Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23200 |
|---|---|
| ensemblid | ENSG00000058063.16 |
| hgncid | 13553 |
| symbol | ATP11B |
| name | ATPase phospholipid transporting 11B (putative) |
| refseq_nuc | NM_014616.3 |
| refseq_prot | NP_055431.1 |
| ensembl_nuc | ENST00000323116.10 |
| ensembl_prot | ENSP00000321195.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 182793504 |
| end | 182921629 |
| strand | + |
| ver | v1.2 |
| region | chr3:182793504-182921629 |
| region5000 | chr3:182788504-182926629 |
| regionname0 | ATP11B_chr3_182793504_182921629 |
| regionname5000 | ATP11B_chr3_182788504_182926629 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1177 | 309 | 76 | 49 | 149 | 13 | 20 | 114 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0002 | 0/0 | 1177 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0003 | 0/0 | 1177 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0004 | 0/0 | 1177 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0005 | 0/0 | 1177 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0006 | 0/0 | 1177 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0007 | 0/0 | 1177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0008 | 0/0 | 1177 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3534 | 259 | 49 | 41 | 141 | 8 | 18 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0002 | 0/0 | 3534 | 50 | 27 | 8 | 8 | 5 | 2 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0003 | 0/0 | 3534 | 4 | 4 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0004 | 0/0 | 3534 | 3 | 2 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0005 | 0/0 | 3534 | 3 | 0 | 0 | 3 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0006 | 0/0 | 3534 | 2 | 0 | 1 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0007 | 0/0 | 3534 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0008 | 0/0 | 3534 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| c0009 | 0/0 | 3534 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 3782 | 107 | 18 | 19 | 60 | 2 | 7 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0002 | 1/0 | 3782 | 80 | 15 | 3 | 50 | 3 | 8 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0003 | 0/0 | 3782 | 48 | 10 | 10 | 25 | 1 | 2 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0004 | 0/0 | 3782 | 31 | 13 | 7 | 4 | 5 | 2 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0005 | 0/0 | 3782 | 11 | 9 | 2 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0006 | 0/0 | 3782 | 11 | 0 | 3 | 7 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0007 | 0/0 | 3781 | 7 | 6 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0008 | 0/0 | 3782 | 6 | 0 | 5 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0009 | 0/0 | 3782 | 5 | 5 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0010 | 0/0 | 3782 | 3 | 3 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0011 | 0/0 | 3782 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0012 | 0/0 | 3782 | 2 | 0 | 0 | 1 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0013 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0014 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0015 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0016 | 0/0 | 3782 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0017 | 0/0 | 3782 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0018 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0019 | 0/0 | 3782 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0020 | 0/0 | 3782 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0021 | 0/0 | 3782 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0022 | 0/0 | 3782 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| t0023 | 0/0 | 3782 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3534 | 259 | 49 | 41 | 141 | 8 | 18 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002 | 0/0 | 3534 | 50 | 27 | 8 | 8 | 5 | 2 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0002c0003 | 0/0 | 3534 | 4 | 4 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0003c0005 | 0/0 | 3534 | 3 | 0 | 0 | 3 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0004c0004 | 0/0 | 3534 | 3 | 2 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0005c0006 | 0/0 | 3534 | 2 | 0 | 1 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0006c0008 | 0/0 | 3534 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0007c0007 | 0/0 | 3534 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0008c0009 | 0/0 | 3534 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 7315 | 104 | 18 | 18 | 59 | 1 | 7 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0002 | 1/0 | 7315 | 75 | 11 | 3 | 49 | 3 | 8 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0003 | 0/0 | 7315 | 47 | 10 | 9 | 25 | 1 | 2 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0005 | 0/0 | 7315 | 11 | 9 | 2 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0006 | 0/0 | 7315 | 4 | 0 | 3 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0008 | 0/0 | 7315 | 6 | 0 | 5 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0011 | 0/0 | 7315 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0012 | 0/0 | 7315 | 2 | 0 | 0 | 1 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0013 | 0/0 | 7315 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0014 | 0/0 | 7315 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0015 | 0/0 | 7325 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0016 | 0/0 | 7315 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0017 | 0/0 | 7315 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0018 | 0/0 | 7315 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0020 | 0/0 | 7315 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0001t0023 | 0/0 | 7315 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0004 | 0/0 | 7315 | 31 | 13 | 7 | 4 | 5 | 2 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0006 | 0/0 | 7315 | 4 | 0 | 0 | 4 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0007 | 0/0 | 7314 | 4 | 4 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0009 | 0/0 | 7315 | 5 | 5 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0010 | 0/0 | 7315 | 3 | 3 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0019 | 0/0 | 7315 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0021 | 0/0 | 7315 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0001c0002t0022 | 0/0 | 7315 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0002c0003t0002 | 0/0 | 7315 | 4 | 4 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0003c0005t0006 | 0/0 | 7315 | 3 | 0 | 0 | 3 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0004c0004t0007 | 0/0 | 7314 | 3 | 2 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0005c0006t0001 | 0/0 | 7315 | 2 | 0 | 1 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0006c0008t0002 | 0/0 | 7315 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0007c0007t0001 | 0/0 | 7315 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| a0008c0009t0003 | 0/0 | 7315 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | copy fasta | chr3 | 182788504 | 182926629 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0187 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0008g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0008g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0008g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0008g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0011g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0012g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0014g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0016g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0017g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0018g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0020g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0001t0023g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0007g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0010g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0010g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0019g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0021g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0001c0002t0022g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0002c0003t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0002c0003t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0002c0003t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0002c0003t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0003c0005t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0003c0005t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0003c0005t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0004c0004t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0004c0004t0007g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0004c0004t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0005c0006t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0005c0006t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0006c0008t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0007c0007t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| a0008c0009t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0004 | g0271 | EUR | GBR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00099 | hp2 | a0001 | c0001 | t0012 | g0013 | EUR | GBR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | GBR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0272 | EUR | GBR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00323 | hp1 | a0001 | c0002 | t0004 | g0294 | EUR | FIN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0159 | EUR | FIN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0256 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01069 | hp1 | a0001 | c0001 | t0008 | g0184 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01069 | hp2 | a0001 | c0002 | t0004 | g0290 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0251 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0186 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0289 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01071 | hp2 | a0001 | c0001 | t0008 | g0185 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01109 | hp1 | a0001 | c0001 | t0016 | g0173 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01169 | hp1 | a0005 | c0006 | t0001 | g0081 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01175 | hp2 | a0001 | c0002 | t0004 | g0298 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0125 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0082 | AMR | PUR | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0257 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01257 | hp1 | a0004 | c0004 | t0007 | g0275 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01261 | hp2 | a0001 | c0002 | t0021 | g0291 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0183 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0300 | AMR | CLM | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01515 | hp2 | a0001 | c0001 | t0023 | g0066 | EUR | IBS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01516 | hp1 | a0001 | c0002 | t0004 | g0308 | EUR | IBS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0083 | EUR | IBS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0307 | EUR | IBS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0288 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0192 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01981 | hp2 | a0001 | c0002 | t0004 | g0301 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0286 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02056 | hp2 | a0001 | c0002 | t0004 | g0285 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02071 | hp1 | a0001 | c0001 | t0013 | g0156 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02132 | hp2 | a0001 | c0001 | t0018 | g0149 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02145 | hp1 | a0001 | c0001 | t0017 | g0158 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CDX | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | CDX | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02257 | hp1 | a0001 | c0002 | t0004 | g0313 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02273 | hp2 | a0008 | c0009 | t0003 | g0180 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0245 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0253 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02451 | hp2 | a0001 | c0002 | t0009 | g0248 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02572 | hp1 | a0001 | c0002 | t0019 | g0297 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02572 | hp2 | a0002 | c0003 | t0002 | g0119 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0120 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02630 | hp2 | a0001 | c0002 | t0007 | g0274 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0280 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0259 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02717 | hp2 | a0002 | c0003 | t0002 | g0117 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02886 | hp2 | a0001 | c0002 | t0022 | g0284 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02895 | hp1 | a0001 | c0002 | t0010 | g0269 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0312 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02922 | hp2 | a0002 | c0003 | t0002 | g0118 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02965 | hp1 | a0001 | c0002 | t0007 | g0279 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02965 | hp2 | a0001 | c0002 | t0007 | g0273 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0314 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02970 | hp2 | a0001 | c0002 | t0007 | g0278 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02976 | hp1 | a0001 | c0002 | t0010 | g0292 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0262 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | ESN | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0001 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0316 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03453 | hp1 | a0001 | c0002 | t0004 | g0315 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03453 | hp2 | a0004 | c0004 | t0007 | g0276 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03486 | hp1 | a0004 | c0004 | t0007 | g0310 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0295 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03579 | hp1 | a0001 | c0002 | t0009 | g0311 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | MSL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | STU | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03688 | hp2 | a0001 | c0002 | t0004 | g0299 | SAS | STU | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03704 | hp1 | a0001 | c0001 | t0008 | g0011 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0200 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | PJL | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0296 | SAS | BEB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0309 | SAS | BEB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | STU | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | STU | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18747 | hp2 | a0006 | c0008 | t0002 | g0237 | EAS | CHB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0254 | AFR | YRI | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18949 | hp1 | a0003 | c0005 | t0006 | g0304 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18956 | hp2 | a0001 | c0002 | t0004 | g0287 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18959 | hp2 | a0001 | c0002 | t0004 | g0306 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18963 | hp1 | a0001 | c0002 | t0006 | g0305 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18989 | hp1 | a0001 | c0001 | t0011 | g0138 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0258 | AFR | LWK | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19054 | hp1 | a0001 | c0002 | t0006 | g0281 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19054 | hp2 | a0001 | c0001 | t0020 | g0078 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19058 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19060 | hp2 | a0001 | c0002 | t0006 | g0303 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19064 | hp1 | a0001 | c0001 | t0011 | g0142 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19074 | hp2 | a0001 | c0002 | t0006 | g0282 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19075 | hp1 | a0003 | c0005 | t0006 | g0283 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19076 | hp1 | a0003 | c0005 | t0006 | g0302 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19076 | hp2 | a0007 | c0007 | t0001 | g0090 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19077 | hp2 | a0001 | c0001 | t0014 | g0124 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19087 | hp2 | a0001 | c0001 | t0015 | g0136 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19240 | hp1 | a0001 | c0002 | t0010 | g0270 | AFR | YRI | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ASW | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0260 | AFR | ASW | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA20805 | hp1 | a0005 | c0006 | t0001 | g0073 | EUR | TSI | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0202 | EUR | TSI | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02109 | hp1 | a0001 | c0002 | t0009 | g0268 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02109 | hp2 | a0001 | c0002 | t0009 | g0247 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02486 | hp2 | a0001 | c0002 | t0009 | g0267 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0261 | AFR | ACB | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | USA | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0293 | AFR | USA | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | USA | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA20300 | hp2 | a0002 | c0003 | t0002 | g0116 | AFR | USA | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | LWK | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0057 | REF | REF | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0187 | REF | REF | ATP11B_chr3_182788504_182926629 | ATP11B | chr3 | 182788504 | 182926629 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:182865550
|
T | A | 1 | a0005 | 2 | HG01169.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.1295T>A | p.Ile432Asn | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 13/30 | 1551/7315 | 1295/3534 | 432/1177 | chr3 | 182865550 | ||
| chr3:182866329
|
A | G | 1 | a0008 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.1505A>G | p.Asn502Ser | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/30 | 1761/7315 | 1505/3534 | 502/1177 | chr3 | 182866329 | ||
| chr3:182869142
|
G | A | 1 | a0004 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1753G>A | p.Ala585Thr | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 16/30 | 2009/7315 | 1753/3534 | 585/1177 | chr3 | 182869142 | ||
| chr3:182872502
|
C | A | 1 | a0007 | 1 | NA19076.hp2 | missense_variant | MODERATE | c.2013C>A | p.Asp671Glu | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/30 | 2269/7315 | 2013/3534 | 671/1177 | chr3 | 182872502 | ||
| chr3:182884806
|
G | A | 1 | a0002 | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
missense_variant | MODERATE | c.2563G>A | p.Ala855Thr | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 22/30 | 2819/7315 | 2563/3534 | 855/1177 | chr3 | 182884806 | ||
| chr3:182887671
|
A | T | 1 | a0006 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.2801A>T | p.His934Leu | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/30 | 3057/7315 | 2801/3534 | 934/1177 | chr3 | 182887671 | ||
| chr3:182889427
|
G | A | 1 | a0003 | 3 | NA18949.hp1 NA19075.hp1 NA19076.hp1 |
missense_variant | MODERATE | c.2861G>A | p.Arg954His | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/30 | 3117/7315 | 2861/3534 | 954/1177 | chr3 | 182889427 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:182896705
|
T | C | 3 | a0001c0002a0003c0005a0004c0004 | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
synonymous_variant | LOW | c.2988T>C | p.Phe996Phe | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 26/30 | 3244/7315 | 2988/3534 | 996/1177 | chr3 | 182896705 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:182793563
|
C | T | 13 | a0001c0001t0001a0001c0001t0006a0001c0001t0012others(10): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-197C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/30 | chr3 | 182793563 | ||||||
| chr3:182793728
|
C | T | 1 | a0001c0001t0018 | 1 | HG02132.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/30 | 32 | chr3 | 182793728 | |||||
| chr3:182918814
|
C | A | 1 | a0001c0001t0005 | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*710C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 710 | chr3 | 182918814 | |||||
| chr3:182918817
|
C | G | 1 | a0001c0001t0023 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*713C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 713 | chr3 | 182918817 | |||||
| chr3:182918883
|
T | C | 1 | a0001c0001t0013 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*779T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 779 | chr3 | 182918883 | |||||
| chr3:182918949
|
G | C | 1 | a0001c0002t0019 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*845G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 845 | chr3 | 182918949 | |||||
| chr3:182919390
|
C | G | 1 | a0001c0002t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1286C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 1286 | chr3 | 182919390 | |||||
| chr3:182919900
|
A | G | 1 | a0001c0001t0017 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1796A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 1796 | chr3 | 182919900 | |||||
| chr3:182920052
|
C | T | 6 | a0001c0002t0004a0001c0002t0009a0001c0002t0010others(3): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1948C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 1948 | chr3 | 182920052 | |||||
| chr3:182920287
|
C | T | 1 | a0001c0002t0021 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2183C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 2183 | chr3 | 182920287 | |||||
| chr3:182920426
|
G | T | 1 | a0001c0001t0020 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2322G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 2322 | chr3 | 182920426 | |||||
| chr3:182920439
|
C | G | 1 | a0001c0001t0016 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2335C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 2335 | chr3 | 182920439 | |||||
| chr3:182920507
|
T | C | 1 | a0001c0002t0019 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2403T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 2403 | chr3 | 182920507 | |||||
| chr3:182920736
|
G | C | 4 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(1): Show | 56 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2632G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 2632 | chr3 | 182920736 | |||||
| chr3:182920764
|
T | G | 1 | a0001c0001t0014 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2660T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 2660 | chr3 | 182920764 | |||||
| chr3:182920788
|
G | A | 1 | a0001c0001t0011 | 2 | NA18989.hp1 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2684G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 2684 | chr3 | 182920788 | |||||
| chr3:182921325
|
AG | A | 2 | a0001c0002t0007a0004c0004t0007 | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3222delG | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 3222 | chr3 | 182921325 | |||||
| chr3:182921333
|
A | G | 7 | a0001c0001t0006a0001c0002t0004a0001c0002t0006others(4): Show | 47 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3229A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 3229 | chr3 | 182921333 | |||||
| chr3:182921379
|
A | G | 1 | a0001c0002t0019 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3275A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 3275 | chr3 | 182921379 | |||||
| chr3:182921484
|
T | C | 1 | a0001c0001t0008 | 6 | HG01069.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3380T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 3380 | chr3 | 182921484 | |||||
| chr3:182921583
|
T | TAAAGTTT others(3): Show |
1 | a0001c0001t0015 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3482_*3491dupAGTT others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 30/30 | 3492 | INFO_REALIGN_3_PRIME | chr3 | 182921583 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:182793802
|
C | T | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+16C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182793802 | ||||||
| chr3:182793945
|
G | A | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.27+159G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182793945 | ||||||
| chr3:182793974
|
C | G | 1 | a0004c0004t0007g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.27+188C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182793974 | ||||||
| chr3:182794055
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.27+269C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794055 | ||||||
| chr3:182794202
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.27+416G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794202 | ||||||
| chr3:182794412
|
C | G | 36 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0280others(33): Show | 39 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.27+626C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794412 | ||||||
| chr3:182794589
|
C | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.27+803C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794589 | ||||||
| chr3:182794636
|
A | T | 1 | a0001c0001t0002g0277 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.27+850A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794636 | ||||||
| chr3:182794651
|
T | C | 1 | a0001c0001t0008g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.27+865T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794651 | ||||||
| chr3:182794793
|
G | A | 1 | a0001c0002t0004g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.27+1007G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794793 | ||||||
| chr3:182794845
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.27+1059G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794845 | ||||||
| chr3:182794946
|
C | G | 5 | a0001c0002t0007g0273a0001c0002t0007g0274a0004c0004t0007g0275others(2): Show | 5 | HG01257.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+1160C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182794946 | ||||||
| chr3:182795034
|
CA | C | 20 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0002g0263others(17): Show | 20 | HG00639.hp2 HG01070.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.27+1263delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182795034 | |||||
| chr3:182795034
|
CAA | C | 38 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(35): Show | 41 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.27+1262_27+1263del others(2): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182795034 | |||||
| chr3:182795179
|
C | CTTG | 45 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(42): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.27+1395_27+1397dup others(3): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182795179 | |||||
| chr3:182795563
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.27+1777T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182795563 | ||||||
| chr3:182795716
|
C | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG00408.hp2 NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.27+1930C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182795716 | ||||||
| chr3:182795924
|
T | A | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+2138T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182795924 | ||||||
| chr3:182795926
|
T | G | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.27+2140T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182795926 | ||||||
| chr3:182796136
|
A | G | 1 | a0001c0002t0004g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.27+2350A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796136 | ||||||
| chr3:182796229
|
CAATGTT | C | 4 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(1): Show | 4 | NA18944.hp1 NA18995.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+2446_27+2451del others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182796229 | |||||
| chr3:182796389
|
C | T | 45 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(42): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.27+2603C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796389 | ||||||
| chr3:182796426
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.27+2640A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796426 | ||||||
| chr3:182796680
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.27+2894A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796680 | ||||||
| chr3:182796687
|
C | A | 1 | a0001c0002t0004g0312 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.27+2901C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796687 | ||||||
| chr3:182796775
|
G | C | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.27+2989G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796775 | ||||||
| chr3:182796848
|
A | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(122): Show | 130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.27+3062A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796848 | ||||||
| chr3:182796876
|
A | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG00735.hp1 HG01433.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.27+3090A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796876 | ||||||
| chr3:182796956
|
G | A | 1 | a0001c0001t0002g0121 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.27+3170G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182796956 | ||||||
| chr3:182797016
|
C | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+3230C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797016 | ||||||
| chr3:182797039
|
A | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+3253A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797039 | ||||||
| chr3:182797090
|
A | G | 2 | a0001c0002t0004g0307a0001c0002t0004g0308 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.27+3304A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797090 | ||||||
| chr3:182797506
|
G | A | 2 | a0001c0001t0008g0011a0001c0001t0008g0125 | 2 | HG01192.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.27+3720G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797506 | ||||||
| chr3:182797577
|
G | A | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+3791G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797577 | ||||||
| chr3:182797677
|
T | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.27+3891T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797677 | ||||||
| chr3:182797707
|
C | CAAAAAAG others(14): Show |
2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.27+3931_27+3951dup others(21): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182797707 | |||||
| chr3:182797707
|
CAAAAAAG | C | 55 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(52): Show | 58 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.27+3945_27+3951del others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182797707 | |||||
| chr3:182797707
|
CAAAAAAG others(7): Show |
C | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27+3938_27+3951del others(14): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182797707 | |||||
| chr3:182797796
|
A | C | 1 | a0001c0002t0004g0306 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.27+4010A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797796 | ||||||
| chr3:182797846
|
G | A | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27+4060G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182797846 | ||||||
| chr3:182798002
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.27+4216T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798002 | ||||||
| chr3:182798005
|
T | C | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.27+4219T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798005 | ||||||
| chr3:182798022
|
A | T | 1 | a0001c0001t0003g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.27+4236A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798022 | ||||||
| chr3:182798484
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.27+4698C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798484 | ||||||
| chr3:182798521
|
T | C | 1 | a0001c0002t0009g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.27+4735T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798521 | ||||||
| chr3:182798605
|
A | G | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27+4819A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798605 | ||||||
| chr3:182798734
|
T | C | 2 | a0001c0002t0004g0271a0001c0002t0004g0272 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.27+4948T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798734 | ||||||
| chr3:182798895
|
T | C | 50 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(47): Show | 53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.27+5109T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182798895 | ||||||
| chr3:182799045
|
A | T | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0309 | 3 | HG02738.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.27+5259A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799045 | ||||||
| chr3:182799059
|
A | G | 1 | a0001c0001t0003g0242 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.27+5273A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799059 | ||||||
| chr3:182799202
|
G | C | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.27+5416G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799202 | ||||||
| chr3:182799281
|
CT | C | 58 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(55): Show | 58 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.27+5511delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182799281 | |||||
| chr3:182799285
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.27+5499T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799285 | ||||||
| chr3:182799309
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.27+5523C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799309 | ||||||
| chr3:182799339
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.27+5553G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799339 | ||||||
| chr3:182799401
|
G | A | 2 | a0001c0002t0004g0280a0001c0002t0022g0284 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.27+5615G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799401 | ||||||
| chr3:182799522
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.27+5736G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799522 | ||||||
| chr3:182799533
|
C | T | 1 | a0001c0001t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.27+5747C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799533 | ||||||
| chr3:182799534
|
G | A | 3 | a0001c0001t0001g0016a0001c0002t0007g0273a0001c0002t0007g0274 | 3 | HG02630.hp2 HG02965.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.27+5748G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799534 | ||||||
| chr3:182799548
|
T | C | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.27+5762T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799548 | ||||||
| chr3:182799707
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.27+5921C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799707 | ||||||
| chr3:182799826
|
A | G | 7 | a0001c0002t0006g0281a0001c0002t0006g0282a0001c0002t0006g0303others(4): Show | 7 | NA18949.hp1 NA18963.hp1 NA19054.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+6040A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799826 | ||||||
| chr3:182799841
|
T | C | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.27+6055T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799841 | ||||||
| chr3:182799904
|
G | A | 45 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(42): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.27+6118G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799904 | ||||||
| chr3:182799909
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.27+6123T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182799909 | ||||||
| chr3:182800067
|
G | A | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.27+6281G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800067 | ||||||
| chr3:182800151
|
C | T | 1 | a0001c0001t0014g0124 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.27+6365C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800151 | ||||||
| chr3:182800168
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.27+6382A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800168 | ||||||
| chr3:182800292
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.27+6506G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800292 | ||||||
| chr3:182800307
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.27+6521A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800307 | ||||||
| chr3:182800390
|
TA | T | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.27+6619delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182800390 | |||||
| chr3:182800392
|
A | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG00735.hp1 HG01433.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.27+6606A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800392 | ||||||
| chr3:182800405
|
A | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.27+6619A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800405 | ||||||
| chr3:182800465
|
C | T | 1 | a0001c0001t0002g0240 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.27+6679C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800465 | ||||||
| chr3:182800556
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.27+6770A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800556 | ||||||
| chr3:182800785
|
A | AT | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 120 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.27+7014dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182800785 | |||||
| chr3:182800785
|
A | ATT | 56 | a0001c0001t0001g0021a0001c0001t0001g0112a0001c0001t0005g0252others(53): Show | 59 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.27+7013_27+7014dup others(2): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182800785 | |||||
| chr3:182800814
|
T | C | 1 | a0002c0003t0002g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.27+7028T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800814 | ||||||
| chr3:182800827
|
C | G | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.27+7041C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800827 | ||||||
| chr3:182800874
|
A | C | 1 | a0001c0001t0001g0021 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.27+7088A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800874 | ||||||
| chr3:182800879
|
C | A | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+7093C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800879 | ||||||
| chr3:182800910
|
C | G | 1 | a0001c0001t0001g0102 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.27+7124C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800910 | ||||||
| chr3:182800962
|
A | G | 1 | a0001c0002t0006g0305 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.27+7176A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800962 | ||||||
| chr3:182800998
|
C | T | 48 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(45): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.27+7212C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182800998 | ||||||
| chr3:182801059
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0098others(4): Show | 8 | HG00639.hp1 HG01934.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.27+7273C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182801059 | ||||||
| chr3:182801094
|
A | C | 1 | a0001c0001t0002g0121 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.27+7308A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182801094 | ||||||
| chr3:182801981
|
C | A | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.27+8195C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182801981 | ||||||
| chr3:182802019
|
A | G | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.27+8233A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802019 | ||||||
| chr3:182802046
|
A | G | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+8260A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802046 | ||||||
| chr3:182802137
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.27+8351A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802137 | ||||||
| chr3:182802334
|
G | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.27+8548G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802334 | ||||||
| chr3:182802525
|
A | G | 52 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(49): Show | 55 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.27+8739A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802525 | ||||||
| chr3:182802560
|
A | G | 52 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(49): Show | 55 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.27+8774A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802560 | ||||||
| chr3:182802636
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.27+8850G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802636 | ||||||
| chr3:182802720
|
G | A | 37 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0127others(34): Show | 37 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.27+8934G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802720 | ||||||
| chr3:182802748
|
C | T | 1 | a0001c0001t0002g0239 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.27+8962C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802748 | ||||||
| chr3:182802833
|
A | G | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.27+9047A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802833 | ||||||
| chr3:182802880
|
T | C | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | NA18962.hp2 NA18968.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+9094T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182802880 | ||||||
| chr3:182803175
|
TTTTCTAA others(13): Show |
T | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024 | 3 | NA18969.hp1 NA18985.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.27+9394_27+9413del others(20): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182803175 | |||||
| chr3:182803267
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.27+9481T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182803267 | ||||||
| chr3:182803339
|
C | T | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.27+9553C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182803339 | ||||||
| chr3:182803355
|
G | T | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.27+9569G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182803355 | ||||||
| chr3:182803449
|
C | T | 8 | a0001c0001t0002g0126a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.27+9663C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182803449 | ||||||
| chr3:182803451
|
G | T | 52 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(49): Show | 55 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.27+9665G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182803451 | ||||||
| chr3:182803473
|
T | C | 52 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(49): Show | 55 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.27+9687T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182803473 | ||||||
| chr3:182803724
|
A | G | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.27+9938A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182803724 | ||||||
| chr3:182804244
|
T | A | 1 | a0001c0001t0002g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.27+10458T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804244 | ||||||
| chr3:182804249
|
C | T | 1 | a0001c0001t0002g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.27+10463C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804249 | ||||||
| chr3:182804388
|
G | A | 1 | a0001c0002t0004g0313 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.27+10602G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804388 | ||||||
| chr3:182804403
|
G | T | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.27+10617G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804403 | ||||||
| chr3:182804407
|
G | A | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+10621G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804407 | ||||||
| chr3:182804476
|
G | C | 1 | a0001c0001t0001g0025 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.27+10690G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804476 | ||||||
| chr3:182804576
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.27+10790C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804576 | ||||||
| chr3:182804628
|
T | G | 2 | a0001c0001t0003g0176a0001c0001t0003g0222 | 2 | NA19070.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.27+10842T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804628 | ||||||
| chr3:182804708
|
C | A | 1 | a0001c0001t0002g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.27+10922C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804708 | ||||||
| chr3:182804734
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.27+10948A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804734 | ||||||
| chr3:182804757
|
C | T | 1 | a0001c0001t0013g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.27+10971C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804757 | ||||||
| chr3:182804810
|
A | G | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.27+11024A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804810 | ||||||
| chr3:182804838
|
G | C | 1 | a0001c0001t0002g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.27+11052G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182804838 | ||||||
| chr3:182804948
|
GTA | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.27+11164_27+11165d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182804948 | |||||
| chr3:182805063
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.27+11277A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805063 | ||||||
| chr3:182805075
|
A | G | 2 | a0001c0001t0002g0240a0001c0001t0003g0221 | 2 | NA18991.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.27+11289A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805075 | ||||||
| chr3:182805076
|
C | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.27+11290C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805076 | ||||||
| chr3:182805161
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0097 | 3 | NA18974.hp1 NA19000.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.27+11375C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805161 | ||||||
| chr3:182805200
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.27+11414A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805200 | ||||||
| chr3:182805262
|
A | G | 2 | a0001c0001t0002g0154a0001c0001t0002g0155 | 2 | NA18973.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.27+11476A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805262 | ||||||
| chr3:182805307
|
A | G | 1 | a0006c0008t0002g0237 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.27+11521A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805307 | ||||||
| chr3:182805600
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.27+11814G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805600 | ||||||
| chr3:182805625
|
C | CT | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.27+11854dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182805625 | |||||
| chr3:182805675
|
G | T | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.27+11889G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805675 | ||||||
| chr3:182805879
|
A | G | 1 | a0001c0001t0005g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.27+12093A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805879 | ||||||
| chr3:182805933
|
T | G | 1 | a0001c0001t0002g0157 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.27+12147T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182805933 | ||||||
| chr3:182806036
|
A | T | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.27+12250A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806036 | ||||||
| chr3:182806080
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 129 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.27+12294A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806080 | ||||||
| chr3:182806090
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG00408.hp2 NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.27+12304A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806090 | ||||||
| chr3:182806153
|
G | T | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.27+12367G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806153 | ||||||
| chr3:182806170
|
G | T | 1 | a0001c0001t0003g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.27+12384G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806170 | ||||||
| chr3:182806266
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.27+12480A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806266 | ||||||
| chr3:182806305
|
A | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | NA18969.hp1 NA18973.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+12519A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806305 | ||||||
| chr3:182806416
|
G | A | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+12630G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806416 | ||||||
| chr3:182806536
|
A | C | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.27+12750A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806536 | ||||||
| chr3:182806725
|
T | C | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.27+12939T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806725 | ||||||
| chr3:182806952
|
A | G | 5 | a0001c0001t0005g0257a0001c0001t0005g0258a0001c0001t0005g0259others(2): Show | 5 | HG01255.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+13166A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182806952 | ||||||
| chr3:182807041
|
TA | T | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.28-13207delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182807041 | |||||
| chr3:182807123
|
C | T | 5 | a0001c0001t0005g0257a0001c0001t0005g0258a0001c0001t0005g0259others(2): Show | 5 | HG01255.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-13137C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807123 | ||||||
| chr3:182807312
|
T | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-12948T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807312 | ||||||
| chr3:182807392
|
A | C | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.28-12868A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807392 | ||||||
| chr3:182807453
|
A | C | 3 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0264 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.28-12807A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807453 | ||||||
| chr3:182807632
|
A | G | 2 | a0001c0001t0005g0255a0001c0001t0005g0256 | 2 | HG00639.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.28-12628A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807632 | ||||||
| chr3:182807700
|
T | C | 1 | a0001c0001t0005g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.28-12560T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807700 | ||||||
| chr3:182807708
|
A | T | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-12552A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807708 | ||||||
| chr3:182807728
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.28-12532G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807728 | ||||||
| chr3:182807771
|
T | G | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.28-12489T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182807771 | ||||||
| chr3:182808118
|
C | T | 45 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(42): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.28-12142C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182808118 | ||||||
| chr3:182808241
|
A | G | 1 | a0002c0003t0002g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.28-12019A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182808241 | ||||||
| chr3:182808406
|
A | G | 3 | a0001c0001t0003g0217a0001c0001t0003g0218a0001c0001t0003g0219 | 3 | NA18964.hp2 NA19012.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.28-11854A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182808406 | ||||||
| chr3:182808740
|
A | G | 12 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(9): Show | 12 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-11520A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182808740 | ||||||
| chr3:182808769
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.28-11491A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182808769 | ||||||
| chr3:182808807
|
C | T | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.28-11453C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182808807 | ||||||
| chr3:182808971
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.28-11289T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182808971 | ||||||
| chr3:182809168
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.28-11092T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809168 | ||||||
| chr3:182809178
|
A | T | 4 | a0001c0002t0010g0270a0004c0004t0007g0275a0004c0004t0007g0276others(1): Show | 4 | HG01257.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-11082A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809178 | ||||||
| chr3:182809209
|
C | T | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.28-11051C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809209 | ||||||
| chr3:182809311
|
C | T | 1 | a0001c0001t0002g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.28-10949C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809311 | ||||||
| chr3:182809397
|
C | T | 162 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.28-10863C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809397 | ||||||
| chr3:182809409
|
T | C | 1 | a0001c0001t0003g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.28-10851T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809409 | ||||||
| chr3:182809410
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 110 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.28-10850G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809410 | ||||||
| chr3:182809457
|
C | T | 39 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(36): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.28-10803C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809457 | ||||||
| chr3:182809471
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.28-10789A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809471 | ||||||
| chr3:182809849
|
G | A | 1 | a0001c0001t0006g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.28-10411G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182809849 | ||||||
| chr3:182810098
|
G | A | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0271others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.28-10162G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810098 | ||||||
| chr3:182810113
|
C | G | 12 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(9): Show | 12 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-10147C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810113 | ||||||
| chr3:182810154
|
A | T | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-10106A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810154 | ||||||
| chr3:182810263
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.28-9997T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810263 | ||||||
| chr3:182810275
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.28-9985C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810275 | ||||||
| chr3:182810276
|
G | A | 1 | a0002c0003t0002g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.28-9984G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810276 | ||||||
| chr3:182810424
|
A | G | 1 | a0001c0002t0022g0284 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.28-9836A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810424 | ||||||
| chr3:182810468
|
C | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.28-9792C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182810468 | ||||||
| chr3:182811083
|
TAATG | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.28-9173_28-9170del others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182811083 | |||||
| chr3:182811208
|
G | A | 2 | a0001c0002t0004g0280a0001c0002t0022g0284 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.28-9052G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182811208 | ||||||
| chr3:182811297
|
A | T | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.28-8963A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182811297 | ||||||
| chr3:182811312
|
T | C | 1 | a0001c0001t0003g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.28-8948T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182811312 | ||||||
| chr3:182811410
|
G | C | 2 | a0004c0004t0007g0275a0004c0004t0007g0276 | 2 | HG01257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.28-8850G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182811410 | ||||||
| chr3:182811448
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.28-8812C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182811448 | ||||||
| chr3:182811937
|
G | A | 6 | a0001c0001t0003g0175a0001c0001t0003g0179a0001c0001t0003g0181others(3): Show | 6 | HG00642.hp1 HG01934.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-8323G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182811937 | ||||||
| chr3:182811982
|
G | A | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.28-8278G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182811982 | ||||||
| chr3:182812381
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-7879A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182812381 | ||||||
| chr3:182812423
|
A | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.28-7837A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182812423 | ||||||
| chr3:182812529
|
C | A | 1 | a0001c0001t0001g0034 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.28-7731C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182812529 | ||||||
| chr3:182812593
|
A | G | 2 | a0004c0004t0007g0275a0004c0004t0007g0276 | 2 | HG01257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.28-7667A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182812593 | ||||||
| chr3:182812643
|
A | G | 48 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(45): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.28-7617A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182812643 | ||||||
| chr3:182812667
|
G | A | 166 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(163): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.28-7593G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182812667 | ||||||
| chr3:182813076
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-7184C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813076 | ||||||
| chr3:182813119
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.28-7141T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813119 | ||||||
| chr3:182813354
|
T | C | 1 | a0001c0001t0005g0255 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.28-6906T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813354 | ||||||
| chr3:182813648
|
C | T | 1 | a0001c0001t0008g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.28-6612C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813648 | ||||||
| chr3:182813688
|
A | G | 1 | a0003c0005t0006g0304 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.28-6572A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813688 | ||||||
| chr3:182813761
|
T | G | 23 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(20): Show | 23 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.28-6499T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813761 | ||||||
| chr3:182813786
|
G | A | 1 | a0001c0001t0005g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.28-6474G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813786 | ||||||
| chr3:182813808
|
A | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 123 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.28-6452A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813808 | ||||||
| chr3:182813852
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.28-6408C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813852 | ||||||
| chr3:182813873
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-6387A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813873 | ||||||
| chr3:182813888
|
C | T | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.28-6372C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182813888 | ||||||
| chr3:182814043
|
A | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-6217A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814043 | ||||||
| chr3:182814151
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0028a0001c0001t0001g0031others(4): Show | 7 | NA18951.hp2 NA18971.hp1 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-6109C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814151 | ||||||
| chr3:182814210
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.28-6050C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814210 | ||||||
| chr3:182814285
|
G | A | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.28-5975G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814285 | ||||||
| chr3:182814566
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0035others(1): Show | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-5694G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814566 | ||||||
| chr3:182814676
|
G | T | 1 | a0001c0001t0005g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.28-5584G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814676 | ||||||
| chr3:182814745
|
G | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.28-5515G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814745 | ||||||
| chr3:182814750
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.28-5510G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814750 | ||||||
| chr3:182814820
|
T | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-5440T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814820 | ||||||
| chr3:182814891
|
G | A | 1 | a0001c0001t0003g0175 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.28-5369G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814891 | ||||||
| chr3:182814895
|
A | G | 1 | a0001c0002t0004g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.28-5365A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814895 | ||||||
| chr3:182814986
|
T | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-5274T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182814986 | ||||||
| chr3:182815315
|
T | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-4945T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182815315 | ||||||
| chr3:182815365
|
A | G | 4 | a0001c0002t0004g0007a0001c0002t0004g0300a0001c0002t0004g0301others(1): Show | 5 | HG01257.hp2 HG01258.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4895A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182815365 | ||||||
| chr3:182815767
|
T | A | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-4493T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182815767 | ||||||
| chr3:182816077
|
C | T | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4183C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182816077 | ||||||
| chr3:182816267
|
A | T | 1 | a0001c0001t0005g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.28-3993A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182816267 | ||||||
| chr3:182816634
|
C | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.28-3626C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182816634 | ||||||
| chr3:182816739
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0086 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.28-3521A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182816739 | ||||||
| chr3:182816751
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.28-3509C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182816751 | ||||||
| chr3:182816993
|
A | G | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-3267A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182816993 | ||||||
| chr3:182817048
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-3212G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817048 | ||||||
| chr3:182817105
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.28-3155A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817105 | ||||||
| chr3:182817256
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | HG00408.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.28-3004A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817256 | ||||||
| chr3:182817274
|
G | GT | 19 | a0001c0001t0001g0019a0001c0001t0001g0112a0001c0001t0001g0115others(16): Show | 21 | HG00558.hp1 HG01175.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.28-2975dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182817274 | |||||
| chr3:182817501
|
G | A | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.28-2759G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817501 | ||||||
| chr3:182817538
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.28-2722C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817538 | ||||||
| chr3:182817557
|
C | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.28-2703C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817557 | ||||||
| chr3:182817587
|
C | T | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.28-2673C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817587 | ||||||
| chr3:182817793
|
C | CT | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-2457dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182817793 | |||||
| chr3:182817833
|
T | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-2427T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182817833 | ||||||
| chr3:182818164
|
T | A | 3 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314 | 5 | HG02257.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-2096T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818164 | ||||||
| chr3:182818179
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-2081A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818179 | ||||||
| chr3:182818189
|
G | A | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.28-2071G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818189 | ||||||
| chr3:182818497
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0106 | 2 | HG00558.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.28-1763G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818497 | ||||||
| chr3:182818656
|
C | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-1604C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818656 | ||||||
| chr3:182818702
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-1558G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818702 | ||||||
| chr3:182818746
|
A | G | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-1514A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818746 | ||||||
| chr3:182818788
|
A | C | 1 | a0001c0001t0001g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.28-1472A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818788 | ||||||
| chr3:182818797
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.28-1463C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818797 | ||||||
| chr3:182818916
|
T | TA | 8 | a0001c0001t0001g0037a0001c0001t0001g0109a0001c0001t0002g0153others(5): Show | 8 | HG02027.hp1 HG02056.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-1329dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182818916 | |||||
| chr3:182818916
|
TA | T | 9 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(6): Show | 9 | HG01255.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.28-1329delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182818916 | |||||
| chr3:182818933
|
A | G | 2 | a0001c0001t0005g0255a0001c0001t0005g0256 | 2 | HG00639.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.28-1327A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182818933 | ||||||
| chr3:182819079
|
C | CT | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(186): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.28-1166dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182819079 | |||||
| chr3:182819079
|
CT | C | 39 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(36): Show | 42 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.28-1166delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | 182819079 | |||||
| chr3:182819107
|
C | T | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.28-1153C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819107 | ||||||
| chr3:182819235
|
A | G | 1 | a0001c0001t0003g0216 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.28-1025A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819235 | ||||||
| chr3:182819262
|
G | A | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.28-998G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819262 | ||||||
| chr3:182819362
|
C | T | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.28-898C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819362 | ||||||
| chr3:182819414
|
T | G | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.28-846T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819414 | ||||||
| chr3:182819515
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.28-745A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819515 | ||||||
| chr3:182819610
|
T | A | 1 | a0001c0002t0004g0271 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.28-650T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819610 | ||||||
| chr3:182819627
|
A | G | 5 | a0001c0002t0007g0273a0001c0002t0007g0274a0004c0004t0007g0275others(2): Show | 5 | HG01257.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-633A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819627 | ||||||
| chr3:182819636
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.28-624A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819636 | ||||||
| chr3:182819637
|
T | C | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-623T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819637 | ||||||
| chr3:182819728
|
C | T | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.28-532C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819728 | ||||||
| chr3:182819759
|
T | C | 1 | a0001c0001t0008g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.28-501T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819759 | ||||||
| chr3:182819861
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-399G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819861 | ||||||
| chr3:182819873
|
G | T | 1 | a0001c0001t0002g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28-387G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819873 | ||||||
| chr3:182819944
|
T | G | 1 | a0001c0001t0001g0092 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.28-316T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182819944 | ||||||
| chr3:182820000
|
C | G | 1 | a0001c0002t0007g0274 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.28-260C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182820000 | ||||||
| chr3:182820041
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.28-219A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | chr3 | 182820041 | ||||||
| chr3:182820400
|
T | G | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG00735.hp1 HG01433.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.144+24T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182820400 | ||||||
| chr3:182820640
|
A | G | 2 | a0001c0001t0002g0151a0001c0001t0002g0172 | 2 | NA18988.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.144+264A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182820640 | ||||||
| chr3:182820670
|
A | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.144+294A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182820670 | ||||||
| chr3:182820775
|
C | T | 16 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(13): Show | 16 | HG00639.hp2 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.144+399C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182820775 | ||||||
| chr3:182820859
|
A | G | 1 | a0001c0001t0005g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.144+483A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182820859 | ||||||
| chr3:182820907
|
A | G | 4 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(1): Show | 4 | HG02145.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.144+531A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182820907 | ||||||
| chr3:182821082
|
T | C | 2 | a0002c0003t0002g0116a0002c0003t0002g0117 | 2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.144+706T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182821082 | ||||||
| chr3:182821402
|
C | T | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+1026C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182821402 | ||||||
| chr3:182821447
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.144+1071T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182821447 | ||||||
| chr3:182821492
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.144+1116G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182821492 | ||||||
| chr3:182821547
|
C | T | 4 | a0001c0001t0002g0130a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG00323.hp2 HG02080.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.144+1171C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182821547 | ||||||
| chr3:182821695
|
C | A | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+1319C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182821695 | ||||||
| chr3:182821785
|
T | A | 1 | a0001c0001t0003g0216 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.144+1409T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182821785 | ||||||
| chr3:182822109
|
CT | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0038a0001c0001t0002g0008others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.144+1747delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 182822109 | |||||
| chr3:182822124
|
A | T | 1 | a0004c0004t0007g0276 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.144+1748A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822124 | ||||||
| chr3:182822144
|
G | C | 1 | a0001c0001t0003g0188 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.144+1768G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822144 | ||||||
| chr3:182822159
|
T | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+1783T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822159 | ||||||
| chr3:182822167
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.144+1791G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822167 | ||||||
| chr3:182822192
|
A | G | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.144+1816A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822192 | ||||||
| chr3:182822225
|
C | T | 2 | a0001c0001t0002g0008a0001c0001t0002g0009 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.144+1849C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822225 | ||||||
| chr3:182822265
|
C | A | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+1889C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822265 | ||||||
| chr3:182822308
|
C | T | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+1932C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822308 | ||||||
| chr3:182822498
|
T | C | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+2122T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822498 | ||||||
| chr3:182822581
|
T | G | 5 | a0001c0002t0007g0273a0001c0002t0007g0274a0004c0004t0007g0275others(2): Show | 5 | HG01257.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+2205T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822581 | ||||||
| chr3:182822620
|
C | T | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+2244C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822620 | ||||||
| chr3:182822761
|
A | G | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.144+2385A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822761 | ||||||
| chr3:182822804
|
G | A | 1 | a0001c0001t0013g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.144+2428G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182822804 | ||||||
| chr3:182823142
|
G | T | 9 | a0001c0001t0005g0254a0001c0001t0005g0255a0001c0001t0005g0256others(6): Show | 9 | HG00639.hp2 HG01255.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.144+2766G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823142 | ||||||
| chr3:182823169
|
T | A | 1 | a0001c0002t0004g0286 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.144+2793T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823169 | ||||||
| chr3:182823224
|
C | T | 1 | a0001c0001t0003g0215 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.144+2848C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823224 | ||||||
| chr3:182823291
|
A | C | 2 | a0001c0001t0002g0130a0001c0001t0002g0160 | 2 | HG03017.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.144+2915A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823291 | ||||||
| chr3:182823303
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.144+2927A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823303 | ||||||
| chr3:182823401
|
G | C | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.144+3025G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823401 | ||||||
| chr3:182823476
|
A | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.144+3100A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823476 | ||||||
| chr3:182823508
|
G | A | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+3132G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823508 | ||||||
| chr3:182823547
|
G | A | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.144+3171G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823547 | ||||||
| chr3:182823553
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.144+3177T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823553 | ||||||
| chr3:182823641
|
G | A | 40 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0127others(37): Show | 40 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.144+3265G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823641 | ||||||
| chr3:182823711
|
G | A | 1 | a0001c0001t0016g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.144+3335G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823711 | ||||||
| chr3:182823746
|
G | A | 23 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(20): Show | 23 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.144+3370G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823746 | ||||||
| chr3:182823755
|
T | C | 1 | a0001c0002t0004g0287 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.144+3379T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823755 | ||||||
| chr3:182823983
|
G | A | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.144+3607G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182823983 | ||||||
| chr3:182824111
|
G | A | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.144+3735G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824111 | ||||||
| chr3:182824150
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.144+3774G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824150 | ||||||
| chr3:182824223
|
T | G | 1 | a0001c0001t0001g0040 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.144+3847T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824223 | ||||||
| chr3:182824261
|
A | G | 6 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(3): Show | 6 | HG01433.hp2 HG02723.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.145-3859A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824261 | ||||||
| chr3:182824339
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.145-3781T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824339 | ||||||
| chr3:182824471
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.145-3649G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824471 | ||||||
| chr3:182824528
|
C | A | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.145-3592C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824528 | ||||||
| chr3:182824731
|
C | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.145-3389C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182824731 | ||||||
| chr3:182825025
|
C | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.145-3095C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825025 | ||||||
| chr3:182825247
|
T | C | 1 | a0001c0002t0009g0248 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.145-2873T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825247 | ||||||
| chr3:182825261
|
T | G | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.145-2859T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825261 | ||||||
| chr3:182825266
|
C | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(167): Show | 177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.145-2854C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825266 | ||||||
| chr3:182825440
|
C | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.145-2680C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825440 | ||||||
| chr3:182825534
|
C | T | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-2586C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825534 | ||||||
| chr3:182825722
|
C | CA | 14 | a0001c0001t0001g0017a0001c0001t0001g0086a0001c0001t0002g0153others(11): Show | 15 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.145-2380dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 182825722 | |||||
| chr3:182825722
|
CAA | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.145-2381_145-2380d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr3 | 182825722 | |||||
| chr3:182825741
|
T | A | 1 | a0001c0002t0004g0312 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.145-2379T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825741 | ||||||
| chr3:182825842
|
G | T | 4 | a0001c0001t0006g0032a0001c0001t0006g0082a0001c0001t0006g0083others(1): Show | 4 | HG01070.hp1 HG01192.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.145-2278G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825842 | ||||||
| chr3:182825856
|
C | T | 1 | a0001c0001t0003g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145-2264C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825856 | ||||||
| chr3:182825875
|
G | A | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(144): Show | 154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.145-2245G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182825875 | ||||||
| chr3:182826229
|
T | G | 1 | a0001c0001t0003g0189 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.145-1891T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182826229 | ||||||
| chr3:182826304
|
T | G | 2 | a0004c0004t0007g0275a0004c0004t0007g0276 | 2 | HG01257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.145-1816T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182826304 | ||||||
| chr3:182826430
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.145-1690A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182826430 | ||||||
| chr3:182826518
|
A | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.145-1602A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182826518 | ||||||
| chr3:182826673
|
C | A | 1 | a0001c0001t0002g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.145-1447C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182826673 | ||||||
| chr3:182826709
|
G | A | 23 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(20): Show | 23 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.145-1411G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182826709 | ||||||
| chr3:182826876
|
A | G | 1 | a0001c0001t0017g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.145-1244A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182826876 | ||||||
| chr3:182827121
|
A | C | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.145-999A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827121 | ||||||
| chr3:182827221
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.145-899A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827221 | ||||||
| chr3:182827233
|
A | T | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.145-887A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827233 | ||||||
| chr3:182827523
|
A | G | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.145-597A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827523 | ||||||
| chr3:182827523
|
A | T | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.145-597A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827523 | ||||||
| chr3:182827536
|
A | G | 1 | a0001c0002t0021g0291 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.145-584A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827536 | ||||||
| chr3:182827644
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.145-476A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827644 | ||||||
| chr3:182827683
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.145-437A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827683 | ||||||
| chr3:182827741
|
T | A | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.145-379T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827741 | ||||||
| chr3:182827814
|
A | T | 1 | a0007c0007t0001g0090 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.145-306A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2/29 | chr3 | 182827814 | ||||||
| chr3:182828229
|
C | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.234+20C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182828229 | ||||||
| chr3:182828511
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.234+302A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182828511 | ||||||
| chr3:182828527
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.234+318T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182828527 | ||||||
| chr3:182828590
|
C | G | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 111 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.234+381C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182828590 | ||||||
| chr3:182828680
|
G | A | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.234+471G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182828680 | ||||||
| chr3:182828909
|
T | C | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.234+700T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182828909 | ||||||
| chr3:182828977
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.235-695A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182828977 | ||||||
| chr3:182829075
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.235-597G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182829075 | ||||||
| chr3:182829179
|
T | C | 2 | a0001c0001t0003g0190a0001c0001t0003g0245 | 2 | HG01346.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.235-493T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182829179 | ||||||
| chr3:182829468
|
G | T | 148 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(145): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.235-204G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182829468 | ||||||
| chr3:182829618
|
G | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0016others(23): Show | 26 | HG00099.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.235-54G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182829618 | ||||||
| chr3:182829641
|
T | C | 1 | a0001c0002t0010g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.235-31T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 3/29 | chr3 | 182829641 | ||||||
| chr3:182830108
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.315+356T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182830108 | ||||||
| chr3:182830120
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.315+368G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182830120 | ||||||
| chr3:182830121
|
C | A | 1 | a0001c0001t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.315+369C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182830121 | ||||||
| chr3:182830314
|
T | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.315+562T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182830314 | ||||||
| chr3:182830322
|
C | CA | 14 | a0001c0001t0002g0126a0001c0001t0002g0161a0001c0001t0002g0165others(11): Show | 16 | HG00735.hp2 HG01167.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.315+587dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 182830322 | |||||
| chr3:182830322
|
CA | C | 9 | a0001c0001t0001g0016a0001c0002t0007g0273a0001c0002t0007g0274others(6): Show | 9 | HG01169.hp1 HG01257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.315+587delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 182830322 | |||||
| chr3:182830418
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.315+666T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182830418 | ||||||
| chr3:182830703
|
A | T | 5 | a0001c0002t0007g0278a0001c0002t0007g0279a0004c0004t0007g0275others(2): Show | 5 | HG01257.hp1 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+951A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182830703 | ||||||
| chr3:182830861
|
A | C | 1 | a0001c0001t0016g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.315+1109A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182830861 | ||||||
| chr3:182831186
|
C | T | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.315+1434C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831186 | ||||||
| chr3:182831187
|
A | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+1435A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831187 | ||||||
| chr3:182831199
|
A | G | 1 | a0001c0001t0002g0150 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.315+1447A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831199 | ||||||
| chr3:182831251
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.315+1499G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831251 | ||||||
| chr3:182831334
|
T | C | 8 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(5): Show | 8 | NA18952.hp2 NA18954.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.315+1582T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831334 | ||||||
| chr3:182831488
|
A | G | 1 | a0001c0001t0002g0239 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.315+1736A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831488 | ||||||
| chr3:182831502
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.315+1750A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831502 | ||||||
| chr3:182831576
|
A | AT | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.315+1835dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr3 | 182831576 | |||||
| chr3:182831579
|
T | A | 1 | a0001c0001t0002g0227 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.315+1827T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831579 | ||||||
| chr3:182831627
|
C | T | 1 | a0001c0001t0002g0226 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.315+1875C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831627 | ||||||
| chr3:182831819
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.315+2067A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831819 | ||||||
| chr3:182831861
|
T | C | 1 | a0001c0002t0004g0314 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.315+2109T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831861 | ||||||
| chr3:182831871
|
C | T | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.315+2119C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831871 | ||||||
| chr3:182831873
|
G | A | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.315+2121G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831873 | ||||||
| chr3:182831888
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.315+2136T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831888 | ||||||
| chr3:182831901
|
C | T | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.315+2149C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182831901 | ||||||
| chr3:182832377
|
A | G | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.315+2625A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182832377 | ||||||
| chr3:182832566
|
G | A | 1 | a0001c0001t0001g0057 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.315+2814G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182832566 | ||||||
| chr3:182832614
|
T | C | 1 | a0001c0001t0012g0013 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.315+2862T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182832614 | ||||||
| chr3:182832633
|
C | G | 2 | a0001c0002t0004g0296a0001c0002t0004g0299 | 2 | HG03688.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.315+2881C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182832633 | ||||||
| chr3:182832766
|
G | A | 2 | a0001c0002t0004g0307a0001c0002t0004g0308 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.315+3014G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182832766 | ||||||
| chr3:182833063
|
G | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 111 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.316-2972G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833063 | ||||||
| chr3:182833103
|
T | G | 9 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(6): Show | 9 | HG01257.hp1 HG02109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.316-2932T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833103 | ||||||
| chr3:182833149
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.316-2886A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833149 | ||||||
| chr3:182833424
|
C | G | 1 | a0001c0001t0002g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.316-2611C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833424 | ||||||
| chr3:182833510
|
G | T | 1 | a0001c0001t0017g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.316-2525G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833510 | ||||||
| chr3:182833612
|
A | C | 10 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0037others(7): Show | 10 | HG00621.hp2 HG00673.hp2 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.316-2423A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833612 | ||||||
| chr3:182833621
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.316-2414G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833621 | ||||||
| chr3:182833835
|
G | T | 2 | a0001c0001t0002g0240a0001c0001t0003g0221 | 2 | NA18991.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.316-2200G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182833835 | ||||||
| chr3:182834091
|
A | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.316-1944A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834091 | ||||||
| chr3:182834460
|
T | C | 1 | a0004c0004t0007g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.316-1575T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834460 | ||||||
| chr3:182834508
|
T | A | 315 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(312): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.316-1527T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834508 | ||||||
| chr3:182834536
|
A | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.316-1499A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834536 | ||||||
| chr3:182834570
|
A | G | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.316-1465A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834570 | ||||||
| chr3:182834609
|
C | T | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.316-1426C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834609 | ||||||
| chr3:182834833
|
A | G | 5 | a0001c0002t0007g0273a0001c0002t0007g0274a0004c0004t0007g0275others(2): Show | 5 | HG01257.hp1 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.316-1202A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834833 | ||||||
| chr3:182834876
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.316-1159G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834876 | ||||||
| chr3:182834945
|
T | G | 1 | a0001c0002t0004g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.316-1090T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182834945 | ||||||
| chr3:182835115
|
C | G | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.316-920C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835115 | ||||||
| chr3:182835210
|
G | A | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG02132.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.316-825G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835210 | ||||||
| chr3:182835367
|
A | C | 1 | a0001c0001t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.316-668A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835367 | ||||||
| chr3:182835416
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.316-619T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835416 | ||||||
| chr3:182835427
|
C | T | 1 | a0001c0001t0002g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.316-608C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835427 | ||||||
| chr3:182835527
|
T | C | 13 | a0001c0001t0003g0176a0001c0001t0003g0190a0001c0001t0003g0191others(10): Show | 13 | HG01255.hp1 HG01346.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.316-508T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835527 | ||||||
| chr3:182835677
|
T | C | 12 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(9): Show | 12 | HG01257.hp1 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.316-358T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835677 | ||||||
| chr3:182835700
|
TA | T | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.316-334delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835700 | ||||||
| chr3:182835885
|
T | G | 1 | a0001c0001t0001g0041 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.316-150T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182835885 | ||||||
| chr3:182836009
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.316-26A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 4/29 | chr3 | 182836009 | ||||||
| chr3:182836215
|
C | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.423+73C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 5/29 | chr3 | 182836215 | ||||||
| chr3:182836260
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.424-82G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 5/29 | chr3 | 182836260 | ||||||
| chr3:182836274
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0012g0020 | 3 | NA18964.hp1 NA19004.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.424-68A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 5/29 | chr3 | 182836274 | ||||||
| chr3:182836493
|
A | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.552+23A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 6/29 | chr3 | 182836493 | ||||||
| chr3:182836555
|
A | G | 1 | a0001c0001t0002g0230 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.552+85A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 6/29 | chr3 | 182836555 | ||||||
| chr3:182836714
|
T | C | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.552+244T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 6/29 | chr3 | 182836714 | ||||||
| chr3:182836766
|
T | C | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.552+296T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 6/29 | chr3 | 182836766 | ||||||
| chr3:182837206
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.656+32A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182837206 | ||||||
| chr3:182837561
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656+387C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182837561 | ||||||
| chr3:182837666
|
T | C | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+492T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182837666 | ||||||
| chr3:182837713
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG00609.hp1 NA18747.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.656+539T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182837713 | ||||||
| chr3:182837937
|
C | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.656+763C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182837937 | ||||||
| chr3:182838199
|
A | G | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.656+1025A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838199 | ||||||
| chr3:182838282
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0086 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.656+1108T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838282 | ||||||
| chr3:182838323
|
T | A | 1 | a0001c0002t0004g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.656+1149T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838323 | ||||||
| chr3:182838390
|
G | C | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.656+1216G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838390 | ||||||
| chr3:182838440
|
C | T | 1 | a0001c0002t0004g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.656+1266C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838440 | ||||||
| chr3:182838461
|
A | C | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.656+1287A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838461 | ||||||
| chr3:182838470
|
A | G | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.656+1296A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838470 | ||||||
| chr3:182838764
|
AAC | A | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.656+1594_656+1595d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182838764 | |||||
| chr3:182838785
|
T | TTA | 5 | a0001c0002t0009g0267a0001c0002t0009g0268a0004c0004t0007g0275others(2): Show | 5 | HG01257.hp1 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.656+1626_656+1627d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182838785 | |||||
| chr3:182838787
|
A | T | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656+1613A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838787 | ||||||
| chr3:182838800
|
T | TATACAC | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.656+1627_656+1628i others(8): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182838800 | |||||
| chr3:182838820
|
G | A | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 110 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.656+1646G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182838820 | ||||||
| chr3:182839056
|
A | G | 34 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.656+1882A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839056 | ||||||
| chr3:182839074
|
A | C | 1 | a0001c0001t0001g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.656+1900A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839074 | ||||||
| chr3:182839084
|
C | T | 1 | a0001c0002t0010g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656+1910C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839084 | ||||||
| chr3:182839118
|
C | G | 1 | a0001c0001t0013g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.656+1944C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839118 | ||||||
| chr3:182839230
|
G | C | 4 | a0001c0001t0002g0130a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG00323.hp2 HG02080.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+2056G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839230 | ||||||
| chr3:182839236
|
A | C | 2 | a0005c0006t0001g0073a0005c0006t0001g0081 | 2 | HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.656+2062A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839236 | ||||||
| chr3:182839372
|
C | T | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.656+2198C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839372 | ||||||
| chr3:182839603
|
T | TTTTTATT others(8): Show |
1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.656+2429_656+2430i others(17): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839603 | ||||||
| chr3:182839604
|
A | ATTTATTT others(8): Show |
128 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(125): Show | 132 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.656+2433_656+2447d others(17): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182839604 | |||||
| chr3:182839604
|
A | ATTTATTT others(13): Show |
9 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(6): Show | 11 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.656+2447_656+2448i others(22): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182839604 | |||||
| chr3:182839604
|
A | ATTTATTT others(18): Show |
33 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(30): Show | 34 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.656+2447_656+2448i others(27): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182839604 | |||||
| chr3:182839604
|
A | ATTTATTT others(23): Show |
1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.656+2447_656+2448i others(32): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182839604 | |||||
| chr3:182839604
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.656+2430A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839604 | ||||||
| chr3:182839696
|
G | A | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.657-2379G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839696 | ||||||
| chr3:182839904
|
C | T | 1 | a0001c0001t0013g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.657-2171C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182839904 | ||||||
| chr3:182840059
|
T | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.657-2016T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182840059 | ||||||
| chr3:182840080
|
C | A | 1 | a0001c0001t0003g0179 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.657-1995C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182840080 | ||||||
| chr3:182840201
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.657-1874T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182840201 | ||||||
| chr3:182840635
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.657-1440A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182840635 | ||||||
| chr3:182840797
|
G | A | 30 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.657-1278G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182840797 | ||||||
| chr3:182840987
|
T | C | 1 | a0001c0002t0004g0280 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.657-1088T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182840987 | ||||||
| chr3:182841298
|
C | A | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.657-777C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841298 | ||||||
| chr3:182841313
|
A | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.657-762A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841313 | ||||||
| chr3:182841385
|
G | T | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657-690G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841385 | ||||||
| chr3:182841495
|
A | G | 1 | a0001c0001t0001g0084 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.657-580A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841495 | ||||||
| chr3:182841615
|
T | G | 5 | a0001c0002t0004g0288a0001c0002t0004g0289a0001c0002t0004g0290others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-460T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841615 | ||||||
| chr3:182841620
|
A | G | 1 | a0001c0002t0010g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.657-455A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841620 | ||||||
| chr3:182841626
|
T | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.657-449T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841626 | ||||||
| chr3:182841709
|
T | A | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.657-366T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841709 | ||||||
| chr3:182841760
|
T | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.657-315T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841760 | ||||||
| chr3:182841805
|
T | C | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.657-270T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841805 | ||||||
| chr3:182841814
|
T | TAAAAATA others(182): Show |
2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.657-261_657-260ins others(189): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841814 | ||||||
| chr3:182841853
|
C | T | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.657-222C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841853 | ||||||
| chr3:182841906
|
G | A | 8 | a0001c0001t0002g0126a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-169G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841906 | ||||||
| chr3:182841913
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0035others(1): Show | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.657-162A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | chr3 | 182841913 | ||||||
| chr3:182841977
|
C | CA | 151 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.657-78dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182841977 | |||||
| chr3:182841977
|
C | CAA | 10 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0042others(7): Show | 10 | HG00642.hp2 HG01099.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.657-79_657-78dupAA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr3 | 182841977 | |||||
| chr3:182842584
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.704+462G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182842584 | ||||||
| chr3:182842865
|
C | A | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.704+743C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182842865 | ||||||
| chr3:182843006
|
A | G | 1 | a0001c0001t0005g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.704+884A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843006 | ||||||
| chr3:182843019
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.704+897A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843019 | ||||||
| chr3:182843258
|
G | T | 4 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314others(1): Show | 6 | HG02257.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.704+1136G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843258 | ||||||
| chr3:182843379
|
C | T | 1 | a0001c0001t0018g0149 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.704+1257C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843379 | ||||||
| chr3:182843408
|
C | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.704+1286C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843408 | ||||||
| chr3:182843590
|
T | A | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.704+1468T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843590 | ||||||
| chr3:182843590
|
T | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.704+1468T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843590 | ||||||
| chr3:182843831
|
C | T | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.705-1627C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843831 | ||||||
| chr3:182843968
|
G | A | 1 | a0001c0002t0009g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.705-1490G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182843968 | ||||||
| chr3:182844087
|
A | C | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.705-1371A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844087 | ||||||
| chr3:182844321
|
G | T | 1 | a0001c0002t0004g0296 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.705-1137G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844321 | ||||||
| chr3:182844402
|
T | C | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.705-1056T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844402 | ||||||
| chr3:182844486
|
T | C | 1 | a0001c0001t0001g0057 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.705-972T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844486 | ||||||
| chr3:182844613
|
T | A | 2 | a0004c0004t0007g0275a0004c0004t0007g0276 | 2 | HG01257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.705-845T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844613 | ||||||
| chr3:182844637
|
A | G | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.705-821A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844637 | ||||||
| chr3:182844716
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.705-742T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844716 | ||||||
| chr3:182844984
|
TTTTTTTT others(3): Show |
T | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.705-464_705-455del others(10): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182844984 | |||||
| chr3:182844985
|
TTTTTTTT others(2): Show |
T | 9 | a0001c0002t0004g0280a0001c0002t0004g0295a0001c0002t0006g0281others(6): Show | 9 | HG02647.hp2 HG02886.hp2 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.705-464_705-456del others(9): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182844985 | |||||
| chr3:182844988
|
TTTTTTA | T | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.705-464_705-459del others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182844988 | |||||
| chr3:182844989
|
TTTTTA | T | 28 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.705-464_705-460del others(5): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182844989 | |||||
| chr3:182844991
|
TTTATTTT others(8): Show |
T | 1 | a0001c0001t0005g0260 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.705-464_705-450del others(15): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182844991 | |||||
| chr3:182844993
|
TA | T | 9 | a0001c0001t0001g0018a0001c0001t0001g0087a0001c0001t0001g0250others(6): Show | 9 | HG00099.hp2 HG00639.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.705-464delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844993 | ||||||
| chr3:182844994
|
A | T | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 121 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.705-464A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844994 | ||||||
| chr3:182844998
|
T | A | 1 | a0001c0001t0002g0153 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.705-460T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182844998 | ||||||
| chr3:182845000
|
T | A | 7 | a0001c0001t0002g0161a0001c0001t0003g0245a0001c0002t0009g0247others(4): Show | 7 | HG02080.hp1 HG02109.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.705-458T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845000 | ||||||
| chr3:182845001
|
T | A | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.705-457T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845001 | ||||||
| chr3:182845006
|
A | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(132): Show | 140 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.705-452A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845006 | ||||||
| chr3:182845006
|
ATTT | A | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.705-445_705-443del others(3): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182845006 | |||||
| chr3:182845006
|
ATTTT | A | 28 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(25): Show | 29 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.705-446_705-443del others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182845006 | |||||
| chr3:182845009
|
T | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 107 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.705-449T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845009 | ||||||
| chr3:182845009
|
T | TA | 10 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.705-449_705-448ins others(1): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845009 | ||||||
| chr3:182845010
|
T | A | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.705-448T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845010 | ||||||
| chr3:182845010
|
T | TA | 4 | a0001c0002t0007g0278a0001c0002t0007g0279a0004c0004t0007g0275others(1): Show | 4 | HG01257.hp1 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.705-448_705-447ins others(1): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845010 | ||||||
| chr3:182845012
|
T | A | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.705-446T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845012 | ||||||
| chr3:182845013
|
TTTA | T | 6 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(3): Show | 6 | HG00639.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.705-442_705-440del others(3): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | 182845013 | |||||
| chr3:182845016
|
A | T | 5 | a0001c0001t0005g0257a0001c0001t0005g0258a0001c0001t0005g0259others(2): Show | 5 | HG01255.hp2 HG02559.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.705-442A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845016 | ||||||
| chr3:182845044
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.705-414A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845044 | ||||||
| chr3:182845091
|
G | A | 1 | a0001c0001t0003g0215 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.705-367G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845091 | ||||||
| chr3:182845093
|
C | G | 1 | a0001c0001t0002g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.705-365C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845093 | ||||||
| chr3:182845098
|
C | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.705-360C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845098 | ||||||
| chr3:182845254
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.705-204G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845254 | ||||||
| chr3:182845261
|
C | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.705-197C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845261 | ||||||
| chr3:182845300
|
C | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.705-158C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | chr3 | 182845300 | ||||||
| chr3:182845618
|
T | G | 5 | a0001c0002t0004g0288a0001c0002t0004g0289a0001c0002t0004g0290others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+96T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182845618 | ||||||
| chr3:182845722
|
A | G | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.769+200A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182845722 | ||||||
| chr3:182845736
|
A | C | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.769+214A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182845736 | ||||||
| chr3:182845759
|
C | T | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+237C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182845759 | ||||||
| chr3:182845797
|
T | C | 1 | a0001c0002t0004g0300 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.769+275T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182845797 | ||||||
| chr3:182845980
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.769+458C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182845980 | ||||||
| chr3:182846204
|
T | A | 9 | a0001c0001t0003g0175a0001c0001t0003g0177a0001c0001t0003g0179others(6): Show | 9 | HG00597.hp1 HG00642.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+682T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182846204 | ||||||
| chr3:182846218
|
C | T | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.769+696C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182846218 | ||||||
| chr3:182846312
|
C | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0250 | 2 | HG02015.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.769+790C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182846312 | ||||||
| chr3:182846325
|
G | T | 2 | a0001c0001t0005g0255a0001c0001t0005g0256 | 2 | HG00639.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.769+803G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182846325 | ||||||
| chr3:182846383
|
ACGTTGCA others(4): Show |
A | 1 | a0001c0001t0003g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.769+863_769+873del others(11): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 182846383 | |||||
| chr3:182846388
|
G | T | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+866G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182846388 | ||||||
| chr3:182846745
|
C | T | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.769+1223C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182846745 | ||||||
| chr3:182847050
|
C | CT | 6 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0002g0157others(3): Show | 6 | HG01109.hp1 HG02738.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-1406dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 182847050 | |||||
| chr3:182847050
|
CT | C | 10 | a0001c0001t0001g0021a0001c0001t0001g0105a0001c0002t0004g0001others(7): Show | 12 | HG01099.hp2 HG02257.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.770-1406delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr3 | 182847050 | |||||
| chr3:182847136
|
T | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.770-1340T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182847136 | ||||||
| chr3:182847469
|
T | C | 2 | a0001c0001t0002g0135a0001c0001t0002g0137 | 2 | HG00408.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.770-1007T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182847469 | ||||||
| chr3:182847525
|
C | T | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.770-951C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182847525 | ||||||
| chr3:182847656
|
G | T | 1 | a0001c0001t0002g0159 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.770-820G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182847656 | ||||||
| chr3:182847822
|
C | T | 2 | a0001c0002t0004g0293a0001c0002t0004g0294 | 2 | HG00323.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.770-654C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182847822 | ||||||
| chr3:182847975
|
A | G | 1 | a0001c0001t0005g0259 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.770-501A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182847975 | ||||||
| chr3:182848126
|
C | T | 1 | a0001c0001t0002g0309 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.770-350C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182848126 | ||||||
| chr3:182848134
|
G | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(150): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.770-342G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182848134 | ||||||
| chr3:182848235
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.770-241G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 9/29 | chr3 | 182848235 | ||||||
| chr3:182848638
|
T | C | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.851+81T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182848638 | ||||||
| chr3:182848747
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.851+190A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182848747 | ||||||
| chr3:182849098
|
G | A | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.851+541G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849098 | ||||||
| chr3:182849253
|
A | T | 1 | a0001c0001t0006g0251 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.851+696A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849253 | ||||||
| chr3:182849368
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.851+811G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849368 | ||||||
| chr3:182849600
|
A | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG00609.hp1 NA18747.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.851+1043A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849600 | ||||||
| chr3:182849612
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.851+1055A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849612 | ||||||
| chr3:182849735
|
A | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.851+1178A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849735 | ||||||
| chr3:182849882
|
C | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0043 | 3 | HG00597.hp2 NA18982.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.851+1325C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849882 | ||||||
| chr3:182849950
|
A | G | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.851+1393A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182849950 | ||||||
| chr3:182850018
|
C | CGTG | 4 | a0001c0001t0006g0032a0001c0001t0006g0082a0001c0001t0006g0083others(1): Show | 4 | HG01070.hp1 HG01192.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.851+1461_851+1462i others(5): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850018 | ||||||
| chr3:182850032
|
G | A | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.851+1475G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850032 | ||||||
| chr3:182850042
|
A | T | 1 | a0001c0001t0003g0205 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.851+1485A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850042 | ||||||
| chr3:182850109
|
A | G | 2 | a0001c0001t0003g0190a0001c0001t0003g0245 | 2 | HG01346.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.851+1552A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850109 | ||||||
| chr3:182850219
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.851+1662T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850219 | ||||||
| chr3:182850246
|
G | A | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.851+1689G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850246 | ||||||
| chr3:182850301
|
C | T | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.851+1744C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850301 | ||||||
| chr3:182850429
|
C | T | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.851+1872C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850429 | ||||||
| chr3:182850661
|
T | G | 3 | a0001c0002t0006g0281a0001c0002t0006g0303a0001c0002t0006g0305 | 3 | NA18963.hp1 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.851+2104T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850661 | ||||||
| chr3:182850809
|
A | G | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.851+2252A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850809 | ||||||
| chr3:182850860
|
A | T | 1 | a0001c0001t0002g0244 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.851+2303A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850860 | ||||||
| chr3:182850874
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.851+2317A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182850874 | ||||||
| chr3:182851075
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.851+2518T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182851075 | ||||||
| chr3:182851084
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.851+2527G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182851084 | ||||||
| chr3:182851240
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.851+2683G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182851240 | ||||||
| chr3:182851264
|
C | A | 27 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(24): Show | 27 | HG00558.hp2 HG02083.hp2 HG02738.hp2 others(24): Show |
intron_variant | MODIFIER | c.851+2707C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182851264 | ||||||
| chr3:182851611
|
G | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.851+3054G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182851611 | ||||||
| chr3:182852086
|
T | C | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.851+3529T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852086 | ||||||
| chr3:182852090
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.851+3533A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852090 | ||||||
| chr3:182852240
|
C | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.851+3683C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852240 | ||||||
| chr3:182852327
|
A | AT | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.851+3772dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182852327 | |||||
| chr3:182852393
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.851+3836G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852393 | ||||||
| chr3:182852411
|
G | C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.851+3854G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852411 | ||||||
| chr3:182852540
|
C | G | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.851+3983C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852540 | ||||||
| chr3:182852852
|
G | A | 1 | a0001c0001t0017g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.851+4295G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852852 | ||||||
| chr3:182852860
|
A | G | 2 | a0001c0001t0002g0169a0001c0001t0002g0264 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.851+4303A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182852860 | ||||||
| chr3:182853001
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.851+4444A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853001 | ||||||
| chr3:182853354
|
C | T | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.852-4524C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853354 | ||||||
| chr3:182853356
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.852-4522C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853356 | ||||||
| chr3:182853457
|
C | T | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.852-4421C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853457 | ||||||
| chr3:182853472
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.852-4406T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853472 | ||||||
| chr3:182853577
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.852-4301A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853577 | ||||||
| chr3:182853669
|
T | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.852-4209T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853669 | ||||||
| chr3:182853747
|
A | G | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-4131A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853747 | ||||||
| chr3:182853823
|
A | G | 1 | a0001c0001t0002g0159 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.852-4055A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853823 | ||||||
| chr3:182853900
|
A | T | 1 | a0001c0002t0010g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.852-3978A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182853900 | ||||||
| chr3:182854060
|
T | C | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.852-3818T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854060 | ||||||
| chr3:182854109
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.852-3769C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854109 | ||||||
| chr3:182854305
|
A | T | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-3573A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854305 | ||||||
| chr3:182854306
|
C | A | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-3572C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854306 | ||||||
| chr3:182854341
|
A | C | 3 | a0001c0002t0006g0281a0001c0002t0006g0303a0001c0002t0006g0305 | 3 | NA18963.hp1 NA19054.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.852-3537A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854341 | ||||||
| chr3:182854425
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.852-3453G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854425 | ||||||
| chr3:182854472
|
AAAAAC | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.852-3381_852-3377d others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854472 | |||||
| chr3:182854752
|
T | TACAC | 3 | a0001c0001t0003g0191a0001c0001t0003g0210a0001c0001t0003g0211 | 3 | HG01255.hp1 HG01433.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.852-3081_852-3078d others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TAC | T | 46 | a0001c0001t0001g0105a0001c0001t0002g0121a0001c0001t0002g0123others(43): Show | 46 | HG00558.hp2 HG00597.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.852-3079_852-3078d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACAC | T | 9 | a0001c0001t0002g0122a0001c0001t0002g0164a0001c0001t0003g0182others(6): Show | 9 | HG01069.hp1 HG03710.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.852-3081_852-3078d others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACAC | T | 26 | a0001c0001t0002g0126a0001c0001t0002g0130a0001c0001t0002g0155others(23): Show | 26 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.852-3083_852-3078d others(8): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(1): Show |
T | 5 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0003g0202others(2): Show | 5 | HG01515.hp1 HG01517.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.852-3085_852-3078d others(10): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(3): Show |
T | 5 | a0001c0001t0002g0153a0001c0001t0005g0253a0001c0001t0011g0138others(2): Show | 5 | HG02451.hp1 HG02451.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.852-3087_852-3078d others(12): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(5): Show |
T | 41 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0132others(38): Show | 41 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.852-3089_852-3078d others(14): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(7): Show |
T | 5 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314others(2): Show | 7 | HG02109.hp2 HG02257.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.852-3091_852-3078d others(16): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(9): Show |
T | 9 | a0001c0001t0002g0134a0001c0001t0002g0146a0001c0001t0002g0147others(6): Show | 9 | HG01109.hp1 HG01496.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.852-3093_852-3078d others(18): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(11): Show |
T | 36 | a0001c0001t0001g0062a0001c0001t0001g0107a0001c0002t0004g0007others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.852-3095_852-3078d others(20): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(13): Show |
T | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 113 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.852-3097_852-3078d others(22): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854752
|
TACACACA others(15): Show |
T | 1 | a0001c0001t0001g0025 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.852-3099_852-3078d others(24): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182854752 | |||||
| chr3:182854862
|
G | C | 3 | a0001c0002t0004g0312a0001c0002t0004g0316a0001c0002t0010g0270 | 3 | HG02896.hp2 HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.852-3016G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854862 | ||||||
| chr3:182854897
|
A | G | 1 | a0001c0002t0006g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.852-2981A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854897 | ||||||
| chr3:182854919
|
C | A | 1 | a0001c0002t0004g0306 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.852-2959C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182854919 | ||||||
| chr3:182855200
|
A | G | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.852-2678A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855200 | ||||||
| chr3:182855248
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.852-2630C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855248 | ||||||
| chr3:182855320
|
C | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.852-2558C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855320 | ||||||
| chr3:182855345
|
C | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.852-2533C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855345 | ||||||
| chr3:182855613
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.852-2265C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855613 | ||||||
| chr3:182855694
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.852-2184A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855694 | ||||||
| chr3:182855839
|
T | C | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.852-2039T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855839 | ||||||
| chr3:182855930
|
G | GA | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.852-1948_852-1947i others(3): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855930 | ||||||
| chr3:182855931
|
G | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.852-1947G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182855931 | ||||||
| chr3:182856102
|
T | C | 1 | a0001c0001t0003g0216 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.852-1776T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182856102 | ||||||
| chr3:182856481
|
G | A | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.852-1397G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182856481 | ||||||
| chr3:182856678
|
G | A | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.852-1200G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182856678 | ||||||
| chr3:182857042
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.852-836A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857042 | ||||||
| chr3:182857238
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0085 | 2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.852-640C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857238 | ||||||
| chr3:182857408
|
A | G | 1 | a0001c0001t0012g0020 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.852-470A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857408 | ||||||
| chr3:182857563
|
T | TA | 110 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.852-302dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | 182857563 | |||||
| chr3:182857576
|
ACT | A | 4 | a0001c0002t0006g0282a0001c0002t0009g0247a0001c0002t0009g0248others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-301_852-300del others(2): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857576 | ||||||
| chr3:182857576
|
ACTT | A | 42 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(39): Show | 45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.852-301_852-299del others(3): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857576 | ||||||
| chr3:182857579
|
T | A | 4 | a0001c0002t0006g0282a0001c0002t0009g0247a0001c0002t0009g0248others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.852-299T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857579 | ||||||
| chr3:182857617
|
C | T | 1 | a0005c0006t0001g0073 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.852-261C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857617 | ||||||
| chr3:182857722
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.852-156G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857722 | ||||||
| chr3:182857843
|
G | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.852-35G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | chr3 | 182857843 | ||||||
| chr3:182858151
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1002+123G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858151 | ||||||
| chr3:182858231
|
G | A | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1002+203G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858231 | ||||||
| chr3:182858321
|
C | A | 1 | a0001c0001t0002g0232 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1002+293C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858321 | ||||||
| chr3:182858453
|
A | C | 1 | a0002c0003t0002g0118 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1002+425A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858453 | ||||||
| chr3:182858525
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1002+497G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858525 | ||||||
| chr3:182858526
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1002+498G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858526 | ||||||
| chr3:182858546
|
C | G | 1 | a0001c0001t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1002+518C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858546 | ||||||
| chr3:182858714
|
T | G | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1003-448T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858714 | ||||||
| chr3:182858858
|
G | A | 1 | a0001c0001t0008g0183 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1003-304G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858858 | ||||||
| chr3:182858909
|
C | G | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1003-253C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858909 | ||||||
| chr3:182858954
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1003-208A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182858954 | ||||||
| chr3:182859038
|
A | G | 1 | a0001c0001t0006g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1003-124A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182859038 | ||||||
| chr3:182859043
|
A | G | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1003-119A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182859043 | ||||||
| chr3:182859135
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1003-27T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 11/29 | chr3 | 182859135 | ||||||
| chr3:182859410
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1200+51G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182859410 | ||||||
| chr3:182859472
|
C | T | 3 | a0003c0005t0006g0283a0003c0005t0006g0302a0003c0005t0006g0304 | 3 | NA18949.hp1 NA19075.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1200+113C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182859472 | ||||||
| chr3:182859757
|
A | G | 261 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(258): Show | 269 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.1200+398A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182859757 | ||||||
| chr3:182859845
|
T | G | 3 | a0001c0001t0002g0231a0001c0001t0002g0233a0001c0001t0002g0234 | 3 | NA18963.hp2 NA18983.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1200+486T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182859845 | ||||||
| chr3:182859948
|
C | CT | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1200+603dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182859948 | |||||
| chr3:182859948
|
CT | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(152): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1200+603delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182859948 | |||||
| chr3:182859970
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1200+611A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182859970 | ||||||
| chr3:182860339
|
G | T | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1200+980G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182860339 | ||||||
| chr3:182860471
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1200+1112T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182860471 | ||||||
| chr3:182860560
|
A | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG00408.hp2 NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1200+1201A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182860560 | ||||||
| chr3:182860566
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1200+1207T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182860566 | ||||||
| chr3:182860684
|
A | C | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+1325A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182860684 | ||||||
| chr3:182860857
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1200+1498C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182860857 | ||||||
| chr3:182860928
|
AT | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0035others(1): Show | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1200+1573delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182860928 | |||||
| chr3:182861061
|
A | T | 8 | a0001c0001t0002g0126a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+1702A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861061 | ||||||
| chr3:182861065
|
C | CT | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(119): Show | 127 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1200+1723dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182861065 | |||||
| chr3:182861065
|
C | CTT | 44 | a0001c0001t0001g0072a0001c0001t0001g0115a0001c0001t0005g0252others(41): Show | 47 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1200+1722_1200+172 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182861065 | |||||
| chr3:182861065
|
C | CTTT | 9 | a0001c0001t0005g0254a0001c0001t0005g0255a0001c0001t0005g0256others(6): Show | 9 | HG00639.hp2 HG01255.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1200+1721_1200+172 others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182861065 | |||||
| chr3:182861190
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1200+1831C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861190 | ||||||
| chr3:182861292
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1200+1933C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861292 | ||||||
| chr3:182861491
|
G | A | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+2132G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861491 | ||||||
| chr3:182861546
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1200+2187C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861546 | ||||||
| chr3:182861858
|
G | T | 1 | a0001c0001t0001g0092 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1200+2499G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861858 | ||||||
| chr3:182861900
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0074 | 3 | HG01261.hp1 HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1200+2541C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861900 | ||||||
| chr3:182861943
|
C | CA | 51 | a0001c0001t0002g0133a0001c0001t0005g0253a0001c0001t0005g0254others(48): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1200+2599dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182861943 | |||||
| chr3:182861943
|
C | CAA | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1200+2598_1200+259 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182861943 | |||||
| chr3:182861964
|
G | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1200+2605G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182861964 | ||||||
| chr3:182862113
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1200+2754C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862113 | ||||||
| chr3:182862155
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0086 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1200+2796C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862155 | ||||||
| chr3:182862245
|
A | ACT | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1200+2888_1200+288 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182862245 | |||||
| chr3:182862279
|
T | TA | 7 | a0001c0001t0002g0157a0001c0001t0002g0171a0001c0001t0017g0158others(4): Show | 7 | HG01257.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+2932dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182862279 | |||||
| chr3:182862290
|
A | C | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1200+2931A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862290 | ||||||
| chr3:182862292
|
C | A | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1200+2933C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862292 | ||||||
| chr3:182862466
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1201-2990C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862466 | ||||||
| chr3:182862477
|
A | G | 8 | a0001c0001t0003g0206a0001c0001t0003g0207a0001c0001t0003g0209others(5): Show | 8 | HG01433.hp2 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201-2979A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862477 | ||||||
| chr3:182862488
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(232): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1201-2968A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862488 | ||||||
| chr3:182862501
|
A | C | 1 | a0001c0001t0001g0096 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1201-2955A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862501 | ||||||
| chr3:182862543
|
C | T | 3 | a0001c0001t0002g0050a0001c0001t0002g0051a0001c0001t0002g0103 | 3 | HG02622.hp2 HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1201-2913C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862543 | ||||||
| chr3:182862615
|
C | T | 4 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(1): Show | 4 | NA18947.hp2 NA18969.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-2841C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862615 | ||||||
| chr3:182862756
|
C | T | 1 | a0001c0001t0002g0122 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1201-2700C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862756 | ||||||
| chr3:182862774
|
C | T | 1 | a0001c0002t0004g0285 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1201-2682C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182862774 | ||||||
| chr3:182862818
|
G | GT | 23 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0040others(20): Show | 23 | HG00621.hp2 HG00639.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1201-2627dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182862818 | |||||
| chr3:182862907
|
C | CATTT | 3 | a0001c0002t0009g0267a0001c0002t0009g0268a0001c0002t0019g0297 | 3 | HG02109.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1201-2528_1201-252 others(8): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr3 | 182862907 | |||||
| chr3:182863001
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0062others(5): Show | 9 | HG02071.hp2 HG02080.hp2 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.1201-2455C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863001 | ||||||
| chr3:182863002
|
G | A | 1 | a0001c0002t0004g0306 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1201-2454G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863002 | ||||||
| chr3:182863056
|
A | G | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1201-2400A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863056 | ||||||
| chr3:182863117
|
C | T | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1201-2339C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863117 | ||||||
| chr3:182863151
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1201-2305G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863151 | ||||||
| chr3:182863155
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1201-2301C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863155 | ||||||
| chr3:182863182
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1201-2274G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863182 | ||||||
| chr3:182863300
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0043 | 2 | HG00597.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1201-2156G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863300 | ||||||
| chr3:182863445
|
C | T | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1201-2011C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863445 | ||||||
| chr3:182863468
|
T | C | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1201-1988T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863468 | ||||||
| chr3:182863538
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1201-1918G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863538 | ||||||
| chr3:182863611
|
C | T | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1201-1845C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863611 | ||||||
| chr3:182863720
|
T | C | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1201-1736T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863720 | ||||||
| chr3:182863804
|
G | T | 1 | a0001c0001t0003g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1201-1652G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863804 | ||||||
| chr3:182863870
|
G | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1201-1586G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863870 | ||||||
| chr3:182863999
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(162): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1201-1457A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182863999 | ||||||
| chr3:182864108
|
C | T | 1 | a0001c0001t0016g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1201-1348C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864108 | ||||||
| chr3:182864271
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1201-1185G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864271 | ||||||
| chr3:182864311
|
A | G | 3 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0264 | 3 | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1201-1145A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864311 | ||||||
| chr3:182864313
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1201-1143A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864313 | ||||||
| chr3:182864494
|
A | G | 1 | a0001c0002t0006g0282 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1201-962A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864494 | ||||||
| chr3:182864578
|
T | C | 1 | a0001c0001t0003g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1201-878T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864578 | ||||||
| chr3:182864783
|
G | A | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1201-673G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864783 | ||||||
| chr3:182864828
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1201-628T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864828 | ||||||
| chr3:182864861
|
C | T | 5 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG01109.hp2 HG01261.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1201-595C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864861 | ||||||
| chr3:182864987
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1201-469C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182864987 | ||||||
| chr3:182865000
|
T | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0074 | 3 | HG01261.hp1 HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1201-456T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182865000 | ||||||
| chr3:182865086
|
A | C | 1 | a0001c0001t0012g0013 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1201-370A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182865086 | ||||||
| chr3:182865216
|
C | T | 4 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0035others(1): Show | 5 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201-240C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182865216 | ||||||
| chr3:182865276
|
T | A | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1201-180T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182865276 | ||||||
| chr3:182865405
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1201-51A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182865405 | ||||||
| chr3:182865426
|
T | C | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1201-30T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 12/29 | chr3 | 182865426 | ||||||
| chr3:182865916
|
G | A | 1 | a0001c0001t0001g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1443+218G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 13/29 | chr3 | 182865916 | ||||||
| chr3:182865931
|
G | A | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1443+233G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 13/29 | chr3 | 182865931 | ||||||
| chr3:182865936
|
TAAGAA | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1443+242_1443+246d others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr3 | 182865936 | |||||
| chr3:182866135
|
G | T | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1444-133G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 13/29 | chr3 | 182866135 | ||||||
| chr3:182866202
|
C | T | 29 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.1444-66C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 13/29 | chr3 | 182866202 | ||||||
| chr3:182866659
|
CTT | C | 53 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(50): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.1619+218_1619+219d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr3 | 182866659 | |||||
| chr3:182866695
|
A | G | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1619+252A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182866695 | ||||||
| chr3:182866787
|
G | C | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1619+344G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182866787 | ||||||
| chr3:182866811
|
AT | A | 12 | a0001c0001t0005g0254a0001c0001t0005g0255a0001c0001t0005g0256others(9): Show | 12 | HG00639.hp2 HG01255.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1619+373delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr3 | 182866811 | |||||
| chr3:182866854
|
AATT | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1619+417_1619+419d others(5): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr3 | 182866854 | |||||
| chr3:182866928
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1620-448T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182866928 | ||||||
| chr3:182866930
|
TA | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-445delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182866930 | ||||||
| chr3:182866931
|
A | T | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1620-445A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182866931 | ||||||
| chr3:182866932
|
T | TA | 115 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1620-444_1620-443i others(3): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182866932 | ||||||
| chr3:182866933
|
T | A | 46 | a0001c0001t0002g0223a0001c0001t0002g0239a0001c0001t0003g0212others(43): Show | 47 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1620-443T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182866933 | ||||||
| chr3:182867103
|
A | G | 1 | a0001c0002t0007g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1620-273A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867103 | ||||||
| chr3:182867145
|
T | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1620-231T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867145 | ||||||
| chr3:182867188
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1620-188T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867188 | ||||||
| chr3:182867199
|
G | GTAAT | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-177_1620-176i others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867199 | ||||||
| chr3:182867202
|
G | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-174G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867202 | ||||||
| chr3:182867204
|
C | CCCA | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-172_1620-171i others(5): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867204 | ||||||
| chr3:182867206
|
G | A | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-170G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867206 | ||||||
| chr3:182867208
|
C | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-168C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867208 | ||||||
| chr3:182867209
|
A | G | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-167A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867209 | ||||||
| chr3:182867211
|
G | A | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-165G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867211 | ||||||
| chr3:182867213
|
G | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-163G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867213 | ||||||
| chr3:182867214
|
C | A | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-162C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867214 | ||||||
| chr3:182867215
|
C | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-161C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867215 | ||||||
| chr3:182867216
|
A | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-160A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867216 | ||||||
| chr3:182867217
|
C | A | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1620-159C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867217 | ||||||
| chr3:182867251
|
A | G | 3 | a0001c0001t0003g0190a0001c0001t0003g0192a0001c0001t0003g0245 | 3 | HG01346.hp1 HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1620-125A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867251 | ||||||
| chr3:182867264
|
T | A | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1620-112T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 14/29 | chr3 | 182867264 | ||||||
| chr3:182867524
|
A | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG00735.hp1 HG01433.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1688+80A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182867524 | ||||||
| chr3:182867579
|
C | CT | 64 | a0001c0001t0001g0093a0001c0001t0002g0128a0001c0001t0002g0143others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.1688+157dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr3 | 182867579 | |||||
| chr3:182867579
|
C | CTT | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(105): Show | 113 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1688+156_1688+157d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr3 | 182867579 | |||||
| chr3:182867579
|
CT | C | 6 | a0001c0001t0002g0146a0001c0001t0002g0166a0001c0001t0002g0226others(3): Show | 6 | HG01069.hp1 HG02135.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1688+157delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr3 | 182867579 | |||||
| chr3:182867712
|
T | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1688+268T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182867712 | ||||||
| chr3:182867898
|
A | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.1688+454A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182867898 | ||||||
| chr3:182868001
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1688+557A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868001 | ||||||
| chr3:182868082
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1688+638G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868082 | ||||||
| chr3:182868328
|
A | G | 8 | a0001c0001t0002g0126a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1689-750A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868328 | ||||||
| chr3:182868383
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1689-695G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868383 | ||||||
| chr3:182868565
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1689-513C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868565 | ||||||
| chr3:182868567
|
C | T | 1 | a0001c0001t0020g0078 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1689-511C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868567 | ||||||
| chr3:182868620
|
A | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.1689-458A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868620 | ||||||
| chr3:182868784
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1689-294G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868784 | ||||||
| chr3:182868854
|
T | A | 1 | a0001c0001t0016g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1689-224T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 15/29 | chr3 | 182868854 | ||||||
| chr3:182869338
|
G | A | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.1866+7G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182869338 | ||||||
| chr3:182869485
|
T | G | 5 | a0001c0002t0004g0271a0001c0002t0004g0272a0001c0002t0004g0295others(2): Show | 5 | HG00099.hp1 HG00140.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1866+154T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182869485 | ||||||
| chr3:182869510
|
C | G | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1866+179C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182869510 | ||||||
| chr3:182869639
|
T | C | 1 | a0001c0001t0003g0182 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1866+308T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182869639 | ||||||
| chr3:182869794
|
T | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1866+463T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182869794 | ||||||
| chr3:182869856
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0097 | 3 | NA18974.hp1 NA19000.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1866+525A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182869856 | ||||||
| chr3:182869878
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1866+547T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182869878 | ||||||
| chr3:182870002
|
A | G | 9 | a0001c0001t0003g0175a0001c0001t0003g0177a0001c0001t0003g0179others(6): Show | 9 | HG00597.hp1 HG00642.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.1866+671A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870002 | ||||||
| chr3:182870083
|
CA | C | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1866+753delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870083 | ||||||
| chr3:182870207
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0019others(3): Show | 7 | HG00558.hp1 HG02165.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1866+876G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870207 | ||||||
| chr3:182870702
|
G | A | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1866+1371G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870702 | ||||||
| chr3:182870708
|
T | G | 1 | a0001c0001t0002g0135 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1866+1377T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870708 | ||||||
| chr3:182870712
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(174): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1866+1381A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870712 | ||||||
| chr3:182870739
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1866+1408C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870739 | ||||||
| chr3:182870860
|
G | A | 7 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(4): Show | 7 | HG02630.hp2 HG02965.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.1867-1496G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870860 | ||||||
| chr3:182870929
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1867-1427A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870929 | ||||||
| chr3:182870982
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1867-1374C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870982 | ||||||
| chr3:182870992
|
C | A | 1 | a0001c0001t0001g0025 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1867-1364C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182870992 | ||||||
| chr3:182871191
|
A | G | 1 | a0002c0003t0002g0116 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1867-1165A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182871191 | ||||||
| chr3:182871426
|
C | T | 2 | a0001c0001t0011g0138a0001c0001t0011g0142 | 2 | NA18989.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1867-930C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182871426 | ||||||
| chr3:182871545
|
T | C | 8 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(5): Show | 8 | HG01257.hp1 HG02109.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1867-811T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182871545 | ||||||
| chr3:182871770
|
T | C | 1 | a0001c0001t0003g0178 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1867-586T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182871770 | ||||||
| chr3:182871908
|
C | T | 2 | a0001c0002t0004g0316a0001c0002t0010g0270 | 2 | HG03225.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1867-448C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182871908 | ||||||
| chr3:182871976
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1867-380C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182871976 | ||||||
| chr3:182872053
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1867-303G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182872053 | ||||||
| chr3:182872199
|
A | G | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.1867-157A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182872199 | ||||||
| chr3:182872278
|
T | C | 1 | a0001c0001t0001g0006 | 2 | NA18943.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1867-78T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 17/29 | chr3 | 182872278 | ||||||
| chr3:182872566
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2048+29C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/29 | chr3 | 182872566 | ||||||
| chr3:182872865
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2048+328A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/29 | chr3 | 182872865 | ||||||
| chr3:182872990
|
A | G | 1 | a0001c0001t0002g0239 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2048+453A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/29 | chr3 | 182872990 | ||||||
| chr3:182873049
|
G | C | 1 | a0001c0001t0003g0189 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2048+512G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/29 | chr3 | 182873049 | ||||||
| chr3:182873359
|
T | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(128): Show | 136 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.2049-453T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/29 | chr3 | 182873359 | ||||||
| chr3:182873621
|
C | T | 5 | a0001c0002t0004g0288a0001c0002t0004g0289a0001c0002t0004g0290others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.2049-191C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/29 | chr3 | 182873621 | ||||||
| chr3:182873625
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.2049-187T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 18/29 | chr3 | 182873625 | ||||||
| chr3:182874185
|
G | C | 3 | a0001c0001t0003g0177a0001c0001t0003g0215a0001c0001t0003g0265 | 3 | HG00597.hp1 NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.2252+170G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182874185 | ||||||
| chr3:182874314
|
A | T | 1 | a0001c0001t0003g0220 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2252+299A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182874314 | ||||||
| chr3:182874499
|
CATTACGA others(1): Show |
C | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2252+485_2252+492d others(10): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182874499 | ||||||
| chr3:182875111
|
T | G | 2 | a0001c0001t0002g0225a0001c0001t0002g0238 | 2 | NA19068.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.2252+1096T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182875111 | ||||||
| chr3:182875238
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.2252+1223T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182875238 | ||||||
| chr3:182875416
|
TTTTGTTG | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2252+1404_2252+141 others(11): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr3 | 182875416 | |||||
| chr3:182876201
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2252+2186C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182876201 | ||||||
| chr3:182876324
|
T | G | 6 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2252+2309T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182876324 | ||||||
| chr3:182876351
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2252+2336T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182876351 | ||||||
| chr3:182876442
|
G | C | 58 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0126others(55): Show | 58 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.2252+2427G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182876442 | ||||||
| chr3:182876836
|
G | A | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2253-2660G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182876836 | ||||||
| chr3:182876997
|
G | A | 1 | a0005c0006t0001g0081 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2253-2499G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182876997 | ||||||
| chr3:182877171
|
A | G | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2253-2325A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182877171 | ||||||
| chr3:182877234
|
G | C | 4 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314others(1): Show | 6 | HG02257.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2253-2262G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182877234 | ||||||
| chr3:182877499
|
G | A | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2253-1997G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182877499 | ||||||
| chr3:182877546
|
G | T | 1 | a0001c0001t0003g0188 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2253-1950G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182877546 | ||||||
| chr3:182877737
|
A | G | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2253-1759A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182877737 | ||||||
| chr3:182878027
|
A | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2253-1469A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182878027 | ||||||
| chr3:182878955
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2253-541T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182878955 | ||||||
| chr3:182879243
|
G | A | 1 | a0001c0002t0010g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2253-253G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 19/29 | chr3 | 182879243 | ||||||
| chr3:182879743
|
G | A | 3 | a0001c0001t0002g0231a0001c0001t0002g0233a0001c0001t0002g0234 | 3 | NA18963.hp2 NA18983.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.2406+94G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182879743 | ||||||
| chr3:182879839
|
A | G | 54 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0126others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.2406+190A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182879839 | ||||||
| chr3:182880211
|
G | A | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.2406+562G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182880211 | ||||||
| chr3:182880267
|
G | C | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2407-612G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182880267 | ||||||
| chr3:182880386
|
A | G | 3 | a0001c0002t0004g0280a0001c0002t0010g0292a0001c0002t0022g0284 | 3 | HG02647.hp2 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2407-493A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182880386 | ||||||
| chr3:182880410
|
A | G | 1 | a0001c0002t0004g0271 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2407-469A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182880410 | ||||||
| chr3:182880502
|
G | A | 1 | a0001c0002t0004g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2407-377G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182880502 | ||||||
| chr3:182880847
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2407-32G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 20/29 | chr3 | 182880847 | ||||||
| chr3:182881065
|
A | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2509+84A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881065 | ||||||
| chr3:182881075
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2509+94A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881075 | ||||||
| chr3:182881195
|
G | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2509+214G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881195 | ||||||
| chr3:182881293
|
G | T | 1 | a0001c0001t0003g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2509+312G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881293 | ||||||
| chr3:182881374
|
C | T | 1 | a0001c0002t0004g0312 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2509+393C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881374 | ||||||
| chr3:182881393
|
C | A | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2509+412C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881393 | ||||||
| chr3:182881413
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2509+432A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881413 | ||||||
| chr3:182881459
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2509+478T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881459 | ||||||
| chr3:182881536
|
T | C | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.2509+555T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881536 | ||||||
| chr3:182881995
|
A | G | 1 | a0001c0001t0003g0241 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2509+1014A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182881995 | ||||||
| chr3:182882173
|
G | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2509+1192G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182882173 | ||||||
| chr3:182882208
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2509+1227C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182882208 | ||||||
| chr3:182882228
|
T | C | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.2509+1247T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182882228 | ||||||
| chr3:182882296
|
TTGA | T | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | NA18962.hp2 NA18968.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2509+1320_2509+132 others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 182882296 | |||||
| chr3:182882536
|
C | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2509+1555C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182882536 | ||||||
| chr3:182882618
|
T | G | 1 | a0001c0001t0005g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2509+1637T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182882618 | ||||||
| chr3:182882857
|
A | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.2509+1876A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182882857 | ||||||
| chr3:182882988
|
G | A | 2 | a0001c0002t0004g0307a0001c0002t0004g0308 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2510-1765G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182882988 | ||||||
| chr3:182883156
|
C | G | 1 | a0001c0001t0018g0149 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2510-1597C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883156 | ||||||
| chr3:182883200
|
G | A | 2 | a0001c0001t0003g0197a0001c0001t0003g0198 | 2 | HG02523.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.2510-1553G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883200 | ||||||
| chr3:182883261
|
C | CT | 8 | a0001c0001t0005g0252a0001c0002t0004g0001a0001c0002t0004g0312others(5): Show | 10 | HG02257.hp1 HG02280.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2510-1479dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 182883261 | |||||
| chr3:182883261
|
C | CTT | 34 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(31): Show | 35 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.2510-1480_2510-147 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 182883261 | |||||
| chr3:182883261
|
CT | C | 8 | a0001c0001t0002g0126a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.2510-1479delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 182883261 | |||||
| chr3:182883302
|
G | T | 3 | a0001c0001t0003g0129a0001c0001t0003g0189a0001c0001t0003g0199 | 3 | HG00673.hp1 NA18975.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.2510-1451G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883302 | ||||||
| chr3:182883344
|
G | A | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2510-1409G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883344 | ||||||
| chr3:182883370
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2510-1383A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883370 | ||||||
| chr3:182883594
|
C | A | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2510-1159C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883594 | ||||||
| chr3:182883677
|
C | T | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2510-1076C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883677 | ||||||
| chr3:182883691
|
C | T | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2510-1062C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883691 | ||||||
| chr3:182883693
|
C | T | 1 | a0001c0001t0006g0251 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2510-1060C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883693 | ||||||
| chr3:182883694
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2510-1059G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883694 | ||||||
| chr3:182883703
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2510-1050C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883703 | ||||||
| chr3:182883727
|
G | A | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.2510-1026G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883727 | ||||||
| chr3:182883756
|
C | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2510-997C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883756 | ||||||
| chr3:182883783
|
G | A | 1 | a0001c0001t0002g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2510-970G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883783 | ||||||
| chr3:182883815
|
C | T | 1 | a0001c0002t0004g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2510-938C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883815 | ||||||
| chr3:182883865
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2510-888G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883865 | ||||||
| chr3:182883886
|
C | T | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2510-867C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883886 | ||||||
| chr3:182883942
|
G | A | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2510-811G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883942 | ||||||
| chr3:182883950
|
G | A | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2510-803G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182883950 | ||||||
| chr3:182883954
|
C | CA | 11 | a0001c0001t0001g0064a0001c0001t0001g0101a0001c0001t0001g0109others(8): Show | 11 | HG01981.hp1 HG02965.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.2510-778dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 182883954 | |||||
| chr3:182883954
|
CA | C | 58 | a0001c0001t0001g0052a0001c0001t0002g0130a0001c0001t0002g0226others(55): Show | 61 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.2510-778delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 182883954 | |||||
| chr3:182883983
|
G | GACTA | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 117 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2510-768_2510-765d others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr3 | 182883983 | |||||
| chr3:182884079
|
T | C | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2510-674T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182884079 | ||||||
| chr3:182884094
|
A | T | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2510-659A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182884094 | ||||||
| chr3:182884450
|
A | C | 2 | a0001c0001t0011g0138a0001c0001t0011g0142 | 2 | NA18989.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2510-303A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182884450 | ||||||
| chr3:182884515
|
T | G | 1 | a0001c0001t0001g0034 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2510-238T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182884515 | ||||||
| chr3:182884522
|
T | C | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2510-231T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182884522 | ||||||
| chr3:182884624
|
A | G | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.2510-129A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 21/29 | chr3 | 182884624 | ||||||
| chr3:182884994
|
T | C | 1 | a0001c0001t0002g0153 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2655+96T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 22/29 | chr3 | 182884994 | ||||||
| chr3:182885270
|
G | A | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2655+372G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 22/29 | chr3 | 182885270 | ||||||
| chr3:182885318
|
A | G | 1 | a0001c0001t0008g0184 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2655+420A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 22/29 | chr3 | 182885318 | ||||||
| chr3:182885582
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2656-369T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 22/29 | chr3 | 182885582 | ||||||
| chr3:182885878
|
A | AT | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.2656-65dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr3 | 182885878 | |||||
| chr3:182885905
|
G | A | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2656-46G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 22/29 | chr3 | 182885905 | ||||||
| chr3:182886103
|
C | G | 4 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(1): Show | 4 | HG02630.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2715+93C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182886103 | ||||||
| chr3:182886515
|
A | G | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2715+505A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182886515 | ||||||
| chr3:182886734
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2715+724A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182886734 | ||||||
| chr3:182886900
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2716-686A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182886900 | ||||||
| chr3:182886932
|
A | G | 1 | a0001c0002t0004g0315 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2716-654A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182886932 | ||||||
| chr3:182887038
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 135 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(132): Show |
intron_variant | MODIFIER | c.2716-548T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182887038 | ||||||
| chr3:182887244
|
G | A | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2716-342G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182887244 | ||||||
| chr3:182887317
|
C | G | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2716-269C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182887317 | ||||||
| chr3:182887364
|
T | C | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2716-222T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182887364 | ||||||
| chr3:182887435
|
C | T | 1 | a0001c0001t0003g0181 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2716-151C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182887435 | ||||||
| chr3:182887537
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2716-49G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 23/29 | chr3 | 182887537 | ||||||
| chr3:182887969
|
C | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843+256C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182887969 | ||||||
| chr3:182887970
|
G | A | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2843+257G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182887970 | ||||||
| chr3:182887992
|
CGT | C | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2843+283_2843+284d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr3 | 182887992 | |||||
| chr3:182888334
|
C | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2843+621C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182888334 | ||||||
| chr3:182888699
|
T | TTTTA | 9 | a0001c0001t0002g0126a0001c0001t0002g0127a0001c0001t0002g0165others(6): Show | 9 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.2844-687_2844-684d others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr3 | 182888699 | |||||
| chr3:182888730
|
T | A | 3 | a0001c0002t0009g0267a0001c0002t0009g0268a0001c0002t0019g0297 | 3 | HG02109.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2844-680T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182888730 | ||||||
| chr3:182888757
|
T | C | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2844-653T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182888757 | ||||||
| chr3:182888858
|
CT | C | 137 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(134): Show | 140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.2844-534delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr3 | 182888858 | |||||
| chr3:182888931
|
T | C | 260 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(257): Show | 268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2844-479T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182888931 | ||||||
| chr3:182889002
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2844-408A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182889002 | ||||||
| chr3:182889010
|
G | A | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.2844-400G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182889010 | ||||||
| chr3:182889044
|
G | T | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.2844-366G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182889044 | ||||||
| chr3:182889191
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.2844-219G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182889191 | ||||||
| chr3:182889231
|
G | A | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2844-179G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182889231 | ||||||
| chr3:182889366
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2844-44A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182889366 | ||||||
| chr3:182889370
|
A | G | 6 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2844-40A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 24/29 | chr3 | 182889370 | ||||||
| chr3:182889623
|
A | G | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2982+75A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182889623 | ||||||
| chr3:182889678
|
A | T | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2982+130A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182889678 | ||||||
| chr3:182890173
|
G | A | 3 | a0001c0001t0002g0140a0001c0001t0002g0150a0001c0001t0002g0152 | 3 | HG02027.hp2 NA18952.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.2982+625G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182890173 | ||||||
| chr3:182890356
|
A | G | 1 | a0001c0001t0006g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2982+808A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182890356 | ||||||
| chr3:182890415
|
GCTATTCC others(6): Show |
G | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2982+872_2982+884d others(15): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr3 | 182890415 | |||||
| chr3:182890634
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2982+1086T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182890634 | ||||||
| chr3:182890678
|
T | C | 4 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314others(1): Show | 6 | HG02257.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.2982+1130T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182890678 | ||||||
| chr3:182890763
|
A | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.2982+1215A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182890763 | ||||||
| chr3:182890783
|
T | A | 1 | a0001c0001t0001g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2982+1235T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182890783 | ||||||
| chr3:182890982
|
A | G | 1 | a0001c0001t0003g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2982+1434A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182890982 | ||||||
| chr3:182891071
|
A | G | 3 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0311 | 3 | HG02109.hp2 HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2982+1523A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182891071 | ||||||
| chr3:182891267
|
G | T | 1 | a0001c0002t0004g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2982+1719G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182891267 | ||||||
| chr3:182891723
|
C | T | 1 | a0001c0001t0008g0184 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2982+2175C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182891723 | ||||||
| chr3:182891802
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2982+2254T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182891802 | ||||||
| chr3:182891846
|
G | A | 7 | a0001c0001t0003g0206a0001c0001t0003g0209a0001c0001t0003g0210others(4): Show | 7 | HG01433.hp2 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.2982+2298G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182891846 | ||||||
| chr3:182891992
|
G | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2982+2444G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182891992 | ||||||
| chr3:182892095
|
A | G | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.2982+2547A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182892095 | ||||||
| chr3:182892241
|
A | G | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.2982+2693A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182892241 | ||||||
| chr3:182892523
|
A | G | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2982+2975A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182892523 | ||||||
| chr3:182892679
|
C | G | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2982+3131C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182892679 | ||||||
| chr3:182892796
|
G | A | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.2982+3248G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182892796 | ||||||
| chr3:182892868
|
C | A | 164 | a0001c0001t0001g0014a0001c0001t0002g0008a0001c0001t0002g0009others(161): Show | 164 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2982+3320C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182892868 | ||||||
| chr3:182893139
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01167.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2983-3561G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893139 | ||||||
| chr3:182893271
|
A | C | 46 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(43): Show | 49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.2983-3429A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893271 | ||||||
| chr3:182893397
|
G | A | 146 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(143): Show | 148 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.2983-3303G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893397 | ||||||
| chr3:182893438
|
A | C | 3 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0309 | 3 | HG02738.hp2 HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2983-3262A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893438 | ||||||
| chr3:182893535
|
G | A | 29 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.2983-3165G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893535 | ||||||
| chr3:182893560
|
T | G | 1 | a0001c0001t0001g0058 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2983-3140T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893560 | ||||||
| chr3:182893833
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2983-2867C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893833 | ||||||
| chr3:182893839
|
G | A | 1 | a0001c0002t0004g0312 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2983-2861G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893839 | ||||||
| chr3:182893955
|
A | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.2983-2745A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182893955 | ||||||
| chr3:182894164
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0021others(6): Show | 11 | HG00639.hp1 HG01934.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.2983-2536C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182894164 | ||||||
| chr3:182894295
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0106 | 2 | HG00558.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2983-2405T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182894295 | ||||||
| chr3:182894752
|
G | A | 1 | a0001c0001t0002g0143 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2983-1948G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182894752 | ||||||
| chr3:182894802
|
G | A | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2983-1898G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182894802 | ||||||
| chr3:182894814
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2983-1886G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182894814 | ||||||
| chr3:182894963
|
C | CA | 141 | a0001c0001t0001g0014a0001c0001t0002g0008a0001c0001t0002g0009others(138): Show | 141 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.2983-1724dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr3 | 182894963 | |||||
| chr3:182895042
|
G | A | 3 | a0001c0001t0003g0177a0001c0001t0003g0215a0001c0001t0003g0265 | 3 | HG00597.hp1 NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.2983-1658G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182895042 | ||||||
| chr3:182895112
|
C | CA | 12 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0022others(9): Show | 12 | HG01175.hp1 HG02132.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.2983-1564dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr3 | 182895112 | |||||
| chr3:182895112
|
CA | C | 10 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0095others(7): Show | 10 | HG01167.hp2 HG01258.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.2983-1564delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr3 | 182895112 | |||||
| chr3:182895112
|
CAA | C | 147 | a0001c0001t0001g0014a0001c0001t0002g0009a0001c0001t0002g0121others(144): Show | 147 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.2983-1565_2983-156 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr3 | 182895112 | |||||
| chr3:182895112
|
CAAA | C | 48 | a0001c0001t0002g0008a0001c0001t0002g0225a0001c0001t0002g0238others(45): Show | 51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.2983-1566_2983-156 others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr3 | 182895112 | |||||
| chr3:182895112
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0002t0007g0274 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2983-1578_2983-156 others(19): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr3 | 182895112 | |||||
| chr3:182895131
|
A | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG00408.hp2 NA18967.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2983-1569A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182895131 | ||||||
| chr3:182895376
|
A | G | 140 | a0001c0001t0001g0014a0001c0001t0002g0008a0001c0001t0002g0009others(137): Show | 140 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2983-1324A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182895376 | ||||||
| chr3:182895648
|
G | A | 140 | a0001c0001t0001g0014a0001c0001t0002g0008a0001c0001t0002g0009others(137): Show | 140 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2983-1052G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182895648 | ||||||
| chr3:182895894
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2983-806G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182895894 | ||||||
| chr3:182895895
|
A | G | 140 | a0001c0001t0001g0014a0001c0001t0002g0008a0001c0001t0002g0009others(137): Show | 140 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.2983-805A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182895895 | ||||||
| chr3:182896015
|
C | T | 1 | a0001c0002t0009g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2983-685C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182896015 | ||||||
| chr3:182896587
|
A | G | 1 | a0001c0001t0017g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2983-113A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182896587 | ||||||
| chr3:182896665
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2983-35A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 25/29 | chr3 | 182896665 | ||||||
| chr3:182896790
|
G | A | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3048+25G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 26/29 | chr3 | 182896790 | ||||||
| chr3:182896851
|
A | G | 3 | a0001c0002t0009g0267a0001c0002t0009g0268a0001c0002t0019g0297 | 3 | HG02109.hp1 HG02486.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.3048+86A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 26/29 | chr3 | 182896851 | ||||||
| chr3:182897125
|
T | G | 1 | a0001c0001t0001g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3049-178T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 26/29 | chr3 | 182897125 | ||||||
| chr3:182897202
|
G | C | 1 | a0001c0001t0008g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3049-101G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 26/29 | chr3 | 182897202 | ||||||
| chr3:182897417
|
A | G | 1 | a0001c0001t0003g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.3152+11A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897417 | ||||||
| chr3:182897604
|
T | A | 40 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(37): Show | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.3152+198T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897604 | ||||||
| chr3:182897639
|
T | A | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3152+233T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897639 | ||||||
| chr3:182897671
|
A | G | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3152+265A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897671 | ||||||
| chr3:182897772
|
G | A | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3152+366G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897772 | ||||||
| chr3:182897799
|
A | G | 3 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314 | 5 | HG02257.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3152+393A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897799 | ||||||
| chr3:182897883
|
A | T | 55 | a0001c0001t0003g0129a0001c0001t0003g0175a0001c0001t0003g0176others(52): Show | 55 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.3152+477A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897883 | ||||||
| chr3:182897952
|
G | A | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3152+546G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182897952 | ||||||
| chr3:182898046
|
A | T | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3153-561A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182898046 | ||||||
| chr3:182898173
|
A | C | 1 | a0001c0001t0003g0179 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3153-434A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182898173 | ||||||
| chr3:182898317
|
A | T | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3153-290A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182898317 | ||||||
| chr3:182898580
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3153-27T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 27/29 | chr3 | 182898580 | ||||||
| chr3:182898798
|
A | G | 2 | a0001c0002t0004g0280a0001c0002t0022g0284 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3318+26A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182898798 | ||||||
| chr3:182899022
|
G | T | 4 | a0001c0001t0002g0130a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG00323.hp2 HG02080.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+250G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899022 | ||||||
| chr3:182899086
|
A | G | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3318+314A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899086 | ||||||
| chr3:182899115
|
A | G | 2 | a0001c0001t0003g0176a0001c0001t0003g0222 | 2 | NA19070.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.3318+343A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899115 | ||||||
| chr3:182899150
|
A | AT | 10 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0048others(7): Show | 10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.3318+399dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182899150 | |||||
| chr3:182899150
|
AT | A | 36 | a0001c0001t0002g0123a0001c0001t0002g0133a0001c0001t0002g0201others(33): Show | 37 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.3318+399delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182899150 | |||||
| chr3:182899150
|
ATT | A | 147 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(144): Show | 149 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.3318+398_3318+399d others(4): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182899150 | |||||
| chr3:182899253
|
T | C | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3318+481T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899253 | ||||||
| chr3:182899280
|
T | G | 1 | a0001c0001t0013g0156 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3318+508T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899280 | ||||||
| chr3:182899283
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3318+511G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899283 | ||||||
| chr3:182899298
|
A | G | 1 | a0001c0001t0001g0068 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3318+526A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899298 | ||||||
| chr3:182899336
|
A | G | 1 | a0001c0002t0007g0273 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3318+564A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899336 | ||||||
| chr3:182899373
|
G | A | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3318+601G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899373 | ||||||
| chr3:182899379
|
C | G | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.3318+607C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899379 | ||||||
| chr3:182899416
|
G | T | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3318+644G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899416 | ||||||
| chr3:182899446
|
T | C | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3318+674T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899446 | ||||||
| chr3:182899816
|
C | A | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3318+1044C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899816 | ||||||
| chr3:182899829
|
A | G | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3318+1057A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182899829 | ||||||
| chr3:182899885
|
C | CGTA | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3318+1114_3318+111 others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182899885 | |||||
| chr3:182900017
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3318+1245A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900017 | ||||||
| chr3:182900118
|
G | A | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3318+1346G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900118 | ||||||
| chr3:182900297
|
A | G | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3318+1525A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900297 | ||||||
| chr3:182900336
|
A | G | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3318+1564A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900336 | ||||||
| chr3:182900497
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3318+1725C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900497 | ||||||
| chr3:182900503
|
G | A | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3318+1731G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900503 | ||||||
| chr3:182900602
|
G | GA | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.3318+1839dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182900602 | |||||
| chr3:182900729
|
T | C | 5 | a0001c0002t0004g0288a0001c0002t0004g0289a0001c0002t0004g0290others(2): Show | 5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.3318+1957T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900729 | ||||||
| chr3:182900860
|
A | G | 3 | a0001c0001t0003g0177a0001c0001t0003g0215a0001c0001t0003g0265 | 3 | HG00597.hp1 NA18959.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.3318+2088A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900860 | ||||||
| chr3:182900996
|
A | G | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3318+2224A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182900996 | ||||||
| chr3:182901149
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3318+2377G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901149 | ||||||
| chr3:182901333
|
C | T | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3318+2561C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901333 | ||||||
| chr3:182901340
|
C | CA | 40 | a0001c0001t0001g0031a0001c0001t0001g0069a0001c0001t0001g0097others(37): Show | 40 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.3318+2581dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182901340 | |||||
| chr3:182901353
|
AC | A | 3 | a0001c0001t0003g0192a0001c0001t0008g0186a0001c0001t0018g0149 | 3 | HG01070.hp2 HG01928.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.3318+2582delC | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901353 | ||||||
| chr3:182901354
|
C | A | 135 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(132): Show | 135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.3318+2582C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901354 | ||||||
| chr3:182901365
|
C | A | 4 | a0001c0001t0001g0088a0001c0001t0002g0223a0001c0001t0002g0228others(1): Show | 4 | NA18949.hp2 NA18951.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+2593C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901365 | ||||||
| chr3:182901425
|
G | A | 157 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.3318+2653G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901425 | ||||||
| chr3:182901477
|
A | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3318+2705A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901477 | ||||||
| chr3:182901531
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(2): Show | 5 | NA18947.hp2 NA18969.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.3318+2759A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901531 | ||||||
| chr3:182901697
|
C | T | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3318+2925C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901697 | ||||||
| chr3:182901791
|
G | A | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3318+3019G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182901791 | ||||||
| chr3:182902223
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3318+3451A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182902223 | ||||||
| chr3:182902397
|
A | G | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3318+3625A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182902397 | ||||||
| chr3:182903086
|
T | C | 1 | a0001c0001t0014g0124 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3318+4314T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903086 | ||||||
| chr3:182903096
|
C | G | 1 | a0001c0001t0003g0177 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3318+4324C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903096 | ||||||
| chr3:182903294
|
C | T | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3318+4522C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903294 | ||||||
| chr3:182903375
|
T | C | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3318+4603T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903375 | ||||||
| chr3:182903390
|
A | T | 1 | a0001c0001t0003g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3318+4618A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903390 | ||||||
| chr3:182903472
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0086 | 2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3318+4700G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903472 | ||||||
| chr3:182903579
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.3318+4807A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903579 | ||||||
| chr3:182903588
|
G | A | 1 | a0001c0002t0009g0248 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3318+4816G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903588 | ||||||
| chr3:182903825
|
A | C | 1 | a0001c0002t0004g0313 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3318+5053A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903825 | ||||||
| chr3:182903863
|
G | A | 1 | a0001c0002t0004g0288 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3318+5091G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182903863 | ||||||
| chr3:182904113
|
G | A | 3 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314 | 5 | HG02257.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3318+5341G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904113 | ||||||
| chr3:182904196
|
T | C | 1 | a0001c0001t0003g0196 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.3318+5424T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904196 | ||||||
| chr3:182904285
|
A | G | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3318+5513A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904285 | ||||||
| chr3:182904354
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3318+5582G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904354 | ||||||
| chr3:182904502
|
G | C | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+5730G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904502 | ||||||
| chr3:182904656
|
G | A | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3318+5884G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904656 | ||||||
| chr3:182904748
|
G | T | 1 | a0001c0002t0007g0274 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3318+5976G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904748 | ||||||
| chr3:182904808
|
G | C | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3318+6036G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904808 | ||||||
| chr3:182904853
|
C | T | 2 | a0001c0002t0009g0267a0001c0002t0009g0268 | 2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.3318+6081C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904853 | ||||||
| chr3:182904888
|
T | TA | 14 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0068others(11): Show | 14 | HG01192.hp2 HG01361.hp1 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.3318+6140dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182904888 | |||||
| chr3:182904888
|
TA | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0049others(10): Show | 14 | HG01070.hp1 HG01167.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.3318+6140delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182904888 | |||||
| chr3:182904903
|
A | G | 1 | a0001c0002t0010g0292 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3318+6131A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904903 | ||||||
| chr3:182904904
|
A | G | 1 | a0003c0005t0006g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3318+6132A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904904 | ||||||
| chr3:182904905
|
A | G | 39 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(36): Show | 42 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.3318+6133A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904905 | ||||||
| chr3:182904911
|
AAG | A | 56 | a0001c0001t0002g0159a0001c0001t0002g0225a0001c0001t0002g0226others(53): Show | 59 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.3318+6140_3318+614 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904911 | ||||||
| chr3:182904912
|
AG | A | 82 | a0001c0001t0002g0009a0001c0001t0002g0121a0001c0001t0002g0122others(79): Show | 82 | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.3318+6142delG | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182904912 | |||||
| chr3:182904913
|
G | A | 62 | a0001c0001t0002g0008a0001c0001t0002g0126a0001c0001t0002g0127others(59): Show | 62 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.3318+6141G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182904913 | ||||||
| chr3:182905444
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3318+6672A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182905444 | ||||||
| chr3:182905577
|
C | G | 1 | a0001c0001t0003g0204 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3318+6805C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182905577 | ||||||
| chr3:182905580
|
C | T | 150 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(147): Show | 150 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.3318+6808C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182905580 | ||||||
| chr3:182905687
|
T | C | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+6915T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182905687 | ||||||
| chr3:182905741
|
G | C | 1 | a0001c0001t0003g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3318+6969G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182905741 | ||||||
| chr3:182905977
|
G | A | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3318+7205G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182905977 | ||||||
| chr3:182906056
|
C | T | 4 | a0001c0001t0002g0130a0001c0001t0002g0159a0001c0001t0002g0160others(1): Show | 4 | HG00323.hp2 HG02080.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.3318+7284C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906056 | ||||||
| chr3:182906223
|
T | C | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3318+7451T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906223 | ||||||
| chr3:182906324
|
G | A | 157 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.3319-7537G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906324 | ||||||
| chr3:182906476
|
T | G | 1 | a0001c0001t0005g0253 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3319-7385T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906476 | ||||||
| chr3:182906525
|
C | A | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3319-7336C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906525 | ||||||
| chr3:182906536
|
C | T | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3319-7325C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906536 | ||||||
| chr3:182906547
|
G | A | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3319-7314G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906547 | ||||||
| chr3:182906776
|
TTA | T | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3319-7084_3319-708 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906776 | ||||||
| chr3:182906777
|
TA | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0036others(4): Show | 7 | HG01069.hp2 HG01099.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3319-7070delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182906777 | |||||
| chr3:182906777
|
TAAA | T | 138 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(135): Show | 138 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.3319-7072_3319-707 others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182906777 | |||||
| chr3:182906826
|
C | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3319-7035C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906826 | ||||||
| chr3:182906830
|
T | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3319-7031T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906830 | ||||||
| chr3:182906855
|
G | A | 2 | a0001c0002t0009g0248a0001c0002t0009g0311 | 2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3319-7006G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906855 | ||||||
| chr3:182906862
|
G | A | 1 | a0004c0004t0007g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3319-6999G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906862 | ||||||
| chr3:182906884
|
C | G | 54 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0126others(51): Show | 54 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.3319-6977C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906884 | ||||||
| chr3:182906956
|
G | A | 1 | a0003c0005t0006g0283 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3319-6905G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906956 | ||||||
| chr3:182906971
|
C | T | 185 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(182): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.3319-6890C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182906971 | ||||||
| chr3:182907085
|
TC | T | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3319-6774delC | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182907085 | |||||
| chr3:182907092
|
CA | C | 157 | a0001c0001t0001g0021a0001c0001t0001g0047a0001c0001t0002g0008others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.3319-6754delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182907092 | |||||
| chr3:182907116
|
G | T | 162 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(159): Show | 162 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.3319-6745G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907116 | ||||||
| chr3:182907162
|
C | T | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3319-6699C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907162 | ||||||
| chr3:182907508
|
A | G | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3319-6353A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907508 | ||||||
| chr3:182907652
|
A | C | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3319-6209A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907652 | ||||||
| chr3:182907654
|
C | T | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3319-6207C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907654 | ||||||
| chr3:182907731
|
A | C | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3319-6130A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907731 | ||||||
| chr3:182907891
|
A | G | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3319-5970A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907891 | ||||||
| chr3:182907970
|
C | A | 1 | a0001c0001t0003g0202 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3319-5891C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907970 | ||||||
| chr3:182907988
|
G | A | 1 | a0001c0002t0004g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3319-5873G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907988 | ||||||
| chr3:182907989
|
T | A | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.3319-5872T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182907989 | ||||||
| chr3:182908015
|
A | G | 1 | a0001c0001t0003g0182 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3319-5846A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908015 | ||||||
| chr3:182908085
|
A | G | 1 | a0001c0001t0002g0131 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.3319-5776A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908085 | ||||||
| chr3:182908098
|
A | G | 1 | a0001c0002t0010g0269 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3319-5763A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908098 | ||||||
| chr3:182908196
|
C | CT | 17 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0035others(14): Show | 18 | HG00621.hp2 HG00735.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.3319-5640dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182908196 | |||||
| chr3:182908196
|
CT | C | 135 | a0001c0001t0001g0045a0001c0001t0001g0071a0001c0001t0001g0087others(132): Show | 135 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.3319-5640delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182908196 | |||||
| chr3:182908205
|
T | C | 1 | a0001c0001t0006g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3319-5656T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908205 | ||||||
| chr3:182908246
|
G | A | 2 | a0001c0001t0003g0193a0001c0001t0003g0195 | 2 | NA18956.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.3319-5615G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908246 | ||||||
| chr3:182908331
|
T | C | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3319-5530T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908331 | ||||||
| chr3:182908926
|
T | C | 1 | a0001c0001t0018g0149 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3319-4935T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908926 | ||||||
| chr3:182908941
|
G | A | 1 | a0001c0002t0009g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3319-4920G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182908941 | ||||||
| chr3:182909166
|
G | A | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3319-4695G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182909166 | ||||||
| chr3:182909522
|
A | C | 1 | a0001c0001t0002g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3319-4339A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182909522 | ||||||
| chr3:182909601
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3319-4260T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182909601 | ||||||
| chr3:182909659
|
A | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3319-4202A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182909659 | ||||||
| chr3:182909914
|
A | T | 5 | a0001c0001t0001g0029a0001c0001t0001g0037a0001c0001t0001g0040others(2): Show | 5 | HG00621.hp2 HG00673.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.3319-3947A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182909914 | ||||||
| chr3:182909998
|
A | G | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3319-3863A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182909998 | ||||||
| chr3:182910071
|
C | CA | 14 | a0001c0001t0002g0141a0001c0001t0002g0147a0001c0001t0002g0151others(11): Show | 14 | HG00621.hp1 HG01109.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.3319-3789dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182910071 | |||||
| chr3:182910071
|
CAGA | C | 20 | a0001c0001t0002g0228a0001c0001t0002g0234a0001c0001t0002g0236others(17): Show | 20 | HG01070.hp2 HG01192.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.3319-3788_3319-378 others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182910071 | |||||
| chr3:182910071
|
CAGAA | C | 61 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(58): Show | 61 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.3319-3788_3319-378 others(8): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182910071 | |||||
| chr3:182910073
|
G | A | 57 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0126others(54): Show | 57 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.3319-3788G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910073 | ||||||
| chr3:182910073
|
G | GA | 17 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0037others(14): Show | 17 | HG01192.hp2 HG01361.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.3319-3766dupA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182910073 | |||||
| chr3:182910073
|
GA | G | 47 | a0001c0001t0001g0059a0001c0001t0005g0254a0001c0001t0005g0255others(44): Show | 50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.3319-3766delA | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182910073 | |||||
| chr3:182910074
|
A | G | 5 | a0001c0002t0004g0288a0001c0002t0004g0299a0001c0002t0004g0301others(2): Show | 5 | HG01884.hp2 HG01981.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.3319-3787A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910074 | ||||||
| chr3:182910075
|
A | G | 29 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(27): Show |
intron_variant | MODIFIER | c.3319-3786A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910075 | ||||||
| chr3:182910315
|
C | T | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3319-3546C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910315 | ||||||
| chr3:182910325
|
C | T | 3 | a0004c0004t0007g0275a0004c0004t0007g0276a0004c0004t0007g0310 | 3 | HG01257.hp1 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3319-3536C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910325 | ||||||
| chr3:182910327
|
G | T | 41 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(38): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.3319-3534G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910327 | ||||||
| chr3:182910658
|
T | C | 1 | a0001c0001t0005g0254 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3319-3203T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910658 | ||||||
| chr3:182910680
|
C | T | 4 | a0001c0001t0002g0134a0001c0001t0002g0146a0001c0001t0002g0147others(1): Show | 4 | NA18947.hp1 NA18951.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.3319-3181C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910680 | ||||||
| chr3:182910993
|
T | C | 7 | a0001c0002t0004g0001a0001c0002t0004g0312a0001c0002t0004g0313others(4): Show | 9 | HG02257.hp1 HG02818.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.3319-2868T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182910993 | ||||||
| chr3:182911245
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3319-2616T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182911245 | ||||||
| chr3:182911271
|
G | GCC | 23 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0002g0152others(20): Show | 23 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.3319-2582_3319-258 others(6): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911271 | |||||
| chr3:182911271
|
G | GCCC | 70 | a0001c0001t0002g0122a0001c0001t0002g0123a0001c0001t0002g0126others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.3319-2583_3319-258 others(7): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911271 | |||||
| chr3:182911271
|
G | GCCCC | 63 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(60): Show | 63 | HG00639.hp2 HG00673.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.3319-2584_3319-258 others(8): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911271 | |||||
| chr3:182911271
|
G | GCCCCC | 25 | a0001c0001t0002g0161a0001c0001t0002g0174a0001c0001t0003g0176others(22): Show | 25 | HG00597.hp1 HG01069.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.3319-2585_3319-258 others(9): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911271 | |||||
| chr3:182911271
|
G | GCCCCCCC others(3): Show |
2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3319-2581_3319-258 others(14): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911271 | |||||
| chr3:182911271
|
G | GCCCCCCC others(4): Show |
1 | a0001c0002t0009g0267 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3319-2581_3319-258 others(15): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911271 | |||||
| chr3:182911271
|
G | GCCCCCCC others(6): Show |
1 | a0001c0002t0009g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3319-2581_3319-258 others(17): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911271 | |||||
| chr3:182911406
|
TATAATC | T | 3 | a0001c0001t0001g0112a0005c0006t0001g0073a0005c0006t0001g0081 | 3 | HG01169.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3319-2450_3319-244 others(10): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911406 | |||||
| chr3:182911445
|
G | C | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3319-2416G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182911445 | ||||||
| chr3:182911505
|
A | G | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3319-2356A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182911505 | ||||||
| chr3:182911680
|
TCTCTC | T | 5 | a0001c0002t0009g0247a0001c0002t0009g0248a0001c0002t0009g0267others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3319-2179_3319-217 others(9): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182911680 | |||||
| chr3:182911713
|
C | T | 1 | a0001c0001t0014g0124 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.3319-2148C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182911713 | ||||||
| chr3:182911961
|
G | T | 4 | a0002c0003t0002g0116a0002c0003t0002g0117a0002c0003t0002g0118others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.3319-1900G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182911961 | ||||||
| chr3:182911967
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3319-1894A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182911967 | ||||||
| chr3:182912067
|
C | G | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3319-1794C>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182912067 | ||||||
| chr3:182912071
|
G | A | 203 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.3319-1790G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182912071 | ||||||
| chr3:182912109
|
T | C | 18 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(15): Show | 18 | HG00639.hp2 HG01255.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.3319-1752T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182912109 | ||||||
| chr3:182912129
|
A | C | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3319-1732A>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182912129 | ||||||
| chr3:182912448
|
C | CT | 10 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0085others(7): Show | 10 | HG01257.hp1 HG02145.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.3319-1402dupT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182912448 | |||||
| chr3:182912448
|
CT | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3319-1402delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182912448 | |||||
| chr3:182912644
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.3319-1217G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182912644 | ||||||
| chr3:182912655
|
T | G | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3319-1206T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182912655 | ||||||
| chr3:182912860
|
C | T | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3319-1001C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182912860 | ||||||
| chr3:182912904
|
GT | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3319-947delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | 182912904 | |||||
| chr3:182913191
|
C | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0026a0001c0001t0001g0035others(4): Show | 8 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.3319-670C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182913191 | ||||||
| chr3:182913220
|
T | C | 7 | a0001c0002t0007g0273a0001c0002t0007g0274a0001c0002t0007g0278others(4): Show | 7 | HG01257.hp1 HG02630.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.3319-641T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182913220 | ||||||
| chr3:182913361
|
T | C | 1 | a0001c0002t0019g0297 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3319-500T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182913361 | ||||||
| chr3:182913582
|
A | T | 1 | a0001c0001t0001g0053 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3319-279A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182913582 | ||||||
| chr3:182913649
|
T | C | 1 | a0001c0001t0002g0159 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3319-212T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182913649 | ||||||
| chr3:182913773
|
G | C | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3319-88G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182913773 | ||||||
| chr3:182913847
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3319-14T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | chr3 | 182913847 | ||||||
| chr3:182914004
|
C | A | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3452+10C>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914004 | ||||||
| chr3:182914235
|
T | A | 2 | a0001c0001t0002g0243a0001c0001t0002g0244 | 2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3452+241T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914235 | ||||||
| chr3:182914356
|
A | T | 1 | a0002c0003t0002g0119 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3452+362A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914356 | ||||||
| chr3:182914356
|
AT | A | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3452+369delT | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr3 | 182914356 | |||||
| chr3:182914438
|
A | G | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3452+444A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914438 | ||||||
| chr3:182914517
|
T | C | 11 | a0001c0001t0005g0252a0001c0001t0005g0253a0001c0001t0005g0254others(8): Show | 11 | HG00639.hp2 HG01255.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3452+523T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914517 | ||||||
| chr3:182914673
|
A | T | 1 | a0001c0001t0002g0137 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3452+679A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914673 | ||||||
| chr3:182914712
|
G | A | 1 | a0001c0002t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3452+718G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914712 | ||||||
| chr3:182914896
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3452+902G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182914896 | ||||||
| chr3:182915039
|
G | A | 1 | a0001c0001t0003g0206 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3452+1045G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915039 | ||||||
| chr3:182915092
|
T | C | 1 | a0008c0009t0003g0180 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.3452+1098T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915092 | ||||||
| chr3:182915216
|
A | T | 4 | a0001c0002t0004g0001a0001c0002t0004g0313a0001c0002t0004g0314others(1): Show | 6 | HG02257.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.3452+1222A>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915216 | ||||||
| chr3:182915264
|
T | C | 30 | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.3452+1270T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915264 | ||||||
| chr3:182915274
|
C | T | 53 | a0001c0002t0004g0001a0001c0002t0004g0007a0001c0002t0004g0120others(50): Show | 56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.3452+1280C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915274 | ||||||
| chr3:182915519
|
G | A | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3452+1525G>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915519 | ||||||
| chr3:182915681
|
A | G | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3452+1687A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915681 | ||||||
| chr3:182915757
|
T | C | 2 | a0001c0001t0002g0162a0001c0001t0002g0163 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3452+1763T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915757 | ||||||
| chr3:182915787
|
T | A | 1 | a0001c0001t0003g0195 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3452+1793T>A | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915787 | ||||||
| chr3:182915939
|
G | T | 157 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(154): Show | 157 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.3452+1945G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182915939 | ||||||
| chr3:182916017
|
T | C | 2 | a0001c0002t0007g0273a0001c0002t0007g0274 | 2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.3453-2006T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182916017 | ||||||
| chr3:182916032
|
T | G | 1 | a0001c0001t0008g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3453-1991T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182916032 | ||||||
| chr3:182916039
|
T | G | 9 | a0001c0001t0005g0254a0001c0001t0005g0255a0001c0001t0005g0256others(6): Show | 9 | HG00639.hp2 HG01255.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.3453-1984T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182916039 | ||||||
| chr3:182916585
|
C | T | 139 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.3453-1438C>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182916585 | ||||||
| chr3:182916637
|
ATAGAAAG others(7): Show |
A | 1 | a0001c0001t0002g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3453-1382_3453-136 others(18): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr3 | 182916637 | |||||
| chr3:182916955
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0043 | 2 | HG00597.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.3453-1068A>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182916955 | ||||||
| chr3:182917040
|
T | C | 3 | a0001c0001t0002g0223a0001c0001t0002g0228a0001c0001t0002g0229 | 3 | NA18949.hp2 NA18974.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.3453-983T>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182917040 | ||||||
| chr3:182917131
|
G | T | 2 | a0001c0002t0007g0278a0001c0002t0007g0279 | 2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3453-892G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182917131 | ||||||
| chr3:182917557
|
G | T | 149 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0121others(146): Show | 149 | HG00323.hp2 HG00408.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.3453-466G>T | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182917557 | ||||||
| chr3:182917844
|
G | C | 1 | a0001c0001t0003g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3453-179G>C | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182917844 | ||||||
| chr3:182917936
|
T | G | 1 | a0001c0001t0002g0160 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3453-87T>G | ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 29/29 | chr3 | 182917936 |