Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 472 |
|---|---|
| ensemblid | ENSG00000149311.21 |
| hgncid | 795 |
| symbol | ATM |
| name | ATM serine/threonine kinase |
| refseq_nuc | NM_000051.4 |
| refseq_prot | NP_000042.3 |
| ensembl_nuc | ENST00000675843.1 |
| ensembl_prot | ENSP00000501606.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 108223067 |
| end | 108369102 |
| strand | + |
| ver | v1.2 |
| region | chr11:108223067-108369102 |
| region5000 | chr11:108218067-108374102 |
| regionname0 | ATM_chr11_108223067_108369102 |
| regionname5000 | ATM_chr11_108218067_108374102 |
| 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 | 3056 | 211 | 33 | 40 | 105 | 10 | 21 | 84 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002 | 0/0 | 3056 | 30 | 27 | 3 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0003 | 0/0 | 3056 | 12 | 0 | 4 | 2 | 3 | 3 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0004 | 0/0 | 3056 | 11 | 10 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0005 | 0/0 | 3056 | 9 | 0 | 0 | 6 | 0 | 3 | 6 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0006 | 0/0 | 3056 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0007 | 0/0 | 3056 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0008 | 0/0 | 3056 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0009 | 0/0 | 3056 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0010 | 0/0 | 3056 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0011 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0012 | 0/0 | 3056 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0013 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0014 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0015 | 0/0 | 3056 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0016 | 0/0 | 3056 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0017 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0018 | 0/0 | 3056 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0019 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0020 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0021 | 0/0 | 3056 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0022 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0023 | 0/0 | 3056 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| 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 | 9171 | 189 | 23 | 35 | 101 | 8 | 20 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0002 | 0/0 | 9171 | 16 | 13 | 3 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0003 | 0/0 | 9171 | 12 | 0 | 4 | 2 | 3 | 3 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0004 | 0/0 | 9171 | 11 | 10 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0005 | 0/0 | 9171 | 9 | 9 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0006 | 0/0 | 9171 | 9 | 0 | 0 | 6 | 0 | 3 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0007 | 0/0 | 9171 | 6 | 6 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0008 | 0/0 | 9171 | 6 | 6 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0009 | 0/0 | 9171 | 5 | 5 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0010 | 0/0 | 9171 | 5 | 3 | 2 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0011 | 0/0 | 9171 | 4 | 3 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0012 | 0/0 | 9171 | 4 | 1 | 0 | 2 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0013 | 0/0 | 9171 | 3 | 2 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0014 | 0/0 | 9171 | 2 | 0 | 1 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0015 | 0/0 | 9171 | 2 | 2 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0016 | 0/0 | 9171 | 2 | 0 | 1 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0017 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0018 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0019 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0020 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0021 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0022 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0023 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0024 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0025 | 0/0 | 9171 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0026 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0027 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0028 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0029 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0030 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0031 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0032 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0033 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0034 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| c0035 | 0/0 | 9171 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| 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 | 3744 | 108 | 12 | 23 | 49 | 12 | 11 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0002 | 1/0 | 3745 | 84 | 21 | 18 | 33 | 1 | 10 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0003 | 0/0 | 3745 | 19 | 16 | 3 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0004 | 0/0 | 3745 | 10 | 9 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0005 | 0/0 | 3745 | 9 | 1 | 0 | 5 | 0 | 3 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0006 | 0/0 | 3746 | 5 | 0 | 1 | 3 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0007 | 0/0 | 3745 | 5 | 0 | 0 | 5 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0008 | 0/0 | 3745 | 5 | 5 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0009 | 0/0 | 3745 | 4 | 1 | 2 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0010 | 0/0 | 3744 | 4 | 3 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0011 | 0/0 | 3745 | 4 | 4 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0012 | 0/0 | 3745 | 4 | 3 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0013 | 0/0 | 3745 | 3 | 0 | 0 | 3 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0014 | 0/0 | 3744 | 3 | 0 | 1 | 0 | 0 | 2 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0015 | 0/0 | 3745 | 3 | 3 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0016 | 0/0 | 3744 | 3 | 2 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0017 | 0/0 | 3744 | 3 | 0 | 0 | 3 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0018 | 0/0 | 3745 | 2 | 0 | 0 | 1 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0019 | 0/0 | 3744 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0020 | 0/0 | 3745 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0021 | 0/0 | 3746 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0022 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0023 | 0/0 | 3744 | 2 | 1 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0024 | 0/0 | 3745 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0025 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0026 | 0/0 | 3744 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0027 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0028 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0029 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0030 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0031 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0032 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0033 | 0/0 | 3746 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0034 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0035 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0036 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0037 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| t0038 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| 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 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| 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 | 9171 | 189 | 23 | 35 | 101 | 8 | 20 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0008 | 0/0 | 9171 | 6 | 6 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0010 | 0/0 | 9171 | 5 | 3 | 2 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0012 | 0/0 | 9171 | 4 | 1 | 0 | 2 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0016 | 0/0 | 9171 | 2 | 0 | 1 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0020 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0024 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0025 | 0/0 | 9171 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0027 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0034 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0002 | 0/0 | 9171 | 16 | 13 | 3 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0005 | 0/0 | 9171 | 9 | 9 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0009 | 0/0 | 9171 | 5 | 5 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0003c0003 | 0/0 | 9171 | 12 | 0 | 4 | 2 | 3 | 3 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0004c0004 | 0/0 | 9171 | 11 | 10 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0005c0006 | 0/0 | 9171 | 9 | 0 | 0 | 6 | 0 | 3 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0006c0007 | 0/0 | 9171 | 6 | 6 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0007c0011 | 0/0 | 9171 | 4 | 3 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0008c0015 | 0/0 | 9171 | 2 | 2 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0008c0029 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0009c0013 | 0/0 | 9171 | 3 | 2 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0010c0014 | 0/0 | 9171 | 2 | 0 | 1 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0011c0017 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0012c0035 | 0/0 | 9171 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0013c0018 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0014c0032 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0015c0019 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0016c0031 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0017c0030 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0018c0028 | 0/0 | 9171 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0019c0022 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0020c0023 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0021c0026 | 0/0 | 9171 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0022c0021 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0023c0033 | 0/0 | 9171 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 12914 | 83 | 7 | 17 | 43 | 8 | 7 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0002 | 1/0 | 12915 | 57 | 5 | 10 | 32 | 0 | 9 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0006 | 0/0 | 12916 | 5 | 0 | 1 | 3 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0007 | 0/0 | 12915 | 5 | 0 | 0 | 5 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0009 | 0/0 | 12915 | 3 | 0 | 2 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0010 | 0/0 | 12914 | 4 | 3 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0011 | 0/0 | 12915 | 4 | 4 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0013 | 0/0 | 12915 | 3 | 0 | 0 | 3 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0014 | 0/0 | 12914 | 3 | 0 | 1 | 0 | 0 | 2 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0016 | 0/0 | 12914 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0017 | 0/0 | 12914 | 3 | 0 | 0 | 3 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0018 | 0/0 | 12915 | 2 | 0 | 0 | 1 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0019 | 0/0 | 12914 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0020 | 0/0 | 12915 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0021 | 0/0 | 12916 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0023 | 0/0 | 12914 | 2 | 1 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0025 | 0/0 | 12915 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0026 | 0/0 | 12914 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0027 | 0/0 | 12914 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0028 | 0/0 | 12914 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0029 | 0/0 | 12916 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0032 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0033 | 0/0 | 12916 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0001t0034 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0008t0002 | 0/0 | 12915 | 4 | 4 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0008t0016 | 0/0 | 12914 | 2 | 2 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0010t0002 | 0/0 | 12915 | 4 | 2 | 2 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0010t0031 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0012t0024 | 0/0 | 12915 | 2 | 0 | 0 | 2 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0012t0037 | 0/0 | 12914 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0012t0038 | 0/0 | 12914 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0016t0002 | 0/0 | 12915 | 2 | 0 | 1 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0020t0001 | 0/0 | 12914 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0024t0001 | 0/0 | 12914 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0025t0001 | 0/0 | 12914 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0027t0002 | 0/0 | 12915 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0001c0034t0002 | 0/0 | 12915 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0002t0003 | 0/0 | 12915 | 16 | 13 | 3 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0005t0003 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0005t0008 | 0/0 | 12915 | 5 | 5 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0005t0015 | 0/0 | 12915 | 3 | 3 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0009t0003 | 0/0 | 12915 | 2 | 2 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0009t0022 | 0/0 | 12915 | 2 | 2 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0002c0009t0035 | 0/0 | 12914 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0003c0003t0001 | 0/0 | 12914 | 12 | 0 | 4 | 2 | 3 | 3 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0004c0004t0004 | 0/0 | 12915 | 10 | 9 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0004c0004t0005 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0005c0006t0005 | 0/0 | 12915 | 8 | 0 | 0 | 5 | 0 | 3 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0005c0006t0030 | 0/0 | 12916 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0006c0007t0001 | 0/0 | 12914 | 5 | 5 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0006c0007t0009 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0007c0011t0002 | 0/0 | 12915 | 4 | 3 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0008c0015t0002 | 0/0 | 12915 | 2 | 2 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0008c0029t0002 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0009c0013t0012 | 0/0 | 12915 | 3 | 2 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0010c0014t0001 | 0/0 | 12914 | 2 | 0 | 1 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0011c0017t0002 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0012c0035t0002 | 0/0 | 12915 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0013c0018t0001 | 0/0 | 12914 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0014c0032t0002 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0015c0019t0001 | 0/0 | 12914 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0016c0031t0002 | 0/0 | 12915 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0017c0030t0002 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0018c0028t0002 | 0/0 | 12915 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0019c0022t0002 | 0/0 | 12915 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0020c0023t0002 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0021c0026t0001 | 0/0 | 12914 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0022c0021t0036 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| a0023c0033t0012 | 0/0 | 12915 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | copy fasta | chr11 | 108218067 | 108374102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0225 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0018 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0006g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0006g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0009g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0009g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0009g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0010g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0011g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0013g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0013g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0014g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0016g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0017g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0017g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0018g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0019g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0019g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0020g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0020g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0021g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0021g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0023g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0023g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0025g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0026g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0027g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0028g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0029g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0032g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0033g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0001t0034g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0008t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0008t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0008t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0008t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0008t0016g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0008t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0010t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0010t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0010t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0010t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0010t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0012t0024g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0012t0024g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0012t0037g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0012t0038g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0016t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0016t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0020t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0024t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0025t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0027t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0001c0034t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0015g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0005t0015g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0009t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0009t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0009t0022g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0009t0022g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0002c0009t0035g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0004c0004t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0005c0006t0030g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0006c0007t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0006c0007t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0006c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0006c0007t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0006c0007t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0006c0007t0009g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0007c0011t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0007c0011t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0007c0011t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0007c0011t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0008c0015t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0008c0015t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0008c0029t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0009c0013t0012g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0009c0013t0012g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0009c0013t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0010c0014t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0010c0014t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0011c0017t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0012c0035t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0013c0018t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0014c0032t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0015c0019t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0016c0031t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0017c0030t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0018c0028t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0019c0022t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0020c0023t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0021c0026t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0022c0021t0036g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| a0023c0033t0012g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | GBR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00099 | hp2 | a0010 | c0014 | t0001 | g0281 | EUR | GBR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00140 | hp2 | a0001 | c0012 | t0038 | g0302 | EUR | GBR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | FIN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00323 | hp2 | a0001 | c0016 | t0002 | g0014 | EUR | FIN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00408 | hp1 | a0021 | c0026 | t0001 | g0230 | EAS | CHS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | CHS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0186 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00642 | hp1 | a0001 | c0016 | t0002 | g0015 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00733 | hp1 | a0001 | c0034 | t0002 | g0055 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00733 | hp2 | a0001 | c0001 | t0026 | g0190 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00738 | hp2 | a0001 | c0010 | t0002 | g0030 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG00741 | hp2 | a0018 | c0028 | t0002 | g0067 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01070 | hp1 | a0002 | c0002 | t0003 | g0138 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01074 | hp1 | a0007 | c0011 | t0002 | g0124 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01074 | hp2 | a0003 | c0003 | t0001 | g0185 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0194 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01081 | hp2 | a0002 | c0002 | t0003 | g0086 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01099 | hp1 | a0001 | c0010 | t0002 | g0029 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01099 | hp2 | a0010 | c0014 | t0001 | g0215 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01109 | hp1 | a0015 | c0019 | t0001 | g0209 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01109 | hp2 | a0001 | c0001 | t0016 | g0009 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01168 | hp2 | a0001 | c0001 | t0014 | g0279 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01175 | hp1 | a0009 | c0013 | t0012 | g0117 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0140 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01243 | hp2 | a0016 | c0031 | t0002 | g0080 | AMR | PUR | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01255 | hp1 | a0001 | c0001 | t0010 | g0220 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0238 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0059 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0191 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01346 | hp1 | a0001 | c0001 | t0009 | g0257 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0192 | EUR | IBS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | IBS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0193 | EUR | IBS | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01891 | hp2 | a0002 | c0009 | t0022 | g0094 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01975 | hp1 | a0001 | c0001 | t0023 | g0058 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02027 | hp1 | a0003 | c0003 | t0001 | g0299 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02055 | hp1 | a0002 | c0005 | t0008 | g0097 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02055 | hp2 | a0002 | c0005 | t0003 | g0096 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02132 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0149 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | CDX | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02257 | hp2 | a0009 | c0013 | t0012 | g0120 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02258 | hp1 | a0002 | c0009 | t0003 | g0135 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02258 | hp2 | a0001 | c0010 | t0002 | g0032 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02280 | hp1 | a0002 | c0009 | t0003 | g0134 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0085 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02451 | hp1 | a0006 | c0007 | t0001 | g0160 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02451 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02523 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02572 | hp1 | a0001 | c0008 | t0016 | g0115 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02572 | hp2 | a0014 | c0032 | t0002 | g0011 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02602 | hp1 | a0005 | c0006 | t0005 | g0173 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02615 | hp1 | a0004 | c0004 | t0004 | g0182 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02615 | hp2 | a0001 | c0010 | t0031 | g0031 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02622 | hp1 | a0001 | c0010 | t0002 | g0053 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02622 | hp2 | a0002 | c0009 | t0035 | g0104 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02630 | hp2 | a0004 | c0004 | t0004 | g0168 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02647 | hp1 | a0002 | c0005 | t0015 | g0100 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0136 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02683 | hp1 | a0001 | c0001 | t0014 | g0275 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02717 | hp1 | a0022 | c0021 | t0036 | g0008 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02717 | hp2 | a0008 | c0015 | t0002 | g0013 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02723 | hp1 | a0006 | c0007 | t0009 | g0162 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0141 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02735 | hp2 | a0012 | c0035 | t0002 | g0027 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02738 | hp1 | a0003 | c0003 | t0001 | g0195 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0077 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02818 | hp1 | a0008 | c0029 | t0002 | g0007 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02818 | hp2 | a0001 | c0012 | t0037 | g0301 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02895 | hp1 | a0001 | c0001 | t0011 | g0155 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02895 | hp2 | a0001 | c0001 | t0034 | g0152 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02896 | hp1 | a0006 | c0007 | t0001 | g0157 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02896 | hp2 | a0002 | c0005 | t0015 | g0099 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02897 | hp1 | a0002 | c0005 | t0015 | g0101 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02897 | hp2 | a0001 | c0001 | t0011 | g0154 | AFR | GWD | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02922 | hp1 | a0009 | c0013 | t0012 | g0119 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02922 | hp2 | a0002 | c0009 | t0022 | g0093 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0221 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02965 | hp2 | a0004 | c0004 | t0004 | g0176 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02970 | hp1 | a0002 | c0002 | t0003 | g0142 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02970 | hp2 | a0008 | c0015 | t0002 | g0012 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02976 | hp1 | a0002 | c0002 | t0003 | g0148 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02976 | hp2 | a0004 | c0004 | t0004 | g0177 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0145 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03098 | hp2 | a0001 | c0008 | t0002 | g0042 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03130 | hp1 | a0006 | c0007 | t0001 | g0161 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03139 | hp1 | a0001 | c0008 | t0016 | g0116 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03139 | hp2 | a0007 | c0011 | t0002 | g0123 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03195 | hp1 | a0002 | c0005 | t0008 | g0098 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03195 | hp2 | a0001 | c0008 | t0002 | g0041 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03209 | hp1 | a0004 | c0004 | t0004 | g0169 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03209 | hp2 | a0001 | c0001 | t0028 | g0290 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03225 | hp1 | a0002 | c0005 | t0008 | g0095 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03225 | hp2 | a0002 | c0002 | t0003 | g0144 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03453 | hp1 | a0004 | c0004 | t0004 | g0184 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03453 | hp2 | a0023 | c0033 | t0012 | g0118 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03486 | hp1 | a0006 | c0007 | t0001 | g0150 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03486 | hp2 | a0002 | c0005 | t0008 | g0102 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03492 | hp1 | a0001 | c0001 | t0014 | g0151 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0143 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03516 | hp2 | a0020 | c0023 | t0002 | g0084 | AFR | ESN | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0197 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03669 | hp1 | a0003 | c0003 | t0001 | g0187 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03688 | hp1 | a0005 | c0006 | t0005 | g0165 | SAS | STU | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | STU | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03942 | hp1 | a0001 | c0001 | t0018 | g0294 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03942 | hp2 | a0005 | c0006 | t0005 | g0174 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | STU | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG04228 | hp2 | a0001 | c0025 | t0001 | g0274 | SAS | STU | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18522 | hp1 | a0017 | c0030 | t0002 | g0126 | AFR | YRI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0147 | AFR | YRI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18906 | hp1 | a0011 | c0017 | t0002 | g0056 | AFR | YRI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18906 | hp2 | a0001 | c0008 | t0002 | g0044 | AFR | YRI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18939 | hp2 | a0005 | c0006 | t0005 | g0172 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18943 | hp1 | a0001 | c0024 | t0001 | g0240 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18953 | hp2 | a0001 | c0001 | t0017 | g0175 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18954 | hp1 | a0001 | c0012 | t0024 | g0303 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0060 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18960 | hp1 | a0005 | c0006 | t0005 | g0171 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18961 | hp1 | a0001 | c0001 | t0033 | g0036 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18962 | hp1 | a0001 | c0001 | t0027 | g0258 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18967 | hp2 | a0001 | c0001 | t0013 | g0025 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18970 | hp1 | a0001 | c0001 | t0019 | g0246 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18974 | hp2 | a0001 | c0001 | t0029 | g0016 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18977 | hp1 | a0013 | c0018 | t0001 | g0231 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18977 | hp2 | a0001 | c0001 | t0006 | g0051 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18980 | hp1 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18980 | hp2 | a0001 | c0020 | t0001 | g0273 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18981 | hp1 | a0001 | c0001 | t0019 | g0253 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0114 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18982 | hp1 | a0001 | c0001 | t0020 | g0048 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18985 | hp1 | a0001 | c0001 | t0025 | g0268 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18985 | hp2 | a0001 | c0001 | t0021 | g0028 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18988 | hp1 | a0001 | c0001 | t0017 | g0071 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18988 | hp2 | a0001 | c0001 | t0013 | g0237 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18989 | hp1 | a0001 | c0001 | t0007 | g0076 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18992 | hp2 | a0005 | c0006 | t0005 | g0166 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19000 | hp2 | a0005 | c0006 | t0030 | g0167 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19030 | hp1 | a0002 | c0005 | t0008 | g0103 | AFR | LWK | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19030 | hp2 | a0004 | c0004 | t0005 | g0004 | AFR | LWK | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19043 | hp1 | a0004 | c0004 | t0004 | g0178 | AFR | LWK | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0222 | AFR | LWK | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19058 | hp1 | a0005 | c0006 | t0005 | g0170 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19060 | hp1 | a0001 | c0001 | t0009 | g0263 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0033 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19067 | hp2 | a0001 | c0001 | t0013 | g0276 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19068 | hp1 | a0001 | c0001 | t0021 | g0020 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19074 | hp2 | a0005 | c0006 | t0005 | g0181 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19075 | hp1 | a0001 | c0001 | t0020 | g0082 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19077 | hp1 | a0001 | c0012 | t0024 | g0300 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19080 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19090 | hp2 | a0019 | c0022 | t0002 | g0023 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19240 | hp1 | a0001 | c0008 | t0002 | g0043 | AFR | YRI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA19240 | hp2 | a0001 | c0001 | t0011 | g0196 | AFR | YRI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ASW | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ASW | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0189 | EUR | TSI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | GIH | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0188 | SAS | GIH | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01123 | hp1 | a0004 | c0004 | t0004 | g0183 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG01123 | hp2 | a0001 | c0027 | t0002 | g0074 | AMR | CLM | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02109 | hp1 | a0004 | c0004 | t0004 | g0180 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0146 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0205 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0139 | AFR | ACB | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03471 | hp1 | a0001 | c0001 | t0032 | g0304 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG03471 | hp2 | a0004 | c0004 | t0004 | g0179 | AFR | MSL | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | USA | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | USA | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20300 | hp1 | a0007 | c0011 | t0002 | g0125 | AFR | USA | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA20300 | hp2 | a0006 | c0007 | t0001 | g0156 | AFR | USA | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0137 | AFR | LWK | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| NA21309 | hp2 | a0007 | c0011 | t0002 | g0122 | AFR | LWK | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0225 | REF | REF | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0018 | REF | REF | ATM_chr11_108218067_108374102 | ATM | chr11 | 108218067 | 108374102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108227819
|
C | A | 1 | a0011 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.116C>A | p.Thr39Lys | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/63 | 266/12915 | 116/9171 | 39/3056 | chr11 | 108227819 | ||
| chr11:108227849
|
C | G | 1 | a0012 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.146C>G | p.Ser49Cys | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/63 | 296/12915 | 146/9171 | 49/3056 | chr11 | 108227849 | ||
| chr11:108235716
|
T | A | 1 | a0002 | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
missense_variant | MODERATE | c.378T>A | p.Asp126Glu | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/63 | 528/12915 | 378/9171 | 126/3056 | chr11 | 108235716 | ||
| chr11:108244000
|
G | C | 1 | a0007 | 4 | HG01074.hp1 HG03139.hp2 NA20300.hp1 others(1): Show |
missense_variant | MODERATE | c.544G>C | p.Val182Leu | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 6/63 | 694/12915 | 544/9171 | 182/3056 | chr11 | 108244000 | ||
| chr11:108250817
|
G | A | 1 | a0013 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.1352G>A | p.Arg451His | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 10/63 | 1502/12915 | 1352/9171 | 451/3056 | chr11 | 108250817 | ||
| chr11:108251006
|
G | A | 1 | a0004 | 11 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(8): Show |
missense_variant | MODERATE | c.1541G>A | p.Gly514Asp | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 10/63 | 1691/12915 | 1541/9171 | 514/3056 | chr11 | 108251006 | ||
| chr11:108251865
|
C | G | 2 | a0009a0023 | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.1636C>G | p.Leu546Val | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 11/63 | 1786/12915 | 1636/9171 | 546/3056 | chr11 | 108251865 | ||
| chr11:108252861
|
C | G | 1 | a0014 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1847C>G | p.Thr616Ser | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/63 | 1997/12915 | 1847/9171 | 616/3056 | chr11 | 108252861 | ||
| chr11:108254034
|
T | C | 1 | a0015 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2119T>C | p.Ser707Pro | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/63 | 2269/12915 | 2119/9171 | 707/3056 | chr11 | 108254034 | ||
| chr11:108257592
|
A | C | 1 | a0016 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2362A>C | p.Ser788Arg | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/63 | 2512/12915 | 2362/9171 | 788/3056 | chr11 | 108257592 | ||
| chr11:108259051
|
C | A | 1 | a0022 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.2442C>A | p.Asp814Glu | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/63 | 2592/12915 | 2442/9171 | 814/3056 | chr11 | 108259051 | ||
| chr11:108267312
|
A | G | 1 | a0017 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.2608A>G | p.Asn870Asp | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/63 | 2758/12915 | 2608/9171 | 870/3056 | chr11 | 108267312 | ||
| chr11:108267318
|
C | T | 2 | a0009a0023 | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
missense_variant | MODERATE | c.2614C>T | p.Pro872Ser | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/63 | 2764/12915 | 2614/9171 | 872/3056 | chr11 | 108267318 | ||
| chr11:108272572
|
A | G | 2 | a0008a0014 | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
missense_variant | MODERATE | c.3118A>G | p.Met1040Val | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 21/63 | 3268/12915 | 3118/9171 | 1040/3056 | chr11 | 108272572 | ||
| chr11:108272729
|
C | G | 1 | a0010 | 2 | HG00099.hp2 HG01099.hp2 |
missense_variant | MODERATE | c.3161C>G | p.Pro1054Arg | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/63 | 3311/12915 | 3161/9171 | 1054/3056 | chr11 | 108272729 | ||
| chr11:108279589
|
A | G | 1 | a0006 | 6 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.3383A>G | p.Gln1128Arg | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/63 | 3533/12915 | 3383/9171 | 1128/3056 | chr11 | 108279589 | ||
| chr11:108289005
|
C | T | 2 | a0004a0005 | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
missense_variant | MODERATE | c.4138C>T | p.His1380Tyr | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 28/63 | 4288/12915 | 4138/9171 | 1380/3056 | chr11 | 108289005 | ||
| chr11:108289623
|
C | T | 1 | a0018 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.4258C>T | p.Leu1420Phe | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/63 | 4408/12915 | 4258/9171 | 1420/3056 | chr11 | 108289623 | ||
| chr11:108289730
|
T | A | 1 | a0019 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.4365T>A | p.Ser1455Arg | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/63 | 4515/12915 | 4365/9171 | 1455/3056 | chr11 | 108289730 | ||
| chr11:108289767
|
G | A | 1 | a0020 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.4402G>A | p.Val1468Ile | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/63 | 4552/12915 | 4402/9171 | 1468/3056 | chr11 | 108289767 | ||
| chr11:108297326
|
A | G | 1 | a0021 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.4949A>G | p.Asn1650Ser | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/63 | 5099/12915 | 4949/9171 | 1650/3056 | chr11 | 108297326 | ||
| chr11:108304735
|
G | A | 1 | a0003 | 12 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(9): Show |
missense_variant | MODERATE | c.5557G>A | p.Asp1853Asn | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/63 | 5707/12915 | 5557/9171 | 1853/3056 | chr11 | 108304735 | ||
| chr11:108315904
|
A | G | 2 | a0011a0016 | 2 | HG01243.hp2 NA18906.hp1 |
missense_variant | MODERATE | c.6088A>G | p.Ile2030Val | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 41/63 | 6238/12915 | 6088/9171 | 2030/3056 | chr11 | 108315904 | ||
| chr11:108327657
|
C | G | 1 | a0011 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.6988C>G | p.Leu2330Val | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/63 | 7138/12915 | 6988/9171 | 2330/3056 | chr11 | 108327657 | ||
| chr11:108327664
|
T | C | 1 | a0023 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.6995T>C | p.Leu2332Pro | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/63 | 7145/12915 | 6995/9171 | 2332/3056 | chr11 | 108327664 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108244065
|
C | T | 1 | a0001c0034 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.609C>T | p.Asp203Asp | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 6/63 | 759/12915 | 609/9171 | 203/3056 | chr11 | 108244065 | ||
| chr11:108244113
|
T | C | 1 | a0002c0002 | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
synonymous_variant | LOW | c.657T>C | p.Cys219Cys | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 6/63 | 807/12915 | 657/9171 | 219/3056 | chr11 | 108244113 | ||
| chr11:108244860
|
C | T | 1 | a0001c0016 | 2 | HG00323.hp2 HG00642.hp1 |
synonymous_variant | LOW | c.735C>T | p.Val245Val | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/63 | 885/12915 | 735/9171 | 245/3056 | chr11 | 108244860 | ||
| chr11:108249043
|
C | G | 1 | a0002c0005 | 9 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
synonymous_variant | LOW | c.1176C>G | p.Gly392Gly | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/63 | 1326/12915 | 1176/9171 | 392/3056 | chr11 | 108249043 | ||
| chr11:108250719
|
A | G | 1 | a0001c0008 | 6 | HG02572.hp1 HG03098.hp2 HG03139.hp1 others(3): Show |
synonymous_variant | LOW | c.1254A>G | p.Gln418Gln | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 10/63 | 1404/12915 | 1254/9171 | 418/3056 | chr11 | 108250719 | ||
| chr11:108256217
|
T | C | 1 | a0001c0020 | 1 | NA18980.hp2 | splice_region_variant&synonymous_variant | LOW | c.2127T>C | p.Ile709Ile | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/63 | 2277/12915 | 2127/9171 | 709/3056 | chr11 | 108256217 | ||
| chr11:108256283
|
C | T | 2 | a0009c0013a0023c0033 | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.2193C>T | p.Tyr731Tyr | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/63 | 2343/12915 | 2193/9171 | 731/3056 | chr11 | 108256283 | ||
| chr11:108268456
|
A | G | 2 | a0009c0013a0023c0033 | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
synonymous_variant | LOW | c.2685A>G | p.Leu895Leu | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/63 | 2835/12915 | 2685/9171 | 895/3056 | chr11 | 108268456 | ||
| chr11:108287648
|
T | C | 1 | a0001c0010 | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
synonymous_variant | LOW | c.4042T>C | p.Leu1348Leu | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/63 | 4192/12915 | 4042/9171 | 1348/3056 | chr11 | 108287648 | ||
| chr11:108292760
|
C | T | 1 | a0001c0027 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.4578C>T | p.Pro1526Pro | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 30/63 | 4728/12915 | 4578/9171 | 1526/3056 | chr11 | 108292760 | ||
| chr11:108310190
|
T | C | 1 | a0001c0012 | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
synonymous_variant | LOW | c.5793T>C | p.Ala1931Ala | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/63 | 5943/12915 | 5793/9171 | 1931/3056 | chr11 | 108310190 | ||
| chr11:108316023
|
T | C | 1 | a0001c0024 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.6108T>C | p.Tyr2036Tyr | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/63 | 6258/12915 | 6108/9171 | 2036/3056 | chr11 | 108316023 | ||
| chr11:108316062
|
T | C | 1 | a0008c0029 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.6147T>C | p.Tyr2049Tyr | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/63 | 6297/12915 | 6147/9171 | 2049/3056 | chr11 | 108316062 | ||
| chr11:108335040
|
A | C | 1 | a0001c0025 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.8082A>C | p.Gly2694Gly | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 55/63 | 8232/12915 | 8082/9171 | 2694/3056 | chr11 | 108335040 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108223106
|
G | A | 21 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(18): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
5_prime_UTR_variant | MODIFIER | c.-111G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/63 | 4519 | chr11 | 108223106 | |||||
| chr11:108365537
|
C | G | 3 | a0001c0012t0024a0001c0012t0037a0001c0012t0038 | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*29C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 29 | chr11 | 108365537 | |||||
| chr11:108365713
|
T | C | 1 | a0001c0001t0025 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*205T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 205 | chr11 | 108365713 | |||||
| chr11:108365780
|
G | A | 2 | a0001c0001t0020a0002c0005t0015 | 5 | HG02647.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*272G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 272 | chr11 | 108365780 | |||||
| chr11:108365879
|
A | G | 2 | a0002c0005t0008a0002c0005t0015 | 8 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*371A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 371 | chr11 | 108365879 | |||||
| chr11:108366029
|
C | CA | 4 | a0001c0001t0006a0001c0001t0021a0001c0001t0029others(1): Show | 9 | HG01257.hp2 HG02132.hp2 HG02738.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*540dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 541 | INFO_REALIGN_3_PRIME | chr11 | 108366029 | ||||
| chr11:108366029
|
CA | C | 28 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(25): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*540delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 540 | INFO_REALIGN_3_PRIME | chr11 | 108366029 | ||||
| chr11:108366038
|
A | G | 1 | a0001c0001t0028 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 530 | chr11 | 108366038 | |||||
| chr11:108366056
|
G | T | 26 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(23): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*548G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 548 | chr11 | 108366056 | |||||
| chr11:108366059
|
T | C | 1 | a0001c0001t0014 | 3 | HG01168.hp2 HG02683.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*551T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 551 | chr11 | 108366059 | |||||
| chr11:108366192
|
T | G | 1 | a0001c0001t0010 | 4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*684T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 684 | chr11 | 108366192 | |||||
| chr11:108366287
|
T | G | 3 | a0001c0012t0024a0001c0012t0037a0001c0012t0038 | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*779T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 779 | chr11 | 108366287 | |||||
| chr11:108366735
|
C | T | 1 | a0001c0001t0027 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1227C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 1227 | chr11 | 108366735 | |||||
| chr11:108366762
|
T | C | 1 | a0001c0010t0031 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1254T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 1254 | chr11 | 108366762 | |||||
| chr11:108366935
|
T | C | 5 | a0001c0001t0034a0004c0004t0004a0004c0004t0005others(2): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1427T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 1427 | chr11 | 108366935 | |||||
| chr11:108367112
|
C | T | 26 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(23): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1604C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 1604 | chr11 | 108367112 | |||||
| chr11:108367307
|
C | T | 1 | a0022c0021t0036 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1799C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 1799 | chr11 | 108367307 | |||||
| chr11:108367390
|
C | G | 1 | a0004c0004t0004 | 10 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1882C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 1882 | chr11 | 108367390 | |||||
| chr11:108367411
|
G | A | 1 | a0002c0009t0022 | 2 | HG01891.hp2 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1903G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 1903 | chr11 | 108367411 | |||||
| chr11:108367588
|
C | T | 2 | a0001c0001t0016a0001c0008t0016 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2080C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 2080 | chr11 | 108367588 | |||||
| chr11:108367707
|
C | G | 4 | a0004c0004t0004a0004c0004t0005a0005c0006t0005others(1): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2199C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 2199 | chr11 | 108367707 | |||||
| chr11:108367728
|
A | G | 4 | a0004c0004t0004a0004c0004t0005a0005c0006t0005others(1): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2220A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 2220 | chr11 | 108367728 | |||||
| chr11:108367732
|
C | T | 1 | a0001c0001t0021 | 2 | NA18985.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2224C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 2224 | chr11 | 108367732 | |||||
| chr11:108367797
|
T | C | 1 | a0001c0012t0037 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2289T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 2289 | chr11 | 108367797 | |||||
| chr11:108367959
|
G | A | 1 | a0001c0001t0032 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2451G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 2451 | chr11 | 108367959 | |||||
| chr11:108368288
|
C | CA | 6 | a0001c0001t0018a0001c0001t0033a0001c0001t0034others(3): Show | 9 | HG01175.hp1 HG02257.hp2 HG02523.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2797dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 2798 | INFO_REALIGN_3_PRIME | chr11 | 108368288 | ||||
| chr11:108368580
|
C | T | 7 | a0002c0002t0003a0002c0005t0003a0002c0005t0008others(4): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3072C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 3072 | chr11 | 108368580 | |||||
| chr11:108368601
|
C | T | 2 | a0009c0013t0012a0023c0033t0012 | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3093C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 3093 | chr11 | 108368601 | |||||
| chr11:108368644
|
A | G | 1 | a0001c0001t0026 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3136A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 3136 | chr11 | 108368644 | |||||
| chr11:108368901
|
G | T | 28 | a0001c0001t0001a0001c0001t0009a0001c0001t0010others(25): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*3393G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 3393 | chr11 | 108368901 | |||||
| chr11:108368903
|
G | A | 1 | a0001c0001t0019 | 2 | NA18970.hp1 NA18981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3395G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 3395 | chr11 | 108368903 | |||||
| chr11:108368921
|
T | C | 2 | a0001c0001t0007a0001c0001t0029 | 6 | NA18959.hp1 NA18973.hp2 NA18974.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3413T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 63/63 | 3413 | chr11 | 108368921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:108223194
|
C | T | 1 | a0001c0001t0032g0304 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.-31+8C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223194 | ||||||
| chr11:108223247
|
A | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+61A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223247 | ||||||
| chr11:108223275
|
T | C | 1 | a0001c0001t0018g0001 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-31+89T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223275 | ||||||
| chr11:108223276
|
C | T | 1 | a0001c0001t0018g0001 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-31+90C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223276 | ||||||
| chr11:108223550
|
G | T | 2 | a0003c0003t0001g0298a0003c0003t0001g0299 | 2 | HG00558.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.-31+364G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223550 | ||||||
| chr11:108223694
|
T | A | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-31+508T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223694 | ||||||
| chr11:108223782
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-31+596C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223782 | ||||||
| chr11:108223811
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-31+625G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223811 | ||||||
| chr11:108223984
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-31+798G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108223984 | ||||||
| chr11:108224011
|
G | A | 1 | a0004c0004t0005g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-31+825G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108224011 | ||||||
| chr11:108224307
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00280.hp2 HG00639.hp2 |
intron_variant | MODIFIER | c.-31+1121G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108224307 | ||||||
| chr11:108224493
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-31+1307A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108224493 | ||||||
| chr11:108224502
|
A | G | 14 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(11): Show | 14 | HG01070.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31+1316A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108224502 | ||||||
| chr11:108224523
|
T | C | 1 | a0008c0029t0002g0007 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-31+1337T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108224523 | ||||||
| chr11:108225053
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-31+1867A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225053 | ||||||
| chr11:108225084
|
C | T | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-31+1898C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225084 | ||||||
| chr11:108225109
|
T | C | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-31+1923T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225109 | ||||||
| chr11:108225264
|
G | A | 1 | a0006c0007t0001g0150 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-31+2078G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225264 | ||||||
| chr11:108225326
|
A | T | 7 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(4): Show | 7 | HG01261.hp1 HG02559.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+2140A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225326 | ||||||
| chr11:108225361
|
A | G | 1 | a0001c0001t0018g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-31+2175A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225361 | ||||||
| chr11:108225376
|
G | T | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-31+2190G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225376 | ||||||
| chr11:108225414
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-30-2181A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225414 | ||||||
| chr11:108225504
|
C | T | 1 | a0001c0001t0001g0292 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-30-2091C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225504 | ||||||
| chr11:108225558
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-30-2037C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225558 | ||||||
| chr11:108225559
|
C | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-30-2036C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225559 | ||||||
| chr11:108225583
|
C | G | 1 | a0017c0030t0002g0126 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-30-2012C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225583 | ||||||
| chr11:108225767
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-30-1828C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225767 | ||||||
| chr11:108225890
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-30-1705A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225890 | ||||||
| chr11:108225974
|
C | T | 4 | a0007c0011t0002g0122a0007c0011t0002g0123a0007c0011t0002g0124others(1): Show | 4 | HG01074.hp1 HG03139.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-1621C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108225974 | ||||||
| chr11:108226035
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-30-1560A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226035 | ||||||
| chr11:108226236
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-30-1359C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226236 | ||||||
| chr11:108226459
|
T | A | 1 | a0001c0001t0014g0151 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-30-1136T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226459 | ||||||
| chr11:108226561
|
T | A | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-30-1034T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226561 | ||||||
| chr11:108226606
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.-30-989A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226606 | ||||||
| chr11:108226639
|
A | C | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-30-956A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226639 | ||||||
| chr11:108226640
|
T | C | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-30-955T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226640 | ||||||
| chr11:108226742
|
C | A | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-30-853C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226742 | ||||||
| chr11:108226776
|
C | T | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-30-819C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226776 | ||||||
| chr11:108226892
|
C | T | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-30-703C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226892 | ||||||
| chr11:108226946
|
C | T | 1 | a0007c0011t0002g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-30-649C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226946 | ||||||
| chr11:108226994
|
A | G | 10 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(7): Show | 10 | HG02074.hp2 HG02165.hp1 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.-30-601A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108226994 | ||||||
| chr11:108227030
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-30-565C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108227030 | ||||||
| chr11:108227082
|
T | G | 1 | a0001c0001t0002g0010 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-30-513T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108227082 | ||||||
| chr11:108227371
|
A | T | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-30-224A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108227371 | ||||||
| chr11:108227415
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30-180C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108227415 | ||||||
| chr11:108227416
|
G | A | 1 | a0001c0012t0024g0300 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-30-179G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108227416 | ||||||
| chr11:108227516
|
A | G | 13 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30-79A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108227516 | ||||||
| chr11:108227551
|
T | C | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-30-44T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 1/62 | chr11 | 108227551 | ||||||
| chr11:108227732
|
TAA | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+37_72+38delAA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 2/62 | chr11 | 108227732 | ||||||
| chr11:108228134
|
T | A | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+246T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228134 | ||||||
| chr11:108228154
|
TTTAG | T | 13 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.185+273_185+276del others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | INFO_REALIGN_3_PRIME | chr11 | 108228154 | |||||
| chr11:108228248
|
G | C | 1 | a0001c0012t0037g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.185+360G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228248 | ||||||
| chr11:108228249
|
T | C | 1 | a0001c0001t0001g0296 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.185+361T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228249 | ||||||
| chr11:108228463
|
G | A | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.185+575G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228463 | ||||||
| chr11:108228504
|
T | C | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+616T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228504 | ||||||
| chr11:108228633
|
A | G | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | HG00408.hp2 HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.186-545A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228633 | ||||||
| chr11:108228647
|
G | A | 2 | a0001c0016t0002g0014a0001c0016t0002g0015 | 2 | HG00323.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.186-531G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228647 | ||||||
| chr11:108228792
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.186-386G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108228792 | ||||||
| chr11:108229161
|
A | G | 9 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 9 | HG01074.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.186-17A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108229161 | ||||||
| chr11:108229171
|
C | T | 2 | a0002c0002t0003g0085a0002c0002t0003g0086 | 2 | HG01081.hp2 HG02280.hp2 |
splice_region_variant&intron_variant | LOW | c.186-7C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 3/62 | chr11 | 108229171 | ||||||
| chr11:108229378
|
G | GT | 153 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.331+69dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108229378 | |||||
| chr11:108229378
|
G | GTT | 7 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(4): Show | 7 | HG00099.hp1 HG00099.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.331+68_331+69dupTT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108229378 | |||||
| chr11:108229500
|
T | A | 1 | a0007c0011t0002g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.331+177T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108229500 | ||||||
| chr11:108229518
|
T | G | 1 | a0001c0012t0024g0300 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.331+195T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108229518 | ||||||
| chr11:108229653
|
A | T | 1 | a0001c0012t0037g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.331+330A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108229653 | ||||||
| chr11:108229832
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.331+509C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108229832 | ||||||
| chr11:108229842
|
G | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.331+519G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108229842 | ||||||
| chr11:108229847
|
AT | A | 9 | a0001c0001t0001g0153a0001c0001t0001g0199a0001c0001t0001g0200others(6): Show | 9 | HG00544.hp1 HG02572.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+541delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108229847 | |||||
| chr11:108230007
|
A | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.331+684A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230007 | ||||||
| chr11:108230036
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.331+713C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230036 | ||||||
| chr11:108230134
|
G | T | 3 | a0008c0015t0002g0013a0008c0029t0002g0007a0014c0032t0002g0011 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.331+811G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230134 | ||||||
| chr11:108230214
|
G | A | 9 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 9 | HG01074.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.331+891G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230214 | ||||||
| chr11:108230221
|
G | T | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.331+898G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230221 | ||||||
| chr11:108230367
|
G | A | 1 | a0001c0001t0001g0201 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.331+1044G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230367 | ||||||
| chr11:108230435
|
C | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.331+1112C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230435 | ||||||
| chr11:108230501
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.331+1178G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230501 | ||||||
| chr11:108230661
|
C | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.331+1338C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230661 | ||||||
| chr11:108230695
|
A | AG | 11 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 11 | HG02132.hp1 HG02451.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+1373dupG | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108230695 | |||||
| chr11:108230765
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.331+1442A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230765 | ||||||
| chr11:108230819
|
A | G | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.331+1496A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230819 | ||||||
| chr11:108230823
|
T | A | 1 | a0001c0001t0001g0203 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.331+1500T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108230823 | ||||||
| chr11:108231072
|
A | G | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+1749A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108231072 | ||||||
| chr11:108231111
|
G | C | 22 | a0001c0001t0017g0175a0001c0001t0034g0152a0004c0004t0004g0168others(19): Show | 22 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(19): Show |
intron_variant | MODIFIER | c.331+1788G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108231111 | ||||||
| chr11:108231192
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.331+1869C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108231192 | ||||||
| chr11:108231335
|
G | A | 11 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 11 | HG02132.hp1 HG02451.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.331+2012G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108231335 | ||||||
| chr11:108231423
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.331+2100C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108231423 | ||||||
| chr11:108231696
|
C | CA | 136 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.331+2396dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108231696 | |||||
| chr11:108231696
|
C | CAA | 13 | a0001c0001t0001g0201a0001c0001t0001g0204a0001c0001t0001g0206others(10): Show | 13 | HG01109.hp1 HG01175.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.331+2395_331+2396d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108231696 | |||||
| chr11:108231696
|
C | CAAA | 10 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(7): Show | 10 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.331+2394_331+2396d others(5): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108231696 | |||||
| chr11:108231696
|
CA | C | 7 | a0001c0001t0002g0113a0001c0001t0034g0152a0002c0009t0035g0104others(4): Show | 7 | HG02257.hp2 HG02622.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.331+2396delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108231696 | |||||
| chr11:108231775
|
G | T | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.331+2452G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108231775 | ||||||
| chr11:108232163
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.331+2840G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232163 | ||||||
| chr11:108232239
|
C | T | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+2916C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232239 | ||||||
| chr11:108232277
|
A | G | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.331+2954A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232277 | ||||||
| chr11:108232314
|
T | G | 1 | a0003c0003t0001g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.331+2991T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232314 | ||||||
| chr11:108232327
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0163 | 2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.331+3004C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232327 | ||||||
| chr11:108232337
|
T | TTTTG | 5 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG02132.hp1 HG03130.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.331+3034_331+3037d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232337 | |||||
| chr11:108232527
|
C | CT | 16 | a0001c0001t0002g0019a0001c0001t0002g0078a0001c0001t0002g0079others(13): Show | 16 | HG02004.hp2 HG02074.hp2 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.332-3113dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232527
|
CT | C | 16 | a0001c0001t0002g0022a0001c0001t0002g0054a0001c0001t0002g0089others(13): Show | 16 | HG00408.hp2 HG00733.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-3113delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232527
|
CTT | C | 46 | a0001c0001t0001g0198a0001c0001t0001g0277a0001c0001t0002g0021others(43): Show | 46 | HG00544.hp2 HG00558.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.332-3114_332-3113d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232527
|
CTTT | C | 53 | a0001c0001t0001g0210a0001c0001t0001g0264a0001c0001t0001g0265others(50): Show | 53 | HG01074.hp1 HG01109.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.332-3115_332-3113d others(5): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232527
|
CTTTT | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.332-3116_332-3113d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232527
|
CTTTTT | C | 14 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0026g0190others(11): Show | 14 | HG00323.hp1 HG00558.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-3117_332-3113d others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232527
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.332-3124_332-3113d others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232527
|
CTTTTTTT others(6): Show |
C | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.332-3125_332-3113d others(15): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232527 | |||||
| chr11:108232530
|
T | C | 6 | a0002c0005t0003g0096a0002c0005t0008g0097a0002c0005t0008g0103others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.332-3140T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232530 | ||||||
| chr11:108232531
|
T | C | 9 | a0002c0002t0003g0146a0002c0002t0003g0147a0002c0005t0008g0095others(6): Show | 9 | HG02109.hp2 HG02280.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.332-3139T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232531 | ||||||
| chr11:108232532
|
T | C | 15 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(12): Show | 15 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.332-3138T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232532 | ||||||
| chr11:108232584
|
A | G | 303 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.332-3086A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232584 | ||||||
| chr11:108232630
|
C | T | 1 | a0001c0001t0009g0263 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.332-3040C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232630 | ||||||
| chr11:108232729
|
G | A | 1 | a0007c0011t0002g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.332-2941G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232729 | ||||||
| chr11:108232846
|
G | A | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-2824G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232846 | ||||||
| chr11:108232884
|
CAG | C | 20 | a0001c0001t0017g0175a0004c0004t0004g0168a0004c0004t0004g0169others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.332-2783_332-2782d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108232884 | |||||
| chr11:108232919
|
A | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-2751A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232919 | ||||||
| chr11:108232965
|
C | T | 1 | a0009c0013t0012g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.332-2705C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232965 | ||||||
| chr11:108232966
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-2704G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232966 | ||||||
| chr11:108232998
|
G | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-2672G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108232998 | ||||||
| chr11:108233018
|
A | T | 5 | a0001c0001t0002g0021a0001c0001t0002g0049a0001c0001t0002g0050others(2): Show | 5 | HG02132.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-2652A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233018 | ||||||
| chr11:108233026
|
C | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-2644C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233026 | ||||||
| chr11:108233106
|
C | A | 1 | a0001c0010t0002g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.332-2564C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233106 | ||||||
| chr11:108233121
|
C | A | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.332-2549C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233121 | ||||||
| chr11:108233210
|
A | G | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.332-2460A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233210 | ||||||
| chr11:108233442
|
A | C | 1 | a0001c0001t0006g0052 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.332-2228A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233442 | ||||||
| chr11:108233569
|
C | CA | 17 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(14): Show | 17 | HG00738.hp2 HG01099.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.332-2080dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108233569 | |||||
| chr11:108233569
|
CA | C | 12 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0002g0081others(9): Show | 12 | HG00140.hp2 HG01109.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.332-2080delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108233569 | |||||
| chr11:108233590
|
A | AT | 14 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(11): Show | 14 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.332-2080_332-2079i others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233590 | ||||||
| chr11:108233750
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.332-1920C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233750 | ||||||
| chr11:108233798
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.332-1872A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233798 | ||||||
| chr11:108233825
|
T | C | 5 | a0001c0001t0002g0021a0001c0001t0002g0049a0001c0001t0002g0050others(2): Show | 5 | HG02132.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.332-1845T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233825 | ||||||
| chr11:108233867
|
GA | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0198a0001c0001t0001g0199others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.332-1795delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108233867 | |||||
| chr11:108233929
|
G | A | 2 | a0001c0001t0001g0223a0001c0001t0001g0267 | 2 | NA18986.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.332-1741G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233929 | ||||||
| chr11:108233971
|
T | C | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-1699T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108233971 | ||||||
| chr11:108234090
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-1580T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234090 | ||||||
| chr11:108234257
|
A | G | 2 | a0003c0003t0001g0192a0003c0003t0001g0193 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.332-1413A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234257 | ||||||
| chr11:108234358
|
A | C | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.332-1312A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234358 | ||||||
| chr11:108234435
|
A | G | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332-1235A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234435 | ||||||
| chr11:108234573
|
A | G | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.332-1097A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234573 | ||||||
| chr11:108234751
|
G | A | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.332-919G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234751 | ||||||
| chr11:108234827
|
C | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-843C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234827 | ||||||
| chr11:108234840
|
T | TA | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.332-819dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108234840 | |||||
| chr11:108234866
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.332-804G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234866 | ||||||
| chr11:108234938
|
A | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.332-732A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234938 | ||||||
| chr11:108234943
|
A | G | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.332-727A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234943 | ||||||
| chr11:108234996
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.332-674A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108234996 | ||||||
| chr11:108235201
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.332-469T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108235201 | ||||||
| chr11:108235259
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.332-411G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108235259 | ||||||
| chr11:108235295
|
C | CA | 34 | a0001c0001t0001g0282a0001c0001t0002g0057a0001c0001t0002g0128others(31): Show | 34 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.332-359dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | INFO_REALIGN_3_PRIME | chr11 | 108235295 | |||||
| chr11:108235511
|
AT | A | 5 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG02132.hp1 HG03130.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.332-158delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108235511 | ||||||
| chr11:108235512
|
T | A | 6 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0157others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.332-158T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108235512 | ||||||
| chr11:108235522
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.332-148T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108235522 | ||||||
| chr11:108235599
|
A | G | 4 | a0001c0001t0001g0259a0001c0001t0001g0284a0001c0001t0001g0285others(1): Show | 4 | HG00099.hp1 HG03834.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.332-71A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 4/62 | chr11 | 108235599 | ||||||
| chr11:108235908
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+74G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108235908 | ||||||
| chr11:108236055
|
C | T | 210 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.496+221C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236055 | ||||||
| chr11:108236281
|
C | T | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+447C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236281 | ||||||
| chr11:108236282
|
G | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.496+448G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236282 | ||||||
| chr11:108236286
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+452G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236286 | ||||||
| chr11:108236390
|
G | A | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.496+556G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236390 | ||||||
| chr11:108236515
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+681G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236515 | ||||||
| chr11:108236534
|
T | TA | 153 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.496+716dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108236534 | |||||
| chr11:108236553
|
G | T | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.496+719G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236553 | ||||||
| chr11:108236654
|
G | A | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.496+820G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236654 | ||||||
| chr11:108236770
|
T | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.496+936T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236770 | ||||||
| chr11:108236850
|
T | C | 6 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0157others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+1016T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236850 | ||||||
| chr11:108236933
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.496+1099G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108236933 | ||||||
| chr11:108237187
|
T | A | 1 | a0001c0001t0001g0005 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.496+1353T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237187 | ||||||
| chr11:108237197
|
G | A | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.496+1363G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237197 | ||||||
| chr11:108237351
|
C | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0214 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.496+1517C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237351 | ||||||
| chr11:108237458
|
A | G | 2 | a0001c0012t0024g0300a0001c0012t0024g0303 | 2 | NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.496+1624A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237458 | ||||||
| chr11:108237459
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.496+1625C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237459 | ||||||
| chr11:108237468
|
C | CT | 11 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(8): Show | 11 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.496+1643dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108237468 | |||||
| chr11:108237789
|
A | G | 1 | a0001c0001t0027g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.496+1955A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237789 | ||||||
| chr11:108237810
|
A | G | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.496+1976A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237810 | ||||||
| chr11:108237899
|
G | GT | 23 | a0001c0001t0002g0010a0001c0001t0002g0019a0001c0001t0002g0022others(20): Show | 23 | HG00544.hp2 HG01123.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.496+2090dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108237899 | |||||
| chr11:108237899
|
G | GTT | 8 | a0001c0001t0016g0009a0001c0008t0016g0116a0002c0009t0022g0094others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.496+2089_496+2090d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108237899 | |||||
| chr11:108237899
|
GTTTT | G | 19 | a0001c0001t0001g0200a0001c0001t0001g0213a0001c0001t0001g0256others(16): Show | 19 | HG00544.hp1 HG01255.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.496+2087_496+2090d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108237899 | |||||
| chr11:108237899
|
GTTTTT | G | 94 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(91): Show | 94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.496+2086_496+2090d others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108237899 | |||||
| chr11:108237899
|
GTTTTTT | G | 42 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(39): Show | 42 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.496+2085_496+2090d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108237899 | |||||
| chr11:108237924
|
TG | T | 3 | a0002c0002t0003g0143a0002c0002t0003g0144a0002c0002t0003g0145 | 3 | HG03098.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.496+2091delG | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237924 | ||||||
| chr11:108237924
|
TGC | T | 13 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(10): Show | 13 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.496+2091_496+2092d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237924 | ||||||
| chr11:108237926
|
C | T | 3 | a0002c0002t0003g0143a0002c0002t0003g0144a0002c0002t0003g0145 | 3 | HG03098.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.496+2092C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237926 | ||||||
| chr11:108237929
|
C | G | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.496+2095C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237929 | ||||||
| chr11:108237930
|
T | C | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.496+2096T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237930 | ||||||
| chr11:108237933
|
G | C | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.496+2099G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108237933 | ||||||
| chr11:108238129
|
G | A | 3 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0038g0302 | 3 | HG00140.hp2 NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.496+2295G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238129 | ||||||
| chr11:108238215
|
C | T | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+2381C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238215 | ||||||
| chr11:108238279
|
AT | A | 13 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.496+2451delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108238279 | |||||
| chr11:108238287
|
T | G | 13 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.496+2453T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238287 | ||||||
| chr11:108238326
|
A | T | 1 | a0001c0001t0002g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.496+2492A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238326 | ||||||
| chr11:108238334
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.496+2500T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238334 | ||||||
| chr11:108238337
|
A | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.496+2503A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238337 | ||||||
| chr11:108238391
|
A | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.496+2557A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238391 | ||||||
| chr11:108238572
|
A | G | 7 | a0002c0002t0003g0139a0002c0002t0003g0140a0002c0002t0003g0141others(4): Show | 7 | HG01243.hp1 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+2738A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238572 | ||||||
| chr11:108238774
|
T | C | 1 | a0001c0001t0013g0025 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.496+2940T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238774 | ||||||
| chr11:108238895
|
A | G | 1 | a0001c0001t0014g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.496+3061A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108238895 | ||||||
| chr11:108239111
|
G | T | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.496+3277G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108239111 | ||||||
| chr11:108239149
|
A | G | 1 | a0001c0010t0002g0032 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.496+3315A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108239149 | ||||||
| chr11:108239212
|
G | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+3378G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108239212 | ||||||
| chr11:108239525
|
A | G | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.496+3691A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108239525 | ||||||
| chr11:108239740
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.496+3906A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108239740 | ||||||
| chr11:108239936
|
A | G | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-4017A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108239936 | ||||||
| chr11:108239997
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0266 | 2 | HG00642.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.497-3956A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108239997 | ||||||
| chr11:108240170
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.497-3783T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108240170 | ||||||
| chr11:108240366
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.497-3587C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108240366 | ||||||
| chr11:108240568
|
T | A | 1 | a0001c0001t0025g0268 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.497-3385T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108240568 | ||||||
| chr11:108240591
|
A | C | 1 | a0002c0002t0003g0138 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.497-3362A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108240591 | ||||||
| chr11:108240628
|
A | G | 1 | a0001c0001t0002g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.497-3325A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108240628 | ||||||
| chr11:108240664
|
T | G | 1 | a0001c0001t0002g0083 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.497-3289T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108240664 | ||||||
| chr11:108240702
|
TA | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.497-3249delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108240702 | |||||
| chr11:108241267
|
C | T | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-2686C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108241267 | ||||||
| chr11:108241295
|
A | G | 1 | a0001c0001t0001g0287 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.497-2658A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108241295 | ||||||
| chr11:108241471
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0214 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.497-2482A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108241471 | ||||||
| chr11:108241609
|
G | A | 3 | a0008c0015t0002g0013a0008c0029t0002g0007a0014c0032t0002g0011 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.497-2344G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108241609 | ||||||
| chr11:108241728
|
GTCTT | G | 21 | a0001c0001t0001g0153a0001c0001t0001g0163a0001c0001t0001g0204others(18): Show | 21 | HG00099.hp1 HG00280.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.497-2211_497-2208d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108241728 | |||||
| chr11:108241738
|
CTTTCT | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.497-2211_497-2207d others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108241738 | |||||
| chr11:108241738
|
CTTTCTT | C | 16 | a0001c0001t0001g0212a0001c0001t0001g0223a0001c0001t0001g0226others(13): Show | 16 | HG00323.hp1 HG00558.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.497-2211_497-2206d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108241738 | |||||
| chr11:108241742
|
C | CTT | 7 | a0001c0001t0002g0069a0001c0010t0002g0029a0001c0010t0002g0030others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.497-2187_497-2186d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108241742 | |||||
| chr11:108241742
|
CT | C | 44 | a0001c0001t0002g0034a0001c0001t0002g0049a0001c0001t0006g0059others(41): Show | 44 | HG00140.hp2 HG01109.hp2 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.497-2186delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108241742 | |||||
| chr11:108241742
|
CTT | C | 26 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(23): Show | 26 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.497-2187_497-2186d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108241742 | |||||
| chr11:108242128
|
CAA | C | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.497-1820_497-1819d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108242128 | |||||
| chr11:108242165
|
T | C | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.497-1788T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242165 | ||||||
| chr11:108242188
|
G | T | 1 | a0001c0001t0002g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.497-1765G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242188 | ||||||
| chr11:108242251
|
G | T | 68 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0153others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.497-1702G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242251 | ||||||
| chr11:108242378
|
G | A | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.497-1575G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242378 | ||||||
| chr11:108242418
|
CATT | C | 6 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0157others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-1532_497-1530d others(5): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | INFO_REALIGN_3_PRIME | chr11 | 108242418 | |||||
| chr11:108242563
|
A | C | 1 | a0002c0002t0003g0147 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.497-1390A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242563 | ||||||
| chr11:108242604
|
C | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.497-1349C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242604 | ||||||
| chr11:108242837
|
A | G | 4 | a0001c0001t0001g0225a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-1116A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242837 | ||||||
| chr11:108242971
|
G | A | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.497-982G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108242971 | ||||||
| chr11:108243181
|
C | G | 1 | a0001c0008t0016g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.497-772C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108243181 | ||||||
| chr11:108243637
|
A | G | 2 | a0011c0017t0002g0056a0016c0031t0002g0080 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.497-316A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108243637 | ||||||
| chr11:108243750
|
T | C | 1 | a0001c0001t0023g0058 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.497-203T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108243750 | ||||||
| chr11:108243779
|
A | G | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.497-174A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108243779 | ||||||
| chr11:108243837
|
G | A | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.497-116G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108243837 | ||||||
| chr11:108243861
|
A | G | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.497-92A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108243861 | ||||||
| chr11:108243905
|
T | G | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.497-48T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 5/62 | chr11 | 108243905 | ||||||
| chr11:108244156
|
T | C | 14 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.662+38T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 6/62 | chr11 | 108244156 | ||||||
| chr11:108244372
|
C | G | 1 | a0002c0002t0003g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.662+254C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 6/62 | chr11 | 108244372 | ||||||
| chr11:108244519
|
C | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.663-269C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 6/62 | chr11 | 108244519 | ||||||
| chr11:108244633
|
AT | A | 300 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.663-144delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 6/62 | INFO_REALIGN_3_PRIME | chr11 | 108244633 | |||||
| chr11:108245051
|
T | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.901+25T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108245051 | ||||||
| chr11:108245253
|
G | A | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.901+227G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108245253 | ||||||
| chr11:108245523
|
A | C | 1 | a0001c0001t0002g0068 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.901+497A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108245523 | ||||||
| chr11:108245685
|
C | G | 1 | a0018c0028t0002g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.901+659C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108245685 | ||||||
| chr11:108245755
|
A | C | 1 | a0018c0028t0002g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.901+729A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108245755 | ||||||
| chr11:108245821
|
C | CT | 15 | a0001c0001t0001g0207a0001c0001t0001g0218a0001c0001t0001g0261others(12): Show | 15 | HG00140.hp2 HG01517.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.901+816dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | INFO_REALIGN_3_PRIME | chr11 | 108245821 | |||||
| chr11:108245886
|
G | A | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.901+860G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108245886 | ||||||
| chr11:108245973
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.901+947T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108245973 | ||||||
| chr11:108246070
|
C | T | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.902-894C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108246070 | ||||||
| chr11:108246156
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.902-808A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108246156 | ||||||
| chr11:108246322
|
A | G | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.902-642A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108246322 | ||||||
| chr11:108246437
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0256 | 3 | NA18982.hp2 NA19004.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.902-527G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108246437 | ||||||
| chr11:108246460
|
C | T | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.902-504C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108246460 | ||||||
| chr11:108246608
|
C | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.902-356C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108246608 | ||||||
| chr11:108246643
|
C | T | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.902-321C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 7/62 | chr11 | 108246643 | ||||||
| chr11:108247405
|
C | T | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.1065+278C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247405 | ||||||
| chr11:108247495
|
C | T | 1 | a0001c0001t0011g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1065+368C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247495 | ||||||
| chr11:108247507
|
T | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.1065+380T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247507 | ||||||
| chr11:108247665
|
C | T | 5 | a0001c0001t0001g0259a0009c0013t0012g0117a0009c0013t0012g0119others(2): Show | 5 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1065+538C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247665 | ||||||
| chr11:108247689
|
G | A | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1065+562G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247689 | ||||||
| chr11:108247734
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065+607T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247734 | ||||||
| chr11:108247752
|
C | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1065+625C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247752 | ||||||
| chr11:108247978
|
C | A | 1 | a0001c0012t0038g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1065+851C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247978 | ||||||
| chr11:108247992
|
A | G | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1065+865A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108247992 | ||||||
| chr11:108248030
|
G | A | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1065+903G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248030 | ||||||
| chr11:108248051
|
A | G | 1 | a0003c0003t0001g0298 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1066-882A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248051 | ||||||
| chr11:108248321
|
C | A | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1066-612C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248321 | ||||||
| chr11:108248614
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1066-319C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248614 | ||||||
| chr11:108248639
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1066-294A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248639 | ||||||
| chr11:108248703
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1066-230A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248703 | ||||||
| chr11:108248745
|
G | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0283a0013c0018t0001g0231 | 3 | NA18963.hp2 NA18977.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1066-188G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248745 | ||||||
| chr11:108248876
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-57G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 8/62 | chr11 | 108248876 | ||||||
| chr11:108249477
|
A | C | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1235+375A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249477 | ||||||
| chr11:108249560
|
C | T | 2 | a0001c0001t0002g0078a0001c0001t0023g0058 | 2 | HG01975.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1235+458C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249560 | ||||||
| chr11:108249595
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1235+493G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249595 | ||||||
| chr11:108249712
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1235+610G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249712 | ||||||
| chr11:108249919
|
G | T | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1236-782G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249919 | ||||||
| chr11:108249922
|
A | T | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1236-779A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249922 | ||||||
| chr11:108249939
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1236-762T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249939 | ||||||
| chr11:108249979
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1236-722T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108249979 | ||||||
| chr11:108250063
|
G | A | 1 | a0003c0003t0001g0187 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1236-638G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108250063 | ||||||
| chr11:108250085
|
G | A | 8 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(5): Show | 8 | HG01175.hp1 HG02257.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1236-616G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108250085 | ||||||
| chr11:108250111
|
AC | A | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236-589delC | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108250111 | ||||||
| chr11:108250141
|
AAT | A | 76 | a0001c0001t0001g0164a0001c0001t0002g0021a0001c0001t0002g0022others(73): Show | 76 | HG00733.hp1 HG00735.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.1236-537_1236-536d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | INFO_REALIGN_3_PRIME | chr11 | 108250141 | |||||
| chr11:108250141
|
AATAT | A | 170 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1236-539_1236-536d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | INFO_REALIGN_3_PRIME | chr11 | 108250141 | |||||
| chr11:108250508
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1236-193C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | chr11 | 108250508 | ||||||
| chr11:108250683
|
C | CT | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1236-3dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 9/62 | INFO_REALIGN_3_PRIME | chr11 | 108250683 | |||||
| chr11:108251184
|
A | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1607+112A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 10/62 | chr11 | 108251184 | ||||||
| chr11:108251428
|
A | G | 1 | a0001c0001t0020g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1607+356A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 10/62 | chr11 | 108251428 | ||||||
| chr11:108251643
|
T | C | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1608-194T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 10/62 | chr11 | 108251643 | ||||||
| chr11:108251829
|
T | C | 1 | a0001c0001t0007g0060 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.1608-8T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 10/62 | chr11 | 108251829 | ||||||
| chr11:108252096
|
T | C | 9 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 9 | HG01074.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1802+65T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 11/62 | chr11 | 108252096 | ||||||
| chr11:108252304
|
G | A | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1802+273G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 11/62 | chr11 | 108252304 | ||||||
| chr11:108252462
|
C | A | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.1803-355C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 11/62 | chr11 | 108252462 | ||||||
| chr11:108252663
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1803-154G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 11/62 | chr11 | 108252663 | ||||||
| chr11:108252680
|
T | C | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1803-137T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 11/62 | chr11 | 108252680 | ||||||
| chr11:108252732
|
A | G | 1 | a0001c0012t0037g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1803-85A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 11/62 | chr11 | 108252732 | ||||||
| chr11:108252915
|
A | G | 2 | a0001c0001t0029g0016a0014c0032t0002g0011 | 2 | HG02572.hp2 NA18974.hp2 |
splice_region_variant&intron_variant | LOW | c.1898+3A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108252915 | ||||||
| chr11:108253050
|
G | A | 1 | a0008c0015t0002g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1898+138G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253050 | ||||||
| chr11:108253088
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1898+176A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253088 | ||||||
| chr11:108253125
|
G | A | 1 | a0004c0004t0004g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1898+213G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253125 | ||||||
| chr11:108253330
|
C | G | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1898+418C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253330 | ||||||
| chr11:108253572
|
G | A | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1899-242G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253572 | ||||||
| chr11:108253652
|
G | A | 3 | a0008c0015t0002g0013a0008c0029t0002g0007a0014c0032t0002g0011 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1899-162G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253652 | ||||||
| chr11:108253691
|
A | G | 1 | a0003c0003t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1899-123A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253691 | ||||||
| chr11:108253759
|
T | G | 3 | a0001c0001t0014g0151a0001c0001t0014g0275a0001c0001t0014g0279 | 3 | HG01168.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1899-55T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 12/62 | chr11 | 108253759 | ||||||
| chr11:108254148
|
A | G | 1 | a0023c0033t0012g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2124+109A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254148 | ||||||
| chr11:108254342
|
A | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2124+303A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254342 | ||||||
| chr11:108254389
|
A | C | 1 | a0001c0001t0002g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2124+350A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254389 | ||||||
| chr11:108254530
|
C | T | 2 | a0001c0001t0006g0051a0001c0001t0006g0052 | 2 | HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2124+491C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254530 | ||||||
| chr11:108254714
|
G | A | 8 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(5): Show | 8 | HG01074.hp1 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2124+675G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254714 | ||||||
| chr11:108254736
|
T | G | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2124+697T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254736 | ||||||
| chr11:108254744
|
C | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.2124+705C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254744 | ||||||
| chr11:108254777
|
G | A | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.2124+738G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254777 | ||||||
| chr11:108254863
|
G | A | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2124+824G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108254863 | ||||||
| chr11:108255129
|
C | A | 1 | a0001c0001t0002g0050 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2125-1086C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108255129 | ||||||
| chr11:108255173
|
A | G | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2125-1042A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108255173 | ||||||
| chr11:108255218
|
G | A | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2125-997G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108255218 | ||||||
| chr11:108255422
|
CT | C | 156 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2125-772delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | INFO_REALIGN_3_PRIME | chr11 | 108255422 | |||||
| chr11:108255422
|
CTT | C | 137 | a0001c0001t0001g0289a0001c0001t0002g0010a0001c0001t0002g0017others(134): Show | 137 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2125-773_2125-772d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | INFO_REALIGN_3_PRIME | chr11 | 108255422 | |||||
| chr11:108255626
|
A | G | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.2125-589A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108255626 | ||||||
| chr11:108255846
|
T | C | 1 | a0001c0001t0033g0036 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2125-369T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108255846 | ||||||
| chr11:108255879
|
C | T | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2125-336C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108255879 | ||||||
| chr11:108256146
|
C | G | 2 | a0011c0017t0002g0056a0016c0031t0002g0080 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2125-69C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 13/62 | chr11 | 108256146 | ||||||
| chr11:108256362
|
A | C | 1 | a0001c0001t0002g0010 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2250+22A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/62 | chr11 | 108256362 | ||||||
| chr11:108256374
|
A | C | 1 | a0001c0001t0002g0010 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2250+34A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/62 | chr11 | 108256374 | ||||||
| chr11:108256415
|
T | C | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | HG00408.hp2 HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2250+75T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/62 | chr11 | 108256415 | ||||||
| chr11:108256561
|
T | C | 303 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2250+221T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/62 | chr11 | 108256561 | ||||||
| chr11:108257319
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2251-162T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/62 | chr11 | 108257319 | ||||||
| chr11:108257364
|
C | CT | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2251-115dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 14/62 | INFO_REALIGN_3_PRIME | chr11 | 108257364 | |||||
| chr11:108258364
|
C | T | 5 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG02132.hp1 HG03130.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.2377-622C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/62 | chr11 | 108258364 | ||||||
| chr11:108258436
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2377-550G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/62 | chr11 | 108258436 | ||||||
| chr11:108258442
|
A | G | 1 | a0005c0006t0005g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2377-544A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/62 | chr11 | 108258442 | ||||||
| chr11:108258618
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG02135.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2377-368A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/62 | chr11 | 108258618 | ||||||
| chr11:108258768
|
T | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2377-218T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/62 | chr11 | 108258768 | ||||||
| chr11:108258872
|
C | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2377-114C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/62 | chr11 | 108258872 | ||||||
| chr11:108258930
|
A | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.2377-56A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 15/62 | chr11 | 108258930 | ||||||
| chr11:108259094
|
T | G | 1 | a0001c0008t0016g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2466+19T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259094 | ||||||
| chr11:108259162
|
T | G | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2466+87T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259162 | ||||||
| chr11:108259304
|
A | G | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2466+229A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259304 | ||||||
| chr11:108259305
|
C | T | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2466+230C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259305 | ||||||
| chr11:108259308
|
T | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2466+233T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259308 | ||||||
| chr11:108259312
|
A | AC | 5 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0038others(2): Show | 5 | HG00544.hp2 NA18939.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2466+241dupC | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108259312 | |||||
| chr11:108259350
|
G | A | 1 | a0001c0001t0014g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2466+275G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259350 | ||||||
| chr11:108259355
|
G | A | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2466+280G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259355 | ||||||
| chr11:108259369
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+294G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259369 | ||||||
| chr11:108259669
|
G | A | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2466+594G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259669 | ||||||
| chr11:108259674
|
A | T | 1 | a0005c0006t0005g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2466+599A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259674 | ||||||
| chr11:108259692
|
A | G | 1 | a0001c0001t0006g0114 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2466+617A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259692 | ||||||
| chr11:108259820
|
C | T | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2466+745C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259820 | ||||||
| chr11:108259847
|
T | C | 2 | a0001c0001t0002g0072a0001c0001t0017g0071 | 2 | NA18988.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2466+772T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259847 | ||||||
| chr11:108259850
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2466+775A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259850 | ||||||
| chr11:108259863
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+788A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259863 | ||||||
| chr11:108259985
|
G | A | 19 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0035others(16): Show | 19 | HG00733.hp1 HG00735.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.2466+910G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108259985 | ||||||
| chr11:108260030
|
C | CT | 15 | a0001c0001t0001g0201a0001c0001t0002g0034a0001c0001t0002g0072others(12): Show | 15 | HG00140.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2466+977dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108260030 | |||||
| chr11:108260030
|
CT | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.2466+977delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108260030 | |||||
| chr11:108260030
|
CTT | C | 7 | a0001c0001t0001g0158a0001c0001t0001g0235a0001c0001t0001g0292others(4): Show | 7 | HG01074.hp2 HG01515.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.2466+976_2466+977d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108260030 | |||||
| chr11:108260074
|
G | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02132.hp1 HG03579.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+999G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260074 | ||||||
| chr11:108260078
|
G | A | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2466+1003G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260078 | ||||||
| chr11:108260345
|
T | C | 7 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(4): Show | 7 | HG01074.hp1 HG01891.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2466+1270T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260345 | ||||||
| chr11:108260379
|
T | G | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2466+1304T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260379 | ||||||
| chr11:108260410
|
G | A | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2466+1335G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260410 | ||||||
| chr11:108260462
|
A | C | 1 | a0007c0011t0002g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2466+1387A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260462 | ||||||
| chr11:108260498
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2466+1423T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260498 | ||||||
| chr11:108260612
|
A | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2466+1537A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260612 | ||||||
| chr11:108260647
|
C | T | 6 | a0005c0006t0005g0166a0005c0006t0005g0170a0005c0006t0005g0171others(3): Show | 6 | NA18939.hp2 NA18960.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.2466+1572C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260647 | ||||||
| chr11:108260648
|
G | A | 9 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2466+1573G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260648 | ||||||
| chr11:108260659
|
G | T | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2466+1584G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260659 | ||||||
| chr11:108260664
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2466+1589G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260664 | ||||||
| chr11:108260782
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2466+1707C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260782 | ||||||
| chr11:108260783
|
G | A | 4 | a0001c0001t0001g0153a0001c0001t0001g0163a0002c0009t0022g0093others(1): Show | 4 | HG01891.hp2 HG02922.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+1708G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260783 | ||||||
| chr11:108260787
|
C | T | 2 | a0001c0001t0021g0020a0001c0001t0021g0028 | 2 | NA18985.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.2466+1712C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260787 | ||||||
| chr11:108260807
|
G | T | 1 | a0001c0001t0001g0287 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2466+1732G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260807 | ||||||
| chr11:108260863
|
C | A | 2 | a0001c0001t0002g0034a0001c0001t0017g0033 | 2 | NA19003.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2466+1788C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260863 | ||||||
| chr11:108260873
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2466+1798G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260873 | ||||||
| chr11:108260882
|
C | T | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2466+1807C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260882 | ||||||
| chr11:108260919
|
T | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2466+1844T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260919 | ||||||
| chr11:108260965
|
C | T | 4 | a0001c0001t0002g0065a0001c0001t0016g0009a0001c0008t0016g0115others(1): Show | 4 | HG01109.hp2 HG02572.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+1890C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260965 | ||||||
| chr11:108260969
|
C | G | 5 | a0001c0001t0001g0254a0009c0013t0012g0117a0009c0013t0012g0119others(2): Show | 5 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2466+1894C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260969 | ||||||
| chr11:108260977
|
G | A | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2466+1902G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260977 | ||||||
| chr11:108260989
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2466+1914G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260989 | ||||||
| chr11:108260992
|
C | A | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2466+1917C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108260992 | ||||||
| chr11:108261002
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2466+1927C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261002 | ||||||
| chr11:108261049
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2466+1974C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261049 | ||||||
| chr11:108261055
|
TG | T | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+1985delG | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108261055 | |||||
| chr11:108261058
|
G | C | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+1983G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261058 | ||||||
| chr11:108261070
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2466+1995T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261070 | ||||||
| chr11:108261087
|
G | T | 1 | a0001c0001t0001g0216 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2466+2012G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261087 | ||||||
| chr11:108261088
|
A | C | 2 | a0001c0001t0006g0051a0001c0001t0006g0052 | 2 | HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2466+2013A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261088 | ||||||
| chr11:108261148
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2466+2073G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261148 | ||||||
| chr11:108261264
|
T | C | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2466+2189T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261264 | ||||||
| chr11:108261332
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2466+2257C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261332 | ||||||
| chr11:108261437
|
G | A | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+2362G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261437 | ||||||
| chr11:108261473
|
A | T | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+2398A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261473 | ||||||
| chr11:108261542
|
A | G | 2 | a0001c0001t0001g0218a0007c0011t0002g0124 | 2 | HG01074.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2466+2467A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261542 | ||||||
| chr11:108261566
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2466+2491A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261566 | ||||||
| chr11:108261568
|
C | G | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2493C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261568 | ||||||
| chr11:108261574
|
G | A | 2 | a0001c0001t0001g0218a0004c0004t0004g0182 | 2 | HG01517.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2466+2499G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261574 | ||||||
| chr11:108261585
|
A | T | 2 | a0001c0001t0001g0218a0007c0011t0002g0124 | 2 | HG01074.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2466+2510A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261585 | ||||||
| chr11:108261605
|
C | T | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2530C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261605 | ||||||
| chr11:108261614
|
C | T | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2539C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261614 | ||||||
| chr11:108261648
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+2573G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261648 | ||||||
| chr11:108261649
|
C | T | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2574C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261649 | ||||||
| chr11:108261666
|
C | T | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2466+2591C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261666 | ||||||
| chr11:108261670
|
C | T | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2595C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261670 | ||||||
| chr11:108261678
|
T | C | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2603T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261678 | ||||||
| chr11:108261684
|
T | C | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2609T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261684 | ||||||
| chr11:108261699
|
C | A | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2466+2624C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261699 | ||||||
| chr11:108261711
|
G | A | 5 | a0001c0001t0001g0207a0001c0001t0001g0261a0001c0001t0018g0001others(2): Show | 5 | HG01074.hp1 HG02523.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2466+2636G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261711 | ||||||
| chr11:108261718
|
G | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2466+2643G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261718 | ||||||
| chr11:108261813
|
C | G | 2 | a0001c0001t0016g0009a0002c0009t0035g0104 | 2 | HG01109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2466+2738C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261813 | ||||||
| chr11:108261817
|
A | C | 2 | a0001c0001t0016g0009a0002c0009t0035g0104 | 2 | HG01109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2466+2742A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261817 | ||||||
| chr11:108261827
|
G | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+2752G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261827 | ||||||
| chr11:108261972
|
A | G | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2466+2897A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108261972 | ||||||
| chr11:108262024
|
A | G | 1 | a0001c0001t0013g0025 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2466+2949A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262024 | ||||||
| chr11:108262026
|
C | T | 1 | a0001c0001t0013g0025 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2466+2951C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262026 | ||||||
| chr11:108262052
|
A | ACACTCTG others(226): Show |
1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2466+2993_2466+299 others(237): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108262052 | |||||
| chr11:108262052
|
A | ACACTCTG others(226): Show |
1 | a0009c0013t0012g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2466+2993_2466+299 others(237): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108262052 | |||||
| chr11:108262052
|
A | ACACTCTG others(229): Show |
1 | a0023c0033t0012g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2466+2993_2466+299 others(240): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108262052 | |||||
| chr11:108262085
|
G | C | 1 | a0001c0001t0010g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2466+3010G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262085 | ||||||
| chr11:108262240
|
C | T | 4 | a0001c0008t0002g0041a0001c0008t0002g0042a0001c0008t0002g0043others(1): Show | 4 | HG03098.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2466+3165C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262240 | ||||||
| chr11:108262277
|
C | T | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+3202C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262277 | ||||||
| chr11:108262315
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2466+3240T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262315 | ||||||
| chr11:108262342
|
G | GA | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2466+3271dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108262342 | |||||
| chr11:108262375
|
T | G | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+3300T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262375 | ||||||
| chr11:108262422
|
C | T | 1 | a0001c0001t0002g0110 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2466+3347C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262422 | ||||||
| chr11:108262464
|
A | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+3389A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262464 | ||||||
| chr11:108262492
|
A | G | 3 | a0001c0001t0002g0021a0001c0001t0002g0049a0001c0001t0002g0050 | 3 | NA18946.hp2 NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.2466+3417A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262492 | ||||||
| chr11:108262507
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.2466+3432C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262507 | ||||||
| chr11:108262616
|
C | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2466+3541C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262616 | ||||||
| chr11:108262800
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2466+3725A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262800 | ||||||
| chr11:108262844
|
A | G | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2466+3769A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262844 | ||||||
| chr11:108262920
|
A | G | 165 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.2466+3845A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108262920 | ||||||
| chr11:108263095
|
G | A | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2466+4020G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263095 | ||||||
| chr11:108263154
|
C | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG02135.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.2467-4017C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263154 | ||||||
| chr11:108263194
|
A | G | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.2467-3977A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263194 | ||||||
| chr11:108263197
|
A | G | 1 | a0001c0008t0016g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2467-3974A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263197 | ||||||
| chr11:108263228
|
C | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2467-3943C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263228 | ||||||
| chr11:108263230
|
G | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2467-3941G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263230 | ||||||
| chr11:108263248
|
C | T | 10 | a0001c0001t0002g0105a0001c0001t0002g0106a0001c0001t0002g0107others(7): Show | 10 | HG02074.hp2 HG02165.hp1 NA18943.hp2 others(7): Show |
intron_variant | MODIFIER | c.2467-3923C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263248 | ||||||
| chr11:108263262
|
G | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02132.hp1 HG03579.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-3909G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263262 | ||||||
| chr11:108263269
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-3902A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263269 | ||||||
| chr11:108263272
|
T | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2467-3899T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263272 | ||||||
| chr11:108263292
|
A | G | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-3879A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263292 | ||||||
| chr11:108263396
|
A | G | 2 | a0003c0003t0001g0187a0003c0003t0001g0188 | 2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2467-3775A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263396 | ||||||
| chr11:108263436
|
C | A | 4 | a0001c0001t0002g0054a0005c0006t0005g0165a0005c0006t0005g0173others(1): Show | 4 | HG00741.hp1 HG02602.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-3735C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263436 | ||||||
| chr11:108263526
|
G | T | 4 | a0002c0002t0003g0141a0002c0002t0003g0142a0002c0002t0003g0145others(1): Show | 4 | HG02145.hp1 HG02723.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-3645G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263526 | ||||||
| chr11:108263640
|
C | A | 1 | a0001c0001t0001g0159 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2467-3531C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263640 | ||||||
| chr11:108263762
|
G | T | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2467-3409G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263762 | ||||||
| chr11:108263808
|
G | A | 2 | a0001c0001t0001g0280a0007c0011t0002g0125 | 2 | NA18995.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2467-3363G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263808 | ||||||
| chr11:108263858
|
C | T | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2467-3313C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263858 | ||||||
| chr11:108263864
|
T | C | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-3307T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263864 | ||||||
| chr11:108263900
|
G | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-3271G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263900 | ||||||
| chr11:108263969
|
A | T | 215 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2467-3202A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108263969 | ||||||
| chr11:108264146
|
A | C | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2467-3025A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264146 | ||||||
| chr11:108264161
|
A | G | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2467-3010A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264161 | ||||||
| chr11:108264195
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2467-2976C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264195 | ||||||
| chr11:108264274
|
C | T | 3 | a0002c0005t0015g0099a0002c0005t0015g0100a0002c0005t0015g0101 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2467-2897C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264274 | ||||||
| chr11:108264331
|
A | G | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2467-2840A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264331 | ||||||
| chr11:108264450
|
C | A | 1 | a0006c0007t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2467-2721C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264450 | ||||||
| chr11:108264519
|
A | G | 11 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2467-2652A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264519 | ||||||
| chr11:108264703
|
C | G | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2467-2468C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264703 | ||||||
| chr11:108264707
|
C | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2467-2464C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264707 | ||||||
| chr11:108264717
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2467-2454G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264717 | ||||||
| chr11:108264763
|
T | C | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2467-2408T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264763 | ||||||
| chr11:108264809
|
A | G | 3 | a0001c0001t0014g0151a0001c0001t0014g0275a0001c0001t0014g0279 | 3 | HG01168.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2467-2362A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264809 | ||||||
| chr11:108264846
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0013g0237 | 2 | NA18988.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.2467-2325A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264846 | ||||||
| chr11:108264883
|
T | C | 1 | a0001c0001t0001g0216 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2467-2288T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264883 | ||||||
| chr11:108264886
|
C | G | 156 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.2467-2285C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264886 | ||||||
| chr11:108264908
|
A | G | 1 | a0002c0009t0003g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2467-2263A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108264908 | ||||||
| chr11:108265098
|
C | T | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2467-2073C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265098 | ||||||
| chr11:108265101
|
A | G | 9 | a0005c0006t0005g0165a0005c0006t0005g0166a0005c0006t0005g0170others(6): Show | 9 | HG02602.hp1 HG03688.hp1 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.2467-2070A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265101 | ||||||
| chr11:108265170
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2467-2001G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265170 | ||||||
| chr11:108265245
|
G | A | 7 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0157others(4): Show | 7 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2467-1926G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265245 | ||||||
| chr11:108265250
|
A | C | 1 | a0010c0014t0001g0281 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2467-1921A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265250 | ||||||
| chr11:108265260
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2467-1911G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265260 | ||||||
| chr11:108265265
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2467-1906G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265265 | ||||||
| chr11:108265288
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.2467-1883T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265288 | ||||||
| chr11:108265313
|
C | G | 1 | a0012c0035t0002g0027 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2467-1858C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265313 | ||||||
| chr11:108265324
|
C | T | 2 | a0001c0001t0001g0283a0003c0003t0001g0195 | 2 | HG02738.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2467-1847C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265324 | ||||||
| chr11:108265433
|
T | G | 1 | a0001c0001t0032g0304 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2467-1738T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265433 | ||||||
| chr11:108265589
|
T | C | 1 | a0001c0001t0001g0225 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2467-1582T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265589 | ||||||
| chr11:108265594
|
C | T | 5 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0038others(2): Show | 5 | HG00544.hp2 NA18939.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2467-1577C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265594 | ||||||
| chr11:108265618
|
A | C | 1 | a0001c0001t0001g0225 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2467-1553A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265618 | ||||||
| chr11:108265621
|
G | A | 1 | a0001c0001t0001g0225 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2467-1550G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265621 | ||||||
| chr11:108265640
|
A | G | 26 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0026others(23): Show | 26 | HG00544.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.2467-1531A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265640 | ||||||
| chr11:108265649
|
A | C | 9 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2467-1522A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265649 | ||||||
| chr11:108265697
|
A | G | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2467-1474A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265697 | ||||||
| chr11:108265704
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2467-1467A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265704 | ||||||
| chr11:108265705
|
A | C | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2467-1466A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265705 | ||||||
| chr11:108265721
|
C | T | 1 | a0001c0010t0002g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2467-1450C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265721 | ||||||
| chr11:108265819
|
C | T | 156 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.2467-1352C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265819 | ||||||
| chr11:108265883
|
A | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0198a0001c0001t0001g0199others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2467-1288A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265883 | ||||||
| chr11:108265920
|
A | G | 1 | a0003c0003t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2467-1251A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265920 | ||||||
| chr11:108265985
|
C | G | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2467-1186C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108265985 | ||||||
| chr11:108266052
|
C | G | 1 | a0001c0012t0038g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2467-1119C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266052 | ||||||
| chr11:108266076
|
T | C | 2 | a0004c0004t0004g0168a0022c0021t0036g0008 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2467-1095T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266076 | ||||||
| chr11:108266163
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.2467-1008C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266163 | ||||||
| chr11:108266164
|
G | A | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-1007G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266164 | ||||||
| chr11:108266167
|
A | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2467-1004A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266167 | ||||||
| chr11:108266185
|
G | A | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2467-986G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266185 | ||||||
| chr11:108266197
|
T | C | 1 | a0003c0003t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2467-974T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266197 | ||||||
| chr11:108266250
|
A | G | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2467-921A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266250 | ||||||
| chr11:108266314
|
A | G | 17 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(14): Show | 17 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.2467-857A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266314 | ||||||
| chr11:108266379
|
G | A | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2467-792G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266379 | ||||||
| chr11:108266419
|
G | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2467-752G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266419 | ||||||
| chr11:108266485
|
TGGGGTG | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-681_2467-676d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108266485 | |||||
| chr11:108266497
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2467-674A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266497 | ||||||
| chr11:108266595
|
C | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2467-576C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266595 | ||||||
| chr11:108266740
|
C | T | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2467-431C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266740 | ||||||
| chr11:108266789
|
A | AT | 38 | a0001c0001t0001g0201a0001c0001t0001g0206a0001c0001t0001g0208others(35): Show | 38 | HG00558.hp2 HG01081.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2467-360dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108266789 | |||||
| chr11:108266789
|
AT | A | 8 | a0001c0001t0001g0223a0001c0001t0001g0228a0001c0001t0001g0260others(5): Show | 8 | HG00323.hp2 HG02523.hp2 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.2467-360delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | INFO_REALIGN_3_PRIME | chr11 | 108266789 | |||||
| chr11:108266792
|
T | G | 2 | a0001c0001t0032g0304a0017c0030t0002g0126 | 2 | HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2467-379T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266792 | ||||||
| chr11:108266825
|
G | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2467-346G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266825 | ||||||
| chr11:108266894
|
C | G | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2467-277C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108266894 | ||||||
| chr11:108267048
|
T | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.2467-123T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108267048 | ||||||
| chr11:108267123
|
G | A | 1 | a0005c0006t0005g0181 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2467-48G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 16/62 | chr11 | 108267123 | ||||||
| chr11:108267420
|
C | T | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.2638+78C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | chr11 | 108267420 | ||||||
| chr11:108267427
|
G | T | 4 | a0001c0008t0002g0041a0001c0008t0002g0042a0001c0008t0002g0043others(1): Show | 4 | HG03098.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2638+85G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | chr11 | 108267427 | ||||||
| chr11:108267518
|
G | C | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2638+176G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | chr11 | 108267518 | ||||||
| chr11:108267653
|
T | C | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.2638+311T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | chr11 | 108267653 | ||||||
| chr11:108267859
|
A | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2638+517A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | chr11 | 108267859 | ||||||
| chr11:108268315
|
CT | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2639-87delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | INFO_REALIGN_3_PRIME | chr11 | 108268315 | |||||
| chr11:108268379
|
CTTAGTG | C | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2639-27_2639-22del others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | INFO_REALIGN_3_PRIME | chr11 | 108268379 | |||||
| chr11:108268393
|
G | T | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.2639-17G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 17/62 | chr11 | 108268393 | ||||||
| chr11:108268637
|
T | TA | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2838+28_2838+29ins others(1): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108268637 | ||||||
| chr11:108268679
|
A | G | 1 | a0002c0002t0003g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2838+70A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108268679 | ||||||
| chr11:108268897
|
A | G | 1 | a0009c0013t0012g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2838+288A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108268897 | ||||||
| chr11:108268900
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2838+291A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108268900 | ||||||
| chr11:108269114
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0214 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2838+505C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269114 | ||||||
| chr11:108269120
|
C | T | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.2838+511C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269120 | ||||||
| chr11:108269271
|
CT | C | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.2838+670delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | INFO_REALIGN_3_PRIME | chr11 | 108269271 | |||||
| chr11:108269300
|
A | G | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2838+691A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269300 | ||||||
| chr11:108269497
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2838+888G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269497 | ||||||
| chr11:108269679
|
T | G | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2838+1070T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269679 | ||||||
| chr11:108269740
|
C | T | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.2838+1131C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269740 | ||||||
| chr11:108269789
|
A | G | 14 | a0001c0001t0026g0190a0001c0001t0028g0290a0003c0003t0001g0185others(11): Show | 14 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2838+1180A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269789 | ||||||
| chr11:108269821
|
A | G | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2838+1212A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269821 | ||||||
| chr11:108269882
|
C | T | 11 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2839-1182C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269882 | ||||||
| chr11:108269924
|
A | G | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2839-1140A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108269924 | ||||||
| chr11:108270182
|
C | T | 153 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.2839-882C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270182 | ||||||
| chr11:108270360
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2839-704A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270360 | ||||||
| chr11:108270381
|
C | G | 1 | a0004c0004t0004g0182 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2839-683C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270381 | ||||||
| chr11:108270393
|
A | G | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2839-671A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270393 | ||||||
| chr11:108270407
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0198a0001c0001t0001g0200others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.2839-657G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270407 | ||||||
| chr11:108270446
|
C | T | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2839-618C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270446 | ||||||
| chr11:108270519
|
G | A | 1 | a0001c0001t0009g0263 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2839-545G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270519 | ||||||
| chr11:108270614
|
T | C | 1 | a0015c0019t0001g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2839-450T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270614 | ||||||
| chr11:108270680
|
T | A | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2839-384T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270680 | ||||||
| chr11:108270727
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2839-337G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270727 | ||||||
| chr11:108270788
|
C | T | 1 | a0005c0006t0005g0181 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2839-276C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270788 | ||||||
| chr11:108270939
|
C | G | 1 | a0002c0009t0022g0094 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2839-125C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270939 | ||||||
| chr11:108270972
|
G | T | 1 | a0002c0002t0003g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2839-92G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270972 | ||||||
| chr11:108270974
|
G | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 101 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(98): Show |
intron_variant | MODIFIER | c.2839-90G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 18/62 | chr11 | 108270974 | ||||||
| chr11:108271228
|
C | CT | 21 | a0001c0001t0001g0233a0001c0001t0001g0244a0001c0001t0001g0245others(18): Show | 21 | HG00140.hp2 HG01496.hp1 HG01975.hp2 others(18): Show |
splice_region_variant&intron_variant | LOW | c.2922-8dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 19/62 | INFO_REALIGN_3_PRIME | chr11 | 108271228 | |||||
| chr11:108271230
|
T | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2922-21T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 19/62 | chr11 | 108271230 | ||||||
| chr11:108271467
|
G | A | 3 | a0008c0015t0002g0013a0008c0029t0002g0007a0014c0032t0002g0011 | 3 | HG02572.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.3077+61G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108271467 | ||||||
| chr11:108271478
|
A | T | 1 | a0001c0001t0001g0234 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3077+72A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108271478 | ||||||
| chr11:108271615
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3077+209C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108271615 | ||||||
| chr11:108271890
|
G | A | 83 | a0001c0001t0001g0003a0001c0001t0001g0198a0001c0001t0001g0200others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.3077+484G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108271890 | ||||||
| chr11:108271947
|
A | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3077+541A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108271947 | ||||||
| chr11:108271959
|
G | A | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3077+553G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108271959 | ||||||
| chr11:108272378
|
G | A | 3 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0092 | 3 | HG00408.hp2 HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.3078-154G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108272378 | ||||||
| chr11:108272393
|
T | G | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3078-139T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108272393 | ||||||
| chr11:108272455
|
C | T | 206 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.3078-77C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108272455 | ||||||
| chr11:108272489
|
A | G | 3 | a0002c0005t0015g0099a0002c0005t0015g0100a0002c0005t0015g0101 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3078-43A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 20/62 | chr11 | 108272489 | ||||||
| chr11:108272706
|
A | C | 1 | a0001c0001t0001g0288 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3154-16A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 21/62 | chr11 | 108272706 | ||||||
| chr11:108273041
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3284+189A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273041 | ||||||
| chr11:108273275
|
C | T | 1 | a0005c0006t0005g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3284+423C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273275 | ||||||
| chr11:108273331
|
C | CT | 14 | a0001c0001t0002g0022a0001c0001t0002g0026a0001c0001t0002g0046others(11): Show | 14 | HG00738.hp2 HG01074.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.3284+506dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
C | CTTTTTTT others(3): Show |
6 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.3284+497_3284+506d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
C | CTTTTTTT others(4): Show |
3 | a0002c0005t0015g0099a0002c0005t0015g0100a0002c0005t0015g0101 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3284+496_3284+506d others(13): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
C | CTTTTTTT others(5): Show |
9 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0139others(6): Show | 9 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3284+495_3284+506d others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
C | CTTTTTTT others(6): Show |
3 | a0002c0002t0003g0140a0002c0002t0003g0142a0002c0002t0003g0146 | 3 | HG01243.hp1 HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3284+494_3284+506d others(15): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
C | CTTTTTTT others(7): Show |
1 | a0002c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3284+493_3284+506d others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
C | CTTTTTTT others(8): Show |
1 | a0002c0002t0003g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3284+492_3284+506d others(17): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
C | CTTTTTTT others(9): Show |
3 | a0002c0002t0003g0086a0002c0009t0003g0134a0002c0009t0003g0135 | 3 | HG01081.hp2 HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3284+491_3284+506d others(18): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
CT | C | 9 | a0001c0001t0001g0236a0001c0001t0002g0037a0001c0001t0002g0050others(6): Show | 9 | HG00323.hp2 HG01257.hp2 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.3284+506delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
CTTTTTTT | C | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.3284+500_3284+506d others(9): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273331
|
CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0223a0001c0001t0001g0254a0001c0001t0001g0289others(6): Show | 9 | HG01168.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.3284+499_3284+506d others(10): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108273331 | |||||
| chr11:108273435
|
C | T | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3284+583C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273435 | ||||||
| chr11:108273600
|
C | T | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.3284+748C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273600 | ||||||
| chr11:108273693
|
A | T | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3284+841A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273693 | ||||||
| chr11:108273835
|
C | G | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3284+983C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273835 | ||||||
| chr11:108273848
|
C | G | 9 | a0005c0006t0005g0165a0005c0006t0005g0166a0005c0006t0005g0170others(6): Show | 9 | HG02602.hp1 HG03688.hp1 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.3284+996C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273848 | ||||||
| chr11:108273919
|
A | G | 2 | a0001c0001t0009g0263a0003c0003t0001g0189 | 2 | NA19060.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3284+1067A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108273919 | ||||||
| chr11:108274008
|
T | G | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3284+1156T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274008 | ||||||
| chr11:108274014
|
G | A | 1 | a0001c0001t0013g0237 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.3284+1162G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274014 | ||||||
| chr11:108274283
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3284+1431G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274283 | ||||||
| chr11:108274293
|
T | A | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3284+1441T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274293 | ||||||
| chr11:108274345
|
TTG | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.3284+1505_3284+150 others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108274345 | |||||
| chr11:108274522
|
C | T | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.3284+1670C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274522 | ||||||
| chr11:108274590
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3284+1738A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274590 | ||||||
| chr11:108274619
|
A | T | 1 | a0001c0001t0001g0295 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3284+1767A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274619 | ||||||
| chr11:108274711
|
T | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3284+1859T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274711 | ||||||
| chr11:108274913
|
T | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.3284+2061T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274913 | ||||||
| chr11:108274969
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3284+2117G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108274969 | ||||||
| chr11:108275013
|
G | A | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3284+2161G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275013 | ||||||
| chr11:108275019
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3284+2167C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275019 | ||||||
| chr11:108275094
|
T | G | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3284+2242T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275094 | ||||||
| chr11:108275428
|
C | T | 11 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3284+2576C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275428 | ||||||
| chr11:108275442
|
GT | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3284+2593delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108275442 | |||||
| chr11:108275521
|
A | G | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3284+2669A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275521 | ||||||
| chr11:108275521
|
A | T | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3284+2669A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275521 | ||||||
| chr11:108275572
|
C | T | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.3284+2720C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275572 | ||||||
| chr11:108275639
|
A | G | 3 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0160 | 3 | HG02451.hp1 HG03486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3284+2787A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108275639 | ||||||
| chr11:108276066
|
C | A | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3284+3214C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276066 | ||||||
| chr11:108276241
|
T | G | 2 | a0001c0001t0006g0051a0001c0001t0006g0052 | 2 | HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.3285-3250T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276241 | ||||||
| chr11:108276354
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3285-3137A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276354 | ||||||
| chr11:108276591
|
T | A | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.3285-2900T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276591 | ||||||
| chr11:108276603
|
T | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3285-2888T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276603 | ||||||
| chr11:108276630
|
G | C | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3285-2861G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276630 | ||||||
| chr11:108276641
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3285-2850G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276641 | ||||||
| chr11:108276699
|
G | C | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3285-2792G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276699 | ||||||
| chr11:108276800
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3285-2691G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276800 | ||||||
| chr11:108276858
|
G | T | 1 | a0019c0022t0002g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.3285-2633G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108276858 | ||||||
| chr11:108277159
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3285-2332A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277159 | ||||||
| chr11:108277204
|
A | G | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3285-2287A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277204 | ||||||
| chr11:108277318
|
C | T | 1 | a0001c0001t0001g0216 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3285-2173C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277318 | ||||||
| chr11:108277380
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3285-2111C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277380 | ||||||
| chr11:108277409
|
G | A | 1 | a0010c0014t0001g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3285-2082G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277409 | ||||||
| chr11:108277457
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0214 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3285-2034C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277457 | ||||||
| chr11:108277538
|
T | C | 195 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.3285-1953T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277538 | ||||||
| chr11:108277557
|
C | T | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3285-1934C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277557 | ||||||
| chr11:108277582
|
C | A | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3285-1909C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277582 | ||||||
| chr11:108277605
|
T | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.3285-1886T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277605 | ||||||
| chr11:108277906
|
G | A | 1 | a0001c0001t0002g0087 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3285-1585G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108277906 | ||||||
| chr11:108278112
|
A | G | 201 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.3285-1379A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278112 | ||||||
| chr11:108278190
|
C | T | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3285-1301C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278190 | ||||||
| chr11:108278480
|
T | G | 2 | a0010c0014t0001g0215a0010c0014t0001g0281 | 2 | HG00099.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.3285-1011T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278480 | ||||||
| chr11:108278779
|
G | A | 1 | a0001c0001t0018g0001 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3285-712G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278779 | ||||||
| chr11:108278781
|
G | A | 1 | a0002c0005t0008g0095 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3285-710G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278781 | ||||||
| chr11:108278803
|
C | T | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3285-688C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278803 | ||||||
| chr11:108278832
|
G | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3285-659G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278832 | ||||||
| chr11:108278895
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0265 | 2 | NA18962.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.3285-596G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | chr11 | 108278895 | ||||||
| chr11:108279480
|
CT | C | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.3285-9delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 22/62 | INFO_REALIGN_3_PRIME | chr11 | 108279480 | |||||
| chr11:108279678
|
A | G | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3402+70A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | chr11 | 108279678 | ||||||
| chr11:108279937
|
A | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.3402+329A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | chr11 | 108279937 | ||||||
| chr11:108280020
|
G | A | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3402+412G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | chr11 | 108280020 | ||||||
| chr11:108280520
|
G | GGT | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3403-459_3403-458d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | INFO_REALIGN_3_PRIME | chr11 | 108280520 | |||||
| chr11:108280542
|
G | A | 192 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.3403-453G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | chr11 | 108280542 | ||||||
| chr11:108280961
|
T | A | 3 | a0001c0001t0009g0238a0001c0001t0009g0257a0015c0019t0001g0209 | 3 | HG01109.hp1 HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.3403-34T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | chr11 | 108280961 | ||||||
| chr11:108280970
|
A | AT | 22 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(19): Show | 22 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.3403-15dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | INFO_REALIGN_3_PRIME | chr11 | 108280970 | |||||
| chr11:108280980
|
T | A | 18 | a0001c0001t0002g0062a0002c0002t0003g0085a0002c0002t0003g0086others(15): Show | 18 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.3403-15T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | chr11 | 108280980 | ||||||
| chr11:108280980
|
T | TA | 163 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.3403-13dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 23/62 | INFO_REALIGN_3_PRIME | chr11 | 108280980 | |||||
| chr11:108281480
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3576+312A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108281480 | ||||||
| chr11:108281673
|
C | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3576+505C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108281673 | ||||||
| chr11:108281855
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.3576+687C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108281855 | ||||||
| chr11:108281918
|
A | G | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.3576+750A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108281918 | ||||||
| chr11:108282128
|
A | AT | 13 | a0001c0001t0001g0200a0001c0001t0001g0255a0001c0001t0002g0017others(10): Show | 13 | HG00140.hp2 HG00544.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.3577-565dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | INFO_REALIGN_3_PRIME | chr11 | 108282128 | |||||
| chr11:108282159
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3577-551G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282159 | ||||||
| chr11:108282251
|
C | T | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3577-459C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282251 | ||||||
| chr11:108282280
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3577-430G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282280 | ||||||
| chr11:108282282
|
C | G | 1 | a0001c0001t0001g0292 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3577-428C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282282 | ||||||
| chr11:108282338
|
A | G | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3577-372A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282338 | ||||||
| chr11:108282346
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3577-364T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282346 | ||||||
| chr11:108282465
|
GTTGGAAA others(3): Show |
G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.3577-242_3577-233d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | INFO_REALIGN_3_PRIME | chr11 | 108282465 | |||||
| chr11:108282546
|
G | C | 3 | a0001c0001t0001g0208a0001c0001t0001g0255a0001c0001t0001g0289 | 3 | NA18955.hp2 NA18967.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3577-164G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282546 | ||||||
| chr11:108282553
|
A | C | 3 | a0001c0001t0009g0238a0001c0001t0009g0257a0015c0019t0001g0209 | 3 | HG01109.hp1 HG01255.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.3577-157A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 24/62 | chr11 | 108282553 | ||||||
| chr11:108282962
|
C | G | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3746+83C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108282962 | ||||||
| chr11:108282994
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3746+115G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108282994 | ||||||
| chr11:108283197
|
C | A | 2 | a0001c0001t0001g0207a0001c0001t0018g0001 | 2 | HG02523.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3746+318C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108283197 | ||||||
| chr11:108283370
|
G | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.3746+491G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108283370 | ||||||
| chr11:108283590
|
A | C | 6 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(3): Show | 6 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3747-637A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108283590 | ||||||
| chr11:108283923
|
G | A | 13 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.3747-304G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108283923 | ||||||
| chr11:108283923
|
G | T | 2 | a0001c0001t0011g0196a0001c0001t0011g0197 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3747-304G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108283923 | ||||||
| chr11:108284193
|
A | G | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3747-34A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 25/62 | chr11 | 108284193 | ||||||
| chr11:108284478
|
G | T | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
splice_region_variant&intron_variant | LOW | c.3993+5G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284478 | ||||||
| chr11:108284521
|
A | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3993+48A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284521 | ||||||
| chr11:108284606
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3993+133A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284606 | ||||||
| chr11:108284633
|
A | G | 1 | a0001c0001t0009g0263 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3993+160A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284633 | ||||||
| chr11:108284637
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3993+164C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284637 | ||||||
| chr11:108284670
|
G | A | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.3993+197G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284670 | ||||||
| chr11:108284796
|
A | C | 1 | a0001c0001t0002g0061 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3993+323A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284796 | ||||||
| chr11:108284925
|
C | G | 1 | a0001c0016t0002g0015 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3993+452C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284925 | ||||||
| chr11:108284940
|
A | T | 1 | a0001c0016t0002g0015 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3993+467A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284940 | ||||||
| chr11:108284972
|
G | A | 1 | a0001c0001t0001g0003 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.3993+499G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108284972 | ||||||
| chr11:108285050
|
C | A | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3993+577C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108285050 | ||||||
| chr11:108285174
|
G | A | 1 | a0001c0001t0021g0020 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3993+701G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108285174 | ||||||
| chr11:108285321
|
CT | C | 205 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.3993+861delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | INFO_REALIGN_3_PRIME | chr11 | 108285321 | |||||
| chr11:108285329
|
T | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3993+856T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108285329 | ||||||
| chr11:108285587
|
A | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.3993+1114A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108285587 | ||||||
| chr11:108285746
|
C | A | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.3993+1273C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108285746 | ||||||
| chr11:108285825
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.3993+1352T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108285825 | ||||||
| chr11:108285982
|
A | C | 5 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG02132.hp1 HG03130.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3993+1509A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108285982 | ||||||
| chr11:108286014
|
C | A | 1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3993+1541C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108286014 | ||||||
| chr11:108286053
|
C | T | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3994-1547C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108286053 | ||||||
| chr11:108286298
|
G | C | 5 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG02132.hp1 HG03130.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.3994-1302G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108286298 | ||||||
| chr11:108286312
|
C | CA | 17 | a0001c0001t0002g0066a0001c0001t0002g0068a0001c0001t0002g0079others(14): Show | 17 | HG00140.hp2 HG00741.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3994-1262dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | INFO_REALIGN_3_PRIME | chr11 | 108286312 | |||||
| chr11:108286312
|
CA | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0158others(147): Show | 150 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.3994-1262delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | INFO_REALIGN_3_PRIME | chr11 | 108286312 | |||||
| chr11:108286312
|
CAA | C | 32 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0201others(29): Show | 32 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.3994-1263_3994-126 others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | INFO_REALIGN_3_PRIME | chr11 | 108286312 | |||||
| chr11:108286458
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3994-1142G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108286458 | ||||||
| chr11:108286514
|
A | C | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3994-1086A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108286514 | ||||||
| chr11:108286701
|
C | T | 1 | a0001c0001t0014g0151 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.3994-899C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108286701 | ||||||
| chr11:108286702
|
G | A | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3994-898G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108286702 | ||||||
| chr11:108287203
|
A | C | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3994-397A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108287203 | ||||||
| chr11:108287378
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3994-222G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108287378 | ||||||
| chr11:108287407
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.3994-193T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108287407 | ||||||
| chr11:108287503
|
G | A | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.3994-97G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 26/62 | chr11 | 108287503 | ||||||
| chr11:108287864
|
G | A | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.4109+149G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | chr11 | 108287864 | ||||||
| chr11:108288062
|
C | T | 1 | a0001c0016t0002g0015 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4109+347C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | chr11 | 108288062 | ||||||
| chr11:108288138
|
C | T | 6 | a0005c0006t0005g0166a0005c0006t0005g0170a0005c0006t0005g0171others(3): Show | 6 | NA18939.hp2 NA18960.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.4109+423C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | chr11 | 108288138 | ||||||
| chr11:108288501
|
C | CT | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.4110-458dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | INFO_REALIGN_3_PRIME | chr11 | 108288501 | |||||
| chr11:108288501
|
C | CTT | 20 | a0001c0001t0025g0268a0004c0004t0004g0168a0004c0004t0004g0169others(17): Show | 20 | HG01123.hp1 HG01175.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.4110-459_4110-458d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | INFO_REALIGN_3_PRIME | chr11 | 108288501 | |||||
| chr11:108288501
|
CT | C | 8 | a0001c0001t0002g0049a0001c0001t0006g0059a0001c0010t0002g0029others(5): Show | 8 | HG00738.hp2 HG01099.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.4110-458delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | INFO_REALIGN_3_PRIME | chr11 | 108288501 | |||||
| chr11:108288503
|
T | TC | 28 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(25): Show | 28 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.4110-474_4110-473i others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | chr11 | 108288503 | ||||||
| chr11:108288504
|
T | C | 1 | a0002c0005t0015g0099 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4110-473T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | chr11 | 108288504 | ||||||
| chr11:108288599
|
CTAAA | C | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.4110-374_4110-371d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | INFO_REALIGN_3_PRIME | chr11 | 108288599 | |||||
| chr11:108288629
|
G | A | 156 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.4110-348G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 27/62 | chr11 | 108288629 | ||||||
| chr11:108289820
|
C | G | 1 | a0001c0001t0018g0001 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4436+19C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108289820 | ||||||
| chr11:108289836
|
C | G | 1 | a0001c0008t0016g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4436+35C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108289836 | ||||||
| chr11:108289897
|
ACT | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4436+99_4436+100de others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108289897 | |||||
| chr11:108289908
|
C | T | 1 | a0002c0002t0003g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4436+107C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108289908 | ||||||
| chr11:108289962
|
A | ATCC | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4436+163_4436+165d others(5): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108289962 | |||||
| chr11:108290309
|
G | A | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4436+508G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290309 | ||||||
| chr11:108290400
|
T | G | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.4436+599T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290400 | ||||||
| chr11:108290466
|
A | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4436+665A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290466 | ||||||
| chr11:108290475
|
T | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.4436+674T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290475 | ||||||
| chr11:108290525
|
A | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.4436+724A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290525 | ||||||
| chr11:108290575
|
T | A | 1 | a0003c0003t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4436+774T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290575 | ||||||
| chr11:108290581
|
T | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.4436+780T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290581 | ||||||
| chr11:108290625
|
G | A | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4436+824G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290625 | ||||||
| chr11:108290638
|
C | CA | 39 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0002g0046others(36): Show | 39 | HG00140.hp2 HG00642.hp1 HG01070.hp1 others(36): Show |
intron_variant | MODIFIER | c.4436+866dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108290638 | |||||
| chr11:108290638
|
C | CAA | 10 | a0001c0012t0024g0300a0002c0002t0003g0145a0002c0002t0003g0146others(7): Show | 10 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.4436+865_4436+866d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108290638 | |||||
| chr11:108290638
|
CA | C | 23 | a0001c0001t0001g0201a0001c0001t0001g0219a0001c0001t0001g0287others(20): Show | 23 | HG00323.hp2 HG00408.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4436+866delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108290638 | |||||
| chr11:108290638
|
CAA | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.4436+865_4436+866d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108290638 | |||||
| chr11:108290638
|
CAAAAAAA others(4): Show |
C | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4436+856_4436+866d others(13): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108290638 | |||||
| chr11:108290654
|
A | G | 1 | a0005c0006t0005g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4436+853A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290654 | ||||||
| chr11:108290656
|
A | G | 4 | a0001c0001t0010g0205a0001c0001t0010g0220a0001c0001t0010g0221others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4436+855A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290656 | ||||||
| chr11:108290657
|
A | G | 1 | a0001c0001t0001g0200 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.4436+856A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290657 | ||||||
| chr11:108290661
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.4436+860A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290661 | ||||||
| chr11:108290825
|
T | A | 1 | a0003c0003t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4436+1024T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290825 | ||||||
| chr11:108290848
|
ACTT | A | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.4436+1050_4436+105 others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | INFO_REALIGN_3_PRIME | chr11 | 108290848 | |||||
| chr11:108290911
|
T | C | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.4436+1110T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290911 | ||||||
| chr11:108290958
|
G | A | 1 | a0005c0006t0005g0181 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4436+1157G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108290958 | ||||||
| chr11:108291275
|
G | C | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4437-1344G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108291275 | ||||||
| chr11:108291752
|
A | C | 1 | a0023c0033t0012g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4437-867A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108291752 | ||||||
| chr11:108292101
|
C | T | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.4437-518C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108292101 | ||||||
| chr11:108292340
|
T | C | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.4437-279T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108292340 | ||||||
| chr11:108292362
|
T | C | 3 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0038g0302 | 3 | HG00140.hp2 NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.4437-257T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108292362 | ||||||
| chr11:108292599
|
T | G | 1 | a0005c0006t0005g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4437-20T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 29/62 | chr11 | 108292599 | ||||||
| chr11:108293006
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.4611+213A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 30/62 | chr11 | 108293006 | ||||||
| chr11:108293178
|
G | C | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4612-135G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 30/62 | chr11 | 108293178 | ||||||
| chr11:108293191
|
G | T | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.4612-122G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 30/62 | chr11 | 108293191 | ||||||
| chr11:108293518
|
C | T | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4776+41C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293518 | ||||||
| chr11:108293877
|
CAA | C | 35 | a0001c0001t0002g0047a0001c0001t0002g0106a0001c0001t0002g0107others(32): Show | 35 | HG01070.hp1 HG01081.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.4776+417_4776+418d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293877 | |||||
| chr11:108293886
|
A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0217a0001c0001t0001g0265 | 3 | HG00639.hp2 NA18962.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.4776+409A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293886 | ||||||
| chr11:108293888
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.4776+411A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293888 | ||||||
| chr11:108293890
|
A | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0216others(9): Show | 12 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.4776+413A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293890 | ||||||
| chr11:108293891
|
AAAAAT | A | 8 | a0001c0001t0028g0290a0003c0003t0001g0195a0006c0007t0001g0150others(5): Show | 8 | HG02451.hp1 HG02723.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.4776+416_4776+420d others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293891 | |||||
| chr11:108293892
|
A | AAT | 10 | a0001c0001t0001g0236a0001c0001t0002g0079a0001c0001t0020g0082others(7): Show | 10 | HG02572.hp2 HG02717.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.4776+416_4776+417i others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293892 | |||||
| chr11:108293892
|
A | AATATATA others(15): Show |
1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4776+416_4776+417i others(24): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293892 | |||||
| chr11:108293892
|
A | AT | 30 | a0001c0001t0001g0204a0001c0001t0001g0225a0001c0001t0001g0226others(27): Show | 30 | HG00408.hp1 HG00558.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.4776+415_4776+416i others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293892 | ||||||
| chr11:108293892
|
A | ATAT | 3 | a0001c0001t0001g0003a0001c0001t0001g0228a0001c0001t0001g0239 | 3 | HG01071.hp2 HG02040.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.4776+415_4776+416i others(5): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293892 | ||||||
| chr11:108293892
|
A | ATATAT | 3 | a0001c0001t0001g0229a0001c0001t0010g0220a0001c0001t0014g0275 | 3 | HG01255.hp1 HG02683.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.4776+415_4776+416i others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293892 | ||||||
| chr11:108293892
|
A | T | 31 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0208others(28): Show | 31 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.4776+415A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293892 | ||||||
| chr11:108293893
|
AAATAT | A | 13 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(10): Show | 13 | HG00558.hp1 HG00733.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.4776+418_4776+422d others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293893 | |||||
| chr11:108293894
|
A | AT | 10 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0247others(7): Show | 10 | HG00140.hp1 HG01169.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.4776+417_4776+418i others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293894 | ||||||
| chr11:108293894
|
A | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.4776+417A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293894 | ||||||
| chr11:108293894
|
AAT | A | 8 | a0002c0002t0003g0147a0002c0009t0003g0134a0002c0009t0003g0135others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.4776+442_4776+443d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293894 | |||||
| chr11:108293894
|
AATAT | A | 9 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4776+440_4776+443d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293894 | |||||
| chr11:108293895
|
ATATAT | A | 10 | a0001c0008t0016g0115a0001c0008t0016g0116a0001c0012t0024g0300others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.4776+419_4776+423d others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293895 | ||||||
| chr11:108293896
|
T | A | 1 | a0001c0001t0002g0010 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4776+419T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293896 | ||||||
| chr11:108293898
|
T | A | 2 | a0009c0013t0012g0119a0009c0013t0012g0120 | 2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4776+421T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293898 | ||||||
| chr11:108293899
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4776+422A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293899 | ||||||
| chr11:108293900
|
T | A | 2 | a0002c0005t0008g0102a0002c0009t0022g0093 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.4776+423T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293900 | ||||||
| chr11:108293902
|
T | A | 4 | a0003c0003t0001g0185a0003c0003t0001g0186a0003c0003t0001g0187others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.4776+425T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293902 | ||||||
| chr11:108293905
|
A | G | 2 | a0001c0001t0011g0196a0001c0001t0011g0197 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4776+428A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293905 | ||||||
| chr11:108293917
|
A | G | 8 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(5): Show | 8 | HG02132.hp1 HG02145.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.4776+440A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293917 | ||||||
| chr11:108293919
|
A | ATATG | 7 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0001t0001g0262others(4): Show | 7 | HG02004.hp1 NA18942.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.4776+443_4776+444i others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293919 | |||||
| chr11:108293919
|
A | ATG | 28 | a0001c0001t0001g0200a0001c0001t0001g0203a0001c0001t0001g0208others(25): Show | 28 | HG00280.hp1 HG00544.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.4776+450_4776+451d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293919 | |||||
| chr11:108293919
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0158others(97): Show | 100 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.4776+442A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293919 | ||||||
| chr11:108293921
|
G | A | 2 | a0005c0006t0005g0173a0005c0006t0005g0174 | 2 | HG02602.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4776+444G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108293921 | ||||||
| chr11:108293943
|
T | TTG | 9 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(6): Show | 9 | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.4776+476_4776+477d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | INFO_REALIGN_3_PRIME | chr11 | 108293943 | |||||
| chr11:108294206
|
A | G | 1 | a0001c0001t0001g0262 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4777-721A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294206 | ||||||
| chr11:108294269
|
T | C | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.4777-658T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294269 | ||||||
| chr11:108294326
|
A | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0198a0001c0001t0001g0200others(80): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.4777-601A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294326 | ||||||
| chr11:108294348
|
A | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.4777-579A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294348 | ||||||
| chr11:108294492
|
T | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.4777-435T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294492 | ||||||
| chr11:108294531
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4777-396G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294531 | ||||||
| chr11:108294646
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4777-281A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294646 | ||||||
| chr11:108294671
|
C | T | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4777-256C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294671 | ||||||
| chr11:108294679
|
G | A | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.4777-248G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294679 | ||||||
| chr11:108294680
|
C | G | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.4777-247C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294680 | ||||||
| chr11:108294706
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4777-221C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294706 | ||||||
| chr11:108294907
|
A | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.4777-20A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 31/62 | chr11 | 108294907 | ||||||
| chr11:108295266
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0163 | 2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.4909+207A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108295266 | ||||||
| chr11:108295338
|
T | G | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.4909+279T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108295338 | ||||||
| chr11:108295431
|
A | G | 3 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0038g0302 | 3 | HG00140.hp2 NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.4909+372A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108295431 | ||||||
| chr11:108295505
|
T | G | 9 | a0005c0006t0005g0165a0005c0006t0005g0166a0005c0006t0005g0170others(6): Show | 9 | HG02602.hp1 HG03688.hp1 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.4909+446T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108295505 | ||||||
| chr11:108295873
|
G | A | 2 | a0001c0008t0002g0041a0001c0008t0002g0044 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4909+814G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108295873 | ||||||
| chr11:108296143
|
T | G | 2 | a0004c0004t0004g0169a0004c0004t0004g0176 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.4909+1084T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108296143 | ||||||
| chr11:108296231
|
TC | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.4910-1054delC | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | INFO_REALIGN_3_PRIME | chr11 | 108296231 | |||||
| chr11:108296256
|
C | CT | 7 | a0001c0001t0001g0283a0001c0001t0023g0002a0001c0012t0024g0300others(4): Show | 7 | HG00140.hp2 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4910-1019dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | INFO_REALIGN_3_PRIME | chr11 | 108296256 | |||||
| chr11:108296318
|
T | C | 2 | a0001c0008t0002g0042a0001c0008t0002g0043 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4910-969T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108296318 | ||||||
| chr11:108296427
|
T | A | 1 | a0001c0001t0001g0254 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4910-860T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108296427 | ||||||
| chr11:108296647
|
GA | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.4910-639delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108296647 | ||||||
| chr11:108296980
|
G | A | 1 | a0003c0003t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4910-307G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108296980 | ||||||
| chr11:108297131
|
T | A | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.4910-156T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108297131 | ||||||
| chr11:108297247
|
T | C | 1 | a0001c0008t0002g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4910-40T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 32/62 | chr11 | 108297247 | ||||||
| chr11:108297601
|
A | G | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5005+219A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108297601 | ||||||
| chr11:108298051
|
G | A | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5005+669G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298051 | ||||||
| chr11:108298097
|
C | T | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5005+715C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298097 | ||||||
| chr11:108298136
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.5005+754A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298136 | ||||||
| chr11:108298268
|
A | C | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.5005+886A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298268 | ||||||
| chr11:108298443
|
C | G | 1 | a0001c0001t0001g0292 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.5005+1061C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298443 | ||||||
| chr11:108298596
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5006-1118G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298596 | ||||||
| chr11:108298777
|
T | C | 4 | a0001c0001t0010g0205a0001c0001t0010g0220a0001c0001t0010g0221others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.5006-937T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298777 | ||||||
| chr11:108298892
|
C | T | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.5006-822C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298892 | ||||||
| chr11:108298966
|
A | G | 2 | a0001c0001t0001g0282a0001c0001t0018g0294 | 2 | HG03927.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.5006-748A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108298966 | ||||||
| chr11:108299272
|
C | G | 1 | a0001c0001t0001g0218 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.5006-442C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108299272 | ||||||
| chr11:108299305
|
TTCTC | T | 18 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(15): Show | 18 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(15): Show |
intron_variant | MODIFIER | c.5006-401_5006-398d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | INFO_REALIGN_3_PRIME | chr11 | 108299305 | |||||
| chr11:108299307
|
C | T | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.5006-407C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108299307 | ||||||
| chr11:108299315
|
CT | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.5006-386delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | INFO_REALIGN_3_PRIME | chr11 | 108299315 | |||||
| chr11:108299316
|
T | TC | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5006-398_5006-397i others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108299316 | ||||||
| chr11:108299544
|
G | A | 131 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.5006-170G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108299544 | ||||||
| chr11:108299576
|
C | T | 6 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0038others(3): Show | 6 | HG00544.hp2 HG03195.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.5006-138C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108299576 | ||||||
| chr11:108299631
|
T | C | 1 | a0001c0001t0002g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.5006-83T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108299631 | ||||||
| chr11:108299646
|
T | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.5006-68T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 33/62 | chr11 | 108299646 | ||||||
| chr11:108300129
|
A | G | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5177+244A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300129 | ||||||
| chr11:108300429
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.5177+544C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300429 | ||||||
| chr11:108300524
|
A | C | 1 | a0019c0022t0002g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.5177+639A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300524 | ||||||
| chr11:108300547
|
G | A | 1 | a0008c0015t0002g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5177+662G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300547 | ||||||
| chr11:108300587
|
T | G | 1 | a0001c0001t0007g0064 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.5177+702T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300587 | ||||||
| chr11:108300735
|
T | G | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.5177+850T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300735 | ||||||
| chr11:108300878
|
C | CT | 16 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0054others(13): Show | 16 | HG00140.hp2 HG00741.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.5178-748dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | INFO_REALIGN_3_PRIME | chr11 | 108300878 | |||||
| chr11:108300878
|
CT | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.5178-748delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | INFO_REALIGN_3_PRIME | chr11 | 108300878 | |||||
| chr11:108300923
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.5178-725C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300923 | ||||||
| chr11:108300964
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5178-684A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108300964 | ||||||
| chr11:108301006
|
C | T | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.5178-642C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108301006 | ||||||
| chr11:108301017
|
C | T | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5178-631C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108301017 | ||||||
| chr11:108301118
|
G | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5178-530G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108301118 | ||||||
| chr11:108301198
|
T | G | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.5178-450T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108301198 | ||||||
| chr11:108301498
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5178-150T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 34/62 | chr11 | 108301498 | ||||||
| chr11:108301939
|
A | C | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.5319+150A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 35/62 | chr11 | 108301939 | ||||||
| chr11:108302271
|
C | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.5319+482C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 35/62 | chr11 | 108302271 | ||||||
| chr11:108302488
|
T | G | 2 | a0001c0001t0011g0154a0001c0001t0011g0155 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5320-365T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 35/62 | chr11 | 108302488 | ||||||
| chr11:108302568
|
A | C | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5320-285A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 35/62 | chr11 | 108302568 | ||||||
| chr11:108302779
|
T | C | 4 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(1): Show | 4 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.5320-74T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 35/62 | chr11 | 108302779 | ||||||
| chr11:108303082
|
A | C | 1 | a0001c0001t0002g0129 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5496+53A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108303082 | ||||||
| chr11:108303323
|
T | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5496+294T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108303323 | ||||||
| chr11:108303446
|
G | A | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.5496+417G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108303446 | ||||||
| chr11:108303464
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.5496+435C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108303464 | ||||||
| chr11:108303954
|
A | G | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5497-721A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108303954 | ||||||
| chr11:108304031
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5497-644G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304031 | ||||||
| chr11:108304078
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5497-597A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304078 | ||||||
| chr11:108304101
|
A | G | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.5497-574A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304101 | ||||||
| chr11:108304111
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5497-564A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304111 | ||||||
| chr11:108304153
|
T | A | 1 | a0001c0001t0011g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5497-522T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304153 | ||||||
| chr11:108304326
|
T | G | 1 | a0001c0001t0001g0003 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.5497-349T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304326 | ||||||
| chr11:108304344
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5497-331A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304344 | ||||||
| chr11:108304383
|
T | C | 10 | a0001c0001t0001g0199a0001c0001t0001g0203a0001c0001t0001g0224others(7): Show | 10 | HG02135.hp2 NA18961.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.5497-292T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304383 | ||||||
| chr11:108304507
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.5497-168T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304507 | ||||||
| chr11:108304563
|
A | G | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5497-112A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304563 | ||||||
| chr11:108304660
|
G | C | 1 | a0001c0001t0002g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5497-15G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304660 | ||||||
| chr11:108304667
|
T | C | 3 | a0003c0003t0001g0191a0003c0003t0001g0192a0003c0003t0001g0193 | 3 | HG01261.hp2 HG01515.hp2 HG01517.hp2 |
splice_region_variant&intron_variant | LOW | c.5497-8T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 36/62 | chr11 | 108304667 | ||||||
| chr11:108305293
|
C | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5674+441C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305293 | ||||||
| chr11:108305347
|
A | G | 2 | a0002c0002t0003g0085a0002c0002t0003g0086 | 2 | HG01081.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.5674+495A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305347 | ||||||
| chr11:108305436
|
C | T | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5674+584C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305436 | ||||||
| chr11:108305464
|
C | T | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5674+612C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305464 | ||||||
| chr11:108305504
|
C | G | 1 | a0001c0001t0006g0059 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.5674+652C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305504 | ||||||
| chr11:108305516
|
G | A | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.5674+664G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305516 | ||||||
| chr11:108305565
|
C | T | 8 | a0002c0005t0008g0095a0002c0005t0008g0097a0002c0005t0008g0098others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.5674+713C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305565 | ||||||
| chr11:108305601
|
C | G | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.5674+749C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305601 | ||||||
| chr11:108305709
|
A | G | 2 | a0003c0003t0001g0192a0003c0003t0001g0193 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.5674+857A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305709 | ||||||
| chr11:108305809
|
G | T | 1 | a0001c0001t0002g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5674+957G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305809 | ||||||
| chr11:108305826
|
T | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5674+974T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305826 | ||||||
| chr11:108305875
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0214 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.5674+1023C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108305875 | ||||||
| chr11:108306204
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5674+1352A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108306204 | ||||||
| chr11:108306370
|
T | A | 105 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.5674+1518T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108306370 | ||||||
| chr11:108306372
|
T | G | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5674+1520T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108306372 | ||||||
| chr11:108306555
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5675-1342T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108306555 | ||||||
| chr11:108306811
|
C | T | 160 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.5675-1086C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108306811 | ||||||
| chr11:108307120
|
C | T | 1 | a0019c0022t0002g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.5675-777C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307120 | ||||||
| chr11:108307181
|
G | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5675-716G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307181 | ||||||
| chr11:108307239
|
C | T | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.5675-658C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307239 | ||||||
| chr11:108307302
|
A | C | 6 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0157others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.5675-595A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307302 | ||||||
| chr11:108307394
|
C | T | 6 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(3): Show | 6 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.5675-503C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307394 | ||||||
| chr11:108307528
|
A | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.5675-369A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307528 | ||||||
| chr11:108307730
|
T | C | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5675-167T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307730 | ||||||
| chr11:108307749
|
C | A | 2 | a0001c0001t0020g0048a0001c0001t0020g0082 | 2 | NA18982.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.5675-148C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 37/62 | chr11 | 108307749 | ||||||
| chr11:108308011
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5762+27G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108308011 | ||||||
| chr11:108308103
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5762+119G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108308103 | ||||||
| chr11:108308382
|
CTTTAT | C | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5762+403_5762+407d others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | INFO_REALIGN_3_PRIME | chr11 | 108308382 | |||||
| chr11:108308418
|
G | A | 1 | a0001c0001t0002g0068 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.5762+434G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108308418 | ||||||
| chr11:108308596
|
A | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.5762+612A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108308596 | ||||||
| chr11:108308647
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.5762+663C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108308647 | ||||||
| chr11:108308656
|
A | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.5762+672A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108308656 | ||||||
| chr11:108309189
|
A | T | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5763-971A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108309189 | ||||||
| chr11:108309686
|
A | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.5763-474A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108309686 | ||||||
| chr11:108310079
|
A | T | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5763-81A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 38/62 | chr11 | 108310079 | ||||||
| chr11:108310438
|
T | C | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5918+123T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108310438 | ||||||
| chr11:108310501
|
T | C | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.5918+186T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108310501 | ||||||
| chr11:108310670
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5918+355G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108310670 | ||||||
| chr11:108310784
|
A | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.5918+469A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108310784 | ||||||
| chr11:108311133
|
AT | A | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.5918+826delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | INFO_REALIGN_3_PRIME | chr11 | 108311133 | |||||
| chr11:108311293
|
C | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5918+978C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108311293 | ||||||
| chr11:108311342
|
G | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.5918+1027G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108311342 | ||||||
| chr11:108311356
|
T | C | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5918+1041T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108311356 | ||||||
| chr11:108311370
|
T | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.5919-1041T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108311370 | ||||||
| chr11:108311445
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.5919-966C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108311445 | ||||||
| chr11:108311676
|
C | T | 1 | a0002c0005t0008g0102 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.5919-735C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108311676 | ||||||
| chr11:108311703
|
C | CA | 7 | a0001c0001t0002g0021a0001c0001t0002g0026a0001c0001t0002g0049others(4): Show | 7 | HG02132.hp2 HG02257.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.5919-695dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | INFO_REALIGN_3_PRIME | chr11 | 108311703 | |||||
| chr11:108311879
|
A | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.5919-532A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108311879 | ||||||
| chr11:108312009
|
A | C | 4 | a0001c0001t0001g0225a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.5919-402A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108312009 | ||||||
| chr11:108312199
|
C | T | 1 | a0001c0001t0002g0079 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.5919-212C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 39/62 | chr11 | 108312199 | ||||||
| chr11:108312553
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.6006+55A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108312553 | ||||||
| chr11:108312686
|
ACT | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.6006+191_6006+192d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | INFO_REALIGN_3_PRIME | chr11 | 108312686 | |||||
| chr11:108312694
|
A | G | 1 | a0002c0005t0003g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6006+196A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108312694 | ||||||
| chr11:108312744
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.6006+246A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108312744 | ||||||
| chr11:108313018
|
G | T | 1 | a0001c0001t0002g0054 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.6006+520G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313018 | ||||||
| chr11:108313130
|
C | T | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6006+632C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313130 | ||||||
| chr11:108313239
|
C | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.6006+741C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313239 | ||||||
| chr11:108313256
|
G | C | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.6006+758G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313256 | ||||||
| chr11:108313324
|
C | T | 1 | a0003c0003t0001g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.6006+826C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313324 | ||||||
| chr11:108313507
|
T | A | 1 | a0001c0001t0029g0016 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.6006+1009T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313507 | ||||||
| chr11:108313704
|
C | G | 14 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.6006+1206C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313704 | ||||||
| chr11:108313777
|
A | G | 1 | a0008c0015t0002g0013 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.6006+1279A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313777 | ||||||
| chr11:108313787
|
G | A | 2 | a0001c0001t0006g0051a0001c0001t0006g0052 | 2 | HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.6006+1289G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313787 | ||||||
| chr11:108313798
|
A | T | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6006+1300A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313798 | ||||||
| chr11:108313867
|
G | A | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.6006+1369G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313867 | ||||||
| chr11:108313874
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.6006+1376C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108313874 | ||||||
| chr11:108314039
|
A | G | 1 | a0001c0001t0027g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6006+1541A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314039 | ||||||
| chr11:108314114
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.6006+1616A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314114 | ||||||
| chr11:108314242
|
A | G | 1 | a0001c0016t0002g0014 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.6007-1581A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314242 | ||||||
| chr11:108314296
|
G | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.6007-1527G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314296 | ||||||
| chr11:108314406
|
C | A | 1 | a0001c0001t0013g0025 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.6007-1417C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314406 | ||||||
| chr11:108314454
|
AT | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.6007-1356delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | INFO_REALIGN_3_PRIME | chr11 | 108314454 | |||||
| chr11:108314476
|
T | C | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.6007-1347T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314476 | ||||||
| chr11:108314522
|
G | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.6007-1301G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314522 | ||||||
| chr11:108314751
|
C | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.6007-1072C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314751 | ||||||
| chr11:108314798
|
G | A | 1 | a0001c0001t0002g0047 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6007-1025G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314798 | ||||||
| chr11:108314805
|
GAAAAT | G | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6007-1017_6007-101 others(9): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108314805 | ||||||
| chr11:108315072
|
C | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.6007-751C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315072 | ||||||
| chr11:108315093
|
A | G | 2 | a0001c0001t0002g0127a0001c0001t0002g0131 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.6007-730A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315093 | ||||||
| chr11:108315160
|
G | T | 1 | a0008c0015t0002g0012 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.6007-663G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315160 | ||||||
| chr11:108315201
|
C | A | 1 | a0001c0001t0002g0047 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.6007-622C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315201 | ||||||
| chr11:108315222
|
A | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.6007-601A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315222 | ||||||
| chr11:108315369
|
G | T | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.6007-454G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315369 | ||||||
| chr11:108315421
|
G | A | 11 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 11 | HG02132.hp1 HG02451.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.6007-402G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315421 | ||||||
| chr11:108315500
|
A | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6007-323A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315500 | ||||||
| chr11:108315508
|
C | G | 2 | a0001c0008t0002g0041a0001c0008t0002g0044 | 2 | HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.6007-315C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315508 | ||||||
| chr11:108315531
|
G | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.6007-292G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315531 | ||||||
| chr11:108315779
|
G | A | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6007-44G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 40/62 | chr11 | 108315779 | ||||||
| chr11:108315926
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.6095+15T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 41/62 | chr11 | 108315926 | ||||||
| chr11:108316144
|
TCACTAGT others(15): Show |
T | 1 | a0001c0001t0020g0082 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.6198+32_6198+53del others(22): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316144 | ||||||
| chr11:108316229
|
T | C | 36 | a0001c0001t0002g0088a0001c0001t0002g0089a0002c0002t0003g0085others(33): Show | 36 | HG01070.hp1 HG01081.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.6198+116T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316229 | ||||||
| chr11:108316243
|
G | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.6198+130G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316243 | ||||||
| chr11:108316423
|
G | A | 10 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(7): Show | 10 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.6198+310G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316423 | ||||||
| chr11:108316512
|
A | G | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6198+399A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316512 | ||||||
| chr11:108316680
|
C | T | 1 | a0001c0001t0006g0059 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.6198+567C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316680 | ||||||
| chr11:108316681
|
G | A | 2 | a0001c0001t0002g0045a0001c0001t0002g0066 | 2 | HG00544.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.6198+568G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316681 | ||||||
| chr11:108316689
|
C | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6198+576C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316689 | ||||||
| chr11:108316725
|
C | T | 2 | a0011c0017t0002g0056a0016c0031t0002g0080 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6198+612C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316725 | ||||||
| chr11:108316753
|
C | CA | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.6199-597dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | INFO_REALIGN_3_PRIME | chr11 | 108316753 | |||||
| chr11:108316753
|
C | CAA | 28 | a0001c0001t0001g0163a0001c0001t0001g0201a0001c0001t0001g0203others(25): Show | 28 | HG01070.hp2 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.6199-598_6199-597d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | INFO_REALIGN_3_PRIME | chr11 | 108316753 | |||||
| chr11:108316785
|
G | C | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.6199-588G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316785 | ||||||
| chr11:108316842
|
C | T | 2 | a0001c0001t0002g0057a0018c0028t0002g0067 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.6199-531C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316842 | ||||||
| chr11:108316878
|
A | C | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.6199-495A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316878 | ||||||
| chr11:108316889
|
G | A | 1 | a0021c0026t0001g0230 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.6199-484G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316889 | ||||||
| chr11:108316906
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.6199-467A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316906 | ||||||
| chr11:108316916
|
A | T | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.6199-457A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316916 | ||||||
| chr11:108316962
|
G | A | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.6199-411G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316962 | ||||||
| chr11:108316965
|
A | G | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6199-408A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108316965 | ||||||
| chr11:108317102
|
T | TA | 205 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0153others(202): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.6199-271_6199-270i others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108317102 | ||||||
| chr11:108317103
|
T | A | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.6199-270T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108317103 | ||||||
| chr11:108317312
|
C | G | 3 | a0001c0001t0014g0151a0001c0001t0014g0275a0001c0001t0014g0279 | 3 | HG01168.hp2 HG02683.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.6199-61C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 42/62 | chr11 | 108317312 | ||||||
| chr11:108317539
|
AT | A | 52 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0016g0009others(49): Show | 52 | HG00140.hp2 HG01070.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.6347+31delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317539 | |||||
| chr11:108317615
|
T | A | 2 | a0009c0013t0012g0119a0023c0033t0012g0118 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6347+94T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317615 | ||||||
| chr11:108317615
|
T | TTA | 12 | a0001c0001t0002g0021a0001c0001t0002g0049a0001c0001t0002g0050others(9): Show | 12 | HG01081.hp2 HG01257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.6347+131_6347+132d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATA | 17 | a0001c0001t0002g0022a0001c0001t0002g0034a0001c0001t0002g0035others(14): Show | 17 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.6347+129_6347+132d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATA | 28 | a0001c0001t0002g0024a0001c0001t0002g0026a0001c0001t0002g0037others(25): Show | 28 | HG00544.hp2 HG00733.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.6347+127_6347+132d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATAT others(1): Show |
10 | a0001c0001t0002g0017a0001c0001t0002g0066a0001c0001t0002g0092others(7): Show | 10 | HG01123.hp2 HG01981.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.6347+125_6347+132d others(10): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATAT others(3): Show |
8 | a0001c0001t0002g0107a0001c0001t0002g0110a0001c0001t0002g0113others(5): Show | 8 | HG01243.hp2 HG01975.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.6347+123_6347+132d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATAT others(5): Show |
4 | a0001c0001t0002g0062a0001c0001t0002g0069a0001c0001t0002g0109others(1): Show | 4 | HG04184.hp1 NA18960.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.6347+121_6347+132d others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATAT others(7): Show |
1 | a0019c0022t0002g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.6347+119_6347+132d others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATAT others(9): Show |
1 | a0001c0008t0002g0044 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.6347+117_6347+132d others(18): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATAT others(11): Show |
2 | a0001c0001t0002g0068a0001c0001t0002g0091 | 2 | HG00408.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.6347+115_6347+132d others(20): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
T | TTATATAT others(13): Show |
1 | a0007c0011t0002g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.6347+113_6347+132d others(22): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
TTA | T | 37 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0208others(34): Show | 37 | HG00140.hp1 HG00738.hp1 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.6347+131_6347+132d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
TTATA | T | 55 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0163others(52): Show | 55 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(52): Show |
intron_variant | MODIFIER | c.6347+129_6347+132d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
TTATATA | T | 21 | a0001c0001t0001g0159a0001c0001t0001g0164a0001c0001t0001g0201others(18): Show | 21 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.6347+127_6347+132d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
TTATATAT others(1): Show |
T | 12 | a0001c0001t0001g0006a0001c0001t0001g0217a0001c0001t0001g0219others(9): Show | 12 | HG00323.hp2 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.6347+125_6347+132d others(10): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317615
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0027g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.6347+121_6347+132d others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317615 | |||||
| chr11:108317640
|
T | C | 1 | a0005c0006t0005g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.6347+119T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317640 | ||||||
| chr11:108317640
|
TATATATA others(7): Show |
T | 3 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032 | 3 | HG00738.hp2 HG01099.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.6347+121_6347+134d others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317640 | |||||
| chr11:108317640
|
TATATATA others(11): Show |
T | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6347+121_6347+138d others(20): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317640 | |||||
| chr11:108317642
|
T | C | 1 | a0005c0006t0005g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.6347+121T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317642 | ||||||
| chr11:108317644
|
T | C | 8 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(5): Show | 8 | HG01257.hp1 HG02132.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.6347+123T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317644 | ||||||
| chr11:108317644
|
TATATATA others(3): Show |
T | 2 | a0001c0010t0002g0053a0001c0010t0031g0031 | 2 | HG02615.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.6347+125_6347+134d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317644 | |||||
| chr11:108317646
|
T | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0153a0001c0001t0001g0158others(13): Show | 16 | HG00738.hp1 HG01071.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.6347+125T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317646 | ||||||
| chr11:108317646
|
TATATATA others(3): Show |
T | 1 | a0001c0012t0024g0300 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.6347+127_6347+136d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317646 | |||||
| chr11:108317646
|
TATATATA others(5): Show |
T | 2 | a0001c0012t0038g0302a0002c0005t0008g0097 | 2 | HG00140.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.6347+127_6347+138d others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317646 | |||||
| chr11:108317648
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0153others(100): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.6347+127T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317648 | ||||||
| chr11:108317648
|
TATATACA others(3): Show |
T | 4 | a0001c0001t0002g0088a0001c0001t0002g0089a0002c0002t0003g0136others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.6347+129_6347+138d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317648 | |||||
| chr11:108317650
|
T | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0153others(113): Show | 116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.6347+129T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317650 | ||||||
| chr11:108317650
|
T | TACACACA others(5): Show |
1 | a0004c0004t0004g0168 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.6347+130_6347+131i others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317650 | |||||
| chr11:108317650
|
T | TACACACA others(7): Show |
1 | a0004c0004t0004g0176 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.6347+130_6347+131i others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317650 | |||||
| chr11:108317650
|
TATACAC | T | 4 | a0002c0002t0003g0144a0002c0009t0003g0134a0002c0009t0003g0135others(1): Show | 4 | HG02258.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.6347+131_6347+136d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317650 | |||||
| chr11:108317650
|
TATACACA others(1): Show |
T | 8 | a0001c0001t0034g0152a0002c0002t0003g0137a0002c0005t0008g0098others(5): Show | 8 | HG02647.hp1 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.6347+131_6347+138d others(10): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317650 | |||||
| chr11:108317652
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0153others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.6347+131T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317652 | ||||||
| chr11:108317652
|
T | TACACACA others(7): Show |
3 | a0004c0004t0004g0169a0004c0004t0004g0182a0004c0004t0004g0183 | 3 | HG01123.hp1 HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.6347+140_6347+153d others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TACACACA others(9): Show |
1 | a0004c0004t0004g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.6347+138_6347+153d others(18): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATACACA others(7): Show |
1 | a0005c0006t0005g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6347+132_6347+133i others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATACACA others(9): Show |
2 | a0004c0004t0004g0177a0004c0004t0004g0180 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6347+132_6347+133i others(18): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATACA others(7): Show |
1 | a0004c0004t0005g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.6347+132_6347+133i others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATACA others(11): Show |
2 | a0004c0004t0004g0178a0004c0004t0004g0184 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6347+132_6347+133i others(20): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(3): Show |
3 | a0001c0001t0002g0079a0001c0001t0002g0083a0001c0001t0007g0073 | 3 | HG02083.hp1 NA19080.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.6347+132_6347+133i others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(13): Show |
4 | a0005c0006t0005g0166a0005c0006t0005g0170a0005c0006t0005g0172others(1): Show | 4 | HG02602.hp1 NA18939.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.6347+132_6347+133i others(22): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(5): Show |
2 | a0001c0001t0002g0057a0018c0028t0002g0067 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.6347+132_6347+133i others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(13): Show |
1 | a0001c0001t0011g0197 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.6347+132_6347+133i others(22): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(15): Show |
2 | a0005c0006t0005g0181a0005c0006t0030g0167 | 2 | NA19000.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.6347+132_6347+133i others(24): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(13): Show |
2 | a0001c0001t0011g0154a0001c0001t0011g0155 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.6347+132_6347+133i others(22): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(17): Show |
1 | a0001c0001t0011g0196 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.6347+132_6347+133i others(26): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
T | TATATATA others(19): Show |
1 | a0005c0006t0005g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.6347+132_6347+133i others(28): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317652
|
TAC | T | 3 | a0002c0002t0003g0139a0011c0017t0002g0056a0017c0030t0002g0126 | 3 | HG02559.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6347+152_6347+153d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108317652 | |||||
| chr11:108317654
|
C | T | 14 | a0001c0001t0002g0078a0002c0002t0003g0085a0002c0002t0003g0086others(11): Show | 14 | HG01081.hp2 HG01891.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.6347+133C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317654 | ||||||
| chr11:108317656
|
C | T | 9 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0139others(6): Show | 9 | HG01081.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.6347+135C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317656 | ||||||
| chr11:108317658
|
C | T | 1 | a0002c0005t0003g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6347+137C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317658 | ||||||
| chr11:108317673
|
A | T | 11 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(8): Show | 11 | HG01071.hp2 HG02074.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.6347+152A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317673 | ||||||
| chr11:108317674
|
C | A | 11 | a0001c0001t0001g0003a0001c0001t0002g0105a0001c0001t0002g0106others(8): Show | 11 | HG01071.hp2 HG02074.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.6347+153C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317674 | ||||||
| chr11:108317675
|
T | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6347+154T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317675 | ||||||
| chr11:108317735
|
T | A | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.6347+214T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317735 | ||||||
| chr11:108317848
|
C | T | 31 | a0001c0001t0002g0088a0001c0001t0002g0089a0002c0002t0003g0085others(28): Show | 31 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.6347+327C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317848 | ||||||
| chr11:108317863
|
T | G | 9 | a0001c0001t0001g0233a0001c0001t0001g0239a0001c0001t0001g0260others(6): Show | 9 | HG00408.hp1 HG01109.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.6347+342T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317863 | ||||||
| chr11:108317984
|
T | G | 8 | a0001c0001t0001g0225a0001c0001t0001g0248a0001c0001t0001g0249others(5): Show | 8 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.6347+463T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108317984 | ||||||
| chr11:108318170
|
T | C | 1 | a0001c0001t0007g0064 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.6347+649T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318170 | ||||||
| chr11:108318179
|
C | T | 3 | a0002c0005t0008g0095a0002c0005t0008g0097a0002c0005t0008g0103 | 3 | HG02055.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.6347+658C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318179 | ||||||
| chr11:108318348
|
C | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.6347+827C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318348 | ||||||
| chr11:108318362
|
T | TAAAAAAA others(11): Show |
2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.6347+852_6347+869d others(20): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108318362 | |||||
| chr11:108318485
|
T | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.6347+964T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318485 | ||||||
| chr11:108318583
|
G | A | 1 | a0001c0008t0002g0041 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.6347+1062G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318583 | ||||||
| chr11:108318796
|
G | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02132.hp1 HG03579.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.6348-1158G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318796 | ||||||
| chr11:108318903
|
C | T | 1 | a0001c0001t0001g0236 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.6348-1051C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318903 | ||||||
| chr11:108318934
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.6348-1020G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108318934 | ||||||
| chr11:108319012
|
C | CA | 14 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.6348-935dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | INFO_REALIGN_3_PRIME | chr11 | 108319012 | |||||
| chr11:108319036
|
G | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0267 | 2 | NA18986.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.6348-918G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108319036 | ||||||
| chr11:108319335
|
G | A | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.6348-619G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108319335 | ||||||
| chr11:108319436
|
C | T | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.6348-518C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108319436 | ||||||
| chr11:108319702
|
T | C | 1 | a0001c0001t0014g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.6348-252T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108319702 | ||||||
| chr11:108319900
|
T | C | 3 | a0001c0001t0001g0235a0001c0001t0001g0241a0001c0001t0001g0242 | 3 | HG00738.hp1 HG01257.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.6348-54T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 43/62 | chr11 | 108319900 | ||||||
| chr11:108320131
|
CA | C | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.6452+75delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 44/62 | INFO_REALIGN_3_PRIME | chr11 | 108320131 | |||||
| chr11:108320307
|
A | T | 2 | a0011c0017t0002g0056a0016c0031t0002g0080 | 2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6452+249A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 44/62 | chr11 | 108320307 | ||||||
| chr11:108320361
|
A | G | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6452+303A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 44/62 | chr11 | 108320361 | ||||||
| chr11:108320409
|
T | C | 5 | a0001c0001t0002g0106a0001c0001t0002g0107a0001c0001t0002g0110others(2): Show | 5 | NA18953.hp1 NA18960.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.6452+351T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 44/62 | chr11 | 108320409 | ||||||
| chr11:108320882
|
AT | A | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.6453-418delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 44/62 | chr11 | 108320882 | ||||||
| chr11:108320886
|
G | A | 4 | a0001c0008t0002g0041a0001c0008t0002g0042a0001c0008t0002g0043others(1): Show | 4 | HG03098.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.6453-415G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 44/62 | chr11 | 108320886 | ||||||
| chr11:108321216
|
G | T | 1 | a0002c0002t0003g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6453-85G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 44/62 | chr11 | 108321216 | ||||||
| chr11:108321432
|
G | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.6572+12G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321432 | ||||||
| chr11:108321600
|
T | C | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.6572+180T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321600 | ||||||
| chr11:108321615
|
T | C | 1 | a0001c0001t0018g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6572+195T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321615 | ||||||
| chr11:108321744
|
C | T | 11 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 11 | HG02132.hp1 HG02451.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.6572+324C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321744 | ||||||
| chr11:108321776
|
G | T | 5 | a0001c0001t0002g0021a0001c0001t0002g0049a0001c0001t0002g0050others(2): Show | 5 | HG02132.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.6572+356G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321776 | ||||||
| chr11:108321786
|
C | CA | 8 | a0001c0001t0001g0210a0001c0001t0001g0217a0001c0001t0001g0265others(5): Show | 8 | HG03516.hp1 HG03516.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.6572+380dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | INFO_REALIGN_3_PRIME | chr11 | 108321786 | |||||
| chr11:108321801
|
C | A | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6572+381C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321801 | ||||||
| chr11:108321803
|
A | T | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6572+383A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321803 | ||||||
| chr11:108321804
|
T | G | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.6572+384T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321804 | ||||||
| chr11:108321885
|
C | T | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.6572+465C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108321885 | ||||||
| chr11:108322249
|
G | A | 1 | a0005c0006t0005g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6572+829G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322249 | ||||||
| chr11:108322257
|
C | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.6572+837C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322257 | ||||||
| chr11:108322294
|
A | G | 2 | a0001c0001t0006g0059a0001c0001t0006g0077 | 2 | HG01257.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.6572+874A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322294 | ||||||
| chr11:108322304
|
C | T | 3 | a0005c0006t0005g0165a0005c0006t0005g0173a0005c0006t0005g0174 | 3 | HG02602.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.6572+884C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322304 | ||||||
| chr11:108322747
|
A | G | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1327A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322747 | ||||||
| chr11:108322748
|
A | T | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1328A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322748 | ||||||
| chr11:108322781
|
C | T | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1361C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322781 | ||||||
| chr11:108322785
|
C | A | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1365C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322785 | ||||||
| chr11:108322815
|
C | T | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1395C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322815 | ||||||
| chr11:108322823
|
T | A | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1403T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322823 | ||||||
| chr11:108322835
|
G | A | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1415G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322835 | ||||||
| chr11:108322841
|
A | G | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.6572+1421A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322841 | ||||||
| chr11:108322847
|
G | A | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1427G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322847 | ||||||
| chr11:108322853
|
C | T | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.6572+1433C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322853 | ||||||
| chr11:108322886
|
G | C | 1 | a0002c0002t0003g0149 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.6572+1466G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322886 | ||||||
| chr11:108322960
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6572+1540C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322960 | ||||||
| chr11:108322997
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0002g0037 | 2 | HG02257.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.6572+1577C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108322997 | ||||||
| chr11:108323297
|
A | G | 5 | a0001c0001t0002g0021a0001c0001t0002g0049a0001c0001t0002g0050others(2): Show | 5 | HG02132.hp2 NA18946.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.6572+1877A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108323297 | ||||||
| chr11:108323346
|
C | T | 199 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.6572+1926C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108323346 | ||||||
| chr11:108323364
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.6572+1944A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108323364 | ||||||
| chr11:108323745
|
T | C | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.6573-1565T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108323745 | ||||||
| chr11:108323801
|
C | A | 218 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.6573-1509C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108323801 | ||||||
| chr11:108323830
|
C | T | 157 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.6573-1480C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108323830 | ||||||
| chr11:108323887
|
G | T | 1 | a0001c0001t0025g0268 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.6573-1423G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108323887 | ||||||
| chr11:108324056
|
GA | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.6573-1245delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | INFO_REALIGN_3_PRIME | chr11 | 108324056 | |||||
| chr11:108324166
|
A | G | 7 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(4): Show | 7 | HG01261.hp1 HG02559.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.6573-1144A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324166 | ||||||
| chr11:108324173
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.6573-1137G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324173 | ||||||
| chr11:108324178
|
C | T | 4 | a0001c0001t0010g0205a0001c0001t0010g0220a0001c0001t0010g0221others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.6573-1132C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324178 | ||||||
| chr11:108324238
|
G | A | 2 | a0001c0001t0023g0002a0001c0001t0034g0152 | 2 | HG02451.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.6573-1072G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324238 | ||||||
| chr11:108324562
|
T | G | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6573-748T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324562 | ||||||
| chr11:108324796
|
C | T | 15 | a0001c0001t0002g0088a0001c0001t0002g0089a0002c0005t0003g0096others(12): Show | 15 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.6573-514C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324796 | ||||||
| chr11:108324951
|
T | C | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.6573-359T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324951 | ||||||
| chr11:108324970
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.6573-340G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108324970 | ||||||
| chr11:108325052
|
A | C | 1 | a0001c0027t0002g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.6573-258A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325052 | ||||||
| chr11:108325186
|
T | A | 1 | a0022c0021t0036g0008 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.6573-124T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325186 | ||||||
| chr11:108325245
|
C | G | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6573-65C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325245 | ||||||
| chr11:108325246
|
A | G | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6573-64A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325246 | ||||||
| chr11:108325246
|
A | T | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6573-64A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325246 | ||||||
| chr11:108325247
|
TAG | T | 3 | a0009c0013t0012g0119a0009c0013t0012g0120a0023c0033t0012g0118 | 3 | HG02257.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6573-62_6573-61del others(2): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325247 | ||||||
| chr11:108325248
|
A | T | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6573-62A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325248 | ||||||
| chr11:108325249
|
G | GT | 13 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116others(10): Show | 13 | HG01109.hp2 HG01123.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.6573-42dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | INFO_REALIGN_3_PRIME | chr11 | 108325249 | |||||
| chr11:108325249
|
G | T | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6573-61G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | chr11 | 108325249 | ||||||
| chr11:108325249
|
GT | G | 232 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.6573-42delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | INFO_REALIGN_3_PRIME | chr11 | 108325249 | |||||
| chr11:108325249
|
GTT | G | 7 | a0001c0001t0001g0210a0001c0001t0001g0248a0001c0001t0001g0262others(4): Show | 7 | HG00140.hp2 HG01070.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.6573-43_6573-42del others(2): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 45/62 | INFO_REALIGN_3_PRIME | chr11 | 108325249 | |||||
| chr11:108325782
|
G | C | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.6807+238G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 46/62 | chr11 | 108325782 | ||||||
| chr11:108325985
|
CATT | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.6808-60_6808-58del others(3): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 46/62 | INFO_REALIGN_3_PRIME | chr11 | 108325985 | |||||
| chr11:108326468
|
C | CT | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.6975+246dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 47/62 | INFO_REALIGN_3_PRIME | chr11 | 108326468 | |||||
| chr11:108326875
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.6975+650G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 47/62 | chr11 | 108326875 | ||||||
| chr11:108327048
|
G | A | 1 | a0001c0034t0002g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.6976-597G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 47/62 | chr11 | 108327048 | ||||||
| chr11:108327373
|
A | G | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.6976-272A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 47/62 | chr11 | 108327373 | ||||||
| chr11:108327392
|
T | A | 1 | a0001c0001t0010g0220 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.6976-253T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 47/62 | chr11 | 108327392 | ||||||
| chr11:108327574
|
C | T | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.6976-71C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 47/62 | chr11 | 108327574 | ||||||
| chr11:108327914
|
T | C | 1 | a0001c0008t0002g0044 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7089+156T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108327914 | ||||||
| chr11:108328008
|
C | T | 1 | a0001c0001t0009g0263 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.7089+250C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108328008 | ||||||
| chr11:108328348
|
G | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0214 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.7089+590G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108328348 | ||||||
| chr11:108328375
|
T | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7089+617T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108328375 | ||||||
| chr11:108328449
|
T | C | 29 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(26): Show | 29 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.7090-572T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108328449 | ||||||
| chr11:108328479
|
C | A | 1 | a0005c0006t0005g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.7090-542C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108328479 | ||||||
| chr11:108328537
|
C | T | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.7090-484C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108328537 | ||||||
| chr11:108328702
|
T | C | 6 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(3): Show | 6 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.7090-319T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 48/62 | chr11 | 108328702 | ||||||
| chr11:108329368
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.7307+130A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329368 | ||||||
| chr11:108329415
|
T | G | 150 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.7307+177T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329415 | ||||||
| chr11:108329455
|
G | A | 6 | a0003c0003t0001g0185a0003c0003t0001g0186a0003c0003t0001g0187others(3): Show | 6 | HG00639.hp1 HG01074.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.7307+217G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329455 | ||||||
| chr11:108329526
|
C | T | 3 | a0005c0006t0005g0165a0005c0006t0005g0173a0005c0006t0005g0174 | 3 | HG02602.hp1 HG03688.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.7307+288C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329526 | ||||||
| chr11:108329557
|
G | T | 1 | a0001c0001t0006g0077 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.7307+319G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329557 | ||||||
| chr11:108329588
|
T | A | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.7307+350T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329588 | ||||||
| chr11:108329687
|
A | G | 21 | a0001c0001t0017g0175a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.7307+449A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329687 | ||||||
| chr11:108329721
|
C | T | 1 | a0002c0005t0003g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.7307+483C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329721 | ||||||
| chr11:108329857
|
TATC | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.7308-354_7308-352d others(5): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | INFO_REALIGN_3_PRIME | chr11 | 108329857 | |||||
| chr11:108329919
|
A | T | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7308-295A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108329919 | ||||||
| chr11:108330019
|
T | C | 2 | a0001c0001t0002g0128a0001c0001t0002g0133 | 2 | HG01261.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.7308-195T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 49/62 | chr11 | 108330019 | ||||||
| chr11:108330495
|
C | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.7515+74C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 50/62 | chr11 | 108330495 | ||||||
| chr11:108330643
|
G | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.7515+222G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 50/62 | chr11 | 108330643 | ||||||
| chr11:108330645
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.7515+224C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 50/62 | chr11 | 108330645 | ||||||
| chr11:108330877
|
A | C | 1 | a0001c0001t0002g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7515+456A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 50/62 | chr11 | 108330877 | ||||||
| chr11:108331160
|
T | C | 1 | a0007c0011t0002g0122 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.7516-284T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 50/62 | chr11 | 108331160 | ||||||
| chr11:108331620
|
A | G | 1 | a0001c0008t0002g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.7629+63A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 51/62 | chr11 | 108331620 | ||||||
| chr11:108331862
|
T | C | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7630-17T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 51/62 | chr11 | 108331862 | ||||||
| chr11:108332045
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.7788+8G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 52/62 | chr11 | 108332045 | ||||||
| chr11:108332185
|
T | G | 1 | a0001c0001t0002g0083 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.7788+148T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 52/62 | chr11 | 108332185 | ||||||
| chr11:108332245
|
G | T | 1 | a0001c0001t0001g0244 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.7788+208G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 52/62 | chr11 | 108332245 | ||||||
| chr11:108332433
|
A | AAATTAAT others(1): Show |
10 | a0004c0004t0005g0004a0005c0006t0005g0165a0005c0006t0005g0166others(7): Show | 10 | HG02602.hp1 HG03688.hp1 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.7789-310_7789-303d others(10): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 52/62 | INFO_REALIGN_3_PRIME | chr11 | 108332433 | |||||
| chr11:108332490
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7789-272A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 52/62 | chr11 | 108332490 | ||||||
| chr11:108332969
|
T | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.7927+69T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 53/62 | chr11 | 108332969 | ||||||
| chr11:108333042
|
G | A | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.7927+142G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 53/62 | chr11 | 108333042 | ||||||
| chr11:108333236
|
G | A | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.7927+336G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 53/62 | chr11 | 108333236 | ||||||
| chr11:108333263
|
C | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.7927+363C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 53/62 | chr11 | 108333263 | ||||||
| chr11:108333526
|
A | G | 84 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0019others(81): Show | 84 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.7928-360A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 53/62 | chr11 | 108333526 | ||||||
| chr11:108333791
|
C | A | 8 | a0002c0005t0008g0095a0002c0005t0008g0097a0002c0005t0008g0098others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.7928-95C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 53/62 | chr11 | 108333791 | ||||||
| chr11:108333839
|
T | C | 1 | a0005c0006t0005g0165 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.7928-47T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 53/62 | chr11 | 108333839 | ||||||
| chr11:108334154
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0198others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.8010+186C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334154 | ||||||
| chr11:108334218
|
GT | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8010+252delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | INFO_REALIGN_3_PRIME | chr11 | 108334218 | |||||
| chr11:108334347
|
G | A | 13 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.8010+379G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334347 | ||||||
| chr11:108334375
|
G | A | 9 | a0005c0006t0005g0165a0005c0006t0005g0166a0005c0006t0005g0170others(6): Show | 9 | HG02602.hp1 HG03688.hp1 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.8010+407G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334375 | ||||||
| chr11:108334491
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8011-478T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334491 | ||||||
| chr11:108334602
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8011-367A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334602 | ||||||
| chr11:108334656
|
G | A | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.8011-313G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334656 | ||||||
| chr11:108334709
|
G | C | 4 | a0001c0001t0010g0205a0001c0001t0010g0220a0001c0001t0010g0221others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8011-260G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334709 | ||||||
| chr11:108334735
|
C | A | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8011-234C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334735 | ||||||
| chr11:108334795
|
G | C | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0265others(1): Show | 4 | NA18954.hp2 NA18962.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.8011-174G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334795 | ||||||
| chr11:108334931
|
A | G | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8011-38A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 54/62 | chr11 | 108334931 | ||||||
| chr11:108335535
|
T | G | 1 | a0005c0006t0005g0171 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.8152-310T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 55/62 | chr11 | 108335535 | ||||||
| chr11:108336446
|
T | C | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8268+485T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108336446 | ||||||
| chr11:108336507
|
T | C | 1 | a0001c0001t0010g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8268+546T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108336507 | ||||||
| chr11:108336577
|
T | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.8268+616T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108336577 | ||||||
| chr11:108336666
|
T | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.8268+705T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108336666 | ||||||
| chr11:108336763
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8268+802C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108336763 | ||||||
| chr11:108336877
|
CAATA | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8268+920_8268+923d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | INFO_REALIGN_3_PRIME | chr11 | 108336877 | |||||
| chr11:108337035
|
C | T | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.8268+1074C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337035 | ||||||
| chr11:108337080
|
G | A | 1 | a0001c0008t0016g0116 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.8268+1119G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337080 | ||||||
| chr11:108337221
|
C | A | 1 | a0012c0035t0002g0027 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.8268+1260C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337221 | ||||||
| chr11:108337268
|
T | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8268+1307T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337268 | ||||||
| chr11:108337449
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8268+1488A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337449 | ||||||
| chr11:108337478
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.8268+1517G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337478 | ||||||
| chr11:108337507
|
C | T | 1 | a0001c0001t0002g0108 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.8268+1546C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337507 | ||||||
| chr11:108337957
|
T | C | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.8268+1996T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108337957 | ||||||
| chr11:108338051
|
T | C | 3 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0016t0002g0015 | 3 | HG00642.hp1 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.8268+2090T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338051 | ||||||
| chr11:108338143
|
G | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0201a0001c0001t0001g0214others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.8268+2182G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338143 | ||||||
| chr11:108338187
|
A | G | 1 | a0005c0006t0030g0167 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.8268+2226A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338187 | ||||||
| chr11:108338276
|
G | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8268+2315G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338276 | ||||||
| chr11:108338285
|
A | G | 1 | a0005c0006t0005g0181 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.8268+2324A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338285 | ||||||
| chr11:108338364
|
A | G | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8268+2403A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338364 | ||||||
| chr11:108338472
|
C | T | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.8268+2511C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338472 | ||||||
| chr11:108338614
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0278 | 2 | NA18942.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.8268+2653C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338614 | ||||||
| chr11:108338633
|
A | G | 202 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.8268+2672A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338633 | ||||||
| chr11:108338656
|
A | T | 1 | a0001c0008t0002g0043 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8268+2695A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338656 | ||||||
| chr11:108338681
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8268+2720G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338681 | ||||||
| chr11:108338881
|
G | T | 1 | a0001c0012t0038g0302 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.8268+2920G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338881 | ||||||
| chr11:108338960
|
T | G | 1 | a0001c0001t0002g0010 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.8268+2999T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108338960 | ||||||
| chr11:108339119
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8268+3158G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339119 | ||||||
| chr11:108339192
|
A | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8268+3231A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339192 | ||||||
| chr11:108339204
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.8268+3243G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339204 | ||||||
| chr11:108339382
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.8268+3421A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339382 | ||||||
| chr11:108339450
|
C | T | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.8268+3489C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339450 | ||||||
| chr11:108339474
|
A | G | 1 | a0006c0007t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.8268+3513A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339474 | ||||||
| chr11:108339531
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.8268+3570T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339531 | ||||||
| chr11:108339643
|
A | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.8269-3579A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339643 | ||||||
| chr11:108339723
|
A | T | 14 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8269-3499A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108339723 | ||||||
| chr11:108340068
|
A | G | 2 | a0001c0001t0002g0057a0018c0028t0002g0067 | 2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.8269-3154A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340068 | ||||||
| chr11:108340080
|
A | G | 6 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0157others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.8269-3142A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340080 | ||||||
| chr11:108340132
|
C | G | 2 | a0001c0001t0021g0020a0001c0001t0021g0028 | 2 | NA18985.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.8269-3090C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340132 | ||||||
| chr11:108340150
|
CTTTAT | C | 26 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0026others(23): Show | 26 | HG00544.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.8269-3068_8269-306 others(9): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | INFO_REALIGN_3_PRIME | chr11 | 108340150 | |||||
| chr11:108340194
|
T | A | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8269-3028T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340194 | ||||||
| chr11:108340241
|
A | C | 14 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8269-2981A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340241 | ||||||
| chr11:108340685
|
T | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.8269-2537T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340685 | ||||||
| chr11:108340710
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8269-2512C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340710 | ||||||
| chr11:108340755
|
A | C | 2 | a0001c0001t0001g0204a0001c0001t0001g0293 | 2 | HG01175.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.8269-2467A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340755 | ||||||
| chr11:108340768
|
A | G | 1 | a0002c0002t0003g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8269-2454A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340768 | ||||||
| chr11:108340793
|
G | A | 1 | a0009c0013t0012g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.8269-2429G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340793 | ||||||
| chr11:108340984
|
C | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.8269-2238C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108340984 | ||||||
| chr11:108341008
|
T | C | 1 | a0004c0004t0005g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8269-2214T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341008 | ||||||
| chr11:108341010
|
T | A | 1 | a0001c0001t0001g0284 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.8269-2212T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341010 | ||||||
| chr11:108341025
|
C | G | 1 | a0001c0001t0001g0224 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.8269-2197C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341025 | ||||||
| chr11:108341069
|
A | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8269-2153A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341069 | ||||||
| chr11:108341323
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.8269-1899C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341323 | ||||||
| chr11:108341366
|
A | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.8269-1856A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341366 | ||||||
| chr11:108341387
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8269-1835T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341387 | ||||||
| chr11:108341547
|
T | A | 9 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(6): Show | 9 | HG01074.hp1 HG01891.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.8269-1675T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341547 | ||||||
| chr11:108341572
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.8269-1650A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341572 | ||||||
| chr11:108341945
|
G | T | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8269-1277G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341945 | ||||||
| chr11:108341965
|
G | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.8269-1257G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108341965 | ||||||
| chr11:108342093
|
G | GT | 10 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(7): Show | 10 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.8269-1120dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | INFO_REALIGN_3_PRIME | chr11 | 108342093 | |||||
| chr11:108342140
|
T | C | 11 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.8269-1082T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108342140 | ||||||
| chr11:108342170
|
G | A | 1 | a0001c0001t0006g0059 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.8269-1052G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108342170 | ||||||
| chr11:108342671
|
C | T | 1 | a0001c0001t0009g0263 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.8269-551C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108342671 | ||||||
| chr11:108342710
|
T | C | 1 | a0001c0001t0002g0083 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.8269-512T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108342710 | ||||||
| chr11:108342953
|
T | C | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.8269-269T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 56/62 | chr11 | 108342953 | ||||||
| chr11:108343448
|
T | C | 4 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(1): Show | 4 | HG02132.hp1 HG03579.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.8418+77T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108343448 | ||||||
| chr11:108343449
|
A | G | 14 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8418+78A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108343449 | ||||||
| chr11:108343677
|
T | C | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8418+306T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108343677 | ||||||
| chr11:108343716
|
T | A | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8418+345T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108343716 | ||||||
| chr11:108343872
|
A | G | 3 | a0001c0001t0023g0002a0001c0001t0034g0152a0022c0021t0036g0008 | 3 | HG02451.hp2 HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8418+501A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108343872 | ||||||
| chr11:108344014
|
A | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0219a0001c0001t0001g0266others(1): Show | 4 | HG00642.hp2 HG01517.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.8418+643A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108344014 | ||||||
| chr11:108344149
|
A | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.8418+778A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108344149 | ||||||
| chr11:108344368
|
A | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.8418+997A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108344368 | ||||||
| chr11:108344670
|
T | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0216a0001c0001t0001g0217others(9): Show | 12 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.8419-1073T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108344670 | ||||||
| chr11:108344979
|
G | A | 1 | a0020c0023t0002g0084 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.8419-764G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108344979 | ||||||
| chr11:108345121
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0264 | 2 | NA18974.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.8419-622A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345121 | ||||||
| chr11:108345256
|
A | G | 1 | a0002c0002t0003g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8419-487A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345256 | ||||||
| chr11:108345278
|
C | T | 2 | a0001c0001t0011g0196a0001c0001t0011g0197 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.8419-465C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345278 | ||||||
| chr11:108345307
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.8419-436T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345307 | ||||||
| chr11:108345321
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8419-422T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345321 | ||||||
| chr11:108345354
|
A | G | 2 | a0001c0008t0002g0042a0001c0008t0002g0043 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.8419-389A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345354 | ||||||
| chr11:108345481
|
G | A | 2 | a0001c0010t0002g0029a0001c0010t0002g0030 | 2 | HG00738.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.8419-262G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345481 | ||||||
| chr11:108345724
|
A | G | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.8419-19A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 57/62 | chr11 | 108345724 | ||||||
| chr11:108346091
|
T | C | 10 | a0001c0001t0001g0199a0001c0001t0001g0203a0001c0001t0001g0224others(7): Show | 10 | HG02135.hp2 NA18961.hp2 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.8584+183T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346091 | ||||||
| chr11:108346322
|
T | G | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.8584+414T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346322 | ||||||
| chr11:108346325
|
T | G | 14 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(11): Show | 14 | HG01123.hp1 HG01175.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.8584+417T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346325 | ||||||
| chr11:108346396
|
A | G | 1 | a0003c0003t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.8584+488A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346396 | ||||||
| chr11:108346398
|
T | G | 10 | a0004c0004t0005g0004a0005c0006t0005g0165a0005c0006t0005g0166others(7): Show | 10 | HG02602.hp1 HG03688.hp1 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.8584+490T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346398 | ||||||
| chr11:108346404
|
T | C | 10 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(7): Show | 10 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.8584+496T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346404 | ||||||
| chr11:108346538
|
C | T | 2 | a0001c0008t0002g0042a0001c0008t0002g0043 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.8584+630C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346538 | ||||||
| chr11:108346657
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.8585-622A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108346657 | ||||||
| chr11:108347050
|
A | T | 10 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(7): Show | 10 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.8585-229A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 58/62 | chr11 | 108347050 | ||||||
| chr11:108347469
|
T | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.8671+104T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108347469 | ||||||
| chr11:108347586
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8671+221G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108347586 | ||||||
| chr11:108347589
|
C | A | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.8671+224C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108347589 | ||||||
| chr11:108347589
|
C | G | 1 | a0001c0001t0001g0256 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.8671+224C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108347589 | ||||||
| chr11:108347944
|
T | C | 2 | a0001c0001t0034g0152a0022c0021t0036g0008 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8671+579T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108347944 | ||||||
| chr11:108348120
|
A | G | 63 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0199others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.8671+755A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348120 | ||||||
| chr11:108348178
|
T | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.8671+813T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348178 | ||||||
| chr11:108348537
|
T | C | 4 | a0001c0008t0002g0041a0001c0008t0002g0042a0001c0008t0002g0043others(1): Show | 4 | HG03098.hp2 HG03195.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.8671+1172T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348537 | ||||||
| chr11:108348612
|
C | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.8671+1247C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348612 | ||||||
| chr11:108348693
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8671+1328G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348693 | ||||||
| chr11:108348703
|
G | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.8671+1338G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348703 | ||||||
| chr11:108348769
|
T | C | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8671+1404T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348769 | ||||||
| chr11:108348818
|
TAGG | T | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.8671+1456_8671+145 others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | INFO_REALIGN_3_PRIME | chr11 | 108348818 | |||||
| chr11:108348914
|
A | T | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.8671+1549A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348914 | ||||||
| chr11:108348968
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.8671+1603T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108348968 | ||||||
| chr11:108349031
|
T | C | 1 | a0009c0013t0012g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.8671+1666T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349031 | ||||||
| chr11:108349060
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.8671+1695C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349060 | ||||||
| chr11:108349061
|
G | A | 11 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(8): Show | 11 | HG02132.hp1 HG02451.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.8671+1696G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349061 | ||||||
| chr11:108349393
|
G | A | 3 | a0002c0009t0022g0093a0002c0009t0022g0094a0009c0013t0012g0117 | 3 | HG01175.hp1 HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8671+2028G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349393 | ||||||
| chr11:108349519
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8671+2154C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349519 | ||||||
| chr11:108349600
|
T | C | 1 | a0001c0034t0002g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.8671+2235T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349600 | ||||||
| chr11:108349641
|
C | T | 10 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(7): Show | 10 | HG01123.hp1 HG02109.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.8671+2276C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349641 | ||||||
| chr11:108349670
|
G | C | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8671+2305G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349670 | ||||||
| chr11:108349716
|
G | A | 1 | a0001c0001t0002g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.8671+2351G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349716 | ||||||
| chr11:108349810
|
G | A | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.8671+2445G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349810 | ||||||
| chr11:108349930
|
C | T | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0198others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.8671+2565C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108349930 | ||||||
| chr11:108350062
|
A | C | 26 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(23): Show | 26 | HG01070.hp1 HG01081.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.8671+2697A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350062 | ||||||
| chr11:108350209
|
G | C | 1 | a0006c0007t0001g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.8671+2844G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350209 | ||||||
| chr11:108350263
|
G | A | 1 | a0001c0012t0037g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8671+2898G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350263 | ||||||
| chr11:108350276
|
A | G | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.8671+2911A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350276 | ||||||
| chr11:108350294
|
G | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.8671+2929G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350294 | ||||||
| chr11:108350372
|
A | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.8671+3007A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350372 | ||||||
| chr11:108350638
|
G | A | 4 | a0001c0001t0010g0205a0001c0001t0010g0220a0001c0001t0010g0221others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8672-3128G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350638 | ||||||
| chr11:108350646
|
G | T | 1 | a0001c0012t0024g0300 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.8672-3120G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350646 | ||||||
| chr11:108350755
|
A | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.8672-3011A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350755 | ||||||
| chr11:108350756
|
G | C | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.8672-3010G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350756 | ||||||
| chr11:108350771
|
T | C | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.8672-2995T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350771 | ||||||
| chr11:108350784
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.8672-2982T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350784 | ||||||
| chr11:108350867
|
A | AC | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.8672-2899_8672-289 others(5): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350867 | ||||||
| chr11:108350869
|
T | A | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.8672-2897T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350869 | ||||||
| chr11:108350938
|
C | G | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.8672-2828C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350938 | ||||||
| chr11:108350949
|
A | G | 1 | a0006c0007t0009g0162 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.8672-2817A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108350949 | ||||||
| chr11:108351270
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8672-2496G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108351270 | ||||||
| chr11:108351322
|
G | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0267 | 2 | NA18986.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.8672-2444G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108351322 | ||||||
| chr11:108351828
|
G | A | 5 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(2): Show | 5 | HG00140.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.8672-1938G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108351828 | ||||||
| chr11:108352074
|
C | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8672-1692C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108352074 | ||||||
| chr11:108352518
|
C | T | 1 | a0001c0012t0037g0301 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8672-1248C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108352518 | ||||||
| chr11:108352601
|
T | C | 2 | a0001c0001t0016g0009a0002c0005t0003g0096 | 2 | HG01109.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.8672-1165T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108352601 | ||||||
| chr11:108352605
|
C | A | 6 | a0006c0007t0001g0150a0006c0007t0001g0156a0006c0007t0001g0157others(3): Show | 6 | HG02451.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.8672-1161C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108352605 | ||||||
| chr11:108352648
|
G | A | 1 | a0009c0013t0012g0117 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.8672-1118G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108352648 | ||||||
| chr11:108352664
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.8672-1102T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108352664 | ||||||
| chr11:108353063
|
G | C | 1 | a0001c0012t0024g0300 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.8672-703G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108353063 | ||||||
| chr11:108353146
|
A | G | 1 | a0013c0018t0001g0231 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.8672-620A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108353146 | ||||||
| chr11:108353155
|
AT | A | 10 | a0001c0001t0002g0034a0001c0001t0002g0088a0001c0001t0002g0089others(7): Show | 10 | HG01074.hp1 HG02486.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.8672-599delT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | INFO_REALIGN_3_PRIME | chr11 | 108353155 | |||||
| chr11:108353211
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.8672-555C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108353211 | ||||||
| chr11:108353300
|
T | C | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8672-466T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108353300 | ||||||
| chr11:108353662
|
G | A | 8 | a0002c0005t0008g0095a0002c0005t0008g0097a0002c0005t0008g0098others(5): Show | 8 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.8672-104G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 59/62 | chr11 | 108353662 | ||||||
| chr11:108353888
|
A | C | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG00099.hp1 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.8786+8A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108353888 | ||||||
| chr11:108353900
|
G | C | 1 | a0001c0001t0002g0068 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.8786+20G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108353900 | ||||||
| chr11:108353908
|
A | G | 2 | a0001c0001t0019g0246a0001c0001t0019g0253 | 2 | NA18970.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.8786+28A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108353908 | ||||||
| chr11:108353970
|
G | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.8786+90G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108353970 | ||||||
| chr11:108354058
|
T | TAC | 8 | a0001c0001t0001g0006a0001c0001t0001g0204a0001c0001t0001g0269others(5): Show | 8 | HG00099.hp2 HG00639.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.8786+188_8786+189d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354058 | |||||
| chr11:108354058
|
T | TACAC | 9 | a0001c0001t0001g0201a0001c0001t0010g0220a0001c0001t0018g0294others(6): Show | 9 | HG00558.hp1 HG00639.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.8786+186_8786+189d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354058 | |||||
| chr11:108354058
|
T | TACACAC | 6 | a0001c0001t0001g0252a0001c0001t0001g0282a0001c0001t0010g0221others(3): Show | 6 | HG00280.hp1 HG00733.hp2 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.8786+184_8786+189d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354058 | |||||
| chr11:108354058
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0214 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.8786+189_8786+190i others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354058 | |||||
| chr11:108354058
|
TACACACA others(13): Show |
T | 4 | a0001c0001t0001g0208a0001c0001t0001g0210a0001c0001t0001g0255others(1): Show | 4 | NA18955.hp2 NA18967.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.8786+190_8786+209d others(22): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354058 | |||||
| chr11:108354060
|
CACACACA others(3): Show |
C | 1 | a0005c0006t0005g0173 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.8786+190_8786+199d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354060 | |||||
| chr11:108354062
|
CACACACA others(1): Show |
C | 12 | a0003c0003t0001g0192a0003c0003t0001g0193a0004c0004t0004g0168others(9): Show | 12 | HG01123.hp1 HG01515.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.8786+190_8786+197d others(10): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354062 | |||||
| chr11:108354064
|
CACACAA | C | 13 | a0001c0001t0001g0285a0001c0001t0017g0175a0001c0001t0019g0246others(10): Show | 13 | HG02615.hp1 HG03209.hp2 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.8786+190_8786+195d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354064 | |||||
| chr11:108354066
|
CACAA | C | 12 | a0001c0001t0001g0213a0001c0001t0001g0225a0001c0001t0001g0284others(9): Show | 12 | HG00099.hp1 HG01978.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.8786+190_8786+193d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354066 | |||||
| chr11:108354068
|
CAA | C | 64 | a0001c0001t0001g0005a0001c0001t0001g0153a0001c0001t0001g0158others(61): Show | 64 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.8786+190_8786+191d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354068 | |||||
| chr11:108354070
|
A | AAC | 68 | a0001c0001t0002g0021a0001c0001t0002g0024a0001c0001t0002g0034others(65): Show | 68 | HG00408.hp2 HG00544.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.8786+225_8786+226d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
A | AACAC | 16 | a0001c0001t0002g0019a0001c0001t0002g0026a0001c0001t0006g0051others(13): Show | 16 | HG00323.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.8786+223_8786+226d others(6): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
A | AACACAC | 4 | a0001c0001t0007g0076a0001c0008t0002g0041a0001c0008t0002g0042others(1): Show | 4 | HG03098.hp2 HG03195.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.8786+221_8786+226d others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
A | AACACACA others(1): Show |
10 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0137others(7): Show | 10 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.8786+219_8786+226d others(10): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
A | AACACACA others(3): Show |
2 | a0002c0002t0003g0138a0002c0002t0003g0144 | 2 | HG01070.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.8786+217_8786+226d others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
A | AACACACA others(5): Show |
2 | a0002c0002t0003g0136a0002c0002t0003g0148 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8786+215_8786+226d others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
A | C | 48 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0201others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.8786+190A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354070 | ||||||
| chr11:108354070
|
AAC | A | 7 | a0001c0001t0002g0063a0001c0001t0023g0002a0001c0001t0032g0304others(4): Show | 7 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.8786+225_8786+226d others(4): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
AACACACA others(5): Show |
A | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.8786+215_8786+226d others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354070
|
AACACACA others(7): Show |
A | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8786+213_8786+226d others(16): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354070 | |||||
| chr11:108354076
|
C | CACACACA others(3): Show |
2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8786+205_8786+206i others(12): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354076 | |||||
| chr11:108354082
|
C | CACACAT | 3 | a0001c0012t0024g0303a0001c0012t0038g0302a0022c0021t0036g0008 | 3 | HG00140.hp2 HG02717.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.8786+207_8786+208i others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | INFO_REALIGN_3_PRIME | chr11 | 108354082 | |||||
| chr11:108354150
|
G | A | 3 | a0001c0001t0002g0061a0001c0001t0002g0065a0001c0001t0002g0121 | 3 | HG01496.hp2 HG02523.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.8786+270G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354150 | ||||||
| chr11:108354479
|
A | T | 2 | a0001c0016t0002g0014a0001c0016t0002g0015 | 2 | HG00323.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.8787-332A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354479 | ||||||
| chr11:108354496
|
T | C | 2 | a0001c0001t0034g0152a0022c0021t0036g0008 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8787-315T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354496 | ||||||
| chr11:108354588
|
T | C | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8787-223T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354588 | ||||||
| chr11:108354646
|
G | A | 1 | a0001c0001t0020g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.8787-165G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354646 | ||||||
| chr11:108354746
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.8787-65G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354746 | ||||||
| chr11:108354756
|
C | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.8787-55C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 60/62 | chr11 | 108354756 | ||||||
| chr11:108354934
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.8850+60A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108354934 | ||||||
| chr11:108354979
|
G | A | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.8850+105G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108354979 | ||||||
| chr11:108355298
|
A | G | 197 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.8850+424A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108355298 | ||||||
| chr11:108355513
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.8850+639C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108355513 | ||||||
| chr11:108355561
|
C | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8850+687C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108355561 | ||||||
| chr11:108355622
|
T | G | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.8850+748T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108355622 | ||||||
| chr11:108355672
|
T | C | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.8850+798T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108355672 | ||||||
| chr11:108355693
|
G | A | 8 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0032g0304others(5): Show | 8 | HG01074.hp1 HG02486.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.8850+819G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108355693 | ||||||
| chr11:108356028
|
G | A | 6 | a0001c0001t0034g0152a0001c0012t0024g0300a0001c0012t0024g0303others(3): Show | 6 | HG00140.hp2 HG02717.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.8850+1154G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356028 | ||||||
| chr11:108356056
|
C | A | 1 | a0016c0031t0002g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.8850+1182C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356056 | ||||||
| chr11:108356128
|
A | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.8850+1254A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356128 | ||||||
| chr11:108356199
|
C | T | 1 | a0023c0033t0012g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.8850+1325C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356199 | ||||||
| chr11:108356200
|
G | A | 1 | a0003c0003t0001g0189 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.8850+1326G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356200 | ||||||
| chr11:108356263
|
C | T | 2 | a0003c0003t0001g0192a0003c0003t0001g0193 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.8850+1389C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356263 | ||||||
| chr11:108356264
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.8850+1390G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356264 | ||||||
| chr11:108356404
|
C | T | 4 | a0001c0001t0001g0225a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+1530C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356404 | ||||||
| chr11:108356407
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.8850+1533G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356407 | ||||||
| chr11:108356451
|
G | A | 1 | a0017c0030t0002g0126 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.8850+1577G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356451 | ||||||
| chr11:108356506
|
A | C | 21 | a0001c0001t0034g0152a0004c0004t0004g0168a0004c0004t0004g0169others(18): Show | 21 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.8850+1632A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356506 | ||||||
| chr11:108356531
|
T | TGTC | 19 | a0001c0001t0002g0024a0001c0001t0002g0063a0001c0001t0002g0066others(16): Show | 19 | HG00408.hp2 HG01975.hp1 HG02004.hp2 others(16): Show |
intron_variant | MODIFIER | c.8850+1658_8850+166 others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | INFO_REALIGN_3_PRIME | chr11 | 108356531 | |||||
| chr11:108356540
|
T | TA | 26 | a0001c0001t0001g0164a0001c0001t0001g0201a0001c0001t0001g0288others(23): Show | 26 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.8850+1686dupA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | INFO_REALIGN_3_PRIME | chr11 | 108356540 | |||||
| chr11:108356540
|
TA | T | 25 | a0001c0001t0001g0158a0001c0001t0001g0245a0001c0001t0001g0254others(22): Show | 25 | HG00140.hp2 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.8850+1686delA | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | INFO_REALIGN_3_PRIME | chr11 | 108356540 | |||||
| chr11:108356541
|
A | T | 12 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0137others(9): Show | 12 | HG01081.hp2 HG01243.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.8850+1667A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356541 | ||||||
| chr11:108356542
|
A | T | 4 | a0002c0002t0003g0136a0002c0002t0003g0138a0002c0002t0003g0143others(1): Show | 4 | HG01070.hp1 HG02109.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.8850+1668A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356542 | ||||||
| chr11:108356555
|
A | C | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8850+1681A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356555 | ||||||
| chr11:108356665
|
G | C | 6 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(3): Show | 6 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.8850+1791G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356665 | ||||||
| chr11:108356717
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8850+1843G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356717 | ||||||
| chr11:108356748
|
T | A | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.8850+1874T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356748 | ||||||
| chr11:108356842
|
C | G | 8 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0001t0001g0262others(5): Show | 8 | HG02004.hp1 NA18942.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.8850+1968C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356842 | ||||||
| chr11:108356898
|
C | T | 2 | a0002c0009t0003g0134a0002c0009t0003g0135 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.8850+2024C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356898 | ||||||
| chr11:108356914
|
C | G | 1 | a0023c0033t0012g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.8850+2040C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356914 | ||||||
| chr11:108356929
|
C | G | 1 | a0001c0001t0007g0064 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.8850+2055C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356929 | ||||||
| chr11:108356953
|
G | A | 2 | a0002c0002t0003g0085a0002c0002t0003g0086 | 2 | HG01081.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.8850+2079G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356953 | ||||||
| chr11:108356986
|
G | A | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8850+2112G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356986 | ||||||
| chr11:108356990
|
G | C | 1 | a0001c0001t0013g0025 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.8850+2116G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356990 | ||||||
| chr11:108356992
|
G | C | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8850+2118G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108356992 | ||||||
| chr11:108357043
|
C | T | 1 | a0002c0005t0003g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8850+2169C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357043 | ||||||
| chr11:108357087
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.8850+2213C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357087 | ||||||
| chr11:108357238
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8850+2364G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357238 | ||||||
| chr11:108357249
|
C | T | 1 | a0001c0001t0017g0175 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.8850+2375C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357249 | ||||||
| chr11:108357258
|
A | T | 29 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(26): Show | 29 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.8850+2384A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357258 | ||||||
| chr11:108357283
|
T | C | 159 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.8850+2409T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357283 | ||||||
| chr11:108357309
|
C | T | 1 | a0019c0022t0002g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.8850+2435C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357309 | ||||||
| chr11:108357317
|
G | A | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8850+2443G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357317 | ||||||
| chr11:108357366
|
G | A | 1 | a0001c0001t0023g0002 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.8850+2492G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357366 | ||||||
| chr11:108357414
|
C | T | 1 | a0001c0001t0016g0009 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8850+2540C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357414 | ||||||
| chr11:108357415
|
G | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8850+2541G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357415 | ||||||
| chr11:108357423
|
C | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0265others(1): Show | 4 | NA18954.hp2 NA18962.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.8850+2549C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357423 | ||||||
| chr11:108357490
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+2616C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357490 | ||||||
| chr11:108357548
|
T | G | 5 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(2): Show | 5 | HG00140.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.8850+2674T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357548 | ||||||
| chr11:108357566
|
T | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0163 | 2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.8850+2692T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357566 | ||||||
| chr11:108357596
|
C | G | 1 | a0005c0006t0005g0174 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.8850+2722C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357596 | ||||||
| chr11:108357597
|
G | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0163 | 2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.8850+2723G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357597 | ||||||
| chr11:108357600
|
C | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0163 | 2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.8850+2726C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357600 | ||||||
| chr11:108357604
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0163 | 2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.8850+2730A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357604 | ||||||
| chr11:108357623
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.8850+2749G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357623 | ||||||
| chr11:108357629
|
T | C | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.8850+2755T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357629 | ||||||
| chr11:108357639
|
T | C | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.8850+2765T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357639 | ||||||
| chr11:108357645
|
C | A | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.8850+2771C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357645 | ||||||
| chr11:108357665
|
G | A | 8 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0001t0001g0262others(5): Show | 8 | HG02004.hp1 NA18942.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.8850+2791G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357665 | ||||||
| chr11:108357699
|
C | T | 6 | a0001c0001t0007g0060a0001c0001t0007g0064a0001c0001t0007g0073others(3): Show | 6 | NA18959.hp1 NA18973.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.8850+2825C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357699 | ||||||
| chr11:108357700
|
G | A | 4 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116others(1): Show | 4 | HG00140.hp2 HG01109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+2826G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357700 | ||||||
| chr11:108357854
|
A | G | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.8850+2980A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357854 | ||||||
| chr11:108357878
|
C | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0163 | 2 | NA18964.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.8850+3004C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357878 | ||||||
| chr11:108357886
|
A | G | 5 | a0001c0001t0002g0108a0009c0013t0012g0117a0009c0013t0012g0119others(2): Show | 5 | HG01175.hp1 HG02165.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.8850+3012A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357886 | ||||||
| chr11:108357907
|
C | T | 6 | a0001c0001t0001g0201a0001c0001t0001g0214a0001c0001t0010g0205others(3): Show | 6 | HG01255.hp1 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.8850+3033C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357907 | ||||||
| chr11:108357926
|
C | T | 1 | a0002c0009t0003g0134 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8850+3052C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108357926 | ||||||
| chr11:108358004
|
G | A | 1 | a0001c0001t0020g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.8850+3130G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358004 | ||||||
| chr11:108358030
|
T | G | 14 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(11): Show | 14 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.8850+3156T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358030 | ||||||
| chr11:108358038
|
C | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.8850+3164C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358038 | ||||||
| chr11:108358045
|
G | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+3171G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358045 | ||||||
| chr11:108358059
|
A | C | 2 | a0001c0012t0024g0300a0001c0012t0024g0303 | 2 | NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.8850+3185A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358059 | ||||||
| chr11:108358060
|
G | A | 2 | a0001c0012t0024g0300a0001c0012t0024g0303 | 2 | NA18954.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.8850+3186G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358060 | ||||||
| chr11:108358138
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+3264T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358138 | ||||||
| chr11:108358225
|
C | T | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.8850+3351C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358225 | ||||||
| chr11:108358250
|
G | T | 2 | a0001c0001t0002g0046a0001c0001t0002g0047 | 2 | HG02135.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.8850+3376G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358250 | ||||||
| chr11:108358263
|
T | C | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8850+3389T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358263 | ||||||
| chr11:108358313
|
G | A | 99 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0019others(96): Show | 99 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.8850+3439G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358313 | ||||||
| chr11:108358366
|
A | G | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8850+3492A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358366 | ||||||
| chr11:108358397
|
C | T | 2 | a0001c0008t0002g0042a0001c0008t0002g0043 | 2 | HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.8850+3523C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358397 | ||||||
| chr11:108358423
|
C | T | 1 | a0001c0027t0002g0074 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.8850+3549C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358423 | ||||||
| chr11:108358425
|
G | C | 1 | a0019c0022t0002g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.8850+3551G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358425 | ||||||
| chr11:108358431
|
G | C | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.8850+3557G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358431 | ||||||
| chr11:108358462
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.8850+3588T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358462 | ||||||
| chr11:108358477
|
C | T | 2 | a0001c0001t0006g0051a0001c0001t0006g0052 | 2 | HG02132.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.8850+3603C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358477 | ||||||
| chr11:108358590
|
A | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.8850+3716A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358590 | ||||||
| chr11:108358599
|
G | A | 5 | a0005c0006t0005g0173a0009c0013t0012g0117a0009c0013t0012g0119others(2): Show | 5 | HG01175.hp1 HG02257.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.8850+3725G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358599 | ||||||
| chr11:108358624
|
G | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0256 | 3 | NA18982.hp2 NA19004.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.8850+3750G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358624 | ||||||
| chr11:108358635
|
A | G | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8850+3761A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358635 | ||||||
| chr11:108358683
|
T | C | 1 | a0001c0001t0017g0175 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.8850+3809T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358683 | ||||||
| chr11:108358687
|
G | T | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+3813G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358687 | ||||||
| chr11:108358704
|
C | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+3830C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358704 | ||||||
| chr11:108358712
|
T | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+3838T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358712 | ||||||
| chr11:108358771
|
A | G | 162 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.8850+3897A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358771 | ||||||
| chr11:108358803
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.8850+3929C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358803 | ||||||
| chr11:108358820
|
G | A | 3 | a0001c0001t0002g0065a0001c0001t0002g0121a0001c0001t0002g0129 | 3 | HG01496.hp2 HG02602.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.8850+3946G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358820 | ||||||
| chr11:108358863
|
G | A | 20 | a0004c0004t0004g0168a0004c0004t0004g0169a0004c0004t0004g0176others(17): Show | 20 | HG01123.hp1 HG02109.hp1 HG02602.hp1 others(17): Show |
intron_variant | MODIFIER | c.8850+3989G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358863 | ||||||
| chr11:108358895
|
C | A | 1 | a0001c0001t0001g0277 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.8850+4021C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108358895 | ||||||
| chr11:108359025
|
A | G | 1 | a0002c0002t0003g0139 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.8850+4151A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359025 | ||||||
| chr11:108359057
|
C | T | 2 | a0001c0001t0001g0226a0005c0006t0005g0174 | 2 | HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.8850+4183C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359057 | ||||||
| chr11:108359072
|
A | G | 1 | a0001c0001t0029g0016 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.8850+4198A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359072 | ||||||
| chr11:108359104
|
T | A | 5 | a0001c0010t0002g0029a0001c0010t0002g0030a0001c0010t0002g0032others(2): Show | 5 | HG00738.hp2 HG01099.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.8850+4230T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359104 | ||||||
| chr11:108359111
|
C | G | 2 | a0001c0008t0016g0115a0001c0008t0016g0116 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8850+4237C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359111 | ||||||
| chr11:108359147
|
T | C | 63 | a0001c0001t0001g0005a0001c0001t0001g0198a0001c0001t0001g0199others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.8850+4273T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359147 | ||||||
| chr11:108359191
|
A | G | 7 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(4): Show | 7 | HG01261.hp1 HG02559.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.8850+4317A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359191 | ||||||
| chr11:108359317
|
A | G | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8850+4443A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359317 | ||||||
| chr11:108359334
|
C | T | 1 | a0002c0005t0008g0102 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.8850+4460C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359334 | ||||||
| chr11:108359408
|
A | G | 1 | a0001c0001t0021g0028 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.8850+4534A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359408 | ||||||
| chr11:108359428
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.8850+4554G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359428 | ||||||
| chr11:108359442
|
G | A | 1 | a0003c0003t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.8850+4568G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359442 | ||||||
| chr11:108359472
|
C | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0089 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.8850+4598C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359472 | ||||||
| chr11:108359473
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8850+4599C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359473 | ||||||
| chr11:108359496
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+4622T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359496 | ||||||
| chr11:108359512
|
C | T | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.8850+4638C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359512 | ||||||
| chr11:108359534
|
C | A | 31 | a0001c0001t0001g0159a0002c0002t0003g0085a0002c0002t0003g0086others(28): Show | 31 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.8850+4660C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359534 | ||||||
| chr11:108359709
|
T | C | 299 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(296): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.8850+4835T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359709 | ||||||
| chr11:108359837
|
G | T | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8850+4963G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359837 | ||||||
| chr11:108359881
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+5007A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359881 | ||||||
| chr11:108359918
|
T | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8850+5044T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359918 | ||||||
| chr11:108359938
|
A | G | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.8850+5064A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359938 | ||||||
| chr11:108359953
|
G | T | 26 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0026others(23): Show | 26 | HG00544.hp2 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.8850+5079G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359953 | ||||||
| chr11:108359983
|
C | G | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-5099C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108359983 | ||||||
| chr11:108360000
|
A | T | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.8851-5082A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360000 | ||||||
| chr11:108360026
|
T | C | 1 | a0001c0001t0010g0205 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.8851-5056T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360026 | ||||||
| chr11:108360037
|
G | A | 1 | a0011c0017t0002g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.8851-5045G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360037 | ||||||
| chr11:108360044
|
C | T | 1 | a0008c0015t0002g0012 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8851-5038C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360044 | ||||||
| chr11:108360068
|
AAGAG | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0019 | 3 | HG01346.hp2 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.8851-5010_8851-500 others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | INFO_REALIGN_3_PRIME | chr11 | 108360068 | |||||
| chr11:108360133
|
A | C | 1 | a0001c0001t0001g0289 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.8851-4949A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360133 | ||||||
| chr11:108360146
|
C | T | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.8851-4936C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360146 | ||||||
| chr11:108360173
|
C | A | 4 | a0001c0012t0024g0300a0001c0012t0024g0303a0001c0012t0037g0301others(1): Show | 4 | HG00140.hp2 HG02818.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-4909C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360173 | ||||||
| chr11:108360253
|
T | C | 1 | a0002c0002t0003g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.8851-4829T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360253 | ||||||
| chr11:108360273
|
G | GT | 155 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.8851-4808dupT | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | INFO_REALIGN_3_PRIME | chr11 | 108360273 | |||||
| chr11:108360350
|
T | C | 1 | a0002c0005t0008g0098 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8851-4732T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360350 | ||||||
| chr11:108360388
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.8851-4694T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360388 | ||||||
| chr11:108360432
|
C | T | 4 | a0001c0001t0010g0205a0001c0001t0010g0220a0001c0001t0010g0221others(1): Show | 4 | HG01255.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-4650C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360432 | ||||||
| chr11:108360445
|
A | T | 1 | a0004c0004t0005g0004 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.8851-4637A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360445 | ||||||
| chr11:108360504
|
T | G | 7 | a0001c0001t0002g0127a0001c0001t0002g0128a0001c0001t0002g0129others(4): Show | 7 | HG01261.hp1 HG02559.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.8851-4578T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360504 | ||||||
| chr11:108360582
|
C | A | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.8851-4500C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360582 | ||||||
| chr11:108360725
|
A | G | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8851-4357A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360725 | ||||||
| chr11:108360726
|
G | A | 16 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(13): Show | 16 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.8851-4356G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360726 | ||||||
| chr11:108360731
|
T | G | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8851-4351T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360731 | ||||||
| chr11:108360744
|
C | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.8851-4338C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360744 | ||||||
| chr11:108360767
|
C | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-4315C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360767 | ||||||
| chr11:108360776
|
A | G | 4 | a0008c0015t0002g0012a0008c0015t0002g0013a0008c0029t0002g0007others(1): Show | 4 | HG02572.hp2 HG02717.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-4306A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360776 | ||||||
| chr11:108360795
|
T | C | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8851-4287T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360795 | ||||||
| chr11:108360823
|
A | G | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8851-4259A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360823 | ||||||
| chr11:108360824
|
A | T | 1 | a0001c0025t0001g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.8851-4258A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360824 | ||||||
| chr11:108360829
|
G | C | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.8851-4253G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360829 | ||||||
| chr11:108360928
|
T | C | 1 | a0001c0001t0028g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.8851-4154T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360928 | ||||||
| chr11:108360951
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-4131A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108360951 | ||||||
| chr11:108361013
|
G | C | 1 | a0001c0001t0002g0109 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.8851-4069G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361013 | ||||||
| chr11:108361022
|
T | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8851-4060T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361022 | ||||||
| chr11:108361034
|
A | G | 2 | a0001c0001t0026g0190a0003c0003t0001g0195 | 2 | HG00733.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.8851-4048A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361034 | ||||||
| chr11:108361051
|
C | T | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8851-4031C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361051 | ||||||
| chr11:108361052
|
T | C | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8851-4030T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361052 | ||||||
| chr11:108361053
|
G | A | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8851-4029G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361053 | ||||||
| chr11:108361131
|
C | G | 1 | a0001c0001t0020g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.8851-3951C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361131 | ||||||
| chr11:108361142
|
T | A | 1 | a0001c0001t0020g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.8851-3940T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361142 | ||||||
| chr11:108361156
|
GACAA | G | 4 | a0003c0003t0001g0185a0003c0003t0001g0186a0003c0003t0001g0187others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-3922_8851-391 others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | INFO_REALIGN_3_PRIME | chr11 | 108361156 | |||||
| chr11:108361223
|
A | G | 17 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(14): Show | 17 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.8851-3859A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361223 | ||||||
| chr11:108361427
|
T | C | 2 | a0001c0001t0034g0152a0022c0021t0036g0008 | 2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.8851-3655T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361427 | ||||||
| chr11:108361485
|
G | A | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8851-3597G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361485 | ||||||
| chr11:108361489
|
A | G | 7 | a0001c0001t0002g0087a0001c0010t0002g0029a0001c0010t0002g0030others(4): Show | 7 | HG00738.hp2 HG01099.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.8851-3593A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361489 | ||||||
| chr11:108361588
|
A | G | 1 | a0002c0005t0003g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8851-3494A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361588 | ||||||
| chr11:108361630
|
T | C | 84 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0019others(81): Show | 84 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.8851-3452T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361630 | ||||||
| chr11:108361649
|
C | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0214 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.8851-3433C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361649 | ||||||
| chr11:108361662
|
A | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-3420A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361662 | ||||||
| chr11:108361737
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.8851-3345C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361737 | ||||||
| chr11:108361748
|
G | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.8851-3334G>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361748 | ||||||
| chr11:108361786
|
C | G | 3 | a0001c0001t0002g0061a0001c0001t0002g0065a0001c0001t0002g0121 | 3 | HG01496.hp2 HG02523.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.8851-3296C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361786 | ||||||
| chr11:108361938
|
A | T | 1 | a0001c0001t0002g0021 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.8851-3144A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108361938 | ||||||
| chr11:108362128
|
A | T | 1 | a0019c0022t0002g0023 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.8851-2954A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362128 | ||||||
| chr11:108362216
|
C | T | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-2866C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362216 | ||||||
| chr11:108362217
|
A | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-2865A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362217 | ||||||
| chr11:108362229
|
C | T | 2 | a0002c0009t0022g0093a0002c0009t0022g0094 | 2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.8851-2853C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362229 | ||||||
| chr11:108362282
|
T | G | 18 | a0001c0001t0001g0006a0001c0001t0001g0201a0001c0001t0001g0214others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.8851-2800T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362282 | ||||||
| chr11:108362333
|
C | A | 8 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0001t0001g0262others(5): Show | 8 | HG02004.hp1 NA18942.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.8851-2749C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362333 | ||||||
| chr11:108362372
|
A | G | 1 | a0001c0001t0027g0258 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.8851-2710A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362372 | ||||||
| chr11:108362392
|
G | A | 14 | a0001c0001t0023g0002a0002c0005t0003g0096a0002c0005t0008g0095others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.8851-2690G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362392 | ||||||
| chr11:108362456
|
A | C | 1 | a0001c0001t0001g0291 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.8851-2626A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362456 | ||||||
| chr11:108362493
|
T | G | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8851-2589T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362493 | ||||||
| chr11:108362497
|
C | G | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-2585C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362497 | ||||||
| chr11:108362512
|
C | T | 1 | a0002c0005t0015g0100 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8851-2570C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362512 | ||||||
| chr11:108362560
|
CAAT | C | 6 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0003g0138others(3): Show | 6 | HG01070.hp1 HG02109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.8851-2521_8851-251 others(7): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362560 | ||||||
| chr11:108362619
|
A | C | 1 | a0014c0032t0002g0011 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.8851-2463A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362619 | ||||||
| chr11:108362730
|
A | T | 1 | a0005c0006t0030g0167 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.8851-2352A>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362730 | ||||||
| chr11:108362777
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-2305T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362777 | ||||||
| chr11:108362811
|
C | G | 2 | a0001c0001t0001g0282a0005c0006t0005g0170 | 2 | HG03927.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.8851-2271C>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362811 | ||||||
| chr11:108362811
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.8851-2271C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362811 | ||||||
| chr11:108362828
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.8851-2254T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362828 | ||||||
| chr11:108362940
|
AAAAGTAT others(3): Show |
A | 1 | a0001c0001t0001g0271 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.8851-2141_8851-213 others(14): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362940 | ||||||
| chr11:108362969
|
AC | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8851-2112delC | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362969 | ||||||
| chr11:108362977
|
C | A | 2 | a0001c0001t0023g0002a0022c0021t0036g0008 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.8851-2105C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108362977 | ||||||
| chr11:108362978
|
AAAAC | A | 3 | a0001c0001t0034g0152a0001c0008t0002g0041a0001c0008t0002g0044 | 3 | HG02895.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.8851-2092_8851-208 others(8): Show |
ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | INFO_REALIGN_3_PRIME | chr11 | 108362978 | |||||
| chr11:108363046
|
C | T | 1 | a0002c0002t0003g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.8851-2036C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363046 | ||||||
| chr11:108363073
|
C | A | 161 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.8851-2009C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363073 | ||||||
| chr11:108363115
|
T | C | 4 | a0009c0013t0012g0117a0009c0013t0012g0119a0009c0013t0012g0120others(1): Show | 4 | HG01175.hp1 HG02257.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.8851-1967T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363115 | ||||||
| chr11:108363212
|
T | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.8851-1870T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363212 | ||||||
| chr11:108363279
|
G | A | 30 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(27): Show | 30 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.8851-1803G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363279 | ||||||
| chr11:108363442
|
T | C | 4 | a0001c0001t0011g0154a0001c0001t0011g0155a0001c0001t0011g0196others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.8851-1640T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363442 | ||||||
| chr11:108363483
|
G | A | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8851-1599G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363483 | ||||||
| chr11:108363493
|
C | A | 1 | a0009c0013t0012g0120 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.8851-1589C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363493 | ||||||
| chr11:108363504
|
T | C | 11 | a0002c0005t0003g0096a0002c0005t0008g0095a0002c0005t0008g0097others(8): Show | 11 | HG02055.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.8851-1578T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363504 | ||||||
| chr11:108363532
|
T | C | 1 | a0001c0001t0034g0152 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8851-1550T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363532 | ||||||
| chr11:108363616
|
A | G | 1 | a0002c0002t0003g0146 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.8851-1466A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363616 | ||||||
| chr11:108363731
|
G | C | 1 | a0002c0009t0035g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8851-1351G>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108363731 | ||||||
| chr11:108364023
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.8851-1059C>T | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364023 | ||||||
| chr11:108364109
|
A | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0198others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.8851-973A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364109 | ||||||
| chr11:108364324
|
T | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0265 | 2 | NA18962.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.8851-758T>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364324 | ||||||
| chr11:108364388
|
C | A | 13 | a0001c0001t0026g0190a0003c0003t0001g0185a0003c0003t0001g0186others(10): Show | 13 | HG00558.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.8851-694C>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364388 | ||||||
| chr11:108364460
|
T | C | 3 | a0001c0001t0016g0009a0001c0008t0016g0115a0001c0008t0016g0116 | 3 | HG01109.hp2 HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.8851-622T>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364460 | ||||||
| chr11:108364538
|
A | G | 29 | a0002c0002t0003g0085a0002c0002t0003g0086a0002c0002t0003g0136others(26): Show | 29 | HG01070.hp1 HG01081.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.8851-544A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364538 | ||||||
| chr11:108364543
|
T | G | 2 | a0001c0001t0020g0048a0001c0001t0020g0082 | 2 | NA18982.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.8851-539T>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364543 | ||||||
| chr11:108364706
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.8851-376A>G | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364706 | ||||||
| chr11:108364836
|
G | A | 3 | a0002c0005t0015g0099a0002c0005t0015g0100a0002c0005t0015g0101 | 3 | HG02647.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.8851-246G>A | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364836 | ||||||
| chr11:108364901
|
A | C | 2 | a0001c0001t0001g0223a0001c0001t0001g0267 | 2 | NA18986.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.8851-181A>C | ATM | ENSG00000149311.21 | transcript | ENST00000675843.1 | protein_coding | 61/62 | chr11 | 108364901 |