Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 83605 |
|---|---|
| ensemblid | ENSG00000136280.17 |
| hgncid | 21708 |
| symbol | CCM2 |
| name | CCM2 scaffold protein |
| refseq_nuc | NM_031443.4 |
| refseq_prot | NP_113631.1 |
| ensembl_nuc | ENST00000258781.11 |
| ensembl_prot | ENSP00000258781.7 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 45000201 |
| end | 45076453 |
| strand | + |
| ver | v1.2 |
| region | chr7:45000201-45076453 |
| region5000 | chr7:44995201-45081453 |
| regionname0 | CCM2_chr7_45000201_45076453 |
| regionname5000 | CCM2_chr7_44995201_45081453 |
| 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 | 444 | 254 | 78 | 47 | 87 | 11 | 29 | 69 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002 | 0/0 | 444 | 41 | 1 | 13 | 18 | 2 | 7 | 13 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0003 | 0/0 | 444 | 13 | 1 | 10 | 2 | 0 | 0 | 2 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0004 | 0/0 | 444 | 5 | 0 | 2 | 0 | 3 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0005 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0006 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0007 | 0/0 | 444 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| 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 | 1/0 | 1335 | 164 | 47 | 28 | 56 | 8 | 24 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0002 | 0/1 | 1335 | 77 | 19 | 19 | 30 | 3 | 5 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0003 | 0/0 | 1335 | 30 | 1 | 12 | 8 | 2 | 7 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0004 | 0/0 | 1335 | 13 | 1 | 10 | 2 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0005 | 0/0 | 1335 | 8 | 0 | 0 | 8 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0006 | 0/0 | 1335 | 7 | 7 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0007 | 0/0 | 1335 | 5 | 0 | 2 | 0 | 3 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0008 | 0/0 | 1335 | 5 | 5 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0009 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0010 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0011 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0012 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0013 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0014 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| c0015 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 530 | 228 | 57 | 42 | 88 | 12 | 27 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| t0002 | 0/0 | 530 | 81 | 20 | 28 | 20 | 4 | 9 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| t0003 | 0/0 | 530 | 2 | 2 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| t0004 | 0/0 | 530 | 2 | 0 | 2 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| t0005 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| t0006 | 0/0 | 530 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| t0007 | 0/0 | 530 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| 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 | 1/0 | 1335 | 164 | 47 | 28 | 56 | 8 | 24 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0002 | 0/1 | 1335 | 77 | 19 | 19 | 30 | 3 | 5 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0006 | 0/0 | 1335 | 7 | 7 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0008 | 0/0 | 1335 | 5 | 5 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0013 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0003 | 0/0 | 1335 | 30 | 1 | 12 | 8 | 2 | 7 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0005 | 0/0 | 1335 | 8 | 0 | 0 | 8 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0009 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0010 | 0/0 | 1335 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0015 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0003c0004 | 0/0 | 1335 | 13 | 1 | 10 | 2 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0004c0007 | 0/0 | 1335 | 5 | 0 | 2 | 0 | 3 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0005c0011 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0006c0012 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0007c0014 | 0/0 | 1335 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1864 | 160 | 47 | 26 | 54 | 8 | 24 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0001t0004 | 0/0 | 1864 | 2 | 0 | 2 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0001t0005 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0001t0006 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0002t0001 | 0/1 | 1864 | 37 | 0 | 4 | 28 | 1 | 3 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0002t0002 | 0/0 | 1864 | 40 | 19 | 15 | 2 | 2 | 2 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0006t0001 | 0/0 | 1864 | 4 | 4 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0006t0003 | 0/0 | 1864 | 2 | 2 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0006t0007 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0008t0001 | 0/0 | 1864 | 5 | 5 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0001c0013t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0003t0002 | 0/0 | 1864 | 30 | 1 | 12 | 8 | 2 | 7 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0005t0002 | 0/0 | 1864 | 8 | 0 | 0 | 8 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0009t0002 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0010t0002 | 0/0 | 1864 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0002c0015t0002 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0003c0004t0001 | 0/0 | 1864 | 13 | 1 | 10 | 2 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0004c0007t0001 | 0/0 | 1864 | 5 | 0 | 2 | 0 | 3 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0005c0011t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0006c0012t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| a0007c0014t0001 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | copy fasta | chr7 | 44995201 | 45081453 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0004g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0006t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0006t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0006t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0006t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0006t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0008t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0008t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0008t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0008t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0008t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0001c0013t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0005t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0009t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0010t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0002c0015t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0003c0004t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0004c0007t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0004c0007t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0004c0007t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0004c0007t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0004c0007t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0005c0011t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0006c0012t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| a0007c0014t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00140 | hp2 | a0004 | c0007 | t0001 | g0300 | EUR | GBR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | FIN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0099 | EUR | FIN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00438 | hp2 | a0002 | c0015 | t0002 | g0085 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00558 | hp2 | a0002 | c0003 | t0002 | g0124 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00609 | hp2 | a0007 | c0014 | t0001 | g0165 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0131 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00642 | hp2 | a0004 | c0007 | t0001 | g0279 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00673 | hp2 | a0002 | c0005 | t0002 | g0083 | EAS | CHS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0058 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0140 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0310 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0157 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01069 | hp2 | a0002 | c0003 | t0002 | g0053 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01070 | hp1 | a0002 | c0003 | t0002 | g0033 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01071 | hp1 | a0002 | c0003 | t0002 | g0038 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0122 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01099 | hp2 | a0002 | c0003 | t0002 | g0081 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01106 | hp1 | a0002 | c0010 | t0002 | g0052 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01109 | hp2 | a0002 | c0003 | t0002 | g0045 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01167 | hp1 | a0002 | c0003 | t0002 | g0032 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01167 | hp2 | a0004 | c0007 | t0001 | g0200 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0159 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01192 | hp2 | a0002 | c0003 | t0002 | g0084 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01261 | hp1 | a0002 | c0003 | t0002 | g0087 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0208 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01358 | hp2 | a0002 | c0003 | t0002 | g0029 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0313 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0024 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01496 | hp2 | a0003 | c0004 | t0001 | g0228 | AMR | CLM | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01515 | hp1 | a0004 | c0007 | t0001 | g0248 | EUR | IBS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0129 | EUR | IBS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01516 | hp2 | a0002 | c0003 | t0002 | g0047 | EUR | IBS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01517 | hp1 | a0002 | c0003 | t0002 | g0046 | EUR | IBS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01517 | hp2 | a0004 | c0007 | t0001 | g0242 | EUR | IBS | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01884 | hp2 | a0001 | c0006 | t0001 | g0059 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0123 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0089 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01928 | hp2 | a0003 | c0004 | t0001 | g0225 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0139 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01952 | hp2 | a0003 | c0004 | t0001 | g0229 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0100 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01975 | hp2 | a0003 | c0004 | t0001 | g0226 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01978 | hp1 | a0003 | c0004 | t0001 | g0224 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01978 | hp2 | a0002 | c0003 | t0002 | g0086 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01981 | hp1 | a0002 | c0003 | t0002 | g0051 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01981 | hp2 | a0003 | c0004 | t0001 | g0230 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01993 | hp1 | a0003 | c0004 | t0001 | g0227 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02004 | hp1 | a0003 | c0004 | t0001 | g0169 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02071 | hp1 | a0002 | c0003 | t0002 | g0298 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02080 | hp1 | a0001 | c0013 | t0001 | g0245 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02129 | hp1 | a0002 | c0003 | t0002 | g0031 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02145 | hp1 | a0001 | c0006 | t0001 | g0161 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02145 | hp2 | a0002 | c0003 | t0002 | g0036 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02280 | hp2 | a0001 | c0006 | t0001 | g0061 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02300 | hp1 | a0003 | c0004 | t0001 | g0201 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0028 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02723 | hp1 | a0001 | c0006 | t0003 | g0077 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02735 | hp1 | a0002 | c0003 | t0002 | g0040 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0305 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02896 | hp1 | a0001 | c0008 | t0001 | g0011 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02897 | hp1 | a0001 | c0008 | t0001 | g0010 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0307 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0063 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02970 | hp2 | a0001 | c0008 | t0001 | g0009 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0048 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03130 | hp1 | a0001 | c0008 | t0001 | g0007 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0158 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0308 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03225 | hp2 | a0001 | c0006 | t0007 | g0162 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03492 | hp1 | a0002 | c0003 | t0002 | g0056 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0311 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0057 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0135 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03927 | hp1 | a0002 | c0003 | t0002 | g0079 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | BEB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04199 | hp1 | a0002 | c0003 | t0002 | g0078 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0299 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | STU | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18522 | hp1 | a0001 | c0006 | t0003 | g0076 | AFR | YRI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0306 | AFR | YRI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18940 | hp1 | a0002 | c0003 | t0002 | g0080 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18943 | hp2 | a0002 | c0005 | t0002 | g0039 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18947 | hp1 | a0003 | c0004 | t0001 | g0193 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18950 | hp1 | a0002 | c0005 | t0002 | g0043 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18953 | hp2 | a0002 | c0005 | t0002 | g0054 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18962 | hp2 | a0002 | c0003 | t0002 | g0044 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18963 | hp1 | a0003 | c0004 | t0001 | g0297 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18963 | hp2 | a0002 | c0009 | t0002 | g0082 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18970 | hp2 | a0002 | c0005 | t0002 | g0041 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0105 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18983 | hp1 | a0006 | c0012 | t0001 | g0196 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18987 | hp1 | a0005 | c0011 | t0001 | g0190 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18993 | hp1 | a0002 | c0003 | t0002 | g0035 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18998 | hp1 | a0002 | c0003 | t0002 | g0037 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0027 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19064 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19064 | hp2 | a0002 | c0005 | t0002 | g0042 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19075 | hp1 | a0002 | c0003 | t0002 | g0030 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19075 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19079 | hp1 | a0002 | c0005 | t0002 | g0050 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19083 | hp1 | a0002 | c0005 | t0002 | g0055 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0312 | AFR | YRI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ASW | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0309 | AFR | ASW | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | TSI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0092 | EUR | TSI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0138 | SAS | GIH | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG03471 | hp2 | a0001 | c0008 | t0001 | g0008 | AFR | MSL | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| HG06807 | hp2 | a0001 | c0006 | t0001 | g0060 | AFR | USA | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0120 | AFR | USA | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0231 | AFR | USA | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0098 | REF | REF | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0049 | REF | REF | CCM2_chr7_44995201_45081453 | CCM2 | chr7 | 44995201 | 45081453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45038379
|
G | A | 1 | a0004 | 5 | HG00140.hp2 HG00642.hp2 HG01167.hp2 others(2): Show |
missense_variant | MODERATE | c.157G>A | p.Val53Ile | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/10 | 290/1864 | 157/1335 | 53/444 | chr7 | 45038379 | ||
| chr7:45064532
|
G | A | 1 | a0002 | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
missense_variant | MODERATE | c.358G>A | p.Val120Ile | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/10 | 491/1864 | 358/1335 | 120/444 | chr7 | 45064532 | ||
| chr7:45068506
|
C | T | 1 | a0007 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.536C>T | p.Ala179Val | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/10 | 669/1864 | 536/1335 | 179/444 | chr7 | 45068506 | ||
| chr7:45069956
|
A | G | 1 | a0006 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.740A>G | p.His247Arg | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/10 | 873/1864 | 740/1335 | 247/444 | chr7 | 45069956 | ||
| chr7:45073522
|
G | A | 1 | a0003 | 13 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(10): Show |
missense_variant | MODERATE | c.866G>A | p.Ser289Asn | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 8/10 | 999/1864 | 866/1335 | 289/444 | chr7 | 45073522 | ||
| chr7:45075837
|
T | A | 1 | a0005 | 1 | NA18987.hp1 | missense_variant | MODERATE | c.1115T>A | p.Ile372Asn | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 1248/1864 | 1115/1335 | 372/444 | chr7 | 45075837 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45063959
|
C | T | 1 | a0002c0015 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.246C>T | p.Pro82Pro | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 3/10 | 379/1864 | 246/1335 | 82/444 | chr7 | 45063959 | ||
| chr7:45064525
|
G | A | 1 | a0001c0006 | 7 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
synonymous_variant | LOW | c.351G>A | p.Ala117Ala | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/10 | 484/1864 | 351/1335 | 117/444 | chr7 | 45064525 | ||
| chr7:45064558
|
G | A | 1 | a0001c0008 | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.384G>A | p.Glu128Glu | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/10 | 517/1864 | 384/1335 | 128/444 | chr7 | 45064558 | ||
| chr7:45069828
|
C | T | 1 | a0001c0013 | 1 | HG02080.hp1 | splice_region_variant&synonymous_variant | LOW | c.612C>T | p.Val204Val | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/10 | 745/1864 | 612/1335 | 204/444 | chr7 | 45069828 | ||
| chr7:45069951
|
C | T | 1 | a0002c0010 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.735C>T | p.Ser245Ser | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/10 | 868/1864 | 735/1335 | 245/444 | chr7 | 45069951 | ||
| chr7:45073571
|
G | A | 3 | a0001c0002a0006c0012a0007c0014 | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
splice_region_variant&synonymous_variant | LOW | c.915G>A | p.Thr305Thr | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 8/10 | 1048/1864 | 915/1335 | 305/444 | chr7 | 45073571 | ||
| chr7:45075982
|
G | A | 2 | a0002c0005a0002c0009 | 9 | HG00673.hp2 NA18943.hp2 NA18950.hp1 others(6): Show |
synonymous_variant | LOW | c.1260G>A | p.Glu420Glu | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 1393/1864 | 1260/1335 | 420/444 | chr7 | 45075982 | ||
| chr7:45076015
|
C | T | 1 | a0002c0009 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.1293C>T | p.Asp431Asp | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 1426/1864 | 1293/1335 | 431/444 | chr7 | 45076015 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45000297
|
G | C | 1 | a0001c0001t0005 | 1 | NA19075.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/10 | 37 | chr7 | 45000297 | |||||
| chr7:45000298
|
C | G | 1 | a0001c0001t0005 | 1 | NA19075.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/10 | 36 | chr7 | 45000298 | |||||
| chr7:45076071
|
G | T | 1 | a0001c0006t0007 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 14 | chr7 | 45076071 | |||||
| chr7:45076168
|
G | A | 1 | a0001c0006t0003 | 2 | HG02723.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*111G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 111 | chr7 | 45076168 | |||||
| chr7:45076174
|
T | C | 6 | a0001c0002t0002a0002c0003t0002a0002c0005t0002others(3): Show | 81 | HG00438.hp2 HG00558.hp2 HG00642.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*117T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 117 | chr7 | 45076174 | |||||
| chr7:45076206
|
C | A | 1 | a0001c0001t0004 | 2 | HG01074.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*149C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 149 | chr7 | 45076206 | |||||
| chr7:45076314
|
G | A | 1 | a0001c0001t0006 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*257G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 10/10 | 257 | chr7 | 45076314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:45000454
|
C | CG | 27 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(24): Show | 27 | HG00438.hp2 HG00673.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.30+102dupG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45000454 | |||||
| chr7:45000454
|
C | CGG | 36 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(33): Show | 36 | HG00323.hp2 HG00558.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.30+101_30+102dupGG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45000454 | |||||
| chr7:45000454
|
C | CGGG | 40 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(37): Show | 41 | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.30+100_30+102dupGG others(1): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45000454 | |||||
| chr7:45000457
|
G | GC | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0004g0003others(1): Show | 4 | HG00323.hp1 HG01074.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+94_30+95insC | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000457 | ||||||
| chr7:45000458
|
G | GA | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+95_30+96insA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000458 | ||||||
| chr7:45000462
|
G | GT | 10 | a0001c0002t0001g0314a0001c0002t0002g0305a0001c0002t0002g0306others(7): Show | 10 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.30+99_30+100insT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000462 | ||||||
| chr7:45000464
|
G | GGT | 24 | a0001c0001t0001g0002a0001c0001t0001g0164a0001c0001t0001g0166others(21): Show | 25 | HG00609.hp2 HG00738.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.30+102_30+103insTG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45000464 | |||||
| chr7:45000464
|
G | GT | 115 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(112): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.30+101_30+102insT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000464 | ||||||
| chr7:45000464
|
G | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0302others(4): Show | 7 | HG00323.hp1 HG00621.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+101G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000464 | ||||||
| chr7:45000608
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.30+245G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000608 | ||||||
| chr7:45000662
|
G | A | 1 | a0001c0001t0004g0003 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.30+299G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000662 | ||||||
| chr7:45000666
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.30+303A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000666 | ||||||
| chr7:45000827
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18948.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.30+464T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000827 | ||||||
| chr7:45000955
|
A | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0301 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.30+592A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45000955 | ||||||
| chr7:45001166
|
C | G | 1 | a0004c0007t0001g0300 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.30+803C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001166 | ||||||
| chr7:45001309
|
C | T | 6 | a0001c0001t0001g0088a0001c0006t0001g0059a0001c0006t0001g0060others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+946C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001309 | ||||||
| chr7:45001417
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+1054C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001417 | ||||||
| chr7:45001512
|
G | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+1149G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001512 | ||||||
| chr7:45001613
|
G | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+1250G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001613 | ||||||
| chr7:45001617
|
A | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.30+1254A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001617 | ||||||
| chr7:45001667
|
A | G | 1 | a0001c0001t0001g0006 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.30+1304A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001667 | ||||||
| chr7:45001701
|
A | AT | 19 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.30+1347dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45001701 | |||||
| chr7:45001716
|
G | T | 1 | a0001c0002t0002g0028 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.30+1353G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001716 | ||||||
| chr7:45001806
|
A | T | 1 | a0004c0007t0001g0300 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.30+1443A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001806 | ||||||
| chr7:45001818
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.30+1455A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45001818 | ||||||
| chr7:45002214
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+1851G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45002214 | ||||||
| chr7:45002337
|
C | T | 2 | a0001c0001t0001g0296a0003c0004t0001g0297 | 2 | NA18947.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.30+1974C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45002337 | ||||||
| chr7:45002567
|
C | CT | 7 | a0001c0001t0001g0002a0001c0001t0001g0182a0001c0001t0001g0183others(4): Show | 8 | HG01243.hp2 HG02027.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+2212dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45002567 | |||||
| chr7:45002617
|
G | A | 6 | a0001c0001t0001g0088a0001c0006t0001g0059a0001c0006t0001g0060others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+2254G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45002617 | ||||||
| chr7:45002650
|
G | A | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+2287G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45002650 | ||||||
| chr7:45002769
|
G | C | 1 | a0001c0001t0001g0189 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.30+2406G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45002769 | ||||||
| chr7:45002989
|
T | C | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+2626T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45002989 | ||||||
| chr7:45003100
|
A | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0293 | 2 | NA18939.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.30+2737A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003100 | ||||||
| chr7:45003215
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+2852A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003215 | ||||||
| chr7:45003319
|
A | C | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0290others(1): Show | 4 | HG02027.hp2 NA18989.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+2956A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003319 | ||||||
| chr7:45003342
|
C | T | 38 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0071others(35): Show | 38 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.30+2979C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003342 | ||||||
| chr7:45003490
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+3127T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003490 | ||||||
| chr7:45003518
|
A | G | 1 | a0002c0003t0002g0058 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.30+3155A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003518 | ||||||
| chr7:45003692
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+3329T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003692 | ||||||
| chr7:45003728
|
CA | C | 231 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.30+3380delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45003728 | |||||
| chr7:45003744
|
C | A | 1 | a0001c0002t0002g0120 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.30+3381C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003744 | ||||||
| chr7:45003908
|
T | C | 18 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(15): Show | 19 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+3545T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45003908 | ||||||
| chr7:45004048
|
T | G | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+3685T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004048 | ||||||
| chr7:45004190
|
A | G | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+3827A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004190 | ||||||
| chr7:45004377
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0179a0001c0001t0001g0186 | 3 | HG02004.hp2 NA18950.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.30+4014A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004377 | ||||||
| chr7:45004534
|
G | C | 3 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009 | 3 | HG02970.hp2 HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.30+4171G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004534 | ||||||
| chr7:45004607
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+4244C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004607 | ||||||
| chr7:45004714
|
C | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+4351C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004714 | ||||||
| chr7:45004842
|
C | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG02080.hp2 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.30+4479C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004842 | ||||||
| chr7:45004890
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.30+4527T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004890 | ||||||
| chr7:45004960
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30+4597C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45004960 | ||||||
| chr7:45004996
|
CA | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.30+4647delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45004996 | |||||
| chr7:45005149
|
T | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0103 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.30+4786T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005149 | ||||||
| chr7:45005220
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.30+4857A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005220 | ||||||
| chr7:45005369
|
G | T | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+5006G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005369 | ||||||
| chr7:45005458
|
C | T | 1 | a0002c0003t0002g0057 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.30+5095C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005458 | ||||||
| chr7:45005552
|
CTT | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+5191_30+5192del others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45005552 | |||||
| chr7:45005592
|
A | C | 15 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+5229A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005592 | ||||||
| chr7:45005699
|
C | T | 8 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0156others(5): Show | 8 | HG01243.hp1 HG02258.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.30+5336C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005699 | ||||||
| chr7:45005769
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+5406A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005769 | ||||||
| chr7:45005829
|
G | C | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+5466G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005829 | ||||||
| chr7:45005921
|
T | G | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.30+5558T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45005921 | ||||||
| chr7:45006113
|
G | A | 1 | a0002c0003t0002g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.30+5750G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006113 | ||||||
| chr7:45006157
|
GA | G | 6 | a0001c0001t0001g0088a0001c0001t0001g0117a0001c0006t0001g0060others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+5802delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45006157 | |||||
| chr7:45006172
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(1): Show | 4 | HG00639.hp1 HG02451.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+5809A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006172 | ||||||
| chr7:45006174
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.30+5811C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006174 | ||||||
| chr7:45006230
|
T | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.30+5867T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006230 | ||||||
| chr7:45006231
|
C | G | 60 | a0001c0001t0001g0069a0001c0002t0001g0013a0001c0002t0001g0014others(57): Show | 60 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.30+5868C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006231 | ||||||
| chr7:45006253
|
C | T | 9 | a0001c0001t0001g0069a0001c0002t0002g0120a0001c0002t0002g0121others(6): Show | 9 | HG01243.hp1 HG02258.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.30+5890C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006253 | ||||||
| chr7:45006258
|
A | G | 1 | a0002c0003t0002g0056 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.30+5895A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006258 | ||||||
| chr7:45006268
|
C | T | 1 | a0001c0006t0001g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.30+5905C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006268 | ||||||
| chr7:45006333
|
C | CT | 216 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.30+5981dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45006333 | |||||
| chr7:45006333
|
C | CTT | 43 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(40): Show | 43 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.30+5980_30+5981dup others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45006333 | |||||
| chr7:45006407
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+6044A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006407 | ||||||
| chr7:45006473
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.30+6110A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006473 | ||||||
| chr7:45006538
|
G | A | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+6175G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45006538 | ||||||
| chr7:45007019
|
T | C | 49 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 49 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.30+6656T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007019 | ||||||
| chr7:45007190
|
T | A | 1 | a0003c0004t0001g0201 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.30+6827T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007190 | ||||||
| chr7:45007232
|
C | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+6869C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007232 | ||||||
| chr7:45007240
|
G | A | 3 | a0001c0001t0001g0166a0001c0001t0001g0202a0001c0001t0001g0203 | 3 | HG00639.hp2 HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.30+6877G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007240 | ||||||
| chr7:45007329
|
G | A | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.30+6966G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007329 | ||||||
| chr7:45007370
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.30+7007G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007370 | ||||||
| chr7:45007371
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+7008C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007371 | ||||||
| chr7:45007789
|
T | TG | 41 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.30+7428dupG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45007789 | |||||
| chr7:45007994
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.30+7631G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45007994 | ||||||
| chr7:45008039
|
A | T | 1 | a0002c0003t0002g0087 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.30+7676A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008039 | ||||||
| chr7:45008039
|
ATT | A | 52 | a0001c0001t0001g0020a0001c0002t0001g0013a0001c0002t0001g0014others(49): Show | 52 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.30+7696_30+7697del others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008039 | |||||
| chr7:45008039
|
ATTT | A | 80 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(77): Show | 81 | HG00280.hp2 HG00639.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.30+7695_30+7697del others(3): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008039 | |||||
| chr7:45008039
|
ATTTT | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+7694_30+7697del others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008039 | |||||
| chr7:45008075
|
C | T | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+7712C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008075 | ||||||
| chr7:45008192
|
C | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+7829C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008192 | ||||||
| chr7:45008201
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.30+7838G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008201 | ||||||
| chr7:45008226
|
G | A | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+7863G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008226 | ||||||
| chr7:45008291
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+7928T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008291 | ||||||
| chr7:45008293
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+7930C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008293 | ||||||
| chr7:45008320
|
T | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+7957T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008320 | ||||||
| chr7:45008329
|
C | T | 1 | a0002c0005t0002g0055 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.30+7966C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008329 | ||||||
| chr7:45008350
|
C | G | 1 | a0001c0001t0001g0287 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.30+7987C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008350 | ||||||
| chr7:45008351
|
A | G | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG01256.hp1 HG02080.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+7988A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008351 | ||||||
| chr7:45008356
|
C | CT | 16 | a0001c0001t0001g0113a0001c0001t0001g0119a0001c0001t0001g0153others(13): Show | 16 | HG00438.hp2 HG01069.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+8020dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008356 | |||||
| chr7:45008356
|
CT | C | 30 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(27): Show | 30 | HG00639.hp1 HG01109.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.30+8020delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008356 | |||||
| chr7:45008356
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.30+8009_30+8020del others(12): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008356 | |||||
| chr7:45008356
|
CTTTTTTT others(6): Show |
C | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0286others(17): Show | 21 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.30+8008_30+8020del others(13): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008356 | |||||
| chr7:45008356
|
CTTTTTTT others(7): Show |
C | 133 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0164others(130): Show | 134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.30+8007_30+8020del others(14): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45008356 | |||||
| chr7:45008425
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.30+8062G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008425 | ||||||
| chr7:45008489
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+8126A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008489 | ||||||
| chr7:45008523
|
C | T | 6 | a0001c0001t0001g0088a0001c0006t0001g0059a0001c0006t0001g0060others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.30+8160C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008523 | ||||||
| chr7:45008573
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+8210A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008573 | ||||||
| chr7:45008602
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.30+8239T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45008602 | ||||||
| chr7:45009018
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+8655T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009018 | ||||||
| chr7:45009131
|
A | G | 1 | a0001c0002t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.30+8768A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009131 | ||||||
| chr7:45009213
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.30+8850A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009213 | ||||||
| chr7:45009250
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+8887A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009250 | ||||||
| chr7:45009311
|
A | AG | 3 | a0001c0002t0002g0101a0001c0002t0002g0102a0001c0002t0002g0140 | 3 | HG00738.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.30+8948_30+8949ins others(1): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009311 | ||||||
| chr7:45009314
|
A | AG | 3 | a0001c0002t0002g0089a0001c0002t0002g0100a0001c0002t0002g0139 | 3 | HG01928.hp1 HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.30+8951_30+8952ins others(1): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009314 | ||||||
| chr7:45009318
|
A | AAAG | 21 | a0001c0001t0001g0074a0001c0001t0001g0088a0001c0001t0001g0104others(18): Show | 21 | HG00741.hp2 HG01433.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.30+8957_30+8958ins others(3): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45009318 | |||||
| chr7:45009318
|
A | AAG | 64 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(61): Show | 65 | HG00639.hp1 HG00735.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.30+8956_30+8957ins others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45009318 | |||||
| chr7:45009318
|
A | AG | 171 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(168): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.30+8955_30+8956ins others(1): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009318 | ||||||
| chr7:45009318
|
A | G | 7 | a0001c0001t0001g0291a0001c0002t0002g0089a0001c0002t0002g0100others(4): Show | 7 | HG00738.hp1 HG01257.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.30+8955A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009318 | ||||||
| chr7:45009320
|
A | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0288 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.30+8957A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009320 | ||||||
| chr7:45009323
|
T | A | 1 | a0002c0003t0002g0030 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.30+8960T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009323 | ||||||
| chr7:45009402
|
G | GT | 49 | a0001c0001t0001g0088a0001c0002t0001g0013a0001c0002t0001g0014others(46): Show | 49 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.30+9059dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45009402 | |||||
| chr7:45009402
|
GT | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.30+9059delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45009402 | |||||
| chr7:45009427
|
C | T | 2 | a0001c0001t0001g0275a0003c0004t0001g0193 | 2 | NA18947.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.30+9064C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009427 | ||||||
| chr7:45009514
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.30+9151C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009514 | ||||||
| chr7:45009523
|
G | A | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(1): Show | 4 | NA18969.hp2 NA18993.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+9160G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009523 | ||||||
| chr7:45009601
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.30+9238A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009601 | ||||||
| chr7:45009636
|
T | C | 3 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0276 | 3 | HG01934.hp1 HG02148.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.30+9273T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009636 | ||||||
| chr7:45009644
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+9281T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009644 | ||||||
| chr7:45009696
|
G | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.30+9333G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009696 | ||||||
| chr7:45009758
|
A | G | 4 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(1): Show | 4 | HG01884.hp1 HG03139.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+9395A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45009758 | ||||||
| chr7:45009913
|
C | CT | 16 | a0001c0001t0001g0145a0001c0002t0001g0141a0001c0002t0002g0012others(13): Show | 16 | HG00741.hp2 HG01192.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.30+9565dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45009913 | |||||
| chr7:45010086
|
T | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0277 | 2 | NA18983.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.30+9723T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010086 | ||||||
| chr7:45010170
|
C | G | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+9807C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010170 | ||||||
| chr7:45010186
|
C | T | 1 | a0001c0002t0002g0089 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.30+9823C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010186 | ||||||
| chr7:45010252
|
A | G | 2 | a0001c0001t0001g0088a0001c0006t0007g0162 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+9889A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010252 | ||||||
| chr7:45010268
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218 | 3 | NA18747.hp1 NA18998.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.30+9905G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010268 | ||||||
| chr7:45010400
|
A | C | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+10037A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010400 | ||||||
| chr7:45010571
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0153 | 2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.30+10208A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010571 | ||||||
| chr7:45010593
|
G | GTA | 3 | a0001c0006t0001g0061a0001c0006t0001g0161a0002c0003t0002g0029 | 3 | HG01358.hp2 HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.30+10244_30+10245d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45010593 | |||||
| chr7:45010595
|
A | G | 1 | a0001c0002t0002g0312 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.30+10232A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010595 | ||||||
| chr7:45010605
|
A | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0176 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.30+10242A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010605 | ||||||
| chr7:45010607
|
A | T | 263 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(260): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.30+10244A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010607 | ||||||
| chr7:45010609
|
T | A | 1 | a0002c0003t0002g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.30+10246T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010609 | ||||||
| chr7:45010728
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.30+10365G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010728 | ||||||
| chr7:45010839
|
A | T | 1 | a0001c0001t0001g0272 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.30+10476A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010839 | ||||||
| chr7:45010850
|
G | A | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+10487G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010850 | ||||||
| chr7:45010890
|
A | C | 1 | a0001c0002t0001g0067 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.30+10527A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45010890 | ||||||
| chr7:45011030
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.30+10667C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011030 | ||||||
| chr7:45011199
|
A | AT | 68 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(65): Show | 69 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.30+10850dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45011199 | |||||
| chr7:45011199
|
AT | A | 10 | a0001c0001t0001g0069a0001c0001t0001g0221a0001c0002t0001g0195others(7): Show | 10 | HG01167.hp1 HG02129.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+10850delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45011199 | |||||
| chr7:45011291
|
A | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+10928A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011291 | ||||||
| chr7:45011309
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0277 | 2 | NA18983.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.30+10946G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011309 | ||||||
| chr7:45011402
|
G | A | 10 | a0001c0001t0001g0168a0001c0001t0001g0180a0001c0001t0001g0181others(7): Show | 10 | HG02027.hp2 NA18956.hp1 NA18960.hp1 others(7): Show |
intron_variant | MODIFIER | c.30+11039G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011402 | ||||||
| chr7:45011433
|
G | A | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+11070G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011433 | ||||||
| chr7:45011464
|
T | C | 1 | a0001c0006t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30+11101T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011464 | ||||||
| chr7:45011508
|
T | A | 3 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212 | 3 | NA18969.hp2 NA18993.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.30+11145T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011508 | ||||||
| chr7:45011704
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+11341A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011704 | ||||||
| chr7:45011795
|
G | A | 1 | a0001c0002t0002g0129 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.30+11432G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011795 | ||||||
| chr7:45011853
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+11490C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011853 | ||||||
| chr7:45011856
|
G | A | 11 | a0003c0004t0001g0169a0003c0004t0001g0201a0003c0004t0001g0208others(8): Show | 11 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+11493G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45011856 | ||||||
| chr7:45012078
|
A | T | 1 | a0001c0001t0001g0271 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.30+11715A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012078 | ||||||
| chr7:45012128
|
A | G | 1 | a0001c0002t0002g0138 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.30+11765A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012128 | ||||||
| chr7:45012130
|
CT | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+11787delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45012130 | |||||
| chr7:45012130
|
CTT | C | 19 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0210others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.30+11786_30+11787d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45012130 | |||||
| chr7:45012274
|
C | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0303 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.30+11911C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012274 | ||||||
| chr7:45012325
|
G | A | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+11962G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012325 | ||||||
| chr7:45012365
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02280.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+12002C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012365 | ||||||
| chr7:45012385
|
C | T | 2 | a0001c0002t0001g0125a0001c0002t0001g0128 | 2 | NA19066.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.30+12022C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012385 | ||||||
| chr7:45012386
|
G | A | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+12023G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012386 | ||||||
| chr7:45012399
|
G | A | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+12036G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012399 | ||||||
| chr7:45012401
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.30+12038T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012401 | ||||||
| chr7:45012534
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.30+12171T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012534 | ||||||
| chr7:45012577
|
G | A | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.30+12214G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012577 | ||||||
| chr7:45012704
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.30+12341G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012704 | ||||||
| chr7:45012721
|
A | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.30+12358A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012721 | ||||||
| chr7:45012753
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.30+12390T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012753 | ||||||
| chr7:45012766
|
G | A | 1 | a0002c0003t0002g0035 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.30+12403G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012766 | ||||||
| chr7:45012899
|
T | C | 11 | a0001c0002t0002g0089a0001c0002t0002g0092a0001c0002t0002g0100others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.30+12536T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012899 | ||||||
| chr7:45012930
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.30+12567C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012930 | ||||||
| chr7:45012995
|
A | G | 1 | a0002c0003t0002g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.30+12632A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45012995 | ||||||
| chr7:45013153
|
CCATGTCT others(3): Show |
C | 1 | a0001c0001t0001g0232 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.30+12793_30+12802d others(12): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45013153 | |||||
| chr7:45013311
|
T | C | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+12948T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013311 | ||||||
| chr7:45013334
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.30+12971G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013334 | ||||||
| chr7:45013416
|
C | T | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+13053C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013416 | ||||||
| chr7:45013486
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30+13123T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013486 | ||||||
| chr7:45013616
|
A | G | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+13253A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013616 | ||||||
| chr7:45013763
|
C | G | 2 | a0001c0002t0001g0125a0001c0002t0001g0128 | 2 | NA19066.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.30+13400C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013763 | ||||||
| chr7:45013843
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+13480T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013843 | ||||||
| chr7:45013865
|
G | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+13502G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45013865 | ||||||
| chr7:45014267
|
G | A | 3 | a0002c0003t0002g0031a0002c0003t0002g0036a0002c0003t0002g0079 | 3 | HG02129.hp1 HG02145.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.30+13904G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014267 | ||||||
| chr7:45014416
|
G | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0164others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.30+14053G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014416 | ||||||
| chr7:45014544
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+14181C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014544 | ||||||
| chr7:45014622
|
C | CT | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.30+14276dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45014622 | |||||
| chr7:45014713
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.30+14350C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014713 | ||||||
| chr7:45014787
|
A | G | 4 | a0001c0001t0001g0088a0001c0006t0001g0061a0001c0006t0001g0161others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.30+14424A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014787 | ||||||
| chr7:45014872
|
T | C | 4 | a0001c0001t0001g0034a0002c0003t0002g0030a0002c0003t0002g0037others(1): Show | 4 | NA18940.hp1 NA18962.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+14509T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014872 | ||||||
| chr7:45014952
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.30+14589A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014952 | ||||||
| chr7:45014976
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+14613T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45014976 | ||||||
| chr7:45015001
|
C | T | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.30+14638C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015001 | ||||||
| chr7:45015044
|
A | T | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+14681A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015044 | ||||||
| chr7:45015165
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.30+14802A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015165 | ||||||
| chr7:45015312
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+14949C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015312 | ||||||
| chr7:45015420
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+15057C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015420 | ||||||
| chr7:45015503
|
G | C | 25 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(22): Show | 25 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.30+15140G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015503 | ||||||
| chr7:45015516
|
T | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+15153T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015516 | ||||||
| chr7:45015615
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+15252G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015615 | ||||||
| chr7:45015655
|
A | T | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.30+15292A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015655 | ||||||
| chr7:45015711
|
G | A | 1 | a0001c0002t0002g0139 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.30+15348G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015711 | ||||||
| chr7:45015713
|
C | T | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.30+15350C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015713 | ||||||
| chr7:45015770
|
T | G | 49 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 49 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.30+15407T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015770 | ||||||
| chr7:45015808
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+15445C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015808 | ||||||
| chr7:45015810
|
C | T | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+15447C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015810 | ||||||
| chr7:45015811
|
G | A | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.30+15448G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015811 | ||||||
| chr7:45015907
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.30+15544G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015907 | ||||||
| chr7:45015979
|
T | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+15616T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45015979 | ||||||
| chr7:45016074
|
A | G | 3 | a0001c0001t0001g0178a0001c0001t0001g0221a0001c0001t0001g0270 | 3 | NA18953.hp1 NA18960.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.30+15711A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016074 | ||||||
| chr7:45016214
|
C | T | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+15851C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016214 | ||||||
| chr7:45016218
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30+15855A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016218 | ||||||
| chr7:45016300
|
A | G | 5 | a0001c0001t0001g0088a0001c0006t0001g0060a0001c0006t0001g0061others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+15937A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016300 | ||||||
| chr7:45016391
|
G | A | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+16028G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016391 | ||||||
| chr7:45016519
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+16156G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016519 | ||||||
| chr7:45016603
|
A | G | 1 | a0001c0002t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.30+16240A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016603 | ||||||
| chr7:45016640
|
C | CT | 6 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(3): Show | 6 | HG00738.hp2 HG01255.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.30+16287dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45016640 | |||||
| chr7:45016717
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30+16354C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016717 | ||||||
| chr7:45016745
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0301 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.30+16382G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016745 | ||||||
| chr7:45016789
|
C | T | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG01256.hp1 HG02080.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.30+16426C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016789 | ||||||
| chr7:45016838
|
G | C | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.30+16475G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016838 | ||||||
| chr7:45016881
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+16518T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016881 | ||||||
| chr7:45016956
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+16593C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016956 | ||||||
| chr7:45016991
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.30+16628G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45016991 | ||||||
| chr7:45017066
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.30+16703G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017066 | ||||||
| chr7:45017125
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.30+16762A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017125 | ||||||
| chr7:45017139
|
C | T | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+16776C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017139 | ||||||
| chr7:45017263
|
A | G | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+16900A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017263 | ||||||
| chr7:45017315
|
A | T | 1 | a0002c0010t0002g0052 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.30+16952A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017315 | ||||||
| chr7:45017535
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+17172G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017535 | ||||||
| chr7:45017565
|
C | CA | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17203dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45017565 | |||||
| chr7:45017566
|
A | G | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+17203A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017566 | ||||||
| chr7:45017652
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+17289G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017652 | ||||||
| chr7:45017664
|
GTATTT | G | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.30+17306_30+17310d others(7): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45017664 | |||||
| chr7:45017729
|
C | T | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+17366C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017729 | ||||||
| chr7:45017960
|
T | A | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.30+17597T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45017960 | ||||||
| chr7:45018009
|
C | T | 2 | a0002c0003t0002g0046a0002c0003t0002g0047 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.30+17646C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018009 | ||||||
| chr7:45018063
|
C | CTG | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+17701_30+17702i others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45018063 | |||||
| chr7:45018144
|
A | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.30+17781A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018144 | ||||||
| chr7:45018179
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30+17816C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018179 | ||||||
| chr7:45018187
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.30+17824G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018187 | ||||||
| chr7:45018192
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.30+17829T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018192 | ||||||
| chr7:45018239
|
G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.30+17876G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018239 | ||||||
| chr7:45018354
|
T | C | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.30+17991T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018354 | ||||||
| chr7:45018464
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+18101C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018464 | ||||||
| chr7:45018764
|
CT | C | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.30+18415delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45018764 | |||||
| chr7:45018766
|
T | G | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+18403T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018766 | ||||||
| chr7:45018821
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG02280.hp1 HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.30+18458G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018821 | ||||||
| chr7:45018849
|
T | C | 1 | a0001c0002t0001g0064 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.30+18486T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018849 | ||||||
| chr7:45018850
|
C | T | 1 | a0001c0002t0001g0064 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.30+18487C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018850 | ||||||
| chr7:45018911
|
C | T | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.30+18548C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018911 | ||||||
| chr7:45018959
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.30+18596C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018959 | ||||||
| chr7:45018960
|
A | G | 2 | a0001c0001t0001g0088a0001c0006t0007g0162 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.30+18597A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45018960 | ||||||
| chr7:45019059
|
C | CT | 25 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0001g0177others(22): Show | 25 | HG01106.hp1 HG01192.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.30+18718dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45019059 | |||||
| chr7:45019059
|
CT | C | 89 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(86): Show | 89 | HG00544.hp1 HG00609.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.30+18718delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45019059 | |||||
| chr7:45019267
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.30+18904A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019267 | ||||||
| chr7:45019376
|
A | G | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-18877A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019376 | ||||||
| chr7:45019377
|
CT | C | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-18873delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45019377 | |||||
| chr7:45019513
|
G | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-18740G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019513 | ||||||
| chr7:45019617
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.31-18636C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019617 | ||||||
| chr7:45019640
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-18613T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019640 | ||||||
| chr7:45019648
|
T | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-18605T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019648 | ||||||
| chr7:45019740
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-18513G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019740 | ||||||
| chr7:45019830
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.31-18423C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019830 | ||||||
| chr7:45019844
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-18409G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019844 | ||||||
| chr7:45019940
|
G | A | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-18313G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019940 | ||||||
| chr7:45019946
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-18307G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45019946 | ||||||
| chr7:45020087
|
GGCCAATA others(8): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-18163_31-18149d others(17): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45020087 | |||||
| chr7:45020112
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-18141T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020112 | ||||||
| chr7:45020201
|
A | G | 1 | a0001c0002t0001g0097 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.31-18052A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020201 | ||||||
| chr7:45020217
|
C | A | 1 | a0001c0002t0002g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.31-18036C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020217 | ||||||
| chr7:45020581
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0179a0001c0001t0001g0186 | 3 | HG02004.hp2 NA18950.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.31-17672C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020581 | ||||||
| chr7:45020649
|
A | G | 41 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.31-17604A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020649 | ||||||
| chr7:45020687
|
C | T | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-17566C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020687 | ||||||
| chr7:45020817
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG00280.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.31-17436T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020817 | ||||||
| chr7:45020836
|
C | T | 70 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(67): Show | 71 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.31-17417C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45020836 | ||||||
| chr7:45020859
|
T | TAG | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-17393_31-17392d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45020859 | |||||
| chr7:45021273
|
T | A | 1 | a0001c0001t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31-16980T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021273 | ||||||
| chr7:45021301
|
G | T | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-16952G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021301 | ||||||
| chr7:45021337
|
C | T | 2 | a0001c0001t0001g0259a0001c0001t0001g0260 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.31-16916C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021337 | ||||||
| chr7:45021393
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.31-16860G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021393 | ||||||
| chr7:45021563
|
C | CA | 31 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(28): Show | 31 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.31-16678dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45021563 | |||||
| chr7:45021571
|
A | T | 15 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(12): Show | 15 | HG00741.hp2 HG01167.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.31-16682A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021571 | ||||||
| chr7:45021572
|
A | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.31-16681A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021572 | ||||||
| chr7:45021576
|
T | A | 5 | a0001c0001t0001g0111a0001c0001t0001g0145a0001c0001t0001g0234others(2): Show | 5 | HG00735.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-16677T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021576 | ||||||
| chr7:45021669
|
G | C | 4 | a0001c0002t0002g0001a0001c0002t0002g0025a0001c0002t0002g0026others(1): Show | 5 | HG02717.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-16584G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021669 | ||||||
| chr7:45021901
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.31-16352A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45021901 | ||||||
| chr7:45022290
|
C | CT | 25 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0107others(22): Show | 25 | HG00673.hp2 HG01106.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.31-15934dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45022290 | |||||
| chr7:45022290
|
CT | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.31-15934delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45022290 | |||||
| chr7:45022290
|
CTT | C | 6 | a0001c0001t0001g0071a0001c0001t0001g0104a0001c0001t0005g0235others(3): Show | 6 | HG01069.hp1 HG01496.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-15935_31-15934d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45022290 | |||||
| chr7:45022290
|
CTTT | C | 9 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 9 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-15936_31-15934d others(5): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45022290 | |||||
| chr7:45022375
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.31-15878C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022375 | ||||||
| chr7:45022376
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.31-15877G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022376 | ||||||
| chr7:45022377
|
G | A | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.31-15876G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022377 | ||||||
| chr7:45022407
|
C | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0004g0003others(1): Show | 4 | HG00323.hp1 HG01074.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-15846C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022407 | ||||||
| chr7:45022467
|
C | T | 1 | a0003c0004t0001g0229 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.31-15786C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022467 | ||||||
| chr7:45022497
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31-15756G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022497 | ||||||
| chr7:45022498
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31-15755G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022498 | ||||||
| chr7:45022552
|
C | T | 2 | a0001c0001t0001g0088a0001c0006t0007g0162 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.31-15701C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022552 | ||||||
| chr7:45022584
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.31-15669G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022584 | ||||||
| chr7:45022803
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31-15450C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022803 | ||||||
| chr7:45022866
|
G | T | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-15387G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022866 | ||||||
| chr7:45022878
|
T | G | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-15375T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022878 | ||||||
| chr7:45022932
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31-15321G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45022932 | ||||||
| chr7:45023002
|
A | G | 1 | a0003c0004t0001g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.31-15251A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023002 | ||||||
| chr7:45023042
|
G | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-15211G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023042 | ||||||
| chr7:45023159
|
T | A | 1 | a0001c0002t0002g0312 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.31-15094T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023159 | ||||||
| chr7:45023229
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-15024G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023229 | ||||||
| chr7:45023287
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.31-14966C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023287 | ||||||
| chr7:45023364
|
A | G | 2 | a0001c0002t0001g0125a0001c0002t0001g0128 | 2 | NA19066.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.31-14889A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023364 | ||||||
| chr7:45023485
|
G | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.31-14768G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023485 | ||||||
| chr7:45023540
|
A | T | 1 | a0002c0003t0002g0086 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.31-14713A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023540 | ||||||
| chr7:45023561
|
C | T | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.31-14692C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023561 | ||||||
| chr7:45023671
|
T | A | 1 | a0001c0006t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.31-14582T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023671 | ||||||
| chr7:45023701
|
G | A | 2 | a0001c0006t0001g0061a0001c0006t0001g0161 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.31-14552G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023701 | ||||||
| chr7:45023723
|
C | CT | 7 | a0001c0001t0001g0073a0001c0001t0001g0154a0001c0001t0001g0177others(4): Show | 7 | HG00639.hp1 HG01256.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-14513dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023723 | |||||
| chr7:45023723
|
CT | C | 67 | a0001c0001t0001g0088a0001c0001t0001g0166a0001c0001t0001g0188others(64): Show | 67 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.31-14513delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023723 | |||||
| chr7:45023787
|
G | GTTTTTTT others(4): Show |
1 | a0001c0008t0001g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.31-14438_31-14428d others(13): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023787 | |||||
| chr7:45023787
|
G | GTTTTTTT others(8): Show |
1 | a0001c0008t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.31-14442_31-14428d others(17): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023787 | |||||
| chr7:45023787
|
GT | G | 42 | a0001c0001t0001g0021a0001c0001t0001g0075a0001c0001t0001g0107others(39): Show | 42 | HG00558.hp1 HG00735.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.31-14428delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023787 | |||||
| chr7:45023787
|
GTT | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0022others(203): Show | 208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.31-14429_31-14428d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023787 | |||||
| chr7:45023787
|
GTTT | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0108others(4): Show | 7 | HG00323.hp1 HG01074.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-14430_31-14428d others(5): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023787 | |||||
| chr7:45023787
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0002t0002g0139 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.31-14442_31-14428d others(17): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023787 | |||||
| chr7:45023787
|
GTTTTTTT others(12): Show |
G | 4 | a0002c0003t0002g0030a0002c0003t0002g0037a0002c0003t0002g0048others(1): Show | 4 | HG03017.hp1 NA18940.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-14446_31-14428d others(21): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45023787 | |||||
| chr7:45023797
|
T | G | 18 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0071others(15): Show | 18 | HG01106.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-14456T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023797 | ||||||
| chr7:45023798
|
T | G | 28 | a0001c0001t0001g0021a0001c0001t0001g0075a0001c0001t0001g0107others(25): Show | 28 | HG00558.hp1 HG00735.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.31-14455T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023798 | ||||||
| chr7:45023799
|
T | G | 203 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0021others(200): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.31-14454T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023799 | ||||||
| chr7:45023800
|
T | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0108others(5): Show | 8 | HG00323.hp1 HG00738.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-14453T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023800 | ||||||
| chr7:45023808
|
T | G | 23 | a0001c0001t0001g0020a0001c0001t0001g0070a0001c0001t0001g0071others(20): Show | 23 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.31-14445T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023808 | ||||||
| chr7:45023809
|
T | G | 193 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0034others(190): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.31-14444T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023809 | ||||||
| chr7:45023810
|
T | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0296others(5): Show | 8 | HG00323.hp1 HG01074.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-14443T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023810 | ||||||
| chr7:45023819
|
T | G | 4 | a0001c0001t0001g0034a0001c0002t0002g0120a0001c0002t0002g0121others(1): Show | 4 | HG01243.hp1 HG02258.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-14434T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023819 | ||||||
| chr7:45023955
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-14298C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023955 | ||||||
| chr7:45023967
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.31-14286C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45023967 | ||||||
| chr7:45024066
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.31-14187C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024066 | ||||||
| chr7:45024100
|
C | T | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-14153C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024100 | ||||||
| chr7:45024226
|
C | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.31-14027C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024226 | ||||||
| chr7:45024357
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0152 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.31-13896A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024357 | ||||||
| chr7:45024435
|
CTTGCTGA others(6): Show |
C | 19 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-13816_31-13804d others(15): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45024435 | |||||
| chr7:45024441
|
G | C | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.31-13812G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024441 | ||||||
| chr7:45024588
|
T | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-13665T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024588 | ||||||
| chr7:45024947
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.31-13306C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024947 | ||||||
| chr7:45024981
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31-13272A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45024981 | ||||||
| chr7:45025091
|
T | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-13162T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025091 | ||||||
| chr7:45025246
|
A | G | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.31-13007A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025246 | ||||||
| chr7:45025323
|
C | T | 82 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(79): Show | 83 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.31-12930C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025323 | ||||||
| chr7:45025534
|
CT | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(265): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.31-12703delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45025534 | |||||
| chr7:45025554
|
A | G | 2 | a0001c0002t0001g0096a0001c0002t0001g0136 | 2 | NA18979.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.31-12699A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025554 | ||||||
| chr7:45025623
|
T | A | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.31-12630T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025623 | ||||||
| chr7:45025785
|
C | CAGCCTTC others(9): Show |
1 | a0001c0002t0001g0141 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.31-12467_31-12452d others(18): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45025785 | |||||
| chr7:45025829
|
C | T | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(1): Show | 4 | NA18969.hp2 NA18993.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-12424C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025829 | ||||||
| chr7:45025931
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.31-12322G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45025931 | ||||||
| chr7:45026050
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-12203T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026050 | ||||||
| chr7:45026375
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.31-11878G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026375 | ||||||
| chr7:45026395
|
GCAAT | G | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-11855_31-11852d others(6): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45026395 | |||||
| chr7:45026432
|
T | C | 41 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.31-11821T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026432 | ||||||
| chr7:45026459
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.31-11794T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026459 | ||||||
| chr7:45026597
|
A | AT | 50 | a0001c0001t0001g0021a0001c0001t0001g0071a0001c0001t0001g0171others(47): Show | 50 | HG00323.hp2 HG00544.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.31-11633dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45026597 | |||||
| chr7:45026597
|
A | ATT | 15 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0002t0001g0068others(12): Show | 16 | HG00438.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.31-11634_31-11633d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45026597 | |||||
| chr7:45026597
|
AT | A | 9 | a0001c0001t0001g0114a0001c0001t0001g0170a0001c0001t0001g0187others(6): Show | 9 | HG01070.hp1 HG01257.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-11633delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45026597 | |||||
| chr7:45026633
|
C | T | 40 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(37): Show | 40 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.31-11620C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026633 | ||||||
| chr7:45026675
|
T | C | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.31-11578T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026675 | ||||||
| chr7:45026833
|
C | G | 1 | a0001c0006t0001g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.31-11420C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026833 | ||||||
| chr7:45026892
|
C | T | 2 | a0001c0001t0001g0088a0001c0006t0007g0162 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.31-11361C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026892 | ||||||
| chr7:45026893
|
G | A | 1 | a0001c0002t0002g0089 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.31-11360G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026893 | ||||||
| chr7:45026936
|
T | G | 1 | a0001c0001t0001g0236 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.31-11317T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45026936 | ||||||
| chr7:45027031
|
A | G | 4 | a0001c0001t0001g0107a0001c0001t0001g0109a0001c0001t0001g0144others(1): Show | 4 | HG02622.hp1 HG02895.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-11222A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027031 | ||||||
| chr7:45027137
|
C | T | 1 | a0002c0003t0002g0031 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.31-11116C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027137 | ||||||
| chr7:45027148
|
C | T | 1 | a0001c0001t0001g0287 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.31-11105C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027148 | ||||||
| chr7:45027219
|
T | C | 310 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(307): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.31-11034T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027219 | ||||||
| chr7:45027219
|
T | G | 1 | a0001c0002t0002g0024 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.31-11034T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027219 | ||||||
| chr7:45027416
|
G | A | 1 | a0006c0012t0001g0196 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.31-10837G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027416 | ||||||
| chr7:45027418
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-10835A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027418 | ||||||
| chr7:45027609
|
G | A | 1 | a0001c0008t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.31-10644G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027609 | ||||||
| chr7:45027668
|
G | C | 82 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(79): Show | 83 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.31-10585G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027668 | ||||||
| chr7:45027997
|
G | A | 1 | a0003c0004t0001g0230 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.31-10256G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45027997 | ||||||
| chr7:45028294
|
A | G | 5 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(2): Show | 5 | HG00140.hp1 HG01099.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9959A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45028294 | ||||||
| chr7:45028400
|
G | A | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9853G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45028400 | ||||||
| chr7:45028513
|
C | T | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.31-9740C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45028513 | ||||||
| chr7:45028523
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0004g0003others(1): Show | 4 | HG00323.hp1 HG01074.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-9730G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45028523 | ||||||
| chr7:45028528
|
G | A | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-9725G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45028528 | ||||||
| chr7:45028656
|
C | CA | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-9588dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45028656 | |||||
| chr7:45028936
|
G | A | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.31-9317G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45028936 | ||||||
| chr7:45028984
|
C | G | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.31-9269C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45028984 | ||||||
| chr7:45029054
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.31-9199C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029054 | ||||||
| chr7:45029185
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-9068T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029185 | ||||||
| chr7:45029228
|
G | A | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.31-9025G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029228 | ||||||
| chr7:45029375
|
A | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.31-8878A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029375 | ||||||
| chr7:45029540
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.31-8713A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029540 | ||||||
| chr7:45029745
|
G | T | 2 | a0001c0002t0001g0141a0001c0002t0001g0142 | 2 | HG02132.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.31-8508G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029745 | ||||||
| chr7:45029985
|
A | C | 49 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 49 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.31-8268A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45029985 | ||||||
| chr7:45030088
|
C | T | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-8165C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030088 | ||||||
| chr7:45030482
|
G | T | 31 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(28): Show | 32 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.31-7771G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030482 | ||||||
| chr7:45030560
|
T | A | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.31-7693T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030560 | ||||||
| chr7:45030747
|
G | A | 49 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(46): Show | 49 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(46): Show |
intron_variant | MODIFIER | c.31-7506G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030747 | ||||||
| chr7:45030770
|
C | G | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-7483C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030770 | ||||||
| chr7:45030849
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.31-7404G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030849 | ||||||
| chr7:45030884
|
C | T | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-7369C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030884 | ||||||
| chr7:45030885
|
G | A | 6 | a0001c0001t0001g0088a0001c0006t0001g0059a0001c0006t0001g0060others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-7368G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030885 | ||||||
| chr7:45030954
|
C | T | 19 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-7299C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030954 | ||||||
| chr7:45030985
|
A | C | 1 | a0001c0006t0001g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.31-7268A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45030985 | ||||||
| chr7:45031050
|
C | T | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-7203C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45031050 | ||||||
| chr7:45031381
|
C | CA | 20 | a0001c0001t0001g0019a0001c0001t0001g0071a0001c0001t0001g0106others(17): Show | 20 | HG00323.hp2 HG00438.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.31-6852dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45031381 | |||||
| chr7:45031381
|
CA | C | 21 | a0001c0001t0001g0069a0001c0001t0001g0108a0001c0001t0001g0177others(18): Show | 22 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.31-6852delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45031381 | |||||
| chr7:45031495
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.31-6758C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45031495 | ||||||
| chr7:45031524
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0301 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.31-6729G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45031524 | ||||||
| chr7:45031935
|
C | G | 6 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0175others(3): Show | 6 | HG00738.hp2 HG01255.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-6318C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45031935 | ||||||
| chr7:45031946
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0288 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.31-6307C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45031946 | ||||||
| chr7:45032157
|
T | C | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.31-6096T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45032157 | ||||||
| chr7:45032262
|
C | A | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-5991C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45032262 | ||||||
| chr7:45032333
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-5920G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45032333 | ||||||
| chr7:45032365
|
A | G | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-5888A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45032365 | ||||||
| chr7:45032482
|
G | A | 1 | a0001c0006t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.31-5771G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45032482 | ||||||
| chr7:45032783
|
G | A | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-5470G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45032783 | ||||||
| chr7:45033044
|
C | CA | 167 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(164): Show | 168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.31-5182dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45033044 | |||||
| chr7:45033044
|
C | CAA | 64 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(61): Show | 64 | HG00140.hp2 HG00558.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.31-5183_31-5182dup others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45033044 | |||||
| chr7:45033044
|
C | CAAA | 19 | a0001c0001t0001g0023a0001c0001t0001g0112a0001c0001t0001g0116others(16): Show | 19 | HG00741.hp2 HG01106.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.31-5184_31-5182dup others(3): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45033044 | |||||
| chr7:45033246
|
G | T | 1 | a0001c0002t0001g0141 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.31-5007G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45033246 | ||||||
| chr7:45033248
|
C | G | 1 | a0001c0002t0001g0141 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.31-5005C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45033248 | ||||||
| chr7:45033250
|
G | C | 1 | a0001c0002t0001g0141 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.31-5003G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45033250 | ||||||
| chr7:45033417
|
T | C | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-4836T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45033417 | ||||||
| chr7:45033568
|
T | A | 1 | a0001c0002t0002g0027 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.31-4685T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45033568 | ||||||
| chr7:45033625
|
C | T | 19 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-4628C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45033625 | ||||||
| chr7:45033813
|
T | TG | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-4439dupG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45033813 | |||||
| chr7:45033819
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.31-4434T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45033819 | ||||||
| chr7:45034134
|
G | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0144a0001c0001t0001g0163 | 3 | HG02622.hp1 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.31-4119G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034134 | ||||||
| chr7:45034146
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.31-4107G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034146 | ||||||
| chr7:45034200
|
A | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-4053A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034200 | ||||||
| chr7:45034209
|
C | CT | 7 | a0001c0001t0001g0020a0001c0001t0001g0117a0001c0001t0001g0147others(4): Show | 7 | HG00609.hp1 HG01109.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.31-4030dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45034209 | |||||
| chr7:45034219
|
T | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.31-4034T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034219 | ||||||
| chr7:45034220
|
T | G | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.31-4033T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034220 | ||||||
| chr7:45034291
|
A | G | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.31-3962A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034291 | ||||||
| chr7:45034304
|
C | A | 19 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-3949C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034304 | ||||||
| chr7:45034423
|
G | A | 1 | a0001c0001t0001g0264 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.31-3830G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034423 | ||||||
| chr7:45034508
|
T | C | 2 | a0002c0003t0002g0030a0002c0003t0002g0080 | 2 | NA18940.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.31-3745T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034508 | ||||||
| chr7:45034512
|
C | CT | 68 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(65): Show | 68 | HG00639.hp1 HG00673.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.31-3718dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45034512 | |||||
| chr7:45034512
|
C | CTT | 166 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.31-3719_31-3718dup others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45034512 | |||||
| chr7:45034512
|
C | CTTT | 37 | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0001g0182others(34): Show | 37 | HG00438.hp1 HG00544.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.31-3720_31-3718dup others(3): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45034512 | |||||
| chr7:45034604
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.31-3649C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034604 | ||||||
| chr7:45034667
|
C | T | 2 | a0001c0006t0001g0061a0001c0006t0001g0161 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.31-3586C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034667 | ||||||
| chr7:45034668
|
G | A | 1 | a0001c0002t0001g0132 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.31-3585G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034668 | ||||||
| chr7:45034677
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0301 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.31-3576C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034677 | ||||||
| chr7:45034709
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.31-3544G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034709 | ||||||
| chr7:45034915
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-3338G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034915 | ||||||
| chr7:45034931
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.31-3322G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034931 | ||||||
| chr7:45034952
|
T | C | 34 | a0001c0001t0001g0019a0001c0001t0001g0166a0001c0001t0001g0167others(31): Show | 34 | HG00280.hp2 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.31-3301T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45034952 | ||||||
| chr7:45035072
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.31-3181C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035072 | ||||||
| chr7:45035135
|
C | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.31-3118C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035135 | ||||||
| chr7:45035149
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-3104T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035149 | ||||||
| chr7:45035198
|
G | A | 1 | a0001c0002t0002g0028 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.31-3055G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035198 | ||||||
| chr7:45035398
|
C | G | 50 | a0001c0001t0001g0034a0001c0001t0001g0164a0001c0001t0001g0170others(47): Show | 50 | HG00558.hp1 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.31-2855C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035398 | ||||||
| chr7:45035439
|
A | G | 1 | a0005c0011t0001g0190 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.31-2814A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035439 | ||||||
| chr7:45035617
|
C | G | 2 | a0001c0001t0001g0249a0001c0001t0001g0280 | 2 | HG02148.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.31-2636C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035617 | ||||||
| chr7:45035629
|
G | A | 1 | a0002c0003t0002g0057 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.31-2624G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035629 | ||||||
| chr7:45035631
|
C | T | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.31-2622C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035631 | ||||||
| chr7:45035651
|
G | A | 2 | a0001c0006t0001g0061a0001c0006t0001g0161 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.31-2602G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035651 | ||||||
| chr7:45035884
|
C | G | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.31-2369C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035884 | ||||||
| chr7:45035913
|
G | A | 11 | a0001c0002t0002g0089a0001c0002t0002g0092a0001c0002t0002g0100others(8): Show | 11 | HG00642.hp1 HG00738.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.31-2340G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035913 | ||||||
| chr7:45035917
|
A | G | 33 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(30): Show | 33 | HG00558.hp2 HG00673.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.31-2336A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45035917 | ||||||
| chr7:45036084
|
A | G | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.31-2169A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036084 | ||||||
| chr7:45036264
|
A | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.31-1989A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036264 | ||||||
| chr7:45036387
|
A | G | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.31-1866A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036387 | ||||||
| chr7:45036392
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.31-1861G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036392 | ||||||
| chr7:45036397
|
AG | A | 5 | a0001c0001t0001g0088a0001c0006t0001g0060a0001c0006t0001g0061others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-1853delG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45036397 | |||||
| chr7:45036709
|
A | G | 3 | a0001c0002t0001g0014a0001c0002t0001g0017a0001c0002t0001g0137 | 3 | HG00741.hp1 HG01070.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.31-1544A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036709 | ||||||
| chr7:45036893
|
T | C | 1 | a0001c0008t0001g0007 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.31-1360T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036893 | ||||||
| chr7:45036913
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.31-1340G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036913 | ||||||
| chr7:45036958
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.31-1295G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45036958 | ||||||
| chr7:45037031
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.31-1222C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037031 | ||||||
| chr7:45037041
|
C | A | 6 | a0002c0003t0002g0029a0002c0003t0002g0033a0002c0003t0002g0038others(3): Show | 6 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-1212C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037041 | ||||||
| chr7:45037207
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.31-1046A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037207 | ||||||
| chr7:45037252
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0219others(2): Show | 5 | HG00738.hp2 HG01255.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-1001C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037252 | ||||||
| chr7:45037351
|
G | A | 1 | a0001c0006t0001g0161 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.31-902G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037351 | ||||||
| chr7:45037375
|
G | A | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-878G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037375 | ||||||
| chr7:45037418
|
C | CT | 55 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(52): Show | 56 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.31-815dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45037418 | |||||
| chr7:45037418
|
C | CTT | 37 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(34): Show | 37 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.31-816_31-815dupTT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45037418 | |||||
| chr7:45037418
|
C | CTTT | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.31-817_31-815dupTT others(1): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45037418 | |||||
| chr7:45037418
|
C | CTTTT | 8 | a0001c0001t0001g0181a0001c0001t0001g0213a0001c0001t0001g0234others(5): Show | 8 | HG01978.hp1 HG01981.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.31-818_31-815dupTT others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 45037418 | |||||
| chr7:45037457
|
G | A | 1 | a0001c0002t0002g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.31-796G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037457 | ||||||
| chr7:45037486
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0154 | 3 | HG00639.hp1 HG02451.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.31-767C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037486 | ||||||
| chr7:45037637
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.31-616C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037637 | ||||||
| chr7:45037662
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.31-591C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037662 | ||||||
| chr7:45037737
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.31-516C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037737 | ||||||
| chr7:45037824
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.31-429G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037824 | ||||||
| chr7:45037825
|
T | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02280.hp1 HG03139.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-428T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037825 | ||||||
| chr7:45037893
|
G | T | 1 | a0001c0001t0006g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.31-360G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 1/9 | chr7 | 45037893 | ||||||
| chr7:45038473
|
G | A | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+47G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45038473 | ||||||
| chr7:45038824
|
T | C | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.204+398T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45038824 | ||||||
| chr7:45039417
|
T | G | 306 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(303): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.204+991T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45039417 | ||||||
| chr7:45039716
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.204+1290A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45039716 | ||||||
| chr7:45039750
|
G | A | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 28 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.204+1324G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45039750 | ||||||
| chr7:45039753
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.204+1327G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45039753 | ||||||
| chr7:45039951
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(269): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.204+1525T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45039951 | ||||||
| chr7:45039967
|
C | T | 19 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+1541C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45039967 | ||||||
| chr7:45040173
|
A | G | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.204+1747A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040173 | ||||||
| chr7:45040207
|
A | G | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.204+1781A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040207 | ||||||
| chr7:45040239
|
C | G | 2 | a0004c0007t0001g0242a0004c0007t0001g0248 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.204+1813C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040239 | ||||||
| chr7:45040240
|
C | T | 1 | a0002c0003t0002g0056 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.204+1814C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040240 | ||||||
| chr7:45040246
|
C | T | 2 | a0003c0004t0001g0201a0003c0004t0001g0225 | 2 | HG01928.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.204+1820C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040246 | ||||||
| chr7:45040252
|
C | T | 1 | a0001c0002t0002g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.204+1826C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040252 | ||||||
| chr7:45040387
|
A | C | 29 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.204+1961A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040387 | ||||||
| chr7:45040493
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.204+2067T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040493 | ||||||
| chr7:45040590
|
T | C | 4 | a0001c0001t0001g0034a0002c0003t0002g0030a0002c0003t0002g0037others(1): Show | 4 | NA18940.hp1 NA18962.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+2164T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040590 | ||||||
| chr7:45040645
|
C | T | 9 | a0001c0001t0001g0164a0001c0001t0001g0172a0001c0001t0001g0178others(6): Show | 9 | HG00609.hp1 HG02004.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+2219C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040645 | ||||||
| chr7:45040754
|
A | AGG | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.204+2333_204+2334d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45040754 | |||||
| chr7:45040779
|
G | A | 1 | a0002c0003t0002g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.204+2353G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040779 | ||||||
| chr7:45040857
|
G | A | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+2431G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040857 | ||||||
| chr7:45040905
|
G | C | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.204+2479G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040905 | ||||||
| chr7:45040938
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+2512C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040938 | ||||||
| chr7:45040949
|
C | G | 2 | a0004c0007t0001g0200a0004c0007t0001g0279 | 2 | HG00642.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.204+2523C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040949 | ||||||
| chr7:45040995
|
A | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.204+2569A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45040995 | ||||||
| chr7:45041087
|
G | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+2661G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041087 | ||||||
| chr7:45041334
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.204+2908G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041334 | ||||||
| chr7:45041511
|
C | G | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG01256.hp1 HG02080.hp2 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+3085C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041511 | ||||||
| chr7:45041576
|
A | G | 1 | a0001c0002t0001g0141 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.204+3150A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041576 | ||||||
| chr7:45041596
|
G | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0186 | 2 | NA18950.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.204+3170G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041596 | ||||||
| chr7:45041672
|
C | T | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.204+3246C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041672 | ||||||
| chr7:45041811
|
A | T | 2 | a0001c0001t0001g0204a0001c0013t0001g0245 | 2 | HG00558.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.204+3385A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041811 | ||||||
| chr7:45041850
|
T | C | 1 | a0001c0002t0002g0126 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.204+3424T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45041850 | ||||||
| chr7:45042004
|
C | T | 2 | a0001c0001t0001g0204a0002c0003t0002g0045 | 2 | HG00558.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.204+3578C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042004 | ||||||
| chr7:45042068
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.204+3642G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042068 | ||||||
| chr7:45042119
|
C | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0103 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.204+3693C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042119 | ||||||
| chr7:45042190
|
C | T | 16 | a0001c0001t0001g0002a0001c0001t0001g0182a0001c0001t0001g0183others(13): Show | 17 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.204+3764C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042190 | ||||||
| chr7:45042220
|
C | T | 6 | a0001c0002t0001g0093a0001c0002t0001g0096a0001c0002t0001g0097others(3): Show | 6 | HG00323.hp2 NA18952.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+3794C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042220 | ||||||
| chr7:45042265
|
C | CAAAAAAA others(2): Show |
126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(123): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.204+3841_204+3849d others(11): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042265
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0001g0254a0001c0001t0001g0275a0001c0001t0001g0276others(4): Show | 7 | HG01934.hp1 HG01981.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+3840_204+3849d others(12): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042265
|
C | CAAAAAAA others(7): Show |
38 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(35): Show | 39 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.204+3849_204+3850i others(16): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042265
|
C | CAAAAAAA others(8): Show |
33 | a0001c0001t0001g0020a0001c0001t0001g0069a0001c0001t0001g0107others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.204+3849_204+3850i others(17): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042265
|
C | CAAAAAAA others(9): Show |
52 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(49): Show | 52 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.204+3849_204+3850i others(18): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042265
|
C | CAAAAAAA others(10): Show |
7 | a0001c0002t0001g0068a0001c0002t0001g0091a0001c0002t0001g0096others(4): Show | 7 | HG00323.hp2 NA18956.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+3849_204+3850i others(19): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042265
|
C | CAAAAAAA others(11): Show |
4 | a0001c0008t0001g0007a0001c0008t0001g0009a0001c0008t0001g0010others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+3849_204+3850i others(20): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042265
|
C | CAAAAAAA others(12): Show |
1 | a0001c0008t0001g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.204+3849_204+3850i others(21): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042265 | |||||
| chr7:45042281
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.204+3855C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042281 | ||||||
| chr7:45042383
|
A | G | 1 | a0001c0002t0001g0132 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.204+3957A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042383 | ||||||
| chr7:45042790
|
G | A | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+4364G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042790 | ||||||
| chr7:45042813
|
TA | T | 6 | a0001c0001t0001g0088a0001c0006t0001g0059a0001c0006t0001g0060others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+4394delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042813 | |||||
| chr7:45042820
|
A | T | 6 | a0001c0001t0001g0088a0001c0006t0001g0059a0001c0006t0001g0060others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+4394A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042820 | ||||||
| chr7:45042826
|
T | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+4400T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042826 | ||||||
| chr7:45042938
|
C | T | 2 | a0001c0006t0001g0061a0001c0006t0001g0161 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.204+4512C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042938 | ||||||
| chr7:45042968
|
C | CT | 6 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0216others(3): Show | 6 | NA18940.hp2 NA18953.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+4560dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042968 | |||||
| chr7:45042968
|
CTTT | C | 165 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(162): Show | 166 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.204+4558_204+4560d others(5): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45042968 | |||||
| chr7:45042971
|
T | C | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.204+4545T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45042971 | ||||||
| chr7:45043047
|
A | G | 33 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(30): Show | 33 | HG00558.hp2 HG00673.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.204+4621A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043047 | ||||||
| chr7:45043178
|
C | G | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.204+4752C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043178 | ||||||
| chr7:45043215
|
C | T | 2 | a0002c0003t0002g0046a0002c0003t0002g0047 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.204+4789C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043215 | ||||||
| chr7:45043466
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+5040C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043466 | ||||||
| chr7:45043579
|
G | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0247 | 2 | HG00609.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.204+5153G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043579 | ||||||
| chr7:45043605
|
G | A | 3 | a0001c0002t0002g0089a0001c0002t0002g0100a0001c0002t0002g0139 | 3 | HG01928.hp1 HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.204+5179G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043605 | ||||||
| chr7:45043628
|
C | CA | 34 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0217others(31): Show | 35 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.204+5216dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45043628 | |||||
| chr7:45043644
|
TGTG | T | 28 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 28 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.204+5220_204+5222d others(5): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45043644 | |||||
| chr7:45043835
|
A | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+5409A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043835 | ||||||
| chr7:45043857
|
T | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+5431T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043857 | ||||||
| chr7:45043874
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.204+5448T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45043874 | ||||||
| chr7:45044005
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.204+5579C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044005 | ||||||
| chr7:45044034
|
T | C | 18 | a0002c0003t0002g0031a0002c0003t0002g0035a0002c0003t0002g0036others(15): Show | 18 | HG00558.hp2 HG00673.hp2 HG02129.hp1 others(15): Show |
intron_variant | MODIFIER | c.204+5608T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044034 | ||||||
| chr7:45044264
|
G | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+5838G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044264 | ||||||
| chr7:45044290
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(202): Show | 206 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.204+5864C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044290 | ||||||
| chr7:45044457
|
G | A | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.204+6031G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044457 | ||||||
| chr7:45044580
|
A | G | 2 | a0001c0001t0004g0003a0001c0001t0004g0004 | 2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.204+6154A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044580 | ||||||
| chr7:45044847
|
T | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+6421T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044847 | ||||||
| chr7:45044855
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.204+6429C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044855 | ||||||
| chr7:45044926
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+6500C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044926 | ||||||
| chr7:45044957
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.204+6531G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45044957 | ||||||
| chr7:45045108
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+6682A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045108 | ||||||
| chr7:45045190
|
T | TAGAGCA | 41 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+6766_204+6771d others(8): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45045190 | |||||
| chr7:45045222
|
T | G | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.204+6796T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045222 | ||||||
| chr7:45045313
|
A | G | 1 | a0003c0004t0001g0225 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.204+6887A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045313 | ||||||
| chr7:45045364
|
TAAAAG | T | 3 | a0001c0002t0002g0101a0001c0002t0002g0102a0001c0002t0002g0140 | 3 | HG00738.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.204+6943_204+6947d others(7): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45045364 | |||||
| chr7:45045380
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0176others(19): Show | 22 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.204+6954G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045380 | ||||||
| chr7:45045383
|
T | TA | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.204+6964dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45045383 | |||||
| chr7:45045520
|
G | A | 1 | a0002c0015t0002g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.204+7094G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045520 | ||||||
| chr7:45045549
|
T | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7123T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045549 | ||||||
| chr7:45045709
|
T | G | 3 | a0001c0002t0002g0122a0001c0002t0002g0157a0001c0002t0002g0159 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.204+7283T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045709 | ||||||
| chr7:45045910
|
G | A | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7484G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45045910 | ||||||
| chr7:45046007
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.204+7581G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046007 | ||||||
| chr7:45046035
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+7609A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046035 | ||||||
| chr7:45046114
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | NA18948.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.204+7688A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046114 | ||||||
| chr7:45046264
|
A | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+7838A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046264 | ||||||
| chr7:45046296
|
T | A | 279 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.204+7870T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046296 | ||||||
| chr7:45046337
|
T | C | 167 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(164): Show | 168 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(165): Show |
intron_variant | MODIFIER | c.204+7911T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046337 | ||||||
| chr7:45046439
|
C | T | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.204+8013C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046439 | ||||||
| chr7:45046639
|
T | C | 19 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0273others(16): Show | 20 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+8213T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046639 | ||||||
| chr7:45046834
|
A | G | 12 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.204+8408A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046834 | ||||||
| chr7:45046841
|
G | T | 1 | a0001c0002t0001g0198 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.204+8415G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45046841 | ||||||
| chr7:45047066
|
A | G | 71 | a0001c0001t0001g0177a0001c0001t0001g0207a0001c0001t0001g0257others(68): Show | 72 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.204+8640A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047066 | ||||||
| chr7:45047314
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+8888C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047314 | ||||||
| chr7:45047387
|
A | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0145 | 3 | HG00735.hp1 HG01106.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.204+8961A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047387 | ||||||
| chr7:45047403
|
G | A | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+8977G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047403 | ||||||
| chr7:45047533
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.204+9107T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047533 | ||||||
| chr7:45047609
|
C | T | 39 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(36): Show | 39 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.204+9183C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047609 | ||||||
| chr7:45047783
|
A | G | 41 | a0001c0001t0001g0170a0001c0001t0001g0192a0002c0003t0002g0029others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+9357A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047783 | ||||||
| chr7:45047937
|
A | G | 1 | a0001c0002t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.204+9511A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047937 | ||||||
| chr7:45047940
|
A | G | 1 | a0001c0002t0001g0134 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.204+9514A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45047940 | ||||||
| chr7:45048067
|
C | CAATAAAT | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+9645_204+9646i others(9): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45048067 | |||||
| chr7:45048219
|
G | T | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.204+9793G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048219 | ||||||
| chr7:45048393
|
A | G | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+9967A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048393 | ||||||
| chr7:45048530
|
C | T | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.204+10104C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048530 | ||||||
| chr7:45048557
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.204+10131G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048557 | ||||||
| chr7:45048607
|
A | G | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.204+10181A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048607 | ||||||
| chr7:45048755
|
G | A | 1 | a0001c0002t0002g0129 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.204+10329G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048755 | ||||||
| chr7:45048758
|
T | TA | 16 | a0001c0001t0001g0206a0001c0002t0002g0001a0001c0002t0002g0024others(13): Show | 17 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.204+10347dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45048758 | |||||
| chr7:45048778
|
T | C | 7 | a0001c0001t0001g0113a0001c0001t0001g0153a0001c0001t0001g0155others(4): Show | 7 | HG01884.hp1 HG02970.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+10352T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048778 | ||||||
| chr7:45048950
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.204+10524T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048950 | ||||||
| chr7:45048994
|
C | G | 1 | a0002c0010t0002g0052 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.204+10568C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45048994 | ||||||
| chr7:45049024
|
T | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+10598T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049024 | ||||||
| chr7:45049038
|
T | C | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.204+10612T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049038 | ||||||
| chr7:45049055
|
C | A | 2 | a0001c0001t0001g0250a0001c0001t0001g0251 | 2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.204+10629C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049055 | ||||||
| chr7:45049419
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+10993C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049419 | ||||||
| chr7:45049467
|
C | T | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.204+11041C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049467 | ||||||
| chr7:45049656
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+11230C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049656 | ||||||
| chr7:45049736
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0006 | 2 | HG00323.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.204+11310C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049736 | ||||||
| chr7:45049773
|
ACT | A | 46 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(43): Show | 46 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.204+11350_204+1135 others(6): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45049773 | |||||
| chr7:45049860
|
A | G | 1 | a0002c0003t0002g0298 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.204+11434A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049860 | ||||||
| chr7:45049970
|
A | G | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.204+11544A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45049970 | ||||||
| chr7:45050127
|
T | C | 130 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 131 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.204+11701T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050127 | ||||||
| chr7:45050128
|
G | A | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.204+11702G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050128 | ||||||
| chr7:45050192
|
A | G | 2 | a0002c0003t0002g0046a0002c0003t0002g0047 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.204+11766A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050192 | ||||||
| chr7:45050261
|
TA | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+11837delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45050261 | |||||
| chr7:45050357
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+11931C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050357 | ||||||
| chr7:45050509
|
G | A | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.204+12083G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050509 | ||||||
| chr7:45050545
|
A | T | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.204+12119A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050545 | ||||||
| chr7:45050653
|
T | A | 1 | a0001c0001t0001g0233 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.204+12227T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050653 | ||||||
| chr7:45050878
|
A | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+12452A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050878 | ||||||
| chr7:45050907
|
G | T | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.204+12481G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050907 | ||||||
| chr7:45050953
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.204+12527C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45050953 | ||||||
| chr7:45051017
|
T | C | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+12591T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051017 | ||||||
| chr7:45051100
|
G | A | 6 | a0001c0001t0001g0069a0001c0008t0001g0007a0001c0008t0001g0008others(3): Show | 6 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+12674G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051100 | ||||||
| chr7:45051105
|
T | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+12679T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051105 | ||||||
| chr7:45051140
|
T | C | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+12714T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051140 | ||||||
| chr7:45051195
|
A | C | 3 | a0001c0001t0001g0107a0001c0001t0001g0144a0001c0001t0001g0163 | 3 | HG02622.hp1 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.205-12723A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051195 | ||||||
| chr7:45051248
|
A | G | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-12670A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051248 | ||||||
| chr7:45051312
|
G | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-12606G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051312 | ||||||
| chr7:45051320
|
T | C | 2 | a0004c0007t0001g0242a0004c0007t0001g0248 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.205-12598T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051320 | ||||||
| chr7:45051341
|
C | T | 2 | a0001c0008t0001g0010a0001c0008t0001g0011 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.205-12577C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051341 | ||||||
| chr7:45051350
|
G | A | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0143others(2): Show | 5 | HG00735.hp1 HG01106.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-12568G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051350 | ||||||
| chr7:45051383
|
G | GTATT | 22 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0001g0153others(19): Show | 22 | HG01243.hp2 HG01433.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.205-12506_205-1250 others(8): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45051383 | |||||
| chr7:45051383
|
G | GTATTTAT others(1): Show |
36 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(33): Show | 36 | HG00735.hp1 HG01106.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.205-12510_205-1250 others(12): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45051383 | |||||
| chr7:45051383
|
G | GTATTTAT others(5): Show |
3 | a0001c0001t0001g0088a0001c0001t0001g0118a0001c0001t0001g0146 | 3 | HG02258.hp1 HG03834.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.205-12514_205-1250 others(16): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45051383 | |||||
| chr7:45051383
|
GTATTTAT others(5): Show |
G | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.205-12514_205-1250 others(16): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45051383 | |||||
| chr7:45051405
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-12513A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051405 | ||||||
| chr7:45051413
|
A | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-12505A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051413 | ||||||
| chr7:45051523
|
T | G | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.205-12395T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051523 | ||||||
| chr7:45051555
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.205-12363G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051555 | ||||||
| chr7:45051585
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-12333C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051585 | ||||||
| chr7:45051646
|
T | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-12272T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051646 | ||||||
| chr7:45051722
|
G | T | 1 | a0001c0002t0001g0142 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.205-12196G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051722 | ||||||
| chr7:45051776
|
T | C | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-12142T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051776 | ||||||
| chr7:45051852
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-12066C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051852 | ||||||
| chr7:45051862
|
C | T | 1 | a0002c0015t0002g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.205-12056C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45051862 | ||||||
| chr7:45052015
|
G | A | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-11903G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052015 | ||||||
| chr7:45052035
|
G | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0179a0001c0001t0001g0186 | 3 | HG02004.hp2 NA18950.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.205-11883G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052035 | ||||||
| chr7:45052048
|
C | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-11870C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052048 | ||||||
| chr7:45052101
|
G | A | 2 | a0002c0003t0002g0053a0002c0003t0002g0084 | 2 | HG01069.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.205-11817G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052101 | ||||||
| chr7:45052103
|
A | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0288 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.205-11815A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052103 | ||||||
| chr7:45052204
|
A | C | 3 | a0001c0001t0001g0170a0001c0001t0001g0192a0001c0001t0001g0244 | 3 | NA18970.hp1 NA19054.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.205-11714A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052204 | ||||||
| chr7:45052278
|
C | T | 1 | a0001c0002t0002g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205-11640C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052278 | ||||||
| chr7:45052287
|
G | A | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.205-11631G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052287 | ||||||
| chr7:45052418
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0103 | 2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.205-11500T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052418 | ||||||
| chr7:45052535
|
C | T | 4 | a0001c0002t0002g0122a0001c0002t0002g0157a0001c0002t0002g0159others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-11383C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052535 | ||||||
| chr7:45052547
|
C | T | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-11371C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052547 | ||||||
| chr7:45052732
|
A | T | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-11186A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052732 | ||||||
| chr7:45052938
|
A | G | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-10980A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052938 | ||||||
| chr7:45052963
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.205-10955C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052963 | ||||||
| chr7:45052974
|
C | T | 3 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0156 | 3 | HG01243.hp1 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.205-10944C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45052974 | ||||||
| chr7:45053121
|
C | G | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.205-10797C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053121 | ||||||
| chr7:45053315
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-10603T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053315 | ||||||
| chr7:45053360
|
C | T | 1 | a0002c0003t0002g0029 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.205-10558C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053360 | ||||||
| chr7:45053361
|
G | A | 2 | a0001c0001t0001g0237a0001c0001t0001g0281 | 2 | HG02071.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.205-10557G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053361 | ||||||
| chr7:45053376
|
T | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-10542T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053376 | ||||||
| chr7:45053392
|
A | C | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-10526A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053392 | ||||||
| chr7:45053468
|
G | C | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.205-10450G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053468 | ||||||
| chr7:45053530
|
G | A | 1 | a0002c0003t0002g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.205-10388G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053530 | ||||||
| chr7:45053588
|
A | G | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-10330A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053588 | ||||||
| chr7:45053599
|
G | A | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-10319G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053599 | ||||||
| chr7:45053680
|
C | T | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.205-10238C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053680 | ||||||
| chr7:45053707
|
C | T | 2 | a0001c0002t0001g0015a0001c0002t0001g0016 | 2 | NA18966.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.205-10211C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053707 | ||||||
| chr7:45053779
|
A | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-10139A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053779 | ||||||
| chr7:45053824
|
G | C | 1 | a0001c0006t0001g0061 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.205-10094G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053824 | ||||||
| chr7:45053840
|
G | T | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.205-10078G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053840 | ||||||
| chr7:45053869
|
T | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-10049T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053869 | ||||||
| chr7:45053951
|
T | G | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.205-9967T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45053951 | ||||||
| chr7:45054076
|
T | C | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-9842T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054076 | ||||||
| chr7:45054084
|
G | A | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-9834G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054084 | ||||||
| chr7:45054235
|
A | G | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.205-9683A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054235 | ||||||
| chr7:45054277
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0271a0001c0001t0001g0294 | 3 | HG02027.hp1 NA18966.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.205-9641G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054277 | ||||||
| chr7:45054481
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-9437A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054481 | ||||||
| chr7:45054486
|
T | TA | 84 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(81): Show | 84 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.205-9421dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45054486 | |||||
| chr7:45054552
|
T | G | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-9366T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054552 | ||||||
| chr7:45054656
|
G | A | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-9262G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054656 | ||||||
| chr7:45054702
|
G | A | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-9216G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054702 | ||||||
| chr7:45054796
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-9122G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45054796 | ||||||
| chr7:45055166
|
G | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-8752G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055166 | ||||||
| chr7:45055217
|
G | A | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-8701G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055217 | ||||||
| chr7:45055248
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-8670A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055248 | ||||||
| chr7:45055277
|
A | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-8641A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055277 | ||||||
| chr7:45055384
|
A | G | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.205-8534A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055384 | ||||||
| chr7:45055407
|
G | A | 2 | a0001c0001t0001g0269a0001c0001t0001g0303 | 2 | HG00621.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.205-8511G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055407 | ||||||
| chr7:45055429
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-8489C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055429 | ||||||
| chr7:45055470
|
C | T | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.205-8448C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055470 | ||||||
| chr7:45055574
|
A | T | 1 | a0004c0007t0001g0300 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.205-8344A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055574 | ||||||
| chr7:45055617
|
G | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-8301G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055617 | ||||||
| chr7:45055733
|
A | G | 52 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(49): Show | 52 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.205-8185A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055733 | ||||||
| chr7:45055996
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-7922C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45055996 | ||||||
| chr7:45056027
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0152 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.205-7891A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056027 | ||||||
| chr7:45056119
|
G | A | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-7799G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056119 | ||||||
| chr7:45056158
|
GTC | G | 12 | a0002c0003t0002g0029a0002c0003t0002g0032a0002c0003t0002g0033others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-7758_205-7757d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45056158 | |||||
| chr7:45056392
|
C | T | 7 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0259others(4): Show | 7 | HG02145.hp1 HG02280.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-7526C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056392 | ||||||
| chr7:45056548
|
G | A | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.205-7370G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056548 | ||||||
| chr7:45056636
|
AATGTC | A | 32 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(29): Show | 32 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.205-7280_205-7276d others(7): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45056636 | |||||
| chr7:45056723
|
A | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-7195A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056723 | ||||||
| chr7:45056729
|
T | A | 6 | a0001c0001t0001g0189a0001c0001t0001g0238a0001c0001t0001g0241others(3): Show | 6 | HG02809.hp1 HG02818.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-7189T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056729 | ||||||
| chr7:45056768
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-7150G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056768 | ||||||
| chr7:45056770
|
T | C | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-7148T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056770 | ||||||
| chr7:45056837
|
G | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-7081G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056837 | ||||||
| chr7:45056930
|
A | T | 1 | a0003c0004t0001g0226 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.205-6988A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45056930 | ||||||
| chr7:45057131
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.205-6787C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057131 | ||||||
| chr7:45057149
|
G | A | 1 | a0003c0004t0001g0231 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.205-6769G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057149 | ||||||
| chr7:45057170
|
C | CT | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.205-6738dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45057170 | |||||
| chr7:45057222
|
G | A | 3 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0145 | 3 | HG00735.hp1 HG01106.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.205-6696G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057222 | ||||||
| chr7:45057222
|
G | C | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-6696G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057222 | ||||||
| chr7:45057312
|
G | A | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.205-6606G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057312 | ||||||
| chr7:45057324
|
G | A | 1 | a0001c0002t0001g0314 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.205-6594G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057324 | ||||||
| chr7:45057412
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-6506C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057412 | ||||||
| chr7:45057452
|
C | T | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.205-6466C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057452 | ||||||
| chr7:45057515
|
T | C | 2 | a0001c0001t0001g0185a0001c0001t0001g0301 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.205-6403T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057515 | ||||||
| chr7:45057569
|
G | C | 5 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0147others(2): Show | 5 | HG01109.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-6349G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057569 | ||||||
| chr7:45057609
|
G | T | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.205-6309G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057609 | ||||||
| chr7:45057835
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.205-6083C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057835 | ||||||
| chr7:45057949
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.205-5969G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45057949 | ||||||
| chr7:45058061
|
T | C | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.205-5857T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058061 | ||||||
| chr7:45058085
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.205-5833A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058085 | ||||||
| chr7:45058099
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.205-5819A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058099 | ||||||
| chr7:45058451
|
T | C | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-5467T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058451 | ||||||
| chr7:45058566
|
G | A | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-5352G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058566 | ||||||
| chr7:45058726
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-5192A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058726 | ||||||
| chr7:45058786
|
T | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-5132T>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058786 | ||||||
| chr7:45058891
|
G | A | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-5027G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058891 | ||||||
| chr7:45058900
|
A | AT | 145 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(142): Show | 145 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.205-5002dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45058900 | |||||
| chr7:45058945
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.205-4973A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45058945 | ||||||
| chr7:45059177
|
G | A | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-4741G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059177 | ||||||
| chr7:45059351
|
GGCAGGAG others(8): Show |
G | 1 | a0001c0008t0001g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.205-4565_205-4551d others(17): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45059351 | |||||
| chr7:45059409
|
C | G | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-4509C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059409 | ||||||
| chr7:45059428
|
AAAAAG | A | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-4486_205-4482d others(7): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45059428 | |||||
| chr7:45059472
|
C | G | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-4446C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059472 | ||||||
| chr7:45059473
|
G | C | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-4445G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059473 | ||||||
| chr7:45059520
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-4398G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059520 | ||||||
| chr7:45059623
|
C | G | 1 | a0001c0001t0001g0273 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.205-4295C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059623 | ||||||
| chr7:45059623
|
C | T | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.205-4295C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059623 | ||||||
| chr7:45059648
|
G | A | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-4270G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059648 | ||||||
| chr7:45059652
|
C | A | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.205-4266C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059652 | ||||||
| chr7:45059691
|
T | C | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.205-4227T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059691 | ||||||
| chr7:45059764
|
A | G | 13 | a0003c0004t0001g0169a0003c0004t0001g0193a0003c0004t0001g0201others(10): Show | 13 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.205-4154A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059764 | ||||||
| chr7:45059851
|
C | T | 40 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(37): Show | 40 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.205-4067C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059851 | ||||||
| chr7:45059907
|
A | G | 13 | a0003c0004t0001g0169a0003c0004t0001g0193a0003c0004t0001g0201others(10): Show | 13 | HG01261.hp2 HG01496.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.205-4011A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45059907 | ||||||
| chr7:45060126
|
T | C | 1 | a0003c0004t0001g0227 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.205-3792T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45060126 | ||||||
| chr7:45060500
|
G | A | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-3418G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45060500 | ||||||
| chr7:45060630
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0281 | 2 | HG02071.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.205-3288G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45060630 | ||||||
| chr7:45060839
|
T | C | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.205-3079T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45060839 | ||||||
| chr7:45060897
|
A | G | 5 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0147others(2): Show | 5 | HG01109.hp1 HG02055.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-3021A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45060897 | ||||||
| chr7:45060987
|
C | T | 205 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0020others(202): Show | 206 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.205-2931C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45060987 | ||||||
| chr7:45061438
|
C | T | 2 | a0001c0001t0001g0209a0001c0001t0001g0288 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.205-2480C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061438 | ||||||
| chr7:45061445
|
T | G | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-2473T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061445 | ||||||
| chr7:45061447
|
T | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-2471T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061447 | ||||||
| chr7:45061456
|
C | CT | 9 | a0001c0002t0002g0305a0001c0002t0002g0306a0001c0002t0002g0307others(6): Show | 9 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.205-2443dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45061456 | |||||
| chr7:45061456
|
CT | C | 50 | a0001c0001t0001g0117a0001c0001t0001g0202a0001c0008t0001g0007others(47): Show | 50 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.205-2443delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45061456 | |||||
| chr7:45061460
|
T | C | 24 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(21): Show | 24 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.205-2458T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061460 | ||||||
| chr7:45061620
|
C | T | 1 | a0001c0001t0001g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.205-2298C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061620 | ||||||
| chr7:45061964
|
T | G | 1 | a0001c0002t0002g0129 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.205-1954T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061964 | ||||||
| chr7:45061982
|
C | A | 1 | a0001c0001t0001g0020 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-1936C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061982 | ||||||
| chr7:45061990
|
T | C | 7 | a0001c0006t0001g0059a0001c0006t0001g0060a0001c0006t0001g0061others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-1928T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45061990 | ||||||
| chr7:45062046
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-1872A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062046 | ||||||
| chr7:45062052
|
T | C | 12 | a0001c0002t0002g0012a0001c0002t0002g0062a0001c0002t0002g0063others(9): Show | 12 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-1866T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062052 | ||||||
| chr7:45062086
|
T | G | 1 | a0001c0001t0001g0265 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.205-1832T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062086 | ||||||
| chr7:45062160
|
G | T | 1 | a0001c0002t0002g0026 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.205-1758G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062160 | ||||||
| chr7:45062177
|
C | T | 79 | a0001c0001t0001g0155a0001c0002t0001g0013a0001c0002t0001g0014others(76): Show | 80 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.205-1741C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062177 | ||||||
| chr7:45062188
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-1730C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062188 | ||||||
| chr7:45062249
|
G | T | 1 | a0002c0003t0002g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.205-1669G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062249 | ||||||
| chr7:45062262
|
C | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-1656C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062262 | ||||||
| chr7:45062289
|
C | T | 1 | a0001c0002t0002g0158 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.205-1629C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062289 | ||||||
| chr7:45062459
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.205-1459C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062459 | ||||||
| chr7:45062677
|
T | G | 1 | a0002c0003t0002g0081 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.205-1241T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062677 | ||||||
| chr7:45062692
|
G | A | 1 | a0001c0006t0007g0162 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-1226G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062692 | ||||||
| chr7:45062719
|
A | C | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.205-1199A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062719 | ||||||
| chr7:45062826
|
C | CA | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.205-1076dupA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45062826 | |||||
| chr7:45062826
|
C | CAA | 11 | a0001c0001t0001g0106a0001c0001t0001g0117a0001c0001t0001g0205others(8): Show | 11 | HG02055.hp1 HG02145.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-1077_205-1076d others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45062826 | |||||
| chr7:45062826
|
CA | C | 76 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(73): Show | 77 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.205-1076delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45062826 | |||||
| chr7:45062880
|
G | A | 4 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0290others(1): Show | 4 | HG02027.hp2 NA18989.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-1038G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45062880 | ||||||
| chr7:45063077
|
C | CT | 46 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(43): Show | 46 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.205-829dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45063077 | |||||
| chr7:45063077
|
CT | C | 42 | a0001c0002t0001g0097a0002c0003t0002g0029a0002c0003t0002g0030others(39): Show | 42 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.205-829delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 45063077 | |||||
| chr7:45063172
|
A | C | 2 | a0001c0006t0001g0061a0001c0006t0001g0161 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.205-746A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063172 | ||||||
| chr7:45063182
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.205-736C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063182 | ||||||
| chr7:45063230
|
G | A | 4 | a0001c0006t0001g0060a0001c0006t0001g0061a0001c0006t0001g0161others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-688G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063230 | ||||||
| chr7:45063548
|
A | G | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.205-370A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063548 | ||||||
| chr7:45063688
|
T | G | 10 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(7): Show | 11 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-230T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063688 | ||||||
| chr7:45063785
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.205-133G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063785 | ||||||
| chr7:45063882
|
A | G | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.205-36A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 2/9 | chr7 | 45063882 | ||||||
| chr7:45064172
|
C | T | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.288+171C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 3/9 | chr7 | 45064172 | ||||||
| chr7:45064353
|
T | C | 1 | a0002c0005t0002g0039 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.289-110T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 3/9 | chr7 | 45064353 | ||||||
| chr7:45064773
|
C | T | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.472+127C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45064773 | ||||||
| chr7:45065024
|
T | C | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.472+378T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065024 | ||||||
| chr7:45065074
|
C | T | 1 | a0002c0003t0002g0298 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.472+428C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065074 | ||||||
| chr7:45065114
|
CTG | C | 7 | a0002c0003t0002g0040a0002c0003t0002g0053a0002c0003t0002g0058others(4): Show | 7 | HG00438.hp2 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.472+474_472+475del others(2): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 45065114 | |||||
| chr7:45065151
|
TAGAATTG others(3): Show |
T | 70 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(67): Show | 70 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.472+531_472+540del others(10): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 45065151 | |||||
| chr7:45065151
|
TAGAATTG others(13): Show |
T | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.472+521_472+540del others(20): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 45065151 | |||||
| chr7:45065329
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.472+683G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065329 | ||||||
| chr7:45065350
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.472+704C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065350 | ||||||
| chr7:45065518
|
T | G | 120 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(117): Show | 121 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.472+872T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065518 | ||||||
| chr7:45065534
|
A | G | 33 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(30): Show | 33 | HG00558.hp2 HG00673.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.472+888A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065534 | ||||||
| chr7:45065547
|
A | G | 12 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.472+901A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065547 | ||||||
| chr7:45065611
|
C | T | 51 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(48): Show | 51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.472+965C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065611 | ||||||
| chr7:45065684
|
G | A | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(10): Show | 13 | HG00639.hp1 HG01109.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.472+1038G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065684 | ||||||
| chr7:45065757
|
G | A | 2 | a0001c0006t0001g0061a0001c0006t0001g0161 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.472+1111G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065757 | ||||||
| chr7:45065816
|
A | G | 1 | a0001c0002t0002g0126 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.472+1170A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065816 | ||||||
| chr7:45065860
|
A | G | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.472+1214A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065860 | ||||||
| chr7:45065968
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0301 | 2 | HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.472+1322G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45065968 | ||||||
| chr7:45066064
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.472+1418A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45066064 | ||||||
| chr7:45066258
|
G | T | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.472+1612G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45066258 | ||||||
| chr7:45066319
|
A | C | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.472+1673A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45066319 | ||||||
| chr7:45066649
|
G | C | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.473-1794G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45066649 | ||||||
| chr7:45066732
|
T | C | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.473-1711T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45066732 | ||||||
| chr7:45066758
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.473-1685G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45066758 | ||||||
| chr7:45066901
|
A | AT | 9 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0154others(6): Show | 9 | HG00639.hp1 HG01256.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.473-1525dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 45066901 | |||||
| chr7:45066901
|
AT | A | 77 | a0001c0001t0001g0183a0001c0002t0001g0013a0001c0002t0001g0014others(74): Show | 78 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.473-1525delT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 45066901 | |||||
| chr7:45066926
|
A | G | 1 | a0001c0002t0002g0123 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.473-1517A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45066926 | ||||||
| chr7:45067116
|
G | T | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.473-1327G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067116 | ||||||
| chr7:45067143
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.473-1300G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067143 | ||||||
| chr7:45067197
|
C | CT | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.473-1233dupT | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 45067197 | |||||
| chr7:45067278
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.473-1165C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067278 | ||||||
| chr7:45067307
|
T | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-1136T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067307 | ||||||
| chr7:45067620
|
G | A | 177 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(174): Show | 178 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.473-823G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067620 | ||||||
| chr7:45067771
|
C | T | 1 | a0001c0002t0002g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.473-672C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067771 | ||||||
| chr7:45067922
|
C | A | 1 | a0001c0006t0001g0060 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.473-521C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067922 | ||||||
| chr7:45067984
|
A | G | 176 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(173): Show | 177 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.473-459A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45067984 | ||||||
| chr7:45068010
|
C | T | 54 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(51): Show | 54 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(51): Show |
intron_variant | MODIFIER | c.473-433C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068010 | ||||||
| chr7:45068218
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.473-225A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068218 | ||||||
| chr7:45068248
|
G | C | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.473-195G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068248 | ||||||
| chr7:45068257
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.473-186G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068257 | ||||||
| chr7:45068269
|
A | G | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.473-174A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068269 | ||||||
| chr7:45068284
|
G | C | 3 | a0001c0001t0001g0020a0001c0006t0003g0076a0001c0006t0003g0077 | 3 | HG02647.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.473-159G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068284 | ||||||
| chr7:45068326
|
G | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0214a0001c0001t0001g0276 | 3 | HG01934.hp1 HG02148.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.473-117G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068326 | ||||||
| chr7:45068348
|
C | G | 2 | a0001c0001t0001g0295a0001c0001t0001g0304 | 2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.473-95C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068348 | ||||||
| chr7:45068366
|
C | T | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.473-77C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068366 | ||||||
| chr7:45068390
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.473-53C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 4/9 | chr7 | 45068390 | ||||||
| chr7:45068964
|
A | G | 1 | a0002c0009t0002g0082 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.609+385A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45068964 | ||||||
| chr7:45069118
|
G | A | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.609+539G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069118 | ||||||
| chr7:45069155
|
A | G | 1 | a0001c0002t0002g0160 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.609+576A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069155 | ||||||
| chr7:45069195
|
A | G | 3 | a0001c0001t0001g0020a0001c0006t0003g0076a0001c0006t0003g0077 | 3 | HG02647.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.609+616A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069195 | ||||||
| chr7:45069279
|
C | T | 125 | a0001c0001t0001g0020a0001c0001t0001g0069a0001c0002t0001g0013others(122): Show | 126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.610-547C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069279 | ||||||
| chr7:45069373
|
A | G | 71 | a0001c0001t0001g0069a0001c0002t0001g0013a0001c0002t0001g0014others(68): Show | 72 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.610-453A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069373 | ||||||
| chr7:45069442
|
T | C | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.610-384T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069442 | ||||||
| chr7:45069536
|
G | A | 1 | a0001c0002t0002g0138 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.610-290G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069536 | ||||||
| chr7:45069546
|
C | T | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.610-280C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | chr7 | 45069546 | ||||||
| chr7:45069594
|
T | TG | 3 | a0001c0001t0001g0020a0001c0006t0003g0076a0001c0006t0003g0077 | 3 | HG02647.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.610-231dupG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 45069594 | |||||
| chr7:45069985
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+24C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45069985 | ||||||
| chr7:45070059
|
G | C | 5 | a0002c0003t0002g0032a0002c0003t0002g0046a0002c0003t0002g0047others(2): Show | 5 | HG01099.hp2 HG01167.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+98G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070059 | ||||||
| chr7:45070285
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.745+324C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070285 | ||||||
| chr7:45070386
|
C | T | 4 | a0001c0002t0002g0001a0001c0002t0002g0025a0001c0002t0002g0026others(1): Show | 5 | HG02717.hp2 HG02818.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.745+425C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070386 | ||||||
| chr7:45070391
|
C | T | 1 | a0001c0006t0001g0059 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.745+430C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070391 | ||||||
| chr7:45070626
|
T | G | 1 | a0001c0001t0001g0276 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.745+665T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070626 | ||||||
| chr7:45070691
|
G | A | 7 | a0002c0003t0002g0029a0002c0003t0002g0033a0002c0003t0002g0038others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.745+730G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070691 | ||||||
| chr7:45070724
|
G | A | 5 | a0001c0002t0002g0120a0001c0002t0002g0121a0001c0002t0002g0123others(2): Show | 5 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.745+763G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070724 | ||||||
| chr7:45070829
|
G | A | 4 | a0001c0001t0001g0020a0001c0006t0001g0059a0001c0006t0003g0076others(1): Show | 4 | HG01884.hp2 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.745+868G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070829 | ||||||
| chr7:45070926
|
T | C | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.745+965T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070926 | ||||||
| chr7:45070928
|
G | A | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.745+967G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45070928 | ||||||
| chr7:45071050
|
C | G | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.745+1089C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071050 | ||||||
| chr7:45071055
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.745+1094G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071055 | ||||||
| chr7:45071352
|
C | A | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.746-1374C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071352 | ||||||
| chr7:45071442
|
GA | G | 6 | a0001c0001t0001g0113a0001c0001t0001g0153a0001c0001t0001g0177others(3): Show | 6 | HG01884.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.746-1283delA | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071442 | ||||||
| chr7:45071474
|
A | T | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.746-1252A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071474 | ||||||
| chr7:45071561
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.746-1165A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071561 | ||||||
| chr7:45071593
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0152 | 2 | HG03710.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.746-1133C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071593 | ||||||
| chr7:45071594
|
G | A | 13 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(10): Show | 13 | HG01256.hp1 HG02080.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.746-1132G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071594 | ||||||
| chr7:45071613
|
T | G | 1 | a0001c0001t0001g0282 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.746-1113T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071613 | ||||||
| chr7:45071704
|
AG | A | 7 | a0002c0003t0002g0040a0002c0003t0002g0053a0002c0003t0002g0058others(4): Show | 7 | HG00438.hp2 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.746-1020delG | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 45071704 | |||||
| chr7:45071883
|
A | T | 119 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(116): Show | 120 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.746-843A>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071883 | ||||||
| chr7:45071897
|
C | T | 46 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(43): Show | 46 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.746-829C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071897 | ||||||
| chr7:45071943
|
G | A | 1 | a0001c0002t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.746-783G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45071943 | ||||||
| chr7:45072099
|
ACTGT | A | 15 | a0001c0002t0002g0001a0001c0002t0002g0024a0001c0002t0002g0025others(12): Show | 16 | HG01069.hp1 HG01071.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.746-622_746-619del others(4): Show |
CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 45072099 | |||||
| chr7:45072279
|
G | A | 3 | a0001c0002t0002g0101a0001c0002t0002g0102a0001c0002t0002g0140 | 3 | HG00738.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.746-447G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072279 | ||||||
| chr7:45072322
|
G | A | 3 | a0001c0002t0002g0122a0001c0002t0002g0157a0001c0002t0002g0159 | 3 | HG01069.hp1 HG01071.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.746-404G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072322 | ||||||
| chr7:45072344
|
A | C | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.746-382A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072344 | ||||||
| chr7:45072471
|
T | G | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.746-255T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072471 | ||||||
| chr7:45072517
|
A | C | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-209A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072517 | ||||||
| chr7:45072521
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.746-205G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072521 | ||||||
| chr7:45072524
|
G | A | 2 | a0001c0001t0001g0295a0001c0001t0001g0304 | 2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.746-202G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072524 | ||||||
| chr7:45072677
|
C | T | 2 | a0001c0006t0003g0076a0001c0006t0003g0077 | 2 | HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.746-49C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 6/9 | chr7 | 45072677 | ||||||
| chr7:45072821
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.803+38G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45072821 | ||||||
| chr7:45072872
|
C | A | 33 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.803+89C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45072872 | ||||||
| chr7:45073046
|
G | C | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.803+263G>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073046 | ||||||
| chr7:45073083
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.803+300G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073083 | ||||||
| chr7:45073113
|
A | G | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.803+330A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073113 | ||||||
| chr7:45073174
|
T | C | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.804-286T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073174 | ||||||
| chr7:45073192
|
A | C | 1 | a0001c0002t0002g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.804-268A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073192 | ||||||
| chr7:45073303
|
T | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(310): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.804-157T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073303 | ||||||
| chr7:45073412
|
A | C | 1 | a0001c0001t0001g0154 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-48A>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073412 | ||||||
| chr7:45073451
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804-9C>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 7/9 | chr7 | 45073451 | ||||||
| chr7:45073625
|
G | T | 3 | a0001c0006t0001g0059a0001c0006t0003g0076a0001c0006t0003g0077 | 3 | HG01884.hp2 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.915+54G>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 8/9 | chr7 | 45073625 | ||||||
| chr7:45073690
|
C | T | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.915+119C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 8/9 | chr7 | 45073690 | ||||||
| chr7:45073744
|
C | T | 11 | a0001c0002t0002g0012a0001c0002t0002g0063a0001c0002t0002g0305others(8): Show | 11 | HG00741.hp2 HG01433.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.915+173C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 8/9 | chr7 | 45073744 | ||||||
| chr7:45073974
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.916-296C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 8/9 | chr7 | 45073974 | ||||||
| chr7:45074490
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1054+82C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45074490 | ||||||
| chr7:45074625
|
A | G | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1054+217A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45074625 | ||||||
| chr7:45074627
|
C | T | 41 | a0002c0003t0002g0029a0002c0003t0002g0030a0002c0003t0002g0031others(38): Show | 41 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1054+219C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45074627 | ||||||
| chr7:45074742
|
A | G | 2 | a0001c0001t0001g0148a0001c0001t0001g0149 | 2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1054+334A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45074742 | ||||||
| chr7:45074813
|
G | A | 1 | a0002c0003t0002g0044 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1054+405G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45074813 | ||||||
| chr7:45075156
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1055-621T>C | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075156 | ||||||
| chr7:45075202
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1055-575G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075202 | ||||||
| chr7:45075206
|
C | T | 2 | a0002c0005t0002g0041a0002c0005t0002g0043 | 2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.1055-571C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075206 | ||||||
| chr7:45075313
|
A | G | 3 | a0001c0002t0002g0101a0001c0002t0002g0102a0001c0002t0002g0140 | 3 | HG00738.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1055-464A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075313 | ||||||
| chr7:45075330
|
G | A | 1 | a0001c0002t0001g0194 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1055-447G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075330 | ||||||
| chr7:45075363
|
G | A | 78 | a0001c0002t0001g0013a0001c0002t0001g0014a0001c0002t0001g0015others(75): Show | 79 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.1055-414G>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075363 | ||||||
| chr7:45075381
|
C | T | 5 | a0001c0008t0001g0007a0001c0008t0001g0008a0001c0008t0001g0009others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1055-396C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075381 | ||||||
| chr7:45075444
|
T | G | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.1055-333T>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075444 | ||||||
| chr7:45075445
|
C | A | 178 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 179 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.1055-332C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075445 | ||||||
| chr7:45075557
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1055-220C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075557 | ||||||
| chr7:45075638
|
A | G | 2 | a0001c0006t0001g0061a0001c0006t0001g0161 | 2 | HG02145.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1055-139A>G | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075638 | ||||||
| chr7:45075680
|
C | A | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1055-97C>A | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075680 | ||||||
| chr7:45075690
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1055-87C>T | CCM2 | ENSG00000136280.17 | transcript | ENST00000258781.11 | protein_coding | 9/9 | chr7 | 45075690 |