | ||||||
chrX:75137646
|
T | C | 1 | a0001c0003t0006g0220 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.168+18459A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137646 | ||||||
chrX:75137767
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+18338C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137767 | ||||||
chrX:75137852
|
T | C | 2 | a0001c0001t0010g0157a0001c0001t0010g0161 | 2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.168+18253A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137852 | ||||||
chrX:75137970
|
T | A | 6 | a0001c0001t0008g0048a0001c0001t0008g0104a0001c0001t0008g0105others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+18135A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75137970 | ||||||
chrX:75138223
|
T | TAC | 2 | a0001c0003t0012g0226a0002c0002t0003g0008 | 2 | HG00735.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.168+17880_168+1788 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138223 | ||||||
chrX:75138223
|
T | TACACAC | 4 | a0001c0003t0006g0221a0001c0003t0006g0222a0001c0003t0006g0223others(1): Show | 4 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+17876_168+1788 others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138223 | ||||||
chrX:75138223
|
TAC | T | 9 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0004g0049others(6): Show | 9 | HG01081.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+17880_168+1788 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138223 | ||||||
chrX:75138223
|
TACAC | T | 76 | a0001c0001t0001g0162a0001c0001t0002g0043a0001c0001t0002g0044others(73): Show | 76 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.168+17878_168+1788 others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138223 | ||||||
chrX:75138223
|
TACACAC | T | 8 | a0001c0001t0001g0035a0001c0001t0001g0120a0001c0001t0004g0111others(5): Show | 8 | HG02129.hp1 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+17876_168+1788 others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138223 | ||||||
chrX:75138223
|
TACACACA others(1): Show |
T | 115 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(112): Show | 116 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.168+17874_168+1788 others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138223 | ||||||
chrX:75138223
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0127 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.168+17872_168+1788 others(14): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138223 | ||||||
chrX:75138272
|
GA | G | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.168+17832delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138272 | ||||||
chrX:75138343
|
T | C | 1 | a0001c0001t0011g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.168+17762A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138343 | ||||||
chrX:75138409
|
T | C | 6 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+17696A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138409 | ||||||
chrX:75138813
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+17292A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138813 | ||||||
chrX:75138900
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.168+17205G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75138900 | ||||||
chrX:75139006
|
C | CAA | 2 | a0001c0003t0012g0226a0001c0003t0012g0227 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+17097_168+1709 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75139006 | ||||||
chrX:75139006
|
C | CAAA | 1 | a0001c0003t0012g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168+17096_168+1709 others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75139006 | ||||||
chrX:75139006
|
CA | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(180): Show | 184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.168+17098delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75139006 | ||||||
chrX:75139006
|
CAA | C | 3 | a0001c0001t0001g0025a0001c0001t0001g0039a0001c0001t0002g0061 | 3 | HG01168.hp1 HG01258.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.168+17097_168+1709 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75139006 | ||||||
chrX:75139168
|
C | G | 59 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.168+16937G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75139168 | ||||||
chrX:75139854
|
G | A | 10 | a0001c0001t0001g0164a0001c0003t0006g0220a0001c0003t0006g0221others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+16251C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75139854 | ||||||
chrX:75140025
|
A | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(120): Show | 124 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.168+16080T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140025 | ||||||
chrX:75140250
|
T | C | 1 | a0001c0001t0013g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.168+15855A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140250 | ||||||
chrX:75140297
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.168+15808C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140297 | ||||||
chrX:75140517
|
T | A | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.168+15588A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140517 | ||||||
chrX:75140530
|
A | AAAGAGAT others(164): Show |
6 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+15574_168+1557 others(175): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140530 | ||||||
chrX:75140530
|
A | AAAGAGAT others(185): Show |
2 | a0001c0003t0012g0225a0001c0003t0012g0227 | 2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.168+15574_168+1557 others(196): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140530 | ||||||
chrX:75140530
|
A | AAAGAGAT others(186): Show |
1 | a0001c0003t0012g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.168+15574_168+1557 others(197): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140530 | ||||||
chrX:75140987
|
CA | C | 1 | a0001c0001t0001g0025 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.168+15117delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75140987 | ||||||
chrX:75141084
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.168+15021A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141084 | ||||||
chrX:75141131
|
T | G | 77 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.168+14974A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141131 | ||||||
chrX:75141251
|
C | T | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.168+14854G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141251 | ||||||
chrX:75141352
|
C | T | 6 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(3): Show | 6 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+14753G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141352 | ||||||
chrX:75141404
|
T | G | 1 | a0002c0002t0003g0016 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.168+14701A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141404 | ||||||
chrX:75141416
|
GT | G | 5 | a0001c0001t0007g0204a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+14688delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141416 | ||||||
chrX:75141643
|
T | C | 2 | a0001c0001t0015g0037a0001c0001t0015g0038 | 2 | HG00673.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.168+14462A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141643 | ||||||
chrX:75141655
|
T | A | 1 | a0002c0002t0003g0017 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.168+14450A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141655 | ||||||
chrX:75141769
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.168+14336C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141769 | ||||||
chrX:75141834
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.168+14271A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141834 | ||||||
chrX:75141949
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.168+14156G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141949 | ||||||
chrX:75141960
|
A | G | 1 | a0002c0002t0003g0008 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.168+14145T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75141960 | ||||||
chrX:75142164
|
C | T | 1 | a0001c0001t0008g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168+13941G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75142164 | ||||||
chrX:75142434
|
G | A | 1 | a0001c0003t0012g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168+13671C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75142434 | ||||||
chrX:75142579
|
C | G | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+13526G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75142579 | ||||||
chrX:75142642
|
T | A | 1 | a0001c0001t0002g0098 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.168+13463A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75142642 | ||||||
chrX:75143125
|
C | G | 1 | a0001c0001t0001g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+12980G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75143125 | ||||||
chrX:75143167
|
A | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(96): Show | 100 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.168+12938T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75143167 | ||||||
chrX:75143192
|
T | G | 2 | a0001c0003t0012g0226a0001c0003t0012g0227 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+12913A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75143192 | ||||||
chrX:75143650
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+12455A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75143650 | ||||||
chrX:75143720
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.168+12385A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75143720 | ||||||
chrX:75143808
|
C | CA | 1 | a0001c0001t0002g0047 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.168+12296dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75143808 | ||||||
chrX:75144060
|
T | A | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+12045A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75144060 | ||||||
chrX:75144387
|
TA | T | 1 | a0001c0001t0001g0126 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.168+11717delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75144387 | ||||||
chrX:75144531
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.168+11574T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75144531 | ||||||
chrX:75144616
|
CT | C | 1 | a0001c0001t0001g0124 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.168+11488delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75144616 | ||||||
chrX:75144616
|
CTT | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(209): Show | 213 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.168+11487_168+1148 others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75144616 | ||||||
chrX:75144808
|
A | G | 1 | a0002c0002t0003g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.168+11297T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75144808 | ||||||
chrX:75145045
|
T | C | 1 | a0001c0001t0008g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.168+11060A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75145045 | ||||||
chrX:75145277
|
C | CA | 1 | a0001c0001t0002g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.168+10827dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75145277 | ||||||
chrX:75145375
|
T | C | 1 | a0001c0001t0014g0160 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.168+10730A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75145375 | ||||||
chrX:75145547
|
T | C | 1 | a0001c0001t0004g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.168+10558A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75145547 | ||||||
chrX:75145799
|
C | T | 59 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(56): Show | 59 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.168+10306G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75145799 | ||||||
chrX:75145919
|
C | A | 1 | a0002c0002t0003g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.168+10186G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75145919 | ||||||
chrX:75146243
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.168+9862C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75146243 | ||||||
chrX:75146373
|
G | C | 1 | a0002c0002t0003g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.168+9732C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75146373 | ||||||
chrX:75146701
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.168+9404T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75146701 | ||||||
chrX:75146716
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+9389T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75146716 | ||||||
chrX:75146932
|
CTAA | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+9170_168+9172d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75146932 | ||||||
chrX:75146976
|
G | GA | 10 | a0001c0001t0004g0111a0001c0003t0006g0220a0001c0003t0006g0221others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.168+9128dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75146976 | ||||||
chrX:75147052
|
A | T | 6 | a0001c0001t0004g0049a0001c0001t0004g0050a0001c0001t0013g0230others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+9053T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147052 | ||||||
chrX:75147053
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+9052G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147053 | ||||||
chrX:75147055
|
C | CA | 2 | a0001c0001t0002g0101a0001c0001t0002g0102 | 2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.168+9049dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147055 | ||||||
chrX:75147055
|
CA | C | 1 | a0001c0001t0007g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+9049delT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147055 | ||||||
chrX:75147107
|
T | C | 9 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.168+8998A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147107 | ||||||
chrX:75147147
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.168+8958A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147147 | ||||||
chrX:75147280
|
A | C | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.168+8825T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147280 | ||||||
chrX:75147511
|
C | T | 5 | a0002c0002t0003g0004a0002c0002t0003g0005a0002c0002t0003g0006others(2): Show | 5 | HG02970.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+8594G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75147511 | ||||||
chrX:75148116
|
AAAAAAAT | A | 2 | a0001c0001t0013g0230a0001c0001t0013g0231 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.168+7982_168+7988d others(9): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75148116 | ||||||
chrX:75148152
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.168+7953T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75148152 | ||||||
chrX:75148346
|
AT | A | 1 | a0002c0002t0003g0020 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.168+7758delA | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75148346 | ||||||
chrX:75148376
|
AC | A | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+7728delG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75148376 | ||||||
chrX:75148897
|
A | G | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+7208T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75148897 | ||||||
chrX:75148971
|
A | C | 1 | a0001c0001t0023g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.168+7134T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75148971 | ||||||
chrX:75149081
|
G | A | 2 | a0001c0001t0016g0216a0001c0001t0016g0217 | 2 | HG01109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.168+7024C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75149081 | ||||||
chrX:75149212
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.168+6893A>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75149212 | ||||||
chrX:75149249
|
A | G | 1 | a0001c0001t0002g0059 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.168+6856T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75149249 | ||||||
chrX:75149799
|
T | C | 1 | a0001c0001t0007g0215 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.168+6306A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75149799 | ||||||
chrX:75149825
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.168+6280A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75149825 | ||||||
chrX:75149849
|
T | G | 1 | a0001c0001t0001g0039 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.168+6256A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75149849 | ||||||
chrX:75150226
|
T | C | 1 | a0001c0001t0007g0204 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.168+5879A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75150226 | ||||||
chrX:75150324
|
A | G | 2 | a0001c0001t0014g0159a0001c0001t0014g0160 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.168+5781T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75150324 | ||||||
chrX:75150474
|
A | G | 1 | a0001c0001t0022g0058 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.168+5631T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75150474 | ||||||
chrX:75150690
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+5415T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75150690 | ||||||
chrX:75150909
|
C | T | 77 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.168+5196G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75150909 | ||||||
chrX:75150966
|
G | A | 2 | a0001c0003t0012g0226a0001c0003t0012g0227 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+5139C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75150966 | ||||||
chrX:75151161
|
T | C | 5 | a0001c0003t0006g0220a0001c0003t0006g0221a0001c0003t0006g0222others(2): Show | 5 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+4944A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75151161 | ||||||
chrX:75151194
|
T | TA | 1 | a0001c0001t0013g0112 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.168+4910dupT | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75151194 | ||||||
chrX:75151224
|
G | A | 1 | a0002c0002t0003g0021 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.168+4881C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75151224 | ||||||
chrX:75151484
|
A | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+4621T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75151484 | ||||||
chrX:75151827
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.168+4278T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75151827 | ||||||
chrX:75151943
|
C | G | 5 | a0001c0001t0007g0204a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+4162G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75151943 | ||||||
chrX:75152159
|
C | T | 5 | a0001c0001t0007g0204a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+3946G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75152159 | ||||||
chrX:75152163
|
A | T | 5 | a0001c0001t0007g0204a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+3942T>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75152163 | ||||||
chrX:75152187
|
T | C | 1 | a0001c0001t0004g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.168+3918A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75152187 | ||||||
chrX:75152461
|
C | T | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.168+3644G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75152461 | ||||||
chrX:75152722
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(114): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.168+3383G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75152722 | ||||||
chrX:75152784
|
T | TA | 1 | a0001c0001t0010g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.168+3320_168+3321i others(3): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75152784 | ||||||
chrX:75152785
|
G | A | 1 | a0001c0001t0010g0161 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.168+3320C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75152785 | ||||||
chrX:75153018
|
A | C | 5 | a0001c0001t0007g0204a0001c0001t0007g0212a0001c0001t0007g0213others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+3087T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153018 | ||||||
chrX:75153323
|
T | G | 3 | a0001c0001t0001g0162a0001c0001t0001g0203a0001c0001t0001g0229 | 3 | HG00323.hp1 HG03491.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.168+2782A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153323 | ||||||
chrX:75153580
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | HG01515.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.168+2525G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153580 | ||||||
chrX:75153747
|
C | T | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+2358G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153747 | ||||||
chrX:75153749
|
T | C | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+2356A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153749 | ||||||
chrX:75153756
|
G | GTA | 1 | a0001c0003t0018g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.168+2348_168+2349i others(4): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153756 | ||||||
chrX:75153756
|
G | GTATA | 7 | a0001c0001t0001g0121a0001c0001t0005g0122a0001c0003t0006g0220others(4): Show | 7 | HG01884.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.168+2348_168+2349i others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153756 | ||||||
chrX:75153756
|
G | GTATATA | 6 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0002g0047others(3): Show | 6 | HG02055.hp1 HG02896.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+2348_168+2349i others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153756 | ||||||
chrX:75153756
|
G | GTATATAT others(1): Show |
51 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0124others(48): Show | 52 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.168+2348_168+2349i others(10): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153756 | ||||||
chrX:75153756
|
G | GTATATAT others(3): Show |
112 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(109): Show | 112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.168+2348_168+2349i others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153756 | ||||||
chrX:75153756
|
G | GTATATAT others(5): Show |
24 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(21): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.168+2348_168+2349i others(14): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153756 | ||||||
chrX:75153756
|
G | GTATATAT others(7): Show |
6 | a0001c0001t0002g0115a0001c0001t0007g0212a0001c0001t0007g0213others(3): Show | 6 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+2348_168+2349i others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153756 | ||||||
chrX:75153758
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(207): Show | 211 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.168+2347C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153758 | ||||||
chrX:75153758
|
G | GTATA | 1 | a0001c0003t0012g0226 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.168+2346_168+2347i others(6): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153758 | ||||||
chrX:75153758
|
G | GTATATA | 1 | a0001c0003t0012g0227 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.168+2346_168+2347i others(8): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153758 | ||||||
chrX:75153758
|
G | GTATATAT others(7): Show |
1 | a0001c0003t0012g0225 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168+2346_168+2347i others(16): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153758 | ||||||
chrX:75153760
|
G | A | 211 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(208): Show | 212 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.168+2345C>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153760 | ||||||
chrX:75153760
|
G | GTATATAT others(13): Show |
1 | a0001c0001t0016g0216 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.168+2344_168+2345i others(22): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153760 | ||||||
chrX:75153760
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0016g0217 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.168+2344_168+2345i others(24): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153760 | ||||||
chrX:75153773
|
T | TATATATA others(3): Show |
1 | a0001c0001t0001g0218 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.168+2331_168+2332i others(12): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153773 | ||||||
chrX:75153799
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.168+2306T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75153799 | ||||||
chrX:75154282
|
T | G | 3 | a0001c0003t0012g0225a0001c0003t0012g0226a0001c0003t0012g0227 | 3 | HG02559.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+1823A>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154282 | ||||||
chrX:75154415
|
C | T | 3 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | NA18965.hp1 NA19058.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.168+1690G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154415 | ||||||
chrX:75154524
|
C | T | 1 | a0001c0006t0002g0046 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.168+1581G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154524 | ||||||
chrX:75154620
|
T | C | 2 | a0001c0003t0012g0226a0001c0003t0012g0227 | 2 | HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.168+1485A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154620 | ||||||
chrX:75154860
|
A | ATATTT | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+1240_168+1244d others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154860 | ||||||
chrX:75154888
|
CAAT | C | 1 | a0001c0001t0024g0116 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.168+1214_168+1216d others(5): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154888 | ||||||
chrX:75154896
|
A | C | 204 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(201): Show | 205 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.168+1209T>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154896 | ||||||
chrX:75154927
|
C | G | 1 | a0001c0001t0002g0045 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.168+1178G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154927 | ||||||
chrX:75154949
|
TC | T | 1 | a0001c0001t0011g0023 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.168+1155delG | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75154949 | ||||||
chrX:75155089
|
C | A | 1 | a0001c0001t0011g0228 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.168+1016G>T | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75155089 | ||||||
chrX:75155490
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+615A>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75155490 | ||||||
chrX:75155625
|
C | T | 77 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(74): Show | 77 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.168+480G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75155625 | ||||||
chrX:75155654
|
C | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+451G>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75155654 | ||||||
chrX:75155692
|
GAATTGCT | G | 2 | a0001c0001t0013g0230a0001c0001t0013g0231 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.168+406_168+412del others(7): Show |
ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75155692 | ||||||
chrX:75155749
|
A | G | 2 | a0001c0001t0002g0043a0001c0001t0002g0044 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.168+356T>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75155749 | ||||||
chrX:75155885
|
G | T | 21 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(18): Show | 21 | HG00621.hp1 HG00673.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.168+220C>A | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75155885 | ||||||
chrX:75156018
|
C | G | 1 | a0001c0001t0001g0022 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.168+87G>C | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75156018 | ||||||
chrX:75156036
|
G | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0024others(210): Show | 214 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.168+69C>G | ABCB7 | ENSG00000131269.19 | transcript | ENST00000373394.8 | protein_coding | 1/15 | chrX | 75156036 |