Search by Gene
| 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 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 752 | 212 | 53 | 42 | 78 | 7 | 30 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0002 | 0/0 | 752 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0003 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0004 | 0/0 | 138 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0005 | 0/0 | 752 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2259 | 201 | 44 | 40 | 78 | 7 | 30 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| c0002 | 0/0 | 2259 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| c0003 | 0/0 | 2259 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| c0004 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| c0005 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| c0006 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| c0007 | 0/0 | 2261 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| c0008 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2340 | 96 | 11 | 12 | 62 | 2 | 9 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0002 | 1/1 | 2334 | 49 | 4 | 21 | 5 | 5 | 12 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0003 | 0/0 | 2344 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0004 | 0/0 | 2335 | 15 | 8 | 1 | 0 | 0 | 6 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0005 | 0/0 | 2341 | 6 | 1 | 1 | 4 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0006 | 0/0 | 2341 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0007 | 0/0 | 2340 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0008 | 0/0 | 2335 | 5 | 3 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0009 | 0/0 | 2339 | 4 | 1 | 1 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0010 | 0/0 | 2339 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0011 | 0/0 | 2341 | 4 | 0 | 0 | 2 | 0 | 2 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0012 | 0/0 | 2342 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0013 | 0/0 | 2336 | 3 | 2 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0014 | 0/0 | 2340 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0015 | 0/0 | 2341 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0016 | 0/0 | 2340 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0017 | 0/0 | 2329 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0018 | 0/0 | 2341 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0019 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0020 | 0/0 | 2340 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0021 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0022 | 0/0 | 2335 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0023 | 0/0 | 2336 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0024 | 0/0 | 2337 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| t0025 | 0/0 | 2336 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 201 | 44 | 40 | 78 | 7 | 30 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0003c0005 | a0003 | c0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0004c0007 | a0004 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0005c0008 | a0005 | c0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 0/0 | 95 | 10 | 12 | 62 | 2 | 9 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 1/1 | 48 | 4 | 20 | 5 | 5 | 12 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 14 | 8 | 0 | 0 | 0 | 6 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0015 | a0001 | c0001 | t0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0016 | a0001 | c0001 | t0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0017 | a0001 | c0001 | t0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0019 | a0001 | c0001 | t0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0020 | a0001 | c0001 | t0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0021 | a0001 | c0001 | t0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0003t0006 | a0001 | c0003 | t0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0003t0012 | a0001 | c0003 | t0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0003t0018 | a0001 | c0003 | t0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0004t0004 | a0001 | c0004 | t0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0001c0006t0002 | a0001 | c0006 | t0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0002c0002t0003 | a0002 | c0002 | t0003 | 0/0 | 17 | 15 | 2 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0003c0005t0001 | a0003 | c0005 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0004c0007t0005 | a0004 | c0007 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| a0005c0008t0017 | a0005 | c0008 | t0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0136 | a0001 | c0001 | t0001 | g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0184 | a0001 | c0001 | t0001 | g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0200 | a0001 | c0001 | t0001 | g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0202 | a0001 | c0001 | t0001 | g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0203 | a0001 | c0001 | t0001 | g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0207 | a0001 | c0001 | t0001 | g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0208 | a0001 | c0001 | t0001 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0209 | a0001 | c0001 | t0001 | g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0210 | a0001 | c0001 | t0001 | g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0211 | a0001 | c0001 | t0001 | g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0218 | a0001 | c0001 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0001g0229 | a0001 | c0001 | t0001 | g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0015 | a0001 | c0001 | t0002 | g0015 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0047 | a0001 | c0001 | t0002 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0057 | a0001 | c0001 | t0002 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0059 | a0001 | c0001 | t0002 | g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0060 | a0001 | c0001 | t0002 | g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0061 | a0001 | c0001 | t0002 | g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0062 | a0001 | c0001 | t0002 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0063 | a0001 | c0001 | t0002 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0064 | a0001 | c0001 | t0002 | g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0065 | a0001 | c0001 | t0002 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0066 | a0001 | c0001 | t0002 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0068 | a0001 | c0001 | t0002 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0069 | a0001 | c0001 | t0002 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0070 | a0001 | c0001 | t0002 | g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0071 | a0001 | c0001 | t0002 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0072 | a0001 | c0001 | t0002 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0073 | a0001 | c0001 | t0002 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0074 | a0001 | c0001 | t0002 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0075 | a0001 | c0001 | t0002 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0076 | a0001 | c0001 | t0002 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0077 | a0001 | c0001 | t0002 | g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0079 | a0001 | c0001 | t0002 | g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0080 | a0001 | c0001 | t0002 | g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0081 | a0001 | c0001 | t0002 | g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0083 | a0001 | c0001 | t0002 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0084 | a0001 | c0001 | t0002 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0087 | a0001 | c0001 | t0002 | g0087 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0088 | a0001 | c0001 | t0002 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0089 | a0001 | c0001 | t0002 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0090 | a0001 | c0001 | t0002 | g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0091 | a0001 | c0001 | t0002 | g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0092 | a0001 | c0001 | t0002 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0093 | a0001 | c0001 | t0002 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0094 | a0001 | c0001 | t0002 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0095 | a0001 | c0001 | t0002 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0096 | a0001 | c0001 | t0002 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0097 | a0001 | c0001 | t0002 | g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0098 | a0001 | c0001 | t0002 | g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0100 | a0001 | c0001 | t0002 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0101 | a0001 | c0001 | t0002 | g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0102 | a0001 | c0001 | t0002 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0110 | a0001 | c0001 | t0002 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0002g0115 | a0001 | c0001 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0049 | a0001 | c0001 | t0004 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0050 | a0001 | c0001 | t0004 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0052 | a0001 | c0001 | t0004 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0053 | a0001 | c0001 | t0004 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0054 | a0001 | c0001 | t0004 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0055 | a0001 | c0001 | t0004 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0067 | a0001 | c0001 | t0004 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0078 | a0001 | c0001 | t0004 | g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0082 | a0001 | c0001 | t0004 | g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0099 | a0001 | c0001 | t0004 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0108 | a0001 | c0001 | t0004 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0109 | a0001 | c0001 | t0004 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0111 | a0001 | c0001 | t0004 | g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0004g0113 | a0001 | c0001 | t0004 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0005g0122 | a0001 | c0001 | t0005 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0005g0135 | a0001 | c0001 | t0005 | g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0005g0146 | a0001 | c0001 | t0005 | g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0005g0177 | a0001 | c0001 | t0005 | g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0005g0196 | a0001 | c0001 | t0005 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0007g0204 | a0001 | c0001 | t0007 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0007g0212 | a0001 | c0001 | t0007 | g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0007g0213 | a0001 | c0001 | t0007 | g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0007g0214 | a0001 | c0001 | t0007 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0007g0215 | a0001 | c0001 | t0007 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0008g0048 | a0001 | c0001 | t0008 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0008g0104 | a0001 | c0001 | t0008 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0008g0105 | a0001 | c0001 | t0008 | g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0008g0106 | a0001 | c0001 | t0008 | g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0008g0107 | a0001 | c0001 | t0008 | g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0009g0027 | a0001 | c0001 | t0009 | g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0009g0036 | a0001 | c0001 | t0009 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0009g0151 | a0001 | c0001 | t0009 | g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0009g0185 | a0001 | c0001 | t0009 | g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0010g0154 | a0001 | c0001 | t0010 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0010g0157 | a0001 | c0001 | t0010 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0010g0161 | a0001 | c0001 | t0010 | g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0010g0201 | a0001 | c0001 | t0010 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0011g0023 | a0001 | c0001 | t0011 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0011g0148 | a0001 | c0001 | t0011 | g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0011g0197 | a0001 | c0001 | t0011 | g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0011g0228 | a0001 | c0001 | t0011 | g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0013g0112 | a0001 | c0001 | t0013 | g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0013g0230 | a0001 | c0001 | t0013 | g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0013g0231 | a0001 | c0001 | t0013 | g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0014g0159 | a0001 | c0001 | t0014 | g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0014g0160 | a0001 | c0001 | t0014 | g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0015g0037 | a0001 | c0001 | t0015 | g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0015g0038 | a0001 | c0001 | t0015 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0016g0216 | a0001 | c0001 | t0016 | g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0016g0217 | a0001 | c0001 | t0016 | g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0017g0086 | a0001 | c0001 | t0017 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0019g0178 | a0001 | c0001 | t0019 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0020g0155 | a0001 | c0001 | t0020 | g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0021g0149 | a0001 | c0001 | t0021 | g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0022g0058 | a0001 | c0001 | t0022 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0023g0114 | a0001 | c0001 | t0023 | g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0024g0116 | a0001 | c0001 | t0024 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0001t0025g0103 | a0001 | c0001 | t0025 | g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0006g0220 | a0001 | c0003 | t0006 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0006g0221 | a0001 | c0003 | t0006 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0006g0222 | a0001 | c0003 | t0006 | g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0006g0223 | a0001 | c0003 | t0006 | g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0006g0224 | a0001 | c0003 | t0006 | g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0012g0225 | a0001 | c0003 | t0012 | g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0012g0226 | a0001 | c0003 | t0012 | g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0012g0227 | a0001 | c0003 | t0012 | g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0003t0018g0219 | a0001 | c0003 | t0018 | g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0004t0004g0002 | a0001 | c0004 | t0004 | g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0001c0006t0002g0046 | a0001 | c0006 | t0002 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0004 | a0002 | c0002 | t0003 | g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0005 | a0002 | c0002 | t0003 | g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0006 | a0002 | c0002 | t0003 | g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0007 | a0002 | c0002 | t0003 | g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0008 | a0002 | c0002 | t0003 | g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0009 | a0002 | c0002 | t0003 | g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0010 | a0002 | c0002 | t0003 | g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0011 | a0002 | c0002 | t0003 | g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0012 | a0002 | c0002 | t0003 | g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0013 | a0002 | c0002 | t0003 | g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0014 | a0002 | c0002 | t0003 | g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0016 | a0002 | c0002 | t0003 | g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0017 | a0002 | c0002 | t0003 | g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0018 | a0002 | c0002 | t0003 | g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0019 | a0002 | c0002 | t0003 | g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0020 | a0002 | c0002 | t0003 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0002c0002t0003g0021 | a0002 | c0002 | t0003 | g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0003c0005t0001g0003 | a0003 | c0005 | t0001 | g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0004c0007t0005g0174 | a0004 | c0007 | t0005 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| a0005c0008t0017g0085 | a0005 | c0008 | t0017 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABCB7_chrX_75046048_75161283 | ABCB7 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | GBR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0064 | EUR | FIN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00609 | hp1 | a0001 | c0001 | t0011 | g0148 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0177 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00673 | hp1 | a0001 | c0001 | t0015 | g0037 | EAS | CHS | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00735 | hp2 | a0002 | c0002 | t0003 | g0008 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG00738 | hp1 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01070 | hp2 | a0001 | c0001 | t0009 | g0185 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0107 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01099 | hp1 | a0001 | c0001 | t0022 | g0058 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0217 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01167 | hp1 | a0001 | c0001 | t0025 | g0103 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0105 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01243 | hp1 | a0001 | c0004 | t0004 | g0002 | AMR | PUR | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0056 | EUR | IBS | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0014 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01884 | hp2 | a0001 | c0003 | t0006 | g0220 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01978 | hp2 | a0001 | c0001 | t0021 | g0149 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02015 | hp1 | a0001 | c0001 | t0013 | g0112 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02055 | hp1 | a0001 | c0001 | t0013 | g0231 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02145 | hp1 | a0001 | c0001 | t0017 | g0086 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | CDX | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02257 | hp1 | a0001 | c0001 | t0010 | g0201 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02273 | hp1 | a0001 | c0006 | t0002 | g0046 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0104 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02572 | hp1 | a0001 | c0003 | t0006 | g0224 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0160 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0157 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02630 | hp1 | a0001 | c0003 | t0012 | g0227 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02647 | hp1 | a0001 | c0003 | t0006 | g0221 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0017 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0154 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02723 | hp2 | a0001 | c0003 | t0006 | g0223 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0197 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0161 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02886 | hp2 | a0001 | c0003 | t0018 | g0219 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02965 | hp1 | a0001 | c0001 | t0020 | g0155 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02970 | hp1 | a0001 | c0003 | t0006 | g0222 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0005 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0020 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0048 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03041 | hp2 | a0001 | c0001 | t0014 | g0159 | AFR | GWD | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0004 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0013 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0018 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03195 | hp2 | a0005 | c0008 | t0017 | g0085 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03225 | hp1 | a0001 | c0003 | t0012 | g0226 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03453 | hp1 | a0002 | c0002 | t0003 | g0021 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03486 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0108 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0109 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0122 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0007 | AFR | ESN | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0078 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0113 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG04184 | hp1 | a0001 | c0001 | t0011 | g0228 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG04199 | hp1 | a0001 | c0001 | t0023 | g0114 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0006 | AFR | YRI | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18747 | hp1 | a0001 | c0001 | t0009 | g0027 | EAS | CHB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | YRI | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18985 | hp1 | a0001 | c0001 | t0011 | g0023 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19012 | hp1 | a0001 | c0001 | t0015 | g0038 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19030 | hp1 | a0001 | c0001 | t0024 | g0116 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0012 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19067 | hp1 | a0004 | c0007 | t0005 | g0174 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19072 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA19091 | hp1 | a0001 | c0001 | t0019 | g0178 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0151 | AFR | ASW | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0106 | AFR | ASW | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | TSI | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | TSI | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0019 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0204 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG02559 | hp2 | a0001 | c0003 | t0012 | g0225 | AFR | ACB | ABCB7_chrX_75046048_75161283 | ABCB7 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0016 | AFR | MSL | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | USA | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA20300 | hp2 | a0001 | c0001 | t0013 | g0230 | AFR | USA | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0216 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 |
| NA21309 | hp2 | a0003 | c0005 | t0001 | g0003 | AFR | LWK | ABCB7_chrX_75046048_75161283 | ABCB7 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0087 | REF | REF | ABCB7_chrX_75046048_75161283 | ABCB7 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0015 | REF | REF | ABCB7_chrX_75046048_75161283 | ABCB7 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | 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_pos_length | cds_pos_length | 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_pos_length | cds_pos_length | 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_pos_length | cds_pos_length | 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 |